Robert W. Taylor

Robert W. Taylor, D. Turnbull, M. Hermanová, 2007, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Quantitative 3D Mapping of the Human Skeletal Muscle Mitochondrial Network

Robert W. Taylor, D. Turnbull, R. Ogden, 2019, Cell reports.

Congenital myasthenic syndrome with mild intellectual disability caused by a recurrent SLC25A1 variant

Robert W. Taylor, H. Lochmüller, R. Horvath, 2019, European Journal of Human Genetics.

Differences in RNA processing underlie the tissue specific phenotype of ISCU myopathy.

Robert W. Taylor, L. Bindoff, Z. Chrzanowska-Lightowlers, 2010, Biochimica et biophysica acta.

Assessment of mitochondrial respiratory chain enzymes in cells and tissues.

Robert W. Taylor, D. Turnbull, Ann E. Frazier, 2020, Methods in cell biology.

A leaky splicing mutation in NFU1 is associated with a particular biochemical phenotype. Consequences for the diagnosis.

Robert W. Taylor, J. A. Arranz, F. Tort, 2016, Mitochondrion (Amsterdam. Print).

Near-identical segregation of mtDNA heteroplasmy in blood, muscle, urinary epithelium, and hair follicles in twins with optic atrophy, ptosis, and intractable epilepsy.

Robert W. Taylor, P. Chinnery, P. Yu-Wai-Man, 2013, JAMA neurology.

Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene.

Robert W. Taylor, D. Turnbull, M. Zeviani, 2006, Brain : a journal of neurology.

Mutant POLG2 disrupts DNA polymerase gamma subunits and causes progressive external ophthalmoplegia.

Robert W. Taylor, D. Turnbull, P. Chinnery, 2006, American journal of human genetics.

The genetic basis of isolated mitochondrial complex II deficiency

Robert W. Taylor, C. Alston, R. Mcfarland, 2020, Molecular genetics and metabolism.

The clinical spectrum of the m.10191T>C mutation in complex I‐deficient Leigh syndrome

Robert W. Taylor, E. Crushell, P. Morrison, 2012, Developmental medicine and child neurology.

Respiratory chain complex I deficiency caused by mitochondrial DNA mutations

Robert W. Taylor, D. Turnbull, A. Compton, 2011, European Journal of Human Genetics.

Recurrent De Novo NAHR Reciprocal Duplications in the ATAD3 Gene Cluster Cause a Neurogenetic Trait with Perturbed Cholesterol and Mitochondrial Metabolism

Robert W. Taylor, J. Lupski, S. Ellard, 2020, American journal of human genetics.

Chromosomal polymorphisms involving telomere fusion, centromeric inactivation and centromere shift in the ant Myrmecia (pilosula) n=1

Robert W. Taylor, H. Imai, 1989, Chromosoma.

Resveratrol attenuates oxidative stress in mitochondrial Complex I deficiency: Involvement of SIRT3.

Robert W. Taylor, A. Slama, A. Lèbre, 2016, Free radical biology & medicine.

muscular dystrophy The role of free radicals in the pathophysiology of

Robert W. Taylor, F. Muntoni, Paul L Huang, 2015 .

Complex I assembly function and fatty acid oxidation enzyme activity of ACAD9 both contribute to disease severity in ACAD9 deficiency.

Robert W. Taylor, A. Munnich, H. Prokisch, 2015, Human molecular genetics.

Novel MTND1 mutations cause isolated exercise intolerance, complex I deficiency and increased assembly factor expression

Laura C. Greaves, Robert W. Taylor, D. Turnbull, 2015, Clinical science.

Quantitative 3D Mapping of the Human Skeletal Muscle Mitochondrial Network

Robert W. Taylor, D. Turnbull, R. Ogden, 2019, Cell reports.

Mutation of OPA1 causes dominant optic atrophy with external ophthalmoplegia, ataxia, deafness and multiple mitochondrial DNA deletions: a novel disorder of mtDNA maintenance.

Robert W. Taylor, D. Turnbull, P. Chinnery, 2008, Brain : a journal of neurology.

Machine learning algorithms reveal the secrets of mitochondrial dynamics

Robert W. Taylor, Jack J Collier, 2021, EMBO molecular medicine.

OPA1 mutations induce mtDNA proliferation in leukocytes of patients with dominant optic atrophy

Robert W. Taylor, M. Larsen, P. Chinnery, 2012, Neurology.

Sensory ataxic neuropathy dysarthria and ophthalmoparesis (SANDO) in a sibling pair with a homozygous p.A467T POLG mutation

Robert W. Taylor, Michael K. Hutchinson, R. Lonergan, 2010, Muscle & nerve.

The natural history of infantile mitochondrial DNA depletion syndrome due to RRM2B deficiency

Robert W. Taylor, A. Rötig, N. Hauser, 2019, Genetics in Medicine.

RRM2B-Related Mitochondrial Disease

Robert W. Taylor, D. Turnbull, R. Pitceathly, 2013 .

Genomic dispersion of 28S rDNA during karyotypic evolution in the ant genusMyrmecia (Formicidae)

Robert W. Taylor, H. Hirai, Masatoshi Yamamoto, 1996, Chromosoma.

Notes on the Remarkable Karyology of the Primitive Ant Nothomyrmecia Macrops, and of the Related Genus Myrmecia (Hymenoptera: Formicidae)

Robert W. Taylor, K. Ogata, M. Kubota, 1990 .

Clinical/scientific Notes Supplemental Data at Neurology.org the M.13051g.a Mitochondrial Dna Mutation Results in Variable Neurology and Activated Mitophagy We Also Have Additional Data Supporting the Same Effect in Fibroblasts from Other Classical Mitochondrial

Robert W. Taylor, S. Hickman, P. Yu-Wai-Man, 2022 .

MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load

Robert W. Taylor, N. Lax, D. Turnbull, 2018, EBioMedicine.

Developmental and Pathological Changes in the Human Cardiac Muscle Mitochondrial DNA Organization, Replication and Copy Number

Robert W. Taylor, D. Turnbull, H. Jacobs, 2010, PloS one.

Copy-choice recombination during mitochondrial L-strand synthesis causes DNA deletions

Robert W. Taylor, E. Larsson, C. Gustafsson, 2019, Nature Communications.

Inosine Triphosphate Pyrophosphohydrolase (ITPA) polymorphic sequence variants in adult hematological malignancy patients and possible association with mitochondrial DNA defects

Robert W. Taylor, M. Zamzami, T. Florin, 2013, Journal of Hematology & Oncology.

Epilepsy due to mutations in the mitochondrial polymerase gamma (POLG) gene: A clinical and molecular genetic review

Robert W. Taylor, R. Mcfarland, Y. Ng, 2016, Epilepsia.

Clinical, morphological, biochemical, imaging and outcome parameters in 21 individuals with mitochondrial maintenance defect related to FBXL4 mutations

Robert W. Taylor, H. Prokisch, N. Hauser, 2015, Journal of Inherited Metabolic Disease.

Lewy body pathology is more prevalent in older individuals with mitochondrial disease than controls

Robert W. Taylor, D. Erskine, N. Lax, 2019, Acta Neuropathologica.

071 Concentric hypertrophic remodelling and subendocardial dysfunction in mitochondrial DNA point mutation carriers

Robert W. Taylor, D. Turnbull, A. Blamire, 2012, Heart.

Isolated distal myopathy of the upper limbs associated with mitochondrial DNA depletion and polymerase gamma mutations.

Robert W. Taylor, F. Pichiorri, G. d’Amati, 2010, Archives of neurology.

POLG1 mutations manifesting as autosomal recessive axonal Charcot-Marie-Tooth disease.

Robert W. Taylor, P. Chinnery, R. de Silva, 2008, Archives of neurology.

POLG 1 Mutations Manifesting as Autosomal Recessive Axonal Charcot-Marie-Tooth Disease

Robert W. Taylor, P. Chinnery, H. Houlden, 2007 .

Scientific and Ethical Issues in Mitochondrial Donation

Robert W. Taylor, D. Turnbull, G. Gorman, 2018, The New bioethics : a multidisciplinary journal of biotechnology and the body.

Further delineation of the phenotypic spectrum of ISCA2 defect: A report of ten new cases.

Robert W. Taylor, N. Kaya, B. Plecko, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Adult-onset cerebellar ataxia due to mutations in CABC1/ADCK3

Robert W. Taylor, P. Chinnery, Hanns Lochmüller, 2011, Journal of Neurology, Neurosurgery & Psychiatry.

Mitochondrial DNA mutations in human disease

Laura C. Greaves, Robert W. Taylor, Robert W. Taylor, 2006, IUBMB life.

Low-dose inhaled nitric oxide in patients with acute lung injury: a randomized controlled trial.

Robert W. Taylor, J. Zimmerman, G. Criner, 2004, JAMA.

CARING FOR THE CRITICALLY ILL PATIENT Low-Dose Inhaled Nitric Oxide in Patients With Acute Lung Injury A Randomized Controlled Trial

Robert W. Taylor, J. Zimmerman, G. Criner, 2004 .

Mitochondrial DNA mutations and human disease.

Robert W. Taylor, D. Turnbull, H. Tuppen, 2010, Biochimica et biophysica acta.

Recent Advances in Mitochondrial Disease.

Robert W. Taylor, D. Turnbull, C. Alston, 2017, Annual review of genomics and human genetics.

Mitochondrial Donation - Which Women Could Benefit?

Robert W. Taylor, D. Turnbull, I. Wilson, 2019, The New England journal of medicine.

Pathogenic variants in MT‐ATP6: A United Kingdom–based mitochondrial disease cohort study

Robert W. Taylor, D. Turnbull, M. Martikainen, 2019, Annals of neurology.

De novo mtDNA point mutations are common and have a low recurrence risk

Robert W. Taylor, H. Smeets, C. D. de Die-Smulders, 2016, Journal of Medical Genetics.

Mitochondrial DNA sequence characteristics modulate the size of the genetic bottleneck

Robert W. Taylor, H. Smeets, M. Zeviani, 2016, Human molecular genetics.

Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factors

Robert W. Taylor, D. Turnbull, H. Cordell, 2018, Annals of clinical and translational neurology.

A national perspective on prenatal testing for mitochondrial disease

Robert W. Taylor, D. Turnbull, J. Poulton, 2014, European Journal of Human Genetics.

Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies.

Beril Talim, Patrick F Chinnery, Robert W Taylor, 2014, JAMA.

Selective inhibition of mutant human mitochondrial DNA replication in vitro by peptide nucleic acids

Robert W. Taylor, D. Turnbull, P. Chinnery, 1997, Nature Genetics.

The Pathology and Treatment of Venereal Diseases

Robert W. Taylor, 1871, Edinburgh Medical Journal.

Mitochondrial DNA defects and selective extraocular muscle involvement in CPEO.

Laura C. Greaves, Robert W. Taylor, D. Turnbull, 2010, Investigative ophthalmology & visual science.

The Ants of Polynesia (Hymenoptera: Formicidae).

Robert W. Taylor, E. Wilson, 2013 .

Biochemical assays of respiratory chain complex activity.

Robert W. Taylor, D. Turnbull, D. Thorburn, 2007, Methods in cell biology.

Rhabdomyolysis andacuteencephalopathy inlate onsetmediumchain acyl-CoA dehydrogenase deficiency

Robert W. Taylor, F. Gabreëls, B. Garavaglia, 2011 .

Endocrine disorders in mitochondrial disease☆

Robert W. Taylor, M. Walker, D. Turnbull, 2013, Molecular and Cellular Endocrinology.

An international classification of inherited metabolic disorders (ICIMD)

Robert W. Taylor, A. Ballabio, E. Bertini, 2020, Journal of inherited metabolic disease.

Thiamine deficiency in childhood with attention to genetic causes: Survival and outcome predictors

Robert W. Taylor, R. Artuch, N. Darín, 2017, Annals of neurology.

Clonal Expansion of Early to Mid-Life Mitochondrial DNA Point Mutations Drives Mitochondrial Dysfunction during Human Ageing

Laura C. Greaves, Robert W. Taylor, D. Turnbull, 2014, PLoS genetics.

Adults with RRM2B-related mitochondrial disease have distinct clinical and molecular characteristics

Robert W. Taylor, D. Turnbull, U. Pohl, 2012, Brain : a journal of neurology.

Retrospective natural history of thymidine kinase 2 deficiency

Robert W. Taylor, S. Dimauro, P. Chinnery, 2018, Journal of Medical Genetics.

Mutations in ELAC2 associated with hypertrophic cardiomyopathy impair mitochondrial tRNA 3′‐end processing

Robert W. Taylor, E. Haan, Pedro Rebelo-Guiomar, 2018, bioRxiv.

A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype

Robert W. Taylor, H. Prokisch, P. Clayton, 2016, Journal of Medical Genetics.

Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies.

Arnold Munnich, Aleksandra Filipovska, Patrick F Chinnery, 2016, American journal of human genetics.

TRMT5 Mutations Cause a Defect in Post-transcriptional Modification of Mitochondrial tRNA Associated with Multiple Respiratory-Chain Deficiencies

Robert W. Taylor, Aaron R D'Souza, M. Minczuk, 2015, American journal of human genetics.

Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutations

Robert W. Taylor, M. Santibanez-Koref, P. Chinnery, 2014, Genetics in Medicine.

Defective i6A37 Modification of Mitochondrial and Cytosolic tRNAs Results from Pathogenic Mutations in TRIT1 and Its Substrate tRNA

Robert W. Taylor, M. Santibanez-Koref, P. Chinnery, 2014, PLoS genetics.

Mutations in FBXL4 cause mitochondrial encephalopathy and a disorder of mitochondrial DNA maintenance.

Robert W. Taylor, W. Craigen, P. Bonnen, 2013, American journal of human genetics.

ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathy.

Robert W. Taylor, M. Minczuk, T. Wieland, 2013, American journal of human genetics.

Adult-onset spinocerebellar ataxia syndromes due to MTATP6 mutations

Robert W. Taylor, P. Chinnery, R. Horvath, 2012, Journal of Neurology, Neurosurgery & Psychiatry.

Detection and quantification of mitochondrial DNA deletions in individual cells by real-time PCR.

Robert W. Taylor, D. Turnbull, P. Chinnery, 2002, Nucleic acids research.

Nuclear genetic disorders of mitochondrial DNA gene expression

Robert W. Taylor, R. Mcfarland, T. Nicholls, 2020 .

Late-onset respiratory failure due to TK2 mutations causing multiple mtDNA deletions

Robert W. Taylor, D. Turnbull, K. J. Krishnan, 2013, Neurology.

MPV17 Loss Causes Deoxynucleotide Insufficiency and Slow DNA Replication in Mitochondria

Robert W. Taylor, G. Elgar, D. Thorburn, 2016, PLoS genetics.

Mutations causing mitochondrial disease: What is new and what challenges remain?

Robert W. Taylor, D. Turnbull, R. Lightowlers, 2015, Science.

Clinical and molecular characteristics of mitochondrial DNA depletion syndrome associated with neonatal cholestasis and liver failure.

Robert W. Taylor, E. Faqeih, A. El-Hattab, 2014, The Journal of pediatrics.

POLG mutations cause decreased mitochondrial DNA repopulation rates following induced depletion in human fibroblasts.

Robert W. Taylor, P. Chinnery, P. Yu-Wai-Man, 2011, Biochimica et biophysica acta.

Molecular genetic investigations identify new clinical phenotypes associated with BCS1L-related mitochondrial disease

Robert W. Taylor, P. Chinnery, R. Horvath, 2019, Human molecular genetics.

A mitochondrial cytochrome b mutation causing severe respiratory chain enzyme deficiency in humans and yeast

Robert W. Taylor, D. Turnbull, L. Nijtmans, 2005, The FEBS journal.

Locating the stem cell niche and tracing hepatocyte lineages in human liver

Laura C. Greaves, Robert W. Taylor, D. Turnbull, 2009, Hepatology.

Karyotype evolution in Australian ants

Robert W. Taylor, R. Crozier, H. Imai, 1977, Chromosoma.

Phase specific Ag-staining of nucleolar organizer regions (NORs) and kinetochores in the Australian ant Myrmecia croslandi

Robert W. Taylor, Y. Satta, T. Shiroishi, 1992 .

Natural History of Leigh Syndrome: A Study of Disease Burden and Progression

Robert W. Taylor, D. Turnbull, E. Wassmer, 2021, Annals of neurology.

LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population

Robert W. Taylor, H. Prokisch, M. Simpson, 2015, Brain : a journal of neurology.

Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number

Robert W. Taylor, M. Simpson, R. Rodenburg, 2016, American journal of human genetics.

Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number

Robert W. Taylor, M. Simpson, R. Rodenburg, 2016, American journal of human genetics.

Kunji ERS, Taylor RW. Recurrent De Novo Dominant Mutations in SLC2SA4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA

Robert W. Taylor, M. Simpson, R. Rodenburg, 2016 .

Recurrent De Novo Dominant Mutations in SLC 2 SA 4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy

Robert W. Taylor, M. Simpson, R. Rodenburg, 2022 .

FBXL4 deficiency increases mitochondrial removal by autophagy

Robert W. Taylor, I. Atanassov, N. Larsson, 2020, EMBO molecular medicine.

Ultrasensitive deletion detection links mitochondrial DNA replication, disease, and aging

Robert W. Taylor, Christopher A. Lavender, T. Kunkel, 2020, Genome biology.

Clinical implementation of RNA sequencing for Mendelian disease diagnostics

Robert W. Taylor, Vicente A. Yépez, J. Gagneur, 2021, Genome Medicine.

The GABA transaminase, ABAT, is essential for mitochondrial nucleoside metabolism.

Robert W. Taylor, S. Lalani, W. Craigen, 2015, Cell metabolism.

Homozygous deletion in MICU1 presenting with fatigue and lethargy in childhood

Robert W. Taylor, V. Mootha, V. Ramesh, 2016, Neurology: Genetics.

A Novel Pathogenic Variant in MT-CO2 Causes an Isolated Mitochondrial Complex IV Deficiency and Late-Onset Cerebellar Ataxia

Robert W. Taylor, A. Schaefer, P. Sarrigiannis, 2019, Journal of clinical medicine.

Clinical, biochemical, and genetic features associated with VARS2‐related mitochondrial disease

Robert W. Taylor, H. Prokisch, H. Mandel, 2018, Human mutation.

Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease

Robert W. Taylor, D. Turnbull, P. Chinnery, 2015, Annals of neurology.

Age-associated mitochondrial DNA mutations cause metabolic remodeling that contributes to accelerated intestinal tumorigenesis

Laura C. Greaves, Robert W. Taylor, D. Turnbull, 2020, Nature Cancer.

Multipotent Basal Stem Cells, Maintained in Localized Proximal Niches, Support Directed Long-Ranging Epithelial Flows in Human Prostates

Laura C. Greaves, Robert W. Taylor, D. Turnbull, 2017, Cell reports.

Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction

Robert W. Taylor, B. Moore, P. Chinnery, 2016, Brain : a journal of neurology.

Novel internally branched, internal alkenes as major components of the cuticular hydrocarbons of the primitive australian antNothomyrmecia macrops Clark (Hymenoptera: Formicidae)

Robert W. Taylor, M. Lacey, P. Jaisson, 1990, Journal of Chemical Ecology.

Mitochondrial DNA mutations induce mitochondrial biogenesis and increase the tumorigenic potential of Hodgkin and Reed-Sternberg cells.

Robert W. Taylor, J. Elson, R. Wiesner, 2020, Carcinogenesis.

Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy

Robert W. Taylor, Carol J. Saunders, C. Saunders, 2018, Human molecular genetics.

A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency

Robert W. Taylor, M. O'sullivan, C. McMahon, 2015, Human Genetics.

Copy-choice recombination during mitochondrial L-strand synthesis causes DNA deletions

Robert W. Taylor, E. Larsson, C. Gustafsson, 2019, Nature Communications.

Identification and characterization of novel MPC1 gene variants causing mitochondrial pyruvate carrier deficiency

Robert W. Taylor, H. Prokisch, R. Mcfarland, 2021, Journal of inherited metabolic disease.

What causes mitochondrial DNA deletions in human cells?

David C Samuels, Patrick F Chinnery, Robert W Taylor, 2008, Nature Genetics.

Novel compound mutations in the mitochondrial translation elongation factor (TSFM) gene cause severe cardiomyopathy with myocardial fibro-adipose replacement

Robert W. Taylor, P. Bonnen, V. Morea, 2019, Scientific Reports.

OXA1L mutations cause mitochondrial encephalopathy and a combined oxidative phosphorylation defect

Robert W. Taylor, N. Lax, P. Bonnen, 2018, EMBO molecular medicine.

Loss‐of‐function mutations in ISCA2 disrupt 4Fe–4S cluster machinery and cause a fatal leukodystrophy with hyperglycinemia and mtDNA depletion

Robert W. Taylor, P. Bonnen, V. Appadurai, 2018, Human mutation.

Characterising a homozygous two‐exon deletion in UQCRH: comparing human and mouse phenotypes

Robert W. Taylor, H. Fuchs, W. Wurst, 2021, EMBO molecular medicine.

The neurology of mitochondrial DNA disease

Robert W. Taylor, D. Turnbull, R. Mcfarland, 2002, The Lancet Neurology.

Multiple neonatal deaths due to a homoplasmic mitochondrial DNA mutation

Robert W. Taylor, D. Turnbull, R. Lightowlers, 2002, Nature Genetics.

NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency.

Robert W. Taylor, H. Dahl, A. Ohtake, 2004, The Journal of clinical investigation.

Gene therapy for the treatment of mitochondrial DNA disorders

Robert W. Taylor, Robert W. Taylor, 2005, Expert opinion on biological therapy.

PPA2-associated sudden cardiac death: extending the clinical and allelic spectrum in 20 new families.

Robert W. Taylor, D. Fisk, R. Weintraub, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

PPA2-associated sudden cardiac death: extending the clinical and allelic spectrum in 20 new families

Robert W. Taylor, W. Chung, D. Fisk, 2021, Genetics in Medicine.

Subcellular origin of mitochondrial DNA deletions in human skeletal muscle

Robert W. Taylor, C. Cooper, D. Turnbull, 2018, Annals of neurology.

Preliminary Evaluation of Clinician Rated Outcome Measures in Mitochondrial Disease

Robert W. Taylor, B. Galna, D. Turnbull, 2015, Journal of neuromuscular diseases.

Mitochondrial DNA deletions in muscle satellite cells: implications for therapies

Robert W. Taylor, D. Turnbull, Hanns Lochmüller, 2013, Human molecular genetics.

SURF1 deficiency: a multi-centre natural history study

Robert W. Taylor, E. Aasheim, S. Rahman, 2013, Orphanet Journal of Rare Diseases.

Making a difference together: reciprocal interactions in C. elegans and zebrafish asymmetric neural development

Robert W. Taylor, C. Chuang, J. Gamse, 2010, Development.

Recombinant Human Interleukin 1 Receptor Antagonist in the Treatment of Patients With Sepsis Syndrome: Results From a Randomized, Double-blind, Placebo-Controlled Trial

R. F. Johnston, Robert W. Taylor, Steven C. Johnson, 1994 .

Mechanisms of field cancerization in the human stomach: the expansion and spread of mutated gastric stem cells.

Laura C. Greaves, Robert W. Taylor, D. Turnbull, 2008, Gastroenterology.

Short peptides from leucyl-tRNA synthetase rescue disease-causing mitochondrial tRNA point mutations

Robert W. Taylor, A. Fiorillo, V. Morea, 2015, Human molecular genetics.

Leigh syndrome caused by mutations in MTFMT is associated with a better prognosis

Robert W. Taylor, H. Smeets, P. Bonnen, 2019, Annals of clinical and translational neurology.

Multiplication of 28S rDNA and NOR activity in chromosome evolution among ants of the Myrmecia pilosula species complex

Robert W. Taylor, Y. Satta, H. Hirai, 1994, Chromosoma.

A Monographic Revision of the Ant Genus Ponera Latreille (Hymenoptera: Formicidae).

Robert W. Taylor, 2015 .

THE NEW GUINEAN SPECIES OF THE ANT GENUS ORECTOGNATHUS FR. SMITH (HYMENOPTERA: FORMICIDAE)

Robert W. Taylor, B. Lowery, 1972 .

Ants of the genus Lordomyrma Emery (1) Generic synonymy, composition and distribution, with notes on Ancyridris Wheeler and Cyphoidris Weber (Hymenoptera: Formicidae: Myrmicinae)

Robert W. Taylor, 2009 .

The nomenclature and distribution of some Australian and New Caledonian ants of the genus Meranoplus Fr. Smith (Hymenoptera: Formicidae: Myrmicinae).

Robert W. Taylor, 1990 .

The m.3291T>C mt-tRNALeu(UUR) mutation is definitely pathogenic and causes multisystem mitochondrial disease

Robert W. Taylor, D. Turnbull, C. Alston, 2013, Journal of the Neurological Sciences.

HUMAN PREDATION ON THE GOPHER TORTOISE ( GOPHERUS POLYPHEMUS ) IN NORTH-CENTRAL FLORIDA

Robert W. Taylor, 2016 .

A Fossil Ant Colony: New Evidence of Social Antiquity

Robert W. Taylor, E. Wilson, 1964 .

Hymenoptera: Formicoidea, Vespoidea and Sphecoidea.

Robert W. Taylor, D. R. Brown, J. Cardale, 1985 .

ANTS OF THE AUSTRALIAN GENUS MESOSTRUMA BROWN (HYMENOPTERA: FORMICIDAE)

Robert W. Taylor, 1973 .

A monographic revision of the rare tropicopolitan ant genus Probolomyrmex Mayr (Hymenoptera: Formicidae)

Robert W. Taylor, 2009 .

Taxonomy and Parataxonomy of Some Fossil Ants (Hymenoptera-Formicidae)

Robert W. Taylor, 1964 .

Ants from Three Remote Oceanic Islands

Robert W. Taylor, E. Wilson, 1961 .

Foraging ecology of the night-active bull ant Myrmecia pyriformis

Robert W. Taylor, J. Zeil, A. Narendra, 2013, Australian Journal of Zoology.

ON THE REMARKABLE KARYOLOGY OF THE PRIMITIVE ANT NOTHOMYRMECIA MACROPS , AND OF THE RELATED GENUS MYRMECIA ( HYMENOPTERA : FORMICIDAE ) BY HIROTAMI

Robert W. Taylor, Y., K. Ogata, 2011 .

Mutations in TOP3A Cause a Bloom Syndrome-like Disorder

Robert W. Taylor, Y. Okazaki, H. Williams, 2018, American journal of human genetics.

Characterization of mtDNA variation in a cohort of South African paediatric patients with mitochondrial disease

Robert W. Taylor, D. Turnbull, J. Elson, 2012, European Journal of Human Genetics.

Mutations in TOP3A Cause a Bloom Syndrome-like Disorder

Robert W. Taylor, Y. Okazaki, H. Williams, 2018, American journal of human genetics.

A novel, pathogenic dinucleotide deletion in the mitochondrial MT-TY gene causing myasthenia-like features

Robert W. Taylor, H. Lochmüller, G. Falkous, 2020, Neuromuscular Disorders.

Mitochondrial Protein Interaction Mapping Identifies Regulators of Respiratory Chain Function.

Robert W. Taylor, M. Westphall, H. Prokisch, 2016, Molecular cell.

SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN)

Robert W. Taylor, I. Harting, T. Meitinger, 2018, Genetics in Medicine.

Mitochondrial stress response triggered by defects in protein synthesis quality control

Robert W. Taylor, S. Seneca, T. Nyman, 2019, Life Science Alliance.

Prevalence of mitochondrial DNA disease in adults

Robert W. Taylor, D. Turnbull, P. Chinnery, 2008, Annals of neurology.

Mitochondrial OXPHOS Biogenesis: Co-Regulation of Protein Synthesis, Import, and Assembly Pathways

Robert W. Taylor, K. Thompson, M. Oláhová, 2020, International journal of molecular sciences.

Mitochondrial tRNA mutations and disease

Robert W Taylor, Robert W. Taylor, J. Elson, 2010, Wiley interdisciplinary reviews. RNA.

Sideroblastic anemia with myopathy secondary to novel, pathogenic missense variants in the YARS2 gene

Robert W. Taylor, F. Norwood, G. Gorman, 2018, Haematologica.

The genetics of mitochondrial disease: dissecting mitochondrial pathology using multi‐omic pipelines

Robert W. Taylor, H. Prokisch, G. Hudson, 2021, The Journal of pathology.

Uniparental isodisomy of chromosome 2 causing MRPL44-related multisystem mitochondrial disease

Robert W. Taylor, Sachit Shah, H. Houlden, 2021, Molecular Biology Reports.

Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies

Arnold Munnich, Aleksandra Filipovska, Patrick F Chinnery, 2016, American journal of human genetics.

Inherited pathogenic mitochondrial DNA mutations and gastrointestinal stem cell populations

Laura C. Greaves, Robert W. Taylor, D. Turnbull, 2018, The Journal of pathology.

Detection of pathogenic splicing events from RNA-sequencing data using dasper

Robert W. Taylor, F. Muntoni, M. Ryten, 2021, bioRxiv.

The isolated carboxy-terminal domain of human mitochondrial leucyl-tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells

Robert W. Taylor, L. Frontali, M. Zeviani, 2014, EMBO molecular medicine.

The molecular pathology of pathogenic mitochondrial tRNA variants

Robert W. Taylor, R. Mcfarland, Uwe Richter, 2021, FEBS letters.

Pigmentary retinopathy, rod–cone dysfunction and sensorineural deafness associated with a rare mitochondrial tRNALys (m.8340G>A) gene variant

Robert W. Taylor, J. Poulton, S. Downes, 2017, British Journal of Ophthalmology.

Sporadic myopathy and exercise intolerance associated with the mitochondrial 8328G>A tRNALys mutation

Robert W. Taylor, D. Turnbull, R. Petty, 2007, Journal of Neurology.

The clinical, biochemical and genetic features associated with RMND1-related mitochondrial disease

Robert W. Taylor, J. Casey, A. Vanderver, 2016, Journal of Medical Genetics.

Compound heterozygous RMND1 gene variants associated with chronic kidney disease, dilated cardiomyopathy and neurological involvement: a case report

Robert W. Taylor, D. Milford, N. Ragge, 2016, BMC Research Notes.

Dysferlin mutations and mitochondrial dysfunction

Robert W. Taylor, D. Turnbull, R. Barresi, 2016, Neuromuscular Disorders.

Diagnosing pediatric mitochondrial disease: lessons from 2,000 exomes

Robert W. Taylor, Vicente A. Yépez, J. Gagneur, 2021, medRxiv.

Bi-allelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency

Robert W. Taylor, Courtney E. French, A. Pagnamenta, 2018, American Journal of Human Genetics.

Bi-allelic Mutations in Phe-tRNA Synthetase Associated with a Multi-system Pulmonary Disease Support Non-translational Function

Robert W. Taylor, W. Chung, A. Borczuk, 2018, American journal of human genetics.

Novel GFM2 variants associated with early-onset neurological presentations of mitochondrial disease and impaired expression of OXPHOS subunits

Robert W. Taylor, H. Prokisch, M. Simpson, 2017, neurogenetics.

Mutations in MDH2, Encoding a Krebs Cycle Enzyme, Cause Early-Onset Severe Encephalopathy

Robert W. Taylor, J. Gagneur, E. Génin, 2016, American journal of human genetics.

Clinical presentation and proteomic signature of patients with TANGO2 mutations

Robert W. Taylor, F. Tort, L. Waddell, 2019, Journal of inherited metabolic disease.

NAD(P)HX dehydratase (NAXD) deficiency: a novel neurodegenerative disorder exacerbated by febrile illnesses

Robert W. Taylor, H. Hakonarson, Yiran Guo, 2018, Brain : a journal of neurology.

Nuclear factors involved in mitochondrial translation cause a subgroup of combined respiratory chain deficiency

Robert W. Taylor, J. Kemp, P. Chinnery, 2010, Brain : a journal of neurology.

Mitochondrial respiratory chain defects and developmental diaphragmatic dysfunction in the neonatal period

Robert W. Taylor, D. Turnbull, J. Wyllie, 2006, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

LONP1 and mtHSP70 cooperate to promote mitochondrial protein folding

Robert W. Taylor, Michael J. Sweredoski, A. Moradian, 2021, Nature communications.

Epilepsy in adults with mitochondrial disease: A cohort study

Robert W. Taylor, N. Lax, D. Turnbull, 2015, Annals of neurology.

Bmi1 enhances skeletal muscle regeneration through MT1-mediated oxidative stress protection in a mouse model of dystrophinopathy

Laura C. Greaves, Robert W. Taylor, F. Muntoni, 2014, The Journal of experimental medicine.

Opening One's Eyes to Mosaicism in Progressive External Ophthalmoplegia

Robert W. Taylor, D. Turnbull, P. Chinnery, 2017, Neurology: Genetics.

Adult-onset Mendelian PEO Associated with Mitochondrial Disease.

Robert W. Taylor, P. Chinnery, G. Gorman, 2014, Journal of neuromuscular diseases.

Interrogating Mitochondrial Biology and Disease Using CRISPR/Cas9 Gene Editing

Robert W. Taylor, A. Pyle, M. Oláhová, 2021, Genes.

Pathogenic SLC25A26 variants impair SAH transport activity causing mitochondrial disease

Robert W. Taylor, M. Moedas, J. Poulton, 2022, Human molecular genetics.

Expanding the phenotype of de novo SLC25A4-linked mitochondrial disease to include mild myopathy

Robert W. Taylor, X. Ortiz-González, Edmund R. S. Kunji, 2018, Neurology: Genetics.

A p.R369G POLG2 mutation associated with adPEO and multiple mtDNA deletions causes decreased affinity between polymerase γ subunits.

Robert W. Taylor, D. Turnbull, W. Copeland, 2012, Mitochondrion.

Adults with RRM 2 B-related mitochondrial disease have distinct clinical and molecular characteristics

Robert W. Taylor, D. Turnbull, U. Pohl, 2012 .

Mitochondrial DNA abnormalities in ophthalmological disease.

Robert W. Taylor, G. Gorman, Robert W. Taylor, 2011, Saudi journal of ophthalmology : official journal of the Saudi Ophthalmological Society.

A novel ANT1 gene mutation with probable germline mosaicism in autosomal dominant progressive external ophthalmoplegia

Robert W. Taylor, P. Chinnery, G. Hudson, 2005, Neuromuscular Disorders.

A novel Twinkle gene mutation in autosomal dominant progressive external ophthalmoplegia

Robert W. Taylor, D. Turnbull, R. Kiefer, 2003, Neuromuscular Disorders.

GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L.

Leena Peltonen, Vineta Fellman, Anu Suomalainen, 2002, American journal of human genetics.

NEW OBSERVATIONS REGARDING THE RETINOPATHY OF GENETICALLY CONFIRMED KEARNS–SAYRE SYNDROME

Robert W. Taylor, I. Kozák, K. Abu-Amero, 2016, Retinal cases & brief reports.

SANDO syndrome in a cohort of 107 patients with CPEO and mitochondrial DNA deletions

Robert W. Taylor, M. Kornhuber, F. Hanisch, 2014, Journal of Neurology, Neurosurgery & Psychiatry.

Mutation of the linker region of the polymerase gamma-1 (POLG1) gene associated with progressive external ophthalmoplegia and Parkinsonism.

Robert W. Taylor, D. Turnbull, Andrew Gibson, 2007, Archives of neurology.

Camptocormia and shuffling gait due to a novel MT-TV mutation: Diagnostic pitfalls

Robert W. Taylor, W. Kunz, G. Falkous, 2017, Neurology: Genetics.

Mitochondrial and inflammatory changes in sporadic inclusion body myositis

Robert W. Taylor, D. Turnbull, J. Grady, 2015, Neuropathology and applied neurobiology.

Complex mitochondrial DNA rearrangements in individual cells from patients with sporadic inclusion body myositis

Robert W. Taylor, D. Turnbull, M. Picard, 2016, Nucleic acids research.

Disease progression in patients with single, large-scale mitochondrial DNA deletions

Robert W. Taylor, D. Turnbull, R. McNally, 2013, Brain : a journal of neurology.

Developmental Consequences of Defective ATG7-Mediated Autophagy in Humans.

Robert W. Taylor, L. Schöls, M. Koenig, 2021, The New England journal of medicine.

Clonally Expanded Mitochondrial DNA Mutations in Epileptic Individuals With Mutated DNA Polymerase &ggr;

Robert W. Taylor, C. Elger, P. Chinnery, 2008, Journal of neuropathology and experimental neurology.

MPV17 mutation causes neuropathy and leukoencephalopathy with multiple mtDNA deletions in muscle

Robert W. Taylor, I. Bodi, R. Hadden, 2012, Neuromuscular Disorders.

A neurological perspective on mitochondrial disease

Robert W. Taylor, D. Turnbull, R. Mcfarland, 2010, The Lancet Neurology.

Structural modeling of tissue-specific mitochondrial alanyl-tRNA synthetase (AARS2) defects predicts differential effects on aminoacylation

Robert W. Taylor, P. Chinnery, R. Horvath, 2015, Front. Genet..

A comparative analysis approach to determining the pathogenicity of mitochondrial tRNA mutations

Robert W. Taylor, J. Elson, C. Alston, 2011, Human mutation.

A Wars2 Mutant Mouse Model Displays OXPHOS Deficiencies and Activation of Tissue-Specific Stress Response Pathways

Robert W. Taylor, R. Cox, H. Cater, 2018, Cell reports.

The genotypic and phenotypic spectrum of MTO1 deficiency

Robert W. Taylor, C. Ross, W. Wasserman, 2018, Molecular genetics and metabolism.

A Wars 2 Mutant Mouse M odel Displays OXPHOS Deficiencies andActivation of Tissue-Specific Stress Response Pathways Graphical

Robert W. Taylor, R. Cox, H. Cater, 2018 .

Taylor RW. Neuropathologic Characterization of Pontocerebellar Hypoplasia Type 6 Associated With Cardiomyopathy and Hydrops Fetalis and Severe Multisystem Respiratory Chain Deficiency due to Novel RARS2

Robert W. Taylor, N. Lax, Soo-Mi Park, 2015 .

MTO1 Mutations are Associated with Hypertrophic Cardiomyopathy and Lactic Acidosis and Cause Respiratory Chain Deficiency in Humans and Yeast

Robert W. Taylor, T. Strom, M. Zeviani, 2013, Human mutation.

ALLOZYME VARIATION, COLONY STRUCTURE AND GENETIC RELATEDNESS IN THE PRIMITIVE ANT NOTHOMYRMECIA MACROPS CLARK (HYMENOPTERA: FORMICIDAE)

Robert W. Taylor, P. S. Ward, Philip S. Ward*, 1981 .

mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease

Robert W. Taylor, D. Turnbull, R. McNally, 2018, EMBO molecular medicine.

A novel m.7539C>T point mutation in the mt-tRNAAsp gene associated with multisystemic mitochondrial disease

Robert W. Taylor, S. Zierz, P. Joshi, 2015, Neuromuscular Disorders.

Accurate Measurement of Mitochondrial DNA Deletion Level and Copy Number Differences in Human Skeletal Muscle

Robert W. Taylor, D. Turnbull, R. Haller, 2014, PloS one.

Adult Onset Leigh Syndrome in the Intensive Care Setting: A Novel Presentation of a C12orf65 Related Mitochondrial Disease

Robert W. Taylor, P. Chinnery, R. Lightowlers, 2015, Journal of neuromuscular diseases.

Progressive deafness–dystonia due to SERAC1 mutations: A study of 67 cases

Robert W. Taylor, W. Chung, H. Prokisch, 2017, Annals of neurology.

Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management

Robert W. Taylor, J. Bourke, D. Turnbull, 2012, European heart journal.

The genetics and pathology of mitochondrial disease

Robert W Taylor, Robert W. Taylor, N. Lax, 2016, The Journal of pathology.

Cardiomyopathies due to homoplasmic mitochondrial tRNA mutations: morphologic and molecular features.

Robert W. Taylor, C. Autore, V. Petrozza, 2013, Human pathology.

Clinical and biochemical features associated with BCS1L mutation

Robert W. Taylor, N. Kaya, D. Çolak, 2013, Journal of Inherited Metabolic Disease.

Mitochondrial respiratory chain disease in children undergoing cardiac transplantation: a prospective study.

Robert W. Taylor, R. Kirk, A. Hasan, 2012, International journal of cardiology.

Forecasting stroke-like episodes and outcomes in mitochondrial disease

Robert W. Taylor, D. Erskine, N. Lax, 2021, Brain : a journal of neurology.

BLOODY FUNNY WASPS! SPECULATIONS ON THE EVOLUTION OF EUSOCIALITY IN ANTS

Robert W. Taylor, 2007 .

Investigating complex I deficiency in Purkinje cells and synapses in patients with mitochondrial disease

Robert W. Taylor, N. Lax, D. Turnbull, 2015, Neuropathology and applied neurobiology.

Sensory neuronopathy in patients harbouring recessive polymerase γ mutations.

Robert W. Taylor, N. Lax, D. Turnbull, 2012, Brain : a journal of neurology.

Structure-activity relationship of a broad-spectrum insect odorant receptor agonist.

Robert W. Taylor, A. Waterson, L. Zwiebel, 2012, ACS chemical biology.

Allosteric Antagonism of Insect Odorant Receptor Ion Channels

Robert W. Taylor, A. Waterson, L. Zwiebel, 2012, PloS one.

Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiency

Robert W. Taylor, T. Meitinger, S. Seneca, 2015, Front. Genet..

2-Deoxy-D-glucose couples mitochondrial DNA replication with mitochondrial fitness and promotes the selection of wild-type over mutant mitochondrial DNA

Iain G. Johnston, Robert W. Taylor, I. Johnston, 2021, Nature Communications.

Mosaic dysfunction of mitophagy in mitochondrial muscle disease

Robert W. Taylor, T. G. McWilliams, A. Suomalainen, 2022, Cell metabolism.

The presence of highly disruptive 16S rRNA mutations in clinical samples indicates a wider role for mutations of the mitochondrial ribosome in human disease

Laura C. Greaves, Robert W. Taylor, R. Lightowlers, 2015, Mitochondrion.

The presence of highly disruptive 16 S rRNA mutations in clinical samples indicates a wider role for mutations of the mitochondrial ribosome in human disease Running Title : Role of the mitoribosomal large subunit rRNA in human disease

Laura C. Greaves, Robert W. Taylor, R. Lightowlers, 2015 .

Long-term survival of neonatal mitochondrial complex III deficiency associated with a novel BCS1L gene mutation.

Robert W. Taylor, D. Turnbull, R. Horvath, 2010, Molecular genetics and metabolism.

Notes on the Ant Genera Romblonella and Willowsiella, with Comments on Their Affinities, and the First Descriptions of Australian Species (Hymenoptera: Formicidae: Myrmicinae)

Robert W. Taylor, 1990 .

Nucleotide pools dictate the identity and frequency of ribonucleotide incorporation in mitochondrial DNA

Robert W. Taylor, C. Gustafsson, M. Falkenberg, 2017, PLoS genetics.

Loss of myelin-associated glycoprotein in kearns-sayre syndrome.

Robert W. Taylor, S. Dimauro, N. Lax, 2012, Archives of neurology.

Impaired mitochondrial biogenesis is a common feature to myocardial hypertrophy and end-stage ischemic heart failure

Robert W. Taylor, C. Nediani, V. Petrozza, 2016, Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.

Narrow SAR in odorant sensing Orco receptor agonists.

Robert W. Taylor, A. Waterson, L. Zwiebel, 2014, Bioorganic & medicinal chemistry letters.

Molecular cloning and biological characterization of novel antimicrobial peptides, pilosulin 3 and pilosulin 4, from a species of the Australian ant genus Myrmecia.

Robert W. Taylor, H. Inagaki, T. Kubo, 2004, Archives of biochemistry and biophysics.

Ants with Attitude: Australian Jack-jumpers of the Myrmecia pilosula species complex, with descriptions of four new species (Hymenoptera: Formicidae: Myrmeciinae).

Robert W. Taylor, Robert W. Taylor, 2015, Zootaxa.

Experimental bases for the minimum interaction theory. I. Chromosome evolution in ants of the Myrmecia pilosula species complex (Hymenoptera: Formicidae: Myrmeciinae)

Robert W. Taylor, R. Crozier, H. Imai, 1994 .

AUSTRALIAN AND MELANESIAN ANTS OF THE GENUS EURHOPALOTHR1X BROWN AND KEMPF–NOTES AND NEW SPECIES (HYMENOPTERA: FORMICIDAE)

Robert W. Taylor, 1980 .

Nothomyrmecia macrops: A Living-Fossil Ant Rediscovered

Robert W. Taylor, Robert W. Taylor, 1978, Science.

The Orientalist Hans Friedrich Overbeck 1882–1942: His Entomological Work, Prisoner-of-War Experiences and Known Photographic Images

Robert W. Taylor, 2014 .

NOTES ON SOME AUSTRALIAN AND MELANESIAN BASICEROTINE ANTS (HYMENOPTERA: FORMICIDAE)

Robert W. Taylor, 1970 .

Endurance training and detraining in mitochondrial myopathies due to single large-scale mtDNA deletions.

Robert W. Taylor, D. Turnbull, M. Barron, 2006, Brain : a journal of neurology.

Resolving complexity in mitochondrial disease: Towards precision medicine.

Robert W. Taylor, R. Mcfarland, A. Lim, 2019, Molecular genetics and metabolism.

Height as a Clinical Biomarker of Disease Burden in Adult Mitochondrial Disease

Robert W. Taylor, D. Turnbull, A. Schaefer, 2017, The Journal of clinical endocrinology and metabolism.

Pseudo‐obstruction, stroke, and mitochondrial dysfunction: A lethal combination

Robert W. Taylor, D. Turnbull, Y. Yiannakou, 2016, Annals of neurology.

The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation—implications for diagnosis and management

Robert W. Taylor, D. Turnbull, S. Rahman, 2013, Journal of Neurology, Neurosurgery & Psychiatry.

Chronic Progressive External Ophthalmoplegia due to a Rare de novo m.12334G>A MT-TL2 Mitochondrial DNA Variant1.

Robert W. Taylor, F. Brett, J. Craig, 2020, Journal of neuromuscular diseases.

Novel MT-ND Gene Variants Causing Adult-Onset Mitochondrial Disease and Isolated Complex I Deficiency

Robert W. Taylor, A. Schaefer, G. Falkous, 2020, Frontiers in Genetics.

A novel mitochondrial m.4414T>C MT-TM gene variant causing progressive external ophthalmoplegia and myopathy

Robert W. Taylor, H. Smeets, G. Falkous, 2019, Neuromuscular Disorders.

Genotypes from patients indicate no paternal mitochondrial DNA contribution

Robert W. Taylor, D. Turnbull, M. Zeviani, 2003, Annals of neurology.

Australasian ants of the subfamily Heteroponerinae (Hymenoptera: Formicidae): (2) the species-group of Heteroponera relicta (Wheeler),with descriptions of nine new species and observations on morphology, biogeography and phylogeny of the genus.

Robert W. Taylor, 2015, Zootaxa.

Australasian ants of the subfamily heteroponerinae (Hymenoptera: Formicidae): (1) General introduction and review of the heteroponera leae (Wheeler, 1923) species group, with descriptions of two new species

Robert W. Taylor, 2011 .

NOMENCLATURE AND DISTRIBUTION OF SOME AUSTRALIAN AND NEW GUINEAN ANTS OF THE SUBFAMILY FORMICINAE (HYMENOPTERA: FORMICIDAE)

Robert W. Taylor, 1992 .

THE NOMENCLATURE AND DISTRIBUTION OF SOME AUSTRALIAN ANTS OF THE GENUS POLYRHACHIS Fr SMITH (HYMENOPTERA: FORMICIDAE: FORMICINAE)

Robert W. Taylor, 1989 .

New asian ants of the Tribe Basicerotini, with an on-line computer interactive key to the twenty-six known Indo-Australian species (Hymenoptera: Formicidae: Myrmicinae)

Robert W. Taylor, 1990 .

Clinically proven mtDNA mutations are not common in those with chronic fatigue syndrome

Robert W. Taylor, J. Elson, F. H. van der Westhuizen, 2017, BMC Medical Genetics.

What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr?

Robert W. Taylor, S. Dimauro, H. Smeets, 2012, Brain : a journal of neurology.

Evidence of severe mitochondrial oxidative stress and a protective effect of low oxygen in mouse models of inherited photoreceptor degeneration.

Robert W. Taylor, R. Mcinnes, D. Turnbull, 2011, Human molecular genetics.

Microangiopathy in the cerebellum of patients with mitochondrial DNA disease

Robert W. Taylor, N. Lax, D. Turnbull, 2012, Brain : a journal of neurology.

Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement

Robert W. Taylor, R. Durbin, T. Wieland, 2015, Annals of clinical and translational neurology.

Resistance training in patients with single, large-scale deletions of mitochondrial DNA.

Robert W. Taylor, D. Turnbull, R. Haller, 2008, Brain : a journal of neurology.

Activated protein C in septic shock: a propensity-matched analysis

Robert W. Taylor, J. O’Brien, F. Sadaka, 2011, Critical care.

The feasibility of muscle mitochondrial respiratory chain phenotyping across the cognitive spectrum in Parkinson's disease

Robert W. Taylor, D. Turnbull, A. Yarnall, 2020, Experimental Gerontology.

Mutations of the mitochondrial carrier translocase channel subunit TIM22 cause early-onset mitochondrial myopathy

Robert W. Taylor, A. Torkamani, E. Ruiz-Pesini, 2018, Human molecular genetics.

Induction of mitochondrial biogenesis is a maladaptive mechanism in mitochondrial cardiomyopathies.

Robert W. Taylor, A. Cossarizza, C. Nediani, 2007, Journal of the American College of Cardiology.

The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families

Robert W. Taylor, S. Mansour, G. Saretzki, 2010, Brain : a journal of neurology.

Mutant POLG2 Disrupts DNA Polymerase γ Subunits and Causes Progressive External Ophthalmoplegia

Robert W. Taylor, D. Turnbull, P. Chinnery, 2006 .

A patient with typical clinical features of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS) but without an obvious genetic cause: a case report

Robert W. Taylor, A. Hellani, K. Abu-Amero, 2009, Journal of medical case reports.

Bridging PNAs can bind preferentially to a deleted mitochondrial DNA template but replication by mitochondrial DNA polymerase gamma in vitro is not impaired.

Robert W. Taylor, D. Turnbull, R. Lightowlers, 2003, Biochimica et biophysica acta.

POLG2 deficiency causes adult‐onset syndromic sensory neuropathy, ataxia and parkinsonism

Robert W. Taylor, G. Stevanin, P. Bonnen, 2016, Annals of clinical and translational neurology.

Cerebellar Ataxia in Patients With Mitochondrial DNA Disease: A Molecular Clinicopathological Study

Robert W. Taylor, N. Lax, D. Turnbull, 2012, Journal of neuropathology and experimental neurology.

Pathogenic mitochondrial mt-tRNAAla variants are uniquely associated with isolated myopathy

Robert W. Taylor, S. Zierz, P. Joshi, 2015, European Journal of Human Genetics.

The diagnosis of mitochondrial muscle disease

Robert W. Taylor, D. Turnbull, M. Barron, 2004, Neuromuscular Disorders.

Clinical , biochemical , and genetic spectrum of seven patients with NFU 1 deficiency

Robert W. Taylor, T. Meitinger, S. Seneca, 2017 .

Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency

Robert W. Taylor, I. Simonic, S. Mehta, 2014, Biochimica et biophysica acta.

Chapter 7 Current and Future Prospects for the Treatment of Mitochondrial Disorders

Robert W. Taylor, D. Turnbull, Robert W. Taylor, 2002 .

A homoplasmic mtDNA variant can influence the phenotype of the pathogenic m.7472Cins MTTS1 mutation: are two mutations better than one?

Robert W. Taylor, M. Elstner, D. Turnbull, 2008, European Journal of Human Genetics.

Comparison of Mitochondrial Mutation Spectra in Ageing Human Colonic Epithelium and Disease: Absence of Evidence for Purifying Selection in Somatic Mitochondrial DNA Point Mutations

Laura C. Greaves, Robert W. Taylor, D. Turnbull, 2012, PLoS genetics.

Anabolic Steroids—Analysis of Dosage Forms from Selected Case Studies from the Los Angeles County Sheriff's Scientific Services Bureau

Robert W. Taylor, E. A'Hearn, S. D. Le, 1991 .

Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults

Robert W. Taylor, J. Bourke, N. Lax, 2015, European heart journal.

The urinary proteome and metabonome differ from normal in adults with mitochondrial disease.

Robert W. Taylor, D. Turnbull, J. Lindon, 2015, Kidney international.

A truncating PET100 variant causing fatal infantile lactic acidosis and isolated cytochrome c oxidase deficiency

Robert W. Taylor, H. Prokisch, R. Lightowlers, 2014, European Journal of Human Genetics.

Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype

Katrien Stouffs, Melanie Bahlo, Holger Prokisch, 2016, American journal of human genetics.

LHON/MELAS overlap syndrome associated with a mitochondrial MTND1 gene mutation

Robert W. Taylor, D. Turnbull, T. Harrower, 2005, European Journal of Human Genetics.

Leigh disease associated with a novel mitochondrial DNA ND5 mutation

Robert W Taylor, Robert W. Taylor, Michael K. Hutchinson, 2002, European Journal of Human Genetics.

SLC25A42‐associated mitochondrial encephalomyopathy: Report of additional founder cases and functional characterization of a novel deletion

Robert W. Taylor, N. Kaya, D. Çolak, 2021, JIMD reports.

Cystic Leukoencephalopathy due to NDUFV1 mutation—A Report of the Phenotype and Its Rare Co-occurrence with Primary Hyperoxaluria

Robert W. Taylor, C. Alston, G. Vadlamani, 2016, Journal of Pediatric Neurology.

The swinging pendulum of biomarkers in mitochondrial disease

Robert W. Taylor, R. Horvath, H. Steele, 2016, Neurology.

A novel point mutation in the mitochondrial tRNATrp gene produces a neurogastrointestinal syndrome

Robert W. Taylor, Margaret A. Johnson, D. Turnbull, 2004, European Journal of Human Genetics.

Changes in the human mitochondrial genome after treatment of malignant disease.

Robert W. Taylor, D. Turnbull, A. Craft, 2003, Mutation research.

Pathogenic mtDNA mutations causing mitochondrial myopathy: The need for muscle biopsy

Robert W. Taylor, D. Turnbull, M. Rose, 2016, Neurology: Genetics.

Distal weakness with respiratory insufficiency caused by the m.8344A > G “MERRF” mutation

Robert W. Taylor, D. Turnbull, B. Chakrabarti, 2014, Neuromuscular Disorders.

Disclosing the functional changes of two genetic alterations in a patient with Chronic Progressive External Ophthalmoplegia: Report of the novel mtDNA m.7486G>A variant

Robert W. Taylor, A. Rego, L. Wong, 2017, Neuromuscular Disorders.

Girao H, Wong LJC, Taylor RW, Grazina M. Disclosing the functional changes of two genetic alterations in a patient with Chronic Progressive External Ophthalmoplegia: Report of the novel mtDNA m.7486G>A

Robert W. Taylor, A. Rego, L. Wong, 2018 .

Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy

Robert W. Taylor, R. Weleber, R. Wibom, 2012, European Journal of Human Genetics.

Mutations in the mitochondrial tRNA Ser(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy This article has been corrected since Advance Online Publication and a corrigendum is also printed in this issue

Robert W. Taylor, R. Weleber, R. Wibom, 2012 .

A novel MT-CO2 variant causing cerebellar ataxia and neuropathy: The role of muscle biopsy in diagnosis and defining pathogenicity

Robert W. Taylor, H. Willison, M. Reilly, 2021, Neuromuscular Disorders.

A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysis

Robert W. Taylor, D. Turnbull, P. Chinnery, 2004, Neuromuscular Disorders.

Bi‐allelic pathogenic variants in NDUFC2 cause early‐onset Leigh syndrome and stalled biogenesis of complex I

Robert W. Taylor, E. Lamantea, I. Wittig, 2020, EMBO molecular medicine.

Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene

Robert W. Taylor, D. Turnbull, P. Smith, 2001, Annals of neurology.

MR-1S Interactswith PET100andPET117 inModule- Based Assembly of Human Cytochrome c Oxidase

Robert W. Taylor, V. Tiranti, M. Zeviani, 2017 .

Familial myopathy: New insights into the T14709C mitochondrial tRNA mutation

Robert W. Taylor, M. Walker, D. Turnbull, 2004, Annals of neurology.

Robert W. Taylor, Ogun Adebali, C. Eraslan, 2020, Molecular genetics and metabolism reports.

Corrigendum: Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations

Robert W. Taylor, J. Armstrong, R. Artuch, 2015, Front. Genet..

Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations

Robert W. Taylor, J. Armstrong, R. Artuch, 2015, Front. Genet..

Sporadic mitochondrial myopathy due to a new mutation in the mitochondrial tRNASer(UCN) gene

Robert W. Taylor, Margaret A. Johnson, D. Turnbull, 2004, Neuromuscular Disorders.

Maternally inherited mitochondrial DNA disease in consanguineous families

Robert W. Taylor, D. Turnbull, I. Hughes, 2011, European Journal of Human Genetics.

Mitochondrial Protein Inte raction Mapping Identifies Regulators of Respiratory Chain Function Graphical

Robert W. Taylor, M. Westphall, H. Prokisch, 2016 .

The adjunctive application of transcranial direct current stimulation in the management of de novo refractory epilepsia partialis continua in adolescent‐onset POLG‐related mitochondrial disease

Robert W. Taylor, D. Turnbull, V. Ramesh, 2018, Epilepsia open.

Cognitive deficits in adult m.3243A>G‐ and m.8344A>G‐related mitochondrial disease: importance of correcting for baseline intellectual ability

Robert W. Taylor, D. Turnbull, A. Schaefer, 2019, Annals of clinical and translational neurology.

The Effect of tRNA[Ser]Sec Isopentenylation on Selenoprotein Expression

Robert W. Taylor, Tsutomu Suzuki, M. Helm, 2021, International journal of molecular sciences.

Noninvasive diagnosis of the 3243A>G mitochondrial DNA mutation using urinary epithelial cells

Robert W. Taylor, D. Turnbull, P. Chinnery, 2004, European Journal of Human Genetics.

A homoplasmic mitochondrial transfer ribonucleic acid mutation as a cause of maternally inherited hypertrophic cardiomyopathy.

Robert W. Taylor, S. Dimauro, D. Turnbull, 2003, Journal of the American College of Cardiology.

Age-associated mitochondrial DNA mutations lead to small but significant changes in cell proliferation and apoptosis in human colonic crypts

Laura C. Greaves, Robert W. Taylor, D. Turnbull, 2010, Aging cell.

A novel mitochondrial DNA tRNAIle (A4267G) mutation in a sporadic patient with mitochondrial myopathy

Robert W. Taylor, D. Turnbull, A. Schaefer, 2002, Neuromuscular Disorders.

Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency: is riboflavin supplementation effective?

Robert W. Taylor, T. Wieland, A. Munnich, 2018, Orphanet Journal of Rare Diseases.

Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in NDUFB11

Robert W. Taylor, S. Cook, J. Ware, 2016, Cold Spring Harbor molecular case studies.

Experimental Strategies Towards Treating Mitochondrial DNA Disorders

Robert W. Taylor, D. Turnbull, L. Craven, 2007, Bioscience reports.

Neuromuscular disease presentation with three genetic defects involving two genomes

Robert W. Taylor, D. Turnbull, J. Goodship, 2009, Neuromuscular Disorders.

Overexpression of human mitochondrial valyl tRNA synthetase can partially restore levels of cognate mt-tRNAVal carrying the pathogenic C25U mutation

Robert W. Taylor, D. Turnbull, R. Lightowlers, 2008, Nucleic acids research.

Sporadic Intragenic Inversion of the Mitochondrial DNA MTND1 Gene Causing Fatal Infantile Lactic Acidosis

C. B. White, Robert W. Taylor, D. Turnbull, 2006, Pediatric Research.

Mitochondrial dysfunction in myofibrillar myopathy

Robert W. Taylor, D. Turnbull, R. Barresi, 2016, Neuromuscular Disorders.

Behr’s Syndrome is Typically Associated with Disturbed Mitochondrial Translation and Mutations in the C12orf65 Gene

Robert W. Taylor, V. Ramesh, M. Santibanez-Koref, 2015, Journal of neuromuscular diseases.

A splice junction mutation in muscle carnitine palmitoyltransferase II deficiency.

Robert W. Taylor, D. Turnbull, Z. Chrzanowska-Lightowlers, 2003, Molecular genetics and metabolism.

Recessive desmin-null muscular dystrophy with central nuclei and mitochondrial abnormalities

Robert W. Taylor, K. Bushby, I. Horrocks, 2013, Acta Neuropathologica.

Preferential amplification of a human mitochondrial DNA deletion in vitro and in vivo

Robert W. Taylor, D. Turnbull, M. Lako, 2018, Scientific Reports.

Time course of normalisation of functional beta cell capacity in DiRECT after weight loss in type 2 diabetes

Benjamin S. Aribisala, Robert W. Taylor, N. Sattar, 2020 .

Bi-allelic variants in the mitochondrial RNase P subunit PRORP cause mitochondrial tRNA processing defects and pleiotropic multisystem presentations

Robert W. Taylor, I. Hochberg, W. Newman, 2021, American journal of human genetics.

ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathy

Robert W. Taylor, Mark T. Handley, A. von Kriegsheim, 2019, PLoS genetics.

ITPase Deficiency Causes Martsolf Syndrome With a Lethal Infantile Dilated Cardiomyopathy

Robert W. Taylor, Mark T. Handley, A. von Kriegsheim, 2018, bioRxiv.

A novel mitochondrial MTND5 frameshift mutation causing isolated complex I deficiency, renal failure and myopathy

Robert W. Taylor, R. Horvath, S. Heales, 2010, Neuromuscular Disorders.

THE ANTS (HYMENOPTERA : FORMICIDAE) OF THE KERMADEC ISLANDS

Robert W. Taylor, 1971 .

ATG7 safeguards human neural integrity

Robert W. Taylor, T. G. McWilliams, Jack J Collier, 2021, Autophagy.

A novel inborn error of the coenzyme Q10 biosynthesis pathway: cerebellar ataxia and static encephalomyopathy due to COQ5 C‐methyltransferase deficiency

Robert W. Taylor, D. Wallace, C. Toro, 2018, Human mutation.

The low abundance of clonally expanded mitochondrial DNA point mutations in aged substantia nigra neurons

Robert W. Taylor, D. Turnbull, C. Morris, 2009, Aging cell.

A novel de novo ACTA1 variant in a patient with nemaline myopathy and mitochondrial Complex I deficiency

Robert W. Taylor, A. Norman, R. Mcfarland, 2019, Neuromuscular Disorders.

Pathogenic Mitochondrial tRNA Point Mutations: Nine Novel Mutations Affirm Their Importance as a Cause of Mitochondrial Disease

Joanna Poulton, Robert W Taylor, Robert W. Taylor, 2013, Human mutation.

Probiotics: Prevention of Severe Pneumonia and Endotracheal Colonization Trial—PROSPECT: a pilot trial

Robert W. Taylor, M. Surette, M. Meade, 2016, Trials.

Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease.

Robert W. Taylor, D. Turnbull, M. Martikainen, 2016, JAMA neurology.

Biallelic Mutations in MTPAP Associated with a Lethal Encephalopathy

Robert W. Taylor, Y. Crow, T. Roscioli, 2019, Neuropediatrics.

Clinical features of the pathogenic m.5540G>A mitochondrial transfer RNA tryptophan gene mutation

Robert W. Taylor, Matthew J. Daniels, D. Mole, 2016, Neuromuscular Disorders.

Early-onset cataracts, spastic paraparesis, and ataxia caused by a novel mitochondrial tRNAGlu (MT-TE) gene mutation causing severe complex I deficiency: a clinical, molecular, and neuropathologic study.

Robert W. Taylor, N. Lax, D. Turnbull, 2013, Journal of neuropathology and experimental neurology.

A novel mitochondrial tRNAGlu (MTTE) gene mutation causing chronic progressive external ophthalmoplegia at low levels of heteroplasmy in muscle

Robert W. Taylor, D. Turnbull, J. Lowe, 2010, Journal of the Neurological Sciences.

The pathogenic m.3243A>T mitochondrial DNA mutation is associated with a variable neurological phenotype

Robert W. Taylor, A. Bender, R. Horvath, 2010, Neuromuscular Disorders.

The investigation and diagnosis of pathogenic mitochondrial DNA mutations in human urothelial cells.

Robert W. Taylor, D. Turnbull, R. Whittaker, 2010, Biochemical and biophysical research communications.

Survey of Students Regarding Zika Infection: Is the Next Generation Aware of the Dangers?

Robert W. Taylor, P. Magnusson, R. Raffa, 2020, Pharmacology & Pharmacy.

False-positive diagnosis of a single, large-scale mitochondrial DNA deletion by Southern blot analysis: the role of neutral polymorphisms.

Robert W. Taylor, A. Krasnianski, S. Zierz, 2004, Genetic testing.

Detection of mitochondrial DNA variation in human cells.

Robert W. Taylor, D. Turnbull, K. J. Krishnan, 2010, Methods in molecular biology.

Pathological mechanisms underlying single large‐scale mitochondrial DNA deletions

Robert W. Taylor, D. Turnbull, R. Haller, 2018, Annals of neurology.

Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy

Robert W. Taylor, R. Weleber, R. Wibom, 2012, European Journal of Human Genetics.

Production of transmitochondrial cybrids containing naturally occurring pathogenic mtDNA variants

Robert W. Taylor, M. Elstner, D. Turnbull, 2006, Nucleic acids research.

Mitochondrial pathology in progressive cerebellar ataxia

Robert W. Taylor, P. Chinnery, R. Horvath, 2015, Cerebellum & Ataxias.

Peripheral neuropathy in patients with CPEO associated with single and multiple mtDNA deletions

Robert W. Taylor, M. Kornhuber, A. Wienke, 2016, Neurology: Genetics.

Neuromuscular Junction Abnormalities in Mitochondrial Disease

Robert W. Taylor, D. Turnbull, R. Whittaker, 2019, Neurology. Clinical practice.

Neuromuscular Junction Abnormalities in Mitochondrial Disease AnObservational Cohort Study

Robert W. Taylor, D. Turnbull, R. Whittaker, 2022 .

Pilosulin 5, a novel histamine-releasing peptide of the Australian ant, Myrmecia pilosula (Jack Jumper Ant).

Robert W. Taylor, M. Wiese, N. Davies, 2008, Archives of biochemistry and biophysics.

Confirming TDP2 mutation in spinocerebellar ataxia autosomal recessive 23 (SCAR23)

Robert W. Taylor, K. Caldecott, A. D. de Brouwer, 2018, Neurology: Genetics.

Con fi rming TDP 2 mutation in spinocerebellar ataxia autosomal recessive 23 ( SCAR 23 )

Robert W. Taylor, D. Niyazov, K. Thompson, 2019 .

Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease.

Robert W. Taylor, R. Horvath, E. Ostergaard, 2021, Human molecular genetics.

The m.5650G>A mitochondrial tRNAAla mutation is pathogenic and causes a phenotype of pure myopathy

Robert W. Taylor, D. Turnbull, K. Bushby, 2008, Neuromuscular Disorders.

Diabetes and Deafness

Robert W. Taylor, D. Turnbull, R. Whittaker, 2007, Diabetes Care.

Ants of the genus Lordomyrma Emery (2) The Japanese L. azumai (Santschi) and six new species from India, Viet Nam and the Philippines (Hymenoptera: Formicidae: Myrmicinae)

Robert W. Taylor, Robert W. Taylor, 2012 .

Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene

Robert W. Taylor, N. Ashley, A. Seller, 2013, European Journal of Human Genetics.

Cytochrome c oxidase-intermediate fibres: Importance in understanding the pathogenesis and treatment of mitochondrial myopathy

Robert W. Taylor, D. Turnbull, R. Haller, 2012, Neuromuscular Disorders.

Biallelic Loss‐of‐Function NDUFA12 Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh‐Like Syndrome to Isolated Optic Atrophy

Robert W. Taylor, K. Bhatia, F. Alkuraya, 2021, Movement disorders clinical practice.

mtDNA disease for the neurologist

Robert W. Taylor, D. Turnbull, R. Whittaker, 2011 .

Robert W. Taylor, D. Turnbull, P. Chinnery, 2008 .

Mitochondrial DNA Disease Prevalence: Still Underrecognized? Reply

Robert W. Taylor, D. Turnbull, P. Chinnery, 2008 .

Exaggerated Status of

Robert W. Taylor, H. Bandelt, A. Salas, 2009 .

A homozygous variant in mitochondrial RNase P subunit PRORP is associated with Perrault syndrome characterized by hearing loss and primary ovarian insufficiency

Robert W. Taylor, I. Hochberg, W. Newman, 2017, bioRxiv.

Early‐onset coenzyme Q10 deficiency associated with ataxia and respiratory chain dysfunction due to novel pathogenic COQ8A variants, including a large intragenic deletion

Robert W. Taylor, G. Gorman, I. Hargreaves, 2020, JIMD reports.

Evidence for the Absence of Worker Behavioral Subcastes in the Sociobiologically Primitive Australian Ant Nothomyrmecia macrops Clark (Hymenoptera: Formicidae: Myrmeciinae)

Robert W. Taylor, Robert W. Taylor, 2014 .

A novel pathogenic m.4412G>A MT-TM mitochondrial DNA variant associated with childhood-onset seizures, myopathy and bilateral basal ganglia changes

Robert W. Taylor, G. Falkous, R. Mcfarland, 2019, Mitochondrion.

Periventricular Calcification, Abnormal Pterins and Dry Thickened Skin: Expanding the Clinical Spectrum of RMND1?

Robert W. Taylor, J. Casey, S. Ennis, 2015, JIMD reports.

Somatic mitochondrial DNA deletions accumulate to high levels in aging human extraocular muscles.

Laura C. Greaves, Robert W. Taylor, D. Turnbull, 2010, Investigative ophthalmology & visual science.

Gut Motility Issues in Critical Illness.

Robert W. Taylor, Robert W. Taylor, 2016, Critical care clinics.

CRITICAL CARE CORE CURRICULUM: AN INTRODUCTION TO CRITICAL CARE FOR MEDICAL STUDENTS

Robert W. Taylor, R. Dellinger, 1990 .

Albinism and a mitochondrial DNA deletion

Robert W. Taylor, E. Glamuzina, A. Vincent, 2020, Ophthalmic genetics.

Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy-like disease

Robert W. Taylor, C. Borchers, V. Ramesh, 2017, Genetics in Medicine.

Decreased male reproductive success in association with mitochondrial dysfunction

Robert W. Taylor, D. Turnbull, M. Martikainen, 2017, European Journal of Human Genetics.

Bilateral paediatric optic neuropathy precipitated by vitamin B12 deficiency and a novel mitochondrial DNA mutation

Robert W. Taylor, J. Ashworth, A. Jalil, 2013, International Ophthalmology.

A Conserved Aspartic Acid Is Important for Agonist (VUAA1) and Odorant/Tuning Receptor-Dependent Activation of the Insect Odorant Co-Receptor (Orco)

Robert W. Taylor, R. Newcomb, L. Zwiebel, 2013, PloS one.

Central venous catheterization.

Robert W. Taylor, J. Newton, D. Sprigings, 2007, Critical care medicine.