M. Gerrits

发表

The Domain II S4-S5 Linker in Nav1.9: A Missense Mutation Enhances Activation, Impairs Fast Inactivation, and Produces Human Painful Neuropathy

Yang Yang, Catharina G. Faber, Sulayman D. Dib-Hajj, 2015, NeuroMolecular Medicine.

Parental repeat length instability in myotonic dystrophy type 1 pre- and protomutations

H. Smeets, C. D. de Die-Smulders, D. Hellebrekers, 2020, European Journal of Human Genetics.

Coccoid forms of Helicobacter pylori are the morphologic manifestation of cell death

J. V. van Strijp, C. Vandenbroucke-Grauls, J. G. Kusters, 1997, Infection and immunity.

Quasispecies development of Helicobacter pylori observed in paired isolates obtained years apart from the same host.

E. Kuipers, M. Blaser, R. V. D. van der Hulst, 2000, The Journal of infectious diseases.

Urease-positive, acid-sensitive mutants of Helicobacter pylori: urease-independent acid resistance involved in growth at low pH.

J. Bijlsma, C. Vandenbroucke-Grauls, J. G. Kusters, 1998, FEMS microbiology letters.

Differential effect of lacosamide on Nav1.7 variants from responsive and non-responsive patients with small fibre neuropathy

H. Smeets, S. Dib-Hajj, S. Waxman, 2020, Brain : a journal of neurology.

Yield of peripheral sodium channels gene screening in pure small fibre neuropathy

H. Smeets, S. Waxman, G. Lauria, 2018, Journal of Neurology, Neurosurgery, and Psychiatry.

No Fabry Disease in Patients Presenting with Isolated Small Fiber Neuropathy

H. Smeets, E. Wolters, A. van den Wijngaard, 2016, PloS one.

Painful neuropathies: the emerging role of sodium channelopathies

S. Waxman, J. Hoeijmakers, M. Gerrits, 2014, Journal of the peripheral nervous system : JPNS.

Gain-of-function mutations in sodium channel Na(v)1.9 in painful neuropathy.

S. Dib-Hajj, S. Waxman, G. Lauria, 2014, Brain : a journal of neurology.

Expression of p53 as predictor for the development of esophageal cancer in achalasia patients.

E. Steyerberg, P. Siersema, H. van Dekken, 2010, Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus.

Structural and functional cardiac changes in myotonic dystrophy type 1: a cardiovascular magnetic resonance study

Y. Pinto, S. Schalla, G. Snoep, 2012, Journal of Cardiovascular Magnetic Resonance.

Helicobacter pylori does not Mediate the Formation of Carcinogenic N‐Nitrosamines

E. Kuipers, J. Kleinjans, J. Dallinga, 2002, Helicobacter.

The G1662S NaV1.8 mutation in small fibre neuropathy: impaired inactivation underlying DRG neuron hyperexcitability

S. Dib-Hajj, S. Waxman, Chongyang Han, 2013, Journal of Neurology, Neurosurgery & Psychiatry.

Small nerve fibres, small hands and small feet: a new syndrome of pain, dysautonomia and acromesomelia in a kindred with a novel NaV1.7 mutation.

S. Dib-Hajj, S. Waxman, G. Lauria, 2012, Brain : a journal of neurology.

Differentially expressed genes in response to amoxicillin in Helicobacter pylori analyzed by RNA arbitrarily primed PCR.

M. Ribeiro, J. G. Kusters, M. Gerrits, 2007, FEMS immunology and medical microbiology.

Multiple Mutations in or Adjacent to the Conserved Penicillin‐Binding Protein Motifs of the Penicillin‐Binding Protein 1A Confer Amoxicillin Resistance to Helicobacter pylori

E. Kuipers, M. Ribeiro, A. H. V. van Vliet, 2006, Helicobacter.

Real-Time PCR Screening for 16S rRNA Mutations Associated with Resistance to Tetracycline in Helicobacter pylori

J. G. Kusters, M. Gerrits, M. Kist, 2005, Antimicrobial Agents and Chemotherapy.

Role of the rdxA and frxA genes in oxygen-dependent metronidazole resistance of Helicobacter pylori.

E. Kuipers, D. Bax, A. H. V. van Vliet, 2004, Journal of medical microbiology.

Detection of high-level tetracycline resistance in clinical isolates of Helicobacter pylori using PCR-RFLP.

E. Kuipers, M. Ribeiro, A. H. V. van Vliet, 2004, FEMS immunology and medical microbiology.

Effects of 16S rRNA Gene Mutations on Tetracycline Resistance in Helicobacter pylori

E. Kuipers, A. H. V. van Vliet, J. G. Kusters, 2003, Antimicrobial Agents and Chemotherapy.

Effects of 16S rRNA gene mutations on tetracycline resistance in Helicobacter pylori.

E. Kuipers, A. H. V. van Vliet, J. G. Kusters, 2003, Antimicrobial agents and chemotherapy.

Alterations in Penicillin-Binding Protein 1A Confer Resistance to β-Lactam Antibiotics in Helicobacter pylori

E. Kuipers, A. V. van Zwet, J. G. Kusters, 2002, Antimicrobial Agents and Chemotherapy.

Nav1.7-related small fiber neuropathy

S. Dib-Hajj, S. Waxman, G. Lauria, 2012, Neurology.

Intra- and interfamily phenotypic diversity in pain syndromes associated with a gain-of-function variant of NaV1.7

S. Dib-Hajj, S. Waxman, G. Lauria, 2011, Molecular pain.

Peripheral Ion Channel Gene Screening in Painful- and Painless-Diabetic Neuropathy

H. Smeets, S. Waxman, E. Salvi, 2022, International journal of molecular sciences.

Gain-of-function Nav1.8 mutations in painful neuropathy

S. Dib-Hajj, S. Waxman, G. Lauria, 2012, Proceedings of the National Academy of Sciences.

Functional profiles of SCN9A variants in dorsal root ganglion neurons and superior cervical ganglion neurons correlate with autonomic symptoms in small fibre neuropathy.

S. Dib-Hajj, S. Waxman, G. Lauria, 2012, Brain : a journal of neurology.

Gain of function NaV1.7 mutations in idiopathic small fiber neuropathy

S. Dib-Hajj, S. Waxman, G. Lauria, 2012, Annals of neurology.

Biomarker-based prediction of inflammatory bowel disease-related colorectal cancer: a case–control study

Hester F. Lingsma, E. Kuipers, E. Steyerberg, 2011, Cellular Oncology.

Molecular Mechanisms of Antibiotic Resistance in Helicobacter pylori

M. Gerrits, 2004 .

16S rRNA Mutation-Mediated Tetracycline Resistance in Helicobacter pylori

E. Kuipers, J. G. Kusters, M. Gerrits, 2002, Antimicrobial Agents and Chemotherapy.

Helicobacter pylori and antimicrobial resistance: molecular mechanisms and clinical implications.

E. Kuipers, A. H. V. van Vliet, J. G. Kusters, 2006, The Lancet. Infectious diseases.

Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers

Peter Devilee, Alfons Meindl, Lesley McGuffog, 2010, Breast Cancer Research.

Hydropathicity-based prediction of pain-causing NaV1.7 variants

Yang Yang, Ronald L. Westra, Dimos Kapetis, 2021, BMC Bioinformatics.

Network topology of NaV1.7 mutations in sodium channel-related painful disorders

Filippo Martinelli-Boneschi, Andrea Zauli, Ronald L. Westra, 2017, BMC Systems Biology.

Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing

H. Smeets, S. Dib-Hajj, S. Waxman, 2020, PloS one.

E. Kuipers, R. Smits, C. J. van der Woude, 2009, Gut.

A gain-of-function sodium channel β2-subunit mutation in painful diabetic neuropathy

S. Dib-Hajj, S. Waxman, G. Lauria, 2019, Molecular pain.

Sodium channel genes in pain-related disorders: phenotype–genotype associations and recommendations for clinical use

C. Woods, S. Dib-Hajj, S. Waxman, 2014, The Lancet Neurology.

Copy number variants from 4800 exomes contribute to ~7% of genetic diagnoses in movement disorders, muscle disorders and neuropathies

R. Pfundt, N. de Leeuw, C. Gilissen, 2023, European Journal of Human Genetics.

Comparison of Pulsed-Field Gel Electrophoresis and Amplified Fragment-Length Polymorphism for Epidemiological Investigations of Common Nosocomial Pathogens

M. Samore, E. D’Agata, Yi-Wei Tang, 2001, Infection Control & Hospital Epidemiology.

Small-Fiber Neuropathy Nav1.8 Mutation Shifts Activation to Hyperpolarized Potentials and Increases Excitability of Dorsal Root Ganglion Neurons

Yang Yang, Stephen G Waxman, S. Dib-Hajj, 2013, The Journal of Neuroscience.

Evidence for SMAD 3 as a modifier of breast cancer risk in BRCA 2 mutation carriers

V. Pankratz, F. Couch, T. Rebbeck, 2010 .

COL6A5 variants in familial neuropathic chronic itch

S. Dib-Hajj, S. Waxman, M. Cocca, 2017, Brain : a journal of neurology.

A novel SCN9A splicing mutation in a compound heterozygous girl with congenital insensitivity to pain, hyposmia and hypogeusia

L. Santoro, M. Nolano, V. Provitera, 2018, Journal of the peripheral nervous system : JPNS.

Expression of pathogenic SCN9A mutations in the zebrafish: A model to study small-fiber neuropathy

H. Smeets, S. Waxman, G. Lauria, 2019, Experimental Neurology.

E. Kuipers, R. Smits, B. Xia, 2022 .

The Domain II S4-S5 Linker in Nav1.9: A Missense Mutation Enhances Activation, Impairs Fast Inactivation, and Produces Human Painful Neuropathy

S. Dib-Hajj, S. Waxman, G. Lauria, 2015, NeuroMolecular Medicine.

Genetic Profiling of Sodium Channels in Diabetic Painful and Painless and Idiopathic Painful and Painless Neuropathies

S. Dib-Hajj, S. Waxman, E. Salvi, 2023, International journal of molecular sciences.

Peripheral Ion Channel Genes Screening in Painful Small Fiber Neuropathy

H. Smeets, S. Waxman, E. Salvi, 2022, International journal of molecular sciences.

TRPA1 rare variants in chronic neuropathic and nociplastic pain patients

M. de Tommaso, S. Dib-Hajj, S. Waxman, 2023, Pain.

Novel SCN9A Mutations in a Compound Heterozygous Girl with Congenital Insensitivity to Pain

C. Haaxma, B. Stunnenberg, M. Gerrits, 2020, Journal of Pediatric Neurology.

Parental repeat length instability in myotonic dystrophy type 1 pre- and protomutations

H. Smeets, C. D. de Die-Smulders, D. Hellebrekers, 2020, European Journal of Human Genetics.

Sodium channel genes in pain-related disorders: phenotype–genotype associations and recommendations for clinical use

S. Dib-Hajj, G. Lauria, M. Gerrits, 2014, The Lancet Neurology.

Small nerve fibres, small hands and small feet: a new syndrome of pain, dysautonomia and acromesomelia in a kindred with a novel NaV1.7 mutation.

S. Dib-Hajj, S. Waxman, G. Lauria, 2012, Brain : a journal of neurology.

Ion Channel Genes in Painful Neuropathies

J. Hoeijmakers, M. Gerrits, Milena Ślęczkowska, 2023, Biomedicines.