D. Chandler

发表

Polymorphisms associated with normal memory variation also affect memory impairment in schizophrenia

S. Wiltshire, J. Badcock, A. Jablensky, 2011, Genes, brain, and behavior.

Impact of the Reelin signaling cascade (Ligands–Receptors–Adaptor Complex) on cognition in schizophrenia

Steven Wiltshire, Leon Flicker, Luba Kalaydjieva, 2012, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Highly variable neural involvement in sphingomyelinase-deficient Niemann-Pick disease caused by an ancestral Gypsy mutation.

J. Bertranpetit, L. Kalaydjieva, P. Seeman, 2006, Brain : a journal of neurology.

N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom.

P K Thomas, F. Baas, A. Rosenthal, 2000, American journal of human genetics.

Promoter polymorphisms in two overlapping 6p25 genes implicate mitochondrial proteins in cognitive deficit in schizophrenia

A. McRae, M. Gill, A. Corvin, 2012, Molecular Psychiatry.

Founder mutation causing infantile GM1-gangliosidosis in the Gypsy population.

L. Kalaydjieva, D. Chandler, I. Kremensky, 2006, Molecular genetics and metabolism.

Impact of Neuritin 1 (NRN1) polymorphisms on fluid intelligence in schizophrenia

L. Palmer, J. Badcock, A. Jablensky, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

N-myc downstream-regulated gene 1 is mutated in hereditary motor and sensory neuropathy-Lom.

F. Baas, A. Rosenthal, D. Gresham, 2000, American journal of human genetics.

Functionally distinct PI 3-kinase pathways regulate myelination in the peripheral nervous system

G. Morahan, F. Lang, L. Kalaydjieva, 2014, The Journal of cell biology.

Hereditary motor and sensory neuropathy – Lom (HMSNL): refined genetic mapping in Romani (Gypsy) families from several European countries

F. Baas, A. Starr, D. Gresham, 2000, Neuromuscular Disorders.

Psychosis susceptibility gene ZNF804A and cognitive performance in schizophrenia.

Michael Gill, Hans-Jürgen Möller, Pierandrea Muglia, 2010, Archives of general psychiatry.

Deleterious GRM1 Mutations in Schizophrenia

P. Visscher, A. Jablensky, L. Kalaydjieva, 2012, PloS one.

Autosomal-recessive congenital cerebellar ataxia is caused by mutations in metabotropic glutamate receptor 1.

Katherine R. Smith, R. Kaneva, M. Bahlo, 2012, American journal of human genetics.

Dating the origin of the CCR5-Delta32 AIDS-resistance allele by the coalescence of haplotypes.

H. Ostrer, D. Goldstein, X. Estivill, 1998, American journal of human genetics.

Dating the Origin of the CCR 5D 32 AIDS-Resistance Allele by the Coalescence of Haplotypes

H. Ostrer, D. Goldstein, X. Estivill, 2007 .

A mutation in an alternative untranslated exon of hexokinase 1 associated with Hereditary Motor and Sensory Neuropathy – Russe (HMSNR)

F. Baas, R. Kaneva, R. Wanders, 2009, European Journal of Human Genetics.

GNE myopathy in Roma patients homozygous for the p.I618T founder mutation

M. Bahlo, H. Goebel, L. Kalaydjieva, 2015, Neuromuscular Disorders.

A Genome-wide Association Analysis of a Broad Psychosis Phenotype Identifies Three Loci for Further Investigation

M. Pirinen, P. Donnelly, C. Spencer, 2014, Biological Psychiatry.

Evidence of aberrant DNA damage response signalling but normal rates of DNA repair in dividing lymphoblasts from patients with schizophrenia

A. Jablensky, M. Lavin, C. Weickert, 2012, The world journal of biological psychiatry : the official journal of the World Federation of Societies of Biological Psychiatry.

Gene mapping in Gypsies identifies a novel demyelinating neuropathy on chromosome 8q24

A. Hristova, L. Middleton, J. Hallmayer, 1996, Nature Genetics.

Ndrg1 in development and maintenance of the myelin sheath

G. Morahan, T. Kilpatrick, L. Kalaydjieva, 2011, Neurobiology of Disease.

Comprehensive analysis of tagging sequence variants in DTNBP1 shows no association with schizophrenia or with its composite neurocognitive endophenotypes

S. Wiltshire, L. Palmer, G. Montgomery, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Carrier rates of the ancestral Indian W24X mutation in GJB2 in the general Gypsy population and individual subisolates.

L. Kalaydjieva, P. Seeman, D. Chandler, 2007, Genetic testing.

A novel locus for autosomal recessive peripheral neuropathy in the EGR2 region on 10q23.

L. Kalaydjieva, P. Thomas, D. Chandler, 2000, American journal of human genetics.

Inherited balanced translocation t(9;17)(q33.2;q25.3) concomitant with a 16p13.1 duplication in a patient with schizophrenia

J. Gécz, A. Jablensky, L. Kalaydjieva, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A novel Gypsy founder mutation, p.Arg1109X in the CMT4C gene, causes variable peripheral neuropathy phenotypes

J. Bertranpetit, Y. Parman, L. Kalaydjieva, 2005, Journal of Medical Genetics.

Congenital cataracts facial dysmorphism neuropathy (CCFDN) syndrome: a novel developmental disorder in Gypsies maps to 18qter

L. Kalaydjieva, D. Chandler, P. Thomas, 1999, European Journal of Human Genetics.

Integrity of genome-wide genotype data from low passage lymphoblastoid cell lines

A. Jablensky, B. Morar, D. Chandler, 2016, Genomics data.

Neuregulin 3 (NRG3) as a susceptibility gene in a schizophrenia subtype with florid delusions and relatively spared cognition

A. Jablensky, F. Waters, M. Dragovic, 2011, Molecular Psychiatry.

The Gitelman syndrome mutation, IVS9+1G>T, is common across Europe.

E. Coto, L. Kalaydjieva, D. Chandler, 2007, Kidney International.

Functionally distinct PI 3-kinase pathways regulate myelination in the peripheral nervous system

G. Morahan, F. Lang, L. Kalaydjieva, 2014, The Journal of cell biology.

The psychosis susceptibility gene ZNF 804 A is associated with less impaired 1 cognitive performance in schizophrenia . 2 3

P. Muglia, I. Giegling, A. Hartmann, 2009 .

A Genome-wide Association Analysis of a Broad Psychosis Phenotype Identifies Three Loci for Further Investigation

Simon C. Potter, M. Pirinen, P. Donnelly, 2014, Biological Psychiatry.

Comprehensive analysis of tagging sequence variants in DTNBP1 shows no association with schizophrenia or with its composite neurocognitive endophenotypes

S. Wiltshire, L. Palmer, G. Montgomery, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The stretcher spontaneous neurodegenerative mutation models Charcot-Marie-Tooth disease type 4D

G. Morahan, T. Kilpatrick, L. Kalaydjieva, 2013, F1000Research.