D. Clair

发表

Large recurrent microdeletions associated with schizophrenia

Thomas W. Mühleisen, Bjarni V. Halldórsson, P. Matthews, 2008, Nature.

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Simon C. Potter, P. Donnelly, C. Spencer, 2007, Nature.

Rare chromosomal deletions and duplications increase risk of schizophrenia

P. Visscher, S. Gabriel, M. Daly, 2008, Nature.

Common variants conferring risk of schizophrenia

Pall I. Olason, P. Matthews, H. Stefánsson, 2009, Nature.

Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls

Jake K. Byrnes, Tomas W. Fitzgerald, P. Donnelly, 2010, Nature.

Synaptic scaffold evolution generated components of vertebrate cognitive complexity

Richard D Emes, D. Clair, L. Saksida, 2012, Nature Neuroscience.

Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging

D. Rujescu, P. Muglia, I. Giegling, 2010, Human Genetics.

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

Manuel A. R. Ferreira, John P. Rice, Edward G. Jones, 2011, Nature Genetics.

Simple Viewing Tests Can Detect Eye Movement Abnormalities That Distinguish Schizophrenia Cases from Controls with Exceptional Accuracy

P. Benson, D. Rujescu, I. Giegling, 2012, Biological Psychiatry.

Association within a family of a balanced autosomal translocation with major mental illness

D. Clair, D. Blackwood, W. Muir, 1990, The Lancet.

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

Manuel A. R. Ferreira, S. Gabriel, M. Daly, 2008, Nature Genetics.

Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder

D. Clair, G. Kirov, D. Grozeva, 2011, Molecular Psychiatry.

Brave New Brain: Conquering Mental Illness in the Era of the Genome

D. Clair, 2002, Heredity.

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

Judy H. Cho, John P. Ferguson, G. Wainrib, 2019, Scientific Reports.

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium

C. Spencer, K. Davis, P. Visscher, 2016, bioRxiv.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

John P. Rice, Melissa J. Green, Robert C. Thompson, 2017, Cell.

Genome-wide association study identifies five new schizophrenia loci

Anders D. Børglum, Peter Donnelly, Jianxin Shi, 2011, Nature Genetics.

Meta-analysis and imputation refines the association of 15q25 with smoking quantity

Inês Barroso, Lowell Satler, Paul Scheet, 2010, Nature Genetics.

Distribution of apolipoprotein E allele frequencies of the Han Chinese in an iodine-deficient mountainous area

D. Clair, S. Duan, Lin He, 2004, Annals of human biology.

A family-based and case-control association study of the NOTCH4 gene and schizophrenia

D. Clair, G. Breen, F. Zou, 2002, Molecular Psychiatry.

Failure to confirm NOTCH4 association with schizophrenia in a large population-based sample from Scotland

Nigel K. Spurr, Ian C. Gray, Michael R. Barnes, 2001, Nature Genetics.

A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia

C. Crombie, G. Fraser, N. Walker, 2010, Molecular Psychiatry.

Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3

C. Crombie, G. Fraser, N. Walker, 2008, European Journal of Human Genetics.

Gene variants associated with schizophrenia in a Norwegian genome-wide study are replicated in a large European cohort.

Elvira Bramon, Leena Peltonen, Morten Mattingsdal, 2010, Journal of psychiatric research.

Association between angiotensin-converting enzyme gene and late onset Alzheimer's disease in Han Chinese

D. Clair, G. Breen, Lin He, 2000, Neuroscience Letters.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

John P. Rice, Melissa J. Green, Robert C. Thompson, 2017, Cell.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

John P. Rice, Melissa J. Green, Robert C. Thompson, 2017, Cell.

Apolipoprotein E Genotype and its Effect on Duration and Severity of Early and Late Onset Alzheimer's Disease

D. Clair, A. Brookes, C. Yates, 1995, British Journal of Psychiatry.

Additional support for schizophrenia linkage on chromosomes 6 and 8: a multicenter study. Schizophrenia Linkage Collaborative Group for Chromosomes 3, 6 and 8.

L. Siever, M. Daly, T. Sigmundsson, 1996, American journal of medical genetics.

Association study and meta-analysis of low-density lipoprotein receptor related protein in Alzheimer's disease

D. Clair, J. Lambert, C. Lendon, 2005, Neuroscience Letters.

LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells

D. Geschwind, D. Rujescu, P. Muglia, 2007, Molecular Psychiatry.

An association study of the neuregulin 1 gene, bipolar affective disorder and psychosis

D. Collier, D. Clair, G. Breen, 2009, Psychiatric genetics.

Chronic idiopathic polyneuropathy presenting in middle or old age : a clinical and electrophysiological study of 75 patients

D. Clair, David, J. Warner, 2022 .

No association between polymorphisms in the lectin-like oxidised low density lipoprotein receptor (ORL1) gene on chromosome 12 and Alzheimer’s disease in a UK cohort

D. Clair, D. Mann, C. Lendon, 2004, Neuroscience Letters.

Interleukin-6 promoter polymorphism: risk and pathology of Alzheimer's disease

D. Clair, D. Mann, J. Lambert, 2004, Neuroscience Letters.

Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis

Tom R. Gaunt, Thomas M. Keane, Hashem A. Shihab, 2019, Nature Communications.

The role of pro-inflammatory factors in mediating the effects on the fetus of prenatal undernutrition: Implications for schizophrenia

D. Clair, Z. Li, G. Feng, 2008, Schizophrenia Research.

Candidate gene association studies of the α4 (CHRNA4) and β2 (CHRNB2) neuronal nicotinic acetylcholine receptor subunit genes in Alzheimer's disease

Carol Brayne, Simon Lovestone, Michael J. Owen, 2004, Neuroscience Letters.

Detection of complement factor B in the cerebrospinal fluid of patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy disease using two-dimensional gel electrophoresis and mass spectrometry

D. Clair, R. Kalaria, M. Ünlü, 2000, Neuroscience Letters.

Microvascular Pathology in Familial Multiinfarct Dementia or CADASIL: Implications for Cerebral Blood Flow

D. Clair, C. Morris, D. Burn, 2001 .

A monoclonal antibody assay technique for plasma and red cell acetylcholinesterase activity in Alzheimer's disease

D. Clair, D. Brock, L. Barron, 1986, Journal of the Neurological Sciences.

DISC1 as a genetic risk factor for schizophrenia and related major mental illness: response to Sullivan

D. Clair, S. McCarthy, J. Roder, 2014, Molecular Psychiatry.

Clinical, psychological and neuroradiological findings in a case of chronic schizophrenia with cognitive impairment and a mis-sense mutation at codon 713 of the β amyloid precursor protein gene

D. Clair, S. Lawrie, G. Goodwin, 1993, Schizophrenia Research.

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

Pall I. Olason, H. Stefánsson, D. Rujescu, 2011, Molecular Psychiatry.

Interplay between DISC1 and GABA Signaling Regulates Neurogenesis in Mice and Risk for Schizophrenia

Joseph H. Callicott, Daniel R. Weinberger, Fengyu Zhang, 2012, Cell.

Crystal structure of 3,3'-commo-bis[undecahydro-1,2-dicarba-3-nickela-closo-dodecaborane], a nickel(IV) complex of the dicarbollide ion

David H. Templeton, D. Clair, Allan Zalkin, 1970 .

Meta-analysis and imputation refines the association of 15q25 with smoking quantity

Tariq Ahmad, Inês Barroso, Lowell Satler, 2010, Nature Genetics.

PREMATURE SENILITY IN DOWN'S SYNDROME

D. Clair, D. Blackwood, 1985, The Lancet.

potential.gical function and changes in P3 event-related Measuring the course of Alzheimer's disease. A longitudinal study

D. Clair, D. Blackwood, I. Blackburn, 2012 .

P3 Abnormality in fragile X syndrome

D. Clair, D. Blackwood, C. Oliver, 1987, Biological Psychiatry.

Evaluation of a Susceptibility Gene for Schizophrenia: Genotype Based Meta-Analysis of RGS4 Polymorphisms from Thirteen Independent Samples

D. Collier, D. Clair, G. Kirov, 2006, Biological Psychiatry.

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

Judy H. Cho, John P. Ferguson, G. Wainrib, 2019, Scientific Reports.

A locus for bipolar affective disorder on chromosome 4p

D. Clair, D. Blackwood, W. Muir, 1996, Nature Genetics.

Localisation of a Susceptibility Locus for Schizophrenia on Chromosome 5

D. Clair, M. Owen, D. Craufurd, 1990, British Journal of Psychiatry.

DNA markers and biological vulnerability markers in families multiply affected with schizophrenia

D. Clair, D. Blackwood, W. Muir, 2005, European Archives of Psychiatry and Clinical Neuroscience.

SCHIZOPHRENIA AND CHROMOSOMES

D. Clair, D. Blackwood, W. Muir, 1989, The Lancet.

No linkage of chromosome 5q11-q13 markers to schizophrenia in Scottish families

H. J. Evans, D. Clair, D. Blackwood, 1989, Nature.

Human leucocyte antigen-A2 increases risk of Alzheimer's disease but does not affect age of onset in a Scottish population

D. Clair, N. Craddock, C. Lendon, 2000, Neuroscience Letters.

GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia

D. Rujescu, S. Cichon, A. Ingason, 2011, Molecular Psychiatry.

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

Minna Männikkö, David Curtis, Peter Holmans, 2016, Nature Neuroscience.

The genetics of the mood disorder spectrum: genome-wide association analyses of over 185,000 cases and 439,000 controls

Melissa J. Green, Robert C. Thompson, Pamela B. Mahon, 2018, bioRxiv.

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

D. Geschwind, D. Rujescu, P. Muglia, 2007, Molecular Psychiatry.

A polygenic resilience score moderates the genetic risk for schizophrenia.

M. Pirinen, P. Donnelly, C. Spencer, 2019, Molecular psychiatry.

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

Hae Kyung Im, Solveig K Sieberts, Kiran Girdhar, 2019, Nature Genetics.

Twin zygosity testing for medical purposes

D. Clair, F. Bamforth, J. Clair, 1998 .

Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia

N. Freimer, R. Ophoff, D. Clair, 2022, Nature Genetics.

A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

John P. Rice, Robert M. Maier, C. Spencer, 2020, Biological Psychiatry.

Association study of a (TG)n dinucleotide repeat at chromosome 15q13.3 and schizophrenia in the Chinese population

D. Clair, Lin He, G. Feng, 2008, Psychiatry Research.

Large-scale analysis of DNA methylation identifies cellular alterations in blood from psychosis patients and molecular biomarkers of treatment-resistant schizophrenia

R. Murray, E. Vassos, D. Collier, 2020, bioRxiv.

Genome-wide Association Study of Clinical Features in the Schizophrenia Psychiatric Genomics Consortium: Confirmation of Polygenic Effect on Negative Symptoms

D. Rujescu, O. Andreassen, R. Ophoff, 2017, bioRxiv.

Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma

H. Stefánsson, A. Sigurdsson, A. Jonasdottir, 2010, Nature Genetics.

Latent Effects of Prenatal Malnutrition on Adult Health

D. Clair, E. Susser, Lin He, 2008, Annals of the New York Academy of Sciences.

UK 10 K Consortium

Tom R. Gaunt, Hashem A. Shihab, Gail P. Clement, 2019 .

Common variant at 16p11.2 conferring risk of psychosis

M. Pirinen, H. Stefánsson, D. Rujescu, 2014, Molecular Psychiatry.

A family-based association study of T1945C polymorphism in the proline dehydrogenase gene and schizophrenia in the Chinese population

D. Clair, Lin He, G. Feng, 2003, Neuroscience Letters.

Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

D. Rujescu, S. Cichon, I. Giegling, 2021, Biological Psychiatry.

Complement genes contribute sex-biased vulnerability in diverse illnesses

Simon C. Potter, Christopher W. Whelan, M. Pirinen, 2020, Nature.

A study of type-1 diabetes associated autoantibodies in schizophrenia

D. Clair, C. Mustard, Jun Wei, 2016, Schizophrenia Research.

Identifying potential risk haplotypes for schizophrenia at the DTNBP1 locus in Han Chinese and Scottish populations

C. Crombie, N. Walker, R. Murray, 2005, Molecular Psychiatry.

Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH 3 causing

D. Clair, M. Viitanen, C. Morris, 2007 .

Screening British CADASIL families for mutations in theNOTCH3 gene

D. Clair, D. Shaw, R. de Lange, 2000, Journal of medical genetics.

5 AN INTEGRATED GENETIC-EPIGENETIC ANALYSIS OF SCHIZOPHRENIA: EVIDENCE FOR CO-LOCALIZATION OF GENETIC ASSOCIATIONS AND DIFFERENTIAL DNA METHYLATION FROM A LARGE META-ANALYSIS OF WHOLE BLOOD DNA

D. Collier, D. Clair, G. Breen, 2019, European Neuropsychopharmacology.

Structural and copy number variants in the human genome: implications for psychiatry

D. Clair, 2013, British Journal of Psychiatry.

Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness

D. Clair, S. Lawrie, A. McIntosh, 2015, Molecular Neuropsychiatry.

Expanding the range of ZNF804A variants conferring risk of psychosis

R A Ophoff, T Sigmundsson, Pall I. Olason, 2011, Molecular Psychiatry.

Apolipoprotein E is a genetic risk factor for fetal iodine deficiency disorder in China

D. Clair, G. Breen, F. Zhang, 2000, Molecular Psychiatry.

Mosaic copy number variation in schizophrenia

D. Clair, G. Kirov, M. Owen, 2013, European Journal of Human Genetics.

Common variants on 8p12 and 1q24.2 confer risk of schizophrenia

Qi Xu, Peng Wang, Dengtang Liu, 2011, Nature Genetics.

Replication Study and Meta-Analysis in European Samples Supports Association of the 3p21.1 Locus with Bipolar Disorder

Thomas W. Mühleisen, H. Stefánsson, D. Rujescu, 2012, Biological Psychiatry.

Strong genetic evidence for a selective influence of GABAA receptors on a component of the bipolar disorder phenotype

P. Donnelly, D. Collier, D. Clair, 2008, Molecular Psychiatry.

BDNF gene is a risk factor for schizophrenia in a Scottish population

C. Crombie, N. Walker, D. Clair, 2005, Molecular Psychiatry.

Population-based and family-based association studies of an (AC)n dinucleotide repeat in α-7 nicotinic receptor subunit gene and schizophrenia

D. Clair, G. He, Lin He, 2006, Schizophrenia Research.

Catechol-O-methyltransferase gene Val/Met functional polymorphism and risk of schizophrenia: A large-scale association study plus meta-analysis

Lin He, Wei-Wei Sun, D. Clair, 2005, Biological Psychiatry.

Family-based association studies of COMT gene polymorphisms and schizophrenia in the Chinese population

D. Clair, G. Breen, G. Feng, 2002, Molecular Psychiatry.

HDAC9 is implicated in schizophrenia and expressed specifically in post-mitotic neurons but not in adult neural stem cells.

Bing Lang, Sanbing Shen, Colin D McCaig, 2012, American journal of stem cells.

Deregulation of EIF4E: a novel mechanism for autism

D. Clair, Z. Miedzybrodzka, S. Shen, 2009, Journal of Medical Genetics.

Autoantibodies in human contacts of SLE dogs.

D. Clair, R. DeHoratius, R. Halliwell, 1980, Arthritis and rheumatism.

DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder

I. Deary, J. Suvisaari, T. Paunio, 2009, Molecular Psychiatry.

Meta-analysis of association between ApoE ε4 allele and schizophrenia

D. Clair, Lin He, Mingqing Xu, 2006, Schizophrenia Research.

Reversal of proliferation deficits caused by chromosome 16p13.11 microduplication through targeting NFκB signaling: an integrated study of patient-derived neuronal precursor cells, cerebral organoids and in vivo brain imaging

D. Clair, S. Lawrie, H. Whalley, 2018, Molecular Psychiatry.

Copy Number Variation and Schizophrenia

D. Clair, David St Clair, 2009 .

autism Deregulation of EIF 4 E : a novel mechanism for

D. Clair, Z. Miedzybrodzka, M. Neves-Pereira, 2009 .

A machine learning case–control classifier for schizophrenia based on DNA methylation in blood

D. Clair, Chathura Gunasekara, C. Coarfa, 2021, Translational Psychiatry.

Synuclein proteins and Alzheimer's disease

D. Clair, A. Brookes, 1994, Trends in Neurosciences.

Linking Prenatal Nutrition to Adult Mental Health

D. Clair, Lin He, K. Harper, 2010 .

Chromosome 21, Down's syndrome and Alzheimer's disease.

D. Clair, 2008 .

Mutation in codon 713 of the β amyloid precursor protein gene presenting with schizophrenia

D. Clair, C. Yates, C. Jones, 1992, Nature Genetics.

Exposure to the Chinese Famine of 1959-1961 Rates of Adult Schizophrenia Following Prenatal

D. Clair, P. Sham, Lin He, 2005 .

Association of APOE gene with schizophrenia in Chinese: a possible risk factor in times of malnutrition

D. Clair, G. Breen, Lin He, 2003, Schizophrenia Research.

Further evidence for the association between G72/G30 genes and schizophrenia in two ethnically distinct populations

D. Clair, S. Duan, F. Zou, 2006, Molecular Psychiatry.

Population-based linkage analysis of schizophrenia and bipolar case–control cohorts identifies a potential susceptibility locus on 19q13

D. Rujescu, P. Muglia, C. Francks, 2010, Molecular Psychiatry.

ADENOIDAL HYPERTROPHY IN HIV-INFECTED PATIENTS

D. Clair, G. Goodwin, R. Brettle, 1988, The Lancet.

At-Risk Variant in TCF7L2 for Type II Diabetes Increases Risk of Schizophrenia

D. Rujescu, S. Cichon, O. Pietiläinen, 2011, Biological Psychiatry.

Confirmation and refinement of an ‘at-risk’ haplotype for schizophrenia suggests the EST cluster, Hs.97362, as a potential susceptibility gene at the Neuregulin-1 locus

D. Clair, P. Scully, A. Corvin, 2004, Molecular Psychiatry.

Family-based association study of the functional monoamine oxidase A gene promoter polymorphism and schizophrenia

D. Clair, Lin He, M. Yang, 2004, Schizophrenia Research.

Magnetic resonance imaging in schizophrenia: Altered brain morphology associated with P300 abnormalities and eye tracking dysfunction

D. Clair, A. Young, W. Muir, 1991, Biological Psychiatry.

Association analysis of the glycogen synthase kinase-3β gene in bipolar disorder

D. Collier, D. Clair, G. Breen, 2006, Neuroscience Letters.

Puerperal Insanity in the 19th and 20th Centuries

Anis-ur-Rehman, D. Clair, C. Platz, 1990, British Journal of Psychiatry.

Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

Kristen K. Dang, D. A. Lewis, C. Spencer, 2019, Nature Genetics.

Prenatal nutrition deficiency reprogramed postnatal gene expression in mammals brain:Implications for schizophrenia

D. Clair, Yun Wang, Qinghe Liu, 2014 .

Study of novel autoantibodies in schizophrenia Running title: Autoantibodies in schizophrenia

D. Clair, C. Mustard, Jun Wei, 2017 .

Pharacogenetic effects of dopamine transporter gene polymorphisms on response to chlorpromazine and clozapine and on extrapyramidal syndrome in schizophrenia

D. Clair, J. Xuan, G. He, 2010, Progress in Neuro-Psychopharmacology and Biological Psychiatry.

Genetic variants in the BDNF gene and therapeutic response to risperidone in schizophrenia patients: a pharmacogenetic study

D. Clair, Lin He, G. Feng, 2010, European Journal of Human Genetics.

Complement genes contribute sex-biased vulnerability in diverse disorders

Christopher W. Whelan, M. Pirinen, C. Spencer, 2020, Nature.

P300 event-related potential abnormalities in borderline personality disorder

D. Clair, D. Blackwood, Kutcher S.P., 1986, Biological Psychiatry.

Association Study of Nonsynonymous Single Nucleotide Polymorphisms in Schizophrenia

H. Stefánsson, D. Rujescu, S. Cichon, 2012, Biological Psychiatry.

Recurrent deletions of ULK 4 in schizophrenia : a novel gene crucial for neuritogenesis and neuronal motility

H. Stefánsson, D. Clair, D. Blackwood, 2013 .

The influence of the e4 allele of the apolipoprotein E gene on childhood IQ, nonverbal reasoning in old age, and lifetime cognitive change

I. Deary, D. Clair, G. Breen, 2003 .

High-resolution mapping of SNCA encoding α-synuclein, the non-Aβ component of Alzheimer’s disease amyloid precursor, to human chromosome 4q21.3→q22 by fluorescence in situ hybridization

Anthony J. Brookes, D. Clair, A. Brookes, 1995 .

P3 and other Long Latency Auditory Evoked Potentials in Presenile Dementia Alzheimer Type and Alcoholic Korsakoff Syndrome

D. Clair, D. Blackwood, J. Christie, 1985, British Journal of Psychiatry.

Candidate Gene Analysis of the Human Natural Killer-1 Carbohydrate Pathway and Perineuronal Nets in Schizophrenia: B3GAT2 Is Associated with Disease Risk and Cortical Surface Area

Anders M. Dale, Elvira Bramon, Ole A. Andreassen, 2011, Biological Psychiatry.

Evidence of Sex-Modulated Association of ZNF804A with Schizophrenia

D. Rujescu, D. Clair, R. Straub, 2011, Biological Psychiatry.

Apolipoprotein E ϵ4 allele frequency in patients with Lewy body dementia, Alzheimer's disease and age-matched controls

D. Clair, A. Brookes, G. Wilcock, 1994, Neuroscience Letters.

Genetics of Alzheimer's Disease

D. Clair, 1994, British Journal of Psychiatry.

Brain-derived neurotrophic factor gene C-270T and Val66Met functional polymorphisms and risk of schizophrenia: A moderate-scale population-based study and meta-analysis

Jurg Ott, Lin He, D. Clair, 2007, Schizophrenia Research.

Apolipoprotein E −491 promoter polymorphism is an independent risk factor for Alzheimer's disease in the Chinese population

D. Clair, G. Feng, J. Zhang, 2003, Neuroscience Letters.

depressionin auditory P3 event-related potential in schizophrenia and

D. Clair, D. Blackwood, J. Christie, 2011 .

Polymorphisms in the TSHR (thyrotropin receptor) gene on chromosome 14q31 are not associated with mental retardation in the iodine-deficient areas of China

D. Clair, S. Duan, Lin He, 2005, Neuroscience Letters.

No association between polymorphisms of methylenetetrahydrofolate reductase gene and schizophrenia in both Chinese and Scottish populations

C. Crombie, N. Walker, D. Collier, 2004, Molecular Psychiatry.

No correlation between HLA-DQ 2.5, DQ 8.1 and DQ 6.2 and circulating levels of antibodies against gliadins in schizophrenia

D. Clair, R. McLean, Jun Wei, 2019, Psychiatry Research.

A survey of rare coding variants in candidate genes in schizophrenia by deep sequencing

D. Clair, S. Lawrie, A. McIntosh, 2013, Molecular Psychiatry.

Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

J. Danesh, M. Daly, M. Hurles, 2016, bioRxiv.

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes.

John P. Rice, Simon C. Potter, Melissa J. Green, 2018, Cell.

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

H. Stefánsson, S. Steinberg, J. Suvisaari, 2019 .

Auditory P300 and eye tracking dysfunction in schizophrenic pedigrees.

J C Duffy, D. Clair, D. Blackwood, 1991, Archives of general psychiatry.

Logical reasoning deficits in schizophrenia

D. Clair, A. Bartolo, V. Goel, 2004, Schizophrenia Research.

Brave New Brain: Conquering Mental Illness in the Era of the Genome

D. Clair, N. Andreasen, Nancy C. Andreasen, 2002, Heredity.

Localization of type 1 diabetes susceptibility to the MHC class I genes HLA-B and HLA-A

Simon C. Potter, C. Spencer, A. Silman, 2007, Nature.

Schizophrenia and affective disorders--cosegregation with a translocation at chromosome 1q42 that directly disrupts brain-expressed genes: clinical and P300 findings in a family.

D J Porteous, D. Clair, D. Blackwood, 2001, American journal of human genetics.

Disruption of two novel genes by a translocation co-segregating with schizophrenia.

Martin S. Taylor, D. Clair, W. Muir, 2000, Human molecular genetics.

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

Thomas W. Mühleisen, A. Hofman, A. Uitterlinden, 2012, Molecular Psychiatry.

Bridging the translational divide: identical cognitive touchscreen testing in mice and humans carrying mutations in a disease-relevant homologous gene

D. Clair, L. Saksida, T. Bussey, 2015, Scientific Reports.

SNP association studies in Alzheimer's disease highlight problems for complex disease analysis.

L. Feuk, D. Clair, A. Brookes, 2001, Trends in genetics : TIG.

The transcriptional factor LBP-1c/CP2/LSF gene on chromosome 12 is a genetic determinant of Alzheimer's disease.

D. Clair, J. Hardy, F. Pasquier, 2000, Human molecular genetics.

A case control and family based association study of the neuregulin1 gene and schizophrenia

D. Clair, Lin He, D. St. Clair, 2004, Journal of Medical Genetics.

Age at first birth in women is genetically associated with increased risk of schizophrenia

Hoffmann, Hartmann, Roussos, 2017, Scientific Reports.

Schizophrenia genetic variants are not associated with intelligence

A F Terwisscha van Scheltinga, S C Bakker, N E M van Haren, 2013, Psychological Medicine.

Tentative association of the serotonin transporter with schizophrenia and unipolar depression but not with bipolar disorder in Han Chinese.

D. Clair, G. Breen, Lin He, 1999, Pharmacogenetics.

Bridging the translational divide : identical cognitive touchscreen testing in mice and humans carrying mutations in a disease-relevant homologous gene

D. Clair, L. Saksida, T. Bussey, 2016 .

The Deiodinase Type 2 (DIO2) Gene and Mental Retardation in Iodine Deficiency

D. Clair, Lin He, T. Guo, 2009 .

Hereditary multi-infarct dementia unlinked to chromosome 19q12 in a large Scottish pedigree: evidence of probable locus heterogeneity.

D. Clair, S. Morris, D. St. Clair, 1995, Journal of medical genetics.

Expanded CAG trinucleotide repeat of Huntington's disease gene in a patient with schizophrenia and normal striatal histology.

D. Clair, 1994 .

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

N. Wray, H. Stefánsson, D. Rujescu, 2019, Nature Genetics.

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

S. Gabriel, M. Daly, D. Collier, 2008, Nature Genetics.

Testing for genetic association between the ZDHHC8 gene locus and susceptibility to schizophrenia: An integrated analysis of multiple datasets

D. Clair, Lin He, Mingqing Xu, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls.

Melissa J. Green, Janice M. Fullerton, Robert C. Thompson, 2019, Biological psychiatry.

Interplay between DISC1 and GABA Signaling Regulates Neurogenesis in Mice and Risk for Schizophrenia

D. Rujescu, D. Clair, J. Callicott, 2012, Cell.

Schizophrenia genetic variants are not associated with intelligence

P. Donnelly, P. Visscher, H. Stefánsson, 2013, Psychological Medicine.

Common variant at 16p11.2 conferring risk of psychosis

M. Pirinen, H. Stefánsson, D. Rujescu, 2014, Molecular Psychiatry.

Latent Effects of Prenatal Malnutrition on Adult Health

D. Clair, E. Susser, Lin He, 2008, Annals of the New York Academy of Sciences.

A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts.

John P. Rice, Warren W. Kretzschmar, Robert M. Maier, 2021, Biological psychiatry.

Sex-Dependent Shared and Non-Shared Genetic Architecture Across Mood and Psychotic Disorders

D. Rujescu, S. Cichon, I. Giegling, 2020, bioRxiv.

Apolipoprotein E ϵ4 allele is a risk factor for late‐onset Alzheimer's disease and vascular dementia in Han Chinese

D. Clair, G. Breen, D. St. Clair, 2001, International journal of geriatric psychiatry.

MULTIVARIATE EYE MOVEMENT PSYCHOPHYSIOLOGY ACCURATELY DIFFERENTIATES SCHIZOPHRENIA CASES FROM UNAFFECTED CONTROLS

P. Benson, D. Rujescu, D. Clair, 2010, Schizophrenia Research.

Visual scanpaths as a generalised deficit in schizophrenia

P. Benson, D. Rujescu, I. Giegling, 2010 .

A polymorphism in the presenilin 1 gene does not modify risk for Alzheimer's disease in a cohort with sporadic early onset

D. Clair, A. Myers, A. Goate, 1997, Neuroscience Letters.

LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

D. Geschwind, D. Rujescu, P. Muglia, 2007, Molecular Psychiatry.

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

Thomas W. Mühleisen, H. Stefánsson, D. Rujescu, 2011 .

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