Citation Impact
Citing Papers
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Identification of a novel neuregulin 1 at-risk haplotype in Han schizophrenia Chinese patients, but no association with the Icelandic/Scottish risk haplotype
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The Molecular Genetics of Schizophrenia
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DNA pooling analysis of ADHD and genes regulating vesicle release of neurotransmitters
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2005
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2000
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2004
Parvalbumin neurons and gamma rhythms enhance cortical circuit performance
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No evidence for association of the dysbindin gene [DTNBP1] with schizophrenia in an Irish population-based study
2003
Association Between a Functional Catechol O-Methyltransferase Gene Polymorphism and Schizophrenia: Meta-Analysis of Case-Control and Family-Based Studies
2003
Association of the dopamine D5 receptor with attention deficit hyperactivity disorder (ADHD) and scores on a continuous performance test (TOVA)
2004
Lack of association of functional cathechol-O-methyltransferase gene polymorphism in schizophrenia
1997
The Genetics of Symptom-Based Phenotypes: Toward a Molecular Classification of Schizophrenia
2008
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1999
The Deacetylase HDAC6 Regulates Aggresome Formation and Cell Viability in Response to Misfolded Protein Stress
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2006
Antibody-Mediated Encephalitis
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A catechol- O -methyltransferase that is essential for auditory function in mice and humans
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Induced chromosome deletions cause hypersociability and other features of Williams–Beuren syndrome in mice
2009
Tbx1 controls cardiac neural crest cell migration during arch artery development by regulatingGbx2expression in the pharyngeal ectoderm
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Neurobiological consequences of maternal cannabis on human fetal development and its neuropsychiatric outcome
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The clinical presentation of attention deficit‐hyperactivity disorder (ADHD) in children with 22q11.2 deletion syndrome
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Diagnosis and Treatment of Parkinson Disease
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Male circumcision: assessment of health benefits and risks.
1998
Evidence for association of schizophrenia with genetic variation in the 8p21.3 gene,PPP3CC, encoding the calcineurin gamma subunit
2003 Nobel
Haplotype relative risk study of catechol-O-methyltransferase (COMT) and attention deficit hyperactivity disorder (ADHD): Association of the high-enzyme activity val allele with adhd impulsive-hyperactive phenotype
1999
Quantum Dot-Based Multiplexed Fluorescence Resonance Energy Transfer
2005 StandoutNobel
Cortical inhibitory neurons and schizophrenia
2005 Standout
p53 suppression partially rescues the mutant phenotype in mouse models of DiGeorge syndrome
2014
22q11 deletion syndrome in adults with schizophrenia
1998
The cell-adhesion G protein-coupled receptor BAI3 is a high-affinity receptor for C1q-like proteins
2011 StandoutNobel
DISC1 splice variants are upregulated in schizophrenia and associated with risk polymorphisms
2009
A General Mechanism for Network-Dosage Compensation in Gene Circuits
2010 StandoutScienceNobel
The genetics of schizophrenia: glutamate not dopamine?
2003
Three phases of DiGeorge/22q11 deletion syndrome pathogenesis during brain development: Patterning, proliferation, and mitochondrial functions of 22q11 genes
2010
The Human Genome Project and Its Impact on Psychiatry
2002
Single-nanometer iron oxide nanoparticles as tissue-permeable MRI contrast agents
2021 StandoutNobel
Catechol-O-methyltransferase (COMT): Biochemistry, Molecular Biology, Pharmacology, and Clinical Efficacy of the New Selective COMT Inhibitors
1999
Influence of Life Stress on Depression: Moderation by a Polymorphism in the 5-HTT Gene
2003 StandoutScience
Linkage disequilibrium on theCOMT gene in French schizophrenics and controls
1999
Virioplankton: Viruses in Aquatic Ecosystems
2000 Standout
Evidence for association of DNA sequence variants in the phosphatidylinositol-4-phosphate 5-kinase IIα gene (PIP5K2A) with schizophrenia
2006
Location of a Major Susceptibility Locus for Familial Schizophrenia on Chromosome 1q21-q22
2000 Science
Temporomandibular Disorders
2008 Standout
The discovery of susceptibility genes for mental disorders
2002
Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development
2012 StandoutNobel
Effect of COMT Val 108/158 Met genotype on frontal lobe function and risk for schizophrenia
2001 Standout
Links between genetics and pathophysiology in the autism spectrum disorders
2011
Dysbindin-1 is reduced in intrinsic, glutamatergic terminals of the hippocampal formation in schizophrenia
2004
Does the Intrapelvic Compartment Syndrome Exist?
1998
Mouse neurexin-1α deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments
2009 StandoutNobel
LINKAGE ANALYSIS IN PSYCHIATRIC DISORDERS : The Emerging Picture
2002
Molecular Genetics of Attention-Deficit/Hyperactivity Disorder
2005 Standout
Fluorescence Resonance Energy Transfer Between Quantum Dot Donors and Dye-Labeled Protein Acceptors
2003 StandoutNobel
Works of Nigel Williams being referenced
Further support for an association between a polymorphic CAG repeat in the hKCa3 gene and schizophrenia
1998
Chromosome 4 workshop summary: Sixth World Congress on Psychiatric Genetics, Bonn, Germany, October 6-10, 1998
1999
Follow-up of genetic linkage findings on chromosome 16p13: evidence of association of N-methyl-D aspartate glutamate receptor 2A gene polymorphism with ADHD
2004
Gene copy number variation in schizophrenia
2007
Operation of the Schizophrenia Susceptibility Gene, Neuregulin 1, Across Traditional Diagnostic Boundaries to Increase Risk for Bipolar Disorder
2005
Strong evidence that GNB1L is associated with schizophrenia
2007
Genomewide Linkage Scan in Schizoaffective Disorder
2005
Determination of the genomic structure and mutation screening in schizophrenic individuals for five subunits of the N-methyl-D-aspartate glutamate receptor
2002
Haplotypes at the dystrobrevin binding protein 1 (DTNBP1) gene locus mediate risk for schizophrenia through reduced DTNBP1 expression
2005
Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis
2010
Molecular Mechanisms in 22q11 Deletion Syndrome
2011
Recent advances in the genetics of schizophrenia
2003
Mutation screening and LD mapping in the VCFS deleted region of chromosome 22q11 in schizophrenia using a novel DNA pooling approach
2002
No evidence for an allelic association between schizophrenia and markers D22S278 and D22S283
1997
A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs
1999
Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools
2002
Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility
2006
Autosome search for schizophrenia susceptibility genes in multiply affected families
1999
DNA Pooling Identifies QTLs on Chromosome 4 for General Cognitive Ability in Children
1999
Is the Dysbindin Gene (DTNBP1) a Susceptibility Gene for Schizophrenia?
2005
Cheap, accurate and rapid allele frequency estimation of single nucleotide polymorphisms by primer extension and DHPLC in DNA pools
2000
Genome scans and microarrays: converging on genes for schizophrenia?
2002
Genotype effects of CHRNA7, CNR1 and COMT in schizophrenia: interactions with tobacco and cannabis use
2007
No evidence for association between a non-synonymous polymorphism in the gene encoding human metabotropic glutamate receptor 7 and schizophrenia
2000
A genomewide linkage study of age at onset in schizophrenia*
2001
Gluteal compartment syndrome following drug overdose
1992
No Association Between Schizophrenia and Polymorphisms in COMT in Two Large Samples
2005
Identification in 2 Independent Samples of a Novel Schizophrenia RiskHaplotype of the Dystrobrevin Binding Protein Gene (DTNBP1)
2004
Multicenter Linkage Study of Schizophrenia Candidate Regions on Chromosomes 5q, 6q, 10p, and 13q: Schizophrenia Linkage Collaborative Group III
2000
A study of chromosome 4p markers and dopamine D5 receptor gene in schizophrenia and bipolar disorder
1998
No evidence for association between polymorphisms in GRM3and schizophrenia
2005
Vascular disease and vascular risk factors in relation to motor features and cognition in early Parkinson's disease
2016
Strong evidence for association between the dystrobrevin binding protein 1 gene (DTNBP1) and schizophrenia in 488 parent-offspring trios from Bulgaria
2004
Support for RGS4 as a susceptibility gene for schizophrenia
2004
Suggestive evidence for linkage of schizophrenia to markers on chromosome 13q14.1-q32
1995
Schizophrenia and functional polymorphisms in the MAOA and COMT genes: No evidence for association or epistasis
2002
The molecular genetics of schizophrenia: new findings promise new insights
2003
Developing and validating Parkinson’s disease subtypes and their motor and cognitive progression
2018
A Haplotype Implicated in Schizophrenia Susceptibility Is Associated with Reduced COMT Expression in Human Brain
2003
Support for Neuregulin 1 as a Susceptibility Gene for Bipolar Disorder and Schizophrenia
2008
Localization of the Gene for Distal Hereditary Motor Neuronopathy VII (dHMN-VII) to Chromosome 2q14
2001
Evidence that interaction between neuregulin 1 and its receptor erbB4 increases susceptibility to schizophrenia
2005
CAG repeat length in the hKCa3 gene and symptom dimensions in schizophrenia
1999
Investigating the Contribution of Common Genetic Variants to the Risk and Pathogenesis of ADHD
2011
Further evidence for high rates of schizophrenia in 22q11.2 deletion syndrome
2014
Support for genetic variation in neuregulin 1 and susceptibility to schizophrenia
2003
Genotyping single nucleotide polymorphisms by primer extension and high performance liquid chromatography
1999
Complications of circumcision
1993
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans: Implications for 22q11 deletion syndrome
2006
No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity
1996
Report of the chromosome 18 workshop
1999
Phage Transfer: A New Player Turns Up in Cholera Infection
1996 Science