Citation Impact
Citing Papers
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
2009 Standout
Human-specific gene ARHGAP11B promotes basal progenitor amplification and neocortex expansion
2015 StandoutScienceNobel
Homeostatic maintenance of natural Foxp3 + CD25+ CD4+ regulatory T cells by interleukin (IL)-2 and induction of autoimmune disease by IL-2 neutralization
2005 StandoutNobel
Serotonin Transporter Genetic Variation and the Response of the Human Amygdala
2002 StandoutScience
Beyond SEM: General Latent Variable Modeling
2002
Deep Brain Stimulation for Treatment-Resistant Depression
2005 Standout
Pregnancy, Delivery, and Neonatal Complications in a Population Cohort of Women With Schizophrenia and Major Affective Disorders
2004
The UK Biobank resource with deep phenotyping and genomic data
2018 StandoutNature
Association study of polymorphisms in synaptic vesicle-associated genes, SYN2 and CPLX2, with schizophrenia
2005
Medication Augmentation after the Failure of SSRIs for Depression
2006 Standout
Schizophrenia risk from complex variation of complement component 4
2016 StandoutNature
No health without mental health
2007 Standout
Altered brain microRNA biogenesis contributes to phenotypic deficits in a 22q11-deletion mouse model
2008
RIM1α and Interacting Proteins Involved in Presynaptic Plasticity Mediate Prepulse Inhibition and Additional Behaviors Linked to Schizophrenia
2010 StandoutNobel
Child abuse: Adolescent records vs. adult recall
1990 Standout
Molecular Characterization of Schizophrenia Viewed by Microarray Analysis of Gene Expression in Prefrontal Cortex
2000
A 3-Mb Map of a Large Segmental Duplication Overlapping the α7-Nicotinic Acetylcholine Receptor Gene (CHRNA7) at Human 15q13–q14
2002
Nicotinic acetylcholine receptors: from structure to brain function
2003
A Genomewide Screen for Schizophrenia Genes in an Isolated Finnish Subpopulation, Suggesting Multiple Susceptibility Loci
1999
Income Differences in Persons Seeking Outpatient Treatment for Mental Disorders
2000
Mouse genetic models for prepulse inhibition: an early review
2002
Cholinergic agonists inhibit HMGB1 release and improve survival in experimental sepsis
2004 Standout
Anatomical and physiological evidence for D1 and D2 dopamine receptor colocalization in neostriatal neurons
2000 StandoutNobel
Linkage and associated studies of schizophrenia
2000
Signal Transduction by the JNK Group of MAP Kinases
2000 Standout
Ultradian rapid cycling in prepubertal and early adolescent bipolarity is not in transmission disequilibrium with val/met COMT alleles
2000
Genetic linkage and association between chromosome 1q and working memory function in schizophrenia
2002
Schizophrenia and the α7 Nicotinic Acetylcholine Receptor
2007
Schizophrenia
2009 Standout
Are the Dorsal and Ventral Hippocampus Functionally Distinct Structures?
2010 Standout
Gene-Environment Interactions in Schizophrenia: Review of Epidemiological Findings and Future Directions
2008
The synapsins: Key actors of synapse function and plasticity
2010
The role of hippocampus in the pathophysiology of bipolar disorder
2007
MicroRNA target site polymorphisms and human disease
2008
Bipolar and major depressive disorder: Neuroimaging the developmental-degenerative divide
2009
Natural Selection in the Great Apes
2016
Global variation in the frequencies of functionally different catechol-O-methyltransferase alleles
1999
Prefrontal neurons and the genetics of schizophrenia
2001
Item response mixture modeling: Application to tobacco dependence criteria
2006
Neurobiology of schizophrenia
1997
cDNA Cloning and Mapping of a Novel Islet-Brain/JNK-Interacting Protein
2000
Relative Risk of Attention Deficits in Siblings of Patients With Schizophrenia
2000
Genome-wide scan for schizophrenia in the Finnish population: evidence for a locus on chromosome 7q22
2000
Molecular Mechanisms of Depression: Perspectives on New Treatment Strategies
2013 Standout
Metazoan MicroRNAs
2018 Standout
Relative risk for cognitive impairments in siblings of patients with schizophrenia
2001
Palmitoylation-dependent neurodevelopmental deficits in a mouse model of 22q11 microdeletion
2008
High Rates of Schizophrenia in Adults With Velo-Cardio-Facial Syndrome
1999
The immunoglobulin superfamily of neuronal cell adhesion molecules: Lessons from animal models and correlation with human disease
2008
Wnt/β-Catenin Signaling: Components, Mechanisms, and Diseases
2009 Standout
Pannexin 1 channels mediate ‘find-me’ signal release and membrane permeability during apoptosis
2010 StandoutNature
A genomewide linkage study of age at onset in schizophrenia*
2001
Should substance use disorders be considered as categorical or dimensional?
2006
Rethinking schizophrenia
2010 StandoutNature
The mammalian pannexin family is homologous to the invertebrate innexin gap junction proteins
2004
Indicators of socioeconomic position (part 2)
2006 Standout
A gene expression atlas of the central nervous system based on bacterial artificial chromosomes
2003 StandoutNature
Environmental animal models for sensorimotor gating deficiencies in schizophrenia: a review
2001
Indicators of socioeconomic position (part 1): Figure 1
2005 Standout
Tissue Multicolor STED Nanoscopy of Presynaptic Proteins in the Calyx of Held
2013 StandoutNobel
Functional mapping and annotation of genetic associations with FUMA
2017 Standout
22q11.2 microdeletions: linking DNA structural variation to brain dysfunction and schizophrenia
2010
The BDNF val66met Polymorphism Affects Activity-Dependent Secretion of BDNF and Human Memory and Hippocampal Function
2003 Standout
The Endophenotype Concept in Psychiatry: Etymology and Strategic Intentions
2003 Standout
The ups and downs of Wnt signaling in prevalent neurological disorders
2006
The interpersonal theory of suicide.
2010 Standout
Thalamic miR-338-3p mediates auditory thalamocortical disruption and its late onset in models of 22q11.2 microdeletion
2016
The glial growth factors deficiency and synaptic destabilization hypothesis of schizophrenia
2002
A Placebo-Controlled Comparison of Lithium and Triiodothyronine Augmentation of Tricyclic Antidepressants in Unipolar Refractory Depression
1993
A Turning Point in Schizophrenia Genetics
1997
Seeking Verisimilitude in a Class: A Systematic Review of Evidence That the Criterial Clinical Symptoms of Schizophrenia Are Taxonic
2009
Genome-wide association studies of brain imaging phenotypes in UK Biobank
2018 Nature
22q11.2 deletion syndrome
2015 Standout
Family-based linkage disequilibrium mapping using SNP marker haplotypes: application to a potential locus for schizophrenia at chromosome 22q11
2000
Positive association between synapsin II and schizophrenia
2004
Schizophrenia genetics at the millennium: cautious optimism
1997
Large-Scale Microarray Studies of Gene Expression in Multiple Regions of the Brain in Schizophrenia and Alzheimer's Disease
2005
Lack of association of functional cathechol-O-methyltransferase gene polymorphism in schizophrenia
1997
Organoid single-cell genomic atlas uncovers human-specific features of brain development
2019 StandoutNatureNobel
Parkinson's Disease
2003 Standout
Quadruplex DNA: sequence, topology and structure
2006 Standout
MDGAs interact selectively with neuroligin-2 but not other neuroligins to regulate inhibitory synapse development
2012 StandoutNobel
Catechol- O -methyltransferase-deficient mice exhibit sexually dimorphic changes in catecholamine levels and behavior
1998
A catechol- O -methyltransferase that is essential for auditory function in mice and humans
2008 StandoutNobel
Cortex mapping reveals regionally specific patterns of genetic and disease-specific gray-matter deficits in twins discordant for schizophrenia
2002
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11.
1995
Integrating Person‐Centered and Variable‐Centered Analyses: Growth Mixture Modeling With Latent Trajectory Classes
2000 Standout
lavaan: AnRPackage for Structural Equation Modeling
2012 Standout
Targeting protein palmitoylation: selective inhibitors and implications in disease
2014
AnFgf8mouse mutant phenocopies human 22q11 deletion syndrome
2002 StandoutNobel
Prevalence, Severity, and Unmet Need for Treatment of Mental Disorders in the World Health Organization World Mental Health Surveys
2004 Standout
The Human Genome Project and Its Impact on Psychiatry
2002
Human-specific endogenous retroviral insert serves as an enhancer for the schizophrenia-linked genePRODH
2013
Click-Chemistry Based High Throughput Screening Platform for Modulators of Ras Palmitoylation
2017 StandoutNobel
Frontotemporal lobar degeneration
1998 Standout
Linkage disequilibrium on theCOMT gene in French schizophrenics and controls
1999
Linkage disequilibrium for schizophrenia at the chromosome 15q13-14 locus of the ?7-nicotinic acetylcholine receptor subunit gene (CHRNA7)
2001
An update on regional brain volume differences associated with mood disorders
2005
No evidence for allelic association between schizophrenia and a polymorphism determining high or low catechol O-methyltransferase activity
1996
Deciding on the Number of Classes in Latent Class Analysis and Growth Mixture Modeling: A Monte Carlo Simulation Study
2007 Standout
Effect of COMT Val 108/158 Met genotype on frontal lobe function and risk for schizophrenia
2001 Standout
Clustering of non-major histocompatibility complex susceptibility candidate loci in human autoimmune diseases
1998
Brief Screening for Family Psychiatric History: The Family History Screen
2000
The Emergence of Modern Neuroscience: Some Implications for Neurology and Psychiatry
2000 StandoutNobel
Seasonality in Psychiatry — A Review*
1992
Emotional processing of fear: Exposure to corrective information.
1986 Standout
Schizophrenia as a Disorder of Neurodevelopment
2002
Mediation Analysis
2006 Standout
The learning theory model of neurosis—A new approach
1976
Neurodevelopmental Outcomes in Children With Congenital Heart Disease: Evaluation and Management
2012 Standout
Mouse neurexin-1α deletion causes correlated electrophysiological and behavioral changes consistent with cognitive impairments
2009 StandoutNobel
LEF-1 is crucial for neutrophil granulocytopoiesis and its expression is severely reduced in congenital neutropenia
2006 Standout
LINKAGE ANALYSIS IN PSYCHIATRIC DISORDERS : The Emerging Picture
2002
Works of Ann E. Pulver being referenced
The power of analysis: Statistical perspectives. Part 2
1988
Risk Factors in Schizophrenia
1992
Psychotic Illness in Patients Diagnosed with Velo-Cardio-Facial Syndrome and Their Relatives
1994
Functional Consequences of PRODH Missense Mutations
2005
Psychotic inpatients' social class and their first admission to state or private psychiatric Baltimore hospitals.
1994
Identification of Sequence Variants and Analysis of the Role of the Catechol-O-Methyl-Transferase Gene in Schizophrenia Susceptibility
1998
Report from the Maryland epidemiology schizophrenia linkage study: No evidence for linkage between schizophrenia and a number of candidate and other genomic regions using a complex dominant model
1994
Hippocampal and ventricular volumes in psychotic and nonpsychotic bipolar patients compared with schizophrenia patients and community control subjects: A pilot study
2005
Search for schizophrenia susceptibility genes
2000
Schizophrenia: A genome scan targets chromosomes 3p and 8p as potential sites of susceptibility genes
1995
Psychiatric morbidity in the relatives of patients with DSM-III schizophreniform disorder: Comparisons with the relatives of schizophrenic and bipolar disorder patients
1991
No missense mutation of WKL1 in a subgroup of probands with schizophrenia
2002
No evidence for linkage between schizophrenia and markers at chromosome 15q13-14
1999
Estimating effects of proband characteristics on familial risk: II. The association between age at onset and familial risk in the Maryland schizophrenia sample
1991
Availability of schizophrenic patients and their families for genetic linkage studies: Findings from the Maryland epidemiology sample
1989
Overrepresentation of rare variants in a specific ethnic group may confuse interpretation of association analyses
2006
Fine Mapping on Chromosome 10q22-q23 Implicates Neuregulin 3 in Schizophrenia
2009
Genome‐wide association study of schizophrenia in Ashkenazi Jews
2015
Linkage and sib-pair analysis reveal a potential schizophrenia susceptibility gene on chromosome 13q32
1996
Differences in social class among psychotic patients at inpatient admission
1995
Risk Factors in Schizophrenia: Season of Birth in Maryland, USA
1983
Human Behavior Genetics
1976
Hyperprolinaemia in patients with deletion (22)(q11.2) syndrome
2000
An Evaluation of the Structure of Schizophrenia Spectrum Personality Disorders
1994