Elliot S Gershon: Influence Statistics

Elliot S Gershon

Elliot S Gershon

Department of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, IL, USA | Department of Psychiatry, Department of Human Genetics, University of Chicago, ...

Elliot S Gershon: Expert Impact

Concepts for which Elliot S Gershon has direct influence: Bipolar disorder , Psychotic disorders , Affective disorders , Affective disorder , Human pair , Affective illness , Attempted suicide .

Elliot S Gershon: KOL impact

Concepts related to the work of other authors for which for which Elliot S Gershon has influence: Bipolar disorder , Dna methylation , Major depression , Gene expression , Anorexia nervosa , Human pair , Mental health .

KOL Resume for Elliot S Gershon

Year
2022

Department of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, IL, USA

University of Chicago, Chicago, IL, United States of America.

2021

Department of Psychiatry, University of Chicago, Chicago, Illinois, USA

University of Chicago, United States

2020

University of Chicago, Department of Psychiatry and Behavioral Neurosciences;

2019

Department of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, IL, United States. Electronic address:

University of Chicago, 5841 S. Maryland Ave, Chicago, IL, 60637, USA.

2018

Department of Psychiatry and Behavioral Neurosciences, University of Chicago, Chicago, IL, USA

2017

Department of Psychiatry, Department of Human Genetics, University of Chicago, United States

University of Chicago;

2016

Department of Psychiatry, University of Chicago, Chicago, IL USA

2015

Department of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, Illinois

2014

Department of Psychiatry and Behavioral Neuroscience; Department of Human Genetics; University of Chicago, Illinois, USA.

2013

From the Department of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago.

Department of Psychiatry, Institute of Human Genetics, The University of Illinois at Chicago, Chicago, IL 60607 (LC, CZ and CL), the Laboratory for Molecular Psychiatry, RIKEN Brain Science Institute, Saitama 351-0198, and Sangenjaya Station Mental Health Clinic, Tokyo 154-0024, Japan (EH), the Department of Neuropsychopharmacology and Hospital Pharmacy, Nagoya University Graduate School of Medicine, Nagoya, 466-8560 Japan (AN), the Department of Psychiatry and Behavioral Neuroscience, The University of Chicago, Chicago, IL 60637 (NAS, MDO, KG, SCD, ESG), and the Department of Cell Biology and Anatomy, Louisiana State University Health Sciences Center, New Orleans, LA 70112 (YPT)

2012

Department of Psychiatry and Behavioral Neuroscience, The University of Chicago, Chicago, IL, US 60637

2011

Department of Psychiatry and Behavioral Neuroscience, The University of Chicago, Chicago, Illinois, United States of America

2010

Department of Human Genetics, The University of Chicago, Chicago, IL 60637, USA

2009

Departments of Psychiatry and Human Genetics, the University of Chicago, Chicago, Illinois, United States of America

Department of Human Genetics, University of Chicago, Chicago, Illinois

2008

Department of Human Genetics, University of Chicago, Chicago, IL 60637, USA

2007

Department of Psychiatry, The University of Chicago, Chicago, Illinois

2006

University of Chicago, Chicago, Illinois

2005

US Department of Health and Human Services, NIMH Genetics Initiative Bipolar Consortium, National Institute of Mental Health, National Institutes of Health, Bethesda, MD, USA

2004

Laboratory of Clinical Science (DLM), National Institute of Mental Health, Bethesda;, USA

2003

Department of Psychiatry (FJM, ESG, JAB), University of Chicago, Chicago, Illinois, USA

2002

Department of Psychiatry, The University of Chicago, Chicago, Illinois, 60637, USA

2001

Department of Psychiatry, University of Chicago, Chicago, III, USA.

2000

Clinical Neurogenetics Branch, National Institute of Mental Health, National Institutes of Health, Bethesda, Maryland

Dept of Psychiatry, University of Chicago, Chicago, IL, USA

1999

Clinical Neurogenetics Branch, National Institute of Mental Health, and Genetic Epidemiology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892; Department of Psychiatry, University of Chicago, Chicago, IL 60637; Center for Neurobiology and Behavior, Department of Psychiatry, University of Pennsylvania, Philadelphia, PA 19104; and Medical and Molecular Genetics and Psychiatry, Indiana University, Indianapolis, IN 46202

National Institute of Mental Health, Bethesda, Maryland

University of Chicago, Illinois

1998

Clinical Neurogenetics Branch, National Institute of Mental Health, Bethesda

1997

Clinical Neurogenetics Branch, National Institute of Mental Health, Bethesda, Maryland, 20892

National Institutes of Mental Health, Bethesda, Maryland

Prominent publications by Elliot S Gershon

KOL-Index: 16736 . BACKGROUND: Difficulty recognizing facial emotions is an important social-cognitive deficit associated with psychotic disorders. It also may reflect a familial risk for psychosis in schizophrenia-spectrum disorders and bipolar disorder. OBJECTIVE: The objectives of this study from the Bipolar-Schizophrenia Network on Intermediate Phenotypes (B-SNIP) consortium were to: 1) compare emotion ...
Known for Bipolar Disorder | Emotion Recognition | Intermediate Phenotypes | Deficits Schizophrenia
KOL-Index: 16367 . OBJECTIVE: Familial neuropsychological deficits are well established in schizophrenia but remain less well characterized in other psychotic disorders. This study from the Bipolar-Schizophrenia Network on Intermediate Phenotypes (B-SNIP) consortium 1) compares cognitive impairment in schizophrenia and bipolar disorder with psychosis, 2) tests a continuum model of cognitive dysfunction in ...
Known for Psychotic Bipolar | Cognitive Impairments | Disorder Schizophrenia | Intermediate Phenotypes
KOL-Index: 14821 . BACKGROUND: Bipolar disorder is a serious and common psychiatric disorder characterized by manic and depressive mood switches and a relapsing and remitting course. The cornerstone of clinical management is stabilization and prophylaxis using mood-stabilizing medications to reduce both manic and depressive symptoms. Lithium remains the gold standard of treatment with the strongest data for ...
Known for Lithium Response | Bipolar Disorder | Genome Wide | Valproic Acid
KOL-Index: 13966 . Measurements of dopamine-beta-hydroxylase (DBH), catechol-O-methyltransferase (COMT), and monoamine oxidase (MAO) along with 27 polymorphic marker phenotypes were available for 162 patients with major affective disorders and 1,125 of their relatives. Levels of enzymes were previously found not to be associated with illness. Pedigree analysis methods for quantitative traits are used to test ...
Known for Dbh Activity | Abo Locus | Linkage Studies | Monoamine Oxidase
KOL-Index: 13167 . An initial genome scan was performed on 540 individuals from 97 families segregating bipolar disorder, collected through the National Institutes of Mental Health Genetics Initiative. We report here affected-sib-pair (ASP) data on 126 marker loci (approximately 68,000 genotypes) mapping to chromosomes 4, 7, 9, 18, 19, 20, and 21q, under three affection status models. Modest increases in ...
Known for Chromosomes Human | Mental Health | Genome Scan | Genetics Initiative
KOL-Index: 12992 . As part of the four-center NIMH Genetics Initiative on Bipolar Disorder we carried out a genomic scan of chromosomes 3, 5, 15, 16,17, and 22. Genotyping was performed on a set of 540 DNAs from 97 families, enriched for affected relative pairs and parents where available. We report here the results of the initial 74 markers that have been typed on this set of DNAs. The average distance ...
Known for Chromosomes Human | Nimh Genetics Initiative | Linkage Bipolar Disorder | Region Chromosome
KOL-Index: 12880 . Linkage evidence suggests that chromosome 13 (13q32-33) contains susceptibility genes for both bipolar disorder and schizophrenia. Recently, genes called "G72" and "G30" were identified, and polymorphisms of these overlapping genes were reported to be associated with schizophrenia. We studied two series of pedigrees with bipolar disorder: the Clinical Neurogenetics (CNG) pedigrees (in ...
Known for G72 G30 | Gene Locus | Bipolar Disorder Schizophrenia | Pedigree Series
KOL-Index: 12840 . OBJECTIVE: Panic attacks are a common complication of affective disorder, although the etiologic relationship of panic and affective symptoms has not been determined. Evidence from a family study suggests that panic attacks and panic disorder may be related genetically to bipolar disorder. This study used diagnostic data from the NIMH Bipolar Disorder Genetics Initiative to assess in a ...
Known for Panic Disorder | Degree Relatives | Comorbid Bipolar | Major Affective
KOL-Index: 12706 . Several previous studies suggest that dysfunction of circadian rhythms may increase susceptibility to bipolar disorder (BP). We conducted an association study of five circadian genes (CRY2, PER1-3, and TIMELESS) in a family collection of 36 trios and 79 quads (Sample I), and 10 circadian genes (ARNTL, ARNTL2, BHLHB2, BHLHB3, CLOCK, CRY1, CSNK1D, CSNK1E, DBP, and NR1D1) in an extended ...
Known for Clock Gene | Bipolar Disorder | Circadian Rhythm | Association Snps
KOL-Index: 12408 . A report on an initial genome screen on 540 individuals in 97 families was collected as part of the NIMH Genetics Initiative on Bipolar Disorder. Families were ascertained to be informative for genetic linkage and underwent a common ascertainment and assessment protocol at four clinical sites. The sample was genotyped for 65 highly polymorphic markers from chromosomes 1, 6, 8, 10, and 12. ...
Known for Human Pair | Chromosomes 1 | Nimh Genetics Initiative | Initial Genome Scan
KOL-Index: 12259 . We report on an initial genome screen of 540 individuals from 97 families collected as part of the NIMH Genetics Initiative Bipolar Group. Among the individuals studied, 232 were diagnosed with bipolar (BP) I, 72 with BPII, 88 with major depressive disorder-recurrent type (UPR), and 32 with schizoaffective disorder, bipolar type (SA/BP). A total of 53 markers on chromosomes 2, 11, 13, 14, ...
Known for Chromosomes 2 | Bipolar Disorder | Human Pair | Genome Screen
KOL-Index: 12038 . We conducted a systematic study of top susceptibility variants from a genome-wide association (GWA) study of bipolar disorder to gain insight into the functional consequences of genetic variation influencing disease risk. We report here the results of experiments to explore the effects of these susceptibility variants on DNA methylation and mRNA expression in human cerebellum samples. ...
Known for Bipolar Disorder | Gene Expression | Trait Loci | Methylation Quantitative
KOL-Index: 11314 . We have investigated whether there is a locus on chromosome 6 that confers an increased susceptibility to schizophrenia using a two-stage approach and nonparametric linkage analysis. Allele sharing identical by descent (IBD) and multipoint maximum likelihood score (MLS) statistics were employed. Results from two tested data sets, a first data set, or genome scanning data set, and a second ...
Known for Susceptibility Locus | Suggestive Evidence | Chromosome 6q | Human Pair

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Department of Psychiatry and Behavioral Neuroscience, University of Chicago, Chicago, IL, USA | Department of Psychiatry, Department of Human Genetics, University of Chicago, Chicago, IL, USA | University of Chicago | Department of Psychiatry, Univer