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Author Details

Jesen Fagerness
Center for Human Genetic Research, Massachusetts General Hospital
2005
48
38
PMIDPaper TitleJournal TitlePublished Year
27138112COMT Val(158) Met genotype is associated with reward learning: a replication study and meta-analysis.Genes Brain Behav2016
25158072Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.Am J Psychiatry2015
26030725Pharmacogenomic and pharmacogenetic-guided therapy as a tool in precision medicine: current state and factors impacting acceptance by stakeholders.Genet Res (Camb)2015
24399358The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data.Brain Imaging Behav2014
25326929Pharmacogenetic-guided psychiatric intervention associated with increased adherence and cost savings.Am J Manag Care2014
25062598Copy number variation in obsessive-compulsive disorder and tourette syndrome: a cross-disorder study.J Am Acad Child Adolesc Psychiatry2014
25033836(Epi)Genetic analyses of age-related macular degeneration: case-control and discordant twin studies.Hum Hered2014
24911414Allele-specific methylation occurs at genetic variants associated with complex disease.PLoS One2014
22889921Genome-wide association study of obsessive-compulsive disorder.Mol Psychiatry2013
23606572Meta-analysis of association between obsessive-compulsive disorder and the 3' region of neuronal glutamate transporter gene SLC1A1.Am J Med Genet B Neuropsychiatr Genet2013
23455636Seven new loci associated with age-related macular degeneration.Nat Genet2013
22889924Genome-wide association study of Tourette's syndrome.Mol Psychiatry2013
22504417Identification of common variants associated with human hippocampal and intracranial volumes.Nat Genet2012
22705344Heritability and genome-wide association study to assess genetic differences between advanced age-related macular degeneration subtypes.Ophthalmology2012
20370803Association between polymorphisms in GRIK2 gene and obsessive-compulsive disorder: a family-based study.CNS Neurosci Ther2011
21917807Corticotropin-releasing hormone receptor type 1 (CRHR1) genetic variation and stress interact to influence reward learning.J Neurosci2011
21665990Common variants near FRK/COL10A1 and VEGFA are associated with advanced age-related macular degeneration.Hum Mol Genet2011
21508513Corticotrophin-releasing hormone type 1 receptor gene (CRHR1) variants predict posttraumatic stress disorder onset and course in pediatric injury patients.Dis Markers2011
21447678Association of variants in the LIPC and ABCA1 genes with intermediate and large drusen and advanced age-related macular degeneration.Invest Ophthalmol Vis Sci2011
21122828ARMS2/HTRA1 locus can confer differential susceptibility to the advanced subtypes of age-related macular degeneration.Am J Ophthalmol2011
21184590Family-based genetic association study of DLGAP3 in Tourette Syndrome.Am J Med Genet B Neuropsychiatr Genet2011
19388002Phenotypic effects of a bipolar liability gene among individuals with major depressive disorder.Am J Med Genet B Neuropsychiatr Genet2010
20528958The impact of mineralocorticoid receptor ISO/VAL genotype (rs5522) and stress on reward learning.Genes Brain Behav2010
20581873Associations of CFHR1-CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent.Nat Genet2010
20385826Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC).Proc Natl Acad Sci U S A2010
20385819Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration.Proc Natl Acad Sci U S A2010
19844262Genetic profile for five common variants associated with age-related macular degeneration in densely affected families: a novel analytic approach.Eur J Hum Genet2010
19621370Variation in TREK1 gene linked to depression-resistant phenotype is associated with potentiated neural responses to rewards in humans.Hum Brain Mapp2010
18685559Variation near complement factor I is associated with risk of advanced AMD.Eur J Hum Genet2009
19117936Prediction model for prevalence and incidence of advanced age-related macular degeneration based on genetic, demographic, and environmental variables.Invest Ophthalmol Vis Sci2009
17876324Further evidence of association between two NET single-nucleotide polymorphisms with ADHD.Mol Psychiatry2008
18937309Sexually dimorphic effects of four genes (COMT, SLC6A2, MAOA, SLC6A4) in genetic associations of ADHD: a preliminary study.Am J Med Genet B Neuropsychiatr Genet2008
18632255Association of SNPs and haplotypes in APOL1, 2 and 4 with schizophrenia.Schizophr Res2008
18288090Pharmacogenetic analysis of genes implicated in rodent models of antidepressant response: association of TREK1 and treatment resistance in the STAR(*)D study.Neuropsychopharmacology2008
18316676Influence of RGS2 on anxiety-related temperament, personality, and brain function.Arch Gen Psychiatry2008
18413575Lack of association between SLITRK1var321 and Tourette syndrome in a large family-based sample.Neurology2008
18180429Family-based association study of lithium-related and other candidate genes in bipolar disorder.Arch Gen Psychiatry2008
17455213Investigation of variation in SNAP-25 and ADHD and relationship to co-morbid major depressive disorder.Am J Med Genet B Neuropsychiatr Genet2007
17894418Association of the SLC1A1 glutamate transporter gene and obsessive-compulsive disorder.Am J Med Genet B Neuropsychiatr Genet2007
17548750Association between treatment-emergent suicidal ideation with citalopram and polymorphisms near cyclic adenosine monophosphate response element binding protein in the STAR*D study.Arch Gen Psychiatry2007
17767156Variation in complement factor 3 is associated with risk of age-related macular degeneration.Nat Genet2007
17300755Clinical and genetic dissection of anger expression and CREB1 polymorphisms in major depressive disorder.Biol Psychiatry2007
17283288A genetic family-based association study of OLIG2 in obsessive-compulsive disorder.Arch Gen Psychiatry2007
17427194Investigation of parent-of-origin effects in ADHD candidate genes.Am J Med Genet B Neuropsychiatr Genet2007
16197923Association between the 5HT1B receptor gene (HTR1B) and the inattentive subtype of ADHD.Biol Psychiatry2006
16936732Common variation in three genes, including a noncoding variant in CFH, strongly influences risk of age-related macular degeneration.Nat Genet2006
16020308A discordant sib-pair linkage analysis of age-related macular degeneration.Ophthalmic Genet2005
15953484The corticotropin-releasing hormone gene and behavioral inhibition in children at risk for panic disorder.Biol Psychiatry2005
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Collaborators

Center for Genomic Medicine, Massachusetts General Hospital
Co-authored papers 17
University of Massachusetts Chan Medical School
Co-authored papers 16
Massachusetts General Hospital
Co-authored papers 14
Center for Quantitative Health, Massachusetts General Hospital
Co-authored papers 13
Tufts University School of Medicine and Tufts Medical Center
Co-authored papers 13
Brigham and Women's Hospital
Co-authored papers 12
Co-authored papers 10
Massachusetts General Hospital
Co-authored papers 9
Co-authored papers 8
Massachusetts General Hospital
Co-authored papers 7
SUNY Upstate Medical University
Co-authored papers 7
Massachusetts Eye and Ear Infirmary
Co-authored papers 7
INSERM U
Co-authored papers 6
Co-authored papers 6
Co-authored papers 6
Massachusetts General Hospital
Co-authored papers 5
University of Paris Est-Creteil
Co-authored papers 5
Johns Hopkins University School of Medicine
Co-authored papers 5
Co-authored papers 5
Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard
Co-authored papers 5
Co-authored papers 5
The Wilmer Eye Institute, Johns Hopkins University School of Medicine
Co-authored papers 5
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Tufts Medical Center
Co-authored papers 5
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Co-authored papers 5
Massachusetts General Hospital and Harvard Medical School
Co-authored papers 5
Northwestern University
Co-authored papers 5
Brigham and Women's Hospital and Harvard Medical School
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