Kimberly Chambert

Broad Institute — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

36h-index26.5kcitations59works0.02yr avg
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Research Topics

Genetic Associations and Epidemiology(21), Genetics and Neurodevelopmental Disorders(20), Genomics and Rare Diseases(16), Genomic variations and chromosomal abnormalities(14), Bipolar Disorder and Treatment(9)

Publications53 total

Genome-wide association study of school grades identifies genetic overlap between language ability, psychopathology and creativity
Scientific Reports·2023· 28 citedOpen Access
Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence
UNC Libraries·2020Open Access
Discovery and Statistical Genotyping of Copy-Number Variation from Whole-Exome Sequencing Depth
UNC Libraries·2020Open Access
A polygenic burden of rare disruptive mutations in schizophrenia
UNC Libraries·2020Open Access
zCall: a rare variant caller for array-based genotyping
UNC Libraries·2020Open Access
Quantifying prion disease penetrance using large population control cohorts
UNC Libraries·2020· 1 citedOpen Access
Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia
UNC Libraries·2020Open Access
Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia
UNC Libraries·2020Open Access
Exome sequencing in schizophrenia-affected parent–offspring trios reveals risk conferred by protein-coding de novo mutations
Nature Neuroscience·2020· 180 citedOpen Access
Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders
Cell·2019· 1.4k citedOpen Access
Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders
Molecular Psychiatry·2019· 46 citedOpen Access
The Genetics of the Mood Disorder Spectrum: Genome-wide Association Analyses of More Than 185,000 Cases and 439,000 Controls
Biological Psychiatry·2019· 202 citedOpen Access
Genome-wide association study identifies 30 loci associated with bipolar disorder
Nature Genetics·2019· 1.6k citedOpen Access
Identification of common genetic risk variants for autism spectrum disorder
Nature Genetics·2019· 2.5k citedOpen Access
Disentangling polygenic associations between attention-deficit/hyperactivity disorder, educational attainment, literacy and language
Translational Psychiatry·2019· 33 citedOpen Access
Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases
Biological Psychiatry·2018· 70 citedOpen Access
Schizophrenia risk conferred by protein-coding <i>de novo</i> mutations
2018· 6 citedOpen Access
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
Nature Genetics·2018· 2.3k citedOpen Access
Contribution of rare copy number variants to bipolar disorder risk is limited to schizoaffective cases
2018· 2 citedOpen Access
Su1089 - Presence of Bile Acids Detected in Human Saliva using a Novel Sensitive Bioanalytical Method: A Comparative Study in Patients with Persistent or Controlled Gerd Symptoms and Healthy Subjects
Gastroenterology·2018
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Frequent Co-authors

Jennifer L. Moran(36), Steven A. McCarroll(31), Pamela Sklar(29), Shaun Purcell(27), Benjamin M. Neale(19), Douglas M. Ruderfer(19), Menachem Fromer(17), Patrick F. Sullivan(17), Sarah E. Bergen(17), Mark J. Daly(15), Eli A. Stahl(15), Felecia Cerrato(13), Stephan Ripke(12), Ashley Dumont(12), Panos Roussos(12), Christina M. Hultman(11), Esben Agerbo(11), Jonas Bybjerg‐Grauholm(11), Daniel P. Howrigan(11), Peter Holmans(11)