Author details

Full Name

Kimberly Chambert

Affiliation

ORCID

Career Start Year

2008

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
31932770	Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations.	Nat Neurosci	2020
30686506	Contribution of Rare Copy Number Variants toÂ Bipolar Disorder Risk Is Limited to Schizoaffective Cases.	Biol Psychiatry	2019
30478444	Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.	Nat Genet	2019
28072414	Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder.	Transl Psychiatry	2017
28719003	Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia.	Am J Med Genet B Neuropsychiatr Genet	2017
27694994	Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.	Nat Neurosci	2016
26791950	Quantifying prion disease penetrance using large population control cohorts.	Sci Transl Med	2016
26503763	Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder.	Mol Psychiatry	2016
26196440	Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.	Transl Psychiatry	2015
25733313	Characterization of bipolar disorder patient-specific induced pluripotent stem cells from a family reveals neurodevelopmental and mRNA expression abnormalities.	Mol Psychiatry	2015
24776740	Copy number variation in schizophrenia in Sweden.	Mol Psychiatry	2014
25279985	Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disorders.	Am J Hum Genet	2014
25426838	Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence.	N Engl J Med	2014
24463508	A polygenic burden of rare disruptive mutations in schizophrenia.	Nature	2014
24463507	De novo mutations in schizophrenia implicate synaptic networks.	Nature	2014
23435088	Using population admixture to help complete maps of the human genome.	Nat Genet	2013
22850628	Cis-acting regulation of brain-specific ANK3 gene expression by a genetic variant associated with bipolar disorder.	Mol Psychiatry	2013
24115684	A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability.	Am J Med Genet B Neuropsychiatr Genet	2013
23938935	Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample.	Mol Psychiatry	2013
23974872	Genome-wide association analysis identifies 13 new risk loci for schizophrenia.	Nat Genet	2013
23933821	Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.	Nat Genet	2013
23321615	Mosaic copy number variation in schizophrenia.	Eur J Hum Genet	2013
22083728	De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.	Mol Psychiatry	2012
22843986	zCall: a rare variant caller for array-based genotyping: genetics and population analysis.	Bioinformatics	2012
23040492	Discovery and statistical genotyping of copy-number variation from whole-exome sequencing depth.	Am J Hum Genet	2012
23128927	Bipolar disorder and a history of suicide attempts with a duplication in 5HTR1A.	Am J Psychiatry	2012
21483432	A family-based study of common polygenic variation and risk of schizophrenia.	Mol Psychiatry	2011
18711365	Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder.	Nat Genet	2008
18317468	Whole-genome association study of bipolar disorder.	Mol Psychiatry	2008