Publications by authors named "Kimberly Chambert"

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Differential Bile Acid Detection in Refractory GERD Patient Saliva Using a Simple and Sensitive Liquid Chromatography Tandem Mass Spectrometry Approach.
Nisha Perez, Kimberly Chambert, Maria Ribadeneira, Mark G Currie, Yan Chen

J Clin Gastroenterol· March 2022

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Exome sequencing in schizophrenia-affected parent-offspring trios reveals risk conferred by protein-coding de novo mutations.
Daniel P Howrigan, Samuel A Rose, Kaitlin E Samocha, Menachem Fromer, Felecia Cerrato, Kimberly Chambert

Nat Neurosci· February 2020

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Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases.
Alexander W Charney, Eli A Stahl, Elaine K Green, Chia-Yen Chen, Jennifer L Moran, Kimberly Chambert

Biol Psychiatry· July 2019

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Genome-wide association study identifies 30 loci associated with bipolar disorder.
Eli A Stahl, Gerome Breen, Andreas J Forstner, Andrew McQuillin, Stephan Ripke, Kimberly Chambert

Nat Genet· May 2019

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Identification of common genetic risk variants for autism spectrum disorder.
Jakob Grove, Stephan Ripke, Thomas D Als, Manuel Mattheisen, Raymond K Walters, Kimberly Chambert

Nat Genet· March 2019

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Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
Ditte Demontis, Raymond K Walters, Joanna Martin, Manuel Mattheisen, Thomas D Als, Kimberly Chambert

Nat Genet· January 2019

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Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia.
Ganna Leonenko, Alexander L Richards, James T Walters, Andrew Pocklington, Kimberly Chambert

Am J Med Genet B Neuropsychiatr Genet· October 2017

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Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.
Giulio Genovese, Menachem Fromer, Eli A Stahl, Douglas M Ruderfer, Kimberly Chambert

Nat Neurosci· November 2016

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Genome-wide association study identifies SESTD1 as a novel risk gene for lithium-responsive bipolar disorder.
J Song, S E Bergen, A Di Florio, R Karlsson, A Charney, K D Chambert, Kimberly Chambert

Mol Psychiatry· September 2016

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Evidence of Common Genetic Overlap Between Schizophrenia and Cognition.
Leon Hubbard, Katherine E Tansey, Dheeraj Rai, Peter Jones, Stephan Ripke, Kimberly D Chambert

Schizophr Bull· May 2016

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Quantifying prion disease penetrance using large population control cohorts.
Eric Vallabh Minikel, Sonia M Vallabh, Monkol Lek, Karol Estrada, Kaitlin E Samocha, Kimberly Chambert

Sci Transl Med· January 2016

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Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia.
Andrew J Pocklington, Elliott Rees, James T R Walters, Jun Han, David H Kavanagh, Kimberly D Chambert

Neuron· June 2015

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De novo CNVs in bipolar affective disorder and schizophrenia.
Lyudmila Georgieva, Elliott Rees, Jennifer L Moran, Kimberly D Chambert, Vihra Milanova

Hum Mol Genet· December 2014

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Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence.
Giulio Genovese, Anna K Kähler, Robert E Handsaker, Johan Lindberg, Samuel A Rose, Kimberly Chambert

N Engl J Med· December 2014

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Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disorders.
Harrison Brand, Vamsee Pillalamarri, Ryan L Collins, Stacey Eggert, Colm O'Dushlaine, Kimberly Chambert

Am J Hum Genet· October 2014

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The penetrance of copy number variations for schizophrenia and developmental delay.
George Kirov, Elliott Rees, James T R Walters, Valentina Escott-Price, Lyudmila Georgieva, Kimberly D Chambert

Biol Psychiatry· March 2014

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CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1.
Elliott Rees, James T R Walters, Kimberly D Chambert, Colm O'Dushlaine, Jin Szatkiewicz

Hum Mol Genet· March 2014

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Analysis of copy number variations at 15 schizophrenia-associated loci.
Elliott Rees, James T R Walters, Lyudmila Georgieva, Anthony R Isles, Kimberly D Chambert

Br J Psychiatry· February 2014

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De novo mutations in schizophrenia implicate synaptic networks.
Menachem Fromer, Andrew J Pocklington, David H Kavanagh, Hywel J Williams, Sarah Dwyer, Kimberly Chambert

Nature· February 2014

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A polygenic burden of rare disruptive mutations in schizophrenia.
Shaun M Purcell, Jennifer L Moran, Menachem Fromer, Douglas Ruderfer, Nadia Solovieff, Kimberly Chambert

Nature· February 2014

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A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability.
Eske M Derks, Muhammad Ayub, Kimberly Chambert, Jurgen Del Favero, Mandy Johnstone

Am J Med Genet B Neuropsychiatr Genet· December 2013

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Genome-wide association analysis identifies 13 new risk loci for schizophrenia.
Stephan Ripke, Colm O'Dushlaine, Kimberly Chambert, Jennifer L Moran, Anna K Kähler

Nat Genet· October 2013

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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.

Nat Genet· September 2013

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Using population admixture to help complete maps of the human genome.
Giulio Genovese, Robert E Handsaker, Heng Li, Nicolas Altemose, Amelia M Lindgren, Kimberly Chambert

Nat Genet· April 2013

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Implication of a rare deletion at distal 16p11.2 in schizophrenia.
Saurav Guha, Elliott Rees, Ariel Darvasi, Dobril Ivanov, Masashi Ikeda, Kimberly D Chambert

JAMA Psychiatry· March 2013

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