Kimberly Chambert

26.8k citations

10 papers · 1.1k indexed · h-index 10

Impact in

Genetics top 5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
Biological Psychiatry

Papers in ⓘ

Genetics 9
- Genomic variations and chromosomal abnormalities 6
- Genomics and Rare Diseases 5
- Genetics and Neurodevelopmental Disorders 4
- Genetic Associations and Epidemiology 3
Molecular Biology 8
- Congenital heart defects research 3
- Gene expression and cancer classification 3
- Epigenetics and DNA Methylation 1
- RNA and protein synthesis mechanisms 1

Co-authors: Jennifer L. Moran (8 shared papers)Steven A. McCarroll (8 shared papers)Shaun Purcell (6 shared papers)Pamela Sklar (5 shared papers)Patrick F. Sullivan (5 shared papers)Menachem Fromer (4 shared papers)Christina M. Hultman (4 shared papers)Douglas M. Ruderfer (3 shared papers)
Journals: The American Journal of Human Genetics (2 papers)American Journal of Medical Genetics Part B Neuropsychiatric Genetics (2 papers)Molecular Psychiatry (2 papers)Nature Neuroscience (1 paper)Nature Genetics (1 paper)
Partner nations: United States United Kingdom Sweden

In The Last Decade

Kimberly Chambert

10 papers receiving 1.1k citations

Peers

Countries citing papers authored by Kimberly Chambert

Since Specialization

Citations

This map shows the geographic impact of Kimberly Chambert's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Kimberly Chambert with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kimberly Chambert more than expected).

Fields of papers citing papers by Kimberly Chambert

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kimberly Chambert. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Kimberly Chambert. The network helps show where Kimberly Chambert may publish in the future.

Co-authors

The 25 scholars most cited alongside Kimberly Chambert, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Kimberly Chambert Line = papers co-authored together Kimberly Chambert links everyone, so they are left out of the graph.

All Works

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10 of 10 papers shown

#	Work
1	Discovery and Statistical Genotyping of Copy-Number Variation from Whole-Exome Sequencing Depth The American Journal of Human Genetics ·Menachem Fromer, Jennifer L. Moran, Kimberly Chambert, Eric Banks, Sarah E. Bergen, Douglas M. Ruderfer, Robert E. Handsaker, Steven A. McCarroll, Michael O’Donovan, Michael J. Owen, George Kirov, Patrick F. Sullivan, Christina M. Hultman, Pamela Sklar, Shaun Purcell	2012	370
2	Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia Nature Neuroscience ·Giulio Genovese, Menachem Fromer, Eli A. Stahl, Douglas M. Ruderfer, Kimberly Chambert, Mikael Landén, Jennifer L. Moran, Shaun Purcell, Pamela Sklar, Patrick F. Sullivan, Christina M. Hultman, Steven A. McCarroll	2016	276
3	Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia Neuron ·Andrew Pocklington, Elliott Rees, James Walters, Jun Han, David H. Kavanagh, Kimberly Chambert, Peter Holmans, Jennifer L. Moran, Steven A. McCarroll, George Kirov, Michael O’Donovan, Michael J. Owen	2015	126
4	zCall: a rare variant caller for array-based genotyping Bioinformatics ·Jacqueline I. Goldstein, Andrew Crenshaw, Jason Carey, George Grant, Jared Maguire, Menachem Fromer, Colm O’Dushlaine, Jennifer L. Moran, Kimberly Chambert, Christine Stevens, Pamela Sklar, Christina M. Hultman, Shaun Purcell, Steven A. McCarroll, Patrick F. Sullivan, Mark J. Daly, Benjamin M. Neale	2012	100
5	Cis-acting regulation of brain-specific ANK3 gene expression by a genetic variant associated with bipolar disorder Molecular Psychiatry ·Erroll H. Rueckert, Douglas Barker, Douglas M. Ruderfer, Sarah E. Bergen, Colm O’Dushlaine, Catherine J. Luce, Steven D. Sheridan, Kraig M. Theriault, Kimberly Chambert, Jennifer L. Moran, Shaun Purcell, Jon M. Madison, Stephen J. Haggarty, Pamela Sklar	2012	69
6	Using population admixture to help complete maps of the human genome Nature Genetics ·Giulio Genovese, Robert E. Handsaker, Heng Li, Nicolas Altemose, Amelia M. Lindgren, Kimberly Chambert, Bogdan Paşaniuc, Alkes L. Price, David Reich, Cynthia C. Morton, Martin R. Pollak, James G. Wilson, Steven A. McCarroll	2013	44
7	Cryptic and Complex Chromosomal Aberrations in Early-Onset Neuropsychiatric Disorders The American Journal of Human Genetics ·Harrison Brand, Vamsee Pillalamarri, Ryan L. Collins, Stacey Eggert, Colm Ó'Dúshláine, Ellen B. Braaten, Matthew R. Stone, Kimberly Chambert, Nathan D. Doty, Carrie Hanscom, Jill A. Rosenfeld, Hillary L. Ditmars, Jessica E. Blais, Ryan E. Mills, Charles Lee, James F. Gusella, Steven A. McCarroll, Jordan W. Smoller, Michael E. Talkowski, Alysa E. Doyle	2014	27
8	Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample Molecular Psychiatry ·Jin Szatkiewicz, Benjamin M. Neale, C O'Dushlaine, Menachem Fromer, Jacqueline I. Goldstein, Jennifer L. Moran, Kimberly Chambert, A Kähler, Patrik K. E. Magnusson, C M Hultman, Pamela Sklar, Shaun Purcell, Steven A. McCarroll, Patrick F. Sullivan	2013	21
9	Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Ganna Leonenko, Alexander Richards, James Walters, Andrew Pocklington, Kimberly Chambert, Mariam M. Al Eissa, Sally I. Sharp, Niamh L. O’Brien, David Curtis, Nicholas Bass, Andrew McQuillin, Christina M. Hultman, Jennifer L. Moran, Steven A. McCarroll, Pamela Sklar, Benjamin M. Neale, Peter Holmans, Michael J. Owen, Patrick F. Sullivan, Michael O’Donovan	2017	16
10	A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Eske M. Derks, Muhammad Ayub, Kimberly Chambert, Jurgen Del‐Favero, Mandy Johnstone, Stuart MacGregor, Alan Maclean, Andrew G. McKechanie, Allan F. McRae, Jennifer L. Moran, Ben Pickard, Shaun Purcell, Pamela Sklar, David StClair, Naomi R. Wray, Peter M. Visscher, Douglas Blackwood	2013	15

About Kimberly Chambert

Kimberly Chambert is a scholar working on Genetics, Molecular Biology, Psychiatry and Mental health, Plant Science and Infectious Diseases, having authored 10 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (4 papers), Congenital heart defects research (3 papers), Genetic Associations and Epidemiology (3 papers), Gene expression and cancer classification (3 papers), Epigenetics and DNA Methylation (1 paper) and RNA and protein synthesis mechanisms (1 paper). The work is most often cited by research in Genetics (704 citations), Biological Psychiatry (26 citations), Cancer Research (134 citations), Molecular Biology (509 citations) and Cellular and Molecular Neuroscience (102 citations). Kimberly Chambert has collaborated with scholars based in United States, United Kingdom and Sweden. Frequent co-authors include Jennifer L. Moran, Steven A. McCarroll, Shaun Purcell, Pamela Sklar, Patrick F. Sullivan, Menachem Fromer, Christina M. Hultman, Douglas M. Ruderfer, Michael O’Donovan and George Kirov. Their work appears in journals such as The American Journal of Human Genetics, American Journal of Medical Genetics Part B Neuropsychiatric Genetics, Molecular Psychiatry, Nature Neuroscience and Nature Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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