Kimberly Chambert

26.8k total citations
10 papers, 1.1k citations indexed

About

Kimberly Chambert is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Kimberly Chambert has authored 10 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 1 paper in Psychiatry and Mental health. Recurrent topics in Kimberly Chambert's work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Kimberly Chambert is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genomics and Rare Diseases (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Kimberly Chambert collaborates with scholars based in United States, United Kingdom and Sweden. Kimberly Chambert's 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 and has published in prestigious journals such as Neuron, Nature Genetics and Nature Neuroscience.

In The Last Decade

Kimberly Chambert

10 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Kimberly Chambert United States	10	704	509	134	104	102	10	1.1k
Nathalie Le Meur France	11	446 0.6×	616 1.2×	100 0.7×	46 0.4×	154 1.5×	14	1.2k
Alissa M. D’Gama United States	12	565 0.8×	753 1.5×	242 1.8×	97 0.9×	104 1.0×	30	1.2k
Anneke T. Vulto-van Silfhout Netherlands	4	959 1.4×	656 1.3×	97 0.7×	112 1.1×	129 1.3×	4	1.3k
Bhooma Thiruvahindrapuram Canada	14	500 0.7×	420 0.8×	74 0.6×	147 1.4×	61 0.6×	47	880
Susan Walker Canada	20	572 0.8×	466 0.9×	97 0.7×	210 2.0×	176 1.7×	48	1.1k
Atsushi Takata Japan	20	563 0.8×	707 1.4×	85 0.6×	114 1.1×	125 1.2×	55	1.2k
Joon‐Yong An South Korea	15	397 0.6×	541 1.1×	145 1.1×	279 2.7×	109 1.1×	49	982
Markus Zweier Switzerland	12	547 0.8×	582 1.1×	38 0.3×	138 1.3×	80 0.8×	23	937
Jean‐Baptiste Rivière Canada	18	575 0.8×	591 1.2×	72 0.5×	101 1.0×	145 1.4×	36	1.2k
Michele Pinelli Italy	19	457 0.6×	745 1.5×	170 1.3×	39 0.4×	199 2.0×	49	1.3k

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-authorship network of co-authors of Kimberly Chambert

This figure shows the co-authorship network connecting the top 25 collaborators of Kimberly Chambert. A scholar is included among the top collaborators of Kimberly Chambert based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Kimberly Chambert. Kimberly Chambert is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

Leonenko, Ganna, Alexander Richards, James Walters, et al.. (2017). Mutation intolerant genes and targets of FMRP are enriched for nonsynonymous alleles in schizophrenia. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 174(7). 724–731. 16 indexed citations

Genovese, Giulio, Menachem Fromer, Eli A. Stahl, et al.. (2016). Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia. Nature Neuroscience. 19(11). 1433–1441. 276 indexed citations

Pocklington, Andrew, Elliott Rees, James Walters, et al.. (2015). Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia. Neuron. 86(5). 1203–1214. 126 indexed citations

Brand, Harrison, Vamsee Pillalamarri, Ryan L. Collins, et al.. (2014). Cryptic and Complex Chromosomal Aberrations in Early-Onset Neuropsychiatric Disorders. The American Journal of Human Genetics. 95(4). 454–461. 27 indexed citations

Szatkiewicz, Jin, Benjamin M. Neale, Menachem Fromer, et al.. (2013). Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample. Molecular Psychiatry. 18(11). 1178–1184. 21 indexed citations

Genovese, Giulio, Robert E. Handsaker, Heng Li, et al.. (2013). Using population admixture to help complete maps of the human genome. Nature Genetics. 45(4). 406–414. 44 indexed citations

Derks, Eske M., Muhammad Ayub, Kimberly Chambert, et al.. (2013). 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. 162(8). 847–854. 15 indexed citations

Fromer, Menachem, Jennifer L. Moran, Kimberly Chambert, et al.. (2012). Discovery and Statistical Genotyping of Copy-Number Variation from Whole-Exome Sequencing Depth. The American Journal of Human Genetics. 91(4). 597–607. 370 indexed citations

Rueckert, Erroll H., Douglas Barker, Douglas M. Ruderfer, et al.. (2012). Cis-acting regulation of brain-specific ANK3 gene expression by a genetic variant associated with bipolar disorder. Molecular Psychiatry. 18(8). 922–929. 69 indexed citations

10.

Goldstein, Jacqueline I., Andrew Crenshaw, Jason Carey, et al.. (2012). zCall: a rare variant caller for array-based genotyping. Bioinformatics. 28(19). 2543–2545. 100 indexed citations

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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