Camille W. Brune

5.3k total citations
16 papers, 2.0k citations indexed

About

Camille W. Brune is a scholar working on Cognitive Neuroscience, Genetics and Clinical Psychology. According to data from OpenAlex, Camille W. Brune has authored 16 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Cognitive Neuroscience, 14 papers in Genetics and 3 papers in Clinical Psychology. Recurrent topics in Camille W. Brune's work include Autism Spectrum Disorder Research (14 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomic variations and chromosomal abnormalities (7 papers). Camille W. Brune is often cited by papers focused on Autism Spectrum Disorder Research (14 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomic variations and chromosomal abnormalities (7 papers). Camille W. Brune collaborates with scholars based in United States and Canada. Camille W. Brune's co-authors include Edwin H. Cook, Bennett Leventhal, Catherine Lord, Susan L. Christian, Jyotsna Sudi, William B. Dobyns, Samer Karamohamed, Judith A. Badner, Norma J. Nowak and T. Conrad Gilliam and has published in prestigious journals such as PLoS ONE, American Journal of Psychiatry and Biological Psychiatry.

In The Last Decade

Camille W. Brune

16 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Camille W. Brune United States	15	1.3k	1.1k	707	343	167	16	2.0k
Olga Peñagarikano Spain	17	1.2k 0.9×	1.2k 1.2×	1.0k 1.4×	533 1.6×	154 0.9×	29	2.6k
Hower Kwon United States	14	978 0.7×	1.6k 1.5×	666 0.9×	101 0.3×	253 1.5×	15	2.4k
Danielle Halpern United States	15	618 0.5×	617 0.6×	350 0.5×	237 0.7×	173 1.0×	30	1.2k
Amy A. Lightbody United States	25	1.6k 1.2×	1.6k 1.5×	624 0.9×	135 0.4×	345 2.1×	49	2.2k
Raija Vanhala Finland	23	889 0.7×	1.5k 1.4×	464 0.7×	111 0.3×	209 1.3×	46	2.1k
Harry H. Wright United States	27	1.3k 1.0×	1.7k 1.6×	672 1.0×	349 1.0×	597 3.6×	58	2.7k
A. Ting Wang United States	11	565 0.4×	634 0.6×	293 0.4×	225 0.7×	161 1.0×	14	1.1k
Maricela Alarcón United States	18	1.3k 1.0×	1.2k 1.1×	627 0.9×	107 0.3×	135 0.8×	24	2.4k
Charlotte Modahl United States	11	525 0.4×	880 0.8×	240 0.3×	668 1.9×	331 2.0×	12	1.6k
Donna M. Werling United States	12	735 0.6×	978 0.9×	383 0.5×	112 0.3×	254 1.5×	18	1.6k

Countries citing papers authored by Camille W. Brune

Since Specialization

Citations

This map shows the geographic impact of Camille W. Brune'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 Camille W. Brune with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Camille W. Brune more than expected).

Fields of papers citing papers by Camille W. Brune

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Camille W. Brune. 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 Camille W. Brune. The network helps show where Camille W. Brune may publish in the future.

Co-authorship network of co-authors of Camille W. Brune

This figure shows the co-authorship network connecting the top 25 collaborators of Camille W. Brune. A scholar is included among the top collaborators of Camille W. Brune 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 Camille W. Brune. Camille W. Brune is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Levy, Tess, Cristan Farmer, Siddharth Srivastava, et al.. (2025). Genetic Subtypes of Phelan-McDermid Syndrome Exhibit Similar Rates of Change Despite Differences in Level of Impairment in Developmental Constructs. American Journal on Intellectual and Developmental Disabilities. 130(5). 395–413. 1 indexed citations

Kistner‐Griffin, Emily, Camille W. Brune, Lea K. Davis, et al.. (2010). Parent-of-origin effects of the serotonin transporter gene associated with autism. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 156(2). 139–144. 38 indexed citations

Kumar, Revati, Jyotsna Sudi, Camille W. Brune, et al.. (2009). A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism. Journal of Medical Genetics. 47(2). 81–90. 39 indexed citations

Owley, Thomas, Camille W. Brune, Jeff Salt, et al.. (2009). A pharmacogenetic study of escitalopram in autism spectrum disorders. Autism Research. 3(1). 1–7. 51 indexed citations

Kumar, Ravinesh A., Christian R. Marshall, Judith A. Badner, et al.. (2009). Association and Mutation Analyses of 16p11.2 Autism Candidate Genes. PLoS ONE. 4(2). e4582–e4582. 73 indexed citations

Delahanty, Ryan, Jing‐Qiong Kang, Camille W. Brune, et al.. (2009). Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism. Molecular Psychiatry. 16(1). 86–96. 84 indexed citations

Brune, Camille W., Soo‐Jeong Kim, Gregory L. Hanna, et al.. (2008). Family‐based association testing of OCD‐associated SNPs of SLC1A1 in an autism sample. Autism Research. 1(2). 108–113. 18 indexed citations

Kim, Soo‐Jeong, Camille W. Brune, Emily O. Kistner, et al.. (2008). Transmission disequilibrium testing of the chromosome 15q11‐q13 region in autism. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(7). 1116–1125. 25 indexed citations

Arking, Dan E., David J. Cutler, Camille W. Brune, et al.. (2008). A Common Genetic Variant in the Neurexin Superfamily Member CNTNAP2 Increases Familial Risk of Autism. The American Journal of Human Genetics. 82(1). 160–164. 434 indexed citations

10.

Christian, Susan L., Camille W. Brune, Jyotsna Sudi, et al.. (2008). Novel Submicroscopic Chromosomal Abnormalities Detected in Autism Spectrum Disorder. Biological Psychiatry. 63(12). 1111–1117. 216 indexed citations

11.

Kumar, Revati, Samer Karamohamed, Jyotsna Sudi, et al.. (2007). Recurrent 16p11.2 microdeletions in autism. Human Molecular Genetics. 17(4). 628–638. 487 indexed citations

12.

Brune, Camille W. & Amanda L. Woodward. (2007). Social Cognition and Social Responsiveness in 10-month-old Infants. Journal of Cognition and Development. 8(2). 133–158. 57 indexed citations

13.

Jacob, Suma, et al.. (2007). Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism. Neuroscience Letters. 417(1). 6–9. 322 indexed citations

14.

Brune, Camille W., Elena Korvatska, Kristina Allen‐Brady, et al.. (2007). Heterogeneous association between engrailed‐2 and autism in the CPEA network. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 147B(2). 187–193. 32 indexed citations

15.

Brune, Camille W., Soo‐Jeong Kim, Jeff Salt, et al.. (2006). 5-HTTLPR Genotype-Specific Phenotype in Children and Adolescents With Autism. American Journal of Psychiatry. 163(12). 2148–2156. 122 indexed citations

16.

Brune, Camille W.. (2006). 5-HTTLPR Genotype-Specific Phenotype in Children and Adolescents With Autism. American Journal of Psychiatry. 163(12). 2148–2148. 30 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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