Christopher D. Brown

9.2k total citations
50 papers, 2.2k citations indexed

About

Christopher D. Brown is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Christopher D. Brown has authored 50 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 20 papers in Genetics and 10 papers in Cancer Research. Recurrent topics in Christopher D. Brown's work include Genetic Associations and Epidemiology (12 papers), RNA Research and Splicing (8 papers) and Epigenetics and DNA Methylation (7 papers). Christopher D. Brown is often cited by papers focused on Genetic Associations and Epidemiology (12 papers), RNA Research and Splicing (8 papers) and Epigenetics and DNA Methylation (7 papers). Christopher D. Brown collaborates with scholars based in United States, Germany and United Kingdom. Christopher D. Brown's co-authors include Kevin P. White, Marco Trizzino, Minal Çalışkan, YoSon Park, Sabina Berretta, Harry Pantazopoulos, Matej Markota, K White, Aurélie Kapusta and Thomas Stricker and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Christopher D. Brown

47 papers receiving 2.2k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Christopher D. Brown 1.2k 567 237 203 150 50 2.2k
David Hoogewijs 1.5k 1.2× 270 0.5× 479 2.0× 174 0.9× 142 0.9× 67 2.8k
Gunnar Houge 1.8k 1.5× 812 1.4× 110 0.5× 134 0.7× 187 1.2× 112 3.3k
Gen Tamiya 1.2k 0.9× 763 1.3× 157 0.7× 356 1.8× 164 1.1× 129 3.4k
Momoki Hirai 1.8k 1.5× 645 1.1× 301 1.3× 151 0.7× 210 1.4× 92 3.1k
Charles R. Lane 1.7k 1.4× 1.1k 1.9× 106 0.4× 83 0.4× 134 0.9× 22 2.9k
Michael B. Gorin 3.0k 2.4× 781 1.4× 359 1.5× 95 0.5× 239 1.6× 147 5.5k
Maya Kasowski 2.0k 1.6× 1.1k 2.0× 448 1.9× 148 0.7× 157 1.0× 14 3.0k
Kenneth W. Gross 2.9k 2.3× 881 1.6× 294 1.2× 83 0.4× 303 2.0× 139 4.7k
Daniel M. Jordan 1.8k 1.4× 1.4k 2.5× 401 1.7× 38 0.2× 239 1.6× 36 3.3k
Michael Lush 1.2k 0.9× 476 0.8× 255 1.1× 127 0.6× 172 1.1× 22 2.3k

Countries citing papers authored by Christopher D. Brown

Since Specialization
Citations

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

Fields of papers citing papers by Christopher D. Brown

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Christopher D. Brown. 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 Christopher D. Brown. The network helps show where Christopher D. Brown may publish in the future.

Co-authorship network of co-authors of Christopher D. Brown

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

All Works

20 of 20 papers shown
1.
Wenz, Brandon M., Yuan He, Nae-Chyun Chen, et al.. (2025). Genotype inference from aggregated chromatin accessibility data reveals genetic regulatory mechanisms. Genome biology. 26(1). 81–81.
2.
Dolui, Sudipto, Christopher D. Brown, Pulkit Khandelwal, et al.. (2024). Regional cerebral blood flow reflects both neurodegeneration and microvascular integrity across the Alzheimer's continuum. Alzheimer s & Dementia. 21(1). e14382–e14382.
3.
Cousins, Katheryn A Q, Magdalena Korecka, Christopher D. Brown, et al.. (2024). Comparison of plasma p‐tau217 and Aβ42/Aβ40 biomarkers by race to detect Alzheimer’s disease. Alzheimer s & Dementia. 20(S8). 1 indexed citations
4.
Gawronski, Katerina A.B., William P. Bone, YoSon Park, et al.. (2023). Evaluating the Contribution of Cell Type–Specific Alternative Splicing to Variation in Lipid Levels. Circulation Genomic and Precision Medicine. 16(3). 248–257. 2 indexed citations
5.
Mechanic‐Hamilton, Dawn, Sudipto Dolui, Sandhitsu R. Das, et al.. (2023). Impact of white matter hyperintensities on structural connectivity and cognition in cognitively intact ADNI participants. Neurobiology of Aging. 135. 79–90. 2 indexed citations
6.
Kelly, Derek E., Shweta Ramdas, Rong Ma, et al.. (2023). The genetic and evolutionary basis of gene expression variation in East Africans. Genome biology. 24(1). 6 indexed citations
7.
Liu, Hongbo, Tomohito Doke, Xin Sheng, et al.. (2022). Epigenomic and transcriptomic analyses define core cell types, genes and targetable mechanisms for kidney disease. Nature Genetics. 54(7). 950–962. 102 indexed citations
8.
Doke, Tomohito, Shizheng Huang, Chengxiang Qiu, et al.. (2021). Transcriptome-wide association analysis identifies DACH1 as a kidney disease risk gene that contributes to fibrosis. Journal of Clinical Investigation. 131(10). 50 indexed citations
9.
He, Yuan, Surya B. Chhetri, Marios Arvanitis, et al.. (2020). sn-spMF: matrix factorization informs tissue-specific genetic regulation of gene expression. Genome biology. 21(1). 235–235. 11 indexed citations
10.
Qiu, Chengxiang, Shizheng Huang, Jihwan Park, et al.. (2018). Renal compartment–specific genetic variation analyses identify new pathways in chronic kidney disease. Nature Medicine. 24(11). 1721–1731. 146 indexed citations
11.
Kember, Rachel L., Liping Hou, Xiao Ji, et al.. (2018). Genetic pleiotropy between mood disorders, metabolic, and endocrine traits in a multigenerational pedigree. Translational Psychiatry. 8(1). 218–218. 14 indexed citations
12.
Kalita, Cynthia A., Christopher D. Brown, Andrew Freiman, et al.. (2018). High-throughput characterization of genetic effects on DNA–protein binding and gene transcription. Genome Research. 28(11). 1701–1708. 25 indexed citations
13.
Stricker, Thomas, Christopher D. Brown, Chaitanya Bandlamudi, et al.. (2017). Robust stratification of breast cancer subtypes using differential patterns of transcript isoform expression. PLoS Genetics. 13(3). e1006589–e1006589. 46 indexed citations
14.
Trizzino, Marco, YoSon Park, Márcia Holsbach Beltrame, et al.. (2017). Transposable elements are the primary source of novelty in primate gene regulation. Genome Research. 27(10). 1623–1633. 149 indexed citations
15.
Ji, Xiao, Rachel L. Kember, Christopher D. Brown, & Maja Bućan. (2016). Increased burden of deleterious variants in essential genes in autism spectrum disorder. Proceedings of the National Academy of Sciences. 113(52). 15054–15059. 34 indexed citations
16.
Pathak, Anand, Katja Seipel, Alexander Pemov, et al.. (2015). Whole exome sequencing reveals a C-terminal germline variant in CEBPA-associated acute myeloid leukemia: 45-year follow up of a large family. Haematologica. 101(7). 846–852. 33 indexed citations
17.
Innocenti, Federico, Gregory M. Cooper, Ian B. Stanaway, et al.. (2011). Identification, Replication, and Functional Fine-Mapping of Expression Quantitative Trait Loci in Primary Human Liver Tissue. PLoS Genetics. 7(5). e1002078–e1002078. 134 indexed citations
18.
Liu, Jiang, Murad Ghanim, Lei Xue, et al.. (2009). Analysis of Drosophila Segmentation Network Identifies a JNK Pathway Factor Overexpressed in Kidney Cancer. Science. 323(5918). 1218–1222. 98 indexed citations
19.
Ricci, Camilla, Leonard Nyadong, Facundo M. Fernández, et al.. (2008). Assessment of hand-held Raman instrumentation for in situ screening for potentially counterfeit artesunate antimalarial tablets by FT-Raman spectroscopy and direct ionization mass spectrometry. Analytica Chimica Acta. 623(2). 178–186. 75 indexed citations
20.
Johnson, David S., Brad Davidson, Christopher D. Brown, William C. Smith, & Arend Sidow. (2004). Noncoding regulatory sequences of Ciona exhibit strong correspondence between evolutionary constraint and functional importance. Genome Research. 14(12). 2448–2456. 57 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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