Kimberly F. Doheny

Also affiliated with Johns Hopkins Medicine

Biochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 1%percentile

8.6Author DataRank

Indexed papers

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Genomic data in the All of Us Research Program

Nature(2024)10.1038/s41586-023-06957-x

Top 2%

8.6DataRank

Top 2%772 citations

Alexander G. Bick, Ginger Metcalf, Kelsey Mayo, Lee Lichtenstein, Shimon Rura +91 more

Papers

Driven by 16 papers — median percentile 98. Top paper: “Genomic data in the All of Us Research Program”.

Genomic data in the All of Us Research Program

Nature(2024)10.1038/s41586-023-06957-x

Top 2%

8.6DataRank

Top 2%772 citations

Alexander G. Bick, Ginger Metcalf, Kelsey Mayo, Lee Lichtenstein, Shimon Rura +91 more

The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities

The American Journal of Human Genetics(2015)10.1016/j.ajhg.2015.06.009

N/A

0.980DataRank · unranked

687 citations

Kati J. Buckingham, Shalini N. Jhangiani, Corinne Boehm, Nara Sobreira, Joshua D. Smith +46 more

Genotoxic colibactin mutational signature in colorectal cancer is associated with clinicopathological features, specific genomic alterations and better survival

medRxiv(2023)10.1101/2023.03.10.23287127

N/A

0.960DataRank · unranked

24 citations

Robert S. Steinfelder, Tabitha A. Harrison, Bernard J. Pope, Syed Hassan Ejaz Zaidi, Conghui Qu +57 more

Common Variants at 9p21 and 8q22 Are Associated with Increased Susceptibility to Optic Nerve Degeneration in Glaucoma

PLoS Genetics(2012)10.1371/journal.pgen.1002654

N/A

0.863DataRank · unranked

314 citations

Brian L. Yaspan, Michael A. Hauser, Jae H. Kang, R. Rand Allingham, Lana M. Olson +52 more

Germline Sequencing DNA Repair Genes in 5545 Men With Aggressive and Nonaggressive Prostate Cancer

JNCI Journal of the National Cancer Institute(2020)10.1093/jnci/djaa132

N/A

0.673DataRank · unranked

88 citations

Tokhir Dadaev, Edward J. Saunders, Xin Sheng, Peggy Wan, Loreall Pooler +25 more

Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program

Genome Medicine(2022)10.1186/s13073-022-01031-z

N/A

0.626DataRank · unranked

64 citations

Donna M. Muzny, Joshua D. Smith, Kimberly Walker, Cynthia L. Neben, Christina M. Lockwood +16 more

Identifying colorectal cancer caused by biallelic MUTYH pathogenic variants using tumor mutational signatures

Nature Communications(2022)10.1038/s41467-022-30916-1

N/A

0.542DataRank · unranked

36 citations

Tabitha A. Harrison, Bernard J. Pope, Syed Hassan Ejaz Zaidi, Conghui Qu, Robert S. Steinfelder +47 more

PhenoDB, GeneMatcher and VariantMatcher, tools for analysis and sharing of sequence data

Orphanet Journal of Rare Diseases(2021)10.1186/s13023-021-01916-z

N/A

0.524DataRank · unranked

32 citations

Renan Paulo Martin, Sean Griffith, Eliete da S. Rodrigues, Corina Antonescu, Jennifer E. Posey +8 more

Clonal hematopoiesis and risk of prostate cancer in large samples of European ancestry men

Human Molecular Genetics(2022)10.1093/hmg/ddac214

N/A

0.396DataRank · unranked

13 citations

Yili Xu, Yao Yu, Kevin T. Nead, Tae‐Beom Kim, Keren Xu +34 more

Exome Array Analysis of 9721 Ischemic Stroke Cases from the SiGN Consortium

Genes(2022)10.3390/genes14010061

N/A

0.254DataRank · unranked

4 citations

Kevin A. Nguyen, Brady Gaynor, Hua Ling, Wei Zhao, Patrick F. McArdle +21 more

Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 818 trios

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.09.009

N/A

0.208DataRank · unranked

3 citations

Sarah W. Curtis, Justin Paschall, Wasiu Lanre Adeyemo, Terri H. Beaty, Azeez Butali +14 more

A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants

UNC Libraries(2021)10.17615/xzx9-fd89

N/A

0.187DataRank · unranked

1 citations

Michael W. Barnhart, Timo T. Valle, Karen L. Mohlke, Michael Boehnke, Heather M. Stringham +36 more

Genomic characterization of colorectal tumors: insights into significantly mutated genes, pathways, and survival outcomes

BMC Cancer(2025)10.1186/s12885-025-15440-x

N/A

0DataRank · unranked

0 citations

Syed Hassan Ejaz Zaidi, H. Yin, Robert S. Steinfelder, Conghui Qu, Elom K. Aglago +47 more

Exome array analysis identifies new loci and low-frequency variants influencing insulin processing and secretion

UNC Libraries(2020)10.17615/63sx-0c91

N/A

0DataRank · unranked

0 citations

Mark J. Daly, Johanna Kuusisto, Francis S. Collins, Markku Laakso, Kimberly F. Doheny +24 more

Common variants in the GDF5-UQCC region are associated with variation in human height

UNC Libraries(2020)10.17615/th6f-r873

N/A

0DataRank · unranked

0 citations

Nicholas J. Timpson, Yoav Ben‐Shlomo, Debbie A. Lawlor, Lori L. Bonnycastle, Laura J. Scott +27 more

Distinguishing syndromic and nonsyndromic cleft palate through analysis of protein-altering de novo variants in 816 trios

medRxiv(2025)10.1101/2025.03.03.25323233

N/A

0DataRank · unranked

0 citations

Sarah W. Curtis, Justin Paschall, Terri H. Beaty, Azeez Butali, Carmen J. Buxó +12 more

Kimberly F. Doheny

Indexed papers

Top data-sharing exemplar

Papers