John D. Overton

Biochemistry, Genetics and Molecular BiologyMedicine

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 2%percentile

2.4Author DataRank

Indexed papers

2in 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 2 indexed papers 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.

Within-sibship GWAS improve estimates of direct genetic effects

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.05.433935

Top 10%

2.2DataRank

Top 10%75 citations

Michel G. Nivard, Tim Morris, Ailin Falkmo Hansen, Humaira Rasheed, Yoonsu Cho +83 more

Papers

Driven by 23 papers — median percentile 63. Top paper: “Within-sibship GWAS improve estimates of direct genetic effects”.

Within-sibship GWAS improve estimates of direct genetic effects

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.05.433935

Top 10%

2.2DataRank

Top 10%75 citations

Michel G. Nivard, Tim Morris, Ailin Falkmo Hansen, Humaira Rasheed, Yoonsu Cho +83 more

A catalog of associations between rare coding variants and COVID-19 outcomes

medRxiv(2020)10.1101/2020.10.28.20221804

N/A

1.3DataRank · unranked

31 citations

Julie Horowitz, Nilanjana Banerjee, Rouel Lanche, Anthony Marcketta, Evan K. Maxwell +75 more

Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity

Science(2021)10.1126/science.abf8683

N/A

0.845DataRank · unranked

278 citations

Ankit Gilani, Olukayode Sosina, Jack A. Kosmicki, Lori Khrimian, Yi‐Ya Fang +55 more

Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank

Nature Genetics(2022)10.1038/s41588-021-01011-w

N/A

0.775DataRank · unranked

174 citations

Seung Hoan Choi, Valerie N. Morrill, Mark Chaffin, James P. Pirruccello, Jennifer L. Halford +65 more

Exome-wide evaluation of rare coding variants using electronic health records identifies new gene–phenotype associations

Nature Medicine(2021)10.1038/s41591-020-1133-8

N/A

0.631DataRank · unranked

66 citations

Anastasia Lucas, Xinyuan Zhang, Kumardeep Chaudhary, Judy H. Cho, Girish N. Nadkarni +36 more

Polygenic Risk of Psychiatric Disorders Exhibits Cross-trait Associations in Electronic Health Record Data From European Ancestry Individuals

Biological Psychiatry(2020)10.1016/j.biopsych.2020.06.026

N/A

0.601DataRank · unranked

54 citations

Alison Merikangas, Shefali S. Verma, Anurag Verma, Renae Judy, Gonçalo R. Abecasis +42 more

Impact of natural selection on global patterns of genetic variation and association with clinical phenotypes at genes involved in SARS-CoV-2 infection

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2123000119

N/A

0.599DataRank · unranked

18 citations

Anurag Verma, Yuanqing Feng, Marcelo C. R. Melo, Michael A. McQuillan, Matthew E.B. Hansen +71 more

Kidney disease genetic risk variants alter lysosomal beta-mannosidase ( MANBA ) expression and disease severity

Science Translational Medicine(2021)10.1126/scitranslmed.aaz1458

N/A

0.593DataRank · unranked

51 citations

Hongliu Yang, Xin Sheng, Yi-An Ko, Chengxiang Qiu, Jihwan Park +23 more

Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants

Science(2025)10.1126/science.adp4753

N/A

0.587DataRank · unranked

49 citations

Amin Abedini, Eunji Ha, Ziyuan Ma, Xin Sheng, Bernhard Dumoulin +94 more

Genome-wide analysis in 756,646 individuals provides first genetic evidence that ACE2 expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease

medRxiv(2020)10.1101/2020.12.14.20248176

N/A

0.561DataRank · unranked

41 citations

Jack A. Kosmicki, Amy Damask, Deepika Sharma, Genevieve H. L. Roberts, Anne E. Justice +54 more

The impact of common and rare genetic variants on bradyarrhythmia development

Nature Genetics(2025)10.1038/s41588-024-01978-2

N/A

0.464DataRank · unranked

21 citations

Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall +95 more

Genetic risk factors for COVID-19 and influenza are largely distinct

Nature Genetics(2024)10.1038/s41588-024-01844-1

N/A

0.406DataRank · unranked

14 citations

Anthony Marcketta, Deepika Sharma, Silvio Alessandro Di Gioia, Samantha Batista, Xiaoman Yang +53 more

Insights from the Biorepository and Integrative Genomics pediatric resource

Nature Communications(2025)10.1038/s41467-025-59375-0

Top 65%

0.208DataRank

Top 65%3 citations

Franco Mársico, Akram Mohammed, Lokesh Chinthala, Ernestine K Amos-Abanyie, Aris Baras +95 more

Exonic Variation and Its Clinical Impact in 7221 Old Order Amish

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.64212

N/A

0DataRank · unranked

0 citations

Ebuka Onyenobi, Joshua P. Lewis, Brady Gaynor, James A. Perry, Kristin A. Maloney +17 more

Biallelic variants in KYNU cause a multisystemic syndrome with hand hyperphalangism

Bone(2020)10.1016/j.bone.2019.115219

N/A

0DataRank · unranked

19 citations

Kristina Cusmano‐Ozog, Rainer Koenig, Manuel Holtgrewe, Banu Nur, Ercan Mıhçı +16 more

MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk

Nature Communications(2020)10.1038/s41467-020-17315-0

N/A

0DataRank · unranked

37 citations

Lars G. Fritsche, Wei Zhou, Joshua Backman, Jack A. Kosmicki, Haocheng Lu +45 more

Germline Mutations in CIDEB and Protection against Liver Disease

New England Journal of Medicine(2022)10.1056/nejmoa2117872

N/A

0DataRank · unranked

125 citations

Mary E. Haas, Jonas B. Nielsen, Olukayode Sosina, Minhee Kim, Parsa Akbari +42 more

ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma

Communications Biology(2022)10.1038/s42003-022-03932-6

N/A

0DataRank · unranked

25 citations

Gaurang Patel, Lauren Gurski, Ariane Ayer, Trikaladarshi Persaud, Matthew Still +95 more

Assessment of genetic susceptibility to multiple primary cancers through whole-exome sequencing in two large multi-ancestry studies

BMC Medicine(2022)10.1186/s12916-022-02535-6

N/A

0DataRank · unranked

18 citations

Linda Kachuri, Rebecca E. Graff, Jovia L. Nierenberg, Khanh K. Thai, Stacey Alexeeff +90 more

Converging evidence from exome sequencing and common variants implicates target genes for osteoporosis

Nature Genetics(2023)10.1038/s41588-023-01444-5

N/A

0DataRank · unranked

27 citations

Olukayode Sosina, Jonas Bovijn, Lætitia Laurent, Vasundhara Sharma, Parsa Akbari +24 more

Risk of lymphoid malignancy associated with cancer predisposition genes

Blood Cancer Journal(2025)10.1038/s41408-025-01283-z

N/A

0DataRank · unranked

8 citations

Raphael Mwangi, Dennis P. Robinson, Cristine Allmer, Allison Rosenthal, Thomas M. Habermann +95 more

Exclusion-based exome sequencing in critically ill adults 18–40 years old has a 24% diagnostic rate and finds racial disparities in access to genetic testing

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.06.007

N/A

0DataRank · unranked

5 citations

Colleen Morse Kripke, Adam J. Mansfield, Alexander Li, Alexander Lopez, Alicia Hawes +95 more

A rare variant in GPR156 associated with depression in a Mennonite pedigree causes habenula hyperactivity and stress sensitivity in mice

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2404754122

N/A

0DataRank · unranked

1 citations

Claudia Gonzaga‐Jauregui, Karlla W. Brigatti, Joop de Jong, Robert Breese, Seung Yeon Ko +34 more

John D. Overton

Indexed papers

Top data-sharing exemplar

Papers