David J. Carey

ORCID: 0000-0001-6404-1950

Also affiliated with Geisinger Health System

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 1%percentile

5.0Author DataRank

Indexed papers

5in 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 5 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.

Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients

PLoS ONE(2020)10.1371/journal.pone.0242182

Top 9%

2.4DataRank

Top 9%43 citations

Jonathan Z. Luo, Alex R. Chang, Joseph B. Leader, Dustin N. Hartzel, Bryn S. Moore +7 more

Papers

Driven by 41 papers — median percentile 76. Top paper: “Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients”.

Electronic health record analysis identifies kidney disease as the leading risk factor for hospitalization in confirmed COVID-19 patients

PLoS ONE(2020)10.1371/journal.pone.0242182

Top 9%

2.4DataRank

Top 9%43 citations

Jonathan Z. Luo, Alex R. Chang, Joseph B. Leader, Dustin N. Hartzel, Bryn S. Moore +7 more

Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis

Nature Genetics(2024)10.1038/s41588-024-01720-y

Top 15%

1.4DataRank

Top 15%63 citations

Garðar Sveinbjörnsson, Marijana Vujković, Anne-Sofie Seidelin, Helene Gellert‐Kristensen, Gustav Ahlberg +47 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

The Genomics of Heart Failure: Design and Rationale of the HERMES Consortium

ESC Heart Failure(2021)10.1002/ehf2.13517

Top 24%

0.829DataRank

Top 24%22 citations

Sonia Shah, Honghuang Lin, Tomasz Czuba, Albert Henry, Daniel I. Swerdlow +95 more

Germline Mutations in CIDEB and Protection against Liver Disease

New England Journal of Medicine(2022)10.1056/nejmoa2117872

N/A

0.728DataRank · unranked

127 citations

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

A Genome-First Approach to Characterize DICER1 Pathogenic Variant Prevalence, Penetrance, and Phenotype

JAMA Network Open(2021)10.1001/jamanetworkopen.2021.0112

N/A

0.578DataRank · unranked

46 citations

Jung Kim, Ana F. Best, Zongming E. Chen, Ying Hu, Jeremy S. Haley +15 more

Rare variant analyses in 51,256 type 2 diabetes cases and 370,487 controls reveal the pathogenicity spectrum of monogenic diabetes genes

Nature Genetics(2024)10.1038/s41588-024-01947-9

N/A

0.564DataRank · unranked

42 citations

Philip Schroeder, Ravi Mandla, Man Li, Lowri Morris, Maheak Vora +21 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

A Genome-First Approach to Estimate Prevalence of Germline Pathogenic Variants and Risk of Pancreatic Cancer in Select Cancer Susceptibility Genes

Cancers(2022)10.3390/cancers14133257

N/A

0.483DataRank · unranked

24 citations

Jung Kim, Jeremy S. Haley, Sun Young Kim, H. Shanker Rao, David J. Carey +3 more

Genome-first approach of the prevalence and cancer phenotypes of pathogenic or likely pathogenic germline TP53 variants

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100242

N/A

0.449DataRank · unranked

19 citations

Natasha T. Strande, Jung Kim, Jeremy S. Haley, Jessica N. Hatton, Megan N. Frone +13 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

A genome-first approach to characterize DICER1 pathogenic variant prevalence, penetrance and cancer, thyroid, and other phenotypes in 2 population-scale cohorts

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101846

Top 50%

0.355DataRank

Top 50%9 citations

Jeremy S. Haley, Jessica N. Hatton, Uyenlinh L Mirshahi, H. Shanker Rao, Mark Ramos +6 more

Genome-first determination of the prevalence and penetrance of eight germline myeloid malignancy predisposition genes: a study of two population-based cohorts

Leukemia(2024)10.1038/s41375-024-02436-y

N/A

0.312DataRank · unranked

7 citations

Jung Kim, Jeremy S. Haley, Mark Ramos, Uyenlinh L Mirshahi, David J. Carey +3 more

Most Fanconi anemia heterozygotes are not at increased cancer risk: A genome-first DiscovEHR cohort population study

Genetics in Medicine(2023)10.1016/j.gim.2023.101042

N/A

0.292DataRank · unranked

6 citations

Burak Altintas, Jeremy S. Haley, Jung Kim, Mark Ramos, David J. Carey +3 more

Germline Pathogenic DROSHA Variants Are Linked to Pineoblastoma and Wilms Tumor Predisposition

Clinical Cancer Research(2025)10.1158/1078-0432.ccr-24-2785

N/A

0.292DataRank · unranked

6 citations

Lisa Golmard, Jung Kim, Riyue Bao, Frank Y. Lin, Angshumoy Roy +32 more

Genomic ascertainment for UBA1 variants and VEXAS syndrome: a population-based study

medRxiv(2022)10.1101/2022.07.27.22277962

N/A

0.241DataRank · unranked

4 citations

Dale L. Bodian, Vandan Shah, Uyenlinh L Mirshahi, Jung Kim, Yi Ding +11 more

Genomic ascertainment of CHEK2 -related cancer predisposition

medRxiv(2024)10.1101/2024.08.07.24311613

N/A

0.179DataRank · unranked

1 citations

Jung Kim, Mark Ramos, Jeremy S. Haley, Diane T. Smelser, H. Shanker Rao +6 more

Increased frequency of CHEK2 germline pathogenic variants among individuals with dermatofibrosarcoma protuberans

Genetics in Medicine Open(2024)10.1016/j.gimo.2024.101895

N/A

0.165DataRank · unranked

2 citations

Jung Kim, Jeremy S. Haley, Hayley P Barker, Piyushkumar A. Mundra, Mandy L. Ballinger +5 more

Improving type 2 diabetes polygenic risk scores by incorporating rare, low-frequency, and population-specific variants

medRxiv(2025)10.1101/2025.11.24.25340878

N/A

0.104DataRank · unranked

1 citations

Alicia Huerta‐Chagoya, Xiaoyu Wang, Maheak Vora, Jiang Li, Lehte Türk +18 more

TERT c.3150 G > C (p.K1050N): a founder Ashkenazi Jewish variant associated with telomere biology disorders

npj Genomic Medicine(2025)10.1038/s41525-025-00501-8

N/A

0.104DataRank · unranked

1 citations

Emília M. Pinto, Tianna Zhao, Logan P Zeigler, Jung Kim, Neelam Giri +18 more

Pharmacologic and Genetic Downregulation of Proprotein Convertase Subtilisin/Kexin Type 9 and Survival From Sepsis

Critical Care Explorations(2023)10.1097/cce.0000000000000997

N/A

0.104DataRank · unranked

1 citations

Garen Manvelian, Alida Coppi, Amy Damask, Michael Cantor, Manuel A. R. Ferreira +35 more

Investigation of cancer predisposition in Fanconi anemia heterozygotes: A DiscovEHR cohort population study.

Journal of Clinical Oncology(2023)10.1200/jco.2023.41.16_suppl.10589

N/A

0DataRank · unranked

0 citations

Burak Altintas, Jeremy S. Haley, Jung Kim, David J. Carey, Douglas R. Stewart +2 more

Supplementary Data 1 from Germline Pathogenic DROSHA Variants Are Linked to Pineoblastoma and Wilms Tumor Predisposition

Figshare(2025)10.1158/1078-0432.29052943

Top 100%

0DataRank

Top 100%0 citations

Lisa Golmard, Jung Kim, Riyue Bao, Frank Y. Lin, Angshumoy Roy +32 more

Supplementary Table Legend 1 from Germline Pathogenic DROSHA Variants Are Linked to Pineoblastoma and Wilms Tumor Predisposition

Figshare(2025)10.1158/1078-0432.29052940

N/A

0DataRank · unranked

0 citations

Lisa Golmard, Jung Kim, Riyue Bao, Frank Y. Lin, Angshumoy Roy +32 more

Figure S1 from Germline Pathogenic DROSHA Variants Are Linked to Pineoblastoma and Wilms Tumor Predisposition

(2025)10.1158/1078-0432.29052958

N/A

0DataRank · unranked

0 citations

Lisa Golmard, Jung Kim, Riyue Bao, Frank Y. Lin, Angshumoy Roy +32 more

Figure S3 from Germline Pathogenic DROSHA Variants Are Linked to Pineoblastoma and Wilms Tumor Predisposition

Figshare(2025)10.1158/1078-0432.29052952

N/A

0DataRank · unranked

0 citations

Lisa Golmard, Jung Kim, Riyue Bao, Frank Y. Lin, Angshumoy Roy +32 more

Figure S2 from Germline Pathogenic DROSHA Variants Are Linked to Pineoblastoma and Wilms Tumor Predisposition

Figshare(2025)10.1158/1078-0432.29052955

N/A

0DataRank · unranked

0 citations

Lisa Golmard, Jung Kim, Riyue Bao, Frank Y. Lin, Angshumoy Roy +32 more

Contributors

Genomic and Personalized Medicine(2009)10.1016/b978-0-12-369420-1.00122-0

N/A

0DataRank · unranked

0 citations

Matthew L. Anderson, Felicita Andreotti, Brian H. Annex, Anthony Antonellis, Dmitri Artemov +272 more

Regulatory Polymorphisms in Human DBH Affect Peripheral Gene Expression and Sympathetic Activity

UNC Libraries(2020)10.17615/sfcz-sw07

N/A

0DataRank · unranked

3 citations

David Weinshenker, James G. Wilson, Murray H. Brilliant, Glenn S. Gerhard, Helena Kuivaniemi +12 more

Polygenic Risk Scores Augment Stroke Subtyping

Neurology Genetics(2021)10.1212/nxg.0000000000000560

N/A

0DataRank · unranked

24 citations

Durgesh Chaudhary, Ayesha Khan, Christoph J. Griessenauer, David J. Carey, Ramin Zand +2 more

A framework for integrated clinical risk assessment using population sequencing data

medRxiv(2021)10.1101/2021.08.12.21261563

N/A

0DataRank · unranked

6 citations

Tho Tran, Jackson R. Bernatchez, Keithen E. Shepard, Christopher Koch, Aniruddh P. Patel +10 more

Independent phenotypic plasticity axes define distinct obesity sub-types

Nature Metabolism(2022)10.1038/s42255-022-00629-2

N/A

0DataRank · unranked

40 citations

Luca Fagnocchi, Stefanos Apostle, Vanessa Wegert, Salvador Casaní-Galdón, Kathrin Landgraf +38 more

Framework From a Multidisciplinary Approach for Transitioning Variants of Unknown Significance From Clinical Genetic Testing in Kidney Disease to a Definitive Classification

Kidney International Reports(2022)10.1016/j.ekir.2022.06.014

N/A

0DataRank · unranked

5 citations

Ahana Bhan, Lotte E. Tholen, Brian Fang, Guoli Chen, Bryn S. Moore +12 more

Contributors

Genomic and Personalized Medicine(2013)10.1016/b978-0-12-382227-7.00124-5

N/A

0DataRank · unranked

0 citations

Minhaz Uddin Ahmed, Sun Hee Ahn, R. Rand Allingham, Jude Alsarraj, Matthew L. Anderson +228 more

Rare GPR37L1 variants reveal potential roles in anxiety and migraine disorders

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.07.05.547546

N/A

0DataRank · unranked

0 citations

Andrea Cippitelli, Yingcai Wang, Oliver B. Pelletier, Ridge Dershem, Jianning Wei +7 more

Applying a genetic risk score model to enhance prediction of future multiple sclerosis diagnosis at first presentation with optic neuritis

Nature Communications(2024)10.1038/s41467-024-44917-9

N/A

0DataRank · unranked

10 citations

Feiyi Wang, Jiang Li, Lauric Ferrat, Uyenlinh L Mirshahi, H. Shanker Rao +11 more

Rare GPR37L1 Variants Reveal Potential Association between GPR37L1 and Disorders of Anxiety and Migraine

Journal of Neuroscience(2024)10.1523/jneurosci.1226-23.2024

N/A

0DataRank · unranked

6 citations

Andrea Cippitelli, Yingcai Wang, Oliver B. Pelletier, Ridge Dershem, Jianning Wei +7 more

Novel polygenic risk score associates with diverticulitis in a multi-institutional, ancestrally diverse cohort

Scientific Reports(2025)10.1038/s41598-025-26455-6

N/A

0DataRank · unranked

1 citations

Thomas E. Ueland, Sarah Abramowitz, John DePaolo, Noah L. Tsao, Jeffrey L. Roberson +8 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

Genome-First Approach to Rare and Common Variant Risk of Thoracic Aortic Aneurysm and Dissection

medRxiv(2025)10.1101/2025.05.18.25327858

N/A

0DataRank · unranked

1 citations

Diane T. Smelser, Dongchuan Guo, Sarah Abramowitz, Gina Biagetti, Renae Judy +12 more

David J. Carey

Indexed papers

Top data-sharing exemplar

Papers