Alan R. Shuldiner

Biochemistry, Genetics and Molecular BiologyHealth Professions

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

3.5Author DataRank

Indexed papers

7in 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 7 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.

A deep catalogue of protein-coding variation in 983,578 individuals

Nature(2024)10.1038/s41586-024-07556-0

Top 11%

1.9DataRank

Top 11%109 citations

Xiaodong Bai, Siying Chen, Suying Bao, Chuanyi Zhang, Manav Kapoor +92 more

Papers

Driven by 67 papers — median percentile 52. Top paper: “Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis”.

Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

Nature(2023)10.1038/s41586-023-05806-1

N/A

2.1DataRank · unranked

107 citations

Jayakrishnan Gopakumar, Bala Bharathi Burugula, Md Mesbah Uddin, Nikolaus Jahn, Julia A. Belk +95 more

A deep catalogue of protein-coding variation in 983,578 individuals

Nature(2024)10.1038/s41586-024-07556-0

Top 11%

1.9DataRank

Top 11%109 citations

Xiaodong Bai, Siying Chen, Suying Bao, Chuanyi Zhang, Manav Kapoor +92 more

Genomewide Association Study of Platelet Reactivity and Cardiovascular Response in Patients Treated With Clopidogrel: A Study by the International Clopidogrel Pharmacogenomics Consortium

Clinical Pharmacology & Therapeutics(2020)10.1002/cpt.1911

N/A

1.6DataRank · unranked

56 citations

Thomas O. Bergmeijer, Li Gong, Jean‐Luc Reny, Joshua P. Lewis, Braxton D. Mitchell +44 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

Defining the role of common variation in the genomic and biological architecture of adult human height

Nature Genetics(2014)10.1038/ng.3097

N/A

1.1DataRank · unranked

2093 citations

Emilio Rodríguez-Ruiz, The PAGE Consortium, Diana O. Perkins, Tonu Esko, Jian Yang +479 more

A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids

Nature Communications(2021)10.1038/s41467-021-23899-y

N/A

1.1DataRank · unranked

45 citations

Michael Mendelson, Rory Wilson, Rahul Gondalia, Roby Joehanes, Elias Salfati +59 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

Mucus sialylation determines intestinal host-commensal homeostasis

Cell(2022)10.1016/j.cell.2022.02.013

N/A

0.821DataRank · unranked

238 citations

Girak Kim, Samantha Shafer, Zuojia Chen, Satoshi Kubo, Yanlong Ji +45 more

Similar burden of pathogenic coding variants in exceptionally long‐lived individuals and individuals without exceptional longevity

Aging Cell(2020)10.1111/acel.13216

Top 25%

0.806DataRank

Top 25%13 citations

Gabriel Lidzbarsky, Sofiya Milman, Tina Gao, Patrick Sin‐Chan, Claudia Gonzaga‐Jauregui +5 more

Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease

Nature Genetics(2022)10.1038/s41588-021-01006-7

N/A

0.780DataRank · unranked

180 citations

Jack A. Kosmicki, Amy Damask, Deepika Sharma, Genevieve H. L. Roberts, Anne E. Justice +89 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

rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysis

Journal of Hepatology(2020)10.1016/j.jhep.2020.08.027

N/A

0.744DataRank · unranked

142 citations

Kushala Abeysekera, Leon A. Adams, Elmar Aigner, Quentin M. Anstee, Jesús M. Bañales +93 more

Extent and distribution of linkage disequilibrium in the Old Order Amish

Genetic Epidemiology(2010)10.1002/gepi.20444

N/A

0.735DataRank · unranked

12 citations

Albert M. Levin, Evadnie Rampersaud, Haiqing Shen, Jeffrey R. O'Connell, Braxton D. Mitchell +3 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

0.731DataRank · unranked

18 citations

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

Depression, stress and regional cerebral blood flow

Journal of Cerebral Blood Flow & Metabolism(2023)10.1177/0271678x221148979

N/A

0.703DataRank · unranked

26 citations

Bhim M. Adhikari, Mark D. Kvarta, Heather Bruce, Eric L. Goldwaser, Yizhou Ma +8 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 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

Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program

Communications Biology(2022)10.1038/s42003-022-03702-4

Top 34%

0.582DataRank

Top 34%16 citations

Sheila M. Gaynor, Emily M. Russell, Kenneth E. Westerman, Laura M. Raffield, Timothy D. Majarian +88 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

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

0.546DataRank · unranked

37 citations

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

Exome Sequencing Identifies A Nonsense Variant inDAOAssociated With Reduced Energy Expenditure in American Indians

The Journal of Clinical Endocrinology & Metabolism(2020)10.1210/clinem/dgaa548

N/A

0.518DataRank · unranked

9 citations

Çiğdem Köroğlu, Anup Nair, Jeff Sutherland, Yunhua L. Muller, Pankaj Kumar +13 more

Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

EBioMedicine(2021)10.1016/j.ebiom.2020.103157

N/A

0.505DataRank · unranked

28 citations

Kelsey Grinde, Jennifer A. Brody, Charles E. Breeze, Laura M. Raffield, Josyf C. Mychaleckyj +68 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 Variation in PEAR1, Cardiovascular Outcomes and Effects of Aspirin in a Healthy Elderly Population

Clinical Pharmacology & Therapeutics(2020)10.1002/cpt.1959

N/A

0.457DataRank · unranked

20 citations

Moeen Riaz, Sophia Xie, Galina Polekhina, Rory Wolfe, Mark Nelson +7 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

Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

Nature Aging(2024)10.1038/s43587-024-00647-7

N/A

0.406DataRank · unranked

14 citations

Michael A. Raddatz, Yash Pershad, Daniel Nachun, Kent D. Taylor, Xiuqing Guo +40 more

The contribution of de novo coding mutations to meningomyelocele

Nature(2025)10.1038/s41586-025-08676-x

N/A

0.396DataRank · unranked

13 citations

Ashna Nisal, Isaac Tang, Chanjae Lee, Ishani Jhamb, Cassidy Wallace +74 more

The genetic determinants of recurrent somatic mutations in 43,693 blood genomes

Science Advances(2023)10.1126/sciadv.abm4945

N/A

0.396DataRank · unranked

13 citations

Cecelia Laurie, Jai Broome, Kent D. Taylor, Xiuqing Guo, Alan R. Shuldiner +82 more

Glucocorticoid Receptor Gene (NR3C1) Polymorphisms and Metabolic Syndrome: Insights from the Mennonite Population

Genes(2023)10.3390/genes14091805

N/A

0.385DataRank · unranked

12 citations

Ana Luiza Sprotte Mira, Eduardo Delabio Auer, Isabela Dall’Oglio Bucco, Carla Eduarda de Lima e Silva, Priscila Ianzen dos Santos +13 more

Clonal hematopoiesis is driven by aberrant activation of TCL1A

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.12.10.471810

N/A

0.360DataRank · unranked

10 citations

Jayakrishnan Gopakumar, Bala Bharathi Burugula, Md Mesbah Uddin, Nikolaus Jahn, Julia A. Belk +95 more

Genome-wide significant risk loci for mood disorders in the Old Order Amish founder population

Molecular Psychiatry(2023)10.1038/s41380-023-02014-1

N/A

0.330DataRank · unranked

8 citations

Kwangmi Ahn, Rachel L. Kember, Fabiana L. Lopes, Evelina Mocci, Juan M. Peralta +14 more

Hemizygous variants in protein phosphatase 1 regulatory subunit 3F (PPP1R3F) are associated with a neurodevelopmental disorder characterized by developmental delay, intellectual disability and autistic features

Human Molecular Genetics(2023)10.1093/hmg/ddad124

N/A

0.312DataRank · unranked

7 citations

Baozhong Xin, Iris Nira Smith, Valerie Sency, Julia Szekely, Anna Alkelai +49 more

Actionable genetic variants in 4,198 Scottish participants from the Orkney and Shetland founder populations and implementation of return of results

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.02.018

N/A

0.312DataRank · unranked

7 citations

Lucija Klaric, Marisa D. Muckian, Kiera Johnston, Camilla Drake, Mihail Halachev +11 more

Association of parity with body mass index and cardiometabolic risk in high-parous women

Menopause The Journal of The North American Menopause Society(2023)10.1097/gme.0000000000002194

N/A

0.292DataRank · unranked

6 citations

Patrick F. McArdle, Kathleen A. Ryan, Melanie Daue, Huichun Xu, Kathryn Hughes Barry +5 more

Missense variants in SORT1 are associated with LDL-C in an Amish population

Journal of Lipid Research(2023)10.1016/j.jlr.2023.100468

N/A

0.269DataRank · unranked

5 citations

Kathryn L. Schueler, Sarah M. King, Joseph Orr, Kathleen A. Ryan, Mark P. Keller +5 more

Randomized evaluation of the loss‐of‐function carboxylesterase 1 (CES1) G143E variant on clopidogrel and ticagrelor pharmacodynamics

Clinical and Translational Science(2024)10.1111/cts.70079

N/A

0.256DataRank · unranked

4 citations

Kathleen A. Ryan, Elizabeth A. Streeten, Hilary B. Whitlatch, Melanie Daue, Keith Tanner +5 more

Next generation sequencing for HLA loci in full heritage Pima Indians of Arizona, Part II: HLA-A, -B, and -C with selected non-classical loci at 4-field resolution from whole genome sequences

Human Immunology(2021)10.1016/j.humimm.2021.03.013

Top 63%

0.216DataRank

Top 63%3 citations

Çiğdem Köroğlu, William C. Knowler, Alan R. Shuldiner, Nehal Gosalia, Cristopher V. Van Hout +4 more

Identification and functional validation of rare coding variants in genes linked to monogenic obesity

Obesity(2024)10.1002/oby.24101

N/A

0.165DataRank · unranked

2 citations

Michael Traurig, Yunhua L. Muller, Samantha E. Day, Paolo Piaggi, Kim Wiedrich +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

0.104DataRank · unranked

1 citations

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

Parkinson’s disease-related motor and non-motor symptoms are not more prevalent in the Lancaster Amish

medRxiv(2020)10.1101/2020.04.13.20064337

N/A

0DataRank · unranked

0 citations

Xuemei Huang, Honglei Chen, Lan Kong, Teodor T. Postolache, John W. Stiller +7 more

Functional characterization of a novel p.Ser76Thr variant in IGFBP4 that associates with body mass index in American Indians

European Journal of Human Genetics(2022)10.1038/s41431-022-01129-3

N/A

0DataRank · unranked

3 citations

Michael S. Saporito, Samantha E. Day, Khushdeep Bandesh, Çiğdem Köroğlu, Sayuko Kobes +7 more

Cerebral blood flow and cardiovascular risk effects on resting brain regional homogeneity

NeuroImage(2022)10.1016/j.neuroimage.2022.119555

N/A

0DataRank · unranked

15 citations

L. Elliot Hong, Zhiwei Zhao, Danny J.J. Wang, Paul M. Thompson, Neda Jahanshad +20 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

NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium

UNC Libraries(2020)10.17615/svd7-zw53

N/A

0DataRank · unranked

0 citations

Lenore J. Launer, Barbara McKnight, Alan R. Shuldiner, Tamara B. Harris, Ulf Gyllensten +27 more

Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation

UNC Libraries(2020)10.17615/frhz-yk87

N/A

0DataRank · unranked

0 citations

Juan M. Peralta, Olivia Weeks, Gudnason, Vilmunder, Kurt Lohman, Andrew D. Johnson +63 more

SuperAger Initiative: unlocking the genetic potential of exceptional longevity

Nature Aging(2023)10.1038/s43587-023-00429-7

N/A

0DataRank · unranked

0 citations

Nir Barzilai, Kara A. Wilson, Odette van der Willik, Stephanie Lederman, Thomas T. Perls +6 more

Prevalence, control, and treatment of diabetes, hypertension, and high cholesterol in the Amish

BMJ Open Diabetes Research & Care(2020)10.1136/bmjdrc-2019-000912

N/A

0DataRank · unranked

23 citations

Kathleen A. Ryan, Elizabeth A. Streeten, Patrick F. McArdle, Melanie Daue, Donna Trubiano +10 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

Contents Vol. 64, 2007

Human Heredity(2007)10.1159/000105467

N/A

0DataRank · unranked

0 citations

John P. A. Ioannidis, Wendy S. Post, Haiqing Shen, Coleen Damcott, Dan E. Arking +20 more

Identification and characterization of human GDF15 knockouts

Nature Metabolism(2024)10.1038/s42255-024-01135-3

N/A

0DataRank · unranked

17 citations

Shareef Khalid, Christopher Koch, Maleeha Khan, Lindsey B. Lamarche, Igor Splawski +32 more

Association Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies

UNC Libraries(2020)10.17615/tb6e-th27

N/A

0DataRank · unranked

0 citations

Christina L. Wassel, Tanja Zeller, Lina Zgaga, Eric Boerwinkle, Ben A. Oostra +95 more

Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

UNC Libraries(2024)10.17615/hd68-ze50

Top 100%

0DataRank

Top 100%0 citations

B.M. Psaty, Leslie J. Baier, Robert B. Wallace, Anna Köttgen, Jiang He +69 more

NFAT5 and SLC4A10 loci associate with plasma osmolality

UNC Libraries(2024)10.17615/86h9-j874

N/A

0DataRank · unranked

0 citations

Priya Srikanth, Péter Vollenweider, Christian Gieger, Ilja M. Nolte, Mariza de Andrade +95 more

Whole genome sequence association analysis of fasting glucose and fasting insulin levels in diverse cohorts from the NHLBI TOPMed program

UNC Libraries(2024)10.17615/75fz-j027

Top 100%

0DataRank

Top 100%0 citations

J.E. Curran, S.L.R. Kardia, Márcio Rodrigues de Almeida, J.B. Meigs, M.R. Irvin +88 more

A multi-ethnic epigenome-wide association study of leukocyte DNA methylation and blood lipids

UNC Libraries(2024)10.17615/6p9v-ms63

N/A

0DataRank · unranked

0 citations

Themistocles L. Assimes, Alan R. Shuldiner, Min-A Jhun, W. Chen, D. Absher +59 more

Author Index Vol. 64, 2007

Human Heredity(2007)10.1159/000105464

N/A

0DataRank · unranked

0 citations

John P. A. Ioannidis, Wendy S. Post, Haiqing Shen, Coleen Damcott, Dan E. Arking +20 more

The landscape of hereditary haemochromatosis risk and diagnosis across the British Isles and Ireland

Nature Communications(2026)10.1038/s41467-025-65511-7

N/A

0DataRank · unranked

0 citations

Benjamin S. Fletcher, Gannie Tzoneva, Alan R. Shuldiner, Edmund Gilbert, James F. Wilson +2 more

Multiple dimensions of stress vs. genetic effects on depression

Translational Psychiatry(2021)10.1038/s41398-021-01369-9

N/A

0DataRank · unranked

6 citations

Heather Bruce, Joshua Chiappelli, Stephanie Hare, Eric L. Goldwaser, Jessica Sewell +12 more

Tailored Approach to Designing a Digital Research Platform for Adults Aged 95 and Older: SuperAgers Family Study

The Journals of Gerontology Series A(2025)10.1093/gerona/glaf016

N/A

0DataRank · unranked

1 citations

Aisha Montgomery, Nir Barzilai, Tina Gao, Kara A. Wilson, Thomas Perls +6 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

A founder variant in TBCB is associated with global developmental delay, autism spectrum, and spastic paraparesis

Genetics in Medicine(2025)10.1016/j.gim.2025.101569

N/A

0DataRank · unranked

0 citations

Chen Itzkovich, Alina Kurolap, Mordechai Shohat, Alexandra Dürr, Jean‐Madeleine de Sainte Agathe +15 more

Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

UNC Libraries(2025)10.17615/cdn0-cm52

N/A

0DataRank · unranked

0 citations

Russell P. Tracy, Jill M. Johnsen, Hind Bouzid, Nicholas L. Smith, Katherine P. Prothro +95 more

Assessment of the potential role of natural selection in type 2 diabetes and related traits across human continental ancestry groups: comparison of phenotypic with genotypic divergence

Diabetologia(2020)10.1007/s00125-020-05272-8

N/A

0DataRank · unranked

6 citations

Cristopher V. Van Hout, Wen‐Chi Hsueh, Alan R. Shuldiner, Sayuko Kobes, Madhumita Sinha +3 more

Genetic versus stress and mood determinants of sleep in the Amish

American Journal of Medical Genetics Part B Neuropsychiatric Genetics(2021)10.1002/ajmg.b.32840

N/A

0DataRank · unranked

3 citations

Peter Kochunov, Joshua Chiappelli, Anya Savransky, Kathleen Carino, Jessica Sewell +10 more

Evidence of Neurovascular Water Exchange and Endothelial Vascular Dysfunction in Schizophrenia: An Exploratory Study

Schizophrenia Bulletin(2023)10.1093/schbul/sbad057

N/A

0DataRank · unranked

21 citations

Danny J.J. Wang, Bhim M. Adhikari, Joshua Chiappelli, Xingfeng Shao, Jiaao Yu +17 more

Alan R. Shuldiner

Indexed papers

Top data-sharing exemplar

Papers