Stella Aslibekyan

University of Alabama at Birmingham

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

5.3Author DataRank

Indexed papers

8in 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 8 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.

Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed

Cell Genomics(2022)10.1016/j.xgen.2021.100084

Top 10%

2.1DataRank

Top 10%82 citations

Matthew P. Conomos, Rebecca Keener, Kruthika Iyer, Joshua S. Weinstock, Lisa R. Yanek +95 more

Papers

Driven by 55 papers — median percentile 62. Top paper: “Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries”.

Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2018)10.1038/s41467-018-04668-w

N/A

3.7DataRank · unranked

109 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed

Cell Genomics(2022)10.1016/j.xgen.2021.100084

Top 10%

2.1DataRank

Top 10%82 citations

Matthew P. Conomos, Rebecca Keener, Kruthika Iyer, Joshua S. Weinstock, Lisa R. Yanek +95 more

Analysis of rare Parkinson’s disease variants in millions of people

npj Parkinson s Disease(2024)10.1038/s41531-023-00608-8

Top 19%

1.1DataRank

Top 19%41 citations

Mary B. Makarious, Sara Bandrés‐Ciga, Hirotaka Iwaki, Stella Aslibekyan, Adam Auton +58 more

Insights From a Large-Scale Whole-Genome Sequencing Study of Systolic Blood Pressure, Diastolic Blood Pressure, and Hypertension

Hypertension(2022)10.1161/hypertensionaha.122.19324

Top 24%

0.842DataRank

Top 24%29 citations

Xiao Sun, Karen He, Michael R. Brown, Sarah A. Gagliano Taliun, Jacklyn N. Hellwege +95 more

GWAS and meta-analysis identifies 49 genetic variants underlying critical COVID-19

Nature(2023)10.1038/s41586-023-06034-3

N/A

0.795DataRank · unranked

199 citations

Konrad Rawlik, Andrew D. Bretherick, Ting Qi, Yang Wu, Isar Nassiri +3013 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

A phenome-wide association and Mendelian randomisation study of alcohol use variants in a diverse cohort comprising over 3 million individuals

EBioMedicine(2024)10.1016/j.ebiom.2024.105086

Top 42%

0.447DataRank

Top 42%13 citations

José Jaime Martínez‐Magaña, Natasia S. Courchesne‐Krak, Renata B. Cupertino, Laura Vilar‐Ribó, Sevim B. Bianchi +66 more

Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries

Nature Communications(2020)10.1038/s41467-020-15236-6

Top 57%

0.275DataRank

Top 57%2 citations

Sanni Ruotsalainen, Robert E. Handsaker, Maris Alver, Jonathan M. Bloom, Timothy Poterba +442 more

The genetic architecture of dog ownership: large-scale genome-wide association study in 97,552 European-ancestry individuals

G3 Genes Genomes Genetics(2024)10.1093/g3journal/jkae116

N/A

0.263DataRank · unranked

3 citations

Robert Karlsson, Shuyang Yao, Patrik K. E. Magnusson, Olesya Ajnakina, Andrew Steptoe +64 more

Genome-wide Study Identifies Association between HLA-B∗55:01 and Self-Reported Penicillin Allergy

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.08.008

N/A

0DataRank · unranked

56 citations

Jonas Bovijn, Neil S. Zheng, Maarja Lepamets, Jenny C. Censin, Tuuli Jürgenson +64 more

Association of Body Mass Index with DNA Methylation and Gene Expression in Blood Cells and Relations to Cardiometabolic Disease: A Mendelian Randomization Approach

UNC Libraries(2020)10.17615/9kkt-zw63

N/A

0DataRank · unranked

2 citations

Weihua Guan, Caroline S. Fox, Erica L. Kleinbrink, Åsa K. Hedman, Yao Chen +44 more

Genetic determinants of daytime napping and effects on cardiometabolic health

medRxiv(2020)10.1101/2020.06.12.20129858

N/A

0DataRank · unranked

17 citations

Iyas Daghlas, Jacqueline M. Lane, Yunru Huang, Miriam S. Udler, Heming Wang +9 more

Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.22.423783

N/A

0DataRank · unranked

11 citations

Peter Dornbos, Mark Chaffin, Dajiang J. Liu, Minxian X. Wang, Margaret Sunitha Selvaraj +95 more

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

Nature Genetics(2022)10.1038/s41588-021-00997-7

N/A

0DataRank · unranked

362 citations

Deepti Jain, Zhili Zheng, TOPMed Anthropometry Working Group, Stella Aslibekyan, Diane M. Becker +95 more

A framework for detecting noncoding rare-variant associations of large-scale whole-genome sequencing studies

Nature Methods(2022)10.1038/s41592-022-01640-x

N/A

0DataRank · unranked

109 citations

Xihao Li, Hufeng Zhou, Sheila M. Gaynor, Margaret Sunitha Selvaraj, Theodore Arapoglou +95 more

Genome-wide association study of REM sleep behavior disorder identifies polygenic risk and brain expression effects

Nature Communications(2022)10.1038/s41467-022-34732-5

N/A

0DataRank · unranked

95 citations

Karl Heilbron, Cornelis Blauwendraat, Regina Hertfelder Reynolds, Eric Yu, Konstantin Senkevich +95 more

Whole genome sequence analysis of blood lipid levels in >66,000 individuals

Nature Communications(2022)10.1038/s41467-022-33510-7

N/A

0DataRank · unranked

75 citations

Xihao Li, Zilin Li, Akhil Pampana, David Zhang, Joseph Park +95 more

Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals

Nature Communications(2022)10.1038/s41467-022-32275-3

N/A

0DataRank · unranked

63 citations

Daniel H. Katz, Julián Ávila-Pacheco, Alexander G. Bick, Akhil Pampana, Jeremy Robbins +95 more

Powerful, scalable and resource-efficient meta-analysis of rare variant associations in large whole genome sequencing studies

Nature Genetics(2022)10.1038/s41588-022-01225-6

N/A

0DataRank · unranked

62 citations

Corbin Quick, Hufeng Zhou, Sheila M. Gaynor, Yaowu Liu, Han Chen +95 more

Using a polygenic score in a family design to understand genetic influences on musicality

Scientific Reports(2022)10.1038/s41598-022-18703-w

N/A

0DataRank · unranked

23 citations

Abdel Abdellaoui, Reyna L. Gordon, Stella Aslibekyan, Adam Auton, Elizabeth Babalola +52 more

Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100163

N/A

0DataRank · unranked

10 citations

Virginia Fisher, Xuan Deng, Jennifer A. Brody, Misa Graff, Elise Lim +57 more

Investigating gene-diet interactions impacting the association between macronutrient intake and glycemic traits

medRxiv(2022)10.1101/2022.07.26.22278077

N/A

0DataRank · unranked

1 citations

Maura E. Walker, Sheila M. Gaynor, Jennifer Wessel, Daniel DiCorpo, Jiantao Ma +66 more

Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease

Nature Genetics(2023)10.1038/s41588-023-01584-8

N/A

0DataRank · unranked

264 citations

Dan Vitale, Diego Véliz Otani, Michelle Mulan Lian, Karl Heilbron, Stella Aslibekyan +95 more

Clonal haematopoiesis and risk of chronic liver disease

Nature(2023)10.1038/s41586-023-05857-4

N/A

0DataRank · unranked

204 citations

Connor A. Emdin, Alexander G. Bick, Seyedeh M. Zekavat, Abhishek Niroula, James P. Pirruccello +95 more

A new method for multiancestry polygenic prediction improves performance across diverse populations

Nature Genetics(2023)10.1038/s41588-023-01501-z

N/A

0DataRank · unranked

96 citations

Jianan Zhan, Jin Jin, Jingning Zhang, Wenxuan Lu, Ruzhang Zhao +65 more

Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

EBioMedicine(2023)10.1016/j.ebiom.2023.104758

N/A

0DataRank · unranked

19 citations

Priyadarshini Kachroo, Tianxiao Huan, David Van Den Berg, Gha Young Lee, Helena Bui +95 more

Investigating Gene–Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits

Diabetes(2023)10.2337/db22-0851

N/A

0DataRank · unranked

16 citations

Maura E. Walker, Sheila M. Gaynor, Jennifer Wessel, Daniel DiCorpo, Jiantao Ma +66 more

Validation of human telomere length trans-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as novel human telomere length regulation genes

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.07.12.548702

N/A

0DataRank · unranked

1 citations

Surya B. Chhetri, Carla J. Connelly, Margaret A. Taub, Matthew P. Conomos, Joshua S. Weinstock +93 more

The shared genetic architecture and evolution of human language and musical rhythm

Nature Human Behaviour(2024)10.1038/s41562-024-02051-y

N/A

0DataRank · unranked

30 citations

Else Eising, Yasmina Mekki, Giacomo Bignardi, Pierre Fontanillas, Stella Aslibekyan +59 more

MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups

Cell Genomics(2024)10.1016/j.xgen.2024.100539

N/A

0DataRank · unranked

27 citations

Jianan Zhan, Jingning Zhang, Ruzhang Zhao, Jared O’Connell, Yunxuan Jiang +65 more

Genome-wide association studies of coffee intake in UK/US participants of European ancestry uncover cohort-specific genetic associations

Neuropsychopharmacology(2024)10.1038/s41386-024-01870-x

N/A

0DataRank · unranked

12 citations

Pierre Fontanillas, Benjamin K. Pham, John J. Meredith, Mariela Jennings, Natasia S. Courchesne‐Krak +57 more

Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

Nature Communications(2024)10.1038/s41467-024-48394-y

N/A

0DataRank · unranked

8 citations

Surya B. Chhetri, Carla J. Connelly, Margaret A. Taub, Matthew P. Conomos, Joshua S. Weinstock +95 more

Bidirectional relationship between olfaction and Parkinson’s disease

npj Parkinson s Disease(2024)10.1038/s41531-024-00838-4

N/A

0DataRank · unranked

4 citations

Sara Bandrés‐Ciga, Karl Heilbron, Stella Aslibekyan, Adam Auton, Elizabeth Babalola +54 more

A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure

UNC Libraries(2024)10.17615/rmgv-6646

N/A

0DataRank · unranked

5 citations

H.J. De Silva, Annette Peters, Matthew Brown, J.D. Faul, Thomas W. Winkler +95 more

A system for phenotype harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) program

UNC Libraries(2024)10.17615/0ea7-3v47

N/A

0DataRank · unranked

0 citations

Nicola L. Hawley, May E. Montasser, P.A. Peyser, Daniel E. Weeks, Braxton D. Mitchell +67 more

Multi-ancestry sleep-by-SNP interaction analysis in 126,926 individuals reveals lipid loci stratified by sleep duration

UNC Libraries(2024)10.17615/f2gw-he44

N/A

0DataRank · unranked

0 citations

Lisa Warsinger Martin, Chen-Huan Yu, Pamela J. Schreiner, Tuomo Rankinen, Sina A. Gharib +95 more

Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants

UNC Libraries(2024)10.17615/xgme-w279

N/A

0DataRank · unranked

0 citations

Meher Preethi Boorgula, Alison E. Fohner, S.S. Rich, Stella Aslibekyan, Merry‐Lynn McDonald +57 more

Genome-Wide Interactions with Dairy Intake for Body Mass Index in Adults of European Descent

UNC Libraries(2024)10.17615/wajp-xh91

Top 100%

0DataRank

Top 100%0 citations

D.K. Arnett, J.I. Rotter, Luigi Ferruci, M. Carola Zillikens, Mika Kähönen +58 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

Whole Blood DNA Methylation Signatures of Diet Are Associated With Cardiovascular Disease Risk Factors and All-Cause Mortality

UNC Libraries(2024)10.17615/m9qy-2s51

N/A

0DataRank · unranked

0 citations

Alice H. Lichtenstein, Yue Zheng, M. FORNAGE, Mike Mendelson, C.M. Sitlani +45 more

Validation of human telomere length multi-ancestry meta-analysis association signals identifies POP5 and KBTBD6 as human telomere length regulation genes

UNC Libraries(2024)10.17615/vs68-ca81

N/A

0DataRank · unranked

0 citations

Ryan L. Minster, Fernando D. Martínez, Dawood Darbar, Juan M. Peralta, Barbara A. Konkle +93 more

Large-scale genome-wide analyses of stuttering

Nature Genetics(2025)10.1038/s41588-025-02267-2

N/A

0DataRank · unranked

11 citations

Alyssa Scartozzi, Douglas M. Shaw, Dillon G. Pruett, Hung‐Hsin Chen, Lauren E. Petty +65 more

A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies

Nature Computational Science(2025)10.1038/s43588-024-00764-8

N/A

0DataRank · unranked

10 citations

Han Chen, Margaret Sunitha Selvaraj, Eric Van Buren, Hufeng Zhou, Yuxuan Wang +95 more

Insights into ancestral diversity in Parkinson’s disease risk: a comparative assessment of polygenic risk scores

npj Parkinson s Disease(2025)10.1038/s41531-025-00967-4

N/A

0DataRank · unranked

5 citations

Spencer Grant, Mary B. Makarious, Inas Elsayed, Arinola O. Sanyaolu, Peter Wild Crea +95 more

Association between polygenic risk and survival in breast cancer patients

BMC Cancer(2025)10.1186/s12885-025-14640-9

N/A

0DataRank · unranked

3 citations

Stefan Groha, Yi Ding, Chris German, Wei Wang, Julie M. Granka +62 more

Whole genome sequence analysis of low-density lipoprotein cholesterol across 246 K individuals

Genome biology(2025)10.1186/s13059-025-03698-0

N/A

0DataRank · unranked

2 citations

Xihao Li, Zilin Li, Eric Van Buren, Sara Haidermota, Darina Postupaka +95 more

Genome-wide association study of delay discounting identifies 11 loci and reveals transdiagnostic associations across mental and physical health

Molecular Psychiatry(2025)10.1038/s41380-025-03356-8

N/A

0DataRank · unranked

2 citations

Renata B. Cupertino, Shreya R. Pakala, Pierre Fontanillas, Mariela Jennings, Jane Yang +75 more

cellSTAAR: incorporating single-cell-sequencing-based functional data to boost power in rare variant association testing of noncoding regions

Nature Methods(2025)10.1038/s41592-025-02919-5

N/A

0DataRank · unranked

0 citations

Yi Zhang, Xihao Li, Margaret Sunitha Selvaraj, Zilin Li, Hufeng Zhou +544 more

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

Nature(2020)10.1038/s41586-020-2819-2

N/A

0DataRank · unranked

748 citations

Joshua S. Weinstock, Satish K. Nandakumar, Charles P. Fulco, Erik L. Bao, Seyedeh M. Zekavat +95 more

Dynamic incorporation of multiple in silico functional annotations empowers rare variant association analysis of large whole-genome sequencing studies at scale

Nature Genetics(2020)10.1038/s41588-020-0676-4

N/A

0DataRank · unranked

292 citations

Zilin Li, Hufeng Zhou, Sheila M. Gaynor, Yaowu Liu, Han Chen +88 more

De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population

Proceedings of the National Academy of Sciences(2020)10.1073/pnas.1902766117

N/A

0DataRank · unranked

112 citations

Douglas P. Loesch, James A. Perry, Nancy L. Heard‐Costa, Daniel Taliun, Brian E. Cade +93 more

Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease

Nature Communications(2020)10.1038/s41467-020-20086-3

N/A

0DataRank · unranked

91 citations

Oren Rom, Ida Surakka, Sarah E. Graham, Wei Zhou, Tanmoy Roychowdhury +95 more

Whole Blood DNA Methylation Signatures of Diet Are Associated With Cardiovascular Disease Risk Factors and All-Cause Mortality

Circulation Genomic and Precision Medicine(2020)10.1161/circgen.119.002766

N/A

0DataRank · unranked

88 citations

Casey M. Rebholz, Kim V.E. Braun, Lindsay M. Reynolds, Stella Aslibekyan, Rui Xia +45 more

Genome-wide association and multi-omic analyses reveal ACTN2 as a gene linked to heart failure

Nature Communications(2020)10.1038/s41467-020-14843-7

N/A

0DataRank · unranked

86 citations

Emmanouil Tampakakis, Yanxiao Zhang, Wei Wang, Adam Auton, Michelle Agee +48 more

Association of Allostatic Load with All-Cause and Cancer Mortality by Race and Body Mass Index in the REGARDS Cohort

Cancers(2020)10.3390/cancers12061695

N/A

0DataRank · unranked

67 citations

Lauren E. Wilson, April Deveaux, Stella Aslibekyan, Mary Cushman, Susan C. Gilchrist +4 more

Stella Aslibekyan

Indexed papers

Top data-sharing exemplar

Papers