Stacey Gabriel

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

16.0Author 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.

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 66 papers — median percentile 68. Top paper: “A genomic mutational constraint map using variation in 76,156 human genomes”.

A genomic mutational constraint map using variation in 76,156 human genomes

Nature(2023)10.1038/s41586-023-06045-0

N/A

9.6DataRank · unranked

1369 citations

Laurent C. Francioli, Julia K. Goodrich, Ryan L. Collins, Masahiro Kanai, Qingbo S. Wang +95 more

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

Determinants of telomere length across human tissues

Science(2020)10.1126/science.aaz6876

N/A

8.6DataRank · unranked

501 citations

Farzana Jasmine, Lin Chen, Meytal Chernoff, Tong Lin, Dayana Delgado +90 more

Proteogenomic characterization of pancreatic ductal adenocarcinoma

Cell(2021)10.1016/j.cell.2021.08.023

N/A

7.9DataRank · unranked

606 citations

Chen Huang, Daniel Cui Zhou, Yingwei Hu, T. Mamie Lih, Sara R. Savage +95 more

Rare coding variants in ten genes confer substantial risk for schizophrenia

Nature(2022)10.1038/s41586-022-04556-w

N/A

7.2DataRank · unranked

900 citations

Timothy Poterba, David Curtis, Huda Akil, Mariam Al Eissa, Jack D. Barchas +95 more

A Quantitative Proteome Map of the Human Body

Cell(2020)10.1016/j.cell.2020.08.036

Top 4%

5.1DataRank

Top 4%487 citations

Meng Wang, Shin Lin, Ruiqi Jian, Xiao Li, Joanne Chan +95 more

High-throughput RNA isoform sequencing using programmed cDNA concatenation

Nature Biotechnology(2023)10.1038/s41587-023-01815-7

N/A

3.9DataRank · unranked

181 citations

Jonathan T. Smith, Kiran Garimella, Mehrtash Babadi, Victoria Popic, Moshe Sade-Feldman +14 more

Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility

Nature Genetics(2022)10.1038/s41588-022-01156-2

N/A

3.7DataRank · unranked

195 citations

Christine Stevens, Guhan Venkataraman, Kai Yuan, Brandon E. Avila, Maria T. Abreu +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

1.6DataRank · unranked

75 citations

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

Chromosome Xq23 is associated with lower atherogenic lipid concentrations and favorable cardiometabolic indices

Nature Communications(2021)10.1038/s41467-021-22339-1

N/A

1.1DataRank · unranked

51 citations

Akhil Pampana, Sarah E. Graham, Sanni Ruotsalainen, James A. Perry, Paul S. de Vries +95 more

Combined tumor and immune signals from genomes or transcriptomes predict outcomes of checkpoint inhibition in melanoma

Cell Reports Medicine(2022)10.1016/j.xcrm.2021.100500

N/A

0.972DataRank · unranked

35 citations

Moshe Sade-Feldman, Jaegil Kim, Chip Stewart, Anna Gonye, Arvind Ravi +34 more

Canonical correlation analysis for multi-omics: Application to cross-cohort analysis

PLoS Genetics(2023)10.1371/journal.pgen.1010517

N/A

0.970DataRank · unranked

40 citations

François Aguet, Kristin G. Ardlie, Jiawen Chen, Elaine Cornell, Dan Cruz +22 more

Estimating epidemiologic dynamics from cross-sectional viral load distributions

Science(2021)10.1126/science.abh0635

N/A

0.832DataRank · unranked

255 citations

Lee Kennedy‐Shaffer, Sanjat Kanjilal, Niall J. Lennon, Stacey Gabriel, Marc Lipsitch +2 more

Structural variation across 138,134 samples in the TOPMed consortium

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.25.525428

Top 27%

0.737DataRank

Top 27%18 citations

Adam C. English, Ginger Metcalf, Jianzhi Yang, Mark J. P. Chaisson, Nathan Pankratz +82 more

Gene expression in African Americans, Puerto Ricans and Mexican Americans reveals ancestry-specific patterns of genetic architecture

Nature Genetics(2023)10.1038/s41588-023-01377-z

N/A

0.694DataRank · unranked

101 citations

Angel C. Y. Mak, Donglei Hu, Celeste Eng, Scott Huntsman, Jennifer R. Elhawary +14 more

Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2023.11.013

N/A

0.679DataRank · unranked

21 citations

François Aguet, Sarah Kim-Hellmuth, Brielin C. Brown, Daniel Nachun, Russell P. Tracy +16 more

Genetic interactions drive heterogeneity in causal variant effect sizes for gene expression and complex traits

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.05.014

N/A

0.663DataRank · unranked

82 citations

Shaila Musharoff, Jeffrey P. Spence, Harold Pimentel, Catherine Tcheandjieu, Hakhamanesh Mostafavi +19 more

Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk

Nature Genetics(2025)10.1038/s41588-025-02074-9

N/A

0.628DataRank · unranked

28 citations

Sean J. Jurgens, Ling Xiao, Matthew C. Hill, Christopher M. Haggerty, Garðar Sveinbjörnsson +95 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

Cross-Site Concordance Evaluation of Tumor DNA and RNA Sequencing Platforms for the CIMAC-CIDC Network

Clinical Cancer Research(2020)10.1158/1078-0432.ccr-20-3251

Top 32%

0.613DataRank

Top 32%15 citations

Jingxin Fu, Carrie Cibulskis, Aashna Jhaveri, Curtis Gumbs, Biswajit Das +41 more

Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes

Nature Neuroscience(2024)10.1038/s41593-024-01747-8

N/A

0.612DataRank · unranked

58 citations

Siwei Chen, Bassel Abou‐Khalil, Zaid Afawi, Quratulain Zulfiqar Ali, Elisabetta Amadori +95 more

Mechanisms of response and resistance to combined decitabine and ipilimumab for advanced myeloid disease

Blood(2023)10.1182/blood.2022018246

N/A

0.593DataRank · unranked

51 citations

Yang Liu, Jacquelyn O. Wolff, Lin Yang, Len Taing, Aashna Jhaveri +32 more

Molecular and cellular features of CTLA-4 blockade for relapsed myeloid malignancies after transplantation

Blood(2021)10.1182/blood.2021010867

N/A

0.564DataRank · unranked

42 citations

Yi Zhang, Alexandra Savell, Teddy Huang, Nicoletta Cieri, Emily M. Thrash +33 more

The functional impact of rare variation across the regulatory cascade

Cell Genomics(2023)10.1016/j.xgen.2023.100401

N/A

0.526DataRank · unranked

15 citations

Nicole M. Ferraro, Benjamin J. Strober, François Aguet, Silva Kasela, Marios Arvanitis +33 more

Prognostically relevant gene signatures of high-grade serous ovarian carcinoma

UNC Libraries(2020)10.17615/c9kk-d491

N/A

0.517DataRank · unranked

4 citations

Martin Köbel, Hailei Zhang, Rehan Akbani, Nianxiang Zhang, Katherine A. Hoadley +27 more

Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program

Circulation Genomic and Precision Medicine(2023)10.1161/circgen.121.003532

Top 38%

0.507DataRank

Top 38%11 citations

Cecelia Laurie, Brandon J. Coombes, Deepti Jain, Matthew P. Conomos, Jennifer A. Brody +30 more

Sequencing of over 100,000 individuals identifies multiple genes and rare variants associated with Crohns disease susceptibility

medRxiv(2021)10.1101/2021.06.15.21258641

N/A

0.500DataRank · unranked

11 citations

Christine Stevens, Guhan Venkataraman, Kai Yuan, Brandon E. Avila, María T. Abreu +95 more

Using viral load and epidemic dynamics to optimize pooled testing in resource constrained settings

medRxiv(2020)10.1101/2020.05.01.20086801

N/A

0.477DataRank · unranked

23 citations

James A. Hay, Brendan Blumenstiel, Maegan Harden, Michelle Cipicchio, Jon Bezney +8 more

Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database

Nature Communications(2025)10.1038/s41467-025-61698-x

Top 44%

0.417DataRank

Top 44%14 citations

Moriel Singer‐Berk, Sarah L. Stenton, Julia K. Goodrich, Michael W. Wilson, Jonah Einson +95 more

Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.09.003

N/A

0.416DataRank · unranked

15 citations

Margaret Sunitha Selvaraj, Xihao Li, Zilin Li, Jacob A. Holdcraft, Donna K. Arnett +69 more

Diet Quality Scores Are Positively Associated with Whole Blood–Derived Mitochondrial DNA Copy Number in the Framingham Heart Study

Journal of Nutrition(2021)10.1093/jn/nxab418

N/A

0.406DataRank · unranked

14 citations

Xue Liu, Yuankai Zhang, Hanning Cheng, Wencheng Gao, Chao‐Qiang Lai +6 more

Whole genome sequencing association analysis of quantitative red blood cell phenotypes: the NHLBI TOPMed program

medRxiv(2020)10.1101/2020.12.09.20246736

N/A

0.360DataRank · unranked

10 citations

Adrienne M. Stilp, Caitlin McHugh, Shuquan Rao, Deepti Jain, Xiuwen Zheng +74 more

Combined tumor and immune signals from genomes or transcriptomes predict outcomes of checkpoint inhibition in melanoma

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.07.03.450733

N/A

0.358DataRank · unranked

7 citations

Moshe Sade-Feldman, Jaegil Kim, Chip Stewart, Anna Gonye, Arvind Ravi +34 more

Structural variation across 138,134 samples in the TOPMed consortium

Research Square(2023)10.21203/rs.3.rs-2515453/v1

N/A

0.345DataRank · unranked

9 citations

Adam C. English, Ginger Metcalf, Jianzhi Yang, Mark J. P. Chaisson, Nathan Pankratz +82 more

Neptune: an environment for the delivery of genomic medicine

Genetics in Medicine(2021)10.1038/s41436-021-01230-w

N/A

0.330DataRank · unranked

8 citations

Victoria Yi, David R. Murdock, Sara E. Kalla, Tsung-Jung Wu, Aniko Sabo +93 more

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

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.10.11.463514

N/A

0.277DataRank · unranked

3 citations

Xihao Li, Zilin Li, Akhil Pampana, David Y Zhang, Joseph Park +80 more

Proteome-Wide Association Studies for Blood Lipids and Comparison with Transcriptome-Wide Association Studies

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.08.17.553749

N/A

0.208DataRank · unranked

3 citations

Boran Gao, Qidi Feng, Ani Manichaikul, Gina M. Peloso, Russell P. Tracy +17 more

Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study

medRxiv(2023)10.1101/2023.06.28.23291966

N/A

0.146DataRank · unranked

1 citations

Margaret Sunitha Selvaraj, Xihao Li, Zilin Li, Jacob A. Holdcraft, Donna K. Arnett +69 more

Proteome-wide association studies for blood lipids and comparison with transcriptome-wide association studies

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100383

N/A

0.128DataRank · unranked

1 citations

Boran Gao, Qidi Feng, Ani Manichaikul, Gina M. Peloso, Russell P. Tracy +17 more

Interaction molecular QTL mapping discovers cellular and environmental modifiers of genetic regulatory effects

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.06.26.546528

N/A

0DataRank · unranked

7 citations

François Aguet, Sarah Kim-Hellmuth, Brielin C. Brown, Daniel Nachun, Russell P. Tracy +16 more

Canonical correlation analysis for multi-omics: Application to cross-cohort analysis

UNC Libraries(2023)10.17615/hthq-e624

N/A

0DataRank · unranked

0 citations

David J. Vandenberg, J. Gustav Smith, Tamar Sofer, Yongmei Liu, Peter Durda +23 more

Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assembly

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.09.07.555775

N/A

0DataRank · unranked

0 citations

Philip M. Boone, Yongqing Huang, Kiran Garimella, Kar‐Tong Tan, Bianca Russell +13 more

Genotyping common, large structural variations in 5,202 genomes using pangenomes, the Giraffe mapper, and the vg toolkit

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.04.412486

N/A

0DataRank · unranked

30 citations

Jean Monlong, Xian Chang, Adam M. Novak, Jordan M. Eizenga, Charles Markello +15 more

Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assembly

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.006

N/A

0DataRank · unranked

23 citations

Philip M. Boone, Yongqing Huang, Kiran Garimella, Kar‐Tong Tan, Bianca Russell +17 more

Dysanapsis Genetic Risk Predicts Lung Function Across the Lifespan

American Journal of Respiratory and Critical Care Medicine(2024)10.1164/rccm.202401-0011oc

N/A

0DataRank · unranked

10 citations

Amirthagowri Ambalavanan, Auyon Ghosh, Zhonglin Li, Kristina L. Buschur, Yanlin Ma +33 more

Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities

Communications Biology(2024)10.1038/s42003-024-06408-x

N/A

0DataRank · unranked

0 citations

Karynne Patterson, Divya Kalra, Marsha M. Wheeler, Yi–Ju Chen, Sara E. Kalla +93 more

Polygenic transcriptome risk scores for COPD and lung function improve cross-ethnic portability of prediction in the NHLBI TOPMed program

UNC Libraries(2024)10.17615/a7t8-mf18

N/A

0DataRank · unranked

0 citations

Stephen S. Rich, Xin Hu, B.E Cade, TOPMed Lung Working Group, Shannon Dugan‐Perez +47 more

Premature Menopause, Clonal Hematopoiesis, and Coronary Artery Disease in Postmenopausal Women

UNC Libraries(2024)10.17615/2ce8-yp94

N/A

0DataRank · unranked

0 citations

A.P Reiner, Michael C. Honigberg, JoAnn E. Manson, James P. Pirruccello, Cecelia Laurie +12 more

Infantile Myelofibrosis and Myeloproliferation with CDC42Dysfunction

Journal of Clinical Immunology(2020)10.1007/s10875-020-00778-7

N/A

0DataRank · unranked

33 citations

Dilnar Mahmut, Ah Ram Kim, Mitsutoshi Nakamura, Nour J. Abdulhay, Satish K. Nandakumar +15 more

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease

PLoS Genetics(2020)10.1371/journal.pgen.1008629

N/A

0DataRank · unranked

169 citations

Mary E. Haas, Amit V. Khera, Krishna G. Aragam, Mark Chaffin, Derek Klarin +37 more

High-throughput RNA isoform sequencing using programmable cDNA concatenation

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.10.01.462818

N/A

0DataRank · unranked

26 citations

Jonathan T. Smith, Kiran Garimella, Mehrtash Babadi, Moshe Sade-Feldman, Michael Gatzen +14 more

Evidence of transmission from fully vaccinated individuals in a large outbreak of the SARS-CoV-2 Delta variant in Provincetown, Massachusetts

medRxiv(2021)10.1101/2021.10.20.21265137

N/A

0DataRank · unranked

9 citations

Lydia A. Krasilnikova, Gage K. Moreno, S. F. Schaffner, Johanna Vostok, Nicholas FitzGerald +75 more

Multiplexed CRISPR-based microfluidic platform for clinical testing of respiratory viruses and identification of SARS-CoV-2 variants

Nature Medicine(2022)10.1038/s41591-022-01734-1

N/A

0DataRank · unranked

306 citations

Meilin Zhu, Catherine Hua, Juliane Weller, Marzieh Ezzaty Mirhashemi, Tien G. Nguyen +45 more

Pangenomics enables genotyping of known structural variants in 5202 diverse genomes

Science(2021)10.1126/science.abg8871

N/A

0DataRank · unranked

419 citations

Jean Monlong, Xian Chang, Adam M. Novak, Jordan M. Eizenga, Charles Markello +15 more

An integrated genomic analysis identifies clinically relevant subtypes of glioblastoma characterized by abnormalities in PDGFRA, IDH1, EGFR and NF1

UNC Libraries(2020)10.17615/qy3p-zp42

N/A

0DataRank · unranked

0 citations

Richard K. Wilson, Katherine A. Hoadley, Gad Getz, Heidi S. Feiler, Jann N. Sarkaria +28 more

Large multiethnic Candidate Gene Study for C-reactive protein levels: identification of a novel association at CD36 in African Americans

UNC Libraries(2020)10.17615/y6gd-gc72

N/A

0DataRank · unranked

0 citations

Stacey Gabriel, Lisa Warsinger Martin, Deborah Farlow, Ethan M. Lange, Ramachandran S. Vasan +27 more

Comprehensive Molecular Portraits of Invasive Lobular Breast Cancer

UNC Libraries(2020)10.17615/s3ab-0w32

N/A

0DataRank · unranked

0 citations

Gordon B. Mills, Nilsa C. Ramirez, Andrew J. Mungall, Hailei Zhang, Nikolaus Schultz +95 more

At-home Testing and Risk Factors for Acquisition of SARS-CoV-2 Infection in a Major US Metropolitan Area

Open Forum Infectious Diseases(2022)10.1093/ofid/ofac505

N/A

0DataRank · unranked

5 citations

Scott Dryden‐Peterson, Andy Kim, Sarah Naz‐McLean, Christina Kelly, Hannah H. Laibinis +10 more

Accounting for population structure in genetic studies of cystic fibrosis

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100117

N/A

0DataRank · unranked

6 citations

Adrienne M. Stilp, William W. Gordon, Jai Broome, Stephanie M. Gogarten, Hua Ling +20 more

At-home Testing and Risk Factors for Acquisition of SARS-CoV-2 Infection in a Major US Metropolitan Area

medRxiv(2022)10.1101/2022.02.02.22269258

Top 100%

0DataRank

Top 100%0 citations

Scott Dryden‐Peterson, Andy Kim, Sarah Naz‐McLean, Christina Kelly, Hannah H. Laibinis +9 more

Integrated genomic characterization of endometrial carcinoma

Carolina Digital Repository (University of North Carolina at Chapel Hill)(2020)10.17615/9sp1-1d11

N/A

0DataRank · unranked

0 citations

Stacey Gabriel, Elaine R. Mardis, Joelle Kalicki-Veizer, David J. Dooling, Rebecca Carlsen +27 more

Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk

Nature Genetics(2023)10.1038/s41588-023-01314-0

N/A

0DataRank · unranked

190 citations

Abril G. Izquierdo, Jing Chen, Richard Packer, Robert J. Hall, Anna L. Guyatt +95 more

Association of Exome Sequences With Cardiovascular Traits among Blacks in the Jackson Heart Study

UNC Libraries(2020)10.17615/a9gj-5z87

N/A

0DataRank · unranked

0 citations

Alex P. Reiner, Mark J. Daly, James G. Wilson, Hao Mei, Joshua D. Smith +14 more

The Somatic Genomic Landscape of Chromophobe Renal Cell Carcinoma

UNC Libraries(2020)10.17615/bd0j-6b91

N/A

0DataRank · unranked

0 citations

Kristen M. Leraas, Angela B. Smith, Michael J. Seiler, A. B. Clarke, Mark A. Jensen +95 more

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease.

Apollo (University of Cambridge)(2020)10.17863/cam.52580

N/A

0DataRank · unranked

0 citations

Mary E. Haas, Amit V. Khera, Krishna G. Aragam, Mark Chaffin, Derek Klarin +37 more

Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants

Genetics(2023)10.1093/genetics/iyad115

N/A

0DataRank · unranked

10 citations

Dafni A. Glinos, Eric Boerwinkle, Peter J. Castaldi, Dawood Darbar, Mariza de Andrade +28 more

Stacey Gabriel

Indexed papers

Top data-sharing exemplar

Papers