Paul L. Auer

Biochemistry, Genetics and Molecular Biology

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

14.6Author DataRank

Indexed papers

14in 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 14 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.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y

Top 3%

7.0DataRank

Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 more

Papers

Driven by 134 papers — median percentile 64. Top paper: “Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data”.

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

7.2DataRank · unranked

363 citations

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

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y

Top 3%

7.0DataRank

Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +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

5.3DataRank · unranked

295 citations

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

Clonal haematopoiesis and risk of chronic liver disease

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

N/A

4.5DataRank · unranked

204 citations

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

A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

Nature Genetics(2021)10.1038/s41588-021-00935-7

N/A

4.0DataRank · unranked

191 citations

Masahiro Kanai, Wanson Choi, Xinyi Li, Saori Sakaue, Kenichi Yamamoto +95 more

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

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

Nature Genetics(2020)10.1038/s41588-020-00713-x

N/A

3.7DataRank · unranked

242 citations

Elena V. Feofanova, Najim Lahrouchi, Ioanna Ntalla, Savita Karthikeyan, James P. Cook +94 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

3.0DataRank · unranked

112 citations

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

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

Genome sequencing unveils a regulatory landscape of platelet reactivity

Nature Communications(2021)10.1038/s41467-021-23470-9

N/A

1.5DataRank · unranked

54 citations

Ming‐Huei Chen, Benjamin A.T. Rodriguez, Lisa R. Yanek, Arunoday Bhan, Brady Gaynor +94 more

Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity

Diabetes(2020)10.2337/db20-0070

N/A

1.5DataRank · unranked

57 citations

Yiying Zhang, Cassandra N. Spracklen, Tugce Karaderi, Lam Opal Huang, Jonathan P. Bradfield +95 more

Whole-Genome Sequencing Association Analyses of Stroke and Its Subtypes in Ancestrally Diverse Populations From Trans-Omics for Precision Medicine Project

Stroke(2021)10.1161/strokeaha.120.031792

Top 16%

1.3DataRank

Top 16%38 citations

Jeffrey W. Haessler, Regina Manansala, Kerri L. Wiggins, Arden Moscati, Alexa Beiser +34 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

1.2DataRank · unranked

63 citations

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

1.1DataRank · unranked

63 citations

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

Deleterious heteroplasmic mitochondrial mutations are associated with an increased risk of overall and cancer-specific mortality

Nature Communications(2023)10.1038/s41467-023-41785-7

N/A

1.1DataRank · unranked

44 citations

Stephanie L. Battle, Wen Shi, Daniela Puiu, Vamsee Pillalamarri, Jiaqi Xie +21 more

Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program

Genome Medicine(2021)10.1186/s13073-021-00917-8

Top 21%

0.976DataRank

Top 21%35 citations

Jiwon Lee, Tamar Sofer, Heming Wang, Man Zhang, Han Chen +94 more

Principles and methods for transferring polygenic risk scores across global populations

Nature Reviews Genetics(2023)10.1038/s41576-023-00637-2

N/A

0.869DataRank · unranked

328 citations

Nilanjan Chatterjee, Jibril Hirbo, Daniel J. Schaid, Iman K. Martin, Iftikhar J. Kullo +12 more

Variant-specific inflation factors for assessing population stratification at the phenotypic variance level

Nature Communications(2021)10.1038/s41467-021-23655-2

N/A

0.840DataRank · unranked

21 citations

Xiuwen Zheng, Cecelia Laurie, Stephanie M. Gogarten, Jennifer A. Brody, Matthew P. Conomos +91 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

Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative

Human Molecular Genetics(2021)10.1093/hmg/ddab252

Top 28%

0.724DataRank

Top 28%20 citations

Yao Hu, Quan Sun, Deepti Jain, Jai Broome, Ming‐Huei Chen +62 more

TOP-LD: A tool to explore linkage disequilibrium with TOPMed whole-genome sequence data

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.04.006

N/A

0.701DataRank · unranked

106 citations

Jonathan D. Rosen, Quan Sun, Jiawen Chen, Marsha M. Wheeler, Ying Zhou +20 more

Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing

Nature Genetics(2023)10.1038/s41588-023-01553-1

N/A

0.681DataRank · unranked

31 citations

Ying Zhou, Adrienne M. Stilp, Jason Bacon, Justin Wong, Zuhal Özcan +46 more

Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2024.12.014

N/A

0.605DataRank · unranked

14 citations

Xiaolong Ma, Adrienne M. Stilp, Fulong Yu, Jason Bacon, Justin Wong +64 more

A genetic association study of circulating coagulation factor VIII and von Willebrand factor levels

Blood(2024)10.1182/blood.2023021452

N/A

0.601DataRank · unranked

23 citations

Paula Reventún, Michael R. Brown, Adam S. Heath, Jennifer E. Huffman, Ngoc‐Quynh Le +90 more

A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry

Breast Cancer Research(2023)10.1186/s13058-023-01691-8

Top 36%

0.538DataRank

Top 36%12 citations

Xiaoliang Wang, Sabine Behrens, Manjeet K. Bolla, Qin Wang, Joe Dennis +95 more

Genomic and phenomic landscape of clonal hematopoiesis in over a million ancestrally diverse participants

medRxiv(2022)10.1101/2022.07.29.22278015

Top 37%

0.528DataRank

Top 37%13 citations

Zhi Yu, Joshua S. Weinstock, Abhishek Niroula, Satoshi Koyama, Tetsushi Nakao +83 more

From GWAS variant to function: A study of ∼148,000 variants for blood cell traits

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100063

N/A

0.523DataRank · unranked

15 citations

Cheynna Crowley, Le Huang, Jia Wen, Jiawen Chen, Erik L. Bao +7 more

ENIGMA CHEK2 gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk

Clinical Cancer Research(2023)10.1158/1078-0432.ccr-23-0212

N/A

0.520DataRank · unranked

31 citations

Petra Kleiblova, Petra Zemánková, Barbora Šťastná, Marketa Janatova, Jana Soukupová +95 more

Rare variant contribution to the heritability of coronary artery disease

Nature Communications(2024)10.1038/s41467-024-52939-6

N/A

0.513DataRank · unranked

16 citations

Shoa L. Clarke, Gaëlle Auguste, Natalie R. Hasbani, Alanna C. Morrison, Adam S. Heath +95 more

Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.007

N/A

0.494DataRank · unranked

26 citations

Caitlin McHugh, Linda M. Polfus, Laura M. Raffield, Meher Preethi Boorgula, Thomas W. Blackwell +88 more

Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study

BMC Genomics(2021)10.1186/s12864-021-07745-5

N/A

0.477DataRank · unranked

23 citations

Stephanie A. Bien, Katherine K. Nishimura, Jeffrey Haessler, Chani J. Hodonsky, Antoine Baldassari +29 more

Interferon gamma-induced protein 10 (IP-10) and cardiovascular disease in African Americans

PLoS ONE(2020)10.1371/journal.pone.0231013

N/A

0.442DataRank · unranked

18 citations

Neil A. Zakai, Paul L. Auer, Mary Cushman, Ethan M. Lange, Emily B. Levitan +8 more

Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factors

Human Molecular Genetics(2022)10.1093/hmg/ddac100

N/A

0.434DataRank · unranked

17 citations

Peng Wei, Jennifer A. Brody, Ming‐Huei Chen, Paul S. de Vries, Jennifer E. Huffman +26 more

Association of clonal hematopoiesis and mosaic chromosomal alterations with solid malignancy incidence and mortality

Cancer(2024)10.1002/cncr.35455

N/A

0.425DataRank · unranked

16 citations

Ying Zhou, Justin Grenet, Samuel K. Handelman, Cynthia Crispino, Laura N. Tarbay +20 more

Whole-genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

Blood(2024)10.1182/blood.2023022596

N/A

0.416DataRank · unranked

15 citations

Jayna Nicholas, Julie Hahn, Adam S. Heath, Laura M. Raffield, Lisa R. Yanek +95 more

Development of a Breast Cancer Risk Prediction Model Integrating Monogenic, Polygenic, and Epidemiologic Risk

Cancer Epidemiology Biomarkers & Prevention(2024)10.1158/1055-9965.epi-24-0594

N/A

0.408DataRank · unranked

8 citations

Nicholas Boddicker, Siddhartha Yadav, Hongyan Huang, Jie Na, Chunling Hu +30 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

Characterization of the phenotypic consequences of the Duffy-null genotype

Blood Advances(2025)10.1182/bloodadvances.2024014399

N/A

0.373DataRank · unranked

11 citations

Megan M. Shuey, Jennifer E. Huffman, Paul L. Auer, Alex P. Reiner, Laura M. Raffield +1 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

Determinants of mosaic chromosomal alteration fitness

Nature Communications(2024)10.1038/s41467-024-48190-8

N/A

0.345DataRank · unranked

9 citations

Taralynn Mack, Hannah Poisner, Yasminka A. Jakubek, Adrienne M. Stilp, Braxton D. Mitchell +39 more

Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-specific effects via GAUDI

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.10.06.511219

N/A

0.345DataRank · unranked

9 citations

Bryce Rowland, Jiawen Chen, Anna V. Mikhaylova, Christy L. Avery, Ulrike Peters +13 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

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

0.330DataRank · unranked

8 citations

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

Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 women

Scientific Reports(2022)10.1038/s41598-022-10121-2

N/A

0.320DataRank · unranked

6 citations

Pooja Middha, Paul L. Auer, Joe Dennis, Alison M. Dunning, Qin Wang +75 more

A General Approach to Adjusting Genetic Studies for Assortative Mating

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.09.01.555983

N/A

0.312DataRank · unranked

7 citations

Regina Manansala, Dhruva Jaishankar, Jonathan Jala, Daniel J. Benjamin, Miles Kimball +4 more

Donor telomeres and their magnitude of shortening post-allogeneic haematopoietic cell transplant impact survival for patients with early-stage leukaemia or myelodysplastic syndrome

EBioMedicine(2025)10.1016/j.ebiom.2025.105641

N/A

0.292DataRank · unranked

6 citations

Hormuzd A. Katki, Tsung‐Po Lai, Paul L. Auer, Casey Dagnall, Caitrin Bupp +11 more

Whole genome sequencing identifies common and rare structural variants contributing to hematologic traits in the NHLBI TOPMed program

medRxiv(2021)10.1101/2021.12.16.21267871

N/A

0.292DataRank · unranked

6 citations

Adrienne M. Stilp, Shuquan Rao, Bjarni V. Halldórsson, Doruk Beyter, Jia Wen +54 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

From GWAS Variant to Function: a Study of ~148,000 Variants for Blood Cell Traits

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.02.16.431409

N/A

0.274DataRank · unranked

4 citations

Cheynna Crowley, Le Huang, Jia Wen, Jiawen Chen, Erik L. Bao +7 more

Author Correction: A high-resolution HLA reference panel capturing global population diversity enables multi-ancestry fine-mapping in HIV host response

Nature Genetics(2021)10.1038/s41588-021-00979-9

N/A

0.246DataRank · unranked

4 citations

Masahiro Kanai, Wanson Choi, Xinyi Li, Saori Sakaue, Kenichi Yamamoto +95 more

Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood

medRxiv(2024)10.1101/2024.04.16.24305851

N/A

0.241DataRank · unranked

4 citations

Xiaolong Ma, Adrienne M. Stilp, Fulong Yu, Jason Bacon, Justin Wong +61 more

Mosaic chromosomal alterations in blood across ancestries via whole-genome sequencing

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.11.07.515222

N/A

0.208DataRank · unranked

3 citations

Ying Zhou, Adrienne M. Stilp, Jason Bacon, Justin Wong, Zuhal Özcan +41 more

Genetic Examination of Hematological Parameters in SARS-CoV-2 Infection and COVID-19

medRxiv(2022)10.1101/2022.02.28.22271562

N/A

0.208DataRank · unranked

3 citations

Quan Sun, Wanjiang Wang, Tyne W. Miller‐Fleming, Nancy J. Cox, Misa Graff +9 more

Genetic determinants and genomic consequences of non-leukemogenic somatic point mutations

Nature Communications(2025)10.1038/s41467-025-64236-x

N/A

0.165DataRank · unranked

2 citations

Sharjeel A. Chaudhry, Μαρία Ιωάννου, Maria Viskadourou, Paula Reventún, Yasminka A. Jakubek +49 more

Integrating whole genome and transcriptome sequencing to characterize the genetic architecture of isoform variation

Nature Communications(2025)10.1038/s41467-025-64336-8

Top 70%

0.165DataRank

Top 70%2 citations

Roby Joehanes, Jiantao Ma, Jiuyong Xie, Jian Yang, Mengyao Wang +20 more

EndoPRS: Incorporating endophenotype information to improve polygenic risk scores for clinical endpoints—A study in asthma

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.03.008

N/A

0.165DataRank · unranked

2 citations

Quan Sun, Franklin P Ockerman, Brian Chen, Laura Y. Zhou, Micah R. Hysong +12 more

Mosaic Loss of Y chromosome associates with lung function, emphysema and epigenetic aging

medRxiv(2025)10.1101/2025.07.30.25332379

N/A

0.165DataRank · unranked

2 citations

Kangjin Kim, Yichen Huang, Jeong H. Yun, Xiaolong Ma, Jason Bacon +25 more

Whole genome sequencing based analysis of inflammation biomarkers in the Trans-Omics for Precision Medicine (TOPMed) consortium.

PubMed(2024)10.1093/hmg/ddae050

N/A

0.165DataRank · unranked

2 citations

Sheila M. Gaynor, Xihao Li, Eric Van Buren, A.M. Stilp, Erin Buth +41 more

Genome-Wide Interaction Analysis of Menopausal Hormone Therapy Use and Breast Cancer Risk Among 62,370 Women

Research Square(2021)10.21203/rs.3.rs-532921/v1

Top 71%

0.126DataRank

Top 71%1 citations

Pooja Middha, Paul L. Auer, Joe Dennis, Alison M. Dunning, Qin Wang +75 more

Whole genome analysis of plasma fibrinogen reveals population-differentiated genetic regulators with putative liver roles

medRxiv(2023)10.1101/2023.06.07.23291095

N/A

0.104DataRank · unranked

1 citations

Jayna Nicolas, Julie Hahn, Adam S. Heath, Laura M. Raffield, Lisa R. Yanek +95 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

0.104DataRank · unranked

1 citations

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

Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits

UNC Libraries(2020)10.17615/aapr-pr41

N/A

0.104DataRank · unranked

1 citations

Niels Grarup, Albert Hofman, Lenore J. Launer, David C. Liewald, Albert V. Smith +76 more

Integrative analysis of sequencing and array genotype data for discovering disease associations with rare mutations

UNC Libraries(2020)10.17615/nngh-g785

Top 78%

0.104DataRank

Top 78%1 citations

D. Y. Lin, Yun Li, Paul L. Auer, Yi‐Juan Hu

Determinants of mosaic chromosomal alteration fitness

medRxiv(2023)10.1101/2023.10.20.23297280

N/A

0.104DataRank · unranked

1 citations

Taralynn Mack, Hannah Poisner, Yasminka A. Jakubek, Adrienne M. Stilp, Braxton D. Mitchell +39 more

Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-19

UNC Libraries(2025)10.17615/w64f-zc73

N/A

0DataRank · unranked

0 citations

Annika Faucon, Quan Sun, Misa Graff, Paul L. Auer, Nancy J. Cox +9 more

Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI

UNC Libraries(2025)10.17615/nrrg-ws98

N/A

0DataRank · unranked

0 citations

Laura M. Raffield, Christy L. Avery, Quan Sun, Anna V. Mikhaylova, Tara C. Matise +13 more

Differences in the Circulating Proteome in Individuals with versus without Sickle Cell Trait

UNC Libraries(2025)10.17615/kwhm-gq49

N/A

0DataRank · unranked

0 citations

Melanie E. Garrett, Morgan E. Grams, Bing Yu, Alex P. Reiner, Genevieve L. Wojcik +17 more

Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing

UNC Libraries(2025)10.17615/mztm-gw84

N/A

0DataRank · unranked

0 citations

Margaret F. Doyle, Jason Bacon, Xiaolong Ma, Nathan Pankratz, Ramachandran S. Vasan +46 more

Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood

UNC Libraries(2025)10.17615/5tss-f273

N/A

0DataRank · unranked

0 citations

Eric Boerwinkle, Yash Pershad, K.E. North, Fulong Yu, Center, Regeneron Genetics +66 more

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

Nature Genetics(2020)10.1038/s41588-019-0537-1

N/A

0DataRank · unranked

189 citations

Laura Fachal, EMBRACE Collaborators, KConFab Investigators, HEBON Investigators, ABCTB Investigators +95 more

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

Nature Genetics(2020)10.1038/s41588-020-0609-2

N/A

0DataRank · unranked

578 citations

Thomas U. Ahearn, Julie Lecarpentier, Daniel R. Barnes, Jonathan Beesley, Guanghao Qi +95 more

Combined Associations of a Polygenic Risk Score and Classical Risk Factors With Breast Cancer Risk

JNCI Journal of the National Cancer Institute(2020)10.1093/jnci/djaa056

N/A

0DataRank · unranked

74 citations

Nasim Mavaddat, Parichoy Pal Choudhury, Amber N. Hurson, Sara Lindström, Sabine Behrens +95 more

Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer

International Journal of Cancer(2020)10.1002/ijc.33206

N/A

0DataRank · unranked

73 citations

Frédéric Amant, Daniela Annibali, Katie A. Ashton, John Attia, Paul L. Auer +89 more

A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

Nature Communications(2020)10.1038/s41467-019-14100-6

N/A

0DataRank · unranked

49 citations

Jean Abraham, Irene L. Andrulis, Hoda Anton‐Culver, Volker Arndt, Alan Ashworth +95 more

Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status

Genetic Epidemiology(2020)10.1002/gepi.22288

N/A

0DataRank · unranked

45 citations

Alexander Gusev, Bogdan Paşaniuc, Lang Wu, Jirong Long, Zomoroda Abu-Full +95 more

Effect of Sickle Cell Trait and APOL1 Genotype on the Association of Soluble uPAR with Kidney Function Measures in Black Americans

Clinical Journal of the American Society of Nephrology(2020)10.2215/cjn.12100720

N/A

0DataRank · unranked

5 citations

Laura M. Raffield, Nora Franceschini, Paul L. Auer, Ethan M. Lange, Deborah A. Nickerson +4 more

Association of exome sequences with plasma C-reactive protein levels in >9000 participants

UNC Libraries(2020)10.17615/003k-2b61

N/A

0DataRank · unranked

2 citations

Cristen J. Willer, Jennifer A. Brody, Eric Boerwinkle, Joshua C. Bis, Jeffery Haessler +27 more

find-tfbs: a tool to identify functional non-coding variants associated with complex human traits using open chromatin maps and phased whole-genome sequences

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.23.394296

N/A

0DataRank · unranked

0 citations

Florian Thibord, Paul L. Auer, John Blangero, Zeynep Coban‐Akdemir, James S. Floyd +11 more

Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension RiskCLINICAL PERSPECTIVE

UNC Libraries(2020)10.17615/ttpw-sn86

N/A

0DataRank · unranked

0 citations

Alex P. Reiner, Donna M. Muzny, Shih‐Jen Hwang, Christopher Newton‐Cheh, Leslie J. Raffel +30 more

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

UNC Libraries(2020)10.17615/vn1s-8a35

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0 citations

Frank J.A. van Rooij, Raha Pazoki, Albert Hofman, Nathan Pankratz, Richard A. Gibbs +51 more

Imputation of Exome Sequence Variants into Population- Based Samples and Blood-Cell-Trait-Associated Loci in African Americans: NHLBI GO Exome Sequencing Project

UNC Libraries(2020)10.17615/gafw-pc57

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Santhi K. Ganesh, Ethan M. Lange, Keolu Fox, Nora Franceschini, Robert B. Wallace +17 more

Genome-wide association study of red blood cell traits in Hispanics/Latinos: The Hispanic Community Health Study/Study of Latinos

UNC Libraries(2020)10.17615/mb9w-yv90

N/A

0DataRank · unranked

0 citations

Lisa M. Brown, Brian L. Browning, Cecilia A. Laurie, Yun Li, Sharon R. Browning +22 more

Association of Low-Frequency and Rare Coding-Sequence Variants with Blood Lipids and Coronary Heart Disease in 56,000 Whites and Blacks

UNC Libraries(2020)10.17615/sbz9-wg52

N/A

0DataRank · unranked

0 citations

Rebecca D. Jackson, Valeska Redon, Gina M. Peloso, Joshua C. Bis, Arend Voorman +27 more

Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases

UNC Libraries(2020)10.17615/s8sd-h432

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Todd L. Edwards, Jin Li, John M. Starr, Eric Boerwinkle, Yingchang Lu +92 more

Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans

UNC Libraries(2020)10.17615/t61g-n927

N/A

0DataRank · unranked

0 citations

Sarah C. Nelson, Adrienne M. Stilp, Robert L. Hanson, Chani J. Hodonsky, Anna Plantinga +33 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

Imputation of coding variants in African Americans: better performance using data from the exome sequencing project

UNC Libraries(2020)10.17615/8p33-rs54

N/A

0DataRank · unranked

0 citations

Alex P. Reiner, Lisa Warsinger Martin, Loı̈c Le Marchand, Steven Buyske, Gonçalo R. Abecasis +30 more

Association of Sickle Cell Trait With Chronic Kidney Disease and Albuminuria in African Americans

UNC Libraries(2020)10.17615/0cmb-g360

N/A

0DataRank · unranked

0 citations

Vimal K. Derebail, Carmen A. Peralta, Pierre Fontanillas, Alexander G. Bick, Adolfo Correa +26 more

Genome-wide Association and Population Genetic Analysis of C-Reactive Protein in African American and Hispanic American Women

UNC Libraries(2020)10.17615/24bs-qj43

N/A

0DataRank · unranked

0 citations

Jennifer G. Robinson, Peters, Ulrike, Paul L. Auer, Alex P. Reiner, Charles Kooperberg +3 more

Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction

UNC Libraries(2020)10.17615/pc2a-ev84

N/A

0DataRank · unranked

0 citations

Jeanette Erdmann, Paul L. Auer, Robert Roberts, John Danesh, Deborah Farlow +27 more

A Population-Based Study of Genes Previously Implicated in Breast Cancer

New England Journal of Medicine(2021)10.1056/nejmoa2005936

N/A

0DataRank · unranked

878 citations

Steven N. Hart, Rohan Gnanaolivu, Hongyan Huang, Kun Y. Lee, Jie Na +55 more

Risk of Breast Cancer Among Carriers of Pathogenic Variants in Breast Cancer Predisposition Genes Varies by Polygenic Risk Score

Journal of Clinical Oncology(2021)10.1200/jco.20.01992

N/A

0DataRank · unranked

95 citations

Eric C. Polley, Steven N. Hart, Hongyan Huang, Chunling Hu, Rohan Gnanaolivu +37 more

Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations

UNC Libraries(2021)10.17615/e6ew-j192

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0DataRank · unranked

27 citations

NHLBI Trans-Omics for Precision Medicine Consortium, H. Qian, C. Montgomery, T.N. Kelly, M.H. Cho +67 more

Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

Breast Cancer Research(2021)10.1186/s13058-021-01450-7

N/A

0DataRank · unranked

23 citations

Maria Escala-Garcia, Jonathan Beesley, Renske Keeman, Sander Canisius, Thomas U. Ahearn +94 more

Soluble Urokinase Plasminogen Activator Receptor: Genetic Variation and Cardiovascular Disease Risk in Black Adults

Circulation Genomic and Precision Medicine(2021)10.1161/circgen.121.003421

N/A

0DataRank · unranked

15 citations

Laura M. Raffield, Anne H. Moxley, Tyne W. Miller‐Fleming, Paul L. Auer, Franceschini, Nora +12 more

Common variants in breast cancer risk loci predispose to distinct tumor subtypes.

Apollo (University of Cambridge)(2021)10.17863/cam.79953

N/A

0DataRank · unranked

6 citations

Haoyu Zhang, Kyriaki Michailidou, Roger L. Milne, Manjeet K. Bolla, Joe Dennis +95 more

Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment.

Apollo (University of Cambridge)(2021)10.17863/cam.75702

N/A

0DataRank · unranked

0 citations

Maria Escala-Garcia, Jonathan Beesley, Renske Keeman, Sander Canisius, Thomas U. Ahearn +95 more

Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol

UNC Libraries(2021)10.17615/shbq-nv48

N/A

0DataRank · unranked

0 citations

Douglas M. Ruderfer, Goo Jun, Ji Zhang, Yun Li, Leslie A. Lange +27 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

Common variants in breast cancer risk loci predispose to distinct tumor subtypes

Breast Cancer Research(2022)10.1186/s13058-021-01484-x

N/A

0DataRank · unranked

32 citations

Haoyu Zhang, Kyriaki Michailidou, Roger L. Milne, Manjeet K. Bolla, Joe Dennis +94 more

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

Nature Communications(2022)10.1038/s41467-022-35354-7

N/A

0DataRank · unranked

18 citations

Adrienne M. Stilp, Shuquan Rao, Bjarni V. Halldórsson, Doruk Beyter, Jia Wen +54 more

Early life trauma and adult leucocyte telomere length

Psychoneuroendocrinology(2022)10.1016/j.psyneuen.2022.105876

N/A

0DataRank · unranked

14 citations

Christine G. Parks, Emily E. Hyde, Paul L. Auer, Amanda M. Simanek, Rebecca Headley Konkel +4 more

Latent Class Models of Early-life Trauma and Incident Breast Cancer

Epidemiology(2022)10.1097/ede.0000000000001507

N/A

0DataRank · unranked

9 citations

Amanda M. Simanek, Katie M. O’Brien, Christine G. Parks, Symielle A. Gaston, Paul L. Auer +5 more

Prenatal Socioeconomic Disadvantage and Epigenetic Alterations at Birth Among Children Born to White British and Pakistani Mothers in the Born in Bradford Study

Epigenetics(2022)10.1080/15592294.2022.2098569

N/A

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3 citations

Regina Manansala, Jennifer M. P. Woo, Helen C.S. Meier, Belinda L. Needham, Paul L. Auer +1 more

Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study

UNC Libraries(2022)10.17615/6q25-sj56

N/A

0DataRank · unranked

2 citations

G.L. Wojcik, B. Thyagarajan, G. Lettre, A.P. Reiner, Q. Sun +30 more

Differences in the Circulating Proteome in Individuals with versus without Sickle Cell Trait

Clinical Journal of the American Society of Nephrology(2023)10.2215/cjn.0000000000000257

N/A

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17 citations

Nora Franceschini, Aditya Surapaneni, Melanie E. Garrett, Usman A. Tahir, Li Hsu +17 more

Associations of a Breast Cancer Polygenic Risk Score With Tumor Characteristics and Survival

Journal of Clinical Oncology(2023)10.1200/jco.22.01978

N/A

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28 citations

Irene L. Andrulis, Stig E. Bojesen, Thilo Dörk, Diana Eccles, Peter A. Fasching +95 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

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19 citations

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

Genetic examination of hematological parameters in SARS-CoV-2 infection and COVID-19

Blood Cells Molecules and Diseases(2023)10.1016/j.bcmd.2023.102782

N/A

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2 citations

Bryce Rowland, Wanjiang Wang, Tyne W. Miller‐Fleming, Nancy J. Cox, Misa Graff +9 more

Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI

Nature Communications(2024)10.1038/s41467-024-45135-z

N/A

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56 citations

Bryce Rowland, Jiawen Chen, Anna V. Mikhaylova, Christy L. Avery, Ulrike Peters +13 more

Admix-kit: an integrated toolkit and pipeline for genetic analyses of admixed populations

Bioinformatics(2024)10.1093/bioinformatics/btae148

N/A

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16 citations

Stephanie M. Gogarten, Joohyun Kim, Xing Hua, Julie‐Alexia Dias, Quan Sun +89 more

Donor germ‐line variants associate with outcomes of allogeneic hematopoietic stem cell transplantation in patients with myelodysplastic syndromes

American Journal of Hematology(2024)10.1002/ajh.27243

N/A

0DataRank · unranked

1 citations

Manzur Farazi, Tao Zhang, Jing Dong, Yung‐Tsi Bolon, Stephen R. Spellman +2 more

Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification

medRxiv(2024)10.1101/2024.09.04.24313051

N/A

0DataRank · unranked

3 citations

Denise G O'Mahony, Michael T. Parsons, Leila Dorling, Joe Dennis, Nicholas Boddicker +95 more

EndoPRS: Incorporating Endophenotype Information to Improve Polygenic Risk Scores for Clinical Endpoints

medRxiv(2024)10.1101/2024.05.23.24307839

N/A

0DataRank · unranked

1 citations

Quan Sun, Frank Ockerman, Brian Chen, Laura Y. Zhou, Hongyuan Cao +10 more

Soluble Urokinase Plasminogen Activator Receptor: Genetic Variation and Cardiovascular Disease Risk in Black Adults

UNC Libraries(2024)10.17615/kv6h-sn71

N/A

0DataRank · unranked

0 citations

L.M. Raffield, T.A. Thornton, K.L. Mohlke, Paul L. Auer, T.W. Miller-Fleming +12 more

Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa

UNC Libraries(2024)10.17615/k3wp-sy78

N/A

0DataRank · unranked

0 citations

D.N. Cooper, A.P. Reiner, A.P. Morris, Eric Young, Cristina Pomilla +52 more

Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program

UNC Libraries(2024)10.17615/m04b-7b81

N/A

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0 citations

Yann Ilboudo, J.A. Brody, Jonathan D. Rosen, A.V. Smith, M. FORNAGE +89 more

Genome-wide interaction analysis of menopausal hormone therapy use and breast cancer risk among 62,370 women

UNC Libraries(2024)10.17615/8eax-6c71

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0 citations

Dong‐Gun Lee, L. Wilkens, Niclas Håkansson, Robert J. MacInnis, Christopher G. Scott +75 more

Combined Associations of a Polygenic Risk Score and Classical Risk Factors with Breast Cancer Risk

Edinburgh Research Explorer (University of Edinburgh)(2024)10.17615/mt16-xj68

N/A

0DataRank · unranked

0 citations

Minouk J. Schoemaker, Hiltrud Brauch, Thomas Brüning, David J. Hunter, Montserrat García‐Closas +95 more

Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

UNC Libraries(2024)10.17615/c9rj-vf19

N/A

0DataRank · unranked

0 citations

Wolfgang Janni, B Rack, D.F. Easton, Per Hall, Clare L. Scott +95 more

A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

Research Explorer (The University of Manchester)(2024)10.17615/dprd-7a14

N/A

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0 citations

Dhanya Ramachandran, John Abraham, Mythily Sachchithananthan, Nadège Presneau, Robert Winqvist +95 more

Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease

UNC Libraries(2024)10.17615/6n4z-q211

N/A

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0 citations

Jacob C. Ulirsch, Alex P. Reiner, Gonçalo R. Abecasis, Joshua D. Smith, Ethan M. Lange +20 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

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0 citations

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

Determinants of mosaic chromosomal alteration fitness

UNC Libraries(2024)10.17615/yx5k-ka41

N/A

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0 citations

Taralynn Mack, Margaret F. Doyle, Yash Pershad, Paul L. Auer, Jeong H. Yun +39 more

Alterations of T Cell Subsets Associated with Sickle Cell Trait

Blood and genomics discovery.(2024)10.70322/bgd.2025.10001

N/A

0DataRank · unranked

0 citations

Laura M. Raffield, Lynette Ekunwe, Nels C. Olson, Paul L. Auer, Margaret F. Doyle +1 more

Association of gene variant type and location with breast cancer risk in the general population

Annals of Oncology(2025)10.1016/j.annonc.2025.04.010

N/A

0DataRank · unranked

8 citations

Nicholas Boddicker, Siddhartha Yadav, Cai-Xia Hu, Steven N. Hart, Christine B. Ambrosone +40 more

Analysis of more than 400,000 women provides case-control evidence for BRCA1 and BRCA2 variant classification

Nature Communications(2025)10.1038/s41467-025-59979-6

N/A

0DataRank · unranked

8 citations

Denise G O'Mahony, Michael T. Parsons, Leila Dorling, Joe Dennis, Nicholas Boddicker +94 more

Methylation profile of individuals with sickle cell trait

Epigenetics(2025)10.1080/15592294.2025.2539234

N/A

0DataRank · unranked

3 citations

Mari Johnson, Yanwei Cai, Li Hsu, Franceschini, Nora, Paul L. Auer +4 more

Genetic study of von Willebrand factor antigen levels ≤ 50 IU/dL identifies variants associated with increased risk of von Willebrand disease and bleeding

Journal of Thrombosis and Haemostasis(2025)10.1016/j.jtha.2025.04.029

N/A

0DataRank · unranked

4 citations

Adam S. Heath, Jennifer E. Huffman, James Baker, Natalie R. Hasbani, Sarah A. Gagliano Taliun +39 more

A Polygenic Risk Score for Late Bladder Toxicity Following Radiotherapy for Non-Metastatic Prostate Cancer

Cancer Epidemiology Biomarkers & Prevention(2025)10.1158/1055-9965.epi-24-1228

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4 citations

Xin Yang, Carson J. Gehl, Gillian C. Barnett, N.G. Burnet, Jenny Chang‐Claude +33 more

Large-scale meta-analysis and precision functional assays identify FANCM regions in which PTVs confer different risks for ER-negative and triple-negative breast cancer

The Breast(2025)10.1016/j.breast.2025.104619

N/A

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1 citations

Gisella Figlioli, Clémence Mooser, Irene Casamassima, Violette Azzoni, Jahnavi Srivatsa +95 more

Genetic drivers and clinical consequences of mosaic chromosomal alterations in 1 million individuals

medRxiv(2025)10.1101/2025.03.05.25323443

N/A

0DataRank · unranked

4 citations

Yash Pershad, Hannah Poisner, Xiaolong Ma, Kali Quade, Caitlyn Vlasschaert +13 more

Race-related host and microbe transcriptomic signatures in triple-negative breast cancer

npj Breast Cancer(2025)10.1038/s41523-025-00806-y

N/A

0DataRank · unranked

0 citations

Susan Duyar‐Ayerdi, Aishwarya Sundaresan, Vinodh Srinivasasainagendra, Chandra Sekhar Pedamallu, Michael Behring +12 more

Paul L. Auer

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