Jennifer A. Smith

University of North Carolina at Chapel Hill

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

9.1Author DataRank

Indexed papers

13in 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 13 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.

Within-sibship GWAS improve estimates of direct genetic effects

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.05.433935

Top 10%

2.2DataRank

Top 10%75 citations

Michel G. Nivard, Tim Morris, Ailin Falkmo Hansen, Humaira Rasheed, Yoonsu Cho +83 more

Papers

Driven by 147 papers — median percentile 63. Top paper: “Evaluation of SARS-CoV-2 serology assays reveals a range of test performance”.

Evaluation of SARS-CoV-2 serology assays reveals a range of test performance

Nature Biotechnology(2020)10.1038/s41587-020-0659-0

N/A

15.0DataRank · unranked

299 citations

Joseph Hiatt, Cody T. Mowery, Brian R. Shy, Ruby Yu, Tori N. Yamamoto +67 more

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

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

N/A

11.6DataRank · unranked

748 citations

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

7.2DataRank · unranked

363 citations

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

Machine Learning Detects Pan-cancer Ras Pathway Activation in The Cancer Genome Atlas

Cell Reports(2018)10.1016/j.celrep.2018.03.046

N/A

5.5DataRank · unranked

186 citations

Francisco Sanchez-Vega, Konnor C. La, Joshua Armenia, Walid K. Chatila, Augustin Luna +869 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

Cerebral small vessel disease genomics and its implications across the lifespan

Nature Communications(2020)10.1038/s41467-020-19111-2

N/A

4.3DataRank · unranked

209 citations

Hideaki Suzuki, Xueqiu Jian, Chloé Sarnowski, Tavia E. Evans, Joshua C. Bis +94 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

Within-sibship GWAS improve estimates of direct genetic effects

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.05.433935

Top 10%

2.2DataRank

Top 10%75 citations

Michel G. Nivard, Tim Morris, Ailin Falkmo Hansen, Humaira Rasheed, Yoonsu Cho +83 more

A multi-ethnic polygenic risk score is associated with hypertension prevalence and progression throughout adulthood

Nature Communications(2022)10.1038/s41467-022-31080-2

N/A

2.1DataRank · unranked

80 citations

Matthew Goodman, Tanika N. Kelly, Tali Elfassy, Kerri L. Wiggins, Joshua C. Bis +32 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

Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts

Diabetes Care(2022)10.2337/dc21-1395

N/A

1.6DataRank · unranked

68 citations

Jessica LeClair, Joanne B. Cole, Chloé Sarnowski, Fariba Ahmadizar, Lawrence F. Bielak +48 more

Model-based assessment of replicability for genome-wide association meta-analysis

Nature Communications(2021)10.1038/s41467-021-21226-z

N/A

1.5DataRank · unranked

40 citations

Yu Jiang, Mengzhen Liu, J. Dylan Weissenkampen, Scott A. Eckert, Lina Yang +125 more

Association of mitochondrial DNA copy number with cardiometabolic diseases

Cell Genomics(2021)10.1016/j.xgen.2021.100006

N/A

1.4DataRank · unranked

62 citations

Ryan J. Longchamps, Kerri L. Wiggins, Laura M. Raffield, Lawrence F. Bielak, Wei Zhao +33 more

Oncogenic Signaling Pathways in The Cancer Genome Atlas

Cell(2018)10.1016/j.cell.2018.03.035

N/A

1.2DataRank · unranked

3322 citations

Marco Mina, Joshua Armenia, Walid K. Chatila, Augustin Luna, Konnor C. La +891 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

Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use

Nature Genetics(2019)10.1038/s41588-018-0307-5

N/A

1.1DataRank · unranked

2128 citations

Mengzhen Liu, HUNT All-In Psychiatry, Yu Jiang, Robbee Wedow, Yue Li +120 more

Discovery and fine-mapping of height loci via high-density imputation of GWASs in individuals of African ancestry

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.02.011

N/A

1.1DataRank · unranked

34 citations

Anne E. Justice, Kristin L. Young, Eirini Marouli, Xinruo Zhang, Rebecca S. Fine +220 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

Downstream Biomarker Effects of Gantenerumab or Solanezumab in Dominantly Inherited Alzheimer Disease

JAMA Neurology(2024)10.1001/jamaneurol.2024.0991

N/A

1.0DataRank · unranked

29 citations

Haiyan Liu, Guoqiao Wang, Xinyu Shi, Tobias Bittner, Marzia A. Scelsi +94 more

50,000 years of Evolutionary History of India: Insights from ~2,700 Whole Genome Sequences

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.02.15.580575

Top 20%

1.0DataRank

Top 20%26 citations

Laurits Skov, Nick Patterson, Wei Zhao, Yuk Yee Lueng, Gerard D. Schellenberg +8 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

Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits—The Hispanic/Latino Anthropometry Consortium

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100099

N/A

0.759DataRank · unranked

25 citations

Mariaelisa Graff, Victoria L. Buchanan, Anne E. Justice, Heather M. Highland, Xiuqing Guo +95 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-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate

Brain(2021)10.1093/brain/awab432

N/A

0.696DataRank · unranked

35 citations

Cécile Duplàa, Dina Vojinović, Hideaki Suzuki, Nuno R. Zilhäo, Shuo Li +61 more

Bayesian Sparse Mediation Analysis with Targeted Penalization of Natural Indirect Effects

Journal of the Royal Statistical Society Series C (Applied Statistics)(2021)10.1111/rssc.12518

N/A

0.694DataRank · unranked

21 citations

Xiang Zhou, Lana X. Garmire, Max T. Aung, Min Zhang, Wei Zhao +7 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

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

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

Deep phenotyping and genomic data from a nationally representative study on dementia in India

Scientific Data(2023)10.1038/s41597-023-01941-6

Top 37%

0.516DataRank

Top 37%20 citations

Sarah Petrosyan, Pranali Khobragade, Joyita Banerjee, Sandy Chien, Bas Weerman +51 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

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

0.393DataRank · unranked

10 citations

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

Large-scale exome array summary statistics resources for glycemic traits to aid effector gene prioritization

Wellcome Open Research(2023)10.12688/wellcomeopenres.18754.1

N/A

0.357DataRank · unranked

7 citations

Natasha Hui Jin Ng, Juan Fernandez, Rebecca S. Fine, Eleanor Wheeler, Jennifer Wessel +95 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

Exome Array Analysis of 9721 Ischemic Stroke Cases from the SiGN Consortium

Genes(2022)10.3390/genes14010061

N/A

0.254DataRank · unranked

4 citations

Kevin A. Nguyen, Brady Gaynor, Hua Ling, Wei Zhao, Patrick F. McArdle +21 more

Epigenetic Aging Clocks and Incident Cardiovascular Outcomes: Results From the MESA

Journal of the American Heart Association(2025)10.1161/jaha.125.044946

Top 61%

0.241DataRank

Top 61%4 citations

Noah Rice, James Russell Pike, Jennifer A. Smith, Jingzhong Ding, Yongmei Liu +3 more

Transcriptome-wide Association Study of Blood Cell Traits in African Ancestry and Hispanic/Latino Populations

Preprints.org(2021)10.20944/preprints202106.0129.v1

N/A

0.196DataRank · unranked

2 citations

Munan Xie, Bryce Rowland, Jonathan D. Rosen, Quan Sun, Amanda L. Tapia +30 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

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

African ancestry genome-wide association study of blood pressure and hypertension identifies 25 novel loci through predicted gene expression

Research Square(2022)10.21203/rs.3.rs-1392991/v1

N/A

0.104DataRank · unranked

1 citations

Jingjing Liang, Ayush Giri, Jacob M. Keaton, Xiao Sun, Eric S. Torstenson +35 more

A Large-Scale Genome-Wide Gene-Sleep Interaction Study in 732,564 Participants Identifies Lipid Loci Explaining Sleep-Associated Lipid Disturbances

medRxiv(2024)10.1101/2024.09.02.24312466

Top 78%

0.104DataRank

Top 78%1 citations

Wenyi Wang, Pavithra Nagarajan, Heming Wang, Michael R. Brown, Amy R. Bentley +95 more

Methods for large‐scale single mediator hypothesis testing: Possible choices and comparisons

Genetic Epidemiology(2022)10.1002/gepi.22510

N/A

0DataRank · unranked

14 citations

Xiang Zhou, Dylan Clark‐Boucher, Wei Hao, Ching‐Ti Liu, Jennifer A. Smith +2 more

Opioid Medication Use and Blood Dna Methylation: Epigenome-Wide Association Meta-Analysis

Epigenomics(2022)10.2217/epi-2022-0353

N/A

0DataRank · unranked

11 citations

Roby Joehanes, Daniel L. McCartney, Minjung Kho, Anke Hüls, Annah B. Wyss +17 more

Rare coding variants in RCN3 are associated with blood pressure

BMC Genomics(2022)10.1186/s12864-022-08356-4

N/A

0DataRank · unranked

10 citations

Tanika N. Kelly, Heming Wang, Jingjing Liang, Luke Zhu, Brian E. Cade +72 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

Assessing the added value of linking electronic health records to improve the prediction of self-reported COVID-19 testing and diagnosis

PLoS ONE(2022)10.1371/journal.pone.0269017

N/A

0DataRank · unranked

2 citations

Jonathan Boss, Maxwell Salvatore, Jennifer A. Smith, Lars G. Fritsche, Bhramar Mukherjee +1 more

The Construction of Multi-ethnic Polygenic Risk Score using Transfer Learning

medRxiv(2022)10.1101/2022.03.08.22272114

N/A

0DataRank · unranked

7 citations

Lars G. Fritsche, Jennifer A. Smith, Bhramar Mukherjee, Seunggeun Lee, Zhangchen Zhao

Educational attainment, health outcomes and mortality: a within-sibship Mendelian randomization study

medRxiv(2022)10.1101/2022.01.11.22268884

N/A

0DataRank · unranked

6 citations

Humaira Rasheed, Paul Remy Jones, Dorret I. Boomsma, David M. Evans, Alexandros Giannelis +23 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

0DataRank · unranked

3 citations

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

The association between mitochondrial DNA copy number, low-density lipoprotein cholesterol, and cardiovascular disease risk

medRxiv(2022)10.1101/2022.10.23.22281418

N/A

0DataRank · unranked

1 citations

Xianbang Sun, Yuankai Zhang, Wenqing Jiang, Lai Meng, Kerri L. Wiggins +40 more

Multi-ancestry genome-wide study identifies effector genes and druggable pathways for coronary artery calcification

Nature Genetics(2023)10.1038/s41588-023-01518-4

N/A

0DataRank · unranked

150 citations

Maxime M. Bos, Hanna J. Barnes, Christian L. Lino Cardenas, Doris Wong, Haojie Lu +84 more

Multi-ancestry transcriptome-wide association analyses yield insights into tobacco use biology and drug repurposing

Nature Genetics(2023)10.1038/s41588-022-01282-x

N/A

0DataRank · unranked

56 citations

Xingyan Wang, Seon-Kyeong Jang, Bryan C. Quach, J. Dylan Weissenkampen, Chachrit Khunsriraksakul +85 more

Evaluating the use of blood pressure polygenic risk scores across race/ethnic background groups

Nature Communications(2023)10.1038/s41467-023-38990-9

N/A

0DataRank · unranked

46 citations

Matthew Goodman, Alyna Khan, Jiongming Wang, Elena V. Feofanova, Joshua C. Bis +38 more

meQTL mapping in the GENOA study reveals genetic determinants of DNA methylation in African Americans

Nature Communications(2023)10.1038/s41467-023-37961-4

N/A

0DataRank · unranked

40 citations

Wei Zhao, Yi-Zhe Wang, Zheng Li, Jerome Choi, Minjung Kho +5 more

Educational attainment, health outcomes and mortality: a within-sibship Mendelian randomization study

International Journal of Epidemiology(2023)10.1093/ije/dyad079

N/A

0DataRank · unranked

39 citations

Humaira Rasheed, Paul Remy Jones, Dorret I. Boomsma, David M. Evans, Alexandros Giannelis +42 more

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

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

N/A

0DataRank · unranked

31 citations

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

Association Between Whole Blood–Derived Mitochondrial DNA Copy Number, Low‐Density Lipoprotein Cholesterol, and Cardiovascular Disease Risk

Journal of the American Heart Association(2023)10.1161/jaha.122.029090

N/A

0DataRank · unranked

30 citations

Xianbang Sun, Yuankai Zhang, Wenqing Jiang, M M Lai, Kerri L. Wiggins +40 more

Methods for mediation analysis with high-dimensional DNA methylation data: Possible choices and comparisons

PLoS Genetics(2023)10.1371/journal.pgen.1011022

N/A

0DataRank · unranked

30 citations

Xiang Zhou, Jiacong Du, Yongmei Liu, Belinda L. Needham, Jennifer A. Smith +2 more

Associations of Early-Life Adversity With Later-Life Epigenetic Aging Profiles in the Multi-Ethnic Study of Atherosclerosis

American Journal of Epidemiology(2023)10.1093/aje/kwad172

N/A

0DataRank · unranked

17 citations

Elizabeth Duffie, Wei Zhao, Scott M. Ratliff, Jingzhong Ding, Ching‐Ti Liu +4 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

0DataRank · unranked

15 citations

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

Circulating metabolites may illustrate relationship of alcohol consumption with cardiovascular disease

BMC Medicine(2023)10.1186/s12916-023-03149-2

N/A

0DataRank · unranked

14 citations

Mengyao Wang, Xue Liu, Jian Rong, Patricia E. Miller, Roby Joehanes +10 more

Epigenome-Wide Meta-Analysis Reveals Differential DNA Methylation Associated With Estimated Glomerular Filtration Rate Among African American Men With HIV

Kidney International Reports(2023)10.1016/j.ekir.2023.02.1085

N/A

0DataRank · unranked

9 citations

Qin Hui, Zeyuan Wang, F. Perry Wilson, Kaku So‐Armah, Matthew S. Freiberg +10 more

Epigenetic Aging Is Associated With Measures of Midlife Muscle Volume and Attenuation in CARDIA Study

The Journals of Gerontology Series A(2023)10.1093/gerona/glad261

N/A

0DataRank · unranked

2 citations

Yinan Zheng, Brian Joyce, Minjung Kho, James G. Terry, Jun Wang +12 more

Structural variation across 138,134 samples in the TOPMed consortium

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

N/A

0DataRank · unranked

9 citations

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

WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE

medRxiv(2023)10.1101/2023.08.21.23293271

N/A

0DataRank · unranked

2 citations

Jennifer A. Brody, Mariaelisa Graff, Heather M. Highland, Nathalie Chami, Hanfei Xu +95 more

Circulating Metabolites May Illustrate Relationship of Alcohol Consumption with Cardiovascular Disease

medRxiv(2023)10.1101/2023.05.24.23290487

N/A

0DataRank · unranked

1 citations

Mengyao Wang, Xue Liu, Jian Rong, Patricia E. Miller, Roby Joehanes +10 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

0DataRank · unranked

1 citations

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

Machine learning models for blood pressure phenotypes combining multiple polygenic risk scores

medRxiv(2023)10.1101/2023.12.13.23299909

N/A

0DataRank · unranked

0 citations

Benjamin Shea, Michael Elgart, Nuzulul Kurniansyah, Genevieve Lyons, Alanna C. Morrison +32 more

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

Blood(2024)10.1182/blood.2023022596

N/A

0DataRank · unranked

15 citations

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

Biological Age, Chronological Age, and Survival in Pulmonary Fibrosis: A Causal Mediation Analysis

American Journal of Respiratory and Critical Care Medicine(2024)10.1164/rccm.202310-1887oc

N/A

0DataRank · unranked

14 citations

John S. Kim, Swaraj Bose, Ayodeji Adegunsoye, A. Linderholm, Ching‐Hsien Chen +15 more

Methylation patterns associated with C-reactive protein in racially and ethnically diverse populations

Epigenetics(2024)10.1080/15592294.2024.2333668

N/A

0DataRank · unranked

9 citations

Ulrike Peters, Yao Hu, Farah Ammous, Christy L. Avery, Emelia J. Benjamin +35 more

Racial and Socioeconomic Disparities Exist in Patients Pursuing Peanut Oral Immunotherapy

The Journal of Allergy and Clinical Immunology In Practice(2024)10.1016/j.jaip.2024.04.040

N/A

0DataRank · unranked

9 citations

Charles F. Schuler, Jonathan P. Troost, Ian Slack, Georgiana Sanders, James R. Baker +3 more

Machine learning models for predicting blood pressure phenotypes by combining multiple polygenic risk scores

Scientific Reports(2024)10.1038/s41598-024-62945-9

N/A

0DataRank · unranked

7 citations

Benjamin Shea, Michael Elgart, Nuzulul Kurniansyah, Genevieve Lyons, Alanna C. Morrison +32 more

Epigenome-wide mediation analysis of the relationship between psychosocial stress and cardiometabolic risk factors in the Health and Retirement Study (HRS)

Clinical Epigenetics(2024)10.1186/s13148-024-01799-4

N/A

0DataRank · unranked

7 citations

Wei Zhao, Scott M. Ratliff, Jiacong Du, Jessica D. Faul, Lauren Schmitz +4 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

Multi-omics and pathway analyses of genome-wide associations implicate regulation and immunity in verbal declarative memory performance

Alzheimer s Research & Therapy(2024)10.1186/s13195-023-01376-6

N/A

0DataRank · unranked

3 citations

Jeannette Simino, Lianna Li, Fan Jiang, Joshua C. Bis, Gail Davies +62 more

Association analysis between an epigenetic alcohol risk score and blood pressure

Clinical Epigenetics(2024)10.1186/s13148-024-01753-4

N/A

0DataRank · unranked

3 citations

Amena Keshawarz, Mengyao Wang, Mi Kyeong Lee, Scott M. Ratliff, Lisha Lin +33 more

The power of genetic diversity in genome-wide association studies of lipids

UNC Libraries(2024)10.17615/539b-tz69

N/A

0DataRank · unranked

5 citations

Joel N. Hirschhorn, Zoltán Kutalik, Sanni Ruotsalainen, Daniela Ruggiero, Prashantha Hebbar +95 more

The expected polygenic risk score (ePRS) framework: an equitable metric for quantifying polygenetic risk via modeling of ancestral makeup

medRxiv(2024)10.1101/2024.03.05.24303738

N/A

0DataRank · unranked

3 citations

Nuzulul Kurniansyah, Matthew Goodman, Brian Spitzer, Jiongming Wang, Adrienne M. Stilp +27 more

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

medRxiv(2024)10.1101/2024.04.16.24305851

N/A

0DataRank · unranked

3 citations

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medRxiv(2024)10.1101/2024.01.03.24300768

N/A

0DataRank · unranked

1 citations

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medRxiv(2024)10.1101/2024.02.29.24303545

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0DataRank · unranked

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Research Square(2024)10.21203/rs.3.rs-4243866/v1

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0DataRank · unranked

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UNC Libraries(2024)10.17615/y07d-kq52

N/A

0DataRank · unranked

0 citations

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UNC Libraries(2024)10.17615/tv1j-wn72

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0DataRank · unranked

0 citations

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UNC Libraries(2024)10.17615/hd68-ze50

Top 100%

0DataRank

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

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0DataRank · unranked

0 citations

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UNC Libraries(2024)10.17615/twaa-ms70

N/A

0DataRank · unranked

0 citations

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UNC Libraries(2024)10.17615/75fz-j027

Top 100%

0DataRank

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UNC Libraries(2024)10.17615/6p9v-ms63

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0DataRank · unranked

0 citations

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UNC Libraries(2024)10.17615/8724-3356

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0DataRank · unranked

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medRxiv(2024)10.1101/2024.09.25.24313663

N/A

0DataRank · unranked

0 citations

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UNC Libraries(2024)10.17615/b6xd-h115

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0DataRank · unranked

32 citations

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Atherosclerosis(2025)10.1016/j.atherosclerosis.2025.120219

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0DataRank · unranked

6 citations

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0DataRank · unranked

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0DataRank · unranked

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0DataRank · unranked

3 citations

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0DataRank · unranked

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1 citations

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0DataRank · unranked

1 citations

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0DataRank · unranked

1 citations

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1 citations

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0 citations

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UNC Libraries(2025)10.17615/mztm-gw84

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0 citations

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0 citations

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0DataRank · unranked

101 citations

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0DataRank · unranked

91 citations

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UNC Libraries(2020)10.17615/tcz3-xa61

N/A

0DataRank · unranked

21 citations

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0DataRank · unranked

20 citations

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0DataRank · unranked

14 citations

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UNC Libraries(2020)10.17615/vygp-he02

N/A

0DataRank · unranked

7 citations

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medRxiv(2020)10.1101/2020.10.29.20221390

N/A

0DataRank · unranked

8 citations

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0DataRank · unranked

5 citations

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bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.23.167759

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0DataRank · unranked

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medRxiv(2020)10.1101/2020.02.10.20021667

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0DataRank · unranked

3 citations

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0DataRank · unranked

0 citations

W. T. Longstreth, Reinhold Schmidt, Paul Freudenberger, Pamela J. Schreiner, Stella Trompet +95 more

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UNC Libraries(2020)10.17615/kwh0-eh07

N/A

0DataRank · unranked

0 citations

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UNC Libraries(2020)10.17615/ca27-5133

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0DataRank · unranked

0 citations

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UNC Libraries(2020)10.17615/gak2-c922

N/A

0DataRank · unranked

0 citations

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UNC Libraries(2020)10.17615/jcdv-pt45

N/A

0DataRank · unranked

0 citations

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0DataRank · unranked

123 citations

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0DataRank · unranked

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0DataRank · unranked

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0DataRank · unranked

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0DataRank · unranked

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Robust, flexible, and scalable tests for Hardy–Weinberg equilibrium across diverse ancestries

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0DataRank · unranked

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0DataRank · unranked

2 citations

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bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.05.27.445969

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medRxiv(2021)10.1101/2021.03.01.21252660

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0DataRank · unranked

11 citations

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medRxiv(2021)10.1101/2021.10.31.21265717

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11 citations

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

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

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0DataRank · unranked

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The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.09.010

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Epigenetic and integrative cross-omics analyses of cerebral white matter hyperintensities on MRI

Brain(2022)10.1093/brain/awac290

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0DataRank · unranked

45 citations

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The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.003

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0DataRank · unranked

43 citations

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Human Reproduction(2022)10.1093/humrep/deac028

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Yvonne T. van der Schouw, Carla H. van Gils, W. M. Monique Verschuren, Frank J. Broekmans, Maria Carolina Borges +14 more

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Nature Human Behaviour(2022)10.1038/s41562-022-01408-5

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0DataRank · unranked

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The Journals of Gerontology Series A(2022)10.1093/gerona/glac041

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0DataRank · unranked

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0DataRank · unranked

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