Brian E. Cade

MedicineBiochemistry, Genetics and Molecular BiologyPsychology

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

12.8Author DataRank

Indexed papers

10in 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 10 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 94 papers — median percentile 69. Top paper: “Inherited causes of clonal haematopoiesis in 97,691 whole genomes”.

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

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

Genetic diversity fuels gene discovery for tobacco and alcohol use

Nature(2022)10.1038/s41586-022-05477-4

N/A

5.9DataRank · unranked

513 citations

Xingyan Wang, Fang Chen, Seon-Kyeong Jang, Mengzhen Liu, Chen Wang +95 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

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

Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

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

N/A

2.1DataRank · unranked

107 citations

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

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

Interaction of obesity polygenic score with lifestyle risk factors in an electronic health record biobank

BMC Medicine(2022)10.1186/s12916-021-02198-9

Top 16%

1.3DataRank

Top 16%40 citations

Nicole Miranda, Brian E. Cade, Tianyi Huang, Susan Redline, Elizabeth W. Karlson +2 more

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

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.021

N/A

1.3DataRank · unranked

70 citations

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

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

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

N/A

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

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

A saturated map of common genetic variants associated with human height

Nature(2022)10.1038/s41586-022-05275-y

N/A

1.0DataRank · unranked

911 citations

Sailaja Vedantam, Eirini Marouli, Julia Sidorenko, Eric Bartell, Saori Sakaue +95 more

The trans-ancestral genomic architecture of glycemic traits

Nature Genetics(2021)10.1038/s41588-021-00852-9

N/A

1.0DataRank · unranked

907 citations

Cassandra N. Spracklen, Gaëlle Marenne, Arushi Varshney, Laura J. Corbin, Jian’an Luan +95 more

The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections

EBioMedicine(2023)10.1016/j.ebiom.2023.104630

N/A

1.0DataRank · unranked

28 citations

Fahrisa I. Maisha, Satu Strausz, Vilma Lammi, Brian E. Cade, Anniina Tervi +88 more

Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

Nature Genetics(2022)10.1038/s41588-022-01058-3

N/A

0.994DataRank · unranked

754 citations

Cassandra N. Spracklen, Weihua Zhang, Maggie C. Y. Ng, Lauren E. Petty, Hidetoshi Kitajima +95 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

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

Association of clonal hematopoiesis with chronic obstructive pulmonary disease

Blood(2021)10.1182/blood.2021013531

N/A

0.818DataRank · unranked

232 citations

Dandi Qiao, Joselyn Rojas, Michael C. Honigberg, Adam S. Sperling, Christopher J. Gibson +39 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

Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH

Diabetologia(2023)10.1007/s00125-023-05922-7

N/A

0.676DataRank · unranked

16 citations

Laura Brenner, Varinderpal Kaur, Katherine Figueroa, Philip Schroeder, Alicia Huerta‐Chagoya +95 more

Polygenic prediction of body mass index and obesity through the life course and across ancestries

Nature Medicine(2025)10.1038/s41591-025-03827-z

N/A

0.665DataRank · unranked

34 citations

Kaitlin H Wade, Qin Hui, Joshua Arias, Xianyong Yin, Malene R. Christiansen +95 more

A System for Phenotype Harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) Program

American Journal of Epidemiology(2021)10.1093/aje/kwab115

N/A

0.631DataRank · unranked

66 citations

Leslie S. Emery, Jai Broome, Erin Buth, Alyna Khan, Cecelia Laurie +67 more

Presence and transmission of mitochondrial heteroplasmic mutations in human populations of European and African ancestry

Mitochondrion(2021)10.1016/j.mito.2021.07.004

N/A

0.624DataRank · unranked

23 citations

Jessica L. Fetterman, Yong Qian, Xianbang Sun, Thomas W. Blackwell, Achilleas Pitsillides +14 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

Genetic determinants of cardiometabolic and pulmonary phenotypes and obstructive sleep apnoea in HCHS/SOL

EBioMedicine(2022)10.1016/j.ebiom.2022.104288

N/A

0.550DataRank · unranked

38 citations

Michael Elgart, Nuzulul Kurniansyah, Brian Spitzer, Heming Wang, Doyoon Kim +9 more

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

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

N/A

0.534DataRank · unranked

11 citations

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

Rare genetic variants explain missing heritability in smoking

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

N/A

0.520DataRank · unranked

31 citations

Luke M. Evans, Allison Fialkowski, Donna K. Arnett, Allison E. Ashley‐Koch, Kathleen C. Barnes +85 more

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

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.007

N/A

0.489DataRank · unranked

25 citations

Dandi Qiao, Wonji Kim, Matthew Moll, Pallavi Balte, Leslie A. Lange +46 more

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

Genetics(2021)10.1093/genetics/iyab044

N/A

0.489DataRank · unranked

25 citations

Thomas W. Blackwell, Jonathon LeFaive, Mariza de Andrade, John Barnard, Kathleen C. Barnes +42 more

Multi-ancestry genome-wide gene–sleep interactions identify novel loci for blood pressure

Molecular Psychiatry(2021)10.1038/s41380-021-01087-0

N/A

0.483DataRank · unranked

24 citations

Raymond Noordam, Brian E. Cade, Karen Schwander, Thomas W. Winkler, Jiwon Lee +95 more

Low oxygen saturation during sleep reduces CD1D and RAB20 expressions that are reversed by CPAP therapy

EBioMedicine(2020)10.1016/j.ebiom.2020.102803

N/A

0.472DataRank · unranked

10 citations

Ruitong Li, Roby Joehanes, Honghuang Lin, Adam C. Gower, Heming Wang +16 more

Assessing the contribution of rare genetic variants to phenotypes of chronic obstructive pulmonary disease using whole-genome sequence data

Human Molecular Genetics(2022)10.1093/hmg/ddac117

N/A

0.455DataRank · unranked

6 citations

Julian Hecker, R. Graham Barr, Eric Boerwinkle, Brian E. Cade, Adolfo Correa +21 more

Leveraging pleiotropy to discover and interpret GWAS results for sleep-associated traits

PLoS Genetics(2022)10.1371/journal.pgen.1010557

N/A

0.434DataRank · unranked

17 citations

Sebastian Akle, Athanasios Teodosiadis, Brian E. Cade, Heming Wang, Tamar Sofer +13 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

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

Targeted Genome Sequencing Identifies Multiple Rare Variants in Caveolin-1 Associated with Obstructive Sleep Apnea

American Journal of Respiratory and Critical Care Medicine(2022)10.1164/rccm.202203-0618oc

N/A

0.414DataRank · unranked

9 citations

Heming Wang, Brian E. Cade, Nuzulul Kurniansyah, Karen He, Jiwon Lee +30 more

Genome-wide association analysis of composite sleep health scores in 413,904 individuals

Communications Biology(2025)10.1038/s42003-025-07514-0

N/A

0.406DataRank · unranked

14 citations

Tariq Faquih, Valentina Paz, Pavithra Nagarajan, Jacqueline M. Lane, Brian Spitzer +21 more

Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

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

N/A

0.406DataRank · unranked

14 citations

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

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

Science Advances(2023)10.1126/sciadv.abm4945

N/A

0.396DataRank · unranked

13 citations

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

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

Rare coding variants in RCN3 are associated with blood pressure

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

N/A

0.360DataRank · unranked

10 citations

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

Clonal hematopoiesis is driven by aberrant activation of TCL1A

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

N/A

0.360DataRank · unranked

10 citations

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

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

An integrated multi-omics analysis of sleep-disordered breathing traits implicates P2XR4 purinergic signaling

Communications Biology(2023)10.1038/s42003-023-04520-y

N/A

0.345DataRank · unranked

7 citations

Danielle A Wallace, Ying Zhang, Bing Yu, Brian E. Cade, Heming Wang +15 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

Polygenic scores for obstructive sleep apnoea reveal pathways contributing to cardiovascular disease

EBioMedicine(2025)10.1016/j.ebiom.2025.105790

N/A

0.292DataRank · unranked

6 citations

Satu Strausz, Geetha Chittoor, Shreyash Gupta, Anne E. Justice, Yana Hrytsenko +30 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

A system for phenotype harmonization in the NHLBI Trans-Omics for Precision Medicine (TOPMed) Program

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.18.146423

N/A

0.269DataRank · unranked

5 citations

Leslie S. Emery, Jai Broome, Erin Buth, Alyna Khan, Cecelia Laurie +67 more

Robust, flexible, and scalable tests for Hardy-Weinberg Equilibrium across diverse ancestries

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

N/A

0.269DataRank · unranked

5 citations

Thomas W. Blackwell, Jonathon LeFaive, Mariza de Andrade, John Barnard, Kathleen C. Barnes +42 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

Genome-wide association analysis of composite sleep health scores in 413,904 individuals

medRxiv(2024)10.1101/2024.02.02.24302211

N/A

0.241DataRank · unranked

4 citations

Tariq Faquih, Valentina Paz, Pavithra Nagarajan, Jacqueline M. Lane, Brian Spitzer +21 more

Multi-ancestry genome-wide gene-sleep interactions identify novel loci for blood pressure

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.29.123505

N/A

0.208DataRank · unranked

3 citations

Raymond Noordam, Brian E. Cade, Karen Schwander, Thomas W. Winkler, Jiwon Lee +95 more

0034 Genetic Variants for Obstructive Sleep Apnea Identified after Modeling Interactions with Daytime Sleepiness

SLEEP(2023)10.1093/sleep/zsad077.0034

N/A

0.165DataRank · unranked

2 citations

Han Chen, Yiyan Zhang, Nuzulul Kurniansyah, Shaun Purcell, Richa Saxena +7 more

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

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

N/A

0.165DataRank · unranked

2 citations

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

A Large-Scale Genome-Wide Study of Gene-Sleep Duration Interactions for Blood Pressure in 811,405 Individuals from Diverse Populations

medRxiv(2024)10.1101/2024.03.07.24303870

N/A

0.104DataRank · unranked

1 citations

Thomas W. Winkler, Amy R. Bentley, Clint L. Miller, Aldi T. Kraja, Karen Schwander +95 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

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

Genome-wide gene by sleepiness interaction analysis for sleep apnea

SLEEP(2025)10.1093/sleep/zsaf212

N/A

0.104DataRank · unranked

1 citations

Nuzulul Kurniansyah, Jiwon Lee, Sina A. Gharib, Yushan Xu, Yiyan Zhang +80 more

A large-scale genome-wide study of gene-sleep duration interactions for blood pressure in 811,405 individuals from diverse populations

Molecular Psychiatry(2025)10.1038/s41380-025-02954-w

Top 78%

0.104DataRank

Top 78%1 citations

Thomas W. Winkler, Amy R. Bentley, Clint L. Miller, Aldi T. Kraja, Karen Schwander +95 more

Breath of Fresh Air: Toward Unraveling the Molecular Underpinnings of Sleep Apnea

American Journal of Respiratory and Critical Care Medicine(2022)10.1164/rccm.202207-1410ed

N/A

0.104DataRank · unranked

1 citations

Sina A. Gharib, Brian E. Cade

Characterization of sleep apnea among a sample of adults from Samoa

medRxiv(2023)10.1101/2023.11.16.23298644

N/A

0.104DataRank · unranked

1 citations

Alysa Pomer, Brian E. Cade, Jenna C. Carlson, Take Naseri, Muagututi‘a Sefuiva Reupena +6 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

Rare coding variants in RCN3 are associated with blood pressure

UNC Libraries(2024)10.17615/y07d-kq52

N/A

0DataRank · unranked

0 citations

C.-T. Liu, A Furniss, R.S. Vasan, P.A. Peyser, Gao Ya +74 more

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

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

N/A

0DataRank · unranked

0 citations

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

Genetic discovery and risk characterization in type 2 diabetes across diverse populations

UNC Libraries(2024)10.17615/jc4m-n673

N/A

0DataRank · unranked

0 citations

G.N. Nadkarni, Christopher S. Carlson, H.M. Highland, Maggie Ng, L. Petty +52 more

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

UNC Libraries(2024)10.17615/mbk9-3d37

Top 100%

0DataRank

Top 100%0 citations

Xihong Lin, Sutapa Mukherjee, J. Rotter, Eric Boerwinkle, Xiuqing Guo +36 more

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

UNC Libraries(2024)10.17615/75fz-j027

Top 100%

0DataRank

Top 100%0 citations

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

A Large-Scale Genome-Wide Study of Gene-Sleep Duration Interactions for Blood Pressure in 811,405 Individuals from Diverse Populations

Research Square(2024)10.21203/rs.3.rs-4163414/v1

Top 100%

0DataRank

Top 100%0 citations

Pavithra Nagarajan, Thomas W. Winkler, Amy R. Bentley, Clint L. Miller, Aldi T. Kraja +95 more

Characterization of sleep apnea among a sample of adults from Samoa

Sleep Epidemiology(2024)10.1016/j.sleepe.2024.100099

N/A

0DataRank · unranked

0 citations

Alysa Pomer, Brian E. Cade, Jenna C. Carlson, Take Naseri, Muagututi‘a Sefuiva Reupena +6 more

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

UNC Libraries(2024)10.17615/vs68-ca81

N/A

0DataRank · unranked

0 citations

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

Gene-Excessive Sleepiness Interactions Suggest Treatment Targets for Obstructive Sleep Apnea Subtype

medRxiv(2024)10.1101/2024.10.25.24316158

N/A

0DataRank · unranked

0 citations

Nuzulul Kurniansyah, Jiwon Lee, Sina A. Gharib, Yushan Xu, Yiyan Zhang +31 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

Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure

UNC Libraries(2020)10.17615/gak2-c922

N/A

0DataRank · unranked

0 citations

Ayush Giri, Brian E. Cade, Heming Wang, Todd L. Edwards, Thu H. Le +13 more

Presence and Transmission of Mitochondrial Heteroplasmic Mutations in Human Populations of European and African Ancestry

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.10.13.337071

N/A

0DataRank · unranked

2 citations

Jessica L. Fetterman, Yong Qian, Xianbang Sun, Kaiyu Yan, Thomas W. Blackwell +15 more

Sleep health, diseases, and pain syndromes: findings from an electronic health record biobank

SLEEP(2020)10.1093/sleep/zsaa189

N/A

0DataRank · unranked

36 citations

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SLEEP(2025)10.1093/sleep/zsaf035

N/A

0DataRank · unranked

3 citations

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UNC Libraries(2025)10.17615/cdn0-cm52

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0DataRank · unranked

0 citations

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SLEEP(2025)10.1093/sleep/zsaf090.1150

N/A

0DataRank · unranked

1 citations

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Research Square(2025)10.21203/rs.3.rs-6025759/v1

N/A

0DataRank · unranked

0 citations

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EBioMedicine(2023)10.1016/j.ebiom.2023.104758

N/A

0DataRank · unranked

19 citations

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Sleep Health(2023)10.1016/j.sleh.2023.11.002

N/A

0DataRank · unranked

6 citations

Susan Redline, Brian E. Cade

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medRxiv(2022)10.1101/2022.05.25.22275570

N/A

0DataRank · unranked

0 citations

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medRxiv(2023)10.1101/2023.02.19.23286148

N/A

0DataRank · unranked

1 citations

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SLEEP(2023)10.1093/sleep/zsad077.0031

N/A

0DataRank · unranked

0 citations

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Nature(2024)10.1038/s41586-024-07019-6

N/A

0DataRank · unranked

537 citations

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medRxiv(2022)10.1101/2022.02.16.22271055

N/A

0DataRank · unranked

15 citations

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JAMIA Open(2022)10.1093/jamiaopen/ooab117

N/A

0DataRank · unranked

19 citations

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SLEEP(2022)10.1093/sleep/zsac121

N/A

0DataRank · unranked

21 citations

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Digital Commons@Becker (Washington University School of Medicine)(2024)10.17615/r2s5-pn26

N/A

0DataRank · unranked

0 citations

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