Braxton D. Mitchell

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

10.1Author 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.

Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies

The Lancet Neurology(2021)10.1016/s1474-4422(21)00031-4

Top 6%

3.8DataRank

Top 6%213 citations

Elodie Persyn, Liisa Tomppo, Sofia Klasson, Vida Abedi, Mark K. Bakker +36 more

Papers

Driven by 130 papers — median percentile 63. 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

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

Meta-Analysis of Genome-Wide Scans Provides Evidence for Sex- and Site-Specific Regulation of Bone Mass

Journal of Bone and Mineral Research(2007)10.1359/jbmr.060806

N/A

4.5DataRank · unranked

168 citations

Mandy Y Ng, Pak C. Sham, Elias Zintzaras, Saskia P. Hagenaars, Hong-Wen Deng +31 more

Genetic basis of lacunar stroke: a pooled analysis of individual patient data and genome-wide association studies

The Lancet Neurology(2021)10.1016/s1474-4422(21)00031-4

Top 6%

3.8DataRank

Top 6%213 citations

Elodie Persyn, Liisa Tomppo, Sofia Klasson, Vida Abedi, Mark K. Bakker +36 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

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

Monogenic and Polygenic Contributions to QTc Prolongation in the Population

Circulation(2022)10.1161/circulationaha.121.057261

N/A

1.7DataRank · unranked

50 citations

Valerie N. Morrill, Sean J. Jurgens, Seung Hoan Choi, Amelia W. Hall, Lu-Chen Weng +34 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

Genomewide Association Study of Platelet Reactivity and Cardiovascular Response in Patients Treated With Clopidogrel: A Study by the International Clopidogrel Pharmacogenomics Consortium

Clinical Pharmacology & Therapeutics(2020)10.1002/cpt.1911

N/A

1.6DataRank · unranked

56 citations

Thomas O. Bergmeijer, Li Gong, Jean‐Luc Reny, Joshua P. Lewis, Braxton D. Mitchell +44 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

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

Evaluating the causal effect of tobacco smoking on white matter brain aging: a two‐sample Mendelian randomization analysis in UK Biobank

Addiction(2022)10.1111/add.16088

Top 24%

0.850DataRank

Top 24%30 citations

Jingtao Wang, Zhenyao Ye, Hongjie Ke, Song Liu, Kathryn S. Hatch +9 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

A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

Nature Genetics(2022)10.1038/s41588-022-01078-z

N/A

0.793DataRank · unranked

197 citations

Shweta Ramdas, Kimberly Lorenz, Xiuqing Guo, Rebecca Darlay, Heather J. Cordell +86 more

rs641738C>T near MBOAT7 is associated with liver fat, ALT and fibrosis in NAFLD: A meta-analysis

Journal of Hepatology(2020)10.1016/j.jhep.2020.08.027

N/A

0.744DataRank · unranked

142 citations

Kushala Abeysekera, Leon A. Adams, Elmar Aigner, Quentin M. Anstee, Jesús M. Bañales +93 more

Extent and distribution of linkage disequilibrium in the Old Order Amish

Genetic Epidemiology(2010)10.1002/gepi.20444

N/A

0.735DataRank · unranked

12 citations

Albert M. Levin, Evadnie Rampersaud, Haiqing Shen, Jeffrey R. O'Connell, Braxton D. Mitchell +3 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

Depression, stress and regional cerebral blood flow

Journal of Cerebral Blood Flow & Metabolism(2023)10.1177/0271678x221148979

N/A

0.703DataRank · unranked

26 citations

Bhim M. Adhikari, Mark D. Kvarta, Heather Bruce, Eric L. Goldwaser, Yizhou Ma +8 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

Population sequencing data reveal a compendium of mutational processes in the human germ line

Science(2021)10.1126/science.aba7408

N/A

0.648DataRank · unranked

74 citations

Ruslan Soldatov, Evan M. Koch, Ryan J. McGinty, Jakob M. Goldmann, Ryan D. Hernandez +38 more

Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

Nature Communications(2024)10.1038/s41467-024-44701-9

N/A

0.648DataRank · unranked

74 citations

Inga Steinbrenner, Yong Li, Melissa Bujnis, Tatsuhiko Naito, Eirini Marouli +95 more

Genome-Wide Association Study Meta-Analysis of Stroke in 22 000 Individuals of African Descent Identifies Novel Associations With Stroke

Stroke(2020)10.1161/strokeaha.120.029123

N/A

0.637DataRank · unranked

69 citations

Hyacinth I. Hyacinth, Joshua C. Bis, Steven J. Kittner, Braxton D. Mitchell, Yu-Ching Cheng +43 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

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

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

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

0.578DataRank · unranked

46 citations

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

Elevated blood pressure accelerates white matter brain aging among late middle-aged women: a Mendelian Randomization study in the UK Biobank

Journal of Hypertension(2023)10.1097/hjh.0000000000003553

Top 37%

0.520DataRank

Top 37%17 citations

Zhenyao Ye, Chen Mo, Jingtao Wang, Song Liu, Si Gao +16 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 sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

EBioMedicine(2021)10.1016/j.ebiom.2020.103157

N/A

0.505DataRank · unranked

28 citations

Kelsey Grinde, Jennifer A. Brody, Charles E. Breeze, Laura M. Raffield, Josyf C. Mychaleckyj +68 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

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

0.442DataRank · unranked

18 citations

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

Functional vs Structural Cortical Deficit Pattern Biomarkers for Major Depressive Disorder

JAMA Psychiatry(2025)10.1001/jamapsychiatry.2025.0192

N/A

0.442DataRank · unranked

18 citations

Bhim M. Adhikari, David B. Keator, Daniel Amen, Si Gao, Nicole R. Karcher +19 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

0.436DataRank · unranked

7 citations

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

A trans-ancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

medRxiv(2021)10.1101/2020.12.26.20248491

N/A

0.425DataRank · unranked

16 citations

Shweta Ramdas, Kimberly Lorenz, Xiuqing Guo, Rebecca Darlay, Heather J. Cordell +85 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-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease

Human Molecular Genetics(2022)10.1093/hmg/ddac290

N/A

0.416DataRank · unranked

15 citations

Xiao Sun, Xuenan Mi, Zhijie Huang, Y.Y. Hsu, James E. Hixson +47 more

Multi-phase, multi-ethnic GWAS uncovers putative loci in predisposition to elite sprint and power performance, health and disease

Biology of Sport(2025)10.5114/biolsport.2025.147015

N/A

0.406DataRank · unranked

11 citations

Noriyuki Fuku, Eri Miyamoto‐Mikami, Masashi Tanaka, Motohiko Miyachi, Haruka Murakami +16 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

Deciphering the causal relationship between blood pressure and regional white matter integrity: A two‐sample Mendelian randomization study

Journal of Neuroscience Research(2023)10.1002/jnr.25205

Top 47%

0.386DataRank

Top 47%9 citations

Chen Mo, Song Liu, Si Gao, Li Feng, Boao Zhao +12 more

Risk factors forToxoplasma gondiiseropositivity in the Old Order Amish

Epidemiology and Infection(2020)10.1017/s0950268820002897

N/A

0.360DataRank · unranked

10 citations

Kathleen A. Ryan, AshimaN Wadhawan, Mary Pavlovich, Maureen Groër, Cecile Punzalan +10 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

0.360DataRank · unranked

10 citations

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

Endophenotype effect sizes support variant pathogenicity in monogenic disease susceptibility genes

Nature Communications(2022)10.1038/s41467-022-32009-5

N/A

0.360DataRank · unranked

10 citations

Valerie N. Morrill, Seung Hoan Choi, Sean J. Jurgens, Giorgio Melloni, Nicholas Marston +39 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

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

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

Monogenic and Polygenic Contributions to QTc Prolongation in the Population

medRxiv(2021)10.1101/2021.06.18.21258578

N/A

0.320DataRank · unranked

5 citations

Valerie N. Morrill, Sean J. Jurgens, Seung Hoan Choi, Amelia Weber Hall, Lu‐Chen Weng +33 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

The copy number variation and stroke (CaNVAS) risk and outcome study

PLoS ONE(2021)10.1371/journal.pone.0248791

Top 57%

0.284DataRank

Top 57%5 citations

Taiwo Adigun, Rufus Akinyemi, Onoja Akpa, Steven Bell, Bowang Chen +31 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

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

Missense variants in SORT1 are associated with LDL-C in an Amish population

Journal of Lipid Research(2023)10.1016/j.jlr.2023.100468

N/A

0.269DataRank · unranked

5 citations

Kathryn L. Schueler, Sarah M. King, Joseph Orr, Kathleen A. Ryan, Mark P. Keller +5 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

Randomized evaluation of the loss‐of‐function carboxylesterase 1 (CES1) G143E variant on clopidogrel and ticagrelor pharmacodynamics

Clinical and Translational Science(2024)10.1111/cts.70079

N/A

0.256DataRank · unranked

4 citations

Kathleen A. Ryan, Elizabeth A. Streeten, Hilary B. Whitlatch, Melanie Daue, Keith Tanner +5 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

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

A Linear Relationship between the Number of Cancers among First-Degree Relatives and the Risk of Multiple Primary Cancers

Cancer Prevention Research(2024)10.1158/1940-6207.capr-24-0062

N/A

0.208DataRank · unranked

3 citations

Kathryn Hughes Barry, Braxton D. Mitchell, Shuo Chen, Yuji Zhang, Laura E. Beane Freeman +2 more

Rare damaging CCR2 variants are associated with lower lifetime cardiovascular risk

medRxiv(2023)10.1101/2023.08.14.23294063

N/A

0.165DataRank · unranked

2 citations

Rainer Malik, Omar El Bounkari, Natalie R. Hasbani, Jiang Li, Jennifer E. Huffman +60 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

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

Genome-Wide Association Study of Radiographic Knee Osteoarthritis in North American Caucasians

UNC Libraries(2024)10.17615/a7hw-qt45

N/A

0.165DataRank · unranked

2 citations

Youfang Liu, Jordan B. Renner, James C. Torner, David T. Felson, C. Kent Kwoh +10 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

The association of SUR1 polymorphisms with acute infarct size: The MRI-GENIE study

Journal of Stroke and Cerebrovascular Diseases(2024)10.1016/j.jstrokecerebrovasdis.2024.108109

N/A

0.104DataRank · unranked

1 citations

Huichun Xu, Brady Gaynor, John W. Cole, Anne‐Katrin Giese, Markus D. Schirmer +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

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

Methylome-wide association analyses of lipids and modifying effects of behavioral factors in diverse race and ethnicity participants

Clinical Epigenetics(2025)10.1186/s13148-025-01859-3

N/A

0.104DataRank · unranked

1 citations

Jeff Haessler, Jessica I. Lundin, Burcu F. Darst, Eric A. Whitsel, Megan L. Grove +32 more

Multiethnic genome-wide meta-analysis of ectopic fat depots identifies loci associated with adipocyte development and differentiation

UNC Libraries(2020)10.17615/frhz-yk87

N/A

0DataRank · unranked

0 citations

Juan M. Peralta, Olivia Weeks, Gudnason, Vilmunder, Kurt Lohman, Andrew D. Johnson +63 more

Evidence of Neurovascular Water Exchange and Endothelial Vascular Dysfunction in Schizophrenia: An Exploratory Study

Schizophrenia Bulletin(2023)10.1093/schbul/sbad057

N/A

0DataRank · unranked

21 citations

Danny J.J. Wang, Bhim M. Adhikari, Joshua Chiappelli, Xingfeng Shao, Jiaao Yu +17 more

Causal Factors for Osteoarthritis: A Scoping Review of Mendelian Randomization Studies

Arthritis Care & Research(2023)10.1002/acr.25252

N/A

0DataRank · unranked

16 citations

Kevin A. Nguyen, Marc C. Hochberg, Braxton D. Mitchell, Eaman Alhassan

NRXN3 Is a Novel Locus for Waist Circumference: A Genome-Wide Association Study from the CHARGE Consortium

UNC Libraries(2020)10.17615/svd7-zw53

N/A

0DataRank · unranked

0 citations

Lenore J. Launer, Barbara McKnight, Alan R. Shuldiner, Tamara B. Harris, Ulf Gyllensten +27 more

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

Genetics(2023)10.1093/genetics/iyad115

N/A

0DataRank · unranked

10 citations

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

Association of parity with body mass index and cardiometabolic risk in high-parous women

Menopause The Journal of The North American Menopause Society(2023)10.1097/gme.0000000000002194

N/A

0DataRank · unranked

6 citations

Patrick F. McArdle, Kathleen A. Ryan, Melanie Daue, Huichun Xu, Kathryn Hughes Barry +5 more

Erratum: Large meta-analysis of genome-wide association studies identifies five loci for lean body mass

UNC Libraries(2020)10.17615/y892-y714

N/A

0DataRank · unranked

0 citations

Wen‐Chi Hsueh, Eric Orwoll, Serkalem Demissie, Liisa Byberg, Arjun Verma +95 more

Genome-wide significant risk loci for mood disorders in the Old Order Amish founder population

Molecular Psychiatry(2023)10.1038/s41380-023-02014-1

N/A

0DataRank · unranked

8 citations

Kwangmi Ahn, Rachel L. Kember, Fabiana L. Lopes, Evelina Mocci, Juan M. Peralta +14 more

Novel Genetic Variants for Cartilage Thickness and Hip Osteoarthritis

UNC Libraries(2020)10.17615/ayp9-a134

N/A

0DataRank · unranked

0 citations

Nancy E. Lane, Elizabeth Barrett‐Connor, Ana M. Valdes, Floris P. J. G. Lafeber, Kenneth Muir +32 more

Genomic risk scores and oral contraceptive-associated ischemic stroke risk: a call for collaboration

Frontiers in Stroke(2023)10.3389/fstro.2023.1143372

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1 citations

Liisa Tomppo, Brady Gaynor, Kathleen A. Ryan, John W. Cole, Braxton D. Mitchell +3 more

An in-depth association analysis of genetic variants within nicotine-related loci: Meeting in middle of GWAS and genetic fine-mapping

Molecular and Cellular Neuroscience(2023)10.1016/j.mcn.2023.103895

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2 citations

Zhenyao Ye, Yezhi Pan, Yuan Zhang, Qiong Wu, Chuan Bi +7 more

Genome-wide meta-analysis identified novel variant associated with hallux valgus in Caucasians

UNC Libraries(2023)10.17615/5s0z-0f43

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1 citations

Michelle S. Yau, Yvonne M. Golightly, Joanne M. Jordan, Braxton D. Mitchell, Marian T. Hannan +5 more

APOE4 poses opposite effects of plasma LDL on white matter integrity in older adults

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.24.563796

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1 citations

Yezhi Pan, Rozalina G. McCoy, Chuan Bi, Chen Mo, Li Feng +14 more

Evidence of survival bias in the association between APOE-Є4 and age of ischemic stroke onset

medRxiv(2023)10.1101/2023.12.01.23294385

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0 citations

Patrick F. McArdle, Paavo Häppölä, Jeffrey Haessler, Charles Kooperberg, Robin Lemmens +8 more

Multi-phase, multi-ethnic GWAS uncovers putative loci in predisposition to human sprint performance, health and disease

medRxiv(2023)10.1101/2023.12.08.23299720

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Noriyuki Fuku, Eri Miyamoto‐Mikami, Masashi Tanaka, Motohiko Miyachi, Haruka Murakami +19 more

Measuring alcohol consumption for genomic meta-analyses of alcohol intake: opportunities and challenges

UNC Libraries(2020)10.17615/4z6y-hr17

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Siiri Bennett, John W. Cole, Qi Sun, Rebecca DeSensi, Rob M. van Dam +33 more

A Guide to Understanding Mendelian Randomization Studies

Arthritis Care & Research(2024)10.1002/acr.25400

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64 citations

Braxton D. Mitchell, Kevin A. Nguyen

Parkinson’s disease-related motor and non-motor symptoms are not more prevalent in the Lancaster Amish

medRxiv(2020)10.1101/2020.04.13.20064337

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0 citations

Xuemei Huang, Honglei Chen, Lan Kong, Teodor T. Postolache, John W. Stiller +7 more

Rare variant enriched identity-by-descent enables the detection of distant relatedness and older divergence between populations

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.05.079541

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2 citations

TOPMed Population Genetics Working Group, Jeffrey R. O’Connell, Braxton D. Mitchell, Timothy D. O’Connor, Amol C. Shetty

Prevalence, control, and treatment of diabetes, hypertension, and high cholesterol in the Amish

BMJ Open Diabetes Research & Care(2020)10.1136/bmjdrc-2019-000912

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23 citations

Kathleen A. Ryan, Elizabeth A. Streeten, Patrick F. McArdle, Melanie Daue, Donna Trubiano +10 more

Long-term exposure to particulate air pollution and brachial artery flow-mediated dilation in the Old Order Amish

Environmental Health(2020)10.1186/s12940-020-00593-y

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10 citations

Jeff D. Yanosky, Dina Huang, Jessica Montressor-Lopez, Robert A. Vogel, Robert M. Reed +3 more

Genome‐wide meta‐analysis identified novel variant associated with hallux valgus in Caucasians

Journal of Foot and Ankle Research(2020)10.1186/s13047-020-0379-1

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11 citations

Michelle S. Yau, Braxton D. Mitchell, Rebecca D. Jackson, Kathleen A. Ryan, Yvonne M. Golightly +5 more

Alternate approach to stroke phenotyping identifies a genetic risk locus for small vessel stroke

European Journal of Human Genetics(2020)10.1038/s41431-020-0580-5

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16 citations

Sander W. van der Laan, Patrick F. McArdle, Rainer Malik, Steven J. Kittner, Braxton D. Mitchell +4 more

Contrasting association pattern of plasma low-density lipoprotein with white matter integrity in APOE4 carriers versus non-carriers

Neurobiology of Aging(2024)10.1016/j.neurobiolaging.2024.08.005

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7 citations

Yezhi Pan, Rozalina G. McCoy, Chuan Bi, Chen Mo, Feng Li +15 more

Evidence of survival bias in the association between APOE-Є4 and age at ischemic stroke onset

Frontiers in Genetics(2024)10.3389/fgene.2024.1392061

N/A

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2 citations

Patrick F. McArdle, Paavo Häppölä, Jeffrey Haessler, Charles Kooperberg, Robin Lemmens +8 more

Impact of Rare and Common Genetic Variants on Diabetes Diagnosis by Hemoglobin A1c in Multi-Ancestry Cohorts: The Trans-Omics for Precision Medicine Program

UNC Libraries(2024)10.17615/4eyj-4q61

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Ramachandran S. Vasan, Ping‐Hsun Wu, Xiuqing Guo, M. O. Goodarzi, Jerome I. Rotter +41 more

Whole-exome sequencing study identifies four novel gene loci associated with diabetic kidney disease

UNC Libraries(2024)10.17615/fpt0-zp94

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0 citations

J.A. Smith, CRIC Study Investigators, Xiuqing Guo, Donald M. Lloyd‐Jones, L.A. Lange +48 more

Rare coding variants in RCN3 are associated with blood pressure

UNC Libraries(2024)10.17615/y07d-kq52

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0 citations

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

Whole genome sequence analyses of eGFR in 23,732 people representing multiple ancestries in the NHLBI trans-omics for precision medicine (TOPMed) consortium

UNC Libraries(2024)10.17615/hd68-ze50

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B.M. Psaty, Leslie J. Baier, Robert B. Wallace, Anna Köttgen, Jiang He +69 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

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0 citations

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

Genetic variants affecting bone mineral density and bone mineral content at multiple skeletal sites in Hispanic children

UNC Libraries(2024)10.17615/90ra-wb17

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0 citations

Diana L. Cousminer, Shelley A. Cole, A.G. Comuzzie, Karin Haack, V. Saroja Voruganti +12 more

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

UNC Libraries(2024)10.17615/xgme-w279

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0 citations

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

Rare Coding Variants Associated With Electrocardiographic Intervals Identify Monogenic Arrhythmia Susceptibility Genes: A Multi-Ancestry Analysis

UNC Libraries(2024)10.17615/c1sy-3719

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0 citations

Brandon K. Fornwalt, Chrissy Austin-Tse, Mark Chaffin, B.E. Cade, J Lee +43 more

Genome-wide meta-analysis of 158,000 individuals of European ancestry identifies three loci associated with chronic back pain

UNC Libraries(2024)10.17615/36rr-ma25

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0 citations

Blair Smith, Magnus K. Karlsson, Michelle S. Yau, Frances M. K. Williams, Traci M. Bartz +32 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

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0 citations

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

Accelerating Heritability, Genetic Correlation, and Genome‐Wide Association Imaging Genetic Analyses in Complex Pedigrees

Human Brain Mapping(2024)10.1002/hbm.70044

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Si Gao, Thomas E. Nichols, Bhim M. Adhikari, Yizhou Ma, Neda Jahanshad +13 more

Seasonal affective disorder and seasonal changes in weight and sleep duration are inversely associated with plasma adiponectin levels

Journal of Psychiatric Research(2020)10.1016/j.jpsychires.2019.12.016

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14 citations

Claudia Gragnoli, Uttam K. Raheja, Søren Snitker, Christopher A. Lowry, Kelly A. Stearns‐Yoder +9 more

Contents Vol. 64, 2007

Human Heredity(2007)10.1159/000105467

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0 citations

John P. A. Ioannidis, Wendy S. Post, Haiqing Shen, Coleen Damcott, Dan E. Arking +20 more

Author Index Vol. 64, 2007

Human Heredity(2007)10.1159/000105464

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0 citations

John P. A. Ioannidis, Wendy S. Post, Haiqing Shen, Coleen Damcott, Dan E. Arking +20 more

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

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

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0 citations

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

Adherence to life’s essential 8 is associated with delayed white matter aging

EBioMedicine(2025)10.1016/j.ebiom.2025.105723

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9 citations

Zhenyao Ye, Yezhi Pan, Rozalina G. McCoy, Braxton D. Mitchell, Peter Kochunov +16 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

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4 citations

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

Multi-ancestry whole genome sequencing analysis of lean body mass

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1 citations

Kuan‐Jui Su, Bodhisattwa Banerjee, Ittai Eres, Yi-Hsiang Hsu, Carolyn Crandall +21 more

Peripheral Microvascular and Cerebral White Matter Dysfunction in Schizophrenia: Implications of a Body-Brain Endothelial Pathophysiology

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1 citations

Alexa Yuen, Wyatt Marshall, Bhim M. Adhikari, Joshua Chiappelli, Andrew van der Vaart +12 more

Exonic Variation and Its Clinical Impact in 7221 Old Order Amish

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.64212

N/A

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0 citations

Ebuka Onyenobi, Joshua P. Lewis, Brady Gaynor, James A. Perry, Kristin A. Maloney +17 more

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

UNC Libraries(2025)10.17615/mztm-gw84

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

Frontal white matter association with sleep quality and the role of stress

Journal of Sleep Research(2022)10.1111/jsr.13669

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16 citations

Peter Kochunov, Mark D. Kvarta, Eric L. Goldwaser, Joshua Chiappelli, Adina Schwartz +13 more

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

UNC Libraries(2025)10.17615/5tss-f273

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0 citations

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

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109 citations

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

Cerebral blood flow and cardiovascular risk effects on resting brain regional homogeneity

NeuroImage(2022)10.1016/j.neuroimage.2022.119555

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15 citations

L. Elliot Hong, Zhiwei Zhao, Danny J.J. Wang, Paul M. Thompson, Neda Jahanshad +20 more

Genetic Fine-Mapping With Dense Linkage Disequilibrium Blocks

Research Square(2021)10.21203/rs.3.rs-649530/v1

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0 citations

Zhenyao Ye, Kathryn S. Hatch, Yuan Zhang, Qiong Wu, Song Liu +7 more

Meta-Analysis of Transcriptome-Wide Association Studies Across 13 Brain Tissues Identified Novel Clusters of Genes Associated with Nicotine Addiction

Preprints.org(2021)10.20944/preprints202111.0386.v1

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3 citations

Mo Chen, Hongjie Ke, Qi Yan, Chixiang Chen, Elliot Hong +5 more

Meta-Analysis of Transcriptome-Wide Association Studies across 13 Brain Tissues Identified Novel Clusters of Genes Associated with Nicotine Addiction

Genes(2021)10.3390/genes13010037

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4 citations

Chen Mo, Hongjie Ke, Qi Yan, Chixiang Chen, Peter Kochunov +5 more

Social and scientific motivations to move beyond groups in allele frequencies: The TOPMed experience

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.07.008

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6 citations

Stephanie M. Gogarten, Stephanie M. Fullerton, Carmen R. Isasi, Braxton D. Mitchell, Kari E. North +5 more

Genetic versus stress and mood determinants of sleep in the Amish

American Journal of Medical Genetics Part B Neuropsychiatric Genetics(2021)10.1002/ajmg.b.32840

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3 citations

Peter Kochunov, Joshua Chiappelli, Anya Savransky, Kathleen Carino, Jessica Sewell +10 more

Multiple dimensions of stress vs. genetic effects on depression

Translational Psychiatry(2021)10.1038/s41398-021-01369-9

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6 citations

Heather Bruce, Joshua Chiappelli, Stephanie Hare, Eric L. Goldwaser, Jessica Sewell +12 more

Identification of novel and rare variants associated with handgrip strength using whole genome sequence data from the NHLBI Trans-Omics in Precision Medicine (TOPMed) Program

PLoS ONE(2021)10.1371/journal.pone.0253611

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8 citations

Han Chen, Mary L. Biggs, Sylvia Wassertheil‐Smoller, Jan Bressler, Marguerite R. Irvin +24 more

Genome‐Wide Association Study Identifies First Locus Associated with Susceptibility to Cerebral Venous Thrombosis

Annals of Neurology(2021)10.1002/ana.26205

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20 citations

Ioana Cotlarciuc, Ida Martinelli, Elvira Grandone, Sini Hiltunen, Erik Lindgren +45 more

Association Between Chromosome 9p21 Variants and the Ankle-Brachial Index Identified by a Meta-Analysis of 21 Genome-Wide Association Studies

UNC Libraries(2020)10.17615/tb6e-th27

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0 citations

Christina L. Wassel, Tanja Zeller, Lina Zgaga, Eric Boerwinkle, Ben A. Oostra +95 more

Braxton D. Mitchell

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