Barry I. Freedman

Also affiliated with University of Chicago Research Bangladesh, Wake Forest University

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 2%percentile

3.5Author DataRank

Indexed papers

7in 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 7 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 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

Papers

Driven by 71 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

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

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

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

Association of Intensive vs Standard Blood Pressure Control With Magnetic Resonance Imaging Biomarkers of Alzheimer Disease

JAMA Neurology(2021)10.1001/jamaneurol.2021.0178

N/A

2.1DataRank · unranked

74 citations

Sarah A. Gaussoin, Raymond Pomponio, Sudipto Dolui, Guray Erus, Clinton B. Wright +91 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

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

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

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

The genetic architecture of type 2 diabetes

Nature(2016)10.1038/nature18642

N/A

1.1DataRank · unranked

1106 citations

Menachem Fromer, Tanya M. Teslovich, Anubha Mahajan, Vineeta Agarwala, Kyle J. Gaulton +334 more

A randomized pilot study to evaluate graft versus fistula vascular access strategy in older patients with advanced kidney disease: results of a feasibility study

Pilot and Feasibility Studies(2020)10.1186/s40814-020-00619-9

N/A

0.760DataRank · unranked

20 citations

Randolph L. Geary, Denise K. Houston, Matthew S. Edwards, Todd W. Robinson, Ross P. Davis +12 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

0.753DataRank · unranked

150 citations

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

Transferability and Fine Mapping of Type 2 Diabetes Loci in African Americans

Diabetes(2013)10.2337/db12-0266

N/A

0.621DataRank · unranked

62 citations

Richa Saxena, Jiang Li, Nicholette D. Palmer, Latchezar Dimitrov, Jianzhao Xu +20 more

Preventing chronic kidney disease and maintaining kidney health: conclusions from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference

Kidney International(2025)10.1016/j.kint.2025.04.005

N/A

0.584DataRank · unranked

48 citations

José Manuel Arreola Guerra, Juliana C.N. Chan, Vivekanand Jha, Holly Kramer, Susanne B. Nicholas +62 more

Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals

Communications Biology(2022)10.1038/s42003-022-03448-z

N/A

0.553DataRank · unranked

39 citations

Humaira Rasheed, Alexander Teumer, Mathias Gorski, Bryce Rowan, Kira J. Stanzick +94 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

Risk for Chronic Kidney Disease Progression After Acute Kidney Injury: Findings From the Chronic Renal Insufficiency Cohort Study

Annals of Internal Medicine(2023)10.7326/m22-3617

N/A

0.529DataRank · unranked

33 citations

Jesse Y. Hsu, Xiaoming Zhang, Lawrence J. Appel, Jing Chen, Debbie L. Cohen +23 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

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

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

End-Stage Renal Disease in African Americans With Lupus Nephritis Is Associated With APOL1

UNC Libraries(2020)10.17615/yd3a-5a16

N/A

0.434DataRank · unranked

17 citations

S. Sam Lim, Daniel J. Birmingham, Lindsey A. Criswell, Neva E. Garner, Hicks, Pamela J. +27 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

Gene Set Enrichment Analsyes Identify Pathways Involved in Genetic Risk for Diabetic Retinopathy

American Journal of Ophthalmology(2021)10.1016/j.ajo.2021.06.014

N/A

0.406DataRank · unranked

14 citations

Gayatri Susarla, Lynn K. Stanwyck, John M. Rouhana, Ashley Li, Samuela Pollack +25 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

Genome-wide association study of vitamin D concentrations and bone mineral density in the African American-Diabetes Heart Study

PLoS ONE(2021)10.1371/journal.pone.0251423

N/A

0.396DataRank · unranked

13 citations

Lingyi Lu, Thomas C. Register, Leon Lenchik, J. Jeffrey Carr, Pamela J. Hicks +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

Genetic variants for head size share genes and pathways with cancer

Cell Reports Medicine(2024)10.1016/j.xcrm.2024.101529

N/A

0.380DataRank · unranked

10 citations

Raymond A. Poot, Tavia E. Evans, Claudia L. Satizábal, Aniket Mishra, Muralidharan Sargurupremraj +95 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

Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes

Circulation Genomic and Precision Medicine(2021)10.1161/circgen.120.003258

N/A

0.360DataRank · unranked

10 citations

Latchezar Dimitrov, Shyh‐Huei Chen, Lawrence F. Bielak, Joshua C. Bis, Mary F. Feitosa +37 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

Kidney Disease, Hypertension Treatment, and Cerebral Perfusion and Structure

American Journal of Kidney Diseases(2021)10.1053/j.ajkd.2021.07.024

N/A

0.313DataRank · unranked

4 citations

Sarah A. Gaussoin, Nicholas M. Pajewski, Greg Zaharchuk, Barry I. Freedman, Stephen R. Rapp +91 more

Genetic variants for head size share genes and pathways with cancer

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.15.191114

N/A

0.312DataRank · unranked

7 citations

Raymond A. Poot, Tavia E. Evans, Claudia L. Satizábal, Aniket Mishra, Sandra Van der Auwera +95 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

Recipient APOL1 Genotype Effects on Outcomes After Kidney Transplantation

American Journal of Kidney Diseases(2021)10.1053/j.ajkd.2021.11.001

N/A

0.269DataRank · unranked

5 citations

Alejandra Mena‐Gutierrez, Lijun Ma, Barry I. Freedman

Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele

Nature Communications(2025)10.1038/s41467-025-58420-2

N/A

0.269DataRank · unranked

5 citations

Jennifer A. Brody, Mariaelisa Graff, Heather M. Highland, Nathalie Chami, Hanfei Xu +93 more

Employment status at transplant influences ethnic disparities in outcomes after deceased donor kidney transplantation

BMC Nephrology(2022)10.1186/s12882-021-02631-4

N/A

0.241DataRank · unranked

4 citations

Sumit Mohan, W. Mark Brown, Stephen O. Pastan, Ajay K. Israni, Robert S. Gaston +8 more

Selecting SNPs informative for African, American Indian and European Ancestry: application to the Family Investigation of Nephropathy and Diabetes (FIND)

BMC Genomics(2016)10.1186/s12864-016-2654-x

N/A

0.218DataRank · unranked

3 citations

Robert C. Williams, Robert C. Elston, Pankaj Kumar, William C. Knowler, Hanna E. Abboud +28 more

Multi-ancestry polygenic risk scores for the prediction of type 2 diabetes and complications in diverse ancestries

The Lancet Diabetes & Endocrinology(2026)10.1016/s2213-8587(25)00405-x

N/A

0.208DataRank · unranked

3 citations

Joohyun Kim, Ravi Mandla, Yingchang Lu, Ken Suzuki, Lauren E Petty +255 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 ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE

medRxiv(2023)10.1101/2023.08.21.23293271

N/A

0.165DataRank · unranked

2 citations

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

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

Metabolomic signatures of cognitive function in a type 2 Diabetes-Enriched cohort

Scientific Reports(2025)10.1038/s41598-025-99606-4

Top 78%

0.104DataRank

Top 78%1 citations

Christina E. Hugenschmidt, Fang‐Chi Hsu, Laura A. Flashman, Jianzhao Xu, Donald W. Bowden +3 more

Urinary Complement proteome strongly linked to diabetic kidney disease progression

Nature Communications(2025)10.1038/s41467-025-62101-5

N/A

0DataRank · unranked

16 citations

Salina Moon, Eiichiro Satake, Daigoro Hirohama, Nicholette D. Palmer, Heather C. Lampert +16 more

Urine Markers of Kidney Tubule Cell Injury and Kidney Function Decline in SPRINT Trial Participants with CKD

Clinical Journal of the American Society of Nephrology(2020)10.2215/cjn.02780319

N/A

0DataRank · unranked

88 citations

Ronit Katz, Vasantha Jotwani, Walter T. Ambrosius, Kalani L. Raphael, William E. Haley +8 more

Apolipoprotein L1 Gene Testing Comes of Age

Kidney360(2020)10.34067/kid.0000162019

N/A

0DataRank · unranked

9 citations

Chris Larsen, Barry I. Freedman

APOL1 Kidney-Risk Variants Induce Mitochondrial Fission.

PubMed(2020)10.1016/j.ekir.2020.03.020

N/A

0DataRank · unranked

44 citations

Hannah C. Ainsworth, James A. Snipes, Mariana Murea, Young A. Choi, Carl D. Langefeld +15 more

Kidney Disease, Intensive Hypertension Treatment, and Risk for Dementia and Mild Cognitive Impairment: The Systolic Blood Pressure Intervention Trial

Journal of the American Society of Nephrology(2020)10.1681/asn.2020010038

N/A

0DataRank · unranked

40 citations

Sarah A. Gaussoin, Nicholas M. Pajewski, Gordon J. Chelune, Barry I. Freedman, Tanya R. Gure +9 more

Meta-analysis of genome-wide linkage scans for renal function traits

UNC Libraries(2020)10.17615/wd26-df09

N/A

0DataRank · unranked

1 citations

Madhumathi Rao, Steven C. Hunt, Shelley A. Cole, Sudha K. Iyengar, Carl D. Langefeld +8 more

A randomized pilot study to evaluate graft-first versus fistula-first vascular access strategy in older patients with advanced kidney disease: results of a feasibility study Pilot and Feasibility Studies

Research Square(2020)10.21203/rs.2.22250/v1

N/A

0DataRank · unranked

0 citations

Randolph L. Geary, Denise K. Houston, Matthew S. Edwards, Todd W. Robinson, Ross P. Davis +11 more

A randomized pilot study to evaluate graft versus fistula vascular access strategy in older patients with advanced kidney disease: results of a feasibility study

Research Square(2020)10.21203/rs.2.22250/v2

N/A

0DataRank · unranked

0 citations

Randolph L. Geary, Denise K. Houston, Matthew S. Edwards, Todd W. Robinson, Ross P. Davis +12 more

Meta-Analysis of Genome-Wide Association Studies in African Americans Provides Insights into the Genetic Architecture of Type 2 Diabetes

UNC Libraries(2020)10.17615/n0t3-7m22

N/A

0DataRank · unranked

0 citations

Xiuqing Guo, Yan V. Sun, Michael A. Nalls, Suzette J. Bielinski, Palmer, Nicholette D. +27 more

Genome-Wide Detection of Allele Specific Copy Number Variation Associated with Insulin Resistance in African Americans from the HyperGEN Study

UNC Libraries(2020)10.17615/wrwb-1632

N/A

0DataRank · unranked

0 citations

Nicholas M. Pajewski, Pankow, Jim, Treva Rice, Donna K. Arnett, Uli Broeckel +9 more

Sickle cell trait is not independently associated with susceptibility to end-stage renal disease in African Americans

UNC Libraries(2020)10.17615/44gk-2q97

N/A

0DataRank · unranked

0 citations

Jasmin Divers, Barry I. Freedman, Donald W. Bowden, Patrick H. Nachman, Lingyi Lu +4 more

APOL1 genotyping in kidney transplantation: to do or not to do, that is the question? (pro)

Kidney International(2021)10.1016/j.kint.2020.11.025

N/A

0DataRank · unranked

8 citations

Emilio D. Poggio, Barry I. Freedman

Factors Influencing Ethnic Disparities in Outcomes after Deceased Donor Kidney Transplantation

Research Square(2021)10.21203/rs.3.rs-852100/v1

N/A

0DataRank · unranked

0 citations

Sumit Mohan, W. Mark Brown, Stephen O. Pastan, Ajay K. Israni, Robert S. Gaston +8 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

Nucleotide variation, haplotype structure, and association with end-stage renal disease of the human interleukin-1 gene cluster

Carolina Digital Repository (University of North Carolina at Chapel Hill)(2023)10.17615/xkqa-ez55

Top 100%

0DataRank

Top 100%0 citations

Douglas Kiger, C.S. Brewer, D. Craig Allred, Carla J. Colicigno, Jeannette T. Bensen +7 more

Multi-ancestry study of blood lipid levels identifies four loci interacting with physical activity

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

N/A

0DataRank · unranked

0 citations

J.M. Norris, Evangelos Evangelou, C.E. Lewis, André G. Uitterlinden, M.Y. Tsai +95 more

Multiethnic Genome-Wide Association Study of Subclinical Atherosclerosis in Individuals With Type 2 Diabetes

UNC Libraries(2024)10.17615/zpcz-6n16

N/A

0DataRank · unranked

0 citations

Mary F. Feitosa, D.W. Bowden, N. Franceschini, L.M. Raffield, Daniël Bos +37 more

HDAC9 is implicated in atherosclerotic aortic calcification and affects vascular smooth muscle cell phenotype

UNC Libraries(2024)10.17615/8v85-pc44

N/A

0DataRank · unranked

0 citations

G. Shelton, Haakon H. Sigurslid, M.F. Feitosa, Sonali Pechlivanis, Christian L. Lino Cardenas +45 more

Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries

UNC Libraries(2024)10.17615/chag-t845

N/A

0DataRank · unranked

0 citations

Hugues Aschard, Kurt K. Lohman, Jiang He, X. Chen, Alisa K. Manning +94 more

Genome-wide association study identifies novel loci for type 2 diabetes-Attributed end-stage kidney disease in African Americans

UNC Libraries(2024)10.17615/mjwt-x036

N/A

0DataRank · unranked

0 citations

W.S. Post, Josyf C. Mychaleckyj, M. FORNAGE, Adrienne Tin, Denyse Thornley‐Brown +22 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

Genetic variants for head size share genes and pathways with cancer

UNC Libraries(2024)10.17615/0jt9-4n49

N/A

0DataRank · unranked

0 citations

Vince D. Calhoun, Manabu Nagata, Raymond A. Poot, Aad van der Lugt, Svenja Caspers +95 more

Association of Collapsing Glomerulopathy with Donor Apolipoprotein L1 Risk Variants in Kidney Allografts from Black Donors

Clinical Journal of the American Society of Nephrology(2025)10.2215/cjn.0000000778

N/A

0DataRank · unranked

0 citations

Alexei Mikhailov, S. Ali Husain, Rachel A. Nuccitelli, Francesca Zanoni, Lili Liu +17 more

Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis

UNC Libraries(2025)10.17615/cdn0-cm52

N/A

0DataRank · unranked

0 citations

Russell P. Tracy, Jill M. Johnsen, Hind Bouzid, Nicholas L. Smith, Katherine P. Prothro +95 more

Barry I. Freedman

Indexed papers

Top data-sharing exemplar

Papers