Eimear E. Kenny

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

44.7Author 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.

A global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

Papers

Driven by 123 papers — median percentile 90. 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

A global reference for human genetic variation

Nature(2015)10.1038/nature15393

Top 1%

10.6DataRank

Top 1%20166 citations

Gonçalo R. Abecasis, Richard M. Durbin, Panagiotis Deloukas, Aravinda Chakravarti, Peter Donnelly +516 more

A brief history of human disease genetics

Nature(2020)10.1038/s41586-019-1879-7

N/A

9.2DataRank · unranked

738 citations

Judy H. Cho, Rory Collins, Nancy J. Cox, Emmanouil T. Dermitzakis, Matthew E. Hurles +13 more

Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel

Nature Communications(2014)10.1038/ncomms4934

Top 2%

8.3DataRank

Top 2%460 citations

Jonathan Marchini, Peter Donnelly, Gerton Lunter, Jonathan L. Marchini, Simon Myers +364 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

The Human Pangenome Project: a global resource to map genomic diversity

Nature(2022)10.1038/s41586-022-04601-8

Top 4%

5.6DataRank

Top 4%571 citations

Lucinda Antonacci-Fulton, Thibaut Hourlier, Heather A. Lawson, Julian K. Lucas, Adam M. Phillippy +36 more

A draft human pangenome reference

Nature(2023)10.1038/s41586-023-05896-x

Top 4%

5.1DataRank

Top 4%1169 citations

Mobin Asri, Jana Ebler, Daniel Doerr, Marina Haukness, Hickey, Glenn +95 more

Pangenome graph construction from genome alignments with Minigraph-Cactus

Nature Biotechnology(2023)10.1038/s41587-023-01793-w

N/A

5.0DataRank · unranked

318 citations

Jean Monlong, Jana Ebler, Adam M. Novak, Jordan M. Eizenga, Yan Gao +94 more

Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations

Nature Medicine(2024)10.1038/s41591-024-02796-z

N/A

4.8DataRank · unranked

196 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Joshua Arias, Gillian M. Belbin +73 more

The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis

Nature Communications(2020)10.1038/s41467-020-15383-w

N/A

4.6DataRank · unranked

223 citations

Lili Liu, Nikol Mladkova, Yifu Li, Hong Ren, Weiming Wang +95 more

Multiscale causal networks identify VGF as a key regulator of Alzheimer’s disease

Nature Communications(2020)10.1038/s41467-020-17405-z

N/A

3.8DataRank · unranked

189 citations

Wei‐Jye Lin, Minghui Wang, Ariella Cohain, Alexander W. Charney, Pei Wang +29 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

FAVOR: functional annotation of variants online resource and annotator for variation across the human genome

Nucleic Acids Research(2022)10.1093/nar/gkac966

Top 8%

2.7DataRank

Top 8%143 citations

Theodore Arapoglou, Xihao Li, Zilin Li, Xiuwen Zheng, Jill E. Moore +20 more

Returning integrated genomic risk and clinical recommendations: The eMERGE study

Genetics in Medicine(2023)10.1016/j.gim.2023.100006

N/A

2.6DataRank · unranked

121 citations

Aimee Allworth, Harris T. Bland, Pedro J. Caraballo, Rex L. Chisholm, Ellen Wright Clayton +95 more

Increased mutation and gene conversion within human segmental duplications

Nature(2023)10.1038/s41586-023-05895-y

N/A

2.1DataRank · unranked

114 citations

Philip C. Dishuck, William T. Harvey, William S. DeWitt, Xavi Guitart, Michael E. Goldberg +108 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

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

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

Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome

Nature Communications(2023)10.1038/s41467-023-37985-w

N/A

1.1DataRank · unranked

51 citations

Michelle T. McNulty, Xiaoyuan Jia, Yask Gupta, Hanna Dêbiec, Yang Luo +65 more

The PRIMED Consortium: Reducing disparities in polygenic risk assessment

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.010

N/A

0.893DataRank · unranked

37 citations

Matthew P. Conomos, Sarah C. Nelson, Sally N. Adebamowo, Ananyo Choudhury, David V. Conti +90 more

Principles and methods for transferring polygenic risk scores across global populations

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

N/A

0.869DataRank · unranked

328 citations

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

Beyond the Human Genome Project: The Age of Complete Human Genome Sequences and Pangenome References

Annual Review of Genomics and Human Genetics(2024)10.1146/annurev-genom-021623-081639

Top 23%

0.864DataRank

Top 23%42 citations

Jordan M. Eizenga, Qiuhui Li, Arun Das, Katharine M. Jenike, Eimear E. Kenny +6 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

Genome-wide polygenic score to predict chronic kidney disease across ancestries

Nature Medicine(2022)10.1038/s41591-022-01869-1

N/A

0.764DataRank · unranked

162 citations

Michael C. Turchin, Amit Patki, Vinodh Srinivasasainagendra, Ning Shang, Rajiv Nadukuru +34 more

Toward a fine-scale population health monitoring system

Cell(2021)10.1016/j.cell.2021.03.034

N/A

0.763DataRank · unranked

161 citations

Sinéad Cullina, Stéphane Wenric, Emily R. Soper, Benjamin Scott Glicksberg, Denis Torre +18 more

Causal effects on complex traits are similar for common variants across segments of different continental ancestries within admixed individuals

Nature Genetics(2023)10.1038/s41588-023-01338-6

N/A

0.727DataRank · unranked

126 citations

Yi Ding, Ziqi Xu, Yue Wu, Arjun Bhattacharya, Rachel Mester +24 more

Recombination between heterologous human acrocentric chromosomes

Nature(2023)10.1038/s41586-023-05976-y

N/A

0.710DataRank · unranked

113 citations

Silvia Buonaiuto, Leonardo Gomes de Lima, Tamara Potapova, Arang Rhie, Sergey Koren +106 more

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

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

N/A

0.701DataRank · unranked

106 citations

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

Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease

Nature Communications(2023)10.1038/s41467-023-43020-9

N/A

0.637DataRank · unranked

69 citations

David J. Friedman, Michelle T. McNulty, Atlas Khan, Brandon M. Lane, Chen Wang +75 more

Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas

Cell Genomics(2024)10.1016/j.xgen.2024.100692

Top 31%

0.635DataRank

Top 31%30 citations

Douglas P. Loesch, Bing Guo, Roland Laboulaye, Diego Véliz-Otani, Jennifer N. French +70 more

An integrative multiomic network model links lipid metabolism to glucose regulation in coronary artery disease

Nature Communications(2021)10.1038/s41467-020-20750-8

N/A

0.626DataRank · unranked

64 citations

William Barrington, Daniel M. Jordan, Noam D. Beckmann, Carmen Argmann, Sander M. Houten +21 more

A common variant in PNPLA3 is associated with age at diagnosis of NAFLD in patients from a multi-ethnic biobank

Journal of Hepatology(2020)10.1016/j.jhep.2020.01.029

N/A

0.621DataRank · unranked

62 citations

Gillian M. Belbin, Elena P. Sorokin, Tielman Van Vleck, Genevieve L. Wojcik, Arden Moscati +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

Kidney multiome-based genetic scorecard reveals convergent coding and regulatory variants

Science(2025)10.1126/science.adp4753

N/A

0.587DataRank · unranked

49 citations

Amin Abedini, Eunji Ha, Ziyuan Ma, Xin Sheng, Bernhard Dumoulin +94 more

Mapping the Human Reference Genome’s Missing Sequence by Three-Way Admixture in Latino Genomes

The American Journal of Human Genetics(2013)10.1016/j.ajhg.2013.07.002

N/A

0.574DataRank · unranked

45 citations

Robert E. Handsaker, Alexandra P. Lewis, Eimear E. Kenny, Steven A. McCarroll, Giulio Genovese

Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

Genetics in Medicine(2023)10.1016/j.gim.2023.100880

N/A

0.564DataRank · unranked

42 citations

Priya N. Marathe, Nicole R. Kelly, Katherine E. Bonini, Monisha Sebastin, Jacqueline A. Odgis +22 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 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

GUÍA: a digital platform to facilitate result disclosure in genetic counseling

Genetics in Medicine(2021)10.1038/s41436-020-01063-z

N/A

0.505DataRank · unranked

28 citations

Jaqueline A. Odgis, Katie M. Gallagher, Jessica Rodriguez, Dana Watnick, Gabrielle Bertier +27 more

MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups

Cell Genomics(2024)10.1016/j.xgen.2024.100539

N/A

0.500DataRank · unranked

27 citations

Jianan Zhan, Jingning Zhang, Ruzhang Zhao, Jared O’Connell, Yunxuan Jiang +65 more

Predicted gene expression in ancestrally diverse populations leads to discovery of susceptibility loci for lifestyle and cardiometabolic traits

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.02.013

N/A

0.484DataRank · unranked

12 citations

Genevieve L. Wojcik, Mariaelisa Graff, Katherine K. Nishimura, Chani J. Hodonsky, Antoine Baldassari +31 more

Hope versus reality: Parent expectations of genomic testing

Patient Education and Counseling(2021)10.1016/j.pec.2021.01.030

N/A

0.470DataRank · unranked

22 citations

Siobhan M. Dolan, Dana Watnick, Katie M. Gallagher, Jacqueline A. Odgis, Sabrina A. Suckiel +7 more

Multi-Ethnic Genome-Wide Association Study of Decomposed Cardioelectric Phenotypes Illustrates Strategies to Identify and Characterize Evidence of Shared Genetic Effects for Complex Traits

Circulation Genomic and Precision Medicine(2020)10.1161/circgen.119.002680

Top 41%

0.466DataRank

Top 41%13 citations

Colleen M. Sitlani, Heather M. Highland, Dan E. Arking, Steven Buyske, Dawood Darbar +27 more

Enrichment analyses identify shared associations for 25 quantitative traits in over 600,000 individuals from seven diverse ancestries

The American Journal of Human Genetics(2022)10.1016/j.ajhg.2022.03.005

N/A

0.449DataRank · unranked

19 citations

Sahar Shahamatdar, Wei Cheng, Selena Zhang, Joseph Paik, Misa Graff +10 more

Estimating heritability explained by local ancestry and evaluating stratification bias in admixture mapping from summary statistics

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.09.012

N/A

0.431DataRank · unranked

8 citations

Xinyue Rui, David V. Conti, Myriam Fornage, Mariaelisa Graff, Jeffrey Haessler +13 more

MUSSEL: Enhanced Bayesian Polygenic Risk Prediction Leveraging Information across Multiple Ancestry Groups

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.12.536510

N/A

0.416DataRank · unranked

15 citations

Jianan Zhan, Jingning Zhang, Ruzhang Zhao, Jared O’Connell, Yunxuan Jiang +11 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

Disease risk and healthcare utilization among ancestrally diverse groups in the Los Angeles region

Nature Medicine(2023)10.1038/s41591-023-02425-1

N/A

0.406DataRank · unranked

14 citations

Arya Boudaie, Ruhollah Shemirani, Joel Mefford, Ella Petter, Alec Chiu +14 more

Leveraging health systems data to characterize a large effect variant conferring risk for liver disease in Puerto Ricans

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.09.016

N/A

0.406DataRank · unranked

14 citations

Stephanie Rutledge, Tetyana Dodatko, Sinéad Cullina, Michael C. Turchin, Sumita Kohli +7 more

Polygenic Risk for Type 2 Diabetes in African Americans

Diabetes(2024)10.2337/db23-0232

N/A

0.404DataRank · unranked

8 citations

Tian Ge, Amit Patki, Vinodh Srinivasasainagendra, Nicole D. Armstrong, Brittney H. Davis +14 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

African-specific alleles modify risk for asthma at the 17q12-q21 locus in African Americans

Genome Medicine(2022)10.1186/s13073-022-01114-x

N/A

0.373DataRank · unranked

11 citations

Matthew Dapas, Arjun Biddanda, Kevin M. Magnaye, Ivy Aneas, Britney A. Helling +45 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

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

TOPORS as a novel causal gene for Joubert syndrome

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63303

N/A

0.355DataRank · unranked

6 citations

Hui‐Qi Qu, Sinéad Cullina, Morgan L. McManus, Elaine H. Zackai, Joseph Glessner +3 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

Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations

medRxiv(2023)10.1101/2023.05.25.23290535

N/A

0.330DataRank · unranked

8 citations

Leah C. Kottyan, Christopher Kachulis, Noura S. Abul‐Husn, Josh Arias, Gillian M. Belbin +71 more

Epigenetic mechanisms underlying variation of IL-6, a well-established inflammation biomarker and risk factor for cardiovascular disease

Atherosclerosis(2025)10.1016/j.atherosclerosis.2025.120219

N/A

0.312DataRank · unranked

7 citations

Ulrike Peters, Yao Hu, Farah Ammous, Emelia J. Benjamin, Joshua C. Bis +31 more

Molecular diagnostic yield of genome sequencing versus targeted gene panel testing in racially and ethnically diverse pediatric patients

medRxiv(2023)10.1101/2023.03.18.23286992

N/A

0.312DataRank · unranked

7 citations

Priya Marathe, Nicole Kelly, Katherine E. Bonini, Monisha Sebastin, Jacqueline A. Odgis +22 more

Admixture mapping of peripheral artery disease in a Dominican population reveals a putative risk locus on 2q35

Frontiers in Genetics(2023)10.3389/fgene.2023.1181167

N/A

0.292DataRank · unranked

6 citations

Genevieve L. Wojcik, Ruhollah Shemirani, Derek Klarin, Bryan R. Gorman, Elena P. Sorokin +9 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

Enrichment analyses identify shared associations for 25 quantitative traits in over 600,000 individuals from seven diverse ancestries

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.20.440612

N/A

0.269DataRank · unranked

5 citations

Sahar Shahamatdar, Wei Cheng, Selena Zhang, Joseph Paik, Misa Graff +10 more

Causal effects on complex traits are similar across segments of different continental ancestries within admixed individuals

medRxiv(2022)10.1101/2022.08.16.22278868

N/A

0.241DataRank · unranked

4 citations

Yi Ding, Ziqi Xu, Yue Wu, Arjun Bhattacharya, Rachel Mester +23 more

Health care utilization of fine-scale identity by descent clusters in a Los Angeles biobank

medRxiv(2022)10.1101/2022.07.12.22277520

N/A

0.241DataRank · unranked

4 citations

Arya Boudaie, Ruhollah Shemirani, Ella Petter, Alec Chiu, Ruth Johnson +10 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

MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.04.001

N/A

0.241DataRank · unranked

4 citations

Yingxi Yang, Jonathan D. Rosen, Jiawen Chen, Xihao Li, Wyliena Guan +22 more

Estimating heritability explained by local ancestry and evaluating stratification bias in admixture mapping from summary statistics

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.10.536252

N/A

0.241DataRank · unranked

4 citations

Xinyue Rui, David V. Conti, Myriam Fornage, Mariaelisa Graff, Jeffrey Haessler +13 more

Genome-wide polygenic score with APOL1 risk genotypes predicts chronic kidney disease across major continental ancestries

medRxiv(2021)10.1101/2021.10.25.21265398

N/A

0.218DataRank · unranked

2 citations

Michael C. Turchin, Amit Patki, Vinodh Srinivasasainagendra, Ning Shang, Rajiv Nadukuru +33 more

Selecting Clustering Algorithms for IBD Mapping

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.08.11.456036

N/A

0.208DataRank · unranked

3 citations

Gillian M. Belbin, Keith Burghardt, Kristina Lerman, Christy L. Avery, Eimear E. Kenny +3 more

Investigating the sources of variable impact of pathogenic variants in monogenic metabolic conditions

Nature Communications(2025)10.1038/s41467-025-60339-7

N/A

0.208DataRank · unranked

3 citations

Richard Border, Boyang Fu, Sinéad Cullina, Nadav Brandes, Seon-Kyeong Jang +7 more

Using the linear references from the pangenome to discover missing autism variants

Nature Communications(2026)10.1038/s41467-026-68378-4

Top 65%

0.208DataRank

Top 65%3 citations

Jiadong Lin, Michelle D. Noyes, Young-Jun Kwon, Isaac Wong, Nidhi Koundinya +252 more

Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease

medRxiv(2023)10.1101/2023.08.02.23293554

N/A

0.208DataRank · unranked

3 citations

David J. Friedman, Michelle T. McNulty, Atlas Khan, Brandon M. Lane, Chen Wang +75 more

Causal effects on complex traits are similar across segments of different continental ancestries within admixed individuals

Research Square(2022)10.21203/rs.3.rs-1950966/v1

N/A

0.188DataRank · unranked

2 citations

Yi Ding, Ziqi Xu, Yue Wu, Arjun Bhattacharya, Rachel Mester +23 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

Assessing efficiency of fine-mapping obesity-associated variants through leveraging ancestry architecture and functional annotation using PAGE and UKBB cohorts

Human Genetics(2023)10.1007/s00439-023-02593-7

N/A

0.165DataRank · unranked

2 citations

Mariaelisa Graff, Heather M. Highland, Roelof A. J. Smit, Zhe Wang, Victoria L. Buchanan +16 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

Rapid response to the alpha-1 adrenergic agent phenylephrine in the perioperative period is impacted by genomics and ancestry

The Pharmacogenomics Journal(2020)10.1038/s41397-020-00194-5

N/A

0.165DataRank · unranked

2 citations

Janina M. Jeff, Thomas T. Joseph, Muh‐Ching Yee, Gillian M. Belbin, Aniwaa Owusu Obeng +6 more

Mediation of Polygenic Asthma Risk Through Gene Expression

Allergy(2025)10.1111/all.70101

N/A

0.165DataRank · unranked

2 citations

Brooke Szczesny, Kanika Kanchan, Erika Esquinca, Meher Preethi Boorgula, Sameer Chavan +25 more

Ancestry Calibration of Polygenic Risk Scores Improves Risk Stratification and Effect Estimation in African American Adults

medRxiv(2025)10.1101/2025.06.18.25329573

N/A

0.123DataRank · unranked

1 citations

Mariah Meyer, Iain R. Konigsberg, Aastha Kakar, Patrick M. Carry, Yun Li +14 more

Physician and informal care use explained by the Pediatric Quality of Life Inventory (PedsQL) in children with suspected genetic disorders

Quality of Life Research(2024)10.1007/s11136-024-03677-1

N/A

0.104DataRank · unranked

1 citations

Nicole Kelly, Ashley Fisher, Samuel F. Hohmann, Noura S. Abul‐Husn, John M. Greally +6 more

General Kernel Machine Methods for Multi‐Omics Integration and Genome‐Wide Association Testing With Related Individuals

Genetic Epidemiology(2025)10.1002/gepi.22610

N/A

0.104DataRank · unranked

1 citations

Ni Zhao, Anna V. Mikhaylova, Angela Zhang, Wodan Ling, Florian Thibord +25 more

Polygenic risk scores lack prognostic value for adults with severe mental illness

medRxiv(2021)10.1101/2021.03.19.21253906

N/A

0.104DataRank · unranked

1 citations

Deepak Kaji, Liam Cotter, Tielman Van Vleck, Gillian M. Belbin, Michael Preuß +20 more

The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children

medRxiv(2020)10.1101/2020.09.02.20186361

N/A

0.104DataRank · unranked

1 citations

Katie M. Gallagher, Sabrina A. Suckiel, Katherine E. Donohue, Michelle A. Ramos, Nicole Kelly +41 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

Genetic identification of a common collagen disease in Puerto Ricans via identity-by-descent mapping in a health system

UNC Libraries(2020)10.17615/mv5t-7356

N/A

0DataRank · unranked

0 citations

Jacqueline A. Odgis, Peters, Ulrike, Ruth J. F. Loos, Eimear E. Kenny, Claudia Schurmann +27 more

The NYCKidSeq project: study protocol for a randomized controlled trial incorporating genomics into the clinical care of diverse New York City children

Research Square(2020)10.21203/rs.3.rs-64844/v1

N/A

0DataRank · unranked

0 citations

Katie M. Gallagher, Sabrina A. Suckiel, Katherine E. Donohue, Michelle A. Ramos, Nicole Kelly +41 more

GenomeDiver: A platform for phenotype-guided medical genomic diagnosis

medRxiv(2020)10.1101/2020.11.22.20236430

N/A

0DataRank · unranked

0 citations

Christian Stolte, Kevin Shi, Faygel Beren, Noura S. Abul‐Husn, Gabrielle Bertier +12 more

GUÍA: a digital platform to facilitate result disclosure in genetic counseling

medRxiv(2020)10.1101/2020.09.14.20194191

N/A

0DataRank · unranked

0 citations

Jaqueline A. Odgis, Katie M. Gallagher, Jessica Rodriguez, Dana Watnick, Gabrielle Bertier +27 more

Evolving knowledge of red flag clinical features associated with TTR p.(Val142Ile) in a diverse electronic health-record-linked biobank

Genetics in Medicine(2024)10.1016/j.gim.2024.101346

N/A

0DataRank · unranked

7 citations

Connor B Benson, Alexandra McClellan, Gillian M. Belbin, Eimear E. Kenny, Noura S. Abul‐Husn +1 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

MagicalRsq-X: A cross-cohort transferable genotype imputation quality metric

UNC Libraries(2025)10.17615/4609-8b83

N/A

0DataRank · unranked

0 citations

Byron C. Jaeger, Michael J. Bamshad, Alex P. Reiner, Yun Li, Jerome I. Rotter +22 more

Variant Classification Concordance using the ACMG-AMP Variant Interpretation Guidelines across Nine Genomic Implementation Research Studies

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.09.011

N/A

0DataRank · unranked

112 citations

Kathleen Muenzen, Leslie G. Biesecker, Kevin M. Bowling, Gregory M. Cooper, Michael O. Dorschner +25 more

The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic results disclosure in diverse families

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.10.016

N/A

0DataRank · unranked

6 citations

Nicole Kelly, Jacqueline A. Odgis, Katie M. Gallagher, Monisha Sebastin, Katherine E. Bonini +18 more

Employing effective recruitment and retention strategies to engage a diverse pediatric population in genomics research

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.10.015

N/A

0DataRank · unranked

4 citations

Katherine E. Bonini, Laura Scarimbolo, Nicole Kelly, Beverly J. Insel, Sabrina A. Suckiel +36 more

Evaluating parental personal utility of pediatric genetic and genomic testing in a diverse, multilingual population

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100321

N/A

0DataRank · unranked

1 citations

Sabrina A. Suckiel, Katherine E. Bonini, Nicole Kelly, Laura Scarimbolo, Beverly J. Insel +22 more

Enrichment analyses identify shared associations for 25 quantitative traits in over 600,000 individuals from seven diverse ancestries

UNC Libraries(2024)10.17615/928h-f622

N/A

0DataRank · unranked

1 citations

Christopher A. Haiman, S Ramachandran, Genevieve L. Wojcik, S. Zhang, U. Peters +10 more

MUSSEL: Enhanced Bayesian polygenic risk prediction leveraging information across multiple ancestry groups

UNC Libraries(2024)10.17615/v37q-5g16

N/A

0DataRank · unranked

1 citations

Ruzhang Zhao, Yunxuan Jiang, Jin Jin, Steven Buyske, Haoyu Zhang +12 more

Identification of copy number variants with genome sequencing: Clinical experiences from the NYCKidSeq program

Clinical Genetics(2023)10.1111/cge.14365

N/A

0DataRank · unranked

6 citations

Amanda Thomas‐Wilson, Priya N. Marathe, Monisha Sebastin, Jacqueline A. Odgis, Miranda Di Biase +24 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

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

UNC Libraries(2024)10.17615/b6xd-h115

N/A

0DataRank · unranked

0 citations

Eimear E. Kenny, Chunyu Liu, Christy L. Avery, On Behalf of the PAGE Study, Nona Sotoodehnia +35 more

Genetics of Latin American Diversity Project: Insights into population genetics and association studies in admixed groups in the Americas

Lume (Universidade Federal do Rio Grande do Sul)(2024)10.17615/anr2-h090

N/A

0DataRank · unranked

0 citations

Carla Luana Dinardo, Bing Guo, Ignácio F. Mata, Jill M. Johnsen, Robert C. Kaplan +73 more

The PRIMED Consortium: Reducing disparities in polygenic risk assessment

UNC Libraries(2024)10.17615/67cq-h633

N/A

0DataRank · unranked

0 citations

John S. Witte, Iman K. Martin, Sally N. Adebamowo, Maggie C. Y. Ng, Eimear E. Kenny +22 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

N/A

0DataRank · unranked

0 citations

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

Left ventricular strain does not differentiate amyloidogenic profiles in at-risk individuals with TTR Val142Ile

medRxiv(2021)10.1101/2021.01.26.21250565

N/A

0DataRank · unranked

1 citations

Wenli Zhao, M. Gavalas, Helen Hashemi, Steve Liao, Eman Rashed +6 more

Association of HSD17B13 and PNPLA3 With Liver Enzymes and Fibrosis in Hispanic/Latino Individuals of Diverse Genetic Ancestries

Clinical Gastroenterology and Hepatology(2023)10.1016/j.cgh.2022.12.025

N/A

0DataRank · unranked

20 citations

Emily R. Soper, Ning Ma, Vikas Pejaver, Scott L. Friedman, Andrea D. Branch +4 more

When families bridge the research-clinical divide: An exploration of values regarding cascade screening in genomic research

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103440

N/A

0DataRank · unranked

1 citations

Lauren Desrosiers, Ann Katherine M. Foreman, Nuriye Sahin‐Hodoglugil, Mary A. Majumder, Candice R. Finnila +9 more

Patient and providers’ perspectives on using the GUÍA digital tool to enhance genomic results disclosure

Genetics in Medicine Open(2025)10.1016/j.gimo.2025.103451

N/A

0DataRank · unranked

1 citations

Sabrina A. Suckiel, Laura Golfinopoulos, Nicole R. Kelly, Katherine E. Bonini, Priya N. Marathe +15 more

Diverse and unselected adults with clinically relevant ACADS variants lack evidence of metabolic disease

Molecular Genetics and Metabolism(2022)10.1016/j.ymgme.2022.106971

N/A

0DataRank · unranked

8 citations

Eimear E. Kenny, Noura S. Abul‐Husn, Margo Sheck Breilyn

Detection of mosaic variants using genome sequencing in a large pediatric cohort

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.63062

N/A

0DataRank · unranked

14 citations

Katie M. Gallagher, Atteeq U. Rehman, Priya Marathe, Katherine E. Bonini, Monisha Sebastin +21 more

Large-scale admixture mapping in the All of Us Research Program improves the characterization of cross-population phenotypic differences

medRxiv(2025)10.1101/2025.04.02.25325115

N/A

0DataRank · unranked

2 citations

Zhuozheng Shi, Kangcheng Hou, Ying Wang, Georgia Mies, Alan J. Aw +7 more

SPC: a SPectral Component approach leveraging Identity-by-Descent graphs to address recent population structure in genomic analysis

medRxiv(2025)10.1101/2025.06.04.25328990

N/A

0DataRank · unranked

2 citations

Gillian M. Belbin, Sinéad Cullina, Christa Caggiano, Christopher R. Gignoux, Noah Zaitlen +2 more

Prediction and Characterization of Genetically Regulated Expression of Target Tissues in Asthma

medRxiv(2025)10.1101/2025.02.06.25321273

N/A

0DataRank · unranked

0 citations

Erika Esquinca, Christopher H. Arehart, Meher P. Boorgula, Brooke Szczesny, Alex Romero +22 more

Prediction and characterization of genetically regulated expression of asthma tissues from African-ancestry populations

Journal of Allergy and Clinical Immunology(2025)10.1016/j.jaci.2025.07.035

N/A

0DataRank · unranked

0 citations

Erika Esquinca, Christopher H. Arehart, Meher P. Boorgula, Brooke Szczesny, Alex Romero +22 more

A Scalable Framework to Integrate Social Determinants of Health into Disease Risk Models using Biobank Survey Data

medRxiv(2025)10.1101/2025.09.29.25336903

N/A

0DataRank · unranked

0 citations

Abhijith Biji, Kathleen D.M. Ferar, Vikas Pejaver, Eimear E. Kenny, Bian Liu +2 more

Rapid detection of identity-by-descent tracts for mega-scale datasets

Nature Communications(2021)10.1038/s41467-021-22910-w

N/A

0DataRank · unranked

56 citations

Gillian M. Belbin, Christy L. Avery, Eimear E. Kenny, Christopher R. Gignoux, José Luis Ambite +1 more

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

UNC Libraries(2025)10.17615/5tss-f273

N/A

0DataRank · unranked

0 citations

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

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

Admixture Mapping of Peripheral Artery Disease in a Dominican Population Reveals a Novel Risk Locus on 2q35

medRxiv(2023)10.1101/2023.03.27.23287788

N/A

0DataRank · unranked

0 citations

Genevieve L. Wojcik, Ruhollah Shemirani, Derek Klarin, Bryan R. Gorman, Elena P. Sorokin +9 more

The NYCKidSeq randomized controlled trial: Impact of GUÍA digitally enhanced genetic counseling in racially and ethnically diverse families

medRxiv(2023)10.1101/2023.07.05.23292193

N/A

0DataRank · unranked

0 citations

Nicole Kelly, Jacqueline A. Odgis, Katie M. Gallagher, Monisha Sebastin, Katherine E. Bonini +18 more

Physician services and costs after disclosure of diagnostic sequencing results in the NYCKidSeq program

Genetics in Medicine(2023)10.1016/j.gim.2023.101011

N/A

0DataRank · unranked

0 citations

Nicole Kelly, Ashley Fisher, Samuel F. Hohmann, Monisha Sebastin, Miranda Di Biase +14 more

A continuum of admixture in the Western Hemisphere revealed by the African Diaspora genome

UNC Libraries(2020)10.17615/svad-an83

N/A

0DataRank · unranked

0 citations

Albert M. Levin, James Graham Wilson, Tina V. Hartert, Christopher O. Olopade, H. Richard Johnston +57 more

Genetic architecture of lipid traits in the Hispanic community health study/study of Latinos

UNC Libraries(2020)10.17615/27xb-g366

N/A

0DataRank · unranked

0 citations

Jill M. Norris, Yun Li, Cathy C. Laurie, Rodriguez, Carlos Jose, Emery, Leslie S. +24 more

Eimear E. Kenny

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