Matthew P. Conomos

Biochemistry, 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 1%percentile

10.4Author DataRank

Indexed papers

4in 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 4 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y

Top 3%

7.0DataRank

Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 more

Papers

Driven by 49 papers — median percentile 81. Top paper: “Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program”.

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

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

Beyond the exome: What’s next in diagnostic testing for Mendelian conditions

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.06.009

N/A

2.2DataRank · unranked

123 citations

Chloe Reuter, Shruti Marwaha, Medhat Mahmoud, Michael Duyzend, Hayk Barseghyan +91 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

Genome sequencing unveils a regulatory landscape of platelet reactivity

Nature Communications(2021)10.1038/s41467-021-23470-9

N/A

1.5DataRank · unranked

54 citations

Ming‐Huei Chen, Benjamin A.T. Rodriguez, Lisa R. Yanek, Arunoday Bhan, Brady Gaynor +94 more

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

Variant-specific inflation factors for assessing population stratification at the phenotypic variance level

Nature Communications(2021)10.1038/s41467-021-23655-2

N/A

0.840DataRank · unranked

21 citations

Xiuwen Zheng, Cecelia Laurie, Stephanie M. Gogarten, Jennifer A. Brody, Matthew P. Conomos +91 more

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

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

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

Systemic Markers of Lung Function and Forced Expiratory Volume in 1 Second Decline across Diverse Cohorts

Annals of the American Thoracic Society(2023)10.1513/annalsats.202210-857oc

N/A

0.556DataRank · unranked

13 citations

Katherine Pratte, Claudia Flexeder, Hans Petersen, Hong Dang, Yanlin Ma +49 more

Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program

Circulation Genomic and Precision Medicine(2023)10.1161/circgen.121.003532

Top 38%

0.507DataRank

Top 38%11 citations

Cecelia Laurie, Brandon J. Coombes, Deepti Jain, Matthew P. Conomos, Jennifer A. Brody +30 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

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

Genetics(2021)10.1093/genetics/iyab044

N/A

0.489DataRank · unranked

25 citations

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

Elucidating mechanisms of genetic cross-disease associations at the PROCR vascular disease locus

Nature Communications(2022)10.1038/s41467-022-28729-3

N/A

0.470DataRank · unranked

22 citations

Lingyan Chen, Paulina J. Stanczyk, Joanna M. M. Howson, Amy M. Mason, Stephen Burgess +91 more

Building a collaborative cloud platform to accelerate heart, lung, blood, and sleep research

Journal of the American Medical Informatics Association(2023)10.1093/jamia/ocad048

N/A

0.442DataRank · unranked

18 citations

Paul Avillach, Rebecca Boyles, Kira Bradford, Steven J. Cox, Brandi N. Davis‐Dusenbery +53 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

A multitrait genetic study of hemostatic factors and hemorrhagic transformation after stroke treatment

Journal of Thrombosis and Haemostasis(2023)10.1016/j.jtha.2023.11.027

N/A

0.330DataRank · unranked

8 citations

Gerard Temprano‐Sagrera, Jara Cárcel‐Márquez, Elena Muiño, Natàlia Cullell, Miquel Lledós +91 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

Data sharing in the PRIMED Consortium: Design, implementation, and recommendations for future policymaking

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.06.004

N/A

0.301DataRank · unranked

5 citations

Quenna Wong, Whitney Hornsby, Matthew P. Conomos, Iftikhar J. Kullo, Bruce M Psaty +28 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

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

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

N/A

0.269DataRank · unranked

5 citations

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

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

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

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

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

GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals

UNC Libraries(2020)10.17615/xn2n-7j45

N/A

0DataRank · unranked

0 citations

Tamar Sofer, Henry J. Lin, Matthew P. Conomos, Nona Sotoodehnia, Eric A. Whitsel +20 more

Population Stratification at the Phenotypic Variance level and Implication for the Analysis of Whole Genome Sequencing Data from Multiple Studies

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.03.03.973420

N/A

0DataRank · unranked

4 citations

Xiuwen Zheng, Cecelia Laurie, Stephanie M. Gogarten, Jennifer A. Brody, Matthew P. Conomos +10 more

Epigenome-wide DNA methylation association study of circulating IgE levels identifies novel targets for asthma

EBioMedicine(2023)10.1016/j.ebiom.2023.104758

N/A

0DataRank · unranked

19 citations

Priyadarshini Kachroo, Tianxiao Huan, David Van Den Berg, Gha Young Lee, Helena Bui +95 more

Genetic Effect on Body Mass Index and Cardiovascular Disease Across Generations

Circulation Genomic and Precision Medicine(2023)10.1161/circgen.122.003858

N/A

0DataRank · unranked

5 citations

Matthew P. Conomos, Ramachandran S. Vasan, James B. Meigs, Josée Dupuis, Ching‐Ti Liu +2 more

Untargeted longitudinal analysis of a wellness cohort identifies markers of metastatic cancer years prior to diagnosis

Scientific Reports(2020)10.1038/s41598-020-73451-z

N/A

0DataRank · unranked

19 citations

Noa Rappaport, Matthew P. Conomos, Gilbert S. Omenn, Jennifer C. Lovejoy, Leroy Hood +2 more

Admix-kit: an integrated toolkit and pipeline for genetic analyses of admixed populations

Bioinformatics(2024)10.1093/bioinformatics/btae148

N/A

0DataRank · unranked

16 citations

Stephanie M. Gogarten, Joohyun Kim, Xing Hua, Julie‐Alexia Dias, Quan Sun +89 more

The power of representation: Statistical analysis of diversity in US Alzheimer's disease genetics data

Alzheimer s & Dementia Translational Research & Clinical Interventions(2024)10.1002/trc2.12462

N/A

0DataRank · unranked

11 citations

Elizabeth Blue, Matthew P. Conomos, Alison E. Fohner, Diane Xue

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

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

A data model for population descriptors in genomic research

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.05.011

N/A

0DataRank · unranked

1 citations

Clement Adebamowo, Stephanie M. Fullerton, Jibril Hirbo, Iain R. Konigsberg, Peter Kraft +20 more

Heterogeneity in statin responses explained by variation in the human gut microbiome

medRxiv(2021)10.1101/2021.12.02.21267193

N/A

0DataRank · unranked

10 citations

Sergey A. Kornilov, Christian Diener, Matthew P. Conomos, Jennifer C. Lovejoy, Paola Sebastiani +7 more

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

UNC Libraries(2025)10.17615/mztm-gw84

N/A

0DataRank · unranked

0 citations

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

Protein prediction for trait mapping in diverse populations

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.08.11.455912

N/A

0DataRank · unranked

3 citations

Elyse Geoffroy, Isabelle Gregga, Ashley J. Mulford, François Aguet, Kristin G. Ardlie +27 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

DUOX2 variants associate with preclinical disturbances in microbiota-immune homeostasis and increased inflammatory bowel disease risk

Journal of Clinical Investigation(2021)10.1172/jci141676

N/A

0DataRank · unranked

83 citations

Andrew T. Magis, Elisa Sheng, Matthew P. Conomos, Min Zhang, Lea S. Garzotto +15 more

Genome-wide Association Study of Platelet Count Identifies Ancestry-Specific Loci in Hispanic/Latino Americans

UNC Libraries(2020)10.17615/t61g-n927

N/A

0DataRank · unranked

0 citations

Sarah C. Nelson, Adrienne M. Stilp, Robert L. Hanson, Chani J. Hodonsky, Anna Plantinga +33 more

Heterogeneity in statin responses explained by variation in the human gut microbiome

Med(2022)10.1016/j.medj.2022.04.007

N/A

0DataRank · unranked

68 citations

Sergey A. Kornilov, Christian Diener, Matthew P. Conomos, Jennifer C. Lovejoy, Paola Sebastiani +7 more

Protein prediction for trait mapping in diverse populations

PLoS ONE(2022)10.1371/journal.pone.0264341

N/A

0DataRank · unranked

30 citations

Elyse Geoffroy, Isabelle Gregga, Ashley Mulford, François Aguet, Kristin G. Ardlie +26 more

Genome-wide association study of dental caries in the Hispanic Communities Health Study/Study of Latinos (HCHS/SOL)

UNC Libraries(2020)10.17615/7r1k-hn33

N/A

0DataRank · unranked

0 citations

Matthew P. Conomos, Timothy A. Thornton, Jean Morrison, Steven Offenbacher, George Papanicolaou +11 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

0DataRank · unranked

18 citations

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

Lymphocyte activation gene-3-associated protein networks are associated with HDL-cholesterol and mortality in the Trans-omics for Precision Medicine program

Communications Biology(2022)10.1038/s42003-022-03304-0

N/A

0DataRank · unranked

9 citations

Honghuang Lin, Chansuk Kang, Chaojie Yang, Stephen S. Rich, Kent D. Taylor +17 more

Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos

UNC Libraries(2020)10.17615/t83e-sv82

N/A

0DataRank · unranked

0 citations

B. S. Weir, Sylvia Wassertheil‐Smoller, Anne E. Justice, Mariaelisa Graff, Martha L. Daviglus +32 more

Matthew P. Conomos

Indexed papers

Top data-sharing exemplar

Papers