Rasika A. Mathias

National Institute of Allergy and Infectious Diseases

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

32.2Author 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 116 papers — median percentile 69. Top paper: “A global reference for human genetic variation”.

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 map of human genome variation from population-scale sequencing

Nature(2010)10.1038/nature09534

Top 2%

9.1DataRank

Top 2%8109 citations

Min Hu, Yuan Chen, Matthew N. Bainbridge, Richard M. Durbin, Si Quang Le +319 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

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

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

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

Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease

Nature Communications(2020)10.1038/s41467-020-20086-3

N/A

1.6DataRank · unranked

91 citations

Oren Rom, Ida Surakka, Sarah E. Graham, Wei Zhou, Tanmoy Roychowdhury +95 more

Whole genome sequence analysis of blood lipid levels in >66,000 individuals

Nature Communications(2022)10.1038/s41467-022-33510-7

N/A

1.6DataRank · unranked

75 citations

Xihao Li, Zilin Li, Akhil Pampana, David Zhang, Joseph Park +95 more

Prospective clinical trial examining the impact of genetic variation in FADS1 on the metabolism of linoleic acid– and ɣ-linolenic acid–containing botanical oils

American Journal of Clinical Nutrition(2020)10.1093/ajcn/nqaa023

N/A

1.4DataRank · unranked

25 citations

Brian Hallmark, Rasika A. Mathias, Tammy L Mustin, Priscilla Ivester, Maggie L Bohannon +5 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

Association of HLA-DRB1∗09:01 with tIgE levels among African-ancestry individuals with asthma

Journal of Allergy and Clinical Immunology(2020)10.1016/j.jaci.2020.01.011

N/A

0.853DataRank · unranked

21 citations

Sophie Limou, Michelle Daya, Wataru Morii, Nicholas Rafaels, Estelle Geffard +26 more

Genome-wide ancestry association testing identifies a common European variant on 6q14.1 as a risk factor for asthma in African American subjects

Journal of Allergy and Clinical Immunology(2012)10.1016/j.jaci.2012.03.045

N/A

0.849DataRank · unranked

29 citations

Daniel Capurso, Elizabeth J. Ampleford, Xingnan Li, Wendy C. Moore, Christopher R. Gignoux +25 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

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

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

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

The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations

Frontiers in Endocrinology(2022)10.3389/fendo.2022.863893

N/A

0.642DataRank · unranked

21 citations

Shing Wan Choi, Nathalie Chami, Eric Boerwinkle, Myriam Fornage, Susan Redline +36 more

Analytical challenges in omics research on asthma and allergy: A National Institute of Allergy and Infectious Diseases workshop

Journal of Allergy and Clinical Immunology(2024)10.1016/j.jaci.2024.01.014

N/A

0.637DataRank · unranked

20 citations

Patrice M. Becker, Matthew C. Altman, Jessica Lasky‐Su, Carole Ober, Karsten Zengler +25 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

FADS genetic and metabolomic analyses identify the ∆5 desaturase (FADS1) step as a critical control point in the formation of biologically important lipids

Scientific Reports(2020)10.1038/s41598-020-71948-1

N/A

0.612DataRank · unranked

58 citations

Rahul Dutta, Michael C. Seeds, Kirsten N. Lake, Brian Hallmark, Rasika A. Mathias +3 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

Building a vertically integrated genomic learning health system: The biobank at the Colorado Center for Personalized Medicine

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2023.12.001

N/A

0.571DataRank · unranked

44 citations

Jonathan A. Shortt, Emily R. Roberts, Joe A. Lesny, Elizabeth Kudron, Meng Lin +49 more

Gene and protein expression in human megakaryocytes derived from induced pluripotent stem cells

Journal of Thrombosis and Haemostasis(2021)10.1111/jth.15334

Top 35%

0.552DataRank

Top 35%11 citations

Margaret A. Taub, Rasika A. Mathias, Lisa R. Yanek, Kanika Kanchan, Vidya Venkatraman +16 more

Late‐life plasma proteins associated with prevalent and incident frailty: A proteomic analysis

Aging Cell(2023)10.1111/acel.13975

N/A

0.546DataRank · unranked

37 citations

Thomas R. Austin, Jennifer A. Schrack, Jingsha Chen, Jeremy Walston, Rasika A. Mathias +10 more

Incorporating genetics in identifying peanut allergy risk and tailoring allergen immunotherapy: A perspective on the genetic findings from the LEAP trial

Journal of Allergy and Clinical Immunology(2023)10.1016/j.jaci.2022.12.819

N/A

0.532DataRank · unranked

11 citations

Kanika Kanchan, Henry T. Bahnson, Carolyn Baloh, Gideon Lack, Gerald T. Nepom +2 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

Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

PLoS ONE(2020)10.1371/journal.pone.0230035

N/A

0.513DataRank · unranked

8 citations

Yi-Ping Fu, Michael R. Brown, Joshua C. Bis, Paul S. de Vries, Mary F. Feitosa +40 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

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

Investigating Gene–Diet Interactions Impacting the Association Between Macronutrient Intake and Glycemic Traits

Diabetes(2023)10.2337/db22-0851

N/A

0.425DataRank · unranked

16 citations

Maura E. Walker, Sheila M. Gaynor, Jennifer Wessel, Daniel DiCorpo, Jiantao Ma +66 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

Epigenetic and proteomic signatures associate with clonal hematopoiesis expansion rate

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

N/A

0.406DataRank · unranked

14 citations

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

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

Science Advances(2023)10.1126/sciadv.abm4945

N/A

0.396DataRank · unranked

13 citations

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

A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies

Nature Computational Science(2025)10.1038/s43588-024-00764-8

N/A

0.393DataRank · unranked

10 citations

Han Chen, Margaret Sunitha Selvaraj, Eric Van Buren, Hufeng Zhou, Yuxuan Wang +95 more

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

Rare coding variants in RCN3 are associated with blood pressure

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

N/A

0.360DataRank · unranked

10 citations

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

Clonal hematopoiesis is driven by aberrant activation of TCL1A

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

N/A

0.360DataRank · unranked

10 citations

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

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

Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-specific effects via GAUDI

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.10.06.511219

N/A

0.345DataRank · unranked

9 citations

Bryce Rowland, Jiawen Chen, Anna V. Mikhaylova, Christy L. Avery, Ulrike Peters +13 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

Structural variation across 138,134 samples in the TOPMed consortium

Research Square(2023)10.21203/rs.3.rs-2515453/v1

N/A

0.345DataRank · unranked

9 citations

Adam C. English, Ginger Metcalf, Jianzhi Yang, Mark J. P. Chaisson, Nathan Pankratz +82 more

Building a Vertically-Integrated Genomic Learning Health System: The Colorado Center for Personalized Medicine Biobank

medRxiv(2022)10.1101/2022.06.09.22276222

N/A

0.330DataRank · unranked

8 citations

Jonathan A. Shortt, Emily R. Roberts, Joe A. Lesny, Elizabeth Kudron, Meng Lin +50 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

FGL1 as a modulator of plasma D‐dimer levels: Exome‐wide marker analysis of plasma tPA, PAI‐1, and D‐dimer

Journal of Thrombosis and Haemostasis(2021)10.1111/jth.15345

N/A

0.292DataRank · unranked

6 citations

Ci Song, Jack Pattee, Benjamin A.T. Rodriguez, Ming‐Huei Chen, Christopher J. O’Donnell +45 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

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

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

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

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

Investigating gene-diet interactions impacting the association between macronutrient intake and glycemic traits

medRxiv(2022)10.1101/2022.07.26.22278077

N/A

0.182DataRank · unranked

1 citations

Maura E. Walker, Sheila M. Gaynor, Jennifer Wessel, Daniel DiCorpo, Jiantao Ma +66 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

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

EndoPRS: Incorporating endophenotype information to improve polygenic risk scores for clinical endpoints—A study in asthma

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.03.008

N/A

0.165DataRank · unranked

2 citations

Quan Sun, Franklin P Ockerman, Brian Chen, Laura Y. Zhou, Micah R. Hysong +12 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

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

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

Omics-oriented research illustrated with the LEAP study and the OASIS bioinformatics tool

Journal of Allergy and Clinical Immunology(2022)10.1016/j.jaci.2022.12.003

N/A

0.104DataRank · unranked

1 citations

Kanika Kanchan, Gautam Shankar, Gerald T. Nepom, Rasika A. Mathias, James A. Perry +1 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

Whole genome sequence association analysis of brain structural volume measures in the NHLBI TOPMed Program highlights novel loci in diverse participants

10.1101/2025.06.11.25329426

N/A

0DataRank · unranked

0 citations

Mohsen Sharifitabar, Alexa Beiser, Claudia L. Satizábal, Thomas H. Mosley, Joanne E. Curran +34 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

Advancing Food Allergy Through Omics Sciences

The Journal of Allergy and Clinical Immunology In Practice(2020)10.1016/j.jaip.2020.07.044

N/A

0DataRank · unranked

20 citations

Kanika Kanchan, Rasika A. Mathias, Supinda Bunyavanich, Haritz Irizar

Large-Scale Genome-Wide Association Studies and Meta-Analyses of Longitudinal Change in Adult Lung Function

UNC Libraries(2020)10.17615/6mem-qn63

N/A

0DataRank · unranked

3 citations

Matthew Kowgier, Tamara B. Harris, Wei Gao, Xiangjun Gu, Rasika A. Mathias +27 more

Genetic loci associated with prevalent and incident myocardial infarction and coronary heart disease in the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.21.959312

N/A

0DataRank · unranked

0 citations

Yi‐Ping Fu, Michael R. Brown, Joshua C. Bis, Paul S. de Vries, Mary F. Feitosa +40 more

find-tfbs: a tool to identify functional non-coding variants associated with complex human traits using open chromatin maps and phased whole-genome sequences

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.23.394296

N/A

0DataRank · unranked

0 citations

Florian Thibord, Paul L. Auer, John Blangero, Zeynep Coban‐Akdemir, James S. Floyd +11 more

Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals

UNC Libraries(2020)10.17615/a384-d483

N/A

0DataRank · unranked

0 citations

Jerome I. Rotter, Alex P. Reiner, André G. Uitterlinden, Gonçalo R. Abecasis, Digna R. Velez Edwards +95 more

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

UNC Libraries(2020)10.17615/m864-xv86

N/A

0DataRank · unranked

0 citations

Lisa R. Yanek, Kjell Nikus, Salman M. Tajuddin, Jussi Hernesniemi, Dawn Waterworth +95 more

Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases

UNC Libraries(2020)10.17615/s8sd-h432

Top 100%

0DataRank

Top 100%0 citations

Todd L. Edwards, Jin Li, John M. Starr, Eric Boerwinkle, Yingchang Lu +92 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

Genome-Wide Association Study of White Blood Cell Count in 16,388 African Americans: the Continental Origins and Genetic Epidemiology Network (COGENT)

UNC Libraries(2020)10.17615/wn5h-av49

N/A

0DataRank · unranked

0 citations

David Couper, Struan F.A. Grant, Tamara B. Harris, Santhi K. Ganesh, Sampath Arepalli +27 more

Current insights into the genetics of food allergy

Journal of Allergy and Clinical Immunology(2021)10.1016/j.jaci.2020.10.039

N/A

0DataRank · unranked

77 citations

Selene M. Clay, Haritz Irizar, Supinda Bunyavanich, Rasika A. Mathias, Kanika Kanchan

Genome-wide association study of asthma, total IgE, and lung function in a cohort of Peruvian children

Journal of Allergy and Clinical Immunology(2021)10.1016/j.jaci.2021.02.035

N/A

0DataRank · unranked

34 citations

Tonya M. Brunetti, Karina Romero, Michelle Daya, Kanika Kanchan, Gautam Shankar +20 more

Polygenic prediction of atopic dermatitis improves with atopic training and filaggrin factors

Journal of Allergy and Clinical Immunology(2021)10.1016/j.jaci.2021.05.034

N/A

0DataRank · unranked

30 citations

Michelle Daya, Monica Campbell, Meher Preethi Boorgula, Nicholas Rafaels, Sameer Chavan +16 more

Discovering metabolite quantitative trait loci in asthma using an isolated population

Journal of Allergy and Clinical Immunology(2021)10.1016/j.jaci.2021.11.002

N/A

0DataRank · unranked

19 citations

Tonya M. Brunetti, Kevin Quinn, Katrina Doenges, Monica Campbell, Christopher H. Arehart +6 more

Secondary Analyses for Genome-wide Association Studies using Expression Quantitative Trait Loci

medRxiv(2021)10.1101/2021.07.20.21260862

N/A

0DataRank · unranked

1 citations

Lisa R. Yanek, Kai Kammers, Kanika Kanchan, Margaret A. Taub, Robert B. Scharpf +5 more

Correction: Identification, Replication, and Fine-Mapping of Loci Associated with Adult Height in Individuals of African Ancestry

UNC Libraries(2021)10.17615/nnk8-vz92

N/A

0DataRank · unranked

0 citations

Angela Britton, Jennifer J. Hu, Christine B. Ambrosone, Larry D. Atwood, Ellen W. Demerath +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

MUC5B, telomere length and longitudinal quantitative interstitial lung changes: the MESA Lung Study

Thorax(2022)10.1136/thorax-2021-218139

N/A

0DataRank · unranked

20 citations

Ani Manichaikul, Eric A. Hoffman, Pallavi Balte, Michaela R. Anderson, Elana J. Bernstein +16 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

Lipid mediators are detectable in the nasal epithelium and differ by asthma status in female subjects

Journal of Allergy and Clinical Immunology(2022)10.1016/j.jaci.2022.02.026

N/A

0DataRank · unranked

17 citations

Jonathan Manke, Monica Campbell, Michael Armstrong, Meher Preethi Boorgula, Gabriela Pimentel Pinheiro +7 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

0DataRank · unranked

11 citations

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

HLA-associated outcomes in peanut oral immunotherapy trials identify mechanistic and clinical determinants of therapeutic success

Frontiers in Immunology(2022)10.3389/fimmu.2022.941839

N/A

0DataRank · unranked

6 citations

Gautam Shankar, Michelle F. Huffaker, Henry T. Bahnson, R. Sharon Chinthrajah, Srinath Sanda +12 more

Telomere shortening and the transition to family caregiving in the Reasons for Geographic and Racial Differences in Stroke (REGARDS) study

PLoS ONE(2022)10.1371/journal.pone.0268689

N/A

0DataRank · unranked

4 citations

Marguerite R. Irvin, William E. Haley, Marcela D. Blinka, Debora Kamin Mukaz, Amit Patki +7 more

A Functional Genomics Pipeline to Identify High-Value Asthma and Allergy CpGs in the Human Methylome

medRxiv(2022)10.1101/2022.05.19.22275204

N/A

0DataRank · unranked

2 citations

Emma E. Thompson, Britney A. Helling, Lyndsey E. Shorey‐Kendrick, Pieter Faber, Tebeb Gebretsadik +17 more

Age at Menopause, Leukocyte Telomere Length, and Coronary Artery Disease in Postmenopausal Women

Circulation Research(2023)10.1161/circresaha.123.322984

N/A

0DataRank · unranked

36 citations

Tetsushi Nakao, Md Mesbah Uddin, Whitney Hornsby, Shriienidhie Ganesh, Aladdin H. Shadyab +12 more

A functional genomics pipeline to identify high-value asthma and allergy CpGs in the human methylome

Journal of Allergy and Clinical Immunology(2023)10.1016/j.jaci.2022.12.828

N/A

0DataRank · unranked

30 citations

Emma E. Thompson, Britney A. Helling, Lyndsey E. Shorey‐Kendrick, Pieter Faber, Tebeb Gebretsadik +17 more

Recent progress in the genetic and epigenetic underpinnings of atopy

Journal of Allergy and Clinical Immunology(2023)10.1016/j.jaci.2022.10.027

N/A

0DataRank · unranked

31 citations

Rasika A. Mathias, Carolyn Baloh

The IL-4Rα Q576R polymorphism is associated with increased severity of atopic dermatitis and exaggerates allergic skin inflammation in mice

Journal of Allergy and Clinical Immunology(2023)10.1016/j.jaci.2023.01.011

N/A

0DataRank · unranked

21 citations

Hazel Wilkie, Mrinmoy Das, Maheshwor Timilshina, Wayne Bainter, Brian Woods +17 more

Evaluating genomic signatures of aging in brain tissue as it relates to Alzheimer’s disease

Scientific Reports(2023)10.1038/s41598-023-41400-1

N/A

0DataRank · unranked

9 citations

Margaret A. Taub, José M. Farfel, Jingyun Yang, Peter Abadir, Philip L. De Jager +4 more

Dietary Sources of Linoleic Acid (LA) Differ by Race/Ethnicity in Adults Participating in the National Health and Nutrition Examination Survey (NHANES) between 2017–2018

Nutrients(2023)10.3390/nu15122779

N/A

0DataRank · unranked

5 citations

Mackenzie K. Senn, Ani Manichaikul, Chaojie Yang, Rasika A. Mathias, Mimi Phan +7 more

Decreased fucosylation impacts epithelial integrity and increases risk for COPD

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.31.564805

N/A

0DataRank · unranked

3 citations

Bonnie Yeung‐Luk, Shreeti Thapa, Kristine Nishida, Arabelis Wally, Baishakhi Ghosh +17 more

The importance of studying genetic ancestry in eosinophilic esophagitis

Journal of Allergy and Clinical Immunology(2023)10.1016/j.jaci.2023.03.010

N/A

0DataRank · unranked

0 citations

Rasika A. Mathias, Christopher R. Gignoux, Katie M. Marker

Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI

Nature Communications(2024)10.1038/s41467-024-45135-z

N/A

0DataRank · unranked

56 citations

Bryce Rowland, Jiawen Chen, Anna V. Mikhaylova, Christy L. Avery, Ulrike Peters +13 more

Multi-omics in nasal epithelium reveals three axes of dysregulation for asthma risk in the African Diaspora populations

Nature Communications(2024)10.1038/s41467-024-48507-7

N/A

0DataRank · unranked

13 citations

Meher Preethi Boorgula, Sameer Chavan, Monica Campbell, Randi K. Johnson, Kai Kammers +32 more

EndoPRS: Incorporating Endophenotype Information to Improve Polygenic Risk Scores for Clinical Endpoints

medRxiv(2024)10.1101/2024.05.23.24307839

N/A

0DataRank · unranked

1 citations

Quan Sun, Frank Ockerman, Brian Chen, Laura Y. Zhou, Hongyuan Cao +10 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

Top 100%

0DataRank

Top 100%0 citations

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

Determinants of mosaic chromosomal alteration fitness

UNC Libraries(2024)10.17615/yx5k-ka41

N/A

0DataRank · unranked

0 citations

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

A rapid accurate approach to inferring pedigrees in endogamous populations

Genetics(2025)10.1093/genetics/iyaf094

N/A

0DataRank · unranked

5 citations

Brooke A. Scelza, Sarah D. Slack, Neus Font‐Porterias, Dana R. Al-Hindi, Rasika A. Mathias +8 more

Cardiovascular-Derived Circulating Cell-Free DNA Fragments Are Associated With Frailty and Increased Cardiovascular Events in Older Adults

The Journals of Gerontology Series A(2025)10.1093/gerona/glaf081

N/A

0DataRank · unranked

3 citations

David W. Sosnowski, Nikita Sivakumar, Alessandra Merino Gomez, Yuqiong Wu, Thomas Laskow +15 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

N/A

0DataRank · unranked

4 citations

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

Mediation of Polygenic Asthma Risk Through Gene Expression

Allergy(2025)10.1111/all.70101

N/A

0DataRank · unranked

1 citations

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

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

Multi-omics in nasal epithelium reveals three axes of dysregulation for asthma risk in the African Diaspora populations

UNC Libraries(2025)10.17615/wd1x-xm13

N/A

0DataRank · unranked

0 citations

Matthew C. Altman, Michelle Daya, Madison S. Cox, Corey Cox, Terri H. Beaty +32 more

Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI

UNC Libraries(2025)10.17615/nrrg-ws98

N/A

0DataRank · unranked

0 citations

Laura M. Raffield, Christy L. Avery, Quan Sun, Anna V. Mikhaylova, Tara C. Matise +13 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

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

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

Rasika A. Mathias

Indexed papers

Top data-sharing exemplar

Papers