Aravinda Chakravarti

Also affiliated with New York University

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

29.2Author DataRank

Indexed papers

6in 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 6 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 47 papers — median percentile 87. 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

Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study

Annals of the Rheumatic Diseases(2011)10.1136/ard.2010.141473

N/A

2.9DataRank · unranked

121 citations

K S Elliott, N. Wrayner, G Zhai, C. Beazley, G. Thorleifsson +108 more

52 Genetic Loci Influencing Myocardial Mass

Journal of the American College of Cardiology(2016)10.1016/j.jacc.2016.07.729

N/A

2.4DataRank · unranked

135 citations

Jessica van Setten, Niek Verweij, Georg Vogler, Matthew T. Maurano, Xinchen Wang +172 more

Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p

Nature Genetics(2022)10.1038/s41588-022-01203-y

N/A

1.3DataRank · unranked

55 citations

Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove +94 more

Defining the role of common variation in the genomic and biological architecture of adult human height

Nature Genetics(2014)10.1038/ng.3097

N/A

1.1DataRank · unranked

2093 citations

Emilio Rodríguez-Ruiz, The PAGE Consortium, Diana O. Perkins, Tonu Esko, Jian Yang +479 more

Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies

Nature Genetics(2009)10.1038/ng.446

N/A

0.984DataRank · unranked

703 citations

Fernando Rivadeneira, Unnur Styrkársdóttir, Karol Estrada, Bjarni V. Halldórsson, J. Brent Richards +33 more

The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities

The American Journal of Human Genetics(2015)10.1016/j.ajhg.2015.06.009

N/A

0.980DataRank · unranked

687 citations

Kati J. Buckingham, Shalini N. Jhangiani, Corinne Boehm, Nara Sobreira, Joshua D. Smith +46 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

Twenty loci associated with bone mineral density identified by large-scale meta-analysis of genome-wide association datasets

Bone(2009)10.1016/j.bone.2009.03.085

N/A

0.535DataRank · unranked

9 citations

Unnur Styrkarsdottir, Bjarni V. Halldorsson, Y. Hsu, Audrey Y. Chu, Y.A. Aulchenko +51 more

Pangenome discovery of missing autism variants

medRxiv(2025)10.1101/2025.07.21.25331932

Top 63%

0.216DataRank

Top 63%3 citations

Jiadong Lin, Michelle D. Noyes, Young-Jun Kwon, Isaac Wong, Nidhi Koundinya +23 more

83 ANALYSIS OF CANDIDATE OSTEOARTHRITIS GENES IN A META-ANALYSIS OF 8 GENOME-WIDE ASSOCIATION STUDIES

Osteoarthritis and Cartilage(2011)10.1016/s1063-4584(11)60110-6

N/A

0.210DataRank · unranked

3 citations

Members of the Rheumatoid Arthritis Challenge Consortium, N.K. Arden, Aravinda Chakravarti, Katharina Domschke, Juan J. Gomez‐Reino Carnota +39 more

356 COMMON VARIANTS IN SKELETAL DYSPLASIA GENES ARE ASSOCIATED WITH OSTEOARTHRITIS

Osteoarthritis and Cartilage(2011)10.1016/s1063-4584(11)60383-x

N/A

0.210DataRank · unranked

3 citations

M. Irving, Katharina Domschke, Unnur Styrkarsdottir, Y. Zhu, Aravinda Chakravarti +34 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

Sequence-based correction of barcode bias in massively parallel reporter assays

Genome Research(2021)10.1101/gr.268599.120

N/A

0DataRank · unranked

7 citations

Ashish Kapoor, Changhee Lee, Michael Mudgett, Michael A. Beer, Aravinda Chakravarti +1 more

Interferon pathway lupus risk alleles modulate risk of death from acute COVID-19

medRxiv(2021)10.1101/2021.11.01.21265766

N/A

0DataRank · unranked

6 citations

Ruth Fernandez‐Ruiz, Theresa Wampler Muskardin, Jacqueline L Paredes, Ashira Blazer, Stephanie Tuminello +7 more

Ret loss-of-function decreases neural crest progenitor proliferation and restricts developmental fate potential during enteric nervous system development

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.12.28.474390

N/A

0DataRank · unranked

3 citations

Sumantra Chatterjee, Gabrielle H. Cannon, Dallas R. Auer, Holly Ross, Aravinda Chakravarti +2 more

Sequence-based correction of barcode bias in massively parallel reporter assays

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.29.442047

N/A

0DataRank · unranked

0 citations

Ashish Kapoor, Changhee Lee, Michael Mudgett, Michael A. Beer, Aravinda Chakravarti +1 more

Interferon pathway lupus risk alleles modulate risk of death from acute COVID-19

Translational research(2022)10.1016/j.trsl.2022.01.007

N/A

0DataRank · unranked

19 citations

Ruth Fernandez‐Ruiz, Theresa Wampler Muskardin, Jacqueline L Paredes, Ashira Blazer, Stephanie Tuminello +7 more

Rare coding variants in RCN3 are associated with blood pressure

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

N/A

0DataRank · unranked

10 citations

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

Quality assessment and refinement of chromatin accessibility data using a sequence-based predictive model

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.02.24.481844

N/A

0DataRank · unranked

4 citations

Yoshiharu Muto, Parker C. Wilson, Aravinda Chakravarti, Benjamin D. Humphreys, Matthew G. Sampson +2 more

Tissue-specific and tissue-agnostic effects of genome sequence variation modulating blood pressure

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.04.19.488795

N/A

0DataRank · unranked

2 citations

Seong Kyu Han, Or Yaacov, Hanna Berk-Rauch, Prabhu Mathiyalagan, Santhi K. Ganesh +2 more

Cardiac muscle-restricted partial loss of Nos1ap expression has limited impact on electro- and echo-cardiographic features

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.09.27.509782

N/A

0DataRank · unranked

0 citations

Dallas R. Auer, Morgan Johnson, Ernesto Sánchez, Holly Ross, Christopher Wård +3 more

Cardiac muscle–restricted partial loss of Nos1ap expression has limited but significant impact on electrocardiographic features

G3 Genes Genomes Genetics(2023)10.1093/g3journal/jkad208

N/A

0DataRank · unranked

5 citations

Dallas R. Auer, Morgan Johnson, Ernesto Sánchez, Holly Ross, Christopher Wård +3 more

Tissue-specific and tissue-agnostic effects of genome sequence variation modulating blood pressure

Cell Reports(2023)10.1016/j.celrep.2023.113351

N/A

0DataRank · unranked

8 citations

Seong Kyu Han, Or Yaacov, Hanna Berk-Rauch, Prabhu Mathiyalagan, Santhi K. Ganesh +2 more

Interleukin-1 receptor antagonist gene ( IL1RN ) variants modulate the cytokine release syndrome and mortality of SARS-CoV-2

medRxiv(2023)10.1101/2023.01.09.23284348

N/A

0DataRank · unranked

3 citations

Christopher M. Petrilli, Samrachana Adhikari, Eduardo Iturrate, Xiyue Li, Stephanie Tuminello +5 more

Interleukin-1 Receptor Antagonist Gene (IL1RN) Variants Modulate the Cytokine Release Syndrome and Mortality of COVID-19

The Journal of Infectious Diseases(2024)10.1093/infdis/jiae031

N/A

0DataRank · unranked

8 citations

Christopher M. Petrilli, Samrachana Adhikari, Eduardo Iturrate, Xiyue Li, Stephanie Tuminello +5 more

Variability in proliferative and migratory defects in Hirschsprung disease-associated RET pathogenic variants

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.02.004

N/A

0DataRank · unranked

4 citations

Sree Dharma, Aravinda Chakravarti, Sumantra Chatterjee, Lauren E. Fries

Sex differences in the developing human cortex intersect with genetic risk of neurodevelopmental disorders

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.09.04.674293

N/A

0DataRank · unranked

9 citations

Yang Sui, Druha Karunakaran, Ally Nicolella, Rachel Leonard, Rebecca Meyer‐Schuman +7 more

The Role of de novo and Ultra-Rare Variants in Hirschsprung Disease (HSCR): Extended Gene Discovery for Risk Profiling of Patients

medRxiv(2025)10.1101/2025.01.07.25320162

N/A

0DataRank · unranked

3 citations

Hanna Berk-Rauch, Sumantra Chatterjee, Aravinda Chakravarti, Mingzhou Fu

Synergistic effects of Ret coding and enhancer loss-of-function alleles cause progressive loss of inhibitory motor neurons in the enteric nervous system

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.01.23.634550

N/A

0DataRank · unranked

3 citations

Gabriel Grullon, Lauren Wilkes, Hanna Berk-Rauch, Aravinda Chakravarti, Sumantra Chatterjee +1 more

Joint disruption of Ret and Ednrb transcription shifts cell fate trajectories in the enteric nervous system in Hirschsprung disease

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2507062122

N/A

0DataRank · unranked

1 citations

Rebecca Chubaryov, Mingzhou Fu, Gabriel Grullon, Aravinda Chakravarti, Ryan D. Fine

A systematic evaluation of 151 candidate genes for their association with osteoporosis and osteoporotic fracture in a meta-analysis of genome-wide association data

Bone(2009)10.1016/j.bone.2009.03.068

N/A

0DataRank · unranked

0 citations

Thomas Quertermous, Unnur Styrkarsdottir, Bjarni V. Halldorsson, Y. Hsu, B. Mullins +47 more

Author Index Vol. 64, 2007

Human Heredity(2007)10.1159/000105464

N/A

0DataRank · unranked

0 citations

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

023 META-ANALYSIS OF GENOME-WIDE ASSOCIATION STUDIES OF OSTEOARTHRITIS

Osteoarthritis and Cartilage(2009)10.1016/s1063-4584(09)60046-7

N/A

0DataRank · unranked

0 citations

Unnur Styrkarsdottir, Hanneke J.M. Kerkhof, Ingileif Jonsdottir, Evangelia E. Tsironi, Y. Zhu +14 more

Contents Vol. 64, 2007

Human Heredity(2007)10.1159/000105467

N/A

0DataRank · unranked

0 citations

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

Analysis of putative cis-regulatory elements regulating blood pressure variation

Human Molecular Genetics(2020)10.1093/hmg/ddaa098

N/A

0DataRank · unranked

13 citations

Dongwon Lee, Thomas J. Hoffmann, Georg Ehret, Dan E. Arking, Dilrini K. Ranatunga +9 more

Multi-ancestry genome-wide association study accounting for gene-psychosocial factor interactions identifies novel loci for blood pressure traits

Human Genetics and Genomics Advances(2020)10.1016/j.xhgg.2020.100013

N/A

0DataRank · unranked

14 citations

Melissa A. Richard, Solomon K. Musani, Yun Ju Sung, Thomas W. Winkler, Karen Schwander +95 more

Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations

UNC Libraries(2020)10.17615/vygp-he02

N/A

0DataRank · unranked

7 citations

Richard S. Cooper, Michele K. Evans, Hua Tang, Alex P. Reiner, Colin A. McKenzie +74 more

Multiple, independent, common variants overlapping known and putative gut enhancers at RET , SEMA3 and NRG1 underlie Hirschsprung disease risk in European ancestry subjects

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.07.138719

N/A

0DataRank · unranked

1 citations

Priyanka Nandakumar, Dallas R. Auer, Maria X. Sosa, Holly Ross, Juli Bollinger +4 more

Rare Exome Sequence Variants in CLCN6 Reduce Blood Pressure Levels and Hypertension RiskCLINICAL PERSPECTIVE

UNC Libraries(2020)10.17615/ttpw-sn86

N/A

0DataRank · unranked

0 citations

Alex P. Reiner, Donna M. Muzny, Shih‐Jen Hwang, Christopher Newton‐Cheh, Leslie J. Raffel +30 more

Rare variants in fox-1 homolog A (RBFOX1) are associated with lower blood pressure

UNC Libraries(2020)10.17615/gak2-c922

N/A

0DataRank · unranked

0 citations

Ayush Giri, Brian E. Cade, Heming Wang, Todd L. Edwards, Thu H. Le +13 more

Pathogenic alleles in microtubule, secretory granule and extracellular matrix-related genes in familial keratoconus

Human Molecular Genetics(2021)10.1093/hmg/ddab075

N/A

0DataRank · unranked

30 citations

Nara Sobreira, Elizabeth Wohler, George Maiti, Nan Hu, Giuliana Silvestri +6 more

Magnitude of Mendelian versus complex inheritance of rare disorders

American Journal of Medical Genetics Part A(2021)10.1002/ajmg.a.62463

N/A

0DataRank · unranked

19 citations

Aravinda Chakravarti

Multiple, independent, common variants at RET, SEMA3 and NRG1 gut enhancers specify Hirschsprung disease risk in European ancestry subjects

Journal of Pediatric Surgery(2021)10.1016/j.jpedsurg.2021.04.010

N/A

0DataRank · unranked

6 citations

Priyanka Nandakumar, Dallas R. Auer, Maria X. Sosa, Holly Ross, Juli Bollinger +4 more

A multi-enhancer RET regulatory code is disrupted in Hirschsprung disease

Genome Research(2021)10.1101/gr.275667.121

N/A

0DataRank · unranked

28 citations

Kameko M. Karasaki, Lauren E. Fries, Ashish Kapoor, Aravinda Chakravarti, Sumantra Chatterjee

Aravinda Chakravarti

Indexed papers

Top data-sharing exemplar

Papers