Aris Baras

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 2%percentile

3.8Author 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.

Within-sibship GWAS improve estimates of direct genetic effects

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.05.433935

Top 10%

2.2DataRank

Top 10%75 citations

Michel G. Nivard, Tim Morris, Ailin Falkmo Hansen, Humaira Rasheed, Yoonsu Cho +83 more

Papers

Driven by 40 papers — median percentile 60. Top paper: “Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants”.

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

Nature Genetics(2022)10.1038/s41588-022-01233-6

N/A

7.7DataRank · unranked

721 citations

Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N. Wolford, Deepak Atri +92 more

Within-sibship GWAS improve estimates of direct genetic effects

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.05.433935

Top 10%

2.2DataRank

Top 10%75 citations

Michel G. Nivard, Tim Morris, Ailin Falkmo Hansen, Humaira Rasheed, Yoonsu Cho +83 more

Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis

Nature Genetics(2024)10.1038/s41588-024-01720-y

Top 15%

1.4DataRank

Top 15%63 citations

Garðar Sveinbjörnsson, Marijana Vujković, Anne-Sofie Seidelin, Helene Gellert‐Kristensen, Gustav Ahlberg +47 more

Efficacy and Safety of Sarilumab in Hospitalized Patients With Coronavirus Disease 2019: A Randomized Clinical Trial

Clinical Infectious Diseases(2022)10.1093/cid/ciac153

N/A

1.3DataRank · unranked

41 citations

David J. Lederer, Rafia Bhore, Negin Hajizadeh, Gerard J. Criner, Romana Hosain +35 more

A large-scale multi-ethnic genome-wide association study of coronary artery disease

Research Square(2021)10.21203/rs.3.rs-275591/v1

N/A

0.561DataRank · unranked

11 citations

Catherine Tcheandjieu, Xiang Zhu, Austin T. Hilliard, Shoa L. Clarke, Valerio Napolioni +77 more

Sequencing of over 100,000 individuals identifies multiple genes and rare variants associated with Crohns disease susceptibility

medRxiv(2021)10.1101/2021.06.15.21258641

N/A

0.500DataRank · unranked

11 citations

Christine Stevens, Guhan Venkataraman, Kai Yuan, Brandon E. Avila, María T. Abreu +95 more

Insights from the Biorepository and Integrative Genomics pediatric resource

Nature Communications(2025)10.1038/s41467-025-59375-0

Top 65%

0.208DataRank

Top 65%3 citations

Franco Mársico, Akram Mohammed, Lokesh Chinthala, Ernestine K Amos-Abanyie, Aris Baras +95 more

Pharmacologic and Genetic Downregulation of Proprotein Convertase Subtilisin/Kexin Type 9 and Survival From Sepsis

Critical Care Explorations(2023)10.1097/cce.0000000000000997

N/A

0.104DataRank · unranked

1 citations

Garen Manvelian, Alida Coppi, Amy Damask, Michael Cantor, Manuel A. R. Ferreira +35 more

Exome-wide evaluation of rare coding variants using electronic health records identifies new gene–phenotype associations

Nature Medicine(2021)10.1038/s41591-020-1133-8

N/A

0DataRank · unranked

65 citations

Anastasia Lucas, Xinyuan Zhang, Kumardeep Chaudhary, Judy H. Cho, Girish N. Nadkarni +36 more

Kidney disease genetic risk variants alter lysosomal beta-mannosidase ( MANBA ) expression and disease severity

Science Translational Medicine(2021)10.1126/scitranslmed.aaz1458

N/A

0DataRank · unranked

50 citations

Hongliu Yang, Xin Sheng, Yi-An Ko, Chengxiang Qiu, Jihwan Park +23 more

The genetic architecture of Plakophilin 2 cardiomyopathy

Genetics in Medicine(2021)10.1038/s41436-021-01233-7

N/A

0DataRank · unranked

36 citations

Anna Kirillova, Chloe Reuter, John Garcia, Hana Zouk, Megan Hawley +28 more

Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants

medRxiv(2021)10.1101/2021.05.24.21257377

N/A

0DataRank · unranked

69 citations

Tao Jiang, Anuj Goel, Stavroula Kanoni, Brooke N. Wolford, Elle M. Weeks +87 more

A trans-ancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

medRxiv(2021)10.1101/2020.12.26.20248491

N/A

0DataRank · unranked

16 citations

Shweta Ramdas, Kimberly Lorenz, Xiuqing Guo, Rebecca Darlay, Heather J. Cordell +85 more

Genetic and Functional Characterization of ANGPTL7 as a Therapeutic Target for Glaucoma

Research Square(2021)10.21203/rs.3.rs-858876/v1

N/A

0DataRank · unranked

0 citations

Gaurang Patel, Lauren Gurski, Ariane Ayer, Trikaladarshi Persaud, Matthew Still +49 more

Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

Nature Medicine(2022)10.1038/s41591-022-01891-3

N/A

0DataRank · unranked

363 citations

Xiang Zhu, Austin T. Hilliard, Shoa L. Clarke, Valerio Napolioni, Shining Ma +78 more

Whole-genome sequencing reveals host factors underlying critical COVID-19

Nature(2022)10.1038/s41586-022-04576-6

N/A

0DataRank · unranked

350 citations

Erola Pairo-Castineira, Konrad Rawlik, A. Stuckey, Christopher A. Odhams, Susan Walker +84 more

Polygenic Risk of Psychiatric Disorders Exhibits Cross-trait Associations in Electronic Health Record Data From European Ancestry Individuals

Biological Psychiatry(2020)10.1016/j.biopsych.2020.06.026

N/A

0DataRank · unranked

54 citations

Alison Merikangas, Shefali S. Verma, Anurag Verma, Renae Judy, Gonçalo R. Abecasis +42 more

A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation

Nature Genetics(2022)10.1038/s41588-022-01078-z

N/A

0DataRank · unranked

195 citations

Shweta Ramdas, Kimberly Lorenz, Xiuqing Guo, Rebecca Darlay, Heather J. Cordell +86 more

Large-scale sequencing identifies multiple genes and rare variants associated with Crohn’s disease susceptibility

Nature Genetics(2022)10.1038/s41588-022-01156-2

N/A

0DataRank · unranked

192 citations

Christine Stevens, Guhan Venkataraman, Kai Yuan, Brandon E. Avila, Maria T. Abreu +95 more

Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank

Nature Genetics(2022)10.1038/s41588-021-01011-w

N/A

0DataRank · unranked

174 citations

Seung Hoan Choi, Valerie N. Morrill, Mark Chaffin, James P. Pirruccello, Jennifer L. Halford +65 more

Germline Mutations in CIDEB and Protection against Liver Disease

New England Journal of Medicine(2022)10.1056/nejmoa2117872

N/A

0DataRank · unranked

125 citations

Mary E. Haas, Jonas B. Nielsen, Olukayode Sosina, Minhee Kim, Parsa Akbari +42 more

Impact of natural selection on global patterns of genetic variation and association with clinical phenotypes at genes involved in SARS-CoV-2 infection

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2123000119

N/A

0DataRank · unranked

18 citations

Anurag Verma, Yuanqing Feng, Marcelo C. R. Melo, Michael A. McQuillan, Matthew E.B. Hansen +71 more

Assessment of genetic susceptibility to multiple primary cancers through whole-exome sequencing in two large multi-ancestry studies

BMC Medicine(2022)10.1186/s12916-022-02535-6

N/A

0DataRank · unranked

18 citations

Linda Kachuri, Rebecca E. Graff, Jovia L. Nierenberg, Khanh K. Thai, Stacey Alexeeff +90 more

Genome-wide association meta-analysis identifies risk loci for abdominal aortic aneurysm and highlights PCSK9 as a therapeutic target

Nature Genetics(2023)10.1038/s41588-023-01510-y

N/A

0DataRank · unranked

100 citations

Derek Klarin, Michael G. Levin, Joshua M. Spin, Yae Hyun Rhee, Alicia Deng +92 more

Converging evidence from exome sequencing and common variants implicates target genes for osteoporosis

Nature Genetics(2023)10.1038/s41588-023-01444-5

N/A

0DataRank · unranked

27 citations

Olukayode Sosina, Jonas Bovijn, Lætitia Laurent, Vasundhara Sharma, Parsa Akbari +24 more

Genetic risk factors for COVID-19 and influenza are largely distinct

Nature Genetics(2024)10.1038/s41588-024-01844-1

N/A

0DataRank · unranked

14 citations

Anthony Marcketta, Deepika Sharma, Silvio Alessandro Di Gioia, Samantha Batista, Xiaoman Yang +53 more

Large-scale genome-wide association study of coronary artery disease in genetically diverse populations

UNC Libraries(2024)10.17615/8zyz-p282

Top 100%

0DataRank

Top 100%0 citations

Shining Ma, J.C. Bis, Noah L. Tsao, Philip S. Tsao, Yi‐Lwun Ho +81 more

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

Science(2025)10.1126/science.adp4753

N/A

0DataRank · unranked

48 citations

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

Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk

Nature Genetics(2025)10.1038/s41588-025-02074-9

N/A

0DataRank · unranked

28 citations

Sean J. Jurgens, Ling Xiao, Matthew C. Hill, Christopher M. Haggerty, Garðar Sveinbjörnsson +95 more

The impact of common and rare genetic variants on bradyarrhythmia development

Nature Genetics(2025)10.1038/s41588-024-01978-2

N/A

0DataRank · unranked

19 citations

Joel Rämö, Sean J. Jurgens, Shaan Khurshid, Mark Chaffin, Amelia Weber Hall +95 more

Risk of lymphoid malignancy associated with cancer predisposition genes

Blood Cancer Journal(2025)10.1038/s41408-025-01283-z

N/A

0DataRank · unranked

8 citations

Raphael Mwangi, Dennis P. Robinson, Cristine Allmer, Allison Rosenthal, Thomas M. Habermann +95 more

Exclusion-based exome sequencing in critically ill adults 18–40 years old has a 24% diagnostic rate and finds racial disparities in access to genetic testing

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.06.007

N/A

0DataRank · unranked

5 citations

Colleen Morse Kripke, Adam J. Mansfield, Alexander Li, Alexander Lopez, Alicia Hawes +95 more

Mucus sialylation determines intestinal host-commensal homeostasis

Cell(2022)10.1016/j.cell.2022.02.013

N/A

0DataRank · unranked

237 citations

Girak Kim, Samantha Shafer, Zuojia Chen, Satoshi Kubo, Yanlong Ji +45 more

MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk

Nature Communications(2020)10.1038/s41467-020-17315-0

N/A

0DataRank · unranked

37 citations

Lars G. Fritsche, Wei Zhou, Joshua Backman, Jack A. Kosmicki, Haocheng Lu +45 more

Identification of Undetected Monogenic Cardiovascular Disorders

Journal of the American College of Cardiology(2020)10.1016/j.jacc.2020.06.037

N/A

0DataRank · unranked

32 citations

Lydia Coulter Kwee, Fawaz Alenezi, Albert Y. Sun, Aris Baras, Teminioluwa Ajayi +10 more

Genome-wide analysis in 756,646 individuals provides first genetic evidence that ACE2 expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease

medRxiv(2020)10.1101/2020.12.14.20248176

N/A

0DataRank · unranked

41 citations

Jack A. Kosmicki, Amy Damask, Deepika Sharma, Genevieve H. L. Roberts, Anne E. Justice +54 more

A catalog of associations between rare coding variants and COVID-19 outcomes

medRxiv(2020)10.1101/2020.10.28.20221804

N/A

0DataRank · unranked

31 citations

Julie Horowitz, Nilanjana Banerjee, Rouel Lanche, Anthony Marcketta, Evan K. Maxwell +75 more

Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity

Science(2021)10.1126/science.abf8683

N/A

0DataRank · unranked

278 citations

Ankit Gilani, Olukayode Sosina, Jack A. Kosmicki, Lori Khrimian, Yi‐Ya Fang +55 more

An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs

Journal of Hepatology(2021)10.1016/j.jhep.2021.04.055

N/A

0DataRank · unranked

186 citations

James J. Fryett, Kazuko Ueno, Rebecca Darlay, Yoshihiro Aiba, Yuki Hitomi +89 more

Disrupting upstream translation in mRNAs is associated with human disease

Nature Communications(2021)10.1038/s41467-021-21812-1

N/A

0DataRank · unranked

70 citations

Joseph Park, Andrew Kromer, Aris Baras, Daniel J. Rader, Marylyn D. Ritchie +3 more

Aris Baras

Indexed papers

Top data-sharing exemplar

Papers