Luca A. Lotta

Biochemistry, Genetics and Molecular BiologyImmunology and MicrobiologyMedicine

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

4.3Author 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 deep catalogue of protein-coding variation in 983,578 individuals

Nature(2024)10.1038/s41586-024-07556-0

Top 11%

1.9DataRank

Top 11%109 citations

Xiaodong Bai, Siying Chen, Suying Bao, Chuanyi Zhang, Manav Kapoor +92 more

Papers

Driven by 36 papers — median percentile 55. 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

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

6.8DataRank · unranked

363 citations

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

Rare and common genetic determinants of metabolic individuality and their effects on human health

Nature Medicine(2022)10.1038/s41591-022-02046-0

N/A

4.1DataRank · unranked

157 citations

Isobel D. Stewart, Victoria P. W. Au Yeung, Maik Pietzner, Johannes Raffler, Maria A. Wörheide +31 more

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

Nature Genetics(2020)10.1038/s41588-020-00713-x

N/A

3.7DataRank · unranked

242 citations

Elena V. Feofanova, Najim Lahrouchi, Ioanna Ntalla, Savita Karthikeyan, James P. Cook +94 more

A deep catalogue of protein-coding variation in 983,578 individuals

Nature(2024)10.1038/s41586-024-07556-0

Top 11%

1.9DataRank

Top 11%109 citations

Xiaodong Bai, Siying Chen, Suying Bao, Chuanyi Zhang, Manav Kapoor +92 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

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

Science(2021)10.1126/science.abf8683

N/A

0.845DataRank · unranked

278 citations

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

The Genomics of Heart Failure: Design and Rationale of the HERMES Consortium

ESC Heart Failure(2021)10.1002/ehf2.13517

Top 24%

0.829DataRank

Top 24%22 citations

Sonia Shah, Honghuang Lin, Tomasz Czuba, Albert Henry, Daniel I. Swerdlow +95 more

Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases

Nature Genetics(2025)10.1038/s41588-024-02072-3

N/A

0.821DataRank · unranked

50 citations

Ida Surakka, Morten S. Olesen, Garðar Sveinbjörnsson, Nicholas Marston, Seung Hoan Choi +95 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

0.793DataRank · unranked

197 citations

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

Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease

Nature Genetics(2022)10.1038/s41588-021-01006-7

N/A

0.780DataRank · unranked

180 citations

Jack A. Kosmicki, Amy Damask, Deepika Sharma, Genevieve H. L. Roberts, Anne E. Justice +89 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

0.775DataRank · unranked

174 citations

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

Divergent role of Mitochondrial Amidoxime Reducing Component 1 (MARC1) in human and mouse

PLoS Genetics(2024)10.1371/journal.pgen.1011179

N/A

0.679DataRank · unranked

15 citations

Lisa M. Shihanian, Ivory J. Mintah, Parnian Bigdelou, Yuliya Livson, Heather M. Brown +14 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

0.637DataRank · unranked

69 citations

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

0.601DataRank · unranked

54 citations

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

0.599DataRank · unranked

18 citations

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

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

The impact of common and rare genetic variants on bradyarrhythmia development

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

N/A

0.464DataRank · unranked

21 citations

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

0.425DataRank · unranked

16 citations

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

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals

UEF eRepo (University of Eastern Finland)(2024)10.17615/k2gw-9005

N/A

0.360DataRank · unranked

10 citations

James R. Staley, M.E. Jørgensen, T. Tuomi, R. Rauramaa, Robin Young +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

Germline Variants Influence Chronic Liver Disease Progression through Distinct Pathways

medRxiv(2025)10.1101/2025.09.16.25335186

N/A

0DataRank · unranked

1 citations

David E. Kaplan, Jonas Ghouse, Bao‐Li Loza, Joseph Brancale, Adam Lewis +68 more

Genome-wide association study of adipocyte lipolysis in the GENetics of adipocyte lipolysis (GENiAL) cohort

Molecular Metabolism(2020)10.1016/j.molmet.2020.01.009

N/A

0DataRank · unranked

16 citations

Veroniqa Lundbäck, Cecilia M. Lindgren, Jian’an Luan, Luca A. Lotta, Claudia Langenberg +4 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

Genome-wide association study of adipocyte lipolysis in the GENetics of adipocyte lipolysis (GENiAL) cohort.

Apollo (University of Cambridge)(2020)10.17863/cam.51590

Top 100%

0DataRank

Top 100%0 citations

Veroniqa Lundbäck, Cecilia M. Lindgren, Jian’an Luan, Luca A. Lotta, Claudia Langenberg +4 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

Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis

Journal of Clinical Investigation(2022)10.1172/jci158788

N/A

0DataRank · unranked

74 citations

Daniel J. Tyrrell, Alexi Vasbinder, Changli Wei, Feriel Presswalla, Hui Wang +37 more

ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma

Communications Biology(2022)10.1038/s42003-022-03932-6

N/A

0DataRank · unranked

25 citations

Gaurang Patel, Lauren Gurski, Ariane Ayer, Trikaladarshi Persaud, Matthew Still +95 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

Framework From a Multidisciplinary Approach for Transitioning Variants of Unknown Significance From Clinical Genetic Testing in Kidney Disease to a Definitive Classification

Kidney International Reports(2022)10.1016/j.ekir.2022.06.014

N/A

0DataRank · unranked

5 citations

Ahana Bhan, Lotte E. Tholen, Brian Fang, Guoli Chen, Bryn S. Moore +12 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

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

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

Luca A. Lotta

Indexed papers

Top data-sharing exemplar

Papers