Carlos A. Aguilar‐Salinas

Also affiliated with National Human Genome Research Institute, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Tecnológico de Monterrey

MedicineBiochemistry, Genetics and Molecular BiologyHealth Professions

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

7.1Author DataRank

Indexed papers

3in 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 3 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 structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8

Top 3%

6.7DataRank

Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Papers

Driven by 28 papers — median percentile 76. Top paper: “A genomic mutational constraint map using variation in 76,156 human genomes”.

A genomic mutational constraint map using variation in 76,156 human genomes

Nature(2023)10.1038/s41586-023-06045-0

N/A

9.6DataRank · unranked

1369 citations

Laurent C. Francioli, Julia K. Goodrich, Ryan L. Collins, Masahiro Kanai, Qingbo S. Wang +95 more

A structural variation reference for medical and population genetics

Nature(2020)10.1038/s41586-020-2287-8

Top 3%

6.7DataRank

Top 3%1180 citations

Harrison Brand, Konrad J. Karczewski, Xuefang Zhao, Jessica Alföldi, Laurent C. Francioli +201 more

Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes

Nature Communications(2020)10.1038/s41467-019-12438-5

N/A

5.6DataRank · unranked

143 citations

James Zou, Beryl B. Cummings, Jessica Alföldi, Laurent C. Francioli, Laura D. Gauthier +174 more

Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals

Nature Communications(2020)10.1038/s41467-019-10717-9

N/A

5.2DataRank · unranked

191 citations

Konrad J. Karczewski, Xiaolei Zhang, Sonia Chothani, Miriam J. Smith, D. Gareth Evans +181 more

The effect of LRRK2 loss-of-function variants in humans

Nature Medicine(2020)10.1038/s41591-020-0893-5

N/A

4.9DataRank · unranked

114 citations

Irina M. Armean, Aaron Kleinman, Jamie L. Marshall, Eric V. Minikel, Julia K. Goodrich +214 more

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

Nature Communications(2021)10.1038/s41467-021-23556-4

N/A

2.7DataRank · unranked

110 citations

Moriel Singer‐Berk, Rachel G. Son, Abigail Sveden, Jordan C. Wood, Eleina England +95 more

The causal effect of obesity on prediabetes and insulin resistance reveals the important role of adipose tissue in insulin resistance

PLoS Genetics(2020)10.1371/journal.pgen.1009018

N/A

2.0DataRank · unranked

71 citations

Marcus Alvarez, Arthur Ko, Yash Bhagat, Elior Rahmani, Brandon Jew +11 more

The mutational constraint spectrum quantified from variation in 141,456 humans

Nature(2020)10.1038/s41586-020-2308-7

N/A

1.4DataRank · unranked

9958 citations

Laurent C. Francioli, Grace Tiao, Beryl B. Cummings, Jessica Alföldi, Qingbo S. Wang +187 more

Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.11.021

N/A

1.3DataRank · unranked

70 citations

Peter Dornbos, Mark Chaffin, Dajiang J. Liu, Minxian Wang, Margaret Sunitha Selvaraj +95 more

Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation

Nature Genetics(2022)10.1038/s41588-022-01058-3

N/A

0.994DataRank · unranked

754 citations

Cassandra N. Spracklen, Weihua Zhang, Maggie C. Y. Ng, Lauren E. Petty, Hidetoshi Kitajima +95 more

Transcript expression-aware annotation improves rare variant interpretation

Nature(2020)10.1038/s41586-020-2329-2

N/A

0.796DataRank · unranked

201 citations

Konrad J. Karczewski, Ditte Demontis, Eleanor G. Seaby, Nicholas A. Watts, Moriel Singer-Berk +177 more

Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits—The Hispanic/Latino Anthropometry Consortium

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100099

N/A

0.759DataRank · unranked

25 citations

Mariaelisa Graff, Victoria L. Buchanan, Anne E. Justice, Heather M. Highland, Xiuqing Guo +95 more

Impact of undiagnosed type 2 diabetes and pre-diabetes on severity and mortality for SARS-CoV-2 infection

BMJ Open Diabetes Research & Care(2021)10.1136/bmjdrc-2020-002026

N/A

0.619DataRank · unranked

61 citations

Omar Yaxmehen Bello‐Chavolla, Edgar Ortiz-Brizuela, Alejandro Campos-Muñoz, Roopa Mehta, Marco Villanueva-Reza +7 more

Rare coding variants in 35 genes associate with circulating lipid levels – a multi-ancestry analysis of 170,000 exomes

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.22.423783

N/A

0.534DataRank · unranked

11 citations

Peter Dornbos, Mark Chaffin, Dajiang J. Liu, Minxian X. Wang, Margaret Sunitha Selvaraj +95 more

Ancestral diversity improves discovery and fine-mapping of genetic loci for anthropometric traits - the Hispanic/Latino Anthropometry Consortium

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.05.27.445969

N/A

0.434DataRank · unranked

17 citations

Mariaelisa Graff, Victoria L. Buchanan, Anne E. Justice, Heather M. Highland, Xiuqing Guo +95 more

The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes

Diabetologia(2023)10.1007/s00125-023-05912-9

N/A

0.434DataRank · unranked

17 citations

Philip Schroeder, Ravi Mandla, Aaron J. Deutsch, Wanying Zhu, Lauren E. Petty +59 more

Exploring penetrance of clinically relevant variants in over 800,000 humans from the Genome Aggregation Database

Nature Communications(2025)10.1038/s41467-025-61698-x

Top 44%

0.417DataRank

Top 44%14 citations

Moriel Singer‐Berk, Sarah L. Stenton, Julia K. Goodrich, Michael W. Wilson, Jonah Einson +95 more

Performance of the enhanced Sampson-NIH equation for VLDL-C and LDL-C in a population with familial combined hyperlipidemia

Atherosclerosis(2023)10.1016/j.atherosclerosis.2023.117364

N/A

0.360DataRank · unranked

10 citations

Arsenio Vargas‐Vázquez, Fabiola Del Razo Olvera, Ivette Cruz‐Bautista, Alexandro J. Martagón, Maureen Sampson +3 more

The power of genetic diversity in genome-wide association studies of lipids

UNC Libraries(2024)10.17615/539b-tz69

N/A

0.269DataRank · unranked

5 citations

Joel N. Hirschhorn, Zoltán Kutalik, Sanni Ruotsalainen, Daniela Ruggiero, Prashantha Hebbar +95 more

The power of TOPMed imputation for the discovery of Latino enriched rare variants associated with type 2 diabetes

medRxiv(2022)10.1101/2022.09.30.22280535

N/A

0.269DataRank · unranked

5 citations

Philip Schroeder, Ravi Mandla, Aaron J. Deutsch, Wanying Zhu, Lauren E. Petty +57 more

Design of a cluster-randomized trial of the effectiveness and cost-effectiveness of metformin on prevention of type 2 diabetes among prediabetic Mexican adults (the PRuDENTE initiative of Mexico City)

Contemporary Clinical Trials(2020)10.1016/j.cct.2020.106067

N/A

0.243DataRank · unranked

3 citations

Sı́món Barquera, Carlos A. Aguilar‐Salinas, Jaime Sepúlveda-Amor, Luz María Sánchez‐Romero, Edgar Denova‐Gutiérrez +8 more

Improving type 2 diabetes polygenic risk scores by incorporating rare, low-frequency, and population-specific variants

medRxiv(2025)10.1101/2025.11.24.25340878

N/A

0.104DataRank · unranked

1 citations

Alicia Huerta‐Chagoya, Xiaoyu Wang, Maheak Vora, Jiang Li, Lehte Türk +18 more

Genetic drivers of heterogeneity in type 2 diabetes pathophysiology

Nature(2024)10.1038/s41586-024-07019-6

N/A

0DataRank · unranked

537 citations

Konstantinos Hatzikotoulas, Lorraine Southam, Henry J. Taylor, Xianyong Yin, Kimberly Lorenz +95 more

Core outcome sets for trials of interventions to prevent and to treat multimorbidity in adults in low and middle-income countries: the COSMOS study

BMJ Global Health(2024)10.1136/bmjgh-2024-015120

N/A

0DataRank · unranked

8 citations

Rubab Ayesha, Jan R. Boehnke, Jamie J Kirkham, Louise Rose, John R. Hurst +55 more

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

medRxiv(2020)10.1101/2020.09.22.20195529

N/A

0DataRank · unranked

11 citations

Moriel Singer‐Berk, Rachel G. Son, Abigail Sveden, Jordan C. Wood, Eleina England +95 more

Molecular Characterization of the Lipid Genome-Wide Association Study Signal on Chromosome 18q11.2 Implicates HNF4A-Mediated Regulation of the TMEM241 GeneHighlights

UNC Libraries(2020)10.17615/3y7x-9f70

N/A

0DataRank · unranked

0 citations

Yash Bhagat, Carlos A. Aguilar‐Salinas, Alejandra Rodríguez, Arthur Ko, Karen L. Mohlke +12 more

Identification of TBX15 as an adipose master trans regulator of abdominal obesity genes

Genome Medicine(2021)10.1186/s13073-021-00939-2

N/A

0DataRank · unranked

46 citations

Zong Miao, Caroline Comenho, Sandhya Rajkumar, Amogha Koka, Seung Hyuk Lee +16 more

The beneficial effect of a comprehensive diabetes care model on high-risk relatives accompanying patients with type 2 diabetes

Primary care diabetes(2022)10.1016/j.pcd.2022.09.008

N/A

0DataRank · unranked

1 citations

Michelle Díaz-Pineda, Alberto Ramírez-García, Neftali Eduardo Antonio‐Villa, Paloma Almeda‐Valdés, Martha Kaufer‐Horwitz +4 more

Carlos A. Aguilar‐Salinas

Indexed papers

Top data-sharing exemplar

Papers