Mariza de Andrade

Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA, Site Investigator

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

9.3Author DataRank

Indexed papers

8in 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 8 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.

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y

Top 3%

7.0DataRank

Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 more

Papers

Driven by 51 papers — median percentile 63. Top paper: “Inherited causes of clonal haematopoiesis in 97,691 whole genomes”.

Inherited causes of clonal haematopoiesis in 97,691 whole genomes

Nature(2020)10.1038/s41586-020-2819-2

N/A

11.6DataRank · unranked

748 citations

Joshua S. Weinstock, Satish K. Nandakumar, Charles P. Fulco, Erik L. Bao, Seyedeh M. Zekavat +95 more

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Nature(2021)10.1038/s41586-021-03205-y

Top 3%

7.0DataRank

Top 3%2322 citations

Daniel Harris, Michael D. Kessler, Jedidiah Carlson, Zachary A. Szpiech, Raúl Torres +95 more

Large-scale replication and heterogeneity in Parkinson disease genetic loci

Neurology(2012)10.1212/wnl.0b013e318264e353

N/A

6.6DataRank · unranked

132 citations

Grazia Annesi, Alexis Brice, Christine Van Broeckhoven, Muin J. Khoury, Maria Bozi +160 more

Genetic diversity fuels gene discovery for tobacco and alcohol use

Nature(2022)10.1038/s41586-022-05477-4

N/A

5.9DataRank · unranked

513 citations

Xingyan Wang, Fang Chen, Seon-Kyeong Jang, Mengzhen Liu, Chen Wang +95 more

A genome- and phenome-wide association study to identify genetic variants influencing platelet count and volume and their pleiotropic effects

Human Genetics(2014)10.1007/s00439-013-1355-7

N/A

5.1DataRank · unranked

148 citations

Joshua C. Denny, Keyue Ding, Hayan Jouni, David R. Crosslin, Mariza de Andrade +15 more

Cerebral small vessel disease genomics and its implications across the lifespan

Nature Communications(2020)10.1038/s41467-020-19111-2

N/A

4.3DataRank · unranked

209 citations

Hideaki Suzuki, Xueqiu Jian, Chloé Sarnowski, Tavia E. Evans, Joshua C. Bis +94 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

Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer

Nature Genetics(2022)10.1038/s41588-022-01115-x

N/A

2.1DataRank · unranked

123 citations

Younghun Han, Yafang Li, Jun Xia, Erping Long, Jiyeon Choi +80 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

Genome sequencing unveils a regulatory landscape of platelet reactivity

Nature Communications(2021)10.1038/s41467-021-23470-9

N/A

1.5DataRank · unranked

54 citations

Ming‐Huei Chen, Benjamin A.T. Rodriguez, Lisa R. Yanek, Arunoday Bhan, Brady Gaynor +94 more

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

Nature Genetics(2012)10.1038/ng.2274

N/A

1.0DataRank · unranked

897 citations

Marie-France Hivert, Robert A Scott, Jonna L Grimsby, Nabila Bouatia-Naji, Han Chen +211 more

Rare deleterious germline variants and risk of lung cancer

npj Precision Oncology(2021)10.1038/s41698-021-00146-7

N/A

1.0DataRank · unranked

34 citations

Jun Xia, James McKay, Spiridon Tsavachidis, Xiangjun Xiao, Margaret R. Spitz +42 more

Whole-genome association analyses of sleep-disordered breathing phenotypes in the NHLBI TOPMed program

Genome Medicine(2021)10.1186/s13073-021-00917-8

Top 21%

0.976DataRank

Top 21%35 citations

Jiwon Lee, Tamar Sofer, Heming Wang, Man Zhang, Han Chen +94 more

International genome-wide meta-analysis identifies new primary biliary cirrhosis risk loci and targetable pathogenic pathways

Nature Communications(2015)10.1038/ncomms9019

N/A

0.860DataRank · unranked

309 citations

Younghun Han, George F. Mells, Yafang Li, Gideon M. Hirschfield, Casey S. Greene +518 more

Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors

Circulation(2022)10.1161/circulationaha.122.059675

N/A

0.701DataRank · unranked

106 citations

Derek Klarin, Jennifer A. Brody, Ming‐Huei Chen, Michael G. Levin, Daniel I. Chasman +82 more

Genome-Wide Association Study of Peripheral Artery Disease

Circulation Genomic and Precision Medicine(2021)10.1161/circgen.119.002862

N/A

0.670DataRank · unranked

86 citations

Alexander Stiby, Moustafa Abdalla, Erin Austin, Stela McLachlan, Efthymia Vlachopoulou +50 more

Brazilian urban population genetic structure reveals a high degree of admixture

European Journal of Human Genetics(2012)10.1038/ejhg.2011.144

N/A

0.670DataRank · unranked

86 citations

Júlia M P Soler, Steven C Greenway, Marcio A A Almeida, Mariza de Andrade, J G Seidman +4 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

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

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

Rare genetic variants explain missing heritability in smoking

Nature Human Behaviour(2022)10.1038/s41562-022-01408-5

N/A

0.520DataRank · unranked

31 citations

Luke M. Evans, Allison Fialkowski, Donna K. Arnett, Allison E. Ashley‐Koch, Kathleen C. Barnes +85 more

Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program

Circulation Genomic and Precision Medicine(2023)10.1161/circgen.121.003532

Top 38%

0.507DataRank

Top 38%11 citations

Cecelia Laurie, Brandon J. Coombes, Deepti Jain, Matthew P. Conomos, Jennifer A. Brody +30 more

Transcriptome-wide association study and Mendelian randomization in pancreatic cancer identifies susceptibility genes and causal relationships with type 2 diabetes and venous thromboembolism

EBioMedicine(2024)10.1016/j.ebiom.2024.105233

N/A

0.497DataRank · unranked

15 citations

Chelsea A. Isom, Yangzi Liu, David-Alexandre Trégouët, Sara Lindström, Lu Wang +52 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

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

Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer

Cancer Research(2021)10.1158/0008-5472.can-20-3196

N/A

0.373DataRank · unranked

11 citations

Claire L. Simpson, Bilal A. Moiz, Claudio W. Pikielny, Candace D. Middlebrooks, Diptasri Mandal +13 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

Neptune: an environment for the delivery of genomic medicine

Genetics in Medicine(2021)10.1038/s41436-021-01230-w

N/A

0.330DataRank · unranked

8 citations

Victoria Yi, David R. Murdock, Sara E. Kalla, Tsung-Jung Wu, Aniko Sabo +93 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

Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection

Scientific Reports(2023)10.1038/s41598-023-45649-4

N/A

0.281DataRank · unranked

3 citations

Taryn O. Hall, Dana C. Crawford, Robb Rowley, Benjamin A. Satterfield, Rongling Li +21 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

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

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

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

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

Genetic Association for Renal Traits among Participants of African Ancestry Reveals New Loci for Renal Function

UNC Libraries(2020)10.17615/1t9q-g098

N/A

0DataRank · unranked

0 citations

Sharon B. Wyatt, Raymond R. Townsend, Josef Coresh, Stephen T. Turner, Thomas H. Mosley +26 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

Lower Cancer Incidence in Amsterdam-I Criteria Families Without Mismatch Repair Deficiency: Familial Colorectal Cancer Type X

UNC Libraries(2020)10.17615/2xsp-an37

N/A

0DataRank · unranked

0 citations

Loı̈c Le Marchand, John A. Baron, John H. Grove, Noralane M. Lindor, Mariza de Andrade +21 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

Multi-Ethnic Genome-Wide Association Study of Cerebral White Matter Hyperintensities on MRI

MURAL - Maynooth University Research Archive Library (National University of Ireland, Maynooth)(2020)10.17615/8trn-p892

N/A

0DataRank · unranked

0 citations

W. T. Longstreth, Reinhold Schmidt, Paul Freudenberger, Pamela J. Schreiner, Stella Trompet +95 more

Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants

Genetics(2023)10.1093/genetics/iyad115

N/A

0DataRank · unranked

10 citations

Dafni A. Glinos, Eric Boerwinkle, Peter J. Castaldi, Dawood Darbar, Mariza de Andrade +28 more

Data from Haplotype and Cell Proliferation Analyses of Candidate Lung Cancer Susceptibility Genes on Chromosome 15q24-25.1

(2023)10.1158/0008-5472.c.6500087.v1

Top 100%

0DataRank

Top 100%0 citations

Pengyuan Liu, Weidong Wen, Michael A. James, Yian Wang, Joan E. Bailey-Wilson +19 more

Data from Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer

(2023)10.1158/0008-5472.c.6513273.v1

N/A

0DataRank · unranked

0 citations

Claire L. Simpson, Bilal A. Moiz, Claudio W. Pikielny, Candace D. Middlebrooks, Diptasri Mandal +13 more

Data from Fine Mapping of Chromosome 6q23-25 Region in Familial Lung Cancer Families Reveals RGS17 as a Likely Candidate Gene

(2023)10.1158/1078-0432.c.6517600.v1

N/A

0DataRank · unranked

0 citations

Daolong Wang, Pengyuan Liu, Haris G. Vikis, Michael James, Yan Lü +37 more

Lung adenocarcinoma patients with ROS1-rearranged tumors by sex and smoking intensity

Heliyon(2024)10.1016/j.heliyon.2024.e28285

N/A

0DataRank · unranked

0 citations

Vinicius Ernani, Dan Liu, Qian Guo, Markay Hopps, Joseph C. Cappelleri +6 more

A system for phenotype harmonization in the National Heart, Lung, and Blood Institute Trans-Omics for Precision Medicine (TOPMed) program

UNC Libraries(2024)10.17615/0ea7-3v47

N/A

0DataRank · unranked

0 citations

Nicola L. Hawley, May E. Montasser, P.A. Peyser, Daniel E. Weeks, Braxton D. Mitchell +67 more

NFAT5 and SLC4A10 loci associate with plasma osmolality

UNC Libraries(2024)10.17615/86h9-j874

N/A

0DataRank · unranked

0 citations

Priya Srikanth, Péter Vollenweider, Christian Gieger, Ilja M. Nolte, Mariza de Andrade +95 more

Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants

UNC Libraries(2024)10.17615/xgme-w279

N/A

0DataRank · unranked

0 citations

Meher Preethi Boorgula, Alison E. Fohner, S.S. Rich, Stella Aslibekyan, Merry‐Lynn McDonald +57 more

Mariza de Andrade

Indexed papers

Top data-sharing exemplar

Papers