Michael Preuß

Also affiliated with Harvard University, Icahn School of Medicine at Mount Sinai

Biochemistry, Genetics and Molecular Biology

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

4.9Author 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.

Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference

Nature Genetics(2024)10.1038/s41588-023-01596-4

Top 9%

2.4DataRank

Top 9%176 citations

Georgina Navoly, Olga Giannakopoulou, Daniel F. Levey, Dóra Koller, Gita A. Pathak +76 more

Papers

Driven by 53 papers — median percentile 63. Top paper: “Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations”.

Trans-ethnic and Ancestry-Specific Blood-Cell Genetics in 746,667 Individuals from 5 Global Populations

Cell(2020)10.1016/j.cell.2020.06.045

N/A

8.3DataRank · unranked

739 citations

Laura M. Raffield, Abdou Mousas, Saori Sakaue, Jennifer E. Huffman, Arden Moscati +95 more

Assessing the contribution of rare variants to complex trait heritability from whole-genome sequence data

Nature Genetics(2022)10.1038/s41588-021-00997-7

N/A

7.2DataRank · unranked

363 citations

Deepti Jain, Zhili Zheng, TOPMed Anthropometry Working Group, Stella Aslibekyan, Diane M. Becker +95 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

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

Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference

Nature Genetics(2024)10.1038/s41588-023-01596-4

Top 9%

2.4DataRank

Top 9%176 citations

Georgina Navoly, Olga Giannakopoulou, Daniel F. Levey, Dóra Koller, Gita A. Pathak +76 more

Multiancestry Genome-Wide Association Study of Aortic Stenosis Identifies Multiple Novel Loci in the Million Veteran Program

Circulation(2023)10.1161/circulationaha.122.061451

N/A

1.9DataRank · unranked

73 citations

Gina M. Peloso, Jason Linefsky, Jayashri Aragam, Ashley Galloway, Vidisha Tanukonda +21 more

Whole genome sequence analysis of blood lipid levels in >66,000 individuals

Nature Communications(2022)10.1038/s41467-022-33510-7

N/A

1.6DataRank · unranked

75 citations

Xihao Li, Zilin Li, Akhil Pampana, David Zhang, Joseph Park +95 more

Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts

Diabetes Care(2022)10.2337/dc21-1395

N/A

1.6DataRank · unranked

68 citations

Jessica LeClair, Joanne B. Cole, Chloé Sarnowski, Fariba Ahmadizar, Lawrence F. Bielak +48 more

Genetic Studies of Leptin Concentrations Implicate Leptin in the Regulation of Early Adiposity

Diabetes(2020)10.2337/db20-0070

N/A

1.5DataRank · unranked

57 citations

Yiying Zhang, Cassandra N. Spracklen, Tugce Karaderi, Lam Opal Huang, Jonathan P. Bradfield +95 more

Host genetic effects in pneumonia

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.12.010

N/A

1.2DataRank · unranked

43 citations

Douglas M. Shaw, Lauren E. Petty, Misa Graff, Ryan J. Bohlender, Hannah G. Polikowsky +13 more

The trans-ancestral genomic architecture of glycemic traits

Nature Genetics(2021)10.1038/s41588-021-00852-9

N/A

1.0DataRank · unranked

907 citations

Cassandra N. Spracklen, Gaëlle Marenne, Arushi Varshney, Laura J. Corbin, Jian’an Luan +95 more

The Polygenic and Monogenic Basis of Blood Traits and Diseases

Cell(2020)10.1016/j.cell.2020.08.008

N/A

0.988DataRank · unranked

722 citations

Erik L. Bao, Parsa Akbari, Caleb A. Lareau, Abdou Mousas, Tao Jiang +95 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

Structural variation across 138,134 samples in the TOPMed consortium

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.25.525428

Top 27%

0.737DataRank

Top 27%18 citations

Adam C. English, Ginger Metcalf, Jianzhi Yang, Mark J. P. Chaisson, Nathan Pankratz +82 more

Whole genome sequence analysis of platelet traits in the NHLBI Trans-Omics for Precision Medicine (TOPMed) initiative

Human Molecular Genetics(2021)10.1093/hmg/ddab252

Top 28%

0.724DataRank

Top 28%20 citations

Yao Hu, Quan Sun, Deepti Jain, Jai Broome, Ming‐Huei Chen +62 more

Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

Cell Genomics(2023)10.1016/j.xgen.2022.100241

N/A

0.710DataRank · unranked

113 citations

Shinichi Namba, Esteban A. Lopera-Maya, Sini Kerminen, Kristin Tsuo, Kristi Läll +83 more

Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing

Nature Genetics(2023)10.1038/s41588-023-01553-1

N/A

0.681DataRank · unranked

31 citations

Ying Zhou, Adrienne M. Stilp, Jason Bacon, Justin Wong, Zuhal Özcan +46 more

Meta-analysis fine-mapping is often miscalibrated at single-variant resolution

Cell Genomics(2022)10.1016/j.xgen.2022.100210

N/A

0.670DataRank · unranked

86 citations

Roy Elzur, Wei Zhou, Kuan-Han Wu, Humaira Rasheed, Kristin Tsuo +91 more

Polygenic prediction of body mass index and obesity through the life course and across ancestries

Nature Medicine(2025)10.1038/s41591-025-03827-z

N/A

0.665DataRank · unranked

34 citations

Kaitlin H Wade, Qin Hui, Joshua Arias, Xianyong Yin, Malene R. Christiansen +95 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

0.628DataRank · unranked

28 citations

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

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

Nature Communications(2022)10.1038/s41467-022-32821-z

N/A

0.596DataRank · unranked

52 citations

Najim Lahrouchi, Aaron Isaacs, ThuyVy Duong, Luisa Foco, Farah Ahmed +95 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

Rare variant contribution to the heritability of coronary artery disease

Nature Communications(2024)10.1038/s41467-024-52939-6

N/A

0.513DataRank · unranked

16 citations

Shoa L. Clarke, Gaëlle Auguste, Natalie R. Hasbani, Alanna C. Morrison, Adam S. Heath +95 more

Whole-genome sequencing in diverse subjects identifies genetic correlates of leukocyte traits: The NHLBI TOPMed program

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.08.007

N/A

0.494DataRank · unranked

26 citations

Caitlin McHugh, Linda M. Polfus, Laura M. Raffield, Meher Preethi Boorgula, Thomas W. Blackwell +88 more

An integrative framework to prioritize genes in more than 500 loci associated with body mass index

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.04.016

N/A

0.489DataRank · unranked

25 citations

Victor Svenstrup, Virginia Diez Obrero, Michael Preuß, Arden Moscati, Joel N. Hirschhorn +2 more

Multi-ethnic genome-wide association analyses of white blood cell and platelet traits in the Population Architecture using Genomics and Epidemiology (PAGE) study

BMC Genomics(2021)10.1186/s12864-021-07745-5

N/A

0.477DataRank · unranked

23 citations

Stephanie A. Bien, Katherine K. Nishimura, Jeffrey Haessler, Chani J. Hodonsky, Antoine Baldassari +29 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

Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed whole-genome sequencing study

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.09.003

N/A

0.416DataRank · unranked

15 citations

Margaret Sunitha Selvaraj, Xihao Li, Zilin Li, Jacob A. Holdcraft, Donna K. Arnett +69 more

The contribution of functional HNF1A variants and polygenic susceptibility to risk of type 2 diabetes in ancestrally diverse populations

Diabetologia(2022)10.1007/s00125-022-05806-2

Top 46%

0.399DataRank

Top 46%8 citations

Michael Preuß, Roelof A. J. Smit, Nathalie Chami, Lise Bjørkhaug, Ingvild Aukrust +3 more

Whole genome sequencing association analysis of quantitative red blood cell phenotypes: the NHLBI TOPMed program

medRxiv(2020)10.1101/2020.12.09.20246736

N/A

0.360DataRank · unranked

10 citations

Adrienne M. Stilp, Caitlin McHugh, Shuquan Rao, Deepti Jain, Xiuwen Zheng +74 more

Structural variation across 138,134 samples in the TOPMed consortium

Research Square(2023)10.21203/rs.3.rs-2515453/v1

N/A

0.345DataRank · unranked

9 citations

Adam C. English, Ginger Metcalf, Jianzhi Yang, Mark J. P. Chaisson, Nathan Pankratz +82 more

Ancestral diversity in lipoprotein(a) studies helps address evidence gaps

Open Heart(2023)10.1136/openhrt-2023-002382

N/A

0.345DataRank · unranked

9 citations

Sofia F. Dimos, Laura M. Raffield, Zhe Wang, Anna F Ballou, Carolina G Downie +29 more

Multi-ancestry GWAS of major depression aids locus discovery, fine-mapping, gene prioritisation, and causal inference

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.07.20.500802

Top 54%

0.311DataRank

Top 54%4 citations

Georgina Navoly, Olga Giannakopoulou, Daniel F. Levey, Dóra Koller, Gita A. Pathak +71 more

Whole genome sequencing identifies common and rare structural variants contributing to hematologic traits in the NHLBI TOPMed program

medRxiv(2021)10.1101/2021.12.16.21267871

N/A

0.292DataRank · unranked

6 citations

Adrienne M. Stilp, Shuquan Rao, Bjarni V. Halldórsson, Doruk Beyter, Jia Wen +54 more

Whole genome sequence analysis of blood lipid levels in >66,000 individuals

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.10.11.463514

N/A

0.277DataRank · unranked

3 citations

Xihao Li, Zilin Li, Akhil Pampana, David Y Zhang, Joseph Park +80 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

Whole genome sequencing analysis of body mass index identifies novel African ancestry-specific risk allele

Nature Communications(2025)10.1038/s41467-025-58420-2

N/A

0.269DataRank · unranked

5 citations

Jennifer A. Brody, Mariaelisa Graff, Heather M. Highland, Nathalie Chami, Hanfei Xu +93 more

Mosaic chromosomal alterations in blood across ancestries via whole-genome sequencing

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.11.07.515222

N/A

0.208DataRank · unranked

3 citations

Ying Zhou, Adrienne M. Stilp, Jason Bacon, Justin Wong, Zuhal Özcan +41 more

WHOLE GENOME SEQUENCING ANALYSIS OF BODY MASS INDEX IDENTIFIES NOVEL AFRICAN ANCESTRY-SPECIFIC RISK ALLELE

medRxiv(2023)10.1101/2023.08.21.23293271

N/A

0.165DataRank · unranked

2 citations

Jennifer A. Brody, Mariaelisa Graff, Heather M. Highland, Nathalie Chami, Hanfei Xu +95 more

Rare variants in long non-coding RNAs are associated with blood lipid levels in the TOPMed Whole Genome Sequencing Study

medRxiv(2023)10.1101/2023.06.28.23291966

N/A

0.146DataRank · unranked

1 citations

Margaret Sunitha Selvaraj, Xihao Li, Zilin Li, Jacob A. Holdcraft, Donna K. Arnett +69 more

Polygenic risk scores lack prognostic value for adults with severe mental illness

medRxiv(2021)10.1101/2021.03.19.21253906

N/A

0.104DataRank · unranked

1 citations

Deepak Kaji, Liam Cotter, Tielman Van Vleck, Gillian M. Belbin, Michael Preuß +20 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

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

The role of polygenic susceptibility to obesity among carriers of pathogenic mutations in MC4R in the UK Biobank population

PLoS Medicine(2020)10.1371/journal.pmed.1003196

N/A

0DataRank · unranked

88 citations

Michael Preuß, Ryan W. Walker, Arden Moscati, Ruth J. F. Loos, Nathalie Chami

Evidence of Novel Susceptibility Variants for Prostate Cancer and a Multiancestry Polygenic Risk Score Associated with Aggressive Disease in Men of African Ancestry

European Urology(2023)10.1016/j.eururo.2023.01.022

N/A

0DataRank · unranked

51 citations

Ravi Madduri, Alex A Rodriguez, Burcu F. Darst, Alisha Chou, Xin Sheng +95 more

BridgePRS leverages shared genetic effects across ancestries to increase polygenic risk score portability

Nature Genetics(2023)10.1038/s41588-023-01583-9

N/A

0DataRank · unranked

52 citations

Shing Wan Choi, Judit García‐González, Tade Souaiaia, Michael Preuß, Paul F. O’Reilly +1 more

A large‐scale transcriptome‐wide association study (TWAS) of 10 blood cell phenotypes reveals complexities of TWAS fine‐mapping

Genetic Epidemiology(2021)10.1002/gepi.22436

N/A

0DataRank · unranked

6 citations

Bryce Rowland, Jonathan D. Rosen, Michael Preuß, Kris Young, Misa Graff +14 more

Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies

Journal of Human Genetics(2021)10.1038/s10038-021-00968-0

N/A

0DataRank · unranked

55 citations

Misa Graff, Bryce Rowland, Jia Wen, Le Huang, Tyne W. Miller‐Fleming +14 more

Genetic subtyping of obesity reveals biological insights into the uncoupling of adiposity from its cardiometabolic comorbidities

Nature Medicine(2025)10.1038/s41591-025-03931-0

N/A

0DataRank · unranked

22 citations

Zhe Wang, Victor Svenstrup, Virginia Diez Obrero, Daiane Hemerich, Yi Huang +14 more

Distinguishing clinical and genetic risk factors for suicidal ideation and behavior in a diverse hospital population

Translational Psychiatry(2025)10.1038/s41398-025-03287-6

N/A

0DataRank · unranked

8 citations

Lauren Lepow, Brian Fennessy, Nakao Iwata, Masashi Ikeda, Takeo Saito +7 more

Whole genome sequencing identifies structural variants contributing to hematologic traits in the NHLBI TOPMed program

Nature Communications(2022)10.1038/s41467-022-35354-7

N/A

0DataRank · unranked

18 citations

Adrienne M. Stilp, Shuquan Rao, Bjarni V. Halldórsson, Doruk Beyter, Jia Wen +54 more

Mosaic chromosomal alterations in blood across ancestries using whole-genome sequencing

UNC Libraries(2025)10.17615/mztm-gw84

N/A

0DataRank · unranked

0 citations

Margaret F. Doyle, Jason Bacon, Xiaolong Ma, Nathan Pankratz, Ramachandran S. Vasan +46 more

Branched chain amino acids harbor distinct and often opposing effects on health and disease

Communications Medicine(2023)10.1038/s43856-023-00382-x

N/A

0DataRank · unranked

7 citations

Annie Green Howard, Harold Lee, Carolina G Downie, Moa P. Lee, Sarah H. Koenigsberg +8 more

Michael Preuß

Indexed papers

Top data-sharing exemplar

Papers