Michael C. Zody

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

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

80.1Author DataRank

Indexed papers

18in 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 18 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.

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

Nature(2007)10.1038/nature05874

Top 1%

12.9DataRank

Top 1%5277 citations

J Stamatoyannopoulos, Simon G. Gregory, T Gingeras, Eoghan Harrington, Zhiping Weng +286 more

Papers

Driven by 48 papers — median percentile 92. Top paper: “Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project”.

Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

Nature(2007)10.1038/nature05874

Top 1%

12.9DataRank

Top 1%5277 citations

J Stamatoyannopoulos, Simon G. Gregory, T Gingeras, Eoghan Harrington, Zhiping Weng +286 more

Initial sequencing and comparative analysis of the mouse genome

Nature(2002)10.1038/nature01262

Top 1%

12.6DataRank

Top 1%7282 citations

Robert H. Waterston, Kerstin Lindblad‐Toh, Julien Lagarde, Josep F. Abril, PANKAJ AGARWAL +189 more

Genome sequence, comparative analysis and haplotype structure of the domestic dog

Nature(2005)10.1038/nature04338

Top 2%

9.2DataRank

Top 2%2636 citations

Claire M. Wade, Tarjei S. Mikkelsen, Elinor K. Karlsson, David B. Jaffe, Michael Kamal +46 more

Genome duplication in the teleost fish Tetraodon nigroviridis reveals the early vertebrate proto-karyotype

Nature(2004)10.1038/nature03025

Top 2%

7.8DataRank

Top 2%2027 citations

Jean-Marc Aury, Frédéric Brunet, Jean-Louis Petit, Nicole Stange-Thomann, Evan Mauceli +69 more

A high-resolution map of human evolutionary constraint using 29 mammals

Nature(2011)10.1038/nature10530

Top 2%

7.6DataRank

Top 2%1227 citations

Genome Institute at Washington University, Manuel Garber, Or Zuk, Alireza Heravi-Moussavi, Wouter Meuleman +49 more

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

Nature Communications(2018)10.1038/s41467-018-06159-4

Top 3%

6.6DataRank

Top 3%260 citations

Yossi Farjoun, Ilya Shlyakhter, Olga Krasheninina, Hyun Min Kang, Daniel P. Howrigan +16 more

High-coverage whole-genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios

Cell(2022)10.1016/j.cell.2022.08.004

Top 3%

6.3DataRank

Top 3%1056 citations

Uday S. Evani, Xuefang Zhao, Anna O. Basile, Haley Abel, Allison A. Regier +37 more

Haplotype-resolved diverse human genomes and integrated analysis of structural variation

Science(2021)10.1126/science.abf7117

Top 4%

5.7DataRank

Top 4%812 citations

Peter A. Audano, Qihui Zhu, Bernardo Rodríguez–Martín, David Porubsky, Marc Jan Bonder +60 more

High coverage whole genome sequencing of the expanded 1000 Genomes Project cohort including 602 trios

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.02.06.430068

Top 4%

5.5DataRank

Top 4%260 citations

Uday S. Evani, Xuefang Zhao, Anna O. Basile, Haley Abel, Allison A. Regier +16 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

High-coverage nanopore sequencing of samples from the 1000 Genomes Project to build a comprehensive catalog of human genetic variation

Genome Research(2024)10.1101/gr.279273.124

Top 13%

1.7DataRank

Top 13%78 citations

Sophia B Gibson, Nikhita Damaraju, Miranda Pg Zalusky, Kendra Hoekzema, David Twesigomwe +42 more

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

bioRxiv (Cold Spring Harbor Laboratory)(2018)10.1101/269316

Top 16%

1.3DataRank

Top 16%34 citations

Yossi Farjoun, David Larson, Olga Krasheninina, Hyun Min Kang, Daniel P. Howrigan +19 more

System-wide transcriptome damage and tissue identity loss in COVID-19 patients

Cell Reports Medicine(2022)10.1016/j.xcrm.2022.100522

N/A

1.2DataRank · unranked

51 citations

Jonathan Foox, Tyler Hether, David Danko, Sarah Warren, Youngmi Kim +43 more

Whole-genome characterization of lung adenocarcinomas lacking alterations in the RTK/RAS/RAF pathway

Cell Reports(2021)10.1016/j.celrep.2021.108707

N/A

1.1DataRank · unranked

32 citations

Xiaotong Yao, Siddhartha Devarakonda, Aditya Deshpande, Jeffrey S. Damrauer, Tiago C. Silva +77 more

Complex genetic variation in nearly complete human genomes

Nature(2025)10.1038/s41586-025-09140-6

Top 19%

1.1DataRank

Top 19%83 citations

Peter Ebert, Peter A. Audano, Mark Loftus, David Porubsky, Feyza Yilmaz +62 more

Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing

Nature Genetics(2013)10.1038/ng.2543

N/A

0.862DataRank · unranked

313 citations

Andreas Gnirke, David B. Jaffe, Veronika Barešová, Nathalie Pochet, Brendan Blumenstiel +43 more

Whole-Genome Sequence Assembly for Mammalian Genomes: Arachne 2

Genome Research(2003)10.1101/gr.828403

N/A

0.829DataRank · unranked

251 citations

Jonathan Butler, Sante Gnerre, Evan Mauceli, Kerstin Lindblad-Toh, Jill P. Mesirov +3 more

Multi-omic analysis of Huntington’s disease reveals a compensatory astrocyte state

Nature Communications(2024)10.1038/s41467-024-50626-0

N/A

0.787DataRank · unranked

39 citations

Ji‐Sun Kwon, Christopher Ng, Kelly Jakubiak, Nacoya Madden, Kenneth Ofori +17 more

Complex genetic variation in nearly complete human genomes

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.09.24.614721

Top 27%

0.741DataRank

Top 27%27 citations

Peter Ebert, Peter A. Audano, Mark Loftus, David Porubsky, Feyza Yilmaz +62 more

Omics Approaches to Investigate the Pathogenesis of Suicide

Biological Psychiatry(2024)10.1016/j.biopsych.2024.05.017

N/A

0.473DataRank · unranked

10 citations

Yang Xiao, Tarjinder Singh, Chenxu Zhu, Mbemba Jabbi, Harry Pantazopoulos +16 more

A comprehensive catalog of 3D genome organization in diverse human genomes facilitates understanding of the impact of structural variation on chromatin structure

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.05.15.540856

Top 49%

0.360DataRank

Top 49%5 citations

Marc Jan Bonder, Sabriya A. Syed, HGSVC Functional Analysis Working Group, Michael C. Zody, Mark J. P. Chaisson +7 more

De novo assembly of 64 haplotype-resolved human genomes of diverse ancestry and integrated analysis of structural variation

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.16.423102

Top 53%

0.322DataRank

Top 53%5 citations

Peter A. Audano, Qihui Zhu, Bernardo Rodríguez–Martín, David Porubsky, Marc Jan Bonder +58 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

taxMaps - Ultra-comprehensive and highly accurate taxonomic classification of short-read data in reasonable time

bioRxiv (Cold Spring Harbor Laboratory)(2017)10.1101/134023

N/A

0.208DataRank · unranked

3 citations

Wayne E. Clarke, Nicolas Robine, Michael C. Zody, André Corvelo

FAVOR 2.0: A reengineered functional annotation of variants online resource for interpreting genomic variation

Nucleic Acids Research(2025)10.1093/nar/gkaf1217

Top 72%

0.115DataRank

Top 72%1 citations

Vineet Verma, Xihao Li, Zilin Li, Nicole Shedd, Thomas Cheng Li +12 more

A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucoma

UNC Libraries(2025)10.17615/vb5g-3265

N/A

0DataRank · unranked

0 citations

Adeyinka Ashaye, Radha Ayyagari, Caitlin McHugh, Susan Williams, Qi N. Cui +55 more

Type 2 and interferon inflammation regulate SARS-CoV-2 entry factor expression in the airway epithelium

Nature Communications(2020)10.1038/s41467-020-18781-2

N/A

0DataRank · unranked

196 citations

Peter DeFord, Yingchun Li, Nathan D. Jackson, Michael T. Montgomery, Jamie L. Everman +23 more

Mapping and characterization of structural variation in 17,795 human genomes

Nature(2020)10.1038/s41586-020-2371-0

N/A

0DataRank · unranked

364 citations

David E. Larson, Allison A. Regier, Colby Chiang, Indraniel Das, Krishna Kanchi +13 more

Somatic variant analysis of linked-reads sequencing data with Lancet

Bioinformatics(2020)10.1093/bioinformatics/btaa888

N/A

0DataRank · unranked

5 citations

Kanika Arora, André Corvelo, Minita Shah, Jennifer Shelton, Michael C. Zody +2 more

Type 2 and interferon inflammation strongly regulate SARS-CoV-2 related gene expression in the airway epithelium

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.04.09.034454

N/A

0DataRank · unranked

69 citations

Peter DeFord, Nathan D. Jackson, Michael T. Montgomery, Jamie L. Everman, Cydney Rios +22 more

Pangenome-based genome inference

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.11.378133

N/A

0DataRank · unranked

25 citations

Wayne E. Clarke, Tobias Rausch, Peter A. Audano, Torsten Houwaart, Jan O. Korbel +5 more

De Novo Mutation in an Enhancer of EBF3 in simplex autism

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.08.28.270751

N/A

0DataRank · unranked

2 citations

Tristan J. Hayeck, Brandon J. Mannion, Sumantra Chatterjee, Marta Byrska-Bishop, Rajeeva Musunuri +16 more

Novel KITLG/SCF regulatory variants are associated with lung function in African American children with asthma

medRxiv(2020)10.1101/2020.02.20.20019588

N/A

0DataRank · unranked

0 citations

Satria P. Sajuthi, Jaehyun Joo, Shujie Xiao, Patrick Sleiman, Marquitta J. White +30 more

Somatic variant analysis of linked-reads sequencing data with Lancet

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.07.04.158063

N/A

0DataRank · unranked

0 citations

Kanika Arora, André Corvelo, Minita Shah, Jennifer Shelton, Michael C. Zody +2 more

Comparison of Illumina and 454 Deep Sequencing in Participants Failing Raltegravir-Based Antiretroviral Therapy

UNC Libraries(2020)10.17615/xcnw-dm02

N/A

0DataRank · unranked

0 citations

Hide, Winston, Daniel R. Kuritzkes, Alyssa Jocson Porter, Michael C. Zody, Saran Vardhanabhuti +10 more

Recent ultra-rare inherited variants implicate new autism candidate risk genes

Nature Genetics(2021)10.1038/s41588-021-00899-8

N/A

0DataRank · unranked

144 citations

Tychele N. Turner, Shwetha C. Murali, PingHsun Hsieh, Arvis Sulovari, Tianyun Wang +38 more

Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism

Human Genomics(2021)10.1186/s40246-021-00342-3

N/A

0DataRank · unranked

35 citations

Tristan J. Hayeck, Zhang Cheng, Sumantra Chatterjee, Brandon J. Mannion, Marta Byrska-Bishop +30 more

Pangenome-based genome inference allows efficient and accurate genotyping across a wide spectrum of variant classes

Nature Genetics(2022)10.1038/s41588-022-01043-w

N/A

0DataRank · unranked

290 citations

Peter Ebert, Wayne E. Clarke, Tobias Rausch, Peter A. Audano, Torsten Houwaart +7 more

Nasal airway transcriptome-wide association study of asthma reveals genetically driven mucus pathobiology

Nature Communications(2022)10.1038/s41467-022-28973-7

N/A

0DataRank · unranked

57 citations

Jamie L. Everman, Nathan D. Jackson, Benjamin Saef, Cydney Rios, Camille M. Moore +20 more

Accounting for population structure in genetic studies of cystic fibrosis

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100117

N/A

0DataRank · unranked

6 citations

Adrienne M. Stilp, William W. Gordon, Jai Broome, Stephanie M. Gogarten, Hua Ling +20 more

Whole genome error-corrected sequencing for sensitive circulating tumor DNA cancer monitoring

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.11.17.516904

N/A

0DataRank · unranked

9 citations

Adam J. Widman, Anushri Arora, Itai Rusinek, William F. Hooper, Rebecca L. Murray +30 more

A multi-cohort genome-wide association study in African ancestry individuals reveals risk loci for primary open-angle glaucoma

Cell(2024)10.1016/j.cell.2023.12.006

N/A

0DataRank · unranked

71 citations

Harini V. Gudiseva, Venkata Ramana Murthy Chavali, Rebecca Salowe, Yuki Bradford, Lindsay Guare +53 more

Rare genetic variation in fibronectin 1 (FN1) protects against APOEε4 in Alzheimer’s disease

Acta Neuropathologica(2024)10.1007/s00401-024-02721-1

N/A

0DataRank · unranked

52 citations

Tamil Iniyan Gunasekaran, Michaël E. Belloy, Dolly Reyes‐Dumeyer, Dörthe Jülich, Hüseyin Tayran +25 more

Impact and characterization of serial structural variations across humans and great apes

Nature Communications(2024)10.1038/s41467-024-52027-9

N/A

0DataRank · unranked

12 citations

Tobias Rausch, Michael Jendrusch, Hufsah Ashraf, Peter A. Audano, Ola Austine +49 more

An integrative TAD catalog in lymphoblastoid cell lines discloses the functional impact of deletions and insertions in human genomes

Genome Research(2024)10.1101/gr.279419.124

N/A

0DataRank · unranked

2 citations

Marc Jan Bonder, Sabriya A. Syed, Matthew Jensen, HGSVC Functional Analysis Working Group, Mark Gerstein +9 more

Mapping and characterization of structural variation in 17,795 human genomes

UNC Libraries(2024)10.17615/bjv3-ys88

Top 100%

0DataRank

Top 100%0 citations

S.S. Rich, Elizabeth L. Appelbaum, Ryan M. Layer, Subra Kugathasan, Scott M. Damrauer +95 more

A rare genetic variant confers resistance to neurodegeneration across multiple neurological disorders by augmenting selective autophagy

Neuron(2025)10.1016/j.neuron.2025.08.018

N/A

0DataRank · unranked

5 citations

Christopher Ng, Serhiy Pankiv, Eddy Albarran, Peter Langfelder, Ana Ramos de Jesus +17 more

Structural and transduction patterns of human-specific polymorphic SVA insertions

Mobile DNA(2025)10.1186/s13100-025-00373-w

N/A

0DataRank · unranked

1 citations

Mark Loftus, Emily C. Golba, Haley Abel, Hufsah Ashraf, Peter A. Audano +64 more

Michael C. Zody

Indexed papers

Top data-sharing exemplar

Papers