Michael C. Zody

75.9k total citations · 2 hit papers
56 papers, 6.0k citations indexed

About

Michael C. Zody is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Michael C. Zody has authored 56 papers receiving a total of 6.0k indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Molecular Biology, 28 papers in Genetics and 14 papers in Plant Science. Recurrent topics in Michael C. Zody's work include Genomics and Phylogenetic Studies (18 papers), Genomics and Rare Diseases (12 papers) and Chromosomal and Genetic Variations (11 papers). Michael C. Zody is often cited by papers focused on Genomics and Phylogenetic Studies (18 papers), Genomics and Rare Diseases (12 papers) and Chromosomal and Genetic Variations (11 papers). Michael C. Zody collaborates with scholars based in United States, Sweden and United Kingdom. Michael C. Zody's co-authors include Kerstin Lindblad‐Toh, Mark J. Daly, Steven A. McCarroll, Eric S. Lander, David Altshuler, Claire M. Wade, Leif Andersson, Edward J. Kulbokas, Matthew R. Henn and Xiao Yang and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Michael C. Zody

55 papers receiving 6.0k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Whole-genome resequencing reveals loci under selection during chicken domestication

2010 761 citations Michael C. Zody, Kerstin Lindblad‐Toh et al. Nature profile →
Common deletion polymorphisms in the human genome

2005 527 citations Michael C. Zody, Mark J. Daly et al. Nature Genetics profile →

Peers

Michael C. Zody

GENET

IMMUN

Robert M. Davies United Kingdom

Andrew Whitwham United Kingdom

Xavier Messeguer Spain

Martin Pollard United States

John Marshall United Kingdom

Valeriu Ohan United Kingdom

Konrad Scheffler South Africa

Merete Fredholm Denmark

Alan Archibald United Kingdom

Bernhard Hirt Germany

Robert M. Davies United Kingdom

Michael C. Zody

2.0k ×0.7

GENET

3.8k ×1.4

1.5k ×1.2

381 ×0.7

IMMUN

569 ×1.1

Citations per year, relative to Michael C. Zody Michael C. Zody (= 1×) peers Robert M. Davies

Countries citing papers authored by Michael C. Zody

Since Specialization

Citations

This map shows the geographic impact of Michael C. Zody's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Michael C. Zody with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael C. Zody more than expected).

Fields of papers citing papers by Michael C. Zody

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael C. Zody. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Michael C. Zody. The network helps show where Michael C. Zody may publish in the future.

Co-authorship network of co-authors of Michael C. Zody

This figure shows the co-authorship network connecting the top 25 collaborators of Michael C. Zody. A scholar is included among the top collaborators of Michael C. Zody based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Michael C. Zody. Michael C. Zody is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Ceroni, Fabiola, Paola Visconti, Annio Posar, et al.. (2024). Genomic analysis of 116 autism families strengthens known risk genes and highlights promising candidates. npj Genomic Medicine. 9(1). 21–21. 10 indexed citations

Boldrini, Maura, Yang Xiao, Tarjinder Singh, et al.. (2024). Omics Approaches to Investigate the Pathogenesis of Suicide. Biological Psychiatry. 96(12). 919–928. 2 indexed citations

Mediavilla, José R., Annie Lee, Michael C. Zody, et al.. (2023). Molecular and Clinical Epidemiology of SARS-CoV-2 Infection among Vaccinated and Unvaccinated Individuals in a Large Healthcare Organization from New Jersey. Viruses. 15(8). 1699–1699. 4 indexed citations

Ebler, Jana, Peter Ebert, Wayne E. Clarke, et al.. (2022). Pangenome-based genome inference allows efficient and accurate genotyping across a wide spectrum of variant classes. Nature Genetics. 54(4). 518–525. 110 indexed citations

Musunuri, Rajeeva, Kanika Arora, André Corvelo, et al.. (2020). Somatic variant analysis of linked-reads sequencing data with Lancet. Bioinformatics. 37(13). 1918–1919. 1 indexed citations

Abel, Haley, David E. Larson, Allison Regier, et al.. (2020). Mapping and characterization of structural variation in 17,795 human genomes. Nature. 583(7814). 83–89. 148 indexed citations

Regier, Allison, Yossi Farjoun, David E. Larson, et al.. (2018). Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects. Nature Communications. 9(1). 4038–4038. 73 indexed citations

Fang, Han, Ewa A. Bergmann, Kanika Arora, et al.. (2016). Indel variant analysis of short-read sequencing data with Scalpel. Nature Protocols. 11(12). 2529–2548. 77 indexed citations

Li, Jonathan Z., Brad Chapman, Patrick Charlebois, et al.. (2014). Comparison of Illumina and 454 Deep Sequencing in Participants Failing Raltegravir-Based Antiretroviral Therapy. PLoS ONE. 9(3). e90485–e90485. 23 indexed citations

10.

Yang, Xiao, et al.. (2013). V-Phaser 2: variant inference for viral populations. BMC Genomics. 14(1). 674–674. 68 indexed citations

11.

Newman, Ruchi M., Thomas Kuntzen, Brian Weiner, et al.. (2012). Whole Genome Pyrosequencing of Rare Hepatitis C Virus Genotypes Enhances Subtype Classification and Identification of Naturally Occurring Drug Resistance Variants. The Journal of Infectious Diseases. 208(1). 17–31. 29 indexed citations

12.

Yang, Xiao, Patrick Charlebois, Sante Gnerre, et al.. (2012). De novo assembly of highly diverse viral populations. BMC Genomics. 13(1). 475–475. 135 indexed citations

13.

Grabherr, Manfred, Evan Mauceli, Wolfgang Ernst, et al.. (2011). Exploiting Nucleotide Composition to Engineer Promoters. PLoS ONE. 6(5). e20136–e20136. 19 indexed citations

14.

Raffaele, Sylvain, Rhys A. Farrer, Liliana M. Cano, et al.. (2010). Genome Evolution Following Host Jumps in the Irish Potato Famine Pathogen Lineage. Science. 330(6010). 1540–1543. 303 indexed citations

15.

Schornack, Sebastián, Edgar Huitema, Liliana M. Cano, et al.. (2009). Ten things to know about oomycete effectors. Molecular Plant Pathology. 10(6). 795–803. 125 indexed citations

16.

Wade, Claire M., Elinor K. Karlsson, Tarjei S. Mikkelsen, Michael C. Zody, & Kerstin Lindblad‐Toh. (2006). 11 The Dog Genome: Sequence, Evolution, and Haplotype Structure. Cold Spring Harbor Monograph Archive. 44. 179–207. 5 indexed citations

17.

Hellmann, Ines, Kay Prüfer, Hongkai Ji, et al.. (2005). Why do human diversity levels vary at a megabase scale?. Genome Research. 15(9). 1222–1231. 126 indexed citations

18.

Taylor, James, Svitlana Tyekucheva, Michael C. Zody, Francesca Chiaromonte, & Kateryna D. Makova. (2005). Strong and Weak Male Mutation Bias at Different Sites in the Primate Genomes: Insights from the Human-Chimpanzee Comparison. Molecular Biology and Evolution. 23(3). 565–573. 69 indexed citations

19.

Jaffe, David B., Jonathan A. Butler, Sante Gnerre, et al.. (2003). Whole-Genome Sequence Assembly for Mammalian Genomes: Arachne 2. Genome Research. 13(1). 91–96. 165 indexed citations

20.

Wade, Claire M., Edward J. Kulbokas, Andrew Kirby, et al.. (2002). The mosaic structure of variation in the laboratory mouse genome. Nature. 420(6915). 574–578. 362 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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