Author

Tom W. Blackwell

University of Michigan

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Genomics· 2 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Organism:human· 3 Approach:statistical model· 3 Assay:whole-genome sequencing· 3 Research Focus:variant effect prediction· 2 Research Focus:variant calling· 1

Frequent Co-Authors

Albert V. SmithiD· 3 shared Alex P. ReineriD· 3 shared Donna K. ArnettiD· 3 shared Jennifer A. SmithiD· 3 shared Jerome I. RotteriD· 3 shared Patricia A. PeyseriD· 3 shared Rasika A. MathiasiD· 3 shared Stephen S. RichiD· 3 shared

Activity by Year

2019-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersGenomics

Albert V. SmithORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Genomic and phenotypic correlates of mosaic loss of chromosome Y in blood

Yasminka A. Jakubek, Xiaolong Ma, Adrienne M. Stilp, Fulong Yu, Jason Bacon, Justin Wong, François Aguet, Kristin Ardlie, Donna K. Arnett, Kathleen Barnes, Joshua C. Bis, Tom W. Blackwell, Lewis C. Becker, Eric Boerwinkle, Russell Paul Bowler, , Paul Livermore Auer

The paper identifies genetic and phenotypic correlates of mosaic loss of chromosome Y in blood using whole genome sequencing data from the TOPMed program.

The American Journal of Human Genetics · Jan 13, 2025Peer-reviewedGenetic & Genomic Medicine

Structural variation across 138,134 samples in the TOPMed consortium

Goo Jun, Adam C. English, Ginger Metcalf, Jianzhi Yang, Mark Chaisson, Nathan Pankratz, Vipin K. Menon, William J. Salerno, Olga A. Krasheninina, Albert V. Smith, John Lane, Tom W. Blackwell, Hyun Min Kang, Sejal Salvi, Qingchang Meng, , Fritz Joachim Sedlazeck

The paper presents a comprehensive catalog of structural variants across 138,134 individuals, identifying novel variants and their associations with cardio-metabolic and hematologic traits.

bioRxiv · Jan 25, 2023 · PreprintGenomics

Loss-of-function genomic variants with impact on liver-related blood traits highlight potential therapeutic targets for cardiovascular disease

Jonas Bille Nielsen, Oren Rom, Ida L. Surakka, Sarah E. Graham, Wei Zhou, Lars G. Fritsche, Sarah A. Gagliano Taliun, Carlo Sidore, Yuhao Liu, Maiken Elvestad Gabrielsen, Anne Heidi Skogholt, Brooke N. Wolford, William Overton, Whitney Hornsby, Akua Acheampong, , Y. Eugene Chen

The paper identifies loss-of-function variants affecting liver-related blood traits that reduce CVD risk without increasing metabolic disease risk, highlighting potential therapeutic targets.

bioRxiv · Apr 2, 2019 · PreprintGenomics