Steven A. McCarroll, Ph.D.
Affiliations: | 2004 | University of California, San Francisco, San Francisco, CA |
Area:
Molecular Biology, GeneticsGoogle:
"Steven McCarroll"
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Publications
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| Genovese G, Rockweiler NB, Gorman BR, et al. (2024) BCFtools/liftover: an accurate and comprehensive tool to convert genetic variants across genome assemblies. Bioinformatics (Oxford, England). 40 |
| Tegtmeyer M, Arora J, Asgari S, et al. (2024) High-dimensional phenotyping to define the genetic basis of cellular morphology. Nature Communications. 15: 347 |
| Maury EA, Sherman MA, Genovese G, et al. (2023) Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent and disruptions. Cell Genomics. 3: 100356 |
| Mukamel RE, Handsaker RE, Sherman MA, et al. (2023) Repeat polymorphisms underlie top genetic risk loci for glaucoma and colorectal cancer. Cell |
| Hujoel MLA, Handsaker RE, Sherman MA, et al. (2023) Hidden protein-altering variants influence diverse human phenotypes. Biorxiv : the Preprint Server For Biology |
| Weiner DJ, Ling E, Erdin S, et al. (2022) Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p. Nature Genetics |
| Hanks SC, Forer L, Schönherr S, et al. (2022) Extent to which array genotyping and imputation with large reference panels approximate deep whole-genome sequencing. American Journal of Human Genetics |
| Trubetskoy V, Pardiñas AF, Qi T, et al. (2022) Mapping genomic loci implicates genes and synaptic biology in schizophrenia. Nature |
| Singh T, Poterba T, Curtis D, et al. (2022) Rare coding variants in ten genes confer substantial risk for schizophrenia. Nature |
| Merkle FT, Ghosh S, Genovese G, et al. (2022) Whole-genome analysis of human embryonic stem cells enables rational line selection based on genetic variation. Cell Stem Cell |