Michael Wigler
Affiliations: | Cold Spring Harbor Laboratory, Cold Spring Harbor, NY |
Area:
Cancer, Molecular BiologyGoogle:
"Michael Wigler"Mean distance: 13.72 (cluster 11) | S | N | B | C | P |
Cross-listing: Chemistry Tree
Parents
Sign in to add mentor| Richard Axel | grad student | CSHL | |
| I. Bernard Weinstein | research scientist | Columbia |
Children
Sign in to add trainee| takashi toda | grad student | (PombeTree) | |
| Javor P. Stolarov | grad student | 2000 | Columbia |
| Mitchell Goldfarb | post-doc | ||
| Linda Van Aelst | post-doc | ||
| Dallan Young | post-doc | CSHL (Cell Biology Tree) | |
| Elizabeth Jane Taparowsky | post-doc | 1981-1984 | CSHL |
| Ira M. Hall | post-doc | 2004-2004 | CSHL |
BETA: Related publications
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Publications
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| Yoon S, Munoz A, Yamrom B, et al. (2021) Rates of contributory de novo mutation in high and low-risk autism families. Communications Biology. 4: 1026 |
| Miyabayashi K, Baker LA, Deschenes A, et al. (2020) Intraductal transplantation models of human pancreatic ductal adenocarcinoma reveal progressive transition of molecular subtypes. Cancer Discovery |
| Baslan T, Kendall J, Volyanskyy K, et al. (2020) Novel insights into breast cancer copy number genetic heterogeneity revealed by single-cell genome sequencing. Elife. 9 |
| Vasudevan A, Baruah PS, Smith JC, et al. (2020) Single-Chromosomal Gains Can Function as Metastasis Suppressors and Promoters in Colon Cancer. Developmental Cell. 52: 413-428.e6 |
| Li S, Kendall J, Park S, et al. (2019) Copolymerization of single cell nucleic acids into balls of acrylamide gel. Genome Research |
| Kumar V, Rosenbaum J, Wang Z, et al. (2017) Partial bisulfite conversion for unique template sequencing. Nucleic Acids Research |
| Krasnitz A, Kendall J, Alexander J, et al. (2017) Early Detection of Cancer in Blood Using Single-Cell Analysis: A Proposal. Trends in Molecular Medicine |
| Fang H, Bergmann EA, Arora K, et al. (2016) Indel variant analysis of short-read sequencing data with Scalpel. Nature Protocols. 11: 2529-2548 |
| Wang Z, Andrews P, Kendall J, et al. (2016) SMASH, a fragmentation and sequencing method for genomic copy number analysis. Genome Research |
| Iossifov I, Levy D, Allen J, et al. (2015) Low load for disruptive mutations in autism genes and their biased transmission. Proceedings of the National Academy of Sciences of the United States of America |