G
Gad Getz
Researcher at Broad Institute
Publications - 627
Citations - 309042
Gad Getz is an academic researcher from Broad Institute. The author has contributed to research in topics: Cancer & Biology. The author has an hindex of 189, co-authored 520 publications receiving 247560 citations. Previous affiliations of Gad Getz include University of Colorado Denver & University of California, San Diego.
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Journal ArticleDOI
Regulation of Transient Site-specific Copy Gain by MicroRNA
TL;DR: It is demonstrated that KDM4A is regulated by hSA-mir-23a-3p, hsa-Mir-23b-3 p, and hsa -mir-137, which are identified as regulators of TSSG and copy gains of a drug resistance gene.
Journal ArticleDOI
Rare Germline Variants in ATM Are Associated with Chronic Lymphocytic Leukemia
Grace Tiao,Ma. Reina Improgo,Ma. Reina Improgo,Ma. Reina Improgo,Siddha Kasar,Siddha Kasar,Siddha Kasar,Weijie Poh,Weijie Poh,Weijie Poh,Atanas Kamburov,Dan-Avi Landau,Dan-Avi Landau,Dan-Avi Landau,Eugen Tausch,Amaro Taylor-Weiner,Carrie Cibulskis,Samira Bahl,Stacey M. Fernandes,Kevin Hoang,Esther Rheinbay,Haesook T. Kim,Jasmin Bahlo,Sandra Robrecht,Kirsten Fischer,Michael Hallek,Stacey Gabriel,Eric S. Lander,Stephan Stilgenbauer,Catherine J. Wu,Catherine J. Wu,Catherine J. Wu,Adam Kiezun,Gad Getz,Gad Getz,Jennifer R. Brown,Jennifer R. Brown,Jennifer R. Brown +37 more
TL;DR: It is hypothesized that CLL heritability might arise from rare coding variants not analyzed in previous studies, which are largely unexplained by traditional linkage or genome-wide association studies.
Journal ArticleDOI
Diverse mutational landscapes in human lymphocytes
Heather E. Machado,Emily G. Mitchell,Nina F. Øbro,Kirsten Kübler,Megan Davies,Daniel Leongamornlert,Alyssa Cull,Francesco Lauria,Mathijs A. Sanders,Alex Cagan,Craig M. McDonald,Miriam Belmonte,Mairi Shepherd,Felipe A. Vieira Braga,Robert Osborne,Krishnaa T. Mahbubani,Inigo Martincorena,Elisa Laurenti,Anthony R. Green,Gad Getz,Paz Polak,Kourosh Saeb-Parsy,Daniel J. Hodson,David G. Kent,Peter J. Campbell +24 more
TL;DR: In this paper , the authors sequenced whole genomes from 717 normal naive and memory B and T cells and haematopoietic stem cells and found that all lymphocyte subsets carried more point mutations and structural variants than stem cells, with higher burdens in memory cells than in naive cells and with T cells accumulating mutations at a higher rate throughout life.
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Quantification of somatic mutation flow across individual cell division events by lineage sequencing.
Yehuda Brody,Robert J. Kimmerling,Yosef E. Maruvka,David Benjamin,Joshua J Elacqua,Joshua J Elacqua,Nicholas J. Haradhvala,Jaegil Kim,Kent W. Mouw,Kent W. Mouw,Kristjana Frangaj,Amnon Koren,Gad Getz,Scott R. Manalis,Paul C. Blainey,Paul C. Blainey +15 more
TL;DR: Lineage sequencing is presented, a new genome sequencing approach that enables somatic event reconstruction by providing quality somatic mutation call sets with resolution as high as the single-cell level in subject lineages and shows that mutations arrive with nonuniform probability across sublineages and that DNA lesion dynamics may cause strong correlations between certain mutations.
Journal ArticleDOI
Accurate estimation of homologue-specific DNA concentration-ratios in cancer samples allows long-range haplotyping
TL;DR: The ability to directly determine haplotypes from cancer samples represents an opportunity to expand reference panels of phased chromosomes, which may have general interest in various population genetic applications and may be exploited to interrogate the relationship between germline risk and cancer phenotype with greater sensitivity than is possible using unphased genotype.