High-throughput mapping of 6,888 <i>RAD51D</i> variants identifies distinct biochemical functions needed for homologous recombination and olaparib response
Kristie Darrah(University of Pittsburgh), Kara A. Bernstein(Columbia University Irving Medical Center), Noah J. Goff(University of Pennsylvania), S. M. Domchek(University of Pennsylvania), Shelby L. Hemker(University of Michigan), Silvia Casadei(University of Washington Medical Center), Yashpal Rawal(The University of Texas at San Antonio Health Science Center), Nicole Banks(Virginia Commonwealth University), Shaun K. Olsen(The University of Texas at San Antonio Health Science Center), Jacob O. Kitzman(University of Michigan), Arjun Kumar(University of Pennsylvania), Ella Roberts(University of Pittsburgh), Caleb Stratton(The University of Texas at San Antonio Health Science Center), Elena Glick(University of Michigan), Patrick Sung(The University of Texas at San Antonio Health Science Center), Katherine Oppenheimer(University of Pittsburgh), Lea M. Starita(University of Washington), Gayatri Ganesan(University of Pennsylvania), Phoebe S. Parker(University of Pennsylvania), Katherine Nathanson(University of Pennsylvania), Matthew W. Snyder(University of Washington)
Cited by 1
Related Papers
Assemblathon 2: evaluating <i>de novo</i> methods of genome assembly in three vertebrate species
|GigaScience|2013|736
Maize Inbreds Exhibit High Levels of Copy Number Variation (CNV) and Presence/Absence Variation (PAV) in Genome Content
|PLoS Genetics|2009|569
HDACs link the DNA damage response, processing of double-strand breaks and autophagy
|Nature|2011|410
Beyond the exome: What’s next in diagnostic testing for Mendelian conditions
|The American Journal of Human Genetics|2023|125
Improving performance of multigene panels for genomic analysis of cancer predisposition
|Genetics in Medicine|2016|92