Marta Byrska-Bishop

2011-2015 Molecular and Cellular Biosciences Pennsylvania State University, State College, PA, United States 
"Marta Byrska-Bishop"
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Wilfert AB, Turner TN, Murali SC, et al. (2021) Recent ultra-rare inherited variants implicate new autism candidate risk genes. Nature Genetics
Padhi EM, Hayeck TJ, Cheng Z, et al. (2021) Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism. Human Genomics. 15: 44
Ebert P, Audano PA, Zhu Q, et al. (2021) Haplotype-resolved diverse human genomes and integrated analysis of structural variation. Science (New York, N.Y.)
Verma A, Bang L, Miller JE, et al. (2018) Human-Disease Phenotype Map Derived from PheWAS across 38,682 Individuals. American Journal of Human Genetics
Basile AO, Byrska-Bishop M, Wallace J, et al. (2018) Novel features and enhancements in BioBin, a tool for the biologically inspired binning and association analysis of rare variants. Bioinformatics (Oxford, England). 34: 527-529
Basile AO, Verma A, Byrska-Bishop M, et al. (2016) PATTERNS IN BIOMEDICAL DATA-HOW DO WE FIND THEM? Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 22: 177-183
Byrska-Bishop M, VanDorn D, Campbell AE, et al. (2015) Pluripotent stem cells reveal erythroid-specific activities of the GATA1 N-terminus. The Journal of Clinical Investigation. 125: 993-1005
Chou ST, Byrska-Bishop M, Tober JM, et al. (2012) Trisomy 21-associated defects in human primitive hematopoiesis revealed through induced pluripotent stem cells. Proceedings of the National Academy of Sciences of the United States of America. 109: 17573-8
Huda S, Soh S, Pilans D, et al. (2012) Microtubule guidance tested through controlled cell geometry. Journal of Cell Science. 125: 5790-9
Stamatoyannopoulos JA, Snyder M, et al. (2012) An encyclopedia of mouse DNA elements (Mouse ENCODE). Genome Biology. 13: 418
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