Chad A. Shaw, Ph.D.
Affiliations: | 2001 | Rice University, Houston, TX |
Area:
Mathematics, StatisticsGoogle:
"Chad Shaw"Parents
Sign in to add mentorMarek Kimmel | grad student | 2001 | Rice University | |
(Genealogical methods for multitype branching processes with applications in biology.) |
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Publications
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Robak LA, Du R, Yuan B, et al. (2020) Integrated sequencing and array comparative genomic hybridization in familial Parkinson disease. Neurology. Genetics. 6: e498 |
Cao Y, Tokita MJ, Chen ES, et al. (2019) A clinical survey of mosaic single nucleotide variants in disease-causing genes detected by exome sequencing. Genome Medicine. 11: 48 |
Madan N, Ghazi AR, Kong X, et al. (2019) Functionalization of CD36 Cardiovascular Disease and Expression Associated Variants by Interdisciplinary High Throughput Analysis. Plos Genetics. 15: e1008287 |
Carvalho CMB, Coban-Akdemir Z, Hijazi H, et al. (2019) Interchromosomal template-switching as a novel molecular mechanism for imprinting perturbations associated with Temple syndrome. Genome Medicine. 11: 25 |
Beck CR, Carvalho CMB, Akdemir ZC, et al. (2019) Megabase Length Hypermutation Accompanies Human Structural Variation at 17p11.2. Cell |
Kong X, Ma L, Chen E, et al. (2019) Identification of the Regulatory Elements and Target Genes of Megakaryopoietic Transcription Factor MEF2C. Thrombosis and Haemostasis |
Zhang J, Li J, Saucier JB, et al. (2019) Non-invasive prenatal sequencing for multiple Mendelian monogenic disorders using circulating cell-free fetal DNA. Nature Medicine |
Callaway DA, Campbell IM, Stover SR, et al. (2018) Prioritization of Candidate Genes for Congenital Diaphragmatic Hernia in a Critical Region on Chromosome 4p16 using a Machine-Learning Algorithm. Journal of Pediatric Genetics. 7: 164-173 |
Coban-Akdemir Z, White JJ, Song X, et al. (2018) Identifying Genes Whose Mutant Transcripts Cause Dominant Disease Traits by Potential Gain-of-Function Alleles. American Journal of Human Genetics |
Madan N, Ghazi A, Kong X, et al. (2018) Identification of the Genetic Variant Responsible for Variable Platelet CD36 Expression By Massively Parallel Reporter Assay Blood. 132: 520-520 |