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Stacey B Gabriel

Showing results (21-30 of 133) with videos related to

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Plos Genetics|April 19, 2012
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autismMaria H Chahrour, Timothy W Yu, Elaine T Lim, et al.
Cancer Discovery|May 16, 2012
High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencingNikhil Wagle, Michael F Berger, Matthew J Davis, et al.
Human Molecular Genetics|January 8, 2011
Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13Minal Çalışkan, Jessica X Chong, Lawrence Uricchio, et al.
Cell Reports|June 30, 2015
Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi AnemiaKimberly A Rickman, Francis P Lach, Avinash Abhyankar, et al.
Nature Genetics|July 19, 2016
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discoveryEric M Scott, Anason Halees, Yuval Itan, et al.
Nucleic Acids Research|January 11, 2013
Discovery and characterization of artifactual mutations in deep coverage targeted capture sequencing data due to oxidative DNA damage during sample preparationMaura Costello, Trevor J Pugh, Timothy J Fennell, et al.
Nature Genetics|June 26, 2012
De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephalyJeong Ho Lee, My Huynh, Jennifer L Silhavy, et al.
Obesity (Silver Spring, Md.)|July 21, 2006
PAI-1 Gene 4G/5G polymorphism and risk of type 2 diabetes in a population-based sampleJames B Meigs, Josée Dupuis, Chunyu Liu, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2026
Genetic Determinants of Pulmonary Artery Size in over 50,000 Subjects with and without COPDVasile Foris, Kangjin Kim, Courtney Tern, et al.
Nature Genetics|September 9, 2008
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVsJoshua M Korn, Finny G Kuruvilla, Steven A McCarroll, et al.
Pageof 14

Showing results (21-30 of 133) with videos related to

Sort By:
Pageof 14
Plos Genetics|April 19, 2012
Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autismMaria H Chahrour, Timothy W Yu, Elaine T Lim, et al.
Cancer Discovery|May 16, 2012
High-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencingNikhil Wagle, Michael F Berger, Matthew J Davis, et al.
Human Molecular Genetics|January 8, 2011
Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13Minal Çalışkan, Jessica X Chong, Lawrence Uricchio, et al.
Cell Reports|June 30, 2015
Deficiency of UBE2T, the E2 Ubiquitin Ligase Necessary for FANCD2 and FANCI Ubiquitination, Causes FA-T Subtype of Fanconi AnemiaKimberly A Rickman, Francis P Lach, Avinash Abhyankar, et al.
Nature Genetics|July 19, 2016
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discoveryEric M Scott, Anason Halees, Yuval Itan, et al.
Nucleic Acids Research|January 11, 2013
Discovery and characterization of artifactual mutations in deep coverage targeted capture sequencing data due to oxidative DNA damage during sample preparationMaura Costello, Trevor J Pugh, Timothy J Fennell, et al.
Nature Genetics|June 26, 2012
De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephalyJeong Ho Lee, My Huynh, Jennifer L Silhavy, et al.
Obesity (Silver Spring, Md.)|July 21, 2006
PAI-1 Gene 4G/5G polymorphism and risk of type 2 diabetes in a population-based sampleJames B Meigs, Josée Dupuis, Chunyu Liu, et al.
Medrxiv : the Preprint Server for Health Sciences|July 10, 2026
Genetic Determinants of Pulmonary Artery Size in over 50,000 Subjects with and without COPDVasile Foris, Kangjin Kim, Courtney Tern, et al.
Nature Genetics|September 9, 2008
Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVsJoshua M Korn, Finny G Kuruvilla, Steven A McCarroll, et al.
Pageof 14