Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Aditya Ekawade"'
Autor:
Tonya Di Sera, Matt Velinder, Alistair Ward, Yi Qiao, Stephanie Georges, Chase Miller, Anders Pitman, Will Richards, Aditya Ekawade, David Viskochil, John C. Carey, Laura Pace, Jim Bale, Stacey L. Clardy, Ashley Andrews, Lorenzo Botto, Gabor Marth
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
Abstract With increasing utilization of comprehensive genomic data to guide clinical care, anticipated to become the standard of care in many clinical settings, the practice of diagnostic medicine is undergoing a notable shift. However, the move from
Externí odkaz:
https://doaj.org/article/e62dd2ea5a434ba3a69d1064890091f2
Autor:
Aditya Ekawade, Matt Velinder, Alistair Ward, Tonya DiSera, Chase Miller, Yi Qiao, Gabor Marth
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-4 (2019)
Abstract When ordering genetic testing or triaging candidate variants in exome and genome sequencing studies, it is critical to generate and test a comprehensive list of candidate genes that succinctly describe the complete and objective phenotypic f
Externí odkaz:
https://doaj.org/article/a5f8b000f48b4ff09815b68f6ca361b5
Autor:
Tonya Di Sera, Matt Velinder, Alistair Ward, Yi Qiao, Stephanie Georges, Chase Miller, Anders Pitman, Will Richards, Aditya Ekawade, David Viskochil, John C. Carey, Laura Pace, Jim Bale, Stacey L. Clardy, Ashley Andrews, Lorenzo Botto, Gabor Marth
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/83ce2aad8ce94366b4e12bbbfe6e3f77
Autor:
Will Richards, Aditya Ekawade, Stacey L. Clardy, Jim Bale, Gabor T. Marth, Yi Qiao, John C. Carey, Anders Pitman, Ashley Andrews, Tonya Di Sera, Alistair Ward, Stephanie Georges, Lorenzo D. Botto, David Viskochil, Laura A. Pace, Chase Miller, Matt Velinder
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-11 (2021)
medRxiv
Scientific Reports
medRxiv
Scientific Reports
With increasing utilization of comprehensive genomic data to guide clinical care, anticipated to become the standard of care in many clinical settings, the practice of diagnostic medicine is undergoing a notable shift. However, the move from single-g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29ca81a06fd91baf29593a3647edf06e
https://doi.org/10.21203/rs.3.rs-402434/v1
https://doi.org/10.21203/rs.3.rs-402434/v1
Autor:
Yi Qiao, Matt Velinder, Tonya DiSera, Aditya Ekawade, Chase Miller, Gabor T. Marth, Alistair Ward
Publikováno v:
BMC Medical Genomics, Vol 12, Iss 1, Pp 1-4 (2019)
BMC Medical Genomics
BMC Medical Genomics
When ordering genetic testing or triaging candidate variants in exome and genome sequencing studies, it is critical to generate and test a comprehensive list of candidate genes that succinctly describe the complete and objective phenotypic features o
A comprehensive list of candidate genes that succinctly describe the complete and objective phenotypic features of disease is critical when both ordering genetic testing and when triaging candidate variants in exome and genome sequencing studies. Gre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85f71ea55109812999cdf895be959268
https://doi.org/10.1101/722843
https://doi.org/10.1101/722843