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Matthew S Lebo

Showing results (31-40 of 69) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 27, 2023
Laboratory perspectives in the development of polygenic risk scores for disease: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)Honey V Reddi, Hannah Wand, Birgit Funke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 27, 2021
Discordant results between conventional newborn screening and genomic sequencing in the BabySeq ProjectMonica H Wojcik, Tian Zhang, Ozge Ceyhan-Birsoy, et al.
Transfusion|December 29, 2018
A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xg<sup>a</sup>William J Lane, Maria Aguad, Robin Smeland-Wagman, et al.
Transfusion|August 9, 2019
Automated typing of red blood cell and platelet antigens from whole exome sequencesWilliam J Lane, Sunitha Vege, Helen H Mah, et al.
American Journal of Human Genetics|January 5, 2019
Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq ProjectOzge Ceyhan-Birsoy, Jaclyn B Murry, Kalotina Machini, et al.
Journal of Pathology Informatics|May 21, 2014
Pathology informatics fellowship training: Focus on molecular pathologyDiana Mandelker, Roy E Lee, Mia Y Platt, et al.
Transfusion|May 31, 2020
Multiple GYPB gene deletions associated with the U- phenotype in those of African ancestryWilliam J Lane, Nicholas S Gleadall, Judith Aeschlimann, et al.
BMC Medical Genetics|February 26, 2015
A systematic approach to the reporting of medically relevant findings from whole genome sequencingHeather M McLaughlin, Ozge Ceyhan-Birsoy, Kurt D Christensen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updatesHana Zouk, Wanfeng Yu, Andrea Oza, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 12, 2021
Randomized prospective evaluation of genome sequencing versus standard-of-care as a first molecular diagnostic testDeanna G Brockman, Christina A Austin-Tse, Renée C Pelletier, et al.
Pageof 7

Showing results (31-40 of 69) with videos related to

Sort By:
Pageof 7
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 27, 2023
Laboratory perspectives in the development of polygenic risk scores for disease: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG)Honey V Reddi, Hannah Wand, Birgit Funke, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 27, 2021
Discordant results between conventional newborn screening and genomic sequencing in the BabySeq ProjectMonica H Wojcik, Tian Zhang, Ozge Ceyhan-Birsoy, et al.
Transfusion|December 29, 2018
A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xg<sup>a</sup>William J Lane, Maria Aguad, Robin Smeland-Wagman, et al.
Transfusion|August 9, 2019
Automated typing of red blood cell and platelet antigens from whole exome sequencesWilliam J Lane, Sunitha Vege, Helen H Mah, et al.
American Journal of Human Genetics|January 5, 2019
Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq ProjectOzge Ceyhan-Birsoy, Jaclyn B Murry, Kalotina Machini, et al.
Journal of Pathology Informatics|May 21, 2014
Pathology informatics fellowship training: Focus on molecular pathologyDiana Mandelker, Roy E Lee, Mia Y Platt, et al.
Transfusion|May 31, 2020
Multiple GYPB gene deletions associated with the U- phenotype in those of African ancestryWilliam J Lane, Nicholas S Gleadall, Judith Aeschlimann, et al.
BMC Medical Genetics|February 26, 2015
A systematic approach to the reporting of medically relevant findings from whole genome sequencingHeather M McLaughlin, Ozge Ceyhan-Birsoy, Kurt D Christensen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 15, 2021
Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updatesHana Zouk, Wanfeng Yu, Andrea Oza, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 12, 2021
Randomized prospective evaluation of genome sequencing versus standard-of-care as a first molecular diagnostic testDeanna G Brockman, Christina A Austin-Tse, Renée C Pelletier, et al.
Pageof 7