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Showing results (741-750 of 809) with videos related to

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Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.
Circulation. Cardiovascular Genetics|June 22, 2014
Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyHonghuang Lin, Min Wang, Jennifer A Brody, et al.
Blood Cancer Discovery|September 25, 2020
Persistence of Drug-Resistant Leukemic Stem Cells and Impaired NK Cell Immunity in CML Patients Depend on <i>MIR300</i> Antiproliferative and PP2A-Activating FunctionsGiovannino Silvestri, Rossana Trotta, Lorenzo Stramucci, et al.
JAMA Oncology|January 30, 2016
Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid TumorsD Williams Parsons, Angshumoy Roy, Yaping Yang, et al.
Nature|October 18, 2021
Exome sequencing and analysis of 454,787 UK Biobank participantsJoshua D Backman, Alexander H Li, Anthony Marcketta, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|November 5, 2021
Molecular and Pathology Features of Colorectal Tumors and Patient Outcomes Are Associated with <i>Fusobacterium nucleatum</i> and Its Subspecies <i>animalis</i>Ivan Borozan, Syed H Zaidi, Tabitha A Harrison, et al.
Neuron|January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersElaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Biorxiv : the Preprint Server for Biology|May 22, 2023
A deep catalog of protein-coding variation in 985,830 individualsKathie Y Sun, Xiaodong Bai, Siying Chen, et al.
Nature Medicine|January 12, 2021
Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associationsJoseph Park, Anastasia M Lucas, Xinyuan Zhang, et al.
Nature Communications|September 13, 2024
NOTCH3 p.Arg1231Cys is markedly enriched in South Asians and associated with strokeJuan Lorenzo Rodriguez-Flores, Shareef Khalid, Neelroop Parikshak, et al.
Pageof 81

Showing results (741-750 of 809) with videos related to

Sort By:
Pageof 81
Plos Genetics|April 18, 2013
Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controlsLi Liu, Aniko Sabo, Benjamin M Neale, et al.
Circulation. Cardiovascular Genetics|June 22, 2014
Strategies to design and analyze targeted sequencing data: cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium Targeted Sequencing StudyHonghuang Lin, Min Wang, Jennifer A Brody, et al.
Blood Cancer Discovery|September 25, 2020
Persistence of Drug-Resistant Leukemic Stem Cells and Impaired NK Cell Immunity in CML Patients Depend on <i>MIR300</i> Antiproliferative and PP2A-Activating FunctionsGiovannino Silvestri, Rossana Trotta, Lorenzo Stramucci, et al.
JAMA Oncology|January 30, 2016
Diagnostic Yield of Clinical Tumor and Germline Whole-Exome Sequencing for Children With Solid TumorsD Williams Parsons, Angshumoy Roy, Yaping Yang, et al.
Nature|October 18, 2021
Exome sequencing and analysis of 454,787 UK Biobank participantsJoshua D Backman, Alexander H Li, Anthony Marcketta, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|November 5, 2021
Molecular and Pathology Features of Colorectal Tumors and Patient Outcomes Are Associated with <i>Fusobacterium nucleatum</i> and Its Subspecies <i>animalis</i>Ivan Borozan, Syed H Zaidi, Tabitha A Harrison, et al.
Neuron|January 29, 2013
Rare complete knockouts in humans: population distribution and significant role in autism spectrum disordersElaine T Lim, Soumya Raychaudhuri, Stephan J Sanders, et al.
Biorxiv : the Preprint Server for Biology|May 22, 2023
A deep catalog of protein-coding variation in 985,830 individualsKathie Y Sun, Xiaodong Bai, Siying Chen, et al.
Nature Medicine|January 12, 2021
Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associationsJoseph Park, Anastasia M Lucas, Xinyuan Zhang, et al.
Nature Communications|September 13, 2024
NOTCH3 p.Arg1231Cys is markedly enriched in South Asians and associated with strokeJuan Lorenzo Rodriguez-Flores, Shareef Khalid, Neelroop Parikshak, et al.
Pageof 81