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Showing results (641-650 of 683) with videos related to

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Nature Communications|June 26, 2019
Pathologic gene network rewiring implicates PPP1R3A as a central regulator in pressure overload heart failurePablo Cordero, Victoria N Parikh, Elizabeth T Chin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2024
Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorderJennefer N Kohler, Nicole R Legro, Dustin Baldridge, et al.
Arxiv|January 7, 2025
GREGoR: Accelerating Genomics for Rare DiseasesMoez Dawood, Ben Heavner, Marsha M Wheeler, et al.
Nature Medicine|June 5, 2019
Identification of rare-disease genes using blood transcriptome sequencing and large control cohortsLaure Frésard, Craig Smail, Nicole M Ferraro, et al.
Plos Genetics|February 10, 2011
The architecture of gene regulatory variation across multiple human tissues: the MuTHER studyAlexandra C Nica, Leopold Parts, Daniel Glass, et al.
Cell|October 1, 2024
Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disordersBo Zhou, Joseph G Arthur, Hanmin Guo, et al.
Nature|November 12, 2025
GREGoR: accelerating genomics for rare diseasesMoez Dawood, Ben Heavner, Marsha M Wheeler, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|February 14, 2018
Transcriptional Profiling of Synovial Macrophages Using Minimally Invasive Ultrasound-Guided Synovial Biopsies in Rheumatoid ArthritisArthur M Mandelin, Philip J Homan, Alexander M Shaffer, et al.
American Journal of Human Genetics|April 3, 2026
Multi-ancestry transcriptome prediction with functionally informed variants in TOPMed MESA improves performance of transcriptome-wide association studiesXiaowei Hu, Daniel S Araujo, Chachrit Khunsriraksakul, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
CHIMERA-DDR: A Machine Learning Framework for Classifying Heterogeneous Mismatch-Repair and Homologous-Recombination Deficiency Patterns in Prostate CancerKomal Sharma, Divin A Wilson, Yu Wang, et al.
Pageof 69

Showing results (641-650 of 683) with videos related to

Sort By:
Pageof 69
Nature Communications|June 26, 2019
Pathologic gene network rewiring implicates PPP1R3A as a central regulator in pressure overload heart failurePablo Cordero, Victoria N Parikh, Elizabeth T Chin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2024
Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorderJennefer N Kohler, Nicole R Legro, Dustin Baldridge, et al.
Arxiv|January 7, 2025
GREGoR: Accelerating Genomics for Rare DiseasesMoez Dawood, Ben Heavner, Marsha M Wheeler, et al.
Nature Medicine|June 5, 2019
Identification of rare-disease genes using blood transcriptome sequencing and large control cohortsLaure Frésard, Craig Smail, Nicole M Ferraro, et al.
Plos Genetics|February 10, 2011
The architecture of gene regulatory variation across multiple human tissues: the MuTHER studyAlexandra C Nica, Leopold Parts, Daniel Glass, et al.
Cell|October 1, 2024
Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disordersBo Zhou, Joseph G Arthur, Hanmin Guo, et al.
Nature|November 12, 2025
GREGoR: accelerating genomics for rare diseasesMoez Dawood, Ben Heavner, Marsha M Wheeler, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|February 14, 2018
Transcriptional Profiling of Synovial Macrophages Using Minimally Invasive Ultrasound-Guided Synovial Biopsies in Rheumatoid ArthritisArthur M Mandelin, Philip J Homan, Alexander M Shaffer, et al.
American Journal of Human Genetics|April 3, 2026
Multi-ancestry transcriptome prediction with functionally informed variants in TOPMed MESA improves performance of transcriptome-wide association studiesXiaowei Hu, Daniel S Araujo, Chachrit Khunsriraksakul, et al.
Biorxiv : the Preprint Server for Biology|November 24, 2025
CHIMERA-DDR: A Machine Learning Framework for Classifying Heterogeneous Mismatch-Repair and Homologous-Recombination Deficiency Patterns in Prostate CancerKomal Sharma, Divin A Wilson, Yu Wang, et al.
Pageof 69