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Matthew N Bainbridge

Showing results (41-50 of 67) with videos related to

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Cancer Discovery|August 13, 2017
Loss of MutL Disrupts CHK2-Dependent Cell-Cycle Control through CDK4/6 to Promote Intrinsic Endocrine Therapy Resistance in Primary Breast CancerSvasti Haricharan, Nindo Punturi, Purba Singh, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 15, 2013
Phenotypic variability of osteogenesis imperfecta type V caused by an IFITM5 mutationJay R Shapiro, Caressa Lietman, Monica Grover, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
A Machine Learning Decision Support Tool Optimizes Whole Genome Sequencing Utilization in a Neonatal Intensive Care UnitEdwin F Juarez, Bennet Peterson, Erica Sanford Kobayashi, et al.
NPJ Digital Medicine|January 30, 2025
A machine learning decision support tool optimizes WGS utilization in a neonatal intensive care unitEdwin F Juarez, Bennet Peterson, Erica Sanford Kobayashi, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|June 28, 2019
Rapid Whole Genome Sequencing Has Clinical Utility in Children in the PICUErica F Sanford, Michelle M Clark, Lauge Farnaes, et al.
Circulation. Cardiovascular Genetics|August 12, 2017
Novel Genetic Triggers and Genotype-Phenotype Correlations in Patients With Left Ventricular NoncompactionKarol Miszalski-Jamka, John L Jefferies, Wojciech Mazur, et al.
Blood|May 23, 2018
Syndromic congenital myelofibrosis associated with a loss-of-function variant in <i>RBSN</i>Pilar L Magoulas, Oleg A Shchelochkov, Matthew N Bainbridge, et al.
The New England Journal of Medicine|October 4, 2013
Clinical whole-exome sequencing for the diagnosis of mendelian disordersYaping Yang, Donna M Muzny, Jeffrey G Reid, et al.
American Journal of Human Genetics|January 24, 2012
Mutations in KAT6B, encoding a histone acetyltransferase, cause Genitopatellar syndromePhilippe M Campeau, Jaeseung C Kim, James T Lu, et al.
Clinical Neuropathology|December 19, 2014
Brain Tumor Epidemiology - A Hub within Multidisciplinary Neuro-oncology. Report on the 15th Brain Tumor Epidemiology Consortium (BTEC) Annual Meeting, Vienna, 2014Adelheid Woehrer, Ching C Lau, Daniela Prayer, et al.
Pageof 7

Showing results (41-50 of 67) with videos related to

Sort By:
Pageof 7
Cancer Discovery|August 13, 2017
Loss of MutL Disrupts CHK2-Dependent Cell-Cycle Control through CDK4/6 to Promote Intrinsic Endocrine Therapy Resistance in Primary Breast CancerSvasti Haricharan, Nindo Punturi, Purba Singh, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 15, 2013
Phenotypic variability of osteogenesis imperfecta type V caused by an IFITM5 mutationJay R Shapiro, Caressa Lietman, Monica Grover, et al.
Medrxiv : the Preprint Server for Health Sciences|July 15, 2024
A Machine Learning Decision Support Tool Optimizes Whole Genome Sequencing Utilization in a Neonatal Intensive Care UnitEdwin F Juarez, Bennet Peterson, Erica Sanford Kobayashi, et al.
NPJ Digital Medicine|January 30, 2025
A machine learning decision support tool optimizes WGS utilization in a neonatal intensive care unitEdwin F Juarez, Bennet Peterson, Erica Sanford Kobayashi, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|June 28, 2019
Rapid Whole Genome Sequencing Has Clinical Utility in Children in the PICUErica F Sanford, Michelle M Clark, Lauge Farnaes, et al.
Circulation. Cardiovascular Genetics|August 12, 2017
Novel Genetic Triggers and Genotype-Phenotype Correlations in Patients With Left Ventricular NoncompactionKarol Miszalski-Jamka, John L Jefferies, Wojciech Mazur, et al.
Blood|May 23, 2018
Syndromic congenital myelofibrosis associated with a loss-of-function variant in <i>RBSN</i>Pilar L Magoulas, Oleg A Shchelochkov, Matthew N Bainbridge, et al.
The New England Journal of Medicine|October 4, 2013
Clinical whole-exome sequencing for the diagnosis of mendelian disordersYaping Yang, Donna M Muzny, Jeffrey G Reid, et al.
American Journal of Human Genetics|January 24, 2012
Mutations in KAT6B, encoding a histone acetyltransferase, cause Genitopatellar syndromePhilippe M Campeau, Jaeseung C Kim, James T Lu, et al.
Clinical Neuropathology|December 19, 2014
Brain Tumor Epidemiology - A Hub within Multidisciplinary Neuro-oncology. Report on the 15th Brain Tumor Epidemiology Consortium (BTEC) Annual Meeting, Vienna, 2014Adelheid Woehrer, Ching C Lau, Daniela Prayer, et al.
Pageof 7