Search research articles
Contact Us
Filters
Showing results (361-370 of 379) with videos related to
Page
of 38
Sort By:
NPJ Genomic Medicine
|
July 2, 2025
Assessing the diagnostic impact of blood transcriptome profiling in a pediatric cohort previously assessed by genome sequencing
Huayun Hou, Kyoko E Yuki, Gregory Costain, et al.
The New England Journal of Medicine
|
December 1, 2006
CD4+ count-guided interruption of antiretroviral treatment
, W M El-Sadr, J D Lundgren, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 29, 2020
Cell-based analysis of CAD variants identifies individuals likely to benefit from uridine therapy
Francisco Del Caño-Ochoa, Bobby G Ng, Malak Abedalthagafi, et al.
American Journal of Respiratory and Critical Care Medicine
|
February 8, 2012
A critical role for muscle ring finger-1 in acute lung injury-associated skeletal muscle wasting
D Clark Files, Franco R D'Alessio, Laura F Johnston, et al.
EMBO Molecular Medicine
|
November 20, 2012
Activation of serum/glucocorticoid-induced kinase 1 (SGK1) is important to maintain skeletal muscle homeostasis and prevent atrophy
Eva Andres-Mateos, Heinrich Brinkmeier, Tyesha N Burks, et al.
JAMA Network Open
|
September 22, 2020
Genome Sequencing as a Diagnostic Test in Children With Unexplained Medical Complexity
Gregory Costain, Susan Walker, Maria Marano, et al.
NPJ Genomic Medicine
|
February 27, 2025
International Precision Child Health Partnership (IPCHiP): an initiative to accelerate discovery and improve outcomes in rare pediatric disease
Katherine B Howell, Susan M White, Amy McTague, et al.
Scientific Reports
|
January 20, 2024
High dimensional predictions of suicide risk in 4.2 million US Veterans using ensemble transfer learning
Sayera Dhaubhadel, Kumkum Ganguly, Ruy M Ribeiro, et al.
American Journal of Human Genetics
|
February 8, 2020
The Canadian Rare Diseases Models and Mechanisms (RDMM) Network: Connecting Understudied Genes to Model Organisms
Kym M Boycott, Philippe M Campeau, Heather E Howley, et al.
Journal of Child Neurology
|
November 17, 2010
Consensus statement on standard of care for congenital muscular dystrophies
Ching H Wang, Carsten G Bonnemann, Anne Rutkowski, et al.
Page
of 38
Search research articles
Search
Showing results (361-370 of 379) with videos related to
Sort By:
Page
of 38
NPJ Genomic Medicine
|
July 2, 2025
Assessing the diagnostic impact of blood transcriptome profiling in a pediatric cohort previously assessed by genome sequencing
Huayun Hou, Kyoko E Yuki, Gregory Costain, et al.
The New England Journal of Medicine
|
December 1, 2006
CD4+ count-guided interruption of antiretroviral treatment
, W M El-Sadr, J D Lundgren, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 29, 2020
Cell-based analysis of CAD variants identifies individuals likely to benefit from uridine therapy
Francisco Del Caño-Ochoa, Bobby G Ng, Malak Abedalthagafi, et al.
American Journal of Respiratory and Critical Care Medicine
|
February 8, 2012
A critical role for muscle ring finger-1 in acute lung injury-associated skeletal muscle wasting
D Clark Files, Franco R D'Alessio, Laura F Johnston, et al.
EMBO Molecular Medicine
|
November 20, 2012
Activation of serum/glucocorticoid-induced kinase 1 (SGK1) is important to maintain skeletal muscle homeostasis and prevent atrophy
Eva Andres-Mateos, Heinrich Brinkmeier, Tyesha N Burks, et al.
JAMA Network Open
|
September 22, 2020
Genome Sequencing as a Diagnostic Test in Children With Unexplained Medical Complexity
Gregory Costain, Susan Walker, Maria Marano, et al.
NPJ Genomic Medicine
|
February 27, 2025
International Precision Child Health Partnership (IPCHiP): an initiative to accelerate discovery and improve outcomes in rare pediatric disease
Katherine B Howell, Susan M White, Amy McTague, et al.
Scientific Reports
|
January 20, 2024
High dimensional predictions of suicide risk in 4.2 million US Veterans using ensemble transfer learning
Sayera Dhaubhadel, Kumkum Ganguly, Ruy M Ribeiro, et al.
American Journal of Human Genetics
|
February 8, 2020
The Canadian Rare Diseases Models and Mechanisms (RDMM) Network: Connecting Understudied Genes to Model Organisms
Kym M Boycott, Philippe M Campeau, Heather E Howley, et al.
Journal of Child Neurology
|
November 17, 2010
Consensus statement on standard of care for congenital muscular dystrophies
Ching H Wang, Carsten G Bonnemann, Anne Rutkowski, et al.
Page
of 38