Search research articles
Contact Us
Filters
Showing results (541-550 of 587) with videos related to
Page
of 59
Sort By:
Human Mutation
|
February 16, 2012
Next-generation genetic testing for retinitis pigmentosa
Kornelia Neveling, Rob W J Collin, Christian Gilissen, et al.
Journal of the American Heart Association
|
March 4, 2020
Interleukin-1 Blockade Inhibits the Acute Inflammatory Response in Patients With ST-Segment-Elevation Myocardial Infarction
Antonio Abbate, Cory R Trankle, Leo F Buckley, et al.
Nature Communications
|
April 14, 2026
Plasma phosphorylated tau 217 and longitudinal trajectories of Aβ, tau, and cognition in cognitively unimpaired older adults
Hyun-Sik Yang, Juliana A U Anzai, Wai-Ying Wendy Yau, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Biomarkers
Annie Li, Hannah M Klinger, Mabel Seto, et al.
European Journal of Heart Failure
|
March 26, 2021
Virtual optimization of guideline-directed medical therapy in hospitalized patients with heart failure with reduced ejection fraction: the IMPLEMENT-HF pilot study
Ankeet S Bhatt, Anubodh S Varshney, Mahan Nekoui, et al.
JAMA Neurology
|
March 3, 2025
Sex Differences in Longitudinal Tau-PET in Preclinical Alzheimer Disease: A Meta-Analysis
Gillian T Coughlan, Hannah M Klinger, Rory Boyle, et al.
European Journal of Human Genetics : EJHG
|
August 15, 2022
Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis
Lisa J Ewans, Andre E Minoche, Deborah Schofield, et al.
Alzheimer'S Research & Therapy
|
July 3, 2024
Identifying longitudinal cognitive resilience from cross-sectional amyloid, tau, and neurodegeneration
Rory Boyle, Diana L Townsend, Hannah M Klinger, et al.
Nature Genetics
|
November 20, 2012
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9
Cristina M Justice, Garima Yagnik, Yoonhee Kim, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 23, 2023
Dominant-negative variants in CBX1 cause a neurodevelopmental disorder
Yukiko Kuroda, Aiko Iwata-Otsubo, Kerith-Rae Dias, et al.
Page
of 59
Search research articles
Search
Showing results (541-550 of 587) with videos related to
Sort By:
Page
of 59
Human Mutation
|
February 16, 2012
Next-generation genetic testing for retinitis pigmentosa
Kornelia Neveling, Rob W J Collin, Christian Gilissen, et al.
Journal of the American Heart Association
|
March 4, 2020
Interleukin-1 Blockade Inhibits the Acute Inflammatory Response in Patients With ST-Segment-Elevation Myocardial Infarction
Antonio Abbate, Cory R Trankle, Leo F Buckley, et al.
Nature Communications
|
April 14, 2026
Plasma phosphorylated tau 217 and longitudinal trajectories of Aβ, tau, and cognition in cognitively unimpaired older adults
Hyun-Sik Yang, Juliana A U Anzai, Wai-Ying Wendy Yau, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
December 24, 2025
Biomarkers
Annie Li, Hannah M Klinger, Mabel Seto, et al.
European Journal of Heart Failure
|
March 26, 2021
Virtual optimization of guideline-directed medical therapy in hospitalized patients with heart failure with reduced ejection fraction: the IMPLEMENT-HF pilot study
Ankeet S Bhatt, Anubodh S Varshney, Mahan Nekoui, et al.
JAMA Neurology
|
March 3, 2025
Sex Differences in Longitudinal Tau-PET in Preclinical Alzheimer Disease: A Meta-Analysis
Gillian T Coughlan, Hannah M Klinger, Rory Boyle, et al.
European Journal of Human Genetics : EJHG
|
August 15, 2022
Whole exome and genome sequencing in mendelian disorders: a diagnostic and health economic analysis
Lisa J Ewans, Andre E Minoche, Deborah Schofield, et al.
Alzheimer'S Research & Therapy
|
July 3, 2024
Identifying longitudinal cognitive resilience from cross-sectional amyloid, tau, and neurodegeneration
Rory Boyle, Diana L Townsend, Hannah M Klinger, et al.
Nature Genetics
|
November 20, 2012
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9
Cristina M Justice, Garima Yagnik, Yoonhee Kim, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
April 23, 2023
Dominant-negative variants in CBX1 cause a neurodevelopmental disorder
Yukiko Kuroda, Aiko Iwata-Otsubo, Kerith-Rae Dias, et al.
Page
of 59