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Medrxiv : the Preprint Server for Health Sciences
|
June 30, 2021
Common and rare variant analyses combined with single-cell multiomics reveal cell-type-specific molecular mechanisms of COVID-19 severity
Sai Zhang, Johnathan Cooper-Knock, Annika K Weimer, et al.
BMC Medicine
|
March 5, 2026
Hypothesis-free evaluation of circulating metabolome provides cell-specific insights regarding the role of energy substrate availability in amyotrophic lateral sclerosis
Elham Alhathli, Johnathan Cooper-Knock, Zain-Ul-Abideen Girach, et al.
Biorxiv : the Preprint Server for Biology
|
August 2, 2024
predicTTE: An accessible and optimal tool for time-to-event prediction in neurological diseases
Marcel Weinreich, Harry McDonough, Nancy Yacovzada, et al.
Neuron
|
January 19, 2022
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis
Sai Zhang, Johnathan Cooper-Knock, Annika K Weimer, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 18, 2024
Deep learning modeling of rare noncoding genetic variants in human motor neurons defines <i>CCDC146</i> as a therapeutic target for ALS
Sai Zhang, Tobias Moll, Jasper Rubin-Sigler, et al.
Genome Biology
|
January 20, 2025
Author Correction: Considerations in the search for epistasis
Marleen Balvert, Johnathan Cooper-Knock, Julian Stamp, et al.
Genome Biology
|
November 20, 2024
Considerations in the search for epistasis
Marleen Balvert, Johnathan Cooper-Knock, Julian Stamp, et al.
Research Square
|
June 12, 2026
Single-nucleus multiomic atlas of ALS primary motor cortex nominates neuroprotective WDR49-expressing astrocytes
Johnathan Cooper-Knock, Sam Bonsall, Rodrigo Kazu, et al.
Heliyon
|
February 6, 2024
Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosis
Calum Harvey, Marcel Weinreich, James A K Lee, et al.
European Journal of Human Genetics : EJHG
|
February 16, 2025
An observational study of pleiotropy and penetrance of amyotrophic lateral sclerosis associated with CAG-repeat expansion of ATXN2
Koen C Demaegd, Aoife Kernan, Johnathan Cooper-Knock, et al.
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Search research articles
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Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Medrxiv : the Preprint Server for Health Sciences
|
June 30, 2021
Common and rare variant analyses combined with single-cell multiomics reveal cell-type-specific molecular mechanisms of COVID-19 severity
Sai Zhang, Johnathan Cooper-Knock, Annika K Weimer, et al.
BMC Medicine
|
March 5, 2026
Hypothesis-free evaluation of circulating metabolome provides cell-specific insights regarding the role of energy substrate availability in amyotrophic lateral sclerosis
Elham Alhathli, Johnathan Cooper-Knock, Zain-Ul-Abideen Girach, et al.
Biorxiv : the Preprint Server for Biology
|
August 2, 2024
predicTTE: An accessible and optimal tool for time-to-event prediction in neurological diseases
Marcel Weinreich, Harry McDonough, Nancy Yacovzada, et al.
Neuron
|
January 19, 2022
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis
Sai Zhang, Johnathan Cooper-Knock, Annika K Weimer, et al.
Medrxiv : the Preprint Server for Health Sciences
|
April 18, 2024
Deep learning modeling of rare noncoding genetic variants in human motor neurons defines <i>CCDC146</i> as a therapeutic target for ALS
Sai Zhang, Tobias Moll, Jasper Rubin-Sigler, et al.
Genome Biology
|
January 20, 2025
Author Correction: Considerations in the search for epistasis
Marleen Balvert, Johnathan Cooper-Knock, Julian Stamp, et al.
Genome Biology
|
November 20, 2024
Considerations in the search for epistasis
Marleen Balvert, Johnathan Cooper-Knock, Julian Stamp, et al.
Research Square
|
June 12, 2026
Single-nucleus multiomic atlas of ALS primary motor cortex nominates neuroprotective WDR49-expressing astrocytes
Johnathan Cooper-Knock, Sam Bonsall, Rodrigo Kazu, et al.
Heliyon
|
February 6, 2024
Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosis
Calum Harvey, Marcel Weinreich, James A K Lee, et al.
European Journal of Human Genetics : EJHG
|
February 16, 2025
An observational study of pleiotropy and penetrance of amyotrophic lateral sclerosis associated with CAG-repeat expansion of ATXN2
Koen C Demaegd, Aoife Kernan, Johnathan Cooper-Knock, et al.
Page
of 3