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J Raphael

Showing results (431-440 of 488) with videos related to

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Brain : a Journal of Neurology|April 22, 2026
Machine learning model based on plasma proteomics for the identification of Parkinson's diseaseBoluwatife Adewale, Ruth Chia, Ruin Moaddel, et al.
Plos Genetics|May 10, 2008
A genome-wide association study identifies protein quantitative trait loci (pQTLs)David Melzer, John R B Perry, Dena Hernandez, et al.
Neuron|December 15, 2010
Exome sequencing reveals VCP mutations as a cause of familial ALSJanel O Johnson, Jessica Mandrioli, Michael Benatar, et al.
Nature Medicine|August 19, 2025
A plasma proteomics-based candidate biomarker panel predictive of amyotrophic lateral sclerosisRuth Chia, Ruin Moaddel, Justin Y Kwan, et al.
Nature Genetics|May 21, 2013
The mutational landscape of adenoid cystic carcinomaAllen S Ho, Kasthuri Kannan, David M Roy, et al.
American Journal of Human Genetics|March 5, 2016
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent MitophagySuzanne Lesage, Valérie Drouet, Elisa Majounie, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 27, 2020
Shared Genetics of Multiple System Atrophy and Inflammatory Bowel DiseaseAlexey A Shadrin, Sören Mucha, David Ellinghaus, et al.
Bioinformatics Advances|August 15, 2024
Current and future directions in network biologyMarinka Zitnik, Michelle M Li, Aydin Wells, et al.
Brain : a Journal of Neurology|June 22, 2023
Large-scale rare variant burden testing in Parkinson's diseaseMary B Makarious, Julie Lake, Vanessa Pitz, et al.
Annals of Neurology|May 29, 2009
SNCA variants are associated with increased risk for multiple system atrophySonja W Scholz, Henry Houlden, Claudia Schulte, et al.
Pageof 49

Showing results (431-440 of 488) with videos related to

Sort By:
Pageof 49
Brain : a Journal of Neurology|April 22, 2026
Machine learning model based on plasma proteomics for the identification of Parkinson's diseaseBoluwatife Adewale, Ruth Chia, Ruin Moaddel, et al.
Plos Genetics|May 10, 2008
A genome-wide association study identifies protein quantitative trait loci (pQTLs)David Melzer, John R B Perry, Dena Hernandez, et al.
Neuron|December 15, 2010
Exome sequencing reveals VCP mutations as a cause of familial ALSJanel O Johnson, Jessica Mandrioli, Michael Benatar, et al.
Nature Medicine|August 19, 2025
A plasma proteomics-based candidate biomarker panel predictive of amyotrophic lateral sclerosisRuth Chia, Ruin Moaddel, Justin Y Kwan, et al.
Nature Genetics|May 21, 2013
The mutational landscape of adenoid cystic carcinomaAllen S Ho, Kasthuri Kannan, David M Roy, et al.
American Journal of Human Genetics|March 5, 2016
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent MitophagySuzanne Lesage, Valérie Drouet, Elisa Majounie, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 27, 2020
Shared Genetics of Multiple System Atrophy and Inflammatory Bowel DiseaseAlexey A Shadrin, Sören Mucha, David Ellinghaus, et al.
Bioinformatics Advances|August 15, 2024
Current and future directions in network biologyMarinka Zitnik, Michelle M Li, Aydin Wells, et al.
Brain : a Journal of Neurology|June 22, 2023
Large-scale rare variant burden testing in Parkinson's diseaseMary B Makarious, Julie Lake, Vanessa Pitz, et al.
Annals of Neurology|May 29, 2009
SNCA variants are associated with increased risk for multiple system atrophySonja W Scholz, Henry Houlden, Claudia Schulte, et al.
Pageof 49