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Patrick May

Showing results (201-210 of 209) with videos related to

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Journal of Parkinson'S Disease|October 11, 2021
Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's DiseaseCloé Domenighetti, Pierre-Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, et al.
Neurology|August 15, 2022
Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence From the COURAGE-PD ConsortiumSandeep Grover, Ashwin Ashok Kumar Sreelatha, Lasse Pihlstrom, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 8, 2022
Dairy Intake and Parkinson's Disease: A Mendelian Randomization StudyCloé Domenighetti, Pierre-Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, et al.
Medrxiv : the Preprint Server for Health Sciences|March 13, 2026
Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant ClassificationTobias Brünger, Ilona Krey, Suyeon Kim, et al.
The Lancet. Neurology|July 24, 2018
Rare coding variants in genes encoding GABA<sub>A</sub> receptors in genetic generalised epilepsies: an exome-based case-control studyPatrick May, Simon Girard, Merle Harrer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 14, 2023
Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and CancersPierre-Emmanuel Sugier, Elise A Lucotte, Cloé Domenighetti, et al.
Brain : a Journal of Neurology|August 25, 2021
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implicationsKatrine M Johannesen, Yuanyuan Liu, Mahmoud Koko, et al.
Nature Genetics|February 16, 2021
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architectureRuth Chia, Marya S Sabir, Sara Bandres-Ciga, et al.
Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Pageof 21

Showing results (201-210 of 209) with videos related to

Sort By:
Pageof 21
You have reached the last page of results.This site can display upto 209 results.
Journal of Parkinson'S Disease|October 11, 2021
Mendelian Randomisation Study of Smoking, Alcohol, and Coffee Drinking in Relation to Parkinson's DiseaseCloé Domenighetti, Pierre-Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, et al.
Neurology|August 15, 2022
Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence From the COURAGE-PD ConsortiumSandeep Grover, Ashwin Ashok Kumar Sreelatha, Lasse Pihlstrom, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|January 8, 2022
Dairy Intake and Parkinson's Disease: A Mendelian Randomization StudyCloé Domenighetti, Pierre-Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, et al.
Medrxiv : the Preprint Server for Health Sciences|March 13, 2026
Gene Portals: A Framework for Integrating Clinical, Functional, and Structural Evidence into Rare Disease Variant ClassificationTobias Brünger, Ilona Krey, Suyeon Kim, et al.
The Lancet. Neurology|July 24, 2018
Rare coding variants in genes encoding GABA<sub>A</sub> receptors in genetic generalised epilepsies: an exome-based case-control studyPatrick May, Simon Girard, Merle Harrer, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 14, 2023
Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and CancersPierre-Emmanuel Sugier, Elise A Lucotte, Cloé Domenighetti, et al.
Brain : a Journal of Neurology|August 25, 2021
Genotype-phenotype correlations in SCN8A-related disorders reveal prognostic and therapeutic implicationsKatrine M Johannesen, Yuanyuan Liu, Mahmoud Koko, et al.
Nature Genetics|February 16, 2021
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architectureRuth Chia, Marya S Sabir, Sara Bandres-Ciga, et al.
Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
Pageof 21