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Patrick May

Showing results (191-200 of 209) with videos related to

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American Journal of Human Genetics|March 28, 2017
Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic FeaturesTeresa Santiago-Sim, Lindsay C Burrage, Frédéric Ebstein, et al.
Nature Genetics|March 10, 2015
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathySteffen Syrbe, Ulrike B S Hedrich, Erik Riesch, et al.
Frontiers in Microbiology|December 11, 2023
A toolbox of machine learning software to support microbiome analysisLaura Judith Marcos-Zambrano, Víctor Manuel López-Molina, Burcu Bakir-Gungor, et al.
Nature Genetics|November 3, 2014
Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromesJulian Schubert, Aleksandra Siekierska, Mélanie Langlois, et al.
Neurology|February 10, 2019
Clinical spectrum of <i>STX1B</i>-related epileptic disordersStefan Wolking, Patrick May, Davide Mei, et al.
NPJ Parkinson'S Disease|May 28, 2026
Genetic variation in antidiabetic drug targets: associations with Parkinson's disease risk and age at onsetKatalin Vincze, Agnieszka Szwajda, Alexander Ploner, et al.
NPJ Parkinson'S Disease|April 20, 2026
Genome-wide association study of copy number variations in Parkinson's diseaseZied Landoulsi, Ashwin Ashok Kumar Sreelatha, Nicole Kuznetsov, et al.
Neurology|July 10, 2024
Association of Body Mass Index and Parkinson Disease: A Bidirectional Mendelian Randomization StudyCloé Domenighetti, Pierre-Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 10, 2022
The Interaction between HLA-DRB1 and Smoking in Parkinson's Disease RevisitedCloé Domenighetti, Venceslas Douillard, Pierre-Emmanuel Sugier, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2024
Genome-wide association study of copy number variations in Parkinson's diseaseZied Landoulsi, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, et al.
Pageof 21

Showing results (191-200 of 209) with videos related to

Sort By:
Pageof 21
American Journal of Human Genetics|March 28, 2017
Biallelic Variants in OTUD6B Cause an Intellectual Disability Syndrome Associated with Seizures and Dysmorphic FeaturesTeresa Santiago-Sim, Lindsay C Burrage, Frédéric Ebstein, et al.
Nature Genetics|March 10, 2015
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathySteffen Syrbe, Ulrike B S Hedrich, Erik Riesch, et al.
Frontiers in Microbiology|December 11, 2023
A toolbox of machine learning software to support microbiome analysisLaura Judith Marcos-Zambrano, Víctor Manuel López-Molina, Burcu Bakir-Gungor, et al.
Nature Genetics|November 3, 2014
Mutations in STX1B, encoding a presynaptic protein, cause fever-associated epilepsy syndromesJulian Schubert, Aleksandra Siekierska, Mélanie Langlois, et al.
Neurology|February 10, 2019
Clinical spectrum of <i>STX1B</i>-related epileptic disordersStefan Wolking, Patrick May, Davide Mei, et al.
NPJ Parkinson'S Disease|May 28, 2026
Genetic variation in antidiabetic drug targets: associations with Parkinson's disease risk and age at onsetKatalin Vincze, Agnieszka Szwajda, Alexander Ploner, et al.
NPJ Parkinson'S Disease|April 20, 2026
Genome-wide association study of copy number variations in Parkinson's diseaseZied Landoulsi, Ashwin Ashok Kumar Sreelatha, Nicole Kuznetsov, et al.
Neurology|July 10, 2024
Association of Body Mass Index and Parkinson Disease: A Bidirectional Mendelian Randomization StudyCloé Domenighetti, Pierre-Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 10, 2022
The Interaction between HLA-DRB1 and Smoking in Parkinson's Disease RevisitedCloé Domenighetti, Venceslas Douillard, Pierre-Emmanuel Sugier, et al.
Medrxiv : the Preprint Server for Health Sciences|September 4, 2024
Genome-wide association study of copy number variations in Parkinson's diseaseZied Landoulsi, Ashwin Ashok Kumar Sreelatha, Claudia Schulte, et al.
Pageof 21