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Jeffrey Kim

Showing results (191-200 of 197) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|November 21, 2023
NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse PopulationsSara Bandres-Ciga, Faraz Faghri, Elisa Majounie, 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.
The New England Journal of Medicine|August 11, 2006
Neonatal-onset multisystem inflammatory disease responsive to interleukin-1beta inhibitionRaphaela Goldbach-Mansky, Natalie J Dailey, Scott W Canna, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 16, 2026
Loeys-Dietz Syndrome: 2026 updated care management primerGretchen MacCarrick, Rana O Afifi, Rebecca Allen, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2023
Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinson's Disease in African and African Admixed PopulationsMie Rizig, Sara Bandres-Ciga, Mary B Makarious, et al.
The Lancet. Neurology|August 26, 2023
Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association studyMie Rizig, Sara Bandres-Ciga, Mary B Makarious, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 30, 2019
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic InsightSara Bandres-Ciga, Sarah Ahmed, Marya S Sabir, et al.
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Showing results (191-200 of 197) with videos related to

Sort By:
Pageof 20
You have reached the last page of results.This site can display upto 197 results.
Medrxiv : the Preprint Server for Health Sciences|November 21, 2023
NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse PopulationsSara Bandres-Ciga, Faraz Faghri, Elisa Majounie, 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.
The New England Journal of Medicine|August 11, 2006
Neonatal-onset multisystem inflammatory disease responsive to interleukin-1beta inhibitionRaphaela Goldbach-Mansky, Natalie J Dailey, Scott W Canna, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 16, 2026
Loeys-Dietz Syndrome: 2026 updated care management primerGretchen MacCarrick, Rana O Afifi, Rebecca Allen, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2023
Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinson's Disease in African and African Admixed PopulationsMie Rizig, Sara Bandres-Ciga, Mary B Makarious, et al.
The Lancet. Neurology|August 26, 2023
Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association studyMie Rizig, Sara Bandres-Ciga, Mary B Makarious, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 30, 2019
The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population-Specific Risk, Differential Haplotype Structures, and Providing Etiologic InsightSara Bandres-Ciga, Sarah Ahmed, Marya S Sabir, et al.
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