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Lynne Krohn

Showing results (1-10 of 47) with videos related to

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Neurobiology of Aging|November 29, 2020
Lack of evidence for association of UQCRC1 with Parkinson's disease in EuropeansKonstantin Senkevich, Sara Bandres-Ciga, Ziv Gan-Or, et al.
Neurobiology of Aging|July 11, 2021
Analysis of PTRHD1 common and rare variants in European patients with Parkinson's diseaseYuri L Sosero, Sara Bandres-Ciga, Ziv Gan-Or, et al.
Neurobiology of Aging|April 20, 2021
Assessment of ANG variants in Parkinson's diseaseFrancis P Grenn, Anni Moore, Sara Bandres-Ciga, et al.
Neurology. Genetics|November 14, 2025
Parkinson Disease <i>SNCA</i> Risk Variants Are Associated With Higher Asymmetric Putamen Dopaminergic DysfunctionSaud Alhusaini, Gabriel Dayanim, Mohamed Kandil, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 11, 2021
Cytokines and Gaucher Biomarkers in Glucocerebrosidase Carriers with and Without Parkinson DiseaseJasmin Galper, Manisha Balwani, Stanley Fahn, et al.
Journal of Human Genetics|September 14, 2019
SPTAN1 variants as a potential cause for autosomal recessive hereditary spastic paraplegiaEtienne Leveille, Mehrdad A Estiar, Lynne Krohn, et al.
Annals of Neurology|January 27, 2021
Heritability Enrichment Implicates Microglia in Parkinson's Disease PathogenesisMaren Stolp Andersen, Sara Bandres-Ciga, Regina H Reynolds, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 11, 2021
Lack of Causal Effects or Genetic Correlation between Restless Legs Syndrome and Parkinson's DiseaseMehrdad A Estiar, Konstantin Senkevich, Eric Yu, et al.
Medrxiv : the Preprint Server for Health Sciences|June 9, 2023
Genome-wide association study stratified by Konstantin Senkevich, Sara Bandres-Ciga, Alejandro Cisterna-García, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 31, 2023
Transcript-aware analysis of rare predicted loss-of-function variants in the UK Biobank elucidate new isoform-trait associationsRachel A Hoffing, Aimee M Deaton, Aaron M Holleman, et al.
Pageof 5

Showing results (1-10 of 47) with videos related to

Sort By:
Pageof 5
Neurobiology of Aging|November 29, 2020
Lack of evidence for association of UQCRC1 with Parkinson's disease in EuropeansKonstantin Senkevich, Sara Bandres-Ciga, Ziv Gan-Or, et al.
Neurobiology of Aging|July 11, 2021
Analysis of PTRHD1 common and rare variants in European patients with Parkinson's diseaseYuri L Sosero, Sara Bandres-Ciga, Ziv Gan-Or, et al.
Neurobiology of Aging|April 20, 2021
Assessment of ANG variants in Parkinson's diseaseFrancis P Grenn, Anni Moore, Sara Bandres-Ciga, et al.
Neurology. Genetics|November 14, 2025
Parkinson Disease <i>SNCA</i> Risk Variants Are Associated With Higher Asymmetric Putamen Dopaminergic DysfunctionSaud Alhusaini, Gabriel Dayanim, Mohamed Kandil, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 11, 2021
Cytokines and Gaucher Biomarkers in Glucocerebrosidase Carriers with and Without Parkinson DiseaseJasmin Galper, Manisha Balwani, Stanley Fahn, et al.
Journal of Human Genetics|September 14, 2019
SPTAN1 variants as a potential cause for autosomal recessive hereditary spastic paraplegiaEtienne Leveille, Mehrdad A Estiar, Lynne Krohn, et al.
Annals of Neurology|January 27, 2021
Heritability Enrichment Implicates Microglia in Parkinson's Disease PathogenesisMaren Stolp Andersen, Sara Bandres-Ciga, Regina H Reynolds, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 11, 2021
Lack of Causal Effects or Genetic Correlation between Restless Legs Syndrome and Parkinson's DiseaseMehrdad A Estiar, Konstantin Senkevich, Eric Yu, et al.
Medrxiv : the Preprint Server for Health Sciences|June 9, 2023
Genome-wide association study stratified by Konstantin Senkevich, Sara Bandres-Ciga, Alejandro Cisterna-García, et al.
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing|December 31, 2023
Transcript-aware analysis of rare predicted loss-of-function variants in the UK Biobank elucidate new isoform-trait associationsRachel A Hoffing, Aimee M Deaton, Aaron M Holleman, et al.
Pageof 5