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J Lubbe

Showing results (61-70 of 75) with videos related to

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Neurobiology of Aging|September 19, 2016
Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's diseaseS J Lubbe, V Escott-Price, A Brice, et al.
Annals of Neurology|March 9, 2018
Recessive mutations in VPS13D cause childhood onset movement disordersJulie Gauthier, Inge A Meijer, Davor Lessel, et al.
Human Molecular Genetics|November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritanceSteven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 1, 2021
Biallelic AOPEP Loss-of-Function Variants Cause Progressive Dystonia with Prominent Limb InvolvementMichael Zech, Kishore R Kumar, Sophie Reining, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 16, 2024
NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse PopulationsSara Bandres-Ciga, Faraz Faghri, Elisa Majounie, et al.
Genome Biology|February 1, 2017
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencingIris E Jansen, Hui Ye, Sasja Heetveld, et al.
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.
Applied Radiation and Isotopes : Including Data, Instrumentation and Methods for Use in Agriculture, Industry and Medicine|March 27, 2012
Results of an international comparison for the activity measurement of 177LuB E Zimmerman, T Altzitzoglou, A Antohe, et al.
Annals of Neurology|November 25, 2020
EIF2AK2 Missense Variants Associated with Early Onset Generalized DystoniaDemy J S Kuipers, Wim Mandemakers, Chin-Song Lu, et al.
The Lancet. Neurology|March 28, 2016
Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association dataKin Y Mok, Una Sheerin, Javier Simón-Sánchez, et al.
Pageof 8

Showing results (61-70 of 75) with videos related to

Sort By:
Pageof 8
Neurobiology of Aging|September 19, 2016
Rare variants analysis of cutaneous malignant melanoma genes in Parkinson's diseaseS J Lubbe, V Escott-Price, A Brice, et al.
Annals of Neurology|March 9, 2018
Recessive mutations in VPS13D cause childhood onset movement disordersJulie Gauthier, Inge A Meijer, Davor Lessel, et al.
Human Molecular Genetics|November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritanceSteven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 1, 2021
Biallelic AOPEP Loss-of-Function Variants Cause Progressive Dystonia with Prominent Limb InvolvementMichael Zech, Kishore R Kumar, Sophie Reining, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 16, 2024
NeuroBooster Array: A Genome-Wide Genotyping Platform to Study Neurological Disorders Across Diverse PopulationsSara Bandres-Ciga, Faraz Faghri, Elisa Majounie, et al.
Genome Biology|February 1, 2017
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencingIris E Jansen, Hui Ye, Sasja Heetveld, et al.
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.
Applied Radiation and Isotopes : Including Data, Instrumentation and Methods for Use in Agriculture, Industry and Medicine|March 27, 2012
Results of an international comparison for the activity measurement of 177LuB E Zimmerman, T Altzitzoglou, A Antohe, et al.
Annals of Neurology|November 25, 2020
EIF2AK2 Missense Variants Associated with Early Onset Generalized DystoniaDemy J S Kuipers, Wim Mandemakers, Chin-Song Lu, et al.
The Lancet. Neurology|March 28, 2016
Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association dataKin Y Mok, Una Sheerin, Javier Simón-Sánchez, et al.
Pageof 8