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J Raphael

Showing results (361-370 of 488) with videos related to

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Plos One|May 23, 2013
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputationAndrew R Wood, John R B Perry, Toshiko Tanaka, et al.
NAR Cancer|August 28, 2023
Co-evolution of <i>AR</i> gene copy number and structural complexity in endocrine therapy resistant prostate cancerAndrej Zivanovic, Jeffrey T Miller, Sarah A Munro, et al.
Medrxiv : the Preprint Server for Health Sciences|October 4, 2023
Long-read sequencing resolves a complex structural variant in <i>PRKN</i> Parkinson's diseaseKensuke Daida, Manabu Funayama, Kimberley J Billingsley, et al.
Brain : a Journal of Neurology|May 31, 2022
Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's diseaseWilliam Zhu, Xiaoping Huang, Esther Yoon, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 6, 2023
Long-Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's DiseaseKensuke Daida, Manabu Funayama, Kimberley J Billingsley, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|April 24, 2020
A multicentre, randomised trial comparing schedules of G-CSF (filgrastim) administration for primary prophylaxis of chemotherapy-induced febrile neutropenia in early stage breast cancerM Clemons, D Fergusson, D Simos, et al.
British Journal of Cancer|September 4, 2025
Recommendations for studying the association of the cancer diagnosis to treatment interval with overall survival: a modified Delphi processMatthew Jalink, Will D King, Benjamin O Anderson, et al.
Neurobiology of Aging|September 5, 2017
Establishing the role of rare coding variants in known Parkinson's disease risk lociIris E Jansen, J Raphael Gibbs, Mike A Nalls, et al.
NPJ Parkinson'S Disease|May 25, 2019
Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onsetKimberley J Billingsley, Ines A Barbosa, Sara Bandrés-Ciga, et al.
Plos Genetics|May 21, 2010
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brainJ Raphael Gibbs, Marcel P van der Brug, Dena G Hernandez, et al.
Pageof 49

Showing results (361-370 of 488) with videos related to

Sort By:
Pageof 49
Plos One|May 23, 2013
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputationAndrew R Wood, John R B Perry, Toshiko Tanaka, et al.
NAR Cancer|August 28, 2023
Co-evolution of <i>AR</i> gene copy number and structural complexity in endocrine therapy resistant prostate cancerAndrej Zivanovic, Jeffrey T Miller, Sarah A Munro, et al.
Medrxiv : the Preprint Server for Health Sciences|October 4, 2023
Long-read sequencing resolves a complex structural variant in <i>PRKN</i> Parkinson's diseaseKensuke Daida, Manabu Funayama, Kimberley J Billingsley, et al.
Brain : a Journal of Neurology|May 31, 2022
Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's diseaseWilliam Zhu, Xiaoping Huang, Esther Yoon, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 6, 2023
Long-Read Sequencing Resolves a Complex Structural Variant in PRKN Parkinson's DiseaseKensuke Daida, Manabu Funayama, Kimberley J Billingsley, et al.
Annals of Oncology : Official Journal of the European Society for Medical Oncology|April 24, 2020
A multicentre, randomised trial comparing schedules of G-CSF (filgrastim) administration for primary prophylaxis of chemotherapy-induced febrile neutropenia in early stage breast cancerM Clemons, D Fergusson, D Simos, et al.
British Journal of Cancer|September 4, 2025
Recommendations for studying the association of the cancer diagnosis to treatment interval with overall survival: a modified Delphi processMatthew Jalink, Will D King, Benjamin O Anderson, et al.
Neurobiology of Aging|September 5, 2017
Establishing the role of rare coding variants in known Parkinson's disease risk lociIris E Jansen, J Raphael Gibbs, Mike A Nalls, et al.
NPJ Parkinson'S Disease|May 25, 2019
Mitochondria function associated genes contribute to Parkinson's Disease risk and later age at onsetKimberley J Billingsley, Ines A Barbosa, Sara Bandrés-Ciga, et al.
Plos Genetics|May 21, 2010
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brainJ Raphael Gibbs, Marcel P van der Brug, Dena G Hernandez, et al.
Pageof 49