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J Raphael

Showing results (471-480 of 488) with videos related to

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Human Molecular Genetics|February 6, 2009
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosisAdriano Chiò, Jennifer C Schymick, Gabriella Restagno, et al.
Neuron|September 28, 2011
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDAlan E Renton, Elisa Majounie, Adrian Waite, et al.
Nature|January 25, 2023
Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomesEsther Rheinbay, Morten Muhlig Nielsen, Federico Abascal, et al.
Nature|February 7, 2020
Analyses of non-coding somatic drivers in 2,658 cancer whole genomesEsther Rheinbay, Morten Muhlig Nielsen, Federico Abascal, et al.
The New England Journal of Medicine|May 3, 2013
Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia, Timothy J Ley, Christopher Miller, et al.
Cell Genomics|October 22, 2024
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic dataSara Saez-Atienzar, Cleide Dos Santos Souza, Ruth Chia, et al.
Nature Genetics|June 25, 2013
Genome-wide meta-analysis identifies new susceptibility loci for migraineVerneri Anttila, Bendik S Winsvold, Padhraig Gormley, 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.
Neuron|May 3, 2024
Genome sequence analyses identify novel risk loci for multiple system atrophyRuth Chia, Anindita Ray, Zalak Shah, et al.
Medrxiv : the Preprint Server for Health Sciences|April 29, 2026
<i>Trans</i> -eQTLs reveal the architecture of human gene regulatory networksC A Robert Warmerdam, Harm-Jan Westra, Adriaan van der Graaf, et al.
Pageof 49

Showing results (471-480 of 488) with videos related to

Sort By:
Pageof 49
Human Molecular Genetics|February 6, 2009
A two-stage genome-wide association study of sporadic amyotrophic lateral sclerosisAdriano Chiò, Jennifer C Schymick, Gabriella Restagno, et al.
Neuron|September 28, 2011
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTDAlan E Renton, Elisa Majounie, Adrian Waite, et al.
Nature|January 25, 2023
Author Correction: Analyses of non-coding somatic drivers in 2,658 cancer whole genomesEsther Rheinbay, Morten Muhlig Nielsen, Federico Abascal, et al.
Nature|February 7, 2020
Analyses of non-coding somatic drivers in 2,658 cancer whole genomesEsther Rheinbay, Morten Muhlig Nielsen, Federico Abascal, et al.
The New England Journal of Medicine|May 3, 2013
Genomic and epigenomic landscapes of adult de novo acute myeloid leukemia, Timothy J Ley, Christopher Miller, et al.
Cell Genomics|October 22, 2024
Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic dataSara Saez-Atienzar, Cleide Dos Santos Souza, Ruth Chia, et al.
Nature Genetics|June 25, 2013
Genome-wide meta-analysis identifies new susceptibility loci for migraineVerneri Anttila, Bendik S Winsvold, Padhraig Gormley, 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.
Neuron|May 3, 2024
Genome sequence analyses identify novel risk loci for multiple system atrophyRuth Chia, Anindita Ray, Zalak Shah, et al.
Medrxiv : the Preprint Server for Health Sciences|April 29, 2026
<i>Trans</i> -eQTLs reveal the architecture of human gene regulatory networksC A Robert Warmerdam, Harm-Jan Westra, Adriaan van der Graaf, et al.
Pageof 49