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Peter Heutink

Showing results (151-160 of 240) with videos related to

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Human Genetics|December 22, 2005
Evidence for novel loci for late-onset Parkinson's disease in a genetic isolate from the NetherlandsAida M Bertoli-Avella, Marieke C J Dekker, Yurii S Aulchenko, et al.
Science (New York, N.Y.)|November 26, 2002
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonismVincenzo Bonifati, Patrizia Rizzu, Marijke J van Baren, et al.
Human Mutation|July 11, 2012
Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunitiesFlorian Mittag, Finja Büchel, Mohamad Saad, et al.
Neurobiology of Disease|December 6, 2021
Novel Machado-Joseph disease-modifying genes and pathways identified by whole-exome sequencingMafalda Raposo, Conceição Bettencourt, Ana Rosa Vieira Melo, et al.
American Journal of Human Genetics|July 8, 2017
A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar AtaxiaAna I Seixas, Joana R Loureiro, Cristina Costa, et al.
Nature|November 1, 2011
Somatic retrotransposition alters the genetic landscape of the human brainJ Kenneth Baillie, Mark W Barnett, Kyle R Upton, et al.
Human Molecular Genetics|April 25, 2002
Mutations in TITF-1 are associated with benign hereditary choreaGuido J Breedveld, Jeroen W F van Dongen, Cesare Danesino, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
Genome-wide association study confirms extant PD risk loci among the DutchJavier Simón-Sánchez, Jacobus J van Hilten, Bart van de Warrenburg, et al.
Molecular Neurodegeneration|July 15, 2022
17q21.31 sub-haplotypes underlying H1-associated risk for Parkinson's disease are associated with LRRC37A/2 expression in astrocytesKathryn R Bowles, Derian A Pugh, Yiyuan Liu, et al.
Molecular Psychiatry|May 17, 2023
Multi-ancestry meta-analysis and fine-mapping in Alzheimer's diseaseJulie Lake, Caroline Warly Solsberg, Jonggeol Jeffrey Kim, et al.
Pageof 24

Showing results (151-160 of 240) with videos related to

Sort By:
Pageof 24
Human Genetics|December 22, 2005
Evidence for novel loci for late-onset Parkinson's disease in a genetic isolate from the NetherlandsAida M Bertoli-Avella, Marieke C J Dekker, Yurii S Aulchenko, et al.
Science (New York, N.Y.)|November 26, 2002
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonismVincenzo Bonifati, Patrizia Rizzu, Marijke J van Baren, et al.
Human Mutation|July 11, 2012
Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunitiesFlorian Mittag, Finja Büchel, Mohamad Saad, et al.
Neurobiology of Disease|December 6, 2021
Novel Machado-Joseph disease-modifying genes and pathways identified by whole-exome sequencingMafalda Raposo, Conceição Bettencourt, Ana Rosa Vieira Melo, et al.
American Journal of Human Genetics|July 8, 2017
A Pentanucleotide ATTTC Repeat Insertion in the Non-coding Region of DAB1, Mapping to SCA37, Causes Spinocerebellar AtaxiaAna I Seixas, Joana R Loureiro, Cristina Costa, et al.
Nature|November 1, 2011
Somatic retrotransposition alters the genetic landscape of the human brainJ Kenneth Baillie, Mark W Barnett, Kyle R Upton, et al.
Human Molecular Genetics|April 25, 2002
Mutations in TITF-1 are associated with benign hereditary choreaGuido J Breedveld, Jeroen W F van Dongen, Cesare Danesino, et al.
European Journal of Human Genetics : EJHG|January 21, 2011
Genome-wide association study confirms extant PD risk loci among the DutchJavier Simón-Sánchez, Jacobus J van Hilten, Bart van de Warrenburg, et al.
Molecular Neurodegeneration|July 15, 2022
17q21.31 sub-haplotypes underlying H1-associated risk for Parkinson's disease are associated with LRRC37A/2 expression in astrocytesKathryn R Bowles, Derian A Pugh, Yiyuan Liu, et al.
Molecular Psychiatry|May 17, 2023
Multi-ancestry meta-analysis and fine-mapping in Alzheimer's diseaseJulie Lake, Caroline Warly Solsberg, Jonggeol Jeffrey Kim, et al.
Pageof 24