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R van Eijk

Showing results (51-60 of 89) with videos related to

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The Pharmacogenomics Journal|October 19, 2019
Pharmacogenetic interactions in amyotrophic lateral sclerosis: a step closer to a cure?Ruben P A van Eijk, Marinus J C Eijkemans, Stavros Nikolakopoulos, et al.
Schizophrenia Research|August 20, 2013
The effect of childhood maltreatment and cannabis use on adult psychotic symptoms is modified by the COMT Val¹⁵⁸Met polymorphismChristiaan H Vinkers, Willemijn A Van Gastel, Christian D Schubart, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|May 3, 2012
A common variant in ERBB4 regulates GABA concentrations in human cerebrospinal fluidJurjen J Luykx, Christiaan H Vinkers, Steven C Bakker, et al.
Nature Genetics|November 14, 1997
BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patientsA Petrij-Bosch, T Peelen, M van Vliet, et al.
Neurology. Genetics|February 12, 2020
Analysis of <i>FUS</i>, <i>PFN2, TDP-43</i>, and <i>PLS3</i> as potential disease severity modifiers in spinal muscular atrophyRenske I Wadman, Marc D Jansen, Chantall A D Curial, et al.
Translational Psychiatry|June 24, 2020
The role of rare compound heterozygous events in autism spectrum disorderBochao Danae Lin, Fabrice Colas, Isaac J Nijman, et al.
Elife|November 19, 2021
Enrichment of <i>SARM1</i> alleles encoding variants with constitutively hyperactive NADase in patients with ALS and other motor nerve disordersJonathan Gilley, Oscar Jackson, Menelaos Pipis, et al.
NAR Genomics and Bioinformatics|February 8, 2021
Cross-reactive probes on Illumina DNA methylation arrays: a large study on ALS shows that a cautionary approach is warranted in interpreting epigenome-wide association studiesPaul J Hop, Ramona A J Zwamborn, Eilis J Hannon, et al.
Scientific Reports|April 13, 2019
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosisAnnelot M Dekker, Frank P Diekstra, Sara L Pulit, et al.
JAMA Ophthalmology|July 6, 2023
Association of Risk Variants in the CFH Gene With Elevated Levels of Coagulation and Complement Factors in Idiopathic Multifocal ChoroiditisEvianne L de Groot, Jeannette Ossewaarde-van Norel, Joke H de Boer, et al.
Pageof 9

Showing results (51-60 of 89) with videos related to

Sort By:
Pageof 9
The Pharmacogenomics Journal|October 19, 2019
Pharmacogenetic interactions in amyotrophic lateral sclerosis: a step closer to a cure?Ruben P A van Eijk, Marinus J C Eijkemans, Stavros Nikolakopoulos, et al.
Schizophrenia Research|August 20, 2013
The effect of childhood maltreatment and cannabis use on adult psychotic symptoms is modified by the COMT Val¹⁵⁸Met polymorphismChristiaan H Vinkers, Willemijn A Van Gastel, Christian D Schubart, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|May 3, 2012
A common variant in ERBB4 regulates GABA concentrations in human cerebrospinal fluidJurjen J Luykx, Christiaan H Vinkers, Steven C Bakker, et al.
Nature Genetics|November 14, 1997
BRCA1 genomic deletions are major founder mutations in Dutch breast cancer patientsA Petrij-Bosch, T Peelen, M van Vliet, et al.
Neurology. Genetics|February 12, 2020
Analysis of <i>FUS</i>, <i>PFN2, TDP-43</i>, and <i>PLS3</i> as potential disease severity modifiers in spinal muscular atrophyRenske I Wadman, Marc D Jansen, Chantall A D Curial, et al.
Translational Psychiatry|June 24, 2020
The role of rare compound heterozygous events in autism spectrum disorderBochao Danae Lin, Fabrice Colas, Isaac J Nijman, et al.
Elife|November 19, 2021
Enrichment of <i>SARM1</i> alleles encoding variants with constitutively hyperactive NADase in patients with ALS and other motor nerve disordersJonathan Gilley, Oscar Jackson, Menelaos Pipis, et al.
NAR Genomics and Bioinformatics|February 8, 2021
Cross-reactive probes on Illumina DNA methylation arrays: a large study on ALS shows that a cautionary approach is warranted in interpreting epigenome-wide association studiesPaul J Hop, Ramona A J Zwamborn, Eilis J Hannon, et al.
Scientific Reports|April 13, 2019
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosisAnnelot M Dekker, Frank P Diekstra, Sara L Pulit, et al.
JAMA Ophthalmology|July 6, 2023
Association of Risk Variants in the CFH Gene With Elevated Levels of Coagulation and Complement Factors in Idiopathic Multifocal ChoroiditisEvianne L de Groot, Jeannette Ossewaarde-van Norel, Joke H de Boer, et al.
Pageof 9