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Peter Heutink

Showing results (131-140 of 240) with videos related to

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Neurobiology of Aging|February 23, 2013
Regional differences in gene expression and promoter usage in aged human brainsLuba M Pardo, Patrizia Rizzu, Margherita Francescatto, et al.
Medrxiv : the Preprint Server for Health Sciences|January 8, 2026
The Global Parkinson's Disease Genetics (GP2) Genome BrowserZih-Hua Fang, Riley H Grant, Dan Vitale, et al.
Lancet (London, England)|February 5, 2011
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies, Michael A Nalls, Vincent Plagnol, et al.
Obesity (Silver Spring, Md.)|October 23, 2010
Melanocortin-4 receptor gene mutations in a Dutch cohort of obese childrenLinda van den Berg, Olivier van Beekum, Peter Heutink, et al.
Scientific Data|December 13, 2018
Author Correction: Transcription start site profiling of 15 anatomical regions of the Macaca mulatta central nervous systemMargherita Francescatto, Marina Lizio, Ingrid Philippens, et al.
Annals of Neurology|November 5, 2003
Variable phenotypic expression and extensive tau pathology in two families with the novel tau mutation L315REsther van Herpen, Sonia M Rosso, Lies-Anne Serverijnen, et al.
European Journal of Human Genetics : EJHG|January 17, 2008
Genome-wide association of major depression: description of samples for the GAIN Major Depressive Disorder Study: NTR and NESDA biobank projectsDorret I Boomsma, Gonneke Willemsen, Patrick F Sullivan, et al.
Cell Reports|June 8, 2022
Drug screen in iPSC-Neurons identifies nucleoside analogs as inhibitors of (G<sub>4</sub>C<sub>2</sub>)<sub>n</sub> expression in C9orf72 ALS/FTDMareike Czuppa, Ashutosh Dhingra, Qihui Zhou, et al.
Neurology|April 5, 2013
NUBPL mutations in patients with complex I deficiency and a distinct MRI patternSietske H Kevelam, Richard J Rodenburg, Nicole I Wolf, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 17, 2009
The role of the brain-derived neurotrophic factor (BDNF) val66met variant in the phenotypic expression of obsessive-compulsive disorder (OCD)Hilga Katerberg, Christine Lochner, Danielle C Cath, et al.
Pageof 24

Showing results (131-140 of 240) with videos related to

Sort By:
Pageof 24
Neurobiology of Aging|February 23, 2013
Regional differences in gene expression and promoter usage in aged human brainsLuba M Pardo, Patrizia Rizzu, Margherita Francescatto, et al.
Medrxiv : the Preprint Server for Health Sciences|January 8, 2026
The Global Parkinson's Disease Genetics (GP2) Genome BrowserZih-Hua Fang, Riley H Grant, Dan Vitale, et al.
Lancet (London, England)|February 5, 2011
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies, Michael A Nalls, Vincent Plagnol, et al.
Obesity (Silver Spring, Md.)|October 23, 2010
Melanocortin-4 receptor gene mutations in a Dutch cohort of obese childrenLinda van den Berg, Olivier van Beekum, Peter Heutink, et al.
Scientific Data|December 13, 2018
Author Correction: Transcription start site profiling of 15 anatomical regions of the Macaca mulatta central nervous systemMargherita Francescatto, Marina Lizio, Ingrid Philippens, et al.
Annals of Neurology|November 5, 2003
Variable phenotypic expression and extensive tau pathology in two families with the novel tau mutation L315REsther van Herpen, Sonia M Rosso, Lies-Anne Serverijnen, et al.
European Journal of Human Genetics : EJHG|January 17, 2008
Genome-wide association of major depression: description of samples for the GAIN Major Depressive Disorder Study: NTR and NESDA biobank projectsDorret I Boomsma, Gonneke Willemsen, Patrick F Sullivan, et al.
Cell Reports|June 8, 2022
Drug screen in iPSC-Neurons identifies nucleoside analogs as inhibitors of (G<sub>4</sub>C<sub>2</sub>)<sub>n</sub> expression in C9orf72 ALS/FTDMareike Czuppa, Ashutosh Dhingra, Qihui Zhou, et al.
Neurology|April 5, 2013
NUBPL mutations in patients with complex I deficiency and a distinct MRI patternSietske H Kevelam, Richard J Rodenburg, Nicole I Wolf, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 17, 2009
The role of the brain-derived neurotrophic factor (BDNF) val66met variant in the phenotypic expression of obsessive-compulsive disorder (OCD)Hilga Katerberg, Christine Lochner, Danielle C Cath, et al.
Pageof 24