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Peter Heutink

Showing results (161-170 of 240) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|May 29, 2002
Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactylyLaura A Lettice, Taizo Horikoshi, Simon J H Heaney, et al.
NPJ Parkinson'S Disease|June 27, 2023
Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)Lara M Lange, Micol Avenali, Melina Ellis, et al.
NPJ Parkinson'S Disease|September 13, 2023
Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)Lara M Lange, Micol Avenali, Melina Ellis, et al.
Nature Neuroscience|November 29, 2018
Publisher Correction: Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric diseaseXianjun Dong, Zhixiang Liao, David Gritsch, et al.
Acta Neuropathologica Communications|July 7, 2022
Distinct cell type-specific protein signatures in GRN and MAPT genetic subtypes of frontotemporal dementiaSuzanne S M Miedema, Merel O Mol, Frank T W Koopmans, et al.
Nature Neuroscience|September 19, 2018
Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric diseaseXianjun Dong, Zhixiang Liao, David Gritsch, et al.
Science (New York, N.Y.)|September 2, 2017
β2-Adrenoreceptor is a regulator of the α-synuclein gene driving risk of Parkinson's diseaseShuchi Mittal, Kjetil Bjørnevik, Doo Soon Im, et al.
Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
Polygenic scores for disease risk are not associated with clinical outcomes in Parkinson's diseaseManuela Mx Tan, Hirotaka Iwaki, Sara Bandres-Ciga, et al.
Human Genetics|October 17, 2007
A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6pMarja W Wessels, Bianca M De Graaf, Titia E Cohen-Overbeek, et al.
Nature Genetics|April 4, 2006
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studiesSusan Service, Joseph DeYoung, Maria Karayiorgou, et al.
Pageof 24

Showing results (161-170 of 240) with videos related to

Sort By:
Pageof 24
Proceedings of the National Academy of Sciences of the United States of America|May 29, 2002
Disruption of a long-range cis-acting regulator for Shh causes preaxial polydactylyLaura A Lettice, Taizo Horikoshi, Simon J H Heaney, et al.
NPJ Parkinson'S Disease|June 27, 2023
Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)Lara M Lange, Micol Avenali, Melina Ellis, et al.
NPJ Parkinson'S Disease|September 13, 2023
Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)Lara M Lange, Micol Avenali, Melina Ellis, et al.
Nature Neuroscience|November 29, 2018
Publisher Correction: Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric diseaseXianjun Dong, Zhixiang Liao, David Gritsch, et al.
Acta Neuropathologica Communications|July 7, 2022
Distinct cell type-specific protein signatures in GRN and MAPT genetic subtypes of frontotemporal dementiaSuzanne S M Miedema, Merel O Mol, Frank T W Koopmans, et al.
Nature Neuroscience|September 19, 2018
Enhancers active in dopamine neurons are a primary link between genetic variation and neuropsychiatric diseaseXianjun Dong, Zhixiang Liao, David Gritsch, et al.
Science (New York, N.Y.)|September 2, 2017
β2-Adrenoreceptor is a regulator of the α-synuclein gene driving risk of Parkinson's diseaseShuchi Mittal, Kjetil Bjørnevik, Doo Soon Im, et al.
Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
Polygenic scores for disease risk are not associated with clinical outcomes in Parkinson's diseaseManuela Mx Tan, Hirotaka Iwaki, Sara Bandres-Ciga, et al.
Human Genetics|October 17, 2007
A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6pMarja W Wessels, Bianca M De Graaf, Titia E Cohen-Overbeek, et al.
Nature Genetics|April 4, 2006
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studiesSusan Service, Joseph DeYoung, Maria Karayiorgou, et al.
Pageof 24