Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)
Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the
Global Parkinson’s Genetics Program (GP2) | npj Parkinson's Disease Skip to main content …
Global Parkinson’s Genetics Program (GP2) | npj Parkinson's Disease Skip to main content …
Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2)
Abstract The Monogenic Network of the Global Parkinson's Genetics Program (GP2) aims to
create an efficient infrastructure to accelerate the identification of novel genetic causes of …
create an efficient infrastructure to accelerate the identification of novel genetic causes of …
Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2)
C Towns, M Richer, S Jasaityte, EJ Stafford… - npj Parkinson's …, 2023 - nature.com
Abstract The Global Parkinson's Genetics Program (GP2) will genotype over 150,000
participants from around the world, and integrate genetic and clinical data for use in large …
participants from around the world, and integrate genetic and clinical data for use in large …
Ten years of the International Parkinson Disease Genomics Consortium: progress and next steps
International Parkinson Disease … - Journal of …, 2020 - content.iospress.com
In June 2009 a small group of investigators met at the annual Movement Disorders Society
meeting in Paris. The explicit goal of this meeting was to discuss a potential research …
meeting in Paris. The explicit goal of this meeting was to discuss a potential research …
[图书][B] Celebrating the Diversity of Genetic Research to Dissect the Pathogenesis of Parkinson's Disease
S Bardien, GD Mellick, N Hattori, OA Ross, S Lesage - 2021 - books.google.com
Celebrating the Diversity of Genetic Research to Dissect the Pathogenesis of Parkinson's
Disease Page 1 CELEBRATING THE DIVERSITY OF GENETIC RESEARCH TO DISSECT THE …
Disease Page 1 CELEBRATING THE DIVERSITY OF GENETIC RESEARCH TO DISSECT THE …
Molecular genetics of Parkinson's disease: Contributions and global trends
M Funayama, K Nishioka, Y Li, N Hattori - Journal of human genetics, 2023 - nature.com
Parkinson's disease (PD) is a neurodegenerative disorder primarily characterized by motor
dysfunction. Aging is the greatest risk factor for developing PD. Recent molecular genetic …
dysfunction. Aging is the greatest risk factor for developing PD. Recent molecular genetic …
WITHDRAWN: Genetics of Parkinson's disease.
CM Lill - Molecular and Cellular Probes, 2020 - europepmc.org
The Publisher regrets that this article is an accidental duplication of an article that has
already been published, DOI of original article: https://doi. org/10.1016/j. mcp. 2016.11. 001 …
already been published, DOI of original article: https://doi. org/10.1016/j. mcp. 2016.11. 001 …
[HTML][HTML] Parkinson disease overview
LC Shukla, J Schulze, J Farlow, ND Pankratz… - GeneReviews® …, 2019 - ncbi.nlm.nih.gov
Parkinson Disease Overview - GeneReviews® - NCBI Bookshelf Your browser does not support
the NLM PubReader view. Go to this page to see a list of supported browsers or return to the …
the NLM PubReader view. Go to this page to see a list of supported browsers or return to the …
The birth of the modern era of Parkinson's disease genetics
AB Singleton, JA Hardy… - Journal of Parkinson's …, 2017 - content.iospress.com
Genetic understanding in Parkinson's disease (PD) has followed a path of hard won
evolution occasionally punctuated by revolution. While it was suggested early on by both …
evolution occasionally punctuated by revolution. While it was suggested early on by both …
Progress in the genetic analysis of Parkinson's disease
A Singleton, J Hardy - Human molecular genetics, 2019 - academic.oup.com
The pace of genetic discovery in complex disease has accelerated exponentially over the
last decade. Our fund of knowledge of the foundational genetics in disease has never been …
last decade. Our fund of knowledge of the foundational genetics in disease has never been …