<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11</volume><submitter>Rajan R</submitter><funding>Michael J. Fox Foundation for Parkinson&amp;apos;s Research</funding><pubmed_abstract>Over the past two decades, our understanding of Parkinson's disease (PD) has been gleaned from the discoveries made in familial and/or sporadic forms of PD in the Caucasian population. The transferability and the clinical utility of genetic discoveries to other ethnically diverse populations are unknown. The Indian population has been under-represented in PD research. The Genetic Architecture of PD in India (GAP-India) project aims to develop one of the largest clinical/genomic bio-bank for PD in India. Specifically, GAP-India project aims to: (1) develop a pan-Indian deeply phenotyped clinical repository of Indian PD patients; (2) perform whole-genome sequencing in 500 PD samples to catalog Indian genetic variability and to develop an Indian PD map for the scientific community; (3) perfor</pubmed_abstract><journal>Frontiers in neurology</journal><pagination>524</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7323575</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease Research.</pubmed_title><pmcid>PMC7323575</pmcid><pubmed_authors>Grover S</pubmed_authors><pubmed_authors>Sturm M</pubmed_authors><pubmed_authors>Divya KP</pubmed_authors><pubmed_authors>Agarwal P</pubmed_authors><pubmed_authors>Ramalingam S</pubmed_authors><pubmed_authors>Bhatt M</pubmed_authors><pubmed_authors>Goyal V</pubmed_authors><pubmed_authors>Kumar N</pubmed_authors><pubmed_authors>Sreeram Prasad AV</pubmed_authors><pubmed_authors>Gasser T</pubmed_authors><pubmed_authors>Satagopam VP</pubmed_authors><pubmed_authors>Schwamborn J</pubmed_authors><pubmed_authors>Riess O</pubmed_authors><pubmed_authors>Pal PK</pubmed_authors><pubmed_authors>Desai S</pubmed_authors><pubmed_authors>Kishore A</pubmed_authors><pubmed_authors>Kumar S</pubmed_authors><pubmed_authors>Ferreira T</pubmed_authors><pubmed_authors>Rajan R</pubmed_authors><pubmed_authors>Mehta S</pubmed_authors><pubmed_authors>Wali GM</pubmed_authors><pubmed_authors>Yadav R</pubmed_authors><pubmed_authors>Kandadai RM</pubmed_authors><pubmed_authors>Chandak GR</pubmed_authors><pubmed_authors>Prashanth LK</pubmed_authors><pubmed_authors>Kumar-Sreelatha A</pubmed_authors><pubmed_authors>Hannussek M</pubmed_authors><pubmed_authors>Shetty K</pubmed_authors><pubmed_authors>Busskamp V</pubmed_authors><pubmed_authors>Borgohain R</pubmed_authors><pubmed_authors>Bartusch F</pubmed_authors><pubmed_authors>Pandey S</pubmed_authors><pubmed_authors>Sharma M</pubmed_authors><pubmed_authors>Madhusoodanan UK</pubmed_authors><pubmed_authors>Kruger J</pubmed_authors><pubmed_authors>Seth P</pubmed_authors><pubmed_authors>Lichtner P</pubmed_authors><pubmed_authors>Kumar H</pubmed_authors><pubmed_authors>Wadia P</pubmed_authors><pubmed_authors>Roeper J</pubmed_authors><pubmed_authors>Kruger R</pubmed_authors><pubmed_authors>Lux-GIANT Consortium</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease Research.</name><description>Over the past two decades, our understanding of Parkinson's disease (PD) has been gleaned from the discoveries made in familial and/or sporadic forms of PD in the Caucasian population. The transferability and the clinical utility of genetic discoveries to other ethnically diverse populations are unknown. The Indian population has been under-represented in PD research. The Genetic Architecture of PD in India (GAP-India) project aims to develop one of the largest clinical/genomic bio-bank for PD in India. Specifically, GAP-India project aims to: (1) develop a pan-Indian deeply phenotyped clinical repository of Indian PD patients; (2) perform whole-genome sequencing in 500 PD samples to catalog Indian genetic variability and to develop an Indian PD map for the scientific community; (3) perfor</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020</publication><modification>2026-04-30T03:52:56.599Z</modification><creation>2020-11-20T08:53:27Z</creation></dates><accession>S-EPMC7323575</accession><cross_references><pubmed>32655481</pubmed><doi>10.3389/fneur.2020.00524</doi></cross_references></HashMap>