<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Cook L</submitter><funding>Parkinson's Foundation</funding><funding>NIA NIH HHS</funding><funding>NINDS NIH HHS</funding><funding>Parkinson’s Foundation</funding><pagination>2668-2679</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11292896</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>147(8)</volume><pubmed_abstract>Variants in seven genes (LRRK2, GBA1, PRKN, SNCA, PINK1, PARK7 and VPS35) have been formally adjudicated as causal contributors to Parkinson's disease; however, individuals with Parkinson's disease are often unaware of their genetic status since clinical testing is infrequently offered. As a result, genetic information is not incorporated into clinical care, and variant-targeted precision medicine trials struggle to enrol people with Parkinson's disease. Understanding the yield of genetic testing using an established gene panel in a large, geographically diverse North American population would help patients, clinicians, clinical researchers, laboratories and insurers better understand the importance of genetics in approaching Parkinson's disease. PD GENEration is an ongoing multi-centre, o</pubmed_abstract><journal>Brain : a journal of neurology</journal><pubmed_title>Parkinson's disease variant detection and disclosure: PD GENEration, a North American study.</pubmed_title><pmcid>PMC11292896</pmcid><funding_grant_id>P30 AG066518</funding_grant_id><funding_grant_id>P30 AG072979</funding_grant_id><funding_grant_id>K08 NS131581</funding_grant_id><pubmed_authors>Marder KS</pubmed_authors><pubmed_authors>Singer C</pubmed_authors><pubmed_authors>Strom SP</pubmed_authors><pubmed_authors>Carbonell J</pubmed_authors><pubmed_authors>Rao SC</pubmed_authors><pubmed_authors>Mencacci NE</pubmed_authors><pubmed_authors>Blauwendraat C</pubmed_authors><pubmed_authors>Wills AM</pubmed_authors><pubmed_authors>Meng Y</pubmed_authors><pubmed_authors>Bressman S</pubmed_authors><pubmed_authors>Alcalay RN</pubmed_authors><pubmed_authors>Schwantes-An TH</pubmed_authors><pubmed_authors>Litvan I</pubmed_authors><pubmed_authors>Nance MA</pubmed_authors><pubmed_authors>Simuni T</pubmed_authors><pubmed_authors>Cruz Vicioso R</pubmed_authors><pubmed_authors>Katus L</pubmed_authors><pubmed_authors>Ghosh Galvelis K</pubmed_authors><pubmed_authors>Hall A</pubmed_authors><pubmed_authors>Shill HA</pubmed_authors><pubmed_authors>Lohmann K</pubmed_authors><pubmed_authors>Hodges PD</pubmed_authors><pubmed_authors>Foroud T</pubmed_authors><pubmed_authors>Mata IF</pubmed_authors><pubmed_authors>Lyons KE</pubmed_authors><pubmed_authors>Verbrugge J</pubmed_authors><pubmed_authors>Cook L</pubmed_authors><pubmed_authors>Quinn JF</pubmed_authors><pubmed_authors>Schwarzschild MA</pubmed_authors><pubmed_authors>Casaceli C</pubmed_authors><pubmed_authors>Beck JC</pubmed_authors><pubmed_authors>Naito A</pubmed_authors><pubmed_authors>Schulze J</pubmed_authors><pubmed_authors>Fernandez HH</pubmed_authors><pubmed_authors>Tropea TF</pubmed_authors><pubmed_authors>Vanegas Arroyave N</pubmed_authors></additional><is_claimable>false</is_claimable><name>Parkinson's disease variant detection and disclosure: PD GENEration, a North American study.</name><description>Variants in seven genes (LRRK2, GBA1, PRKN, SNCA, PINK1, PARK7 and VPS35) have been formally adjudicated as causal contributors to Parkinson's disease; however, individuals with Parkinson's disease are often unaware of their genetic status since clinical testing is infrequently offered. As a result, genetic information is not incorporated into clinical care, and variant-targeted precision medicine trials struggle to enrol people with Parkinson's disease. Understanding the yield of genetic testing using an established gene panel in a large, geographically diverse North American population would help patients, clinicians, clinical researchers, laboratories and insurers better understand the importance of genetics in approaching Parkinson's disease. PD GENEration is an ongoing multi-centre, o</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2026-06-23T03:13:44.078Z</modification><creation>2025-02-19T02:27:20.835Z</creation></dates><accession>S-EPMC11292896</accession><cross_references><pubmed>39074992</pubmed><doi>10.1093/brain/awae142</doi></cross_references></HashMap>