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Public Health Genomics and Precision Health Knowledge Base (v9.0)
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Precision Health Database|Search|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
Last data update: May 18, 2024
. (Total: 63881 Documents since 2012)
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RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses.
Emil K Gustavsson et al. Lancet Neurol 2024
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Factors Influencing Patient Disclosure of Parkinson's Disease Genetic Testing Results to Relatives.
Jeanine Schulze et al. Mov Disord Clin Pract 2024
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HFE genotypes, haemochromatosis diagnosis and clinical outcomes at age 80 years: a prospective cohort study in the UK Biobank.
Mitchell R Lucas et al. BMJ Open 2024 14(3) e081926
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Levodopa-induced dyskinesia in early-onset Parkinson's disease (EOPD) associates with glucocerebrosidase mutation: A next-generation sequencing study in EOPD patients in Thailand.
Sekh Thanprasertsuk et al. PLoS One 2023 18(10) e0293516
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Challenges of Parkinson's disease GWASs in African people.
Samia Ben Sassi et al. Lancet Neurol 2023 22(11) 975-976
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Genetic literacy and attitude towards genetic testing in patients with Parkinson's disease and their caregivers: A review of literature.
Sneha D Kamath et al. Parkinsonism Relat Disord 2023 105853
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Risk factor for Parkinson's discovered in genes from people of African descent
J Hamilton, NPR, September 24, 2023
Caffeine intake interacts with Asian gene variants in Parkinson's disease: a study in 4488 subjects.
Yi-Lin Ong et al. Lancet Reg Health West Pac 2023 40100877
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Readiness for Parkinson's disease genetic testing and counseling in patients and their relatives in urban settings in the Dominican Republic.
Margaret Hackl et al. NPJ Parkinsons Dis 2023 9(1) 126
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Genome-wide Analysis of Motor Progression in Parkinson Disease.
Alejandro Martínez Carrasco et al. Neurol Genet 2023 9(5) e200092
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Genetic Testing in Parkinson's Disease.
Gian Pal et al. Mov Disord 2023
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International Genetic Testing and Counseling Practices for Parkinson's Disease.
Rachel Saunders-Pullman et al. Mov Disord 2023
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Shared genetic risk loci between Alzheimer's disease and related dementias, Parkinson's disease, and amyotrophic lateral sclerosis.
Michael Wainberg et al. Alzheimers Res Ther 2023 15(1) 113
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Providing Genetic Testing and Genetic Counseling for Parkinson’s Disease to the Community
L Cook et al, Genetics in Medicine, June 8, 2023
Implementation of Exome Sequencing in Clinical Practice for Neurological Disorders.
María Isabel Alvarez-Mora et al. Genes (Basel) 2023 14(4)
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Advancing the Genetics of Lewy Body Disorders with Disease-Modifying Treatments in Mind.
Gilberto Levy et al. Advanced genetics (Hoboken, N.J.) 2023 3(4) 2200011
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Differences in survival across monogenic forms of Parkinson's disease.
Aymeric Lanore et al. Annals of neurology 2023
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Association between RIT2 rs16976358 Polymorphism and Autism Spectrum Disorder in Asian Populations: A Meta-analysis.
Jing Wang et al. BioMed research international 2023 20238886927
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An exploration of knowledge, risk perceptions, and communication in a family with multiple genetic risks for Parkinson's disease.
Daykin Emily C et al. Journal of genetic counseling 2023
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Participant perspective on the recall-by-genotype research approach: a mixed-method embedded study with participants of the CHRIS study.
Biasiotto Roberta et al. European journal of human genetics : EJHG 2023
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Motor and non-motor features in Parkinson's Disease patients carrying GBA gene mutations.
De Michele Giovanna et al. Acta neurologica Belgica 2023
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Screening for the FMR1 premutation in Greek patients with late-onset movement disorders.
Kartanou Chrisoula et al. Parkinsonism & related disorders 2022 107105253
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Calculating variant penetrance from family history of disease and average family size in population-scale data.
Spargo Thomas P et al. Genome medicine 2022 14(1) 141
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Early-Onset Parkinson's Disease: Creating the Right Environment for a Genetic Disorder.
Kolicheski Ana et al. Journal of Parkinson's disease 2022
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Tools for communicating risk for Parkinson's disease.
Cook Lola et al. NPJ Parkinson's disease 2022 8(1) 164
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Association of rare PPARGC1A variants with Parkinson's disease risk.
Li Li-Zhi et al. Journal of human genetics 2022
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Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence From the COURAGE-PD Consortium.
Grover Sandeep et al. Neurology 2022 99(7) e698-e710
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GPNMB confers risk for Parkinson's disease through interaction with α-synuclein.
Diaz-Ortiz Maria E et al. Science (New York, N.Y.) 2022 377(6608) eabk0637
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Epigenetic Clock Acceleration Is Linked to Age at Onset of Parkinson's Disease.
Tang Xuelin et al. Movement disorders : official journal of the Movement Disorder Society 2022
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Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions.
Schumacher-Schuh Artur Francisco et al. Movement disorders : official journal of the Movement Disorder Society 2022
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Page last reviewed:
Feb 1, 2024
Page last updated:
May 18, 2024
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Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
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National Center on Birth Defects and Developmental Disabilities
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