Gene-based burden analysis of damaging private variants in PRKN, PARK7 and PINK1 in Parkinson's disease cohorts of European descent-Reference-Cited by-同舟云学术

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Gene-based burden analysis of damaging private variants in PRKN, PARK7 and PINK1 in Parkinson's disease cohorts of European descent

Published:2022-11 Issue: Volume:119 Page:136-138
ISSN:0197-4580
Container-title:Neurobiology of Aging
language:en
Short-container-title:Neurobiology of Aging

Author:

Hu Jing,Waters Cheryl H.,Spiegelman Dan,Fon Edward A.,Yu Eric,Asayesh Farnaz,Krohn Lynne,Saini Prabhjyot,Alcalay Roy N.,Hassin-Baer Sharon,Gan-Or Ziv,Krainc Dimitri,Zhang BaoRong,Bustos Bernabe I.,Lubbe Steven J.

Publisher

Elsevier BV

Subject

Geriatrics and Gerontology,Developmental Biology,Neurology (clinical),Aging,General Neuroscience

Reference15 articles.

1. Next Generation Sequencing of Pooled Samples: Guideline for Variants’ Filtering;Anand;Sci. Rep.,2016

2. Autosomal recessive Parkinsonism;Bonifati;Parkinsonism Relat. Disord.,2012

3. Private variants in PRKN are associated with late-onset Parkinson's disease;Hopfner;Parkinsonism Relat Disord,2020

4. The mutational constraint spectrum quantified from variation in 141,456 humans;Karczewski;Nature,2020

5. Genotype-phenotype relations for the Parkinson's disease genes Parkin, PINK1, DJ1: MDSGene systematic review;Kasten;Mov. Disord.,2018

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