Evidence of mutations inRIC3acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes

CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study

(2015) Manabu Funayama et al.   LANCET NEUROLOGY

Progress in unraveling the genetic etiology of Parkinson disease in a genomic era

(2015) Aline Verstraeten et al.   TRENDS IN GENETICS

Nicotinic acetylcholine receptors in human genetic disease

(2014) Christian P. Schaaf   GENETICS IN MEDICINE

Genetic modifiers of cognitive maintenance among older adults

(2014) Jennifer S. Yokoyama et al.   HUMAN BRAIN MAPPING

A genome-wide association study of brain lesion distribution in multiple sclerosis

(2013) Pierre-Antoine Gourraud et al.   BRAIN

DJ-1Variants in Indian Parkinson’s Disease Patients

(2013) Tamal Sadhukhan et al.   DISEASE MARKERS

DNAJC13 mutations in Parkinson disease

(2013) Carles Vilariño-Güell et al.   HUMAN MOLECULAR GENETICS

VPS35 and EIF4G1 mutations are rare in Parkinson's disease among Indians

(2013) Sumedha Sudhaman et al.   NEUROBIOLOGY OF AGING

Genetics of Parkinson's Disease

(2013) C. Klein et al.   Cold Spring Harbor Perspectives in Medicine

Parkinson's Disease: Gene Therapies

(2013) P. G. Coune et al.   Cold Spring Harbor Perspectives in Medicine

wANNOVAR: annotating genetic variants for personal genomes via the web

(2012) Xiao Chang et al.   JOURNAL OF MEDICAL GENETICS

An integrated map of genetic variation from 1,092 human genomes

(2012)   NATURE

Database resources of the National Center for Biotechnology Information

(2012)   NUCLEIC ACIDS RESEARCH

A comprehensive framework for prioritizing variants in exome sequencing studies of Mendelian diseases

(2012) Miao-Xin Li et al.   NUCLEIC ACIDS RESEARCH

Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease

(2011) Marie-Christine Chartier-Harlin et al.   AMERICAN JOURNAL OF HUMAN GENETICS

VPS35 Mutations in Parkinson Disease

(2011) Carles Vilariño-Güell et al.   AMERICAN JOURNAL OF HUMAN GENETICS

A framework for variation discovery and genotyping using next-generation DNA sequencing data

(2011) Mark A DePristo et al.   NATURE GENETICS

Role of Mendelian genes in “sporadic” Parkinson's disease

(2011) Suzanne Lesage et al.   PARKINSONISM & RELATED DISORDERS

Autosomal dominant Parkinson's disease

(2011) Christina Sundal et al.   PARKINSONISM & RELATED DISORDERS

BEDTools: a flexible suite of utilities for comparing genomic features

(2010) Aaron R. Quinlan et al.   BIOINFORMATICS

Ric-3 Promotes  7 Nicotinic Receptor Assembly and Trafficking through the ER Subcompartment of Dendrites

(2010) J. K. Alexander et al.   JOURNAL OF NEUROSCIENCE

The Sequence Alignment/Map format and SAMtools

(2009) H. Li et al.   BIOINFORMATICS

Fast and accurate short read alignment with Burrows-Wheeler transform

(2009) H. Li et al.   BIOINFORMATICS

Molecular pathogenesis of Parkinson disease: insights from genetic studies

(2009) Thomas Gasser   EXPERT REVIEWS IN MOLECULAR MEDICINE

Evaluation of PINK1 variants in Indian Parkinson's disease patients

(2009) Arindam Biswas et al.   PARKINSONISM & RELATED DISORDERS

RIC-3 and nicotinic acetylcholine receptors: Biogenesis, properties, and diversity

(2008) Millet Treinin   Biotechnology Journal