EIF4G1is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohorts: Table1

Analysis of EIF4G1 in ethnic Chinese

(2013) Kai Li et al.   BMC Neurology

Mutations inEIF4G1are not a common cause of Parkinson's disease

(2013) A. Siitonen et al.   EUROPEAN JOURNAL OF NEUROLOGY

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

(2013) Sumedha Sudhaman et al.   NEUROBIOLOGY OF AGING

The importance of rare DNA variation in neurologic disease: Cautionary tale

(2013) J. L. Haines   NEUROLOGY

Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease

(2013) K. Nuytemans et al.   NEUROLOGY

EIF4G1 Ala502Val and Arg1205His variants in Chinese patients with Parkinson disease

(2013) Lamei Yuan et al.   NEUROSCIENCE LETTERS

Sequence variants in eukaryotic translation initiation factor 4-gamma (eIF4G1) are associated with Lewy body dementia

(2012) Shinsuke Fujioka et al.   ACTA NEUROPATHOLOGICA

EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?

(2012) Suzanne Lesage et al.   NEUROBIOLOGY OF AGING

Analysis of EIF4G1 in Parkinson's disease among Asians

(2012) Yi Zhao et al.   NEUROBIOLOGY OF AGING

VPS35 Asp620Asn and EIF4G1 Arg1205His mutations are rare in Parkinson disease from Southwest China

(2012) YongPing Chen et al.   NEUROBIOLOGY OF AGING

Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson’s disease

(2012) Eva C. Schulte et al.   NEUROGENETICS

Study of the genetic variability in a Parkinson's Disease gene: EIF4G1

(2012) Arianna Tucci et al.   NEUROSCIENCE LETTERS

Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease

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

Milestones in PD genetics

(2011) Thomas Gasser et al.   MOVEMENT DISORDERS

Identification of low-frequency variants associated with gout and serum uric acid levels

(2011) Patrick Sulem et al.   NATURE GENETICS

A rare variant in MYH6 is associated with high risk of sick sinus syndrome

(2011) Hilma Holm et al.   NATURE GENETICS

Genetic characteristics of leucine-rich repeat kinase 2 (LRRK2) associated Parkinson’s disease

(2011) Soraya Bardien et al.   PARKINSONISM & RELATED DISORDERS

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

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

Oxidative Stress in Parkinson's Disease

(2010) Chun Zhou et al.   Annals of the New York Academy of Sciences

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

eIF4GI links nutrient sensing by mTOR to cell proliferation and inhibition of autophagy

(2008) Francisco Ramírez-Valle et al.   JOURNAL OF CELL BIOLOGY

Detection of sharing by descent, long-range phasing and haplotype imputation

(2008) Augustine Kong et al.   NATURE GENETICS