LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago. (Q35070498)

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English	LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago.	scientific article

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scholarly article

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PubMed publication ID

6 August 2017

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LRRK2 G2019S in families with Parkinson disease who originated from Europe and the Middle East: evidence of two distinct founding events beginning two millennia ago. (English)

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Europe PubMed Central

PubMed publication ID

6 August 2017

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Parkinson's disease

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based on heuristic

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Cyrus P Zabetian

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6 August 2017

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John G Nutt

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Stewart A Factor

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Stewart A Factor

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6 August 2017

John W. Roberts

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John W Roberts

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Dora Yearout

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6 August 2017

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Ali Samii

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Haydeh Payami

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Alida Griffith

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6 August 2017

Carolyn M Hutter

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Carolyn M Hutter

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Berta C Leis

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6 August 2017

Karen L Edwards

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Karen L Edwards

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author name string

Alexis N Lopez

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6 August 2017

Thomas D Bird

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6 August 2017

Donald S Higgins

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6 August 2017

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publication date

17 August 2006

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6 August 2017

American Journal of Human Genetics

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6 August 2017

79

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6 August 2017

4

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6 August 2017

752-758

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6 August 2017

The G6055A (G2019S) mutation in LRRK2 is frequent in both early and late onset Parkinson's disease and originates from a common ancestor

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

8 July 2018

Cross-cultural estimation of the human generation interval for use in genetics-based population divergence studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

8 July 2018

Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

8 July 2018

Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation

1 reference

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8 July 2018

A common LRRK2 mutation in idiopathic Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

8 July 2018

Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

8 July 2018

Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

8 July 2018

Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

8 July 2018

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

1 reference

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8 July 2018

Genetic anthropology of the colorectal cancer-susceptibility allele APC I1307K: evidence of genetic drift within the Ashkenazim

1 reference

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8 July 2018

Alzheimer's disease and Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

8 July 2018

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

8 July 2018

The mutation rate in the human mtDNA control region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

8 July 2018

Age estimate of the N370S mutation causing Gaucher disease in Ashkenazi Jews and European populations: A reappraisal of haplotype data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

8 July 2018

New estimates of intergenerational time intervals for the calculation of age and origins of mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

8 July 2018

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

8 July 2018

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

8 July 2018

The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

8 July 2018

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

27 September 2018

Parkinson's disease and LRRK2: frequency of a common mutation in U.S. movement disorder clinics

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

27 September 2018

LRRK2 haplotype analyses in European and North African families with Parkinson disease: a common founder for the G2019S mutation dating from the 13th century

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

27 September 2018

A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

27 September 2018

MAP-O-MAT: internet-based linkage mapping.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

27 September 2018

Estimating the age of rare disease mutations: the example of Triple-A syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

27 September 2018

Age estimates of two common mutations causing factor XI deficiency: recent genetic drift is not necessary for elevated disease incidence among Ashkenazi Jews

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1592578

27 September 2018

Identification and haplotype analysis of LRRK2 G2019S in Japanese patients with Parkinson disease

1 reference

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9 December 2018

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/16960813

12 December 2020

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A common founder for amyotrophic lateral sclerosis type 8 (ALS8) in the Brazilian population

1 reference

https://pubmed.ncbi.nlm.nih.gov/16960813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

LRRK2G2019S as a Cause of Parkinson's Disease in North African Arabs

1 reference

https://pubmed.ncbi.nlm.nih.gov/16960813

12 December 2020

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inferred from PubMed ID database lookup

Increased risk of Parkinson's disease in parents and siblings of patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/16960813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial Parkinson's disease: a clinical genetic analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/16960813

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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Europe PubMed Central

PubMed publication ID

6 August 2017

PMC publication ID

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Europe PubMed Central

PubMed publication ID

6 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 August 2017

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