Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries (Q47273363)

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scientific article published on 13 March 2009

Ashkenazi Parkinson’s disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries

Language	Label	Description	Also known as
English	Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries	scientific article published on 13 March 2009	Ashkenazi Parkinson’s disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries

Statements

scholarly article

1 reference

Europe PubMed Central

13 January 2018

http://europepmc.org/abstract/MED/19283415

Ashkenazi Parkinson's disease patients with the LRRK2 G2019S mutation share a common founder dating from the second to fifth centuries (English)

1 reference

Europe PubMed Central

13 January 2018

http://europepmc.org/abstract/MED/19283415

Parkinson's disease

1 reference

based on heuristic

inferred from title

Cyrus P Zabetian

4

1 reference

Europe PubMed Central

13 January 2018

http://europepmc.org/abstract/MED/19283415

3

object named as

Nir Giladi

1 reference

Europe PubMed Central

13 January 2018

Avi Orr-Urtreger

5

object named as

Avi Orr-Urtreger

1 reference

Europe PubMed Central

13 January 2018

1

object named as

Anat Bar-Shira

1 reference

Europe PubMed Central

13 January 2018

http://europepmc.org/abstract/MED/19283415

author name string

Carolyn M Hutter

2

1 reference

Europe PubMed Central

13 January 2018

http://europepmc.org/abstract/MED/19283415

publication date

13 March 2009

1 reference

Europe PubMed Central

13 January 2018

http://europepmc.org/abstract/MED/19283415

1 reference

Europe PubMed Central

13 January 2018

http://europepmc.org/abstract/MED/19283415

10

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Europe PubMed Central

13 January 2018

http://europepmc.org/abstract/MED/19283415

355-358

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Europe PubMed Central

13 January 2018

http://europepmc.org/abstract/MED/19283415

4

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Europe PubMed Central

13 January 2018

http://europepmc.org/abstract/MED/19283415

https://scigraph.springernature.com/pub.10.1007/s10048-009-0186-0

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The carrier frequency of the BRCA1 185delAG mutation is approximately 1 percent in Ashkenazi Jewish individuals

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A founding LRRK2 haplotype shared by Tunisian, US, European and Middle Eastern families with Parkinson's disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The ancestry of LRRK2 Gly2019Ser parkinsonism

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular pathogenesis of Parkinson disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

LRRK2 mutations in patients with Parkinson's disease from Peru and Uruguay

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

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/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 185delAG BRCA1 mutation originated before the dispersion of Jews in the diaspora and is not limited to Ashkenazim

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Could the 185delAG BRCA1 mutation be an ancient Jewish mutation?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High prevalence of LRRK2 mutations in familial and sporadic Parkinson's disease in Portugal

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The LRRK2 G2019S mutation in Ashkenazi Jews with Parkinson disease: is there a gender effect?

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of Parkinson's disease in Europe: A collaborative study of population-based cohorts. Neurologic Diseases in the Elderly Research Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/19283415

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10048-009-0186-0

1 reference

Europe PubMed Central

13 January 2018

http://europepmc.org/abstract/MED/19283415

1 reference

Europe PubMed Central

13 January 2018

http://europepmc.org/abstract/MED/19283415

ResearchGate publication ID

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