(Q33649391)

28 July 2017

title

Lrrk2 R1441G-related Parkinson's disease: evidence of a common founding event in the seventh century in Northern Spain (English)

1 reference

28 July 2017

1 reference

18

1 reference

28 July 2017

14

Joseph Jankovic

1 reference

28 July 2017

0 references

16

Karen L Edwards

1 reference

28 July 2017

Ignacio F Mata

1

1 reference

28 July 2017

Carolyn M Hutter

2

1 reference

28 July 2017

María C González-Fernández

3

1 reference

28 July 2017

Marian M de Pancorbo

4

1 reference

28 July 2017

Elena Lezcano

5

1 reference

28 July 2017

Cecilia Huerta

6

1 reference

28 July 2017

Marta Blazquez

7

1 reference

28 July 2017

Renee Ribacoba

8

1 reference

28 July 2017

Luis M Guisasola

9

1 reference

28 July 2017

Carlos Salvador

10

1 reference

28 July 2017

Juan C Gómez-Esteban

11

1 reference

28 July 2017

Juan J Zarranz

12

1 reference

28 July 2017

Jon Infante

13

1 reference

28 July 2017

Hao Deng

15

1 reference

28 July 2017

Victoria Alvarez

17

1 reference

28 July 2017

publication date

24 March 2009

1 reference

28 July 2017

1 reference

28 July 2017

volume

10

1 reference

28 July 2017

issue

4

1 reference

28 July 2017

page(s)

347-353

1 reference

Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism

28 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

Parkinson's disease: clinical features and diagnosis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

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.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

The mitochondrial lineage U8a reveals a Paleolithic settlement in the Basque country

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

Genetics of Parkinson disease: paradigm shifts and future prospects.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease*.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

A common LRRK2 mutation in idiopathic Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

MPTP as a mitochondrial neurotoxic model of Parkinson's disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

Patterns of Human Genetic Diversity: Implications for Human Evolutionary History and Disease

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

The mutation rate in the human mtDNA control region

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

Recent male-mediated gene flow over a linguistic barrier in Iberia, suggested by analysis of a Y-chromosomal DNA polymorphism

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

Human genomic diversity in Europe: a summary of recent research and prospects for the future

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

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

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

Molecular evidence of founder effects of fatal familial insomnia through SNP haplotypes around the D178N mutation

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

Mitochondrial DNA haplogroup diversity in Basques: a reassessment based on HVI and HVII polymorphisms.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

Genetic analysis of LRRK2 mutations in patients with Parkinson disease

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

Allelic frequencies of 13 STR loci in autochthonous Basques from the province of Vizcaya (Spain).

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

LRRK2 R1441G in Spanish patients with Parkinson's disease.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

Lrrk2-associated parkinsonism is a major cause of disease in Northern Spain

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

LRRK2 mutations in Parkinson disease

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

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

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2821036

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

10 December 2018

1 reference

12 December 2020

Parkinson's disease due to the R1441G mutation in Dardarin: a founder effect in the Basques

1 reference

12 December 2020

The Basques according to polymorphic Alu insertions

1 reference

12 December 2020

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

1 reference

12 December 2020

Familial Parkinson's disease: a clinical genetic analysis

1 reference

12 December 2020

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

1 reference

12 December 2020

A Common Haplotype Associated with the Basque 2362AG-TCATCT Mutation in the Muscular Calpain-3 Gene

1 reference

12 December 2020

10.1007/S10048-009-0187-Z

Identifiers

DOI

1 reference

release_6yfrwqljszf4th54tx2efyvvcy

28 July 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/6yfrwqljszf4th54tx2efyvvcy

24 November 2022

mapped directly with Wikidata item

PMC publication ID

2821036

1 reference

28 July 2017

1 reference