(Q57309530)

9

object named as

Jeffrey R. Gulcher

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author name string

Hjörvar Pétursson

2

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Thorlákur Jónsson

3

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Hreinn Stefánsson

4

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Hrefna S. Jóhannsdóttir

5

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Jesus Sainz

6

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Michael L. Frigge

7

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Augustine Kong

8

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Kári Stefánsson

10

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Sigurlaug Sveinbjörnsdóttir

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

11

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publication date

20 September 2002

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published in

Annals of Neurology

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volume

52

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page(s)

549-555

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issue

5

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cites work

1 reference

A susceptibility locus for Parkinson's disease maps to chromosome 2p13.

21 January 2018

1 reference

The ubiquitin pathway in Parkinson's disease.

21 January 2018

1 reference

A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

21 January 2018

1 reference

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

21 January 2018

1 reference

Chromosome 6-linked autosomal recessive early-onset Parkinsonism: linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family. The French Parkinson's Disease Genetics Study

21 January 2018

1 reference

Association between early-onset Parkinson's disease and mutations in the parkin gene

21 January 2018

1 reference

Localization of a novel locus for autosomal recessive early-onset parkinsonism, PARK6, on human chromosome 1p35-p36

21 January 2018

1 reference

Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36.

21 January 2018

1 reference

A new locus for Parkinson's disease (PARK8) maps to chromosome 12p11.2-q13.1.

21 January 2018

1 reference

Parkinson disease in twins: an etiologic study

21 January 2018

1 reference

Familial Aggregation of Parkinson's Disease in Iceland

21 January 2018

1 reference

Genome-wide scan for Parkinson's disease: the GenePD Study

21 January 2018

1 reference

Complete genomic screen in Parkinson disease: evidence for multiple genes.

21 January 2018

1 reference

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

21 January 2018

1 reference

Cerebral palsy in Iceland

21 January 2018

1 reference

Parkinsonism: onset, progression, and mortality

21 January 2018

1 reference

Protection of privacy by third-party encryption in genetic research in Iceland

21 January 2018

1 reference

Localization of a susceptibility gene for common forms of stroke to 5q12

21 January 2018

1 reference

Olfactory receptor-gene clusters, genomic-inversion polymorphisms, and common chromosome rearrangements

21 January 2018

1 reference

Allele-sharing models: LOD scores and accurate linkage tests

21 January 2018

1 reference

Allegro, a new computer program for multipoint linkage analysis

21 January 2018

1 reference

A class of tests for linkage using affected pedigree members

21 January 2018

1 reference

Large upward bias in estimation of locus-specific effects from genomewide scans

21 January 2018

1 reference

Familial aggregation of Parkinson's disease in a Finnish population

21 January 2018

1 reference

Familial aggregation of Parkinson's disease: A population-based case-control study in Europe

21 January 2018

1 reference

The role of inheritance in sporadic Parkinson's disease: evidence from a longitudinal study of dopaminergic function in twins.

21 January 2018

1 reference

Lewy bodies and parkinsonism in families with parkin mutations

21 January 2018

1 reference

Age at onset in two common neurodegenerative diseases is genetically controlled

21 January 2018

1 reference

A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor

21 January 2018

1 reference