(Q33321350)

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An evaluation of the performance of HapMap SNP data in a Shanghai Chinese population: analyses of allele frequency, linkage disequilibrium pattern and tagging SNPs transferability on chromosome 1q21-q25

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scholarly article

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Europe PubMed Central

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3 January 2020

An evaluation of the performance of HapMap SNP data in a Shanghai Chinese population: analyses of allele frequency, linkage disequilibrium pattern and tagging SNPs transferability on chromosome 1q21-q25 (English)

1 reference

Europe PubMed Central

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3 January 2020

1 reference

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inferred from title

linkage disequilibrium

1 reference

based on heuristic

inferred from title

1

1 reference

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3 January 2020

Matthew J. Farrer

1 reference

ORCID Public Data File 2021

author name string

Weiping Jia

2

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3 January 2020

Weihua Zhang

3

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3 January 2020

Congrong Wang

4

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3 January 2020

Rong Zhang

5

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3 January 2020

Jie Wang

6

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3 January 2020

Xiaojing Ma

7

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3 January 2020

International Type 2 Diabetes 1q Consortium

8

1 reference

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3 January 2020

Kunsan Xiang

9

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3 January 2020

publication date

27 February 2008

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3 January 2020

1 reference

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3 January 2020

9

1 reference

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3 January 2020

19

1 reference

Europe PubMed Central

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3 January 2020

https://scigraph.springernature.com/pub.10.1186/1471-2350-9-19

0 references

Significant variation in haplotype block structure but conservation in tagSNP patterns among global populations

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21 June 2018

Similarity of the allele frequency and linkage disequilibrium pattern of single nucleotide polymorphisms in drug-related gene loci between Thai and northern East Asian populations: implications for tagging SNP selection in Thais

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21 June 2018

Comparison of linkage disequilibrium patterns between the HapMap CEPH samples and a family-based cohort of Northern European descent

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21 June 2018

An evaluation of the performance of tag SNPs derived from HapMap in a Caucasian population

1 reference

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21 June 2018

Linkage disequilibrium sharing and haplotype-tagged SNP portability between populations.

1 reference

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21 June 2018

On the utility of data from the International HapMap Project for Australian association studies.

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21 June 2018

Evaluating HapMap SNP data transferability in a large-scale genotyping project involving 175 cancer-associated genes

1 reference

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21 June 2018

An evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data sets

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21 June 2018

A haplotype map of the human genome

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21 June 2018

Factors affecting statistical power in the detection of genetic association

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21 June 2018

A note on exact tests of Hardy-Weinberg equilibrium

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21 June 2018

Linkage disequilibrium patterns and tagSNP transferability among European populations

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21 June 2018

Genetic evidence supports demic diffusion of Han culture

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21 June 2018

Haploview: analysis and visualization of LD and haplotype maps

1 reference

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21 June 2018

Integrating ethics and science in the International HapMap Project

1 reference

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21 June 2018

The complex interplay among factors that influence allelic association.

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21 June 2018

The International HapMap Project

1 reference

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21 June 2018

Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium

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21 June 2018

The structure of haplotype blocks in the human genome

1 reference

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21 June 2018

Association study designs for complex diseases

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21 June 2018

Genetic relationship of populations in China

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21 June 2018

Gm and Km allotypes in 74 Chinese populations: a hypothesis of the origin of the Chinese nation

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21 June 2018

Alpha-synuclein in Lewy bodies

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21 January 2018

alpha-Synuclein in filamentous inclusions of Lewy bodies from Parkinson's disease and dementia with lewy bodies

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21 January 2018

Filamentous alpha-synuclein inclusions link multiple system atrophy with Parkinson's disease and dementia with Lewy bodies.

1 reference

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21 January 2018

Glial cytoplasmic inclusions in white matter oligodendrocytes of multiple system atrophy brains contain insoluble alpha-synuclein.

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21 January 2018

Synphilin-1 associates with alpha-synuclein and promotes the formation of cytosolic inclusions

1 reference

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21 January 2018

Immunocytochemical localization of synphilin-1, an alpha-synuclein-associated protein, in neurodegenerative disorders.

1 reference

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21 January 2018

Synphilin-1 is developmentally localized to synaptic terminals, and its association with synaptic vesicles is modulated by alpha-synuclein

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21 January 2018

Parkin ubiquitinates the alpha-synuclein-interacting protein, synphilin-1: implications for Lewy-body formation in Parkinson disease

1 reference

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21 January 2018

Organization of the human synphilin-1 gene, a candidate for Parkinson's disease

1 reference

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21 January 2018

Sequence conservation between mouse and human synphilin-1

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21 January 2018

Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease

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21 January 2018

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

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21 January 2018

Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations

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21 January 2018

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21 January 2018

Diagnostic criteria for Parkinson disease

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21 January 2018

No pathogenic mutations in the synphilin-1 gene in Parkinson's disease

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21 January 2018

Ubiquitylation of synphilin-1 and alpha-synuclein by SIAH and its presence in cellular inclusions and Lewy bodies imply a role in Parkinson's disease

1 reference

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21 January 2018

Parkin mediates nonclassical, proteasomal-independent ubiquitination of synphilin-1: implications for Lewy body formation

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21 January 2018

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21 January 2018

Tag SNPs chosen from HapMap perform well in several population isolates

1 reference

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31 October 2018

Sample size calculations for population- and family-based case-control association studies on marker genotypes.

1 reference

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31 October 2018

Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms

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31 October 2018

Genetic Analysis of Synphilin-1 in Familial Parkinson's Disease

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21 January 2018

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21 January 2018

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31 October 2018

Comparative study of the linkage disequilibrium of an ENCODE region, chromosome 7p15, in Korean, Japanese, and Han Chinese samples

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12 December 2020

based on heuristic

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Identifiers

10.1186/1471-2350-9-19

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Europe PubMed Central

25 July 2017

10.1186/1471-2156-9-19

1 reference

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3 January 2020

Dimensions Publication ID

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https://scigraph.springernature.com/pub.10.1186/1471-2350-9-19

9 September 2019

1 reference

Europe PubMed Central

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3 January 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18302794%20AND%20SRC:MED&resulttype=core&format=json

3 January 2020

reason for deprecated rank

incorrect identifier value

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