CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration (Q24681526)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16936733%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

title

CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16936733%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

1 reference

10

1 reference

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29 December 2019

Gonçalo Abecasis

11

1 reference

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29 December 2019

3

Mohammad Othman

1 reference

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29 December 2019

7

Yun Li

1 reference

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29 December 2019

author name string

Mingyao Li

1

1 reference

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29 December 2019

Pelin Atmaca-Sonmez

2

1 reference

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29 December 2019

Kari E H Branham

4

1 reference

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29 December 2019

Ritu Khanna

5

1 reference

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29 December 2019

Michael S Wade

6

1 reference

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29 December 2019

Liming Liang

8

1 reference

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29 December 2019

Sepideh Zareparsi

9

1 reference

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29 December 2019

language of work or name

English

0 references

publication date

27 August 2006

1 reference

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29 December 2019

1 reference

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29 December 2019

volume

38

1 reference

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29 December 2019

issue

9

1 reference

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29 December 2019

page(s)

1049-1054

1 reference

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Cigarette smoking strongly modifies the association of LOC387715 and age-related macular degeneration

29 December 2019

cites work

1 reference

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7 April 2017

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Susceptibility genes for age-related maculopathy on chromosome 10q26

7 April 2017

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7 April 2017

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Complement factor H polymorphism in age-related macular degeneration

7 April 2017

1 reference

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A New Statistical Method for Haplotype Reconstruction from Population Data

7 April 2017

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Complement factor H variant increases the risk of age-related macular degeneration

7 April 2017

1 reference

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Complement factor H polymorphism and age-related macular degeneration

7 April 2017

1 reference

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

7 April 2017

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Efficient study designs for test of genetic association using sibship data and unrelated cases and controls

7 April 2017

1 reference

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Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk

28 September 2017

1 reference

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Meta-analysis of genome scans of age-related macular degeneration

28 September 2017

1 reference

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Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration

28 September 2017

1 reference

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Joint modeling of linkage and association: identifying SNPs responsible for a linkage signal

28 September 2017

1 reference

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Genetic inheritance of gene expression in human cell lines

28 September 2017

1 reference

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28 September 2017

1 reference

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Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data

28 September 2017

1 reference

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A genomewide scan for age-related macular degeneration provides evidence for linkage to several chromosomal regions

28 September 2017

1 reference

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28 September 2017

1 reference

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An international classification and grading system for age-related maculopathy and age-related macular degeneration. The International ARM Epidemiological Study Group

28 September 2017

1 reference

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Linkage strategies for genetically complex traits. I. Multilocus models

28 September 2017

1 reference

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Detecting disease-predisposing variants: the haplotype method

28 September 2017

1 reference

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30 May 2018

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Risk factors for age-related macular degeneration: Pooled findings from three continents.

21 January 2018

1 reference

Ten-year incidence of age-related maculopathy and smoking and drinking: the Beaver Dam Eye Study

21 January 2018

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21 January 2018

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Testing association of statistically inferred haplotypes with discrete and continuous traits in samples of unrelated individuals.

21 January 2018

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Leber congenital amaurosis and retinitis pigmentosa with Coats-like exudative vasculopathy are associated with mutations in the crumbs homologue 1 (CRB1) gene

21 January 2018

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21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16936733

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Risk factors of age-related maculopathy in a population 70 years of age or older

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/16936733

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NG1871

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16936733%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

29 December 2019

1040680942

0 references

1 reference

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16936733%20AND%20SRC:MED&resulttype=core&format=json

29 December 2019

2 references

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16936733%20AND%20SRC:MED&resulttype=core&format=json