(Q34307274)

1 August 2017

Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration (English)

1 reference

1 August 2017

0 references

67

1 reference

Margaret A. Pericak-Vance

1 August 2017

51

Margaret A Pericak-Vance

0 references

Mark Lathrop

39

Mark Lathrop

1 reference

1 August 2017

Felix Grassmann

25

0 references

Arvydas Maminishkis

Arvydas Maminishkis

11

0 references

Jacqueline Ramke

Jacqueline Ramke

30

0 references

Robert N. Fariss

Robert N Fariss

3

0 references

Samuel G. Jacobson

Samuel G Jacobson

52

0 references

Bernhard H Weber

Bernhard H Weber

57

0 references

Daniel E. Weeks

Daniel E Weeks

62

0 references

Lindsay A. Farrer

Lindsay A Farrer

36

0 references

Ivana K Kim

Ivana K Kim

29

0 references

Sudha Iyengar

Sudha K Iyengar

56

0 references

Andrew J Lotery

Andrew Lotery

16

0 references

Dwight Stambolian

61

Dwight Stambolian

1 reference

1 August 2017

58

Jonathan L Haines

1 reference

1 August 2017

13

Matthew Brooks

1 reference

1 August 2017

1

Rinki Ratnapriya

2 references

ORCID Public Data File 2021

1 August 2017

Mohammad Othman

9

Mohammad Othman

1 reference

1 August 2017

64

Emily Y Chew

1 reference

1 August 2017

50

Chi-Chao Chan

1 reference

1 August 2017

47

Yvette Conley

1 reference

1 August 2017

49

Donald J Zack

1 reference

1 August 2017

66

Gonçalo R Abecasis

1 reference

1 August 2017

15

Albert O Edwards

1 reference

1 August 2017

4

Kari E Branham

1 reference

1 August 2017

43

Stephanie A Hagstrom

1 reference

1 August 2017

38

Neal S Peachey

1 reference

1 August 2017

60

Margaret M Deangelis

1 reference

1 August 2017

65

John R Heckenlively

1 reference

1 August 2017

41

Robert P Igo

1 reference

1 August 2017

32

Joanna E Merriam

1 reference

1 August 2017

44

Yoichiro Kamatani

1 reference

1 August 2017

21

Denise J Morgan

1 reference

1 August 2017

22

Margaux A Morrison

1 reference

1 August 2017

20

Debra A Schaumberg

1 reference

1 August 2017

27

Giuliana Silvestri

1 reference

1 August 2017

23

Eric Souied

1 reference

1 August 2017

18

Barbara J Truitt

1 reference

1 August 2017

24

Evangelia E Tsironi

1 reference

1 August 2017

55

Rando Allikmets

1 reference

1 August 2017

59

Thierry Léveillard

1 reference

1 August 2017

7

Yuri V Sergeev

1 reference

1 August 2017

33

John C Merriam

1 reference

1 August 2017

35

Lana M Olson

1 reference

1 August 2017

46

Yingda Jiang

1 reference

1 August 2017

28

Hendrik P N Scholl

1 reference

1 August 2017

12

Naushin H Waseem

1 reference

1 August 2017

6

Christina F Chakarova

1 reference

1 August 2017

63

Shomi S Bhattacharya

1 reference

1 August 2017

Xiaowei Zhan

2

1 reference

1 August 2017

David Zipprer

5

1 reference

1 August 2017

Maria M Campos

8

1 reference

1 August 2017

James S Friedman

10

1 reference

1 August 2017

Harsha K Rajasimha

14

1 reference

1 August 2017

Barbara E Klein

17

1 reference

1 August 2017

Bingshan Li

19

1 reference

1 August 2017

Gerald A Fishman

26

1 reference

1 August 2017

Jingsheng Tuo

31

1 reference

1 August 2017

Kyu Hyung Park

34

1 reference

1 August 2017

Matthew P Johnson

37

1 reference

1 August 2017

Robert V Baron

40

1 reference

1 August 2017

Ronald Klein

42

1 reference

1 August 2017

Tammy M Martin

45

1 reference

1 August 2017

Jose-Alan Sahel

48

1 reference

1 August 2017

Michael B Gorin

53

1 reference

1 August 2017

Michael L Klein

54

1 reference

1 August 2017

4 June 2014

1 reference

1 August 2017

Human Molecular Genetics

1 reference

1 August 2017

23

1 reference

1 August 2017

21

1 reference

1 August 2017

5827-5837

1 reference

Distilling pathophysiology from complex disease genetics

1 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Identification of a rare coding variant in complement 3 associated with age-related macular degeneration

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Seven new loci associated with age-related macular degeneration

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Genetic studies of age-related macular degeneration: lessons, challenges, and opportunities for disease management

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Spatial distribution of the pathways of cholesterol homeostasis in human retina

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Genetic insights into age-related macular degeneration: controversies addressing risk, causality, and therapeutics

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Rare and common variants: twenty arguments

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Prospective assessment of genetic effects on progression to different stages of age-related macular degeneration using multistate Markov models

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

The mystery of missing heritability: Genetic interactions create phantom heritability

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

A rare penetrant mutation in CFH confers high risk of age-related macular degeneration.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

The oil spill in ageing Bruch membrane

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

A CTRP5 gene S163R mutation knock-in mouse model for late-onset retinal degeneration

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Fibrillin assemblies: extracellular determinants of tissue formation and fibrosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Beals-Hecht syndrome and choroidal neovascularization.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

LocusZoom: regional visualization of genome-wide association scan results

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

METAL: fast and efficient meta-analysis of genomewide association scans

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Uncovering the roles of rare variants in common disease through whole-genome sequencing

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Genome-wide association study of advanced age-related macular degeneration identifies a role of the hepatic lipase gene (LIPC)

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Genetic variants near TIMP3 and high-density lipoprotein-associated loci influence susceptibility to age-related macular degeneration

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

A generalized family-based association test for dichotomous traits

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Biogenesis and function of fibrillin assemblies

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

The Sequence Alignment/Map format and SAMtools

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Fast and accurate short read alignment with Burrows-Wheeler transform

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Unraveling a multifactorial late-onset disease: from genetic susceptibility to disease mechanisms for age-related macular degeneration

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

The SWISS-MODEL Repository and associated resources

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Fibrillin-rich microfibrils: Structural determinants of morphogenetic and homeostatic events

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Current concepts of ocular manifestations in Marfan syndrome

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Macular degeneration: recent advances and therapeutic opportunities.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Late-onset macular degeneration and long anterior lens zonules result from a CTRP5 gene mutation.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Decreased thickness and integrity of the macular elastic layer of Bruch's membrane correspond to the distribution of lesions associated with age-related macular degeneration.

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Fibrillin-1 and fibrillin-2 show temporal and tissue-specific regulation of expression in developing elastic tissues

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Tissue inhibitor of metalloproteinases-3 (TIMP-3) is a binding partner of epithelial growth factor-containing fibulin-like extracellular matrix protein 1 (EFEMP1). Implications for macular degenerations

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Measuring inconsistency in meta-analyses

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Mutation in a short-chain collagen gene, CTRP5, results in extracellular deposit formation in late-onset retinal degeneration: a genetic model for age-related macular degeneration

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

A novel function for tissue inhibitor of metalloproteinases-3 (TIMP3): inhibition of angiogenesis by blockage of VEGF binding to VEGF receptor-2

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Aberrant accumulation of EFEMP1 underlies drusen formation in Malattia Leventinese and age-related macular degeneration

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

An integrated hypothesis that considers drusen as biomarkers of immune-mediated processes at the RPE-Bruch's membrane interface in aging and age-related macular degeneration

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Further evidence for an association of ABCR alleles with age-related macular degeneration. The International ABCR Screening Consortium

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Early drusen formation in the normal and aging eye and their relation to age related maculopathy: a clinicopathological study

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Accumulation of tissue inhibitor of metalloproteinases-3 in human eyes with Sorsby's fundus dystrophy or retinitis pigmentosa

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

SMART: identification and annotation of domains from signalling and extracellular protein sequences

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Mutations in the tissue inhibitor of metalloproteinases-3 (TIMP3) in patients with Sorsby's fundus dystrophy

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Bruch's membrane change with age

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4189898

Comparison of morphology of human macular and peripheral Bruch's membrane in older eyes

28 July 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU276

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU276

Ocular findings of Beals syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU276

Transforming growth factor‐β induces expression of vascular endothelial growth factor in human retinal pigment epithelial cells: Involvement of mitogen‐activated protein kinases

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU276

A functional variant in the CFI gene confers a high risk of age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU276

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU276

A rare nonsynonymous sequence variant in C3 is associated with high risk of age-related macular degeneration

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU276

Age-related macular degeneration

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24899048

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Clustering of FBN2 mutations in patients with congenital contractural arachnodactyly indicates an important role of the domains encoded by exons 24 through 34 during human development

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24899048

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1093/HMG/DDU276

1 reference

1 August 2017

1 reference

1 August 2017

1 reference