Literature DB >> 15136529

Genetics and ARMD.

Ian M MacDonald, Matthew A Lines.   

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Year:  2004        PMID： 15136529      PMCID： PMC400700          DOI： 10.1503/cmaj.1040494

Source DB:  PubMed          Journal:  CMAJ        ISSN： 0820-3946            Impact factor:   8.262


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  8 in total

Review 1.  Simple and complex ABCR: genetic predisposition to retinal disease.

Authors:  R Allikmets
Journal:  Am J Hum Genet       Date:  2000-09-01       Impact factor: 11.025

Review 2.  Age-related macular degeneration: etiology, pathogenesis, and therapeutic strategies.

Authors:  Jayakrishna Ambati; Balamurali K Ambati; Sonia H Yoo; Sean Ianchulev; Anthony P Adamis
Journal:  Surv Ophthalmol       Date:  2003 May-Jun       Impact factor: 6.048

3.  Age-related macular degeneration: armed against ARMD.

Authors:  Erica Weir
Journal:  CMAJ       Date:  2004-02-17       Impact factor: 8.262

4.  Genetic risk of age-related maculopathy. Population-based familial aggregation study.

Authors:  C C Klaver; R C Wolfs; J J Assink; C M van Duijn; A Hofman; P T de Jong
Journal:  Arch Ophthalmol       Date:  1998-12

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

Authors:  R Allikmets
Journal:  Nat Genet       Date:  1997-09       Impact factor: 38.330

6.  Prospective study of dietary fat and the risk of age-related macular degeneration.

Authors:  E Cho; S Hung; W C Willett; D Spiegelman; E B Rimm; J M Seddon; G A Colditz; S E Hankinson
Journal:  Am J Clin Nutr       Date:  2001-02       Impact factor: 7.045

7.  A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy.

Authors:  K Zhang; M Kniazeva; M Han; W Li; Z Yu; Z Yang; Y Li; M L Metzker; R Allikmets; D J Zack; L E Kakuk; P S Lagali; P W Wong; I M MacDonald; P A Sieving; D J Figueroa; C P Austin; R J Gould; R Ayyagari; K Petrukhin
Journal:  Nat Genet       Date:  2001-01       Impact factor: 38.330

8.  Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.

Authors:  Matthew A Lines; Marc Hébert; Kerry E McTaggart; Sarah J Flynn; Matthew T Tennant; Ian M MacDonald
Journal:  Ophthalmology       Date:  2002-10       Impact factor: 12.079
  8 in total

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