Literature DB >> 17661825

Mutations in the CHX10 gene in non-syndromic microphthalmia/anophthalmia patients from Qatar.

M Faiyaz-Ul-Haque, S H E Zaidi, M S Al-Mureikhi, I Peltekova, L-C Tsui, A S Teebi.   

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Year:  2007        PMID： 17661825     DOI： 10.1111/j.1399-0004.2007.00846.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


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  15 in total

1.  Genetic architecture of natural variation in visual senescence in Drosophila.

Authors:  Mary Anna Carbone; Akihiko Yamamoto; Wen Huang; Rachel A Lyman; Tess Brune Meadors; Ryoan Yamamoto; Robert R H Anholt; Trudy F C Mackay
Journal:  Proc Natl Acad Sci U S A       Date:  2016-10-10       Impact factor: 11.205

2.  FOXE3 plays a significant role in autosomal recessive microphthalmia.

Authors:  Linda M Reis; Rebecca C Tyler; Adele Schneider; Tanya Bardakjian; Joan M Stoler; Serge B Melancon; Elena V Semina
Journal:  Am J Med Genet A       Date:  2010-03       Impact factor: 2.802

3.  Regulation of WNT Signaling by VSX2 During Optic Vesicle Patterning in Human Induced Pluripotent Stem Cells.

Authors:  Elizabeth E Capowski; Lynda S Wright; Kun Liang; M Joseph Phillips; Kyle Wallace; Anna Petelinsek; Anna Hagstrom; Isabel Pinilla; Katarzyna Borys; Jessica Lien; Jee Hong Min; Sunduz Keles; James A Thomson; David M Gamm
Journal:  Stem Cells       Date:  2016-07-05       Impact factor: 6.277

4.  Use of genome-wide SNP homozygosity mapping in small pedigrees to identify new mutations in VSX2 causing recessive microphthalmia and a semidominant inner retinal dystrophy.

Authors:  Sibel Ugur Iseri; Alexander W Wyatt; Gudrun Nürnberg; Christian Kluck; Peter Nürnberg; Graham E Holder; Ed Blair; Alison Salt; Nicola K Ragge
Journal:  Hum Genet       Date:  2010-04-23       Impact factor: 4.132

5.  Modeling human retinal development with patient-specific induced pluripotent stem cells reveals multiple roles for visual system homeobox 2.

Authors:  M Joseph Phillips; Enio T Perez; Jessica M Martin; Samantha T Reshel; Kyle A Wallace; Elizabeth E Capowski; Ruchira Singh; Lynda S Wright; Eric M Clark; Patrick M Barney; Ron Stewart; Sarah J Dickerson; Michael J Miller; E Ferda Percin; James A Thomson; David M Gamm
Journal:  Stem Cells       Date:  2014-06       Impact factor: 6.277

6.  A genome-wide linkage scan in Tunisian families identifies a novel locus for non-syndromic posterior microphthalmia to chromosome 2q37.1.

Authors:  Mounira Hmani-Aifa; Salma Ben Salem; Zeineb Benzina; Walid Bouassida; Riadh Messaoud; Khalil Turki; Moncef Khairallah; Ahmed Rebaï; Faïza Fakhfekh; Peter Söderkvist; Hammadi Ayadi
Journal:  Hum Genet       Date:  2009-06-14       Impact factor: 4.132

7.  Vsx2 controls eye organogenesis and retinal progenitor identity via homeodomain and non-homeodomain residues required for high affinity DNA binding.

Authors:  Changjiang Zou; Edward M Levine
Journal:  PLoS Genet       Date:  2012-09-20       Impact factor: 5.917

8.  Mutations in the LHX2 gene are not a frequent cause of micro/anophthalmia.

Authors:  Annaïck Desmaison; Adeline Vigouroux; Claudine Rieubland; Christine Peres; Patrick Calvas; Nicolas Chassaing
Journal:  Mol Vis       Date:  2010-12-18       Impact factor: 2.367

9.  VSX2 mutations in autosomal recessive microphthalmia.

Authors:  Linda M Reis; Ayesha Khan; Ariana Kariminejad; Farhad Ebadi; Rebecca C Tyler; Elena V Semina
Journal:  Mol Vis       Date:  2011-09-28       Impact factor: 2.367

10.  Nucleome Dynamics during Retinal Development.

Authors:  Jackie L Norrie; Marybeth S Lupo; Beisi Xu; Issam Al Diri; Marc Valentine; Daniel Putnam; Lyra Griffiths; Jiakun Zhang; Dianna Johnson; John Easton; Ying Shao; Victoria Honnell; Sharon Frase; Shondra Miller; Valerie Stewart; Xin Zhou; Xiang Chen; Michael A Dyer
Journal:  Neuron       Date:  2019-09-04       Impact factor: 17.173
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