Associated Papers
Molecular genetics of primary open-angle glaucoma.
Yadav M et al.
Indian Journal of Ophthalmology, 2023
Whole-exome sequencing analysis in a case of primary congenital glaucoma due to the partial uniparental isodisomy.
Zavarzadeh PG et al.
Genomics & Informatics, 2022
Genetic pleiotropy between mood disorders, metabolic, and endocrine traits in a multigenerational pedigree.
Kember RL et al.
Translational Psychiatry, 2018
30315151 (PubMed )
Supplement: 41398_2018_226_MOESM2_ESM.xlsx › Supplemental_Table_6
Analysis of protein-coding genetic variation in 60,706 humans.
Lek M et al.
Nature, 2016
27535533 (PubMed )
Supplement: NIHMS798561-supplement-supp_table20.xlsx › SI_Table_20
Mutation analysis of seven known glaucoma-associated genes in Chinese patients with glaucoma.
Huang X et al.
Investigative Ophthalmology & Visual Science, 2014
Association of eNOS polymorphisms with primary angle-closure glaucoma.
Awadalla MS et al.
Investigative Ophthalmology & Visual Science, 2013
Evaluation of NTF4 as a causative gene for primary open-angle glaucoma.
Chen LJ et al.
Molecular Vision, 2012
Variations in NTF4, VAV2, and VAV3 genes are not involved with primary open-angle and primary angle-closure glaucomas in an indian population.
Rao KN et al.
Investigative Ophthalmology & Visual Science, 2010
Identification of a novel mutation in the NTF4 gene that causes primary open-angle glaucoma in a Chinese population.
Vithana EN et al.
Molecular Vision, 2010
No evidence of association of heterozygous NTF4 mutations in patients with primary open-angle glaucoma.
Liu Y et al.
American Journal of Human Genetics, 2010
Heterozygous NTF4 mutations impairing neurotrophin-4 signaling in patients with primary open-angle glaucoma.
Pasutto F et al.
American Journal of Human Genetics, 2009
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