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Humaira Ayub

Showing results (11-20 of 20) with videos related to

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Plos One|August 15, 2014
Association of a polymorphism in the BIRC6 gene with pseudoexfoliative glaucomaHumaira Ayub, Shazia Micheal, Farah Akhtar, et al.
Plos One|November 19, 2014
Exome sequencing identifies three novel candidate genes implicated in intellectual disabilityZehra Agha, Zafar Iqbal, Maleeha Azam, et al.
Annals of Human Genetics|March 22, 2019
Association of rs10490924 in ARMS2/HTRA1 with age-related macular degeneration in the Pakistani populationHumaira Ayub, Sobia Shafique, Aisha Azam, et al.
Plos One|June 21, 2014
Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani familiesSobia Shafique, Saima Siddiqi, Margit Schraders, et al.
Molecular Vision|April 6, 2013
Exome sequencing identifies a novel and a recurrent BBS1 mutation in Pakistani families with Bardet-Biedl syndromeMuhammad Ajmal, Muhammad Imran Khan, Kornelia Neveling, et al.
Plos One|March 17, 2015
Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistanMaleeha Maria, Muhammad Ajmal, Maleeha Azam, et al.
Human Molecular Genetics|April 16, 2019
The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndromeDaniel Berner, Ursula Hoja, Matthias Zenkel, et al.
Nature Communications|August 15, 2025
Functionally deficient UBOX5 variants and primary angle-closure glaucomaZheng Li, Wee Ling Chng, Zhehao Liu, et al.
Nature Genetics|April 12, 2016
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucomaChiea Chuen Khor, Tan Do, Hongyan Jia, et al.
Nature Genetics|May 30, 2017
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility lociTin Aung, Mineo Ozaki, Mei Chin Lee, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Plos One|August 15, 2014
Association of a polymorphism in the BIRC6 gene with pseudoexfoliative glaucomaHumaira Ayub, Shazia Micheal, Farah Akhtar, et al.
Plos One|November 19, 2014
Exome sequencing identifies three novel candidate genes implicated in intellectual disabilityZehra Agha, Zafar Iqbal, Maleeha Azam, et al.
Annals of Human Genetics|March 22, 2019
Association of rs10490924 in ARMS2/HTRA1 with age-related macular degeneration in the Pakistani populationHumaira Ayub, Sobia Shafique, Aisha Azam, et al.
Plos One|June 21, 2014
Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani familiesSobia Shafique, Saima Siddiqi, Margit Schraders, et al.
Molecular Vision|April 6, 2013
Exome sequencing identifies a novel and a recurrent BBS1 mutation in Pakistani families with Bardet-Biedl syndromeMuhammad Ajmal, Muhammad Imran Khan, Kornelia Neveling, et al.
Plos One|March 17, 2015
Homozygosity mapping and targeted sanger sequencing reveal genetic defects underlying inherited retinal disease in families from pakistanMaleeha Maria, Muhammad Ajmal, Maleeha Azam, et al.
Human Molecular Genetics|April 16, 2019
The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndromeDaniel Berner, Ursula Hoja, Matthias Zenkel, et al.
Nature Communications|August 15, 2025
Functionally deficient UBOX5 variants and primary angle-closure glaucomaZheng Li, Wee Ling Chng, Zhehao Liu, et al.
Nature Genetics|April 12, 2016
Genome-wide association study identifies five new susceptibility loci for primary angle closure glaucomaChiea Chuen Khor, Tan Do, Hongyan Jia, et al.
Nature Genetics|May 30, 2017
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility lociTin Aung, Mineo Ozaki, Mei Chin Lee, et al.
Pageof 2