Zubair Ahmed
University of Maryland
H-index: 55
North America-United States
Top articles of Zubair Ahmed
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
Syntaxin 4 is essential for hearing in human and zebrafish | Human Molecular Genetics | Isabelle Schrauwen Amama Ghaffar Thashi Bharadwaj Khadim Shah Sakina Rehman | 2023/4/1 |
Appraisal of climate change and source of heavy metals, sediments in water of the Kunhar River watershed, Pakistan | Natural Hazards | Shan-e-hyder Soomro Xiaotao Shi Jiali Guo Caihong Hu Haider M Zwain | 2023/3 |
Regulation of Protocadherin-15 function in the outer retina by alternative splicing of cytoplasmic domain | Investigative Ophthalmology & Visual Science | Sehar Riaz Saumil Sethna Saima Riazuddin Livia Carvalho Zubair Ahmed | 2022/6/1 |
Protocadherin 15 suppresses oligodendrocyte progenitor cell proliferation and promotes motility through distinct signalling pathways | Communications Biology | Yilan Zhen Carlie L Cullen Raphael Ricci Benjamin S Summers Sakina Rehman | 2022/5/30 |
Delineating the Molecular and Phenotypic Spectrum of the CNGA3-Related Cone Photoreceptor Disorder in Pakistani Families | Stefan Barakat K Lanko FJ Guzmán-Vega A Jackson R Ramakrishnan | 2021 | |
Identification of Frameshift Variants in POLH Gene Causing Xeroderma Pigmentosum in Two Consanguineous Pakistani Families | Genes | Ghazala Y Zamani Ranjha Khan Noreen Karim Zubair M Ahmed Muhammad Naeem | 2022/3/19 |
Molecular mechanisms underlying CIB function in inner-ear mechanotransduction | Biophysical Journal | Wei-Hsiang Weng Jonathan Montgomery Sanket Walujkar Jeffrey M Lotthammer Arnaud PJ Giese | 2022/2/11 |
Biallelic in-frame deletion of SOX4 is associated with developmental delay, hypotonia and intellectual disability | European Journal of Human Genetics | Amama Ghaffar Faiza Rasheed Muhammad Rashid Hans van Bokhoven Zubair M Ahmed | 2022/2 |
Corneal structural changes in congenital glaucoma | Eye & contact lens | Jennifer Drechsler Adrianna Lee Snehaa Maripudi Laura Kueny Moran R Levin | 2022/1/1 |
Long-term anatomic and visual outcomes of planned preterm delivery and treatment of Norrie disease | Ophthalmic Surgery, Lasers and Imaging Retina | Robert A Sisk Virginia Miraldi-Utz Terry L Schwartz Robert B Hufnagel Zubair M Ahmed | 2022/8/1 |
ADAMTS1, MPDZ, MVD, and SEZ6: candidate genes for autosomal recessive nonsyndromic hearing impairment | European Journal of Human Genetics | Thashi Bharadwaj Isabelle Schrauwen Sakina Rehman Khurram Liaqat Anushree Acharya | 2022/1 |
Genetic association analysis of 269 rare diseases reveals novel aetiologies | medRxiv | Daniel Greene Genomics England Research Consortium Daniela Pirri Karen Frudd Ege Sackey | 2022/6/14 |
Identification and computational analysis of novel pathogenic variants in Pakistani families with diverse epidermolysis bullosa phenotypes | Biomolecules | Fehmida F Khan Naima Khan Sakina Rehman Amir Ejaz Uzma Ali | 2021/4/22 |
Novel Homozygous Missense Variant in GJA3 Connexin Domain Causing Congenital Nuclear and Cortical Cataracts | International Journal of Molecular Sciences | Abdullah Y Hassan Sairah Yousaf Moran R Levin Osamah J Saeedi Saima Riazuddin | 2021/12/27 |
MODULATION OF mTORCI ACTIVITY AND AUTOPHAGY VIA CIB2-RHEB INTERACTION | 2021/9/23 | ||
Genetic causes of oculocutaneous albinism in Pakistani population | Genes | Zureesha Sajid Sairah Yousaf Yar M Waryah Tauqeer A Mughal Tasleem Kausar | 2021/3/28 |
Putting the pieces together: the hair cell transduction complex | Jeffrey R Holt Mélanie Tobin Johannes Elferich Eric Gouaux Angela Ballesteros | 2021/12/1 | |
Biallelic variants in TMEM222 cause a new autosomal recessive neurodevelopmental disorder | Genetics in Medicine | Daniel L Polla Mohammad Ali Farazi Fard Zahra Tabatabaei Parham Habibzadeh Olga A Levchenko | 2021/7 |
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 | Daniel J Klionsky Amal Kamal Abdel-Aziz Sara Abdelfatah Mahmoud Abdellatif Asghar Abdoli | 2021/1/2 | |
Identification and Computational Analysis of Rare Variants of Known Hearing Loss Genes Present in Five Deaf Members of a Pakistani Kindred | Genes | Irum Badshah Saleem Muhammad Shareef Masoud Muhammad Qasim Muhammad Ali Zubair M Ahmed | 2021/11/30 |
