Zubair M Ahmed (Z M Ahmed)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 31

Top Venues

Genes

Communications biology

Nature medicine

International journal of molecular sciences

This page only lists publications with an associated author ORCID identifier.

Publications

Muhammad A Usmani, Amama Ghaffar, Mohsin Shahzad, Javed Akram, Aisha I Majeed, Kausar Malik, Khushbakht Fatima, Asma A Khan, Zubair M Ahmed, Sheikh Riazuddin, Saima Riazuddin
A Missense Variant in HACE1 Is Associated with Intellectual Disability, Epilepsy, Spasticity, and Psychomotor Impairment in a Pakistani Kindred. Genes 15 (5) (2024)
Amama Ghaffar, Tehmeena Akhter, Petter Strømme, Doriana Misceo, Amjad Khan, Eirik Frengen, Muhammad Umair, Bertrand Isidor, Benjamin Cogné, Asma A Khan, Ange-Line Bruel, Arthur Sorlin, Paul Kuentz, Christine Chiaverini, A Micheil Innes, Michael Zech, Marek Baláž, Petra Havrankova, Robert Jech, Zubair M Ahmed, Sheikh Riazuddin, Saima Riazuddin
Variants of NAV3, a neuronal morphogenesis protein, cause intellectual disability, developmental delay, and microcephaly. Communications biology 7 (1) (2024)
Arnaud P J Giese, Andrew Parker, Sakina Rehman, Steve D M Brown, Saima Riazuddin, Craig W Vander Kooi, Michael R Bowl, Zubair M Ahmed
CIB2 function is distinct from Whirlin in the development of cochlear stereocilia staircase pattern. bioRxiv : the preprint server for biology (2024)
Ayesha Yousaf, Sairah Yousaf, Asra S Shabbir, Rafia Yousaf, Saima Riazuddin, Rehan S Shaikh, Regie Lyn P Santos-Cortez, Zubair M Ahmed
Identification of rare missense variants in the BSN gene co-segregating with chronic otitis media in a consanguineous Pakistani family. Molecular genetics & genomic medicine 12 (9) (2024)
Amama Ghaffar, Tehmeena Akhter, Petter Strømme, Doriana Misceo, Amjad Khan, Eirik Frengen, Muhammad Umair, Bertrand Isidor, Benjamin Cogné, Asma A Khan, Ange-Line Bruel, Arthur Sorlin, Paul Kuentz, Christine Chiaverini, A Micheil Innes, Michael Zech, Marek Baláž, Petra Havrankova, Robert Jech, Zubair M Ahmed, Sheikh Riazuddin, Saima Riazuddin
Variants of NAV3, a neuronal morphogenesis protein, cause intellectual disability, developmental delay, and microcephaly. Communications biology 7 (1) (2024)
Muhammad A Usmani, Amama Ghaffar, Mohsin Shahzad, Javed Akram, Aisha I Majeed, Kausar Malik, Khushbakht Fatima, Asma A Khan, Zubair M Ahmed, Sheikh Riazuddin, Saima Riazuddin
A Missense Variant in HACE1 Is Associated with Intellectual Disability, Epilepsy, Spasticity, and Psychomotor Impairment in a Pakistani Kindred. Genes 15 (5) (2024)
Arnaud P J Giese, Andrew Parker, Sakina Rehman, Steve D M Brown, Saima Riazuddin, Craig W Vander Kooi, Michael R Bowl, Zubair M Ahmed
CIB2 function is distinct from Whirlin in the development of cochlear stereocilia staircase pattern. bioRxiv : the preprint server for biology (2024)
Amama Ghaffar, Tehmeena Akhter, Petter Strømme, Doriana Misceo, Amjad Khan, Eirik Frengen, Muhammad Umair, Bertrand Isidor, Benjamin Cogné, Asma A Khan, Ange-Line Bruel, Arthur Sorlin, Paul Kuentz, Christine Chiaverini, A Micheil Innes, Michael Zech, Marek Baláž, Petra Havrankova, Robert Jech, Zubair M Ahmed, Sheikh Riazuddin, Saima Riazuddin
Variants of NAV3, a neuronal morphogenesis protein, cause intellectual disability, developmental delay, and microcephaly. Communications biology 7 (1) (2024)
Amama Ghaffar, Tehmeena Akhter, Petter Strømme, Doriana Misceo, Amjad Khan, Eirik Frengen, Muhammad Umair, Bertrand Isidor, Benjamin Cogné, Asma A Khan, Ange-Line Bruel, Arthur Sorlin, Paul Kuentz, Christine Chiaverini, A Micheil Innes, Michael Zech, Marek Baláž, Petra Havrankova, Robert Jech, Zubair M Ahmed, Sheikh Riazuddin, Saima Riazuddin
Variants of NAV3, a neuronal morphogenesis protein, cause intellectual disability, developmental delay, and microcephaly. Communications biology 7 (1) (2024)
Muhammad A Usmani, Amama Ghaffar, Mohsin Shahzad, Javed Akram, Aisha I Majeed, Kausar Malik, Khushbakht Fatima, Asma A Khan, Zubair M Ahmed, Sheikh Riazuddin, Saima Riazuddin
A Missense Variant in HACE1 Is Associated with Intellectual Disability, Epilepsy, Spasticity, and Psychomotor Impairment in a Pakistani Kindred. Genes 15 (5) (2024)
Muhammad A Usmani, Amama Ghaffar, Mohsin Shahzad, Javed Akram, Aisha I Majeed, Kausar Malik, Khushbakht Fatima, Asma A Khan, Zubair M Ahmed, Sheikh Riazuddin, Saima Riazuddin
A Missense Variant in HACE1 Is Associated with Intellectual Disability, Epilepsy, Spasticity, and Psychomotor Impairment in a Pakistani Kindred. Genes 15 (5) (2024)
Daniel Greene, null null, Daniela Pirri, Karen Frudd, Ege Sackey, Mohammed Al-Owain, Arnaud P J Giese, Khushnooda Ramzan, Sehar Riaz, Itaru Yamanaka, Nele Boeckx, Chantal Thys, Bruce D Gelb, Paul Brennan, Verity Hartill, Julie Harvengt, Tomoki Kosho, Sahar Mansour, Mitsuo Masuno, Takako Ohata, Helen Stewart, Khalid Taibah, Claire L S Turner, Faiqa Imtiaz, Saima Riazuddin, Takayuki Morisaki, Pia Ostergaard, Bart L Loeys, Hiroko Morisaki, Zubair M Ahmed, Graeme M Birdsey, Kathleen Freson, Andrew Mumford, Ernest Turro
Genetic association analysis of 77,539 genomes reveals rare disease etiologies. Nature medicine 29 (3) (2023)
Daniel Greene, null null, Daniela Pirri, Karen Frudd, Ege Sackey, Mohammed Al-Owain, Arnaud P J Giese, Khushnooda Ramzan, Sehar Riaz, Itaru Yamanaka, Nele Boeckx, Chantal Thys, Bruce D Gelb, Paul Brennan, Verity Hartill, Julie Harvengt, Tomoki Kosho, Sahar Mansour, Mitsuo Masuno, Takako Ohata, Helen Stewart, Khalid Taibah, Claire L S Turner, Faiqa Imtiaz, Saima Riazuddin, Takayuki Morisaki, Pia Ostergaard, Bart L Loeys, Hiroko Morisaki, Zubair M Ahmed, Graeme M Birdsey, Kathleen Freson, Andrew Mumford, Ernest Turro
Genetic association analysis of 77,539 genomes reveals rare disease etiologies. Nature medicine (2023)
Daniel Greene, null null, Daniela Pirri, Karen Frudd, Ege Sackey, Mohammed Al-Owain, Arnaud P J Giese, Khushnooda Ramzan, Sehar Riaz, Itaru Yamanaka, Nele Boeckx, Chantal Thys, Bruce D Gelb, Paul Brennan, Verity Hartill, Julie Harvengt, Tomoki Kosho, Sahar Mansour, Mitsuo Masuno, Takako Ohata, Helen Stewart, Khalid Taibah, Claire L S Turner, Faiqa Imtiaz, Saima Riazuddin, Takayuki Morisaki, Pia Ostergaard, Bart L Loeys, Hiroko Morisaki, Zubair M Ahmed, Graeme M Birdsey, Kathleen Freson, Andrew Mumford, Ernest Turro
Genetic association analysis of 77,539 genomes reveals rare disease etiologies. Nature medicine 29 (3) (2023)
Rafaqat Ishaq, Muhammad Ilyas, Umme Habiba, Muhammad Noor Ul Amin, Sadia Saeed, Ghazala Kaukab Raja, Pakeeza Arzoo Shaiq, Zubair M Ahmed
Whole Exome Sequencing Reveals Clustering of Variants of Known Vitiligo Genes in Multiplex Consanguineous Pakistani Families. Genes 14 (5) (2023)
Daniel Greene, null null, Daniela Pirri, Karen Frudd, Ege Sackey, Mohammed Al-Owain, Arnaud P J Giese, Khushnooda Ramzan, Sehar Riaz, Itaru Yamanaka, Nele Boeckx, Chantal Thys, Bruce D Gelb, Paul Brennan, Verity Hartill, Julie Harvengt, Tomoki Kosho, Sahar Mansour, Mitsuo Masuno, Takako Ohata, Helen Stewart, Khalid Taibah, Claire L S Turner, Faiqa Imtiaz, Saima Riazuddin, Takayuki Morisaki, Pia Ostergaard, Bart L Loeys, Hiroko Morisaki, Zubair M Ahmed, Graeme M Birdsey, Kathleen Freson, Andrew Mumford, Ernest Turro
Genetic association analysis of 77,539 genomes reveals rare disease etiologies. Nature medicine 29 (3) (2023)
Ghazala Y Zamani, Ranjha Khan, Noreen Karim, Zubair M Ahmed, Muhammad Naeem
Identification of Frameshift Variants in POLH Gene Causing Xeroderma Pigmentosum in Two Consanguineous Pakistani Families. Genes 13 (3) (2022)
Sairah Yousaf, Nabeela Tariq, Zureesha Sajid, Shakeel A Sheikh, Tasleem Kausar, Yar M Waryah, Rehan S Shaikh, Ali Muhammad Waryah, Saumil Sethna, Saima Riazuddin, Zubair M Ahmed
Delineating the Molecular and Phenotypic Spectrum of the CNGA3 -Related Cone Photoreceptor Disorder in Pakistani Families. Genes 13 (4) (2022)
Yilan Zhen, Carlie L Cullen, Raphael Ricci, Benjamin S Summers, Sakina Rehman, Zubair M Ahmed, Antoinette Y Foster, Ben Emery, Robert Gasperini, Kaylene M Young
Protocadherin 15 suppresses oligodendrocyte progenitor cell proliferation and promotes motility through distinct signalling pathways. Communications biology 5 (1) (2022)
Saumil Sethna, Wadih M Zein, Sehar Riaz, Arnaud Pj Giese, Julie M Schultz, Todd Duncan, Robert B Hufnagel, Carmen C Brewer, Andrew J Griffith, T Michael Redmond, Saima Riazuddin, Thomas B Friedman, Zubair M Ahmed
Proposed therapy, developed in a Pcdh15-deficient mouse, for progressive loss of vision in human Usher syndrome. eLife 10 (2021)
Fehmida F Khan, Naima Khan, Sakina Rehman, Amir Ejaz, Uzma Ali, Muhammad Erfan, Zubair M Ahmed, Muhammad Naeem
Identification and Computational Analysis of Novel Pathogenic Variants in Pakistani Families with Diverse Epidermolysis Bullosa Phenotypes. Biomolecules 11 (5) (2021)
Abdullah Y Hassan, Sairah Yousaf, Moran R Levin, Osamah J Saeedi, Saima Riazuddin, Janet L Alexander, Zubair M Ahmed
Novel Homozygous Missense Variant in GJA3 Connexin Domain Causing Congenital Nuclear and Cortical Cataracts. International journal of molecular sciences 23 (1) (2021)
Priya Jarwar, Shakeel Ahmed Sheikh, Yar Muhammad Waryah, Ikram Uddin Ujjan, Saima Riazuddin, Ali Muhammad Waryah, Zubair M Ahmed
Biallelic Variants in EPHA2 Identified in Three Large Inbred Families with Early-Onset Cataract. International journal of molecular sciences 22 (19) (2021)
Amama Ghaffar, Faiza Rasheed, Muhammad Rashid, Hans van Bokhoven, Zubair M Ahmed, Sheikh Riazuddin, Saima Riazuddin
Biallelic in-frame deletion of SOX4 is associated with developmental delay, hypotonia and intellectual disability. European journal of human genetics : EJHG (2021)
Irum Badshah Saleem, Muhammad Shareef Masoud, Muhammad Qasim, Muhammad Ali, Zubair M Ahmed
Identification and Computational Analysis of Rare Variants of Known Hearing Loss Genes Present in Five Deaf Members of a Pakistani Kindred. Genes 12 (12) (2021)
Zureesha Sajid, Sairah Yousaf, Yar M Waryah, Tauqeer A Mughal, Tasleem Kausar, Mohsin Shahzad, Ali R Rao, Ansar Ahmed Abbasi, Rehan Sadiq Shaikh, Ali Muhammad Waryah, Saima Riazuddin, Zubair M Ahmed
Genetic Causes of Oculocutaneous Albinism in Pakistani Population. Genes 12 (4) (2021)
Sairah Yousaf, Saumil Sethna, Muhammad A Chaudhary, Rehan S Shaikh, Saima Riazuddin, Zubair M Ahmed
Molecular characterization of SLC24A5 variants and evaluation of Nitisinone treatment efficacy in a zebrafish model of OCA6. Pigment cell & melanoma research 33 (4) (2020)
Daniel N Frank, Arnaud P J Giese, Lena Hafren, Tori C Bootpetch, Talitha Karisse L Yarza, Matthew J Steritz, Melquiadesa Pedro, Patrick John Labra, Kathleen A Daly, Ma Leah C Tantoco, Wasyl Szeremeta, Maria Rina T Reyes-Quintos, Niaz Ahankoob, Erasmo Gonzalo D V Llanes, Harold S Pine, Sairah Yousaf, Diana Ir, Elisabet Einarsdottir, Rhodieleen Anne R de la Cruz, Nanette R Lee, Rachelle Marie A Nonato, Charles E Robertson, Kimberly Mae C Ong, Jose Pedrito M Magno, Alessandra Nadine E Chiong, Ma Carmina Espiritu-Chiong, Maria Luz San Agustin, Teresa Luisa G Cruz, Generoso T Abes, Michael J Bamshad, Eva Maria Cutiongco-de la Paz, Juha Kere, Deborah A Nickerson, Karen L Mohlke, Saima Riazuddin, Abner Chan, Petri S Mattila, Suzanne M Leal, Allen F Ryan, Zubair M Ahmed, Tasnee Chonmaitree, Michele M Sale, Charlotte M Chiong, Regie Lyn P Santos-Cortez
Otitis media susceptibility and shifts in the head and neck microbiome due to SPINK5 variants. Journal of medical genetics 58 (7) (2020)
Saba Zafar, Mohsin Shahzad, Rafaqat Ishaq, Ayesha Yousaf, Rehan Sadiq Shaikh, Javed Akram, Zubair M Ahmed, Saima Riazuddin
Novel Mutations in CLPP, LARS2, CDH23, and COL4A5 Identified in Familial Cases of Prelingual Hearing Loss. Genes 11 (9) (2020)
S Yousaf, S A Sheikh, S Riazuddin, Ali Muhammad Waryah, Zubair M Ahmed
INPP5K variant causes autosomal recessive congenital cataract in a Pakistani family. Clinical genetics 93 (3) (2018)
Osamah Saeedi, Sairah Yousaf, Joby Tsai, Kathleen Palmer, Saima Riazuddin, Zubair M Ahmed
Delineation of Novel Compound Heterozygous Variants in LTBP2 Associated with Juvenile Open Angle Glaucoma. Genes 9 (11) (2018)

Zubair M Ahmed.css-eqlu8i{font-size:small;padding-left:4px;} (Z M Ahmed)

Publication Activity (10 Years)

Top Topics

Top Venues

Zubair M Ahmed (Z M Ahmed)