Biallelic variants in WARS1 cause a highly variable neurodevelopmental syndrome and implicate a critical exon for normal auditory function
Lin, Sheng‐Jia, Vona, Barbara, Porter, Hillary M., Izadi, Mahmoud, Huang, Kevin, Lacassie, Yves, Rosenfeld, Jill A., Khan, Saadullah, Petree, Cassidy, Ali, Tayyiba A., Muhammad, Nazif, Khan, Sher A., Muhammad, Noor, Liu, Pengfei, Haymon, Marie‐Louise, Rüschendorf, Franz, Kong, Il‐Keun, Schnapp, Linda, Shur, Natasha, Chorich, Lynn, Layman, Lawrence, Haaf, Thomas, Pourkarimi, Ehsan, Kim, Hyung‐Goo, Varshney, Gaurav K.
Published in Human mutation (01.10.2022)
Published in Human mutation (01.10.2022)
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Biallelic mutations in FLG, TGM1, and STS genes segregated with different types of ichthyoses in eight families of Pakistani origin
Khan, Niamatullah, Shah, Khadim, Fozia, Fozia, Khan, Sher A., Muhammad, Nazif, Nasir, Abdul, Ahmad, Ijaz, Rehman, Zia U., Jan, Abid, Muhammad, Noor, Khan, Saadullah
Published in International journal of dermatology (01.05.2023)
Published in International journal of dermatology (01.05.2023)
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Journal Article
Variants in HCFC1 and MN1 genes causing intellectual disability in two Pakistani families
Hussain, Syeda Iqra, Muhammad, Nazif, Shah, Shahbaz Ali, Rehman, Adil U, Khan, Sher Alam, Saleha, Shamim, Khan, Yar Muhammad, Muhammad, Noor, Khan, Saadullah, Wasif, Naveed
Published in BMC medical genomics (02.07.2024)
Published in BMC medical genomics (02.07.2024)
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Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability
Hussain, Syeda Iqra, Muhammad, Nazif, Shah, Salah Ud Din, Fardous, Fardous, Khan, Sher Alam, Khan, Niamatullah, Rehman, Adil U, Siddique, Mehwish, Wasan, Shoukat Ali, Niaz, Rooh, Ullah, Hafiz, Khan, Niamat, Muhammad, Noor, Mirza, Muhammad Usman, Wasif, Naveed, Khan, Saadullah
Published in BMC neurology (04.10.2023)
Published in BMC neurology (04.10.2023)
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Autosomal recessive variants c.953A>C and c.97-1G>C in NSUN2 causing intellectual disability: a molecular dynamics simulation study of loss-of-function mechanisms
Muhammad, Nazif, Hussain, Syeda Iqra, Rehman, Zia Ur, Khan, Sher Alam, Jan, Samin, Khan, Niamatullah, Muzammal, Muhammad, Abbasi, Sumra Wajid, Kakar, Naseebullah, Rehman, Zia Ur, Khan, Muzammil Ahmad, Mirza, Muhammad Usman, Muhammad, Noor, Khan, Saadullah, Wasif, Naveed
Published in Frontiers in neurology (25.05.2023)
Published in Frontiers in neurology (25.05.2023)
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A novel nonsense variant in SLC24A4 causing a rare form of amelogenesis imperfecta in a Pakistani family
Khan, Sher Alam, Khan, Muhammad Adnan, Muhammad, Nazif, Bashir, Hina, Khan, Niamat, Muhammad, Noor, Yilmaz, Rüstem, Khan, Saadullah, Wasif, Naveed
Published in BMC medical genetics (07.05.2020)
Published in BMC medical genetics (07.05.2020)
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Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome
Nawaz, Hamed, Mujahid, Khan, Sher Alam, Bibi, Farhana, Waqas, Ahmed, Bari, Abdul, Fardous, Khan, Niamatullah, Muhammad, Nazif, Khan, Amjad, Paracha, Sohail Aziz, Alam, Qamre, Kamal, Mohammad Azhar, Rafeeq, Misbahuddin M, Muhammad, Noor, Haq, Fayaz Ul, Khan, Shazia, Mahmood, Arif, Khan, Saadullah, Umair, Muhammad
Published in Genes (19.05.2023)
Published in Genes (19.05.2023)
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Association of sequence variants in frizzled-6 with autosomal recessive nail dysplasia (NDNC-10) in Pashtun families
Khan, Saadullah, Khan, Anwar Kamal, Hamid, Malaika, Nazif, Muhammad, Abbas, Muhammad, Khan, Sher Alam, Khan, Bushra, Khan, Muzammil Ahmad, Jan, Abid, Khattak, Baharullah, Ullah, Waheed, Muhammad, Noor
Published in Journal of the Pakistan Medical Association (01.01.2020)
Published in Journal of the Pakistan Medical Association (01.01.2020)
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Journal Article
Glycine Improved Cryopreserved Spermatozoa Quality in Achai Bull
Nazif, Muhammad Sohail, Rehman, Zia ur, Khan, Humayun, Khan, Farhan Anwar, Hussain, Tarique, Ahmad, Adnan, Farmanullah, Husnain, Ali, Muhammad, Safdar, Murtaza, Ghulam, Gang, Liu
Published in BioMed research international (04.08.2022)
Published in BioMed research international (04.08.2022)
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Molecular insight into CREBBP and TANGO2 variants causing intellectual disability
Hussain, Syeda Iqra, Muhammad, Nazif, Khan, Niamatullah, Khan, Mobeen, Fardous, Fardous, Tahir, Raheel, Yasin, Muhammad, Khan, Sher Alam, Saleha, Shamim, Muhammad, Noor, Wasif, Naveed, Khan, Saadullah
Published in The journal of gene medicine (01.01.2024)
Published in The journal of gene medicine (01.01.2024)
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Front Cover, Volume 43, Issue 10
Lin, Sheng‐Jia, Vona, Barbara, Porter, Hillary M., Izadi, Mahmoud, Huang, Kevin, Lacassie, Yves, Rosenfeld, Jill A., Khan, Saadullah, Petree, Cassidy, Ali, Tayyiba A., Muhammad, Nazif, Khan, Sher A., Muhammad, Noor, Liu, Pengfei, Haymon, Marie‐Louise, Rüschendorf, Franz, Kong, Il‐Keun, Schnapp, Linda, Shur, Natasha, Chorich, Lynn, Layman, Lawrence, Haaf, Thomas, Pourkarimi, Ehsan, Kim, Hyung‐Goo, Varshney, Gaurav K.
Published in Human mutation (01.10.2022)
Published in Human mutation (01.10.2022)
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Pertumbuhan Selada Merah (Lactuca sativa L. var. Red Rapid) dan Selada Hijau (Lactuca sativa L. Grand Rapids) dengan Sistem Hidroponik Apung dengan Pemberian Dosis Pupuk Organik Cair (POC) Bioslurry dan AB Mix yang Berbeda
Anwary, Muhammad Nazif, Slamet, W, Kusmiyati, Florentina
Published in Buletin Anatomi dan Fisiologi (31.08.2019)
Published in Buletin Anatomi dan Fisiologi (31.08.2019)
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