Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability von Khan, Muzammil Ahmad, Rafiq, Muhammad Arshad, Noor, Abdul, Hussain, Shobbir, Flores, Joana V., Rupp, Verena, Vincent, Akshita K., Malli, Roland, Ali, Ghazanfar, Khan, Falak Sher, Ishak, Gisele E., Doherty, Dan, Weksberg, Rosanna, Ayub, Muhammad, Windpassinger, Christian, Ibrahim, Shahnaz, Frye, Michaela, Ansar, Muhammad, Vincent, John B.

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Alopecia‐mental retardation syndrome: Molecular genetics of a rare neuro‐dermal disorder von Muzammal, Muhammad, Ahmad, Safeer, Ali, Muhammad Zeeshan, Khan, Muzammil Ahmad

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Type IA topoisomerases can be "magicians" for both DNA and RNA in all domains of life von Ahmad, Muzammil, Xu, Dongyi, Wang, Weidong

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Comments on “Management of diabetic macular edema patients in clinical practice in Spain” von Nahaboo Solim, Muzammil Ahmad

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A homozygous ARMC3 splicing variant causes asthenozoospermia and flagellar disorganization in a consanguineous family von Rahim, Fazal, Tao, Liu, Khan, Khalid, Ali, Imtiaz, Zeb, Aurang, Khan, Ihsan, Dil, Sobia, Abbas, Tanveer, Hussain, Ansar, Zubair, Muhammad, Zhang, Huan, Hui, Ma, Khan, Muzammil Ahmad, Shah, Wasim, Shi, Qinghua

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Mutations in the Alpha 1,2-Mannosidase Gene, MAN1B1, Cause Autosomal-Recessive Intellectual Disability von Rafiq, Muhammad Arshad, Kuss, Andreas W., Puettmann, Lucia, Noor, Abdul, Ramiah, Annapoorani, Ali, Ghazanfar, Hu, Hao, Kerio, Nadir Ali, Xiang, Yong, Garshasbi, Masoud, Khan, Muzammil Ahmad, Ishak, Gisele E., Weksberg, Rosanna, Ullmann, Reinhard, Tzschach, Andreas, Kahrizi, Kimia, Mahmood, Khalid, Naeem, Farooq, Ayub, Muhammad, Moremen, Kelley W., Vincent, John B., Ropers, Hans Hilger, Ansar, Muhammad, Najmabadi, Hossein

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Explosion pressure and duration prediction using machine learning: A comparative study using classical models with Adam‐optimized neural network von Idris, Ahmad Muzammil, Rusli, Risza, Mohamed, Moamen Elsayed, Ramli, Ahmad Fakrul, Nasif, Mohammad Shakir, Lim, Jeng Shiun

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Optimizing Spectrum Utilization and Security in SAS-Enabled CBRS Systems for Enhanced 5G Performance von Abbass, Waseem, Ahmad Khan, Muzammil, Hussain Farooqi, Ashfaq, Nawaz, Waqas, Abbas, Nasim, Ali, Zulfiqar

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Secured Dynamic Request Scheduling and Optimal CSP Selection for Analyzing Cloud Service Performance Using Intelligent Approaches von Khan, Muzammil Ahmad, Khan, Shariq Mahmood, Subramaniam, Siva Kumar

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Exome sequence analysis identifies a homozygous, pathogenic, frameshift variant in the MAN2B1 gene underlying clinical variant of α-mannosidosis von Hashmi, Jamil Amjad, Latif, Muhammad, Balahmar, Reham M, Ali, Muhammad Zeeshan, Alfadhli, Fatima, Khan, Muzammil Ahmad, Basit, Sulman

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The molecular genetics of UV-Sensitive syndrome: A rare dermal anomaly von Muzammal, Muhammad, Ali, Muhammad Zeeshan, Ahmad, Safeer, Huma, Shawana, Ahmad, Sohail, Abbasi, Ansar Ahmad, Khan, Saadullah, Khan, Muzammil Ahmad

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Analysis of a non‐lethal biallelic frameshift mutation in ZMPSTE24 reveals utilization of alternative translation initiation codons von Kaufmann, Lukas, Pilic, Johannes, Auinger, Lisa, Mayer, Anna‐Lena, Blatterer, Jasmin, Semmler‐Bruckner, Johann, Abbas, Safdar, Rehman, Khurram, Ayaz, Muhammad, Graier, Wolfgang F., Malli, Roland, Petek, Erwin, Wagner, Klaus, Al Kaissi, Ali, Khan, Muzammil Ahmad, Windpassinger, Christian

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Topoisomerase 3β interacts with RNAi machinery to promote heterochromatin formation and transcriptional silencing in Drosophila von Lee, Seung Kyu, Xue, Yutong, Shen, Weiping, Zhang, Yongqing, Joo, Yuyoung, Ahmad, Muzammil, Chinen, Madoka, Ding, Yi, Ku, Wai Lim, De, Supriyo, Lehrmann, Elin, Becker, Kevin G., Lei, Elissa P., Zhao, Keji, Zou, Sige, Sharov, Alexei, Wang, Weidong

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Mutation screening of multiple Pakistani MCPH families revealed novel and recurrent protein‐truncating mutations of ASPM von Hussain, Sadam, Nawaz, Amjad, Hamid, Malaika, Ullah, Waseem, Khan, Iqbal Nawaz, Afshan, Mehak, Rehman, Adil, Nawaz, Hamid, Halswick, Julia, Rehman, Shoaib‐ur, Ahmad, Sohail, Muzammal, Muhammad, Muhammad, Noor, Jan, Abid, Khan, Saadullah, Windpassinger, Christian, Khan, Muzammil Ahmad

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Carbon Emission Pinch Analysis: an application to the transportation sector in Iskandar Malaysia for 2025 von Ramli, Ahmad Fakrul, Muis, Zarina Ab, Ho, Wai Shin, Idris, Ahmad Muzammil, Mohtar, Aminullah

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Exome Sequencing Identified Molecular Determinants of Retinal Dystrophies in Nine Consanguineous Pakistani Families von Tehreem, Raeesa, Chen, Iris, Shah, Mudassar Raza, Li, Yumei, Khan, Muzammil Ahmad, Afshan, Kiran, Chen, Rui, Firasat, Sabika

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Comment on homozygosity mapping of a consanguineous Pakistani family affected with oculocutaneous albinism to Tyrosinase gene von Khan, Muzammil Ahmad

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Machine Learning Approach to Classification of Online Users by Exploiting Information Seeking Behavior von Kanwal, Moona, Khan, Najeed A., Ismat, Najma, Khan, Aftab A., Khan, Muzammil Ahmad

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Clinical outcomes and safety of Diphoterine® irrigation for chemical eye injury: A single-centre experience in the United Kingdom von Nahaboo Solim, Muzammil Ahmad, Lupion-Duran, Teresa Maria, Rana-Rahman, Romeela, Patel, Trushar, Ah-Kine, Desiree, Ting, Darren S. J.

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Genetics of Human Isolated Acromesomelic Dysplasia von Khan, Saadullah, Basit, Sulman, Khan, Muzammil Ahmed, Muhammad, Noor, Ahmad, Wasim

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