Arif Mahmood

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 20

Top Topics

Autism Spectrum Disorder

Intellectual Disability

Top Venues

Medicina (Kaunas, Lithuania)

Clinical genetics

Molecules (Basel, Switzerland)

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

Publications

Muhammad Riaz, Ashfaq Ur Rehman, Muhammad Waqas, Asaad Khalid, Ashraf N Abdalla, Arif Mahmood, Junjian Hu, Abdul Wadood
A Novel Approach to Develop New and Potent Inhibitors for the Simultaneous Inhibition of Protease and Helicase Activities of HCV NS3/4A Protease: A Computational Approach. Molecules (Basel, Switzerland) 28 (3) (2023)
Kun Chen, Haoyang Wang, Iqra Ilyas, Arif Mahmood, Lijun Hou
Microglia and Astrocytes Dysfunction and Key Neuroinflammation-Based Biomarkers in Parkinson's Disease. Brain sciences 13 (4) (2023)
Asmat Ullah, Abid Ali Shah, Fibhaa Syed, Arif Mahmood, Hassan Ur Rehman, Beenish Khurshid, Abdus Samad, Wasim Ahmad, Sulman Basit
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in CYB5R3 Gene in Patients with Methemoglobinemia. Medicina (Kaunas, Lithuania) 59 (2) (2023)
Asmat Ullah, Abid Ali Shah, Fibhaa Syed, Arif Mahmood, Hassan Ur Rehman, Beenish Khurshid, Abdus Samad, Wasim Ahmad, Sulman Basit
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in CYB5R3 Gene in Patients with Methemoglobinemia. Medicina (Kaunas, Lithuania) 59 (2) (2023)
Kun Chen, Haoyang Wang, Iqra Ilyas, Arif Mahmood, Lijun Hou
Microglia and Astrocytes Dysfunction and Key Neuroinflammation-Based Biomarkers in Parkinson's Disease. Brain sciences 13 (4) (2023)
Zhaoyang Meng, Ran You, Arif Mahmood, Fancheng Yan, Yanling Wang
Application of Proteomics Analysis and Animal Models in Optic Nerve Injury Diseases. Brain sciences 13 (3) (2023)
Muhammad Riaz, Ashfaq Ur Rehman, Muhammad Waqas, Asaad Khalid, Ashraf N Abdalla, Arif Mahmood, Junjian Hu, Abdul Wadood
A Novel Approach to Develop New and Potent Inhibitors for the Simultaneous Inhibition of Protease and Helicase Activities of HCV NS3/4A Protease: A Computational Approach. Molecules (Basel, Switzerland) 28 (3) (2023)
Asmat Ullah, Abid Ali Shah, Fibhaa Syed, Arif Mahmood, Hassan Ur Rehman, Beenish Khurshid, Abdus Samad, Wasim Ahmad, Sulman Basit
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in CYB5R3 Gene in Patients with Methemoglobinemia. Medicina (Kaunas, Lithuania) 59 (2) (2023)
Muhammad Riaz, Ashfaq Ur Rehman, Muhammad Waqas, Asaad Khalid, Ashraf N Abdalla, Arif Mahmood, Junjian Hu, Abdul Wadood
A Novel Approach to Develop New and Potent Inhibitors for the Simultaneous Inhibition of Protease and Helicase Activities of HCV NS3/4A Protease: A Computational Approach. Molecules (Basel, Switzerland) 28 (3) (2023)
Zhaoyang Meng, Ran You, Arif Mahmood, Fancheng Yan, Yanling Wang
Application of Proteomics Analysis and Animal Models in Optic Nerve Injury Diseases. Brain sciences 13 (3) (2023)
Asmat Ullah, Abid Ali Shah, Fibhaa Syed, Arif Mahmood, Hassan Ur Rehman, Beenish Khurshid, Abdus Samad, Wasim Ahmad, Sulman Basit
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in CYB5R3 Gene in Patients with Methemoglobinemia. Medicina (Kaunas, Lithuania) 59 (2) (2023)
Asmat Ullah, Abid Ali Shah, Fibhaa Syed, Arif Mahmood, Hassan Ur Rehman, Beenish Khurshid, Abdus Samad, Wasim Ahmad, Sulman Basit
Molecular Dynamic Simulation Analysis of a Novel Missense Variant in CYB5R3 Gene in Patients with Methemoglobinemia. Medicina (Kaunas, Lithuania) 59 (2) (2023)
Duoduo Xu, Qiqi Shao, Chen Zhou, Arif Mahmood, Jizhou Zhang
In Silico Analysis of nsSNPs of Human KRAS Gene and Protein Modeling Using Bioinformatic Tools. ACS omega 8 (14) (2023)
Syed Mansoor Jan, Aamir Fahira, Yongyong Shi, Mohammad Imran Khan, Alam Jamal, Arif Mahmood, Sulaiman Shams, Zahida Parveen, Junjian Hu, Muhammad Umair, Abdul Wadood
Integrative Genomic Analysis of m6a-SNPs Identifies Potential Functional Variants Associated with Alzheimer's Disease. ACS omega 8 (14) (2023)
Sumayya Mustafa, Safdar Abbas, Arif Mahmood, Ali Zaman Khan, Shah Zeb, Amjad Khan, Muhammad Umair
A novel de novo variant in the PHF21A causes craniofacial abnormalities, intellectual disability and skeletal manifestations. Clinical genetics (2023)
Hamed Nawaz, null Mujahid, Sher Alam Khan, Farhana Bibi, Ahmed Waqas, Abdul Bari, null Fardous, Niamatullah Khan, Nazif Muhammad, Amjad Khan, Sohail Aziz Paracha, Qamre Alam, Mohammad Azhar Kamal, Misbahuddin M Rafeeq, Noor Muhammad, Fayaz Ul Haq, Shazia Khan, Arif Mahmood, Saadullah Khan, Muhammad Umair
Biallelic Variants in Seven Different Genes Associated with Clinically Suspected Bardet-Biedl Syndrome. Genes 14 (5) (2023)
Sumayya Mustafa, Safdar Abbas, Arif Mahmood, Ali Zaman Khan, Shah Zeb, Amjad Khan, Muhammad Umair
A Novel de novo Variant in the PHF21A causes craniofacial abnormalities, intellectual disability and skeletal manifestations. Clinical genetics (2023)
Arif Mahmood, Abdus Samad, Abid Ali Shah, Abdul Wadood, Afnan Alkathiri, Mohammed Ali Alshehri, Mohammad Zubair Alam, Taimur Hussain, Pei He, Muhammad Umair
A novel biallelic variant in the Popeye domain-containing protein 1 (POPDC1) underlies limb girdle muscle dystrophy type 25. Clinical genetics (2022)
Abid Ali Shah, Marryam Amjad, Jawad-Ul Hassan, Asmat Ullah, Arif Mahmood, Huiyin Deng, Yasir Ali, Fouzia Gul, Kun Xia
Molecular Insights into the Role of Pathogenic nsSNPs in GRIN2B Gene Provoking Neurodevelopmental Disorders. Genes 13 (8) (2022)
Arif Mahmood, Abid Ali Shah, Muhammad Umair, Yiming Wu, Amjad Khan
Recalling the pathology of Parkinson's disease; lacking exact figure of prevalence and genetic evidence in Asia with an alarming outcome: A time to step-up. Clinical genetics 100 (6) (2021)