Asmat Ullah

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 15

Top Topics

Clinical Evaluation

Intellectual Disability

Candida Albicans

Top Venues

Medicina (Kaunas, Lithuania)

International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience

Antioxidants (Basel, Switzerland)

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

Publications

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)
Warda Akbar, Asmat Ullah, Nighat Haider, Sufyan Suleman, Fati Ullah Khan, Abid Ali Shah, Muhammad Atif Sikandar, Sulman Basit, Wasim Ahmad
Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmia. The journal of gene medicine (2023)
Muhammad Bilal, Hammal Khan, Muhammad Javed Khan, Tobias B Haack, Rebecca Buchert, Khurram Liaqat, Kifayat Ullah, Sohail Ahmed, Thashi Bharadwaj, Anushree Acharya, Susana Peralta, null Najumuddin, Hamid Ali, Muhammad Sharif Hasni, Isabelle Schrauwen, Asmat Ullah, Wasim Ahmad, Regie Lyn P Santos-Cortez
Variants in EFCAB7 underlie nonsyndromic postaxial polydactyly. European journal of human genetics : EJHG (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)
Abu Bakar, Sulaiman Shams, Nousheen Bibi, Asmat Ullah, Wasim Ahmad, Musharraf Jelani, Osama Yousef Muthaffar, Angham Abdulrhman Abdulkareem, Turki S Abujamel, Absarul Haque, Muhammad Imran Naseer, Bushra Khan
A Novel Homozygous Nonsense Variant in the DYM Underlies Dyggve-Melchior-Clausen Syndrome in Large Consanguineous Family. Genes 14 (2) (2023)
Abu Bakar, Sulaiman Shams, Nousheen Bibi, Asmat Ullah, Wasim Ahmad, Musharraf Jelani, Osama Yousef Muthaffar, Angham Abdulrhman Abdulkareem, Turki S Abujamel, Absarul Haque, Muhammad Imran Naseer, Bushra Khan
A Novel Homozygous Nonsense Variant in the DYM Underlies Dyggve-Melchior-Clausen Syndrome in Large Consanguineous Family. Genes 14 (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)
Abu Bakar, Sulaiman Shams, Nousheen Bibi, Asmat Ullah, Wasim Ahmad, Musharraf Jelani, Osama Yousef Muthaffar, Angham Abdulrhman Abdulkareem, Turki S Abujamel, Absarul Haque, Muhammad Imran Naseer, Bushra Khan
A Novel Homozygous Nonsense Variant in the DYM Underlies Dyggve-Melchior-Clausen Syndrome in Large Consanguineous Family. Genes 14 (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)
Asmat Ullah, Evelina Stankevic, Louise Aas Holm, Sara E Stinson, Helene Bæk Juel, Cilius Esmann Fonvig, Morten A V Lund, Cæcilie Trier, Line Engelbrechtsen, Lars H Ängquist, Anna E Jonsson, Oluf Pedersen, Niels Grarup, Jens-Christian Holm, Torben Hansen
Genetics of Plasma Bilirubin and Associations between Bilirubin and Cardiometabolic Risk Profiles in Danish Children and Adolescents. Antioxidants (Basel, Switzerland) 12 (8) (2023)
Nadia Waheed, Maryam Naseer, Nighat Haider, Sufyan Suleman, Asmat Ullah
Whole exome sequencing identified a novel splice donor site variant in interleukin 2 receptor alpha chain. Immunogenetics (2022)
Asmat Ullah, Abid Ali Shah, Majed Alluqmani, Nighat Haider, Hasan Aman, Fatima Alfadhli, Ahmed M Almatrafi, Alia M Albalawi, Jai Krishin, Fati Ullah Khan, Bilal Ali Anjam, null Abdullah, Elionora Peña Lozano, Abdus Samad, Wasim Ahmad, Torben Hansen, Kun Xia, Sulman Basit
Clinical and genetic characterization of patients segregating variants in KPTN, MINPP1, NGLY1, AP4B1, and SON underlying neurodevelopmental disorders: Genetic and phenotypic expansion. International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 82 (8) (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)
Farah Bibi, Nighat Haider, Shahab Ud Din, Muqadar Shah, Jai Krishin, Naila Qayyum, Ghazala Kaukab Raja, Henry Houlden, Wasim Ahmad, Tanwir Khaliq, Asmat Ullah
Sequence variants in three genes underlying leukodystrophy in Pakistani families. International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience (2020)