Sohail Ahmed

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个人简介

Sohail Ahmed currently works at the Institute of Biochemistry, University of Baluchistan. Sohail does research in Genetics, Human Biology and Molecular Biology. Their current project is 'Human molecular genetics'.

研究兴趣

论文共 8 篇作者统计合作学者相似作者

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Delineating the Disease Boundaries: Homozygous CDC14A Variants Underlying Nonsyndromic Hearing Loss and Hearing Impairment Infertile Male Syndrome

Zamrud Zehri,Hammal Khan,Sohail Ahmed,Muhammad Javed Khan,Nisar Ahmed Shahwani,Shoaib Nawaz, Muhammad Umair

MOLECULAR SYNDROMOLOGYno. 4 (2024): 269-274

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Novel Pathogenic Variants in HR Underlie Atrichia with Papular Lesions in a Cohort of 10 Families

Kifayat Ullah,Sohail Ahmed,Nicole Cesarato,Xing Xiong, Maria Taj, Naushaba Manan,Maria Wehner,Muhammad Javed Khan,Hammal Khan,Sabba Mehmood,Muhammad Sharif Hasni, Dariusz Michna, Rehmana Waris,Henning Hamm,Regina C. Betz,Wasim Ahmad,Imran Ullah

The Journal of Dermatology (2024)

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Clinical and Genetic Investigation of 14 Families with Various Forms of Short Stature Syndromes

Fati Ullah Khan,Hammal Khan,Kifayat Ullah,Shoaib Nawaz,Muhammad Javed Khan,Sohail Ahmed,Muhammad Ilyas, Amjad Ali,Imran Ullah, Aamir Sohail,Shabir Hussain,Farooq Ahmad, Raza Sufyan,Amir Hayat, Tooba Hanif,Fatima Bibi, Maria Hayat, Rehmat Ullah, Inam Ullah Khan,Raja Hussain Ali,Muhammad Sharif Hasni,Hamid Ali,Muhammad Bilal,Susana Peralta,Rebecca Buchert,Zamrud Zehri, Gul Hassan, Khurrum Liaqat,Muhammad Zahid,Khadim Shah, Outi Mikitie,Tobias B. Haack,Weizhen Ji,Saquib A. Lakhani,Muhammad Ansar,Wasim Ahmad

CLINICAL GENETICSno. 3 (2024): 347-353

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A Novel Variant in the Cyto-Tail of SMO Gene Underlying Isolated Postaxial Polydactyly

Muhammad Javed Khan, Hammal Abdullah,Hammal Khan,Atteaya Zaman,Sohail Ahmed, Palwasha Iqbal,Muhammad Bilal,Kifayat Ullah,Muhammad Sharif Hasni,Imran Ullah,Emily Kathryn Mis,Saquib Ali Lakhani,Wasim Ahmad

MOLECULAR SYNDROMOLOGY (2024)

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Unraveling the Genetic Basis of Congenital Limb Anomalies in Eight Families

Inam Ullah Khan, Abdullah,Hammal Khan, Amjad Ali, Ayesha Sani,Fati Ullah Khan, Muhammad Tahir Ullah,Sohail Ahmed, Romana Liaqat, Awais Haider,Kifayat Ullah, Naseeb Ullah, Muhammad Sajid Khan, Shabir Hussain,Imran Ullah,Asmat Ullah, Mariam Anees, Outi Makitie, Wasim Ahmad

Clinical genetics (2024)

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Greig Cephalopolysyndactyly Syndrome: Phenotypic Variability Associated with Variants in Two Different Domains of GLI3