Farooq Ahmad

ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 3

Top Venues

Clinical genetics

Genes

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

Publications

Fati Ullah Khan, Hammal Khan, Kifayat Ullah, Shoaib Nawaz, null Abdullah, Muhammad Javed Khan, Sohail Ahmed, Muhammad Ilyas, Amjad Ali, Imran Ullah, Aamir Sohail, Shabir Hussain, Farooq Ahmad, null Faisal, 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, Khurram Liaqat, Muhammad Zahid, Khadim Shah, Outi Mikitie, Tobias B Haack, Weizhen Ji, Saquib A Lakhani, Muhammad Ansar, Wasim Ahmad
Clinical and genetic investigation of 14 families with various forms of short stature syndromes. Clinical genetics 106 (3) (2024)
Fati Ullah Khan, Hammal Khan, Kifayat Ullah, Shoaib Nawaz, null Abdullah, Muhammad Javed Khan, Sohail Ahmed, Muhammad Ilyas, Amjad Ali, Imran Ullah, Aamir Sohail, Shabir Hussain, Farooq Ahmad, null Faisal, 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, Khurram Liaqat, Muhammad Zahid, Khadim Shah, Outi Mikitie, Tobias B Haack, Weizhen Ji, Saquib A Lakhani, Muhammad Ansar, Wasim Ahmad
Clinical and genetic investigation of 14 families with various forms of short stature syndromes. Clinical genetics (2024)
Amjad Khan, Zhichiao Miao, Muhammad Umair, Amir Ullah, Mohammad A Alshabeeb, Muhammad Bilal, Farooq Ahmad, Gudrun A Rappold, Muhammad Ansar, Raphaël Carapito
Two Cases of Recessive Intellectual Disability Caused by NDST1 and METTL23 Variants. Genes 11 (9) (2020)

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Publication Activity (10 Years)

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Farooq Ahmad