Reading between the (Genetic) Lines: How Epigenetics is Unlocking Novel Therapies for Type 1 Diabetes

por Akil, Ammira-Sarah AL-Shabeeb, Jerman, Laila F., Yassin, Esraa, Padmajeya, Sujitha S., Al-Kurbi, Alya, Fakhro, Khalid A.
Publicado 2020

Ethnic-specific association of amylase gene copy number with adiposity traits in a large Middle Eastern biobank

por Rossi, Niccolo’, Aliyev, Elbay, Visconti, Alessia, Akil, Ammira S. A., Syed, Najeeb, Aamer, Waleed, Padmajeya, Sujitha S., Falchi, Mario, Fakhro, Khalid A.
Publicado 2021

A de novo start-loss in EFTUD2 associated with mandibulofacial dysostosis with microcephaly: case report

por Kohailan, Muhammad, Al-Saei, Omayma, Padmajeya, Sujitha, Aamer, Waleed, Elbashir, Najwa, Al-Shabeeb Akil, Ammira, Kamboh, Abdul-Rauf, Fakhro, Khalid
Publicado 2022

Patterns and distribution of de novo mutations in multiplex Middle Eastern families

por Kohailan, Muhammad, Aamer, Waleed, Syed, Najeeb, Padmajeya, Sujitha, Hussein, Sura, Sayed, Amira, Janardhanan, Jyothi, Palaniswamy, Sasirekha, El hajj, Nady, Al-Shabeeb Akil, Ammira, Fakhro, Khalid A.
Publicado 2022