Association of Homozygous PROP1 Mutation in a Saudi Family with Combined Pituitary Hormone Deficiency

por Almatrafi, Ahmed M., Hibshi, Ali M., Basit, Sulman
Publicado 2023

KMT2C, a histone methyltransferase, is mutated in a family segregating non-syndromic primary failure of tooth eruption

por Assiry, Ali A., Albalawi, Alia M., Zafar, Muhammad S., Khan, Siraj D., Ullah, Anhar, Almatrafi, Ahmed, Ramzan, Khushnooda, Basit, Sulman
Publicado 2019

Identification of a class of human cancer germline genes with transcriptional silencing refractory to the hypomethylating drug 5-aza-2′-deoxycytidine.

por Almatrafi, Ahmed, Feichtinger, Julia, Vernon, Ellen G., Escobar, Natalia Gomez, Wakeman, Jane A., Larcombe, Lee D., McFarlane, Ramsay J.
Publicado 2014

Meta-analysis of clinical data using human meiotic genes identifies a novel cohort of highly restricted cancer-specific marker genes

por Feichtinger, Julia, Aldeailej, Ibrahim, Anderson, Rebecca, Almutairi, Mikhlid, Almatrafi, Ahmed, Alsiwiehri, Naif, Griffiths, Keith, Stuart, Nicholas, Wakeman, Jane A., Larcombe, Lee, McFarlane, Ramsay J.
Publicado 2012

Investigating the pathogenic SNPs in BLM helicase and their biological consequences by computational approach

por Alzahrani, Faisal A., Ahmed, Firoz, Sharma, Monika, Rehan, Mohd, Mahfuz, Maryam, Baeshen, Mohammed N., Hawsawi, Yousef, Almatrafi, Ahmed, Alsagaby, Suliman Abdallah, Kamal, Mohammad Azhar, Warsi, Mohiuddin Khan, Choudhry, Hani, Jamal, Mohammad Sarwar
Publicado 2020