Exome sequencing identifies novel and known mutations in families with intellectual disability

por Rasheed, Memoona, Khan, Valeed, Harripaul, Ricardo, Siddiqui, Maimoona, Malik, Madiha Amin, Ullah, Zahid, Zahid, Muhammad, Vincent, John B., Ansar, Muhammad
Publicado 2021

Genomic Characterization of SARS-CoV2 from Peshawar Pakistan Using Next-Generation Sequencing

por Afridi, Ome Kalsoom, Bibi, Nousheen, Haider, Syed Adnan, Sabiha, Bibi, Jan, Hanifullah, Khan, Abid Ali, Akhter, Shireen, Khan, Valeed, Ali, Johar
Publicado 2022

Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and mice

por Rawlins, Lettie E., Almousa, Hashem, Khan, Shazia, Collins, Stephan C., Milev, Miroslav P., Leslie, Joseph, Saint-Dic, Djenann, Khan, Valeed, Hincapie, Ana Maria, Day, Jacob O., McGavin, Lucy, Rowley, Christine, Harlalka, Gaurav V., Vancollie, Valerie E., Ahmad, Wasim, Lelliott, Christopher J., Gul, Asma, Yalcin, Binnaz, Crosby, Andrew H., Sacher, Michael, Baple, Emma L.
Publicado 2022