Saudi Familial Hypercholesterolemia Patients With Rare LDLR Stop Gain Variant Showed Variable Clinical Phenotype and Resistance to Multiple Drug Regimen

by Zuhier Ahmed Awan, Zuhier Ahmed Awan, Omran M. Rashidi, Omran M. Rashidi, Omran M. Rashidi, Bandar Ali Al-Shehri, Bandar Ali Al-Shehri, Kaiser Jamil, Ramu Elango, Ramu Elango, Jumana Y. Al-Aama, Jumana Y. Al-Aama, Robert A. Hegele, Babajan Banaganapalli, Babajan Banaganapalli, Noor A. Shaik, Noor A. Shaik
Published 2021-06-01

Whole exome sequencing identifies rare biallelic ALMS1 missense and stop gain mutations in familial Alström syndrome patients

by Naglaa M. Kamal, Ahmed N. Sahly, Babajan Banaganapalli, Omran M. Rashidi, Preetha J. Shetty, Jumana Y. Al-Aama, Noor A. Shaik, Ramu Elango, Omar I. Saadah
Published 2020-01-01

Whole exome sequencing of a Saudi family and systems biology analysis identifies CPED1 as a putative causative gene to Celiac Disease

by Hifaa A. Bokhari, Noor Ahmad Shaik, Babajan Banaganapalli, Khalidah Khalid Nasser, Hossain Ibrahim Ageel, Ali Saad Al Shamrani, Omran M. Rashidi, Omar Yaseen Al Ghubayshi, Jilani Shaik, Aftab Ahmad, Nuha Mohammad Alrayes, Jumana Yousuf Al-Aama, Ramu Elango, Omar Ibrahim Saadah
Published 2020-06-01

Exome sequencing and metabolomic analysis of a chronic kidney disease and hearing loss patient family revealed RMND1 mutation induced sphingolipid metabolism defects

by Nagwa E.A. Gaboon, Babajan Banaganapalli, Khalidah Nasser, Mohammed Razeeth, Mosab S. Alsaedi, Omran M. Rashidi, Lereen S. Abdelwehab, Turki Saad Alahmadi, Osama Y. Safdar, Jilani Shaik, Hani M.Z. Choudhry, Huda Husain Al-numan, Mohammad Imran Khan, Jumana Y. Al-Aama, Ramu Elango, Noor A. Shaik
Published 2020-01-01