Computational Protein Phenotype Characterization of IL10RA Mutations Causative to Early Onset Inflammatory Bowel Disease (IBD)

por Al-Abbasi, Fahad A., Mohammed, Kaleemuddin, Sadath, Saida, Banaganapalli, Babajan, Nasser, Khalidah, Shaik, Noor A.
Publicado 2018

Integrative weighted molecular network construction from transcriptomics and genome wide association data to identify shared genetic biomarkers for COPD and lung cancer

por Banaganapalli, Babajan, Mallah, Bayan, Alghamdi, Kawthar Saad, Albaqami, Walaa F., Alshaer, Dalal Sameer, Alrayes, Nuha, Elango, Ramu, Shaik, Noor A.
Publicado 2022

Multilevel systems biology analysis of lung transcriptomics data identifies key miRNAs and potential miRNA target genes for SARS-CoV-2 infection

por Banaganapalli, Babajan, Al-Rayes, Nuha, Awan, Zuhier Ahmed, Alsulaimany, Faten A., Alamri, Abdulhakeem S., Elango, Ramu, Malik, Md Zubbair, Shaik, Noor A.
Publicado 2021

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

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

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

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

Identification of key regulatory genes connected to NF-κB family of proteins in visceral adipose tissues using gene expression and weighted protein interaction network

por Sabir, Jamal S. M., El Omri, Abdelfatteh, Shaik, Noor A., Banaganapalli, Babajan, Al-Shaeri, Majed A., Alkenani, Naser A., Hajrah, Nahid H., Awan, Zuhier A., Zrelli, Houda, Elango, Ramu, Khan, Muhummadh
Publicado 2019

The genetic association study of TP53 polymorphisms in Saudi obese patients

por Sabir, Jamal S.M., El Omri, Abdelfatteh, Shaik, Noor A., Banaganapalli, Babajan, Hajrah, Nahid H., Zrelli, Houda, Arfaoui, Leila, Awan, Zuhier A., Shaikh Omar, Abdulkader M., Mohammed, Arif, Alharbi, Mona G., Alhebshi, Alawiah M., Jansen, Robert K., Khan, Muhummadh
Publicado 2019

Unraveling the role of salt-sensitivity genes in obesity with integrated network biology and co-expression analysis

por Sabir, Jamal Sabir M., El Omri, Abdelfatteh, Banaganapalli, Babajan, Aljuaid, Nada, Omar, Abdulkader M. Shaikh, Altaf, Abdulmalik, Hajrah, Nahid H., Zrelli, Houda, Arfaoui, Leila, Elango, Ramu, Alharbi, Mona G., Alhebshi, Alawiah M., Jansen, Robert K., Shaik, Noor A., Khan, Muhummadh
Publicado 2020

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

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