Computational Molecular Phenotypic Analysis of PTPN22 (W620R), IL6R (D358A), and TYK2 (P1104A) Gene Mutations of Rheumatoid Arthritis

per Shaik, Noor Ahmad, Banaganapalli, Babajan
Publicat a Front Genet (2019)

Insights from Streptococcus pneumoniae glucose kinase structural model

per Mulakayala, Chaitanya, Banaganapalli, Babajan Nawaz, Anuradha, CM, Chitta, Suresh Kumar
Publicat 2009

Ursolic acid rich Ocimum sanctum L leaf extract loaded nanostructured lipid carriers ameliorate adjuvant induced arthritis in rats by inhibition of COX-1, COX-2, TNF-α and IL-1: Ph...

per Ahmad, Aftab, Abuzinadah, Mohammed F., Alkreathy, Huda M., Banaganapalli, Babajan, Mujeeb, Mohd
Publicat a PLoS One (2018)

Design and evaluation of new chemotherapeutics of aloe-emodin (AE) against the deadly cancer disease: an in silico study

per Mulakayala, Chaitanya, Banaganapalli, Babajan, Mulakayala, Naveen, Pulaganti, Madhusudana, C.M., Anuradha, Chitta, Suresh Kumar
Publicat 2013

In-Silico Analysis of Inflammatory Bowel Disease (IBD) GWAS Loci to Novel Connections

per Mesbah-Uddin, Md., Elango, Ramu, Banaganapalli, Babajan, Shaik, Noor Ahmad, Al-Abbasi, Fahad A.
Publicat a PLoS One (2015)

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

per Al-Abbasi, Fahad A., Mohammed, Kaleemuddin, Sadath, Saida, Banaganapalli, Babajan, Nasser, Khalidah, Shaik, Noor A.
Publicat a Front Genet (2018)

Molecular designing, virtual screening and docking study of novel curcumin analogue as mutation (S769L and K846R) selective inhibitor for EGFR

per Shaik, Noor Ahmad, Al-Kreathy, Huda M., Ajabnoor, Ghada M., Verma, Prashant Kumar, Banaganapalli, Babajan
Publicat a Saudi J Biol Sci (2019)

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

per Banaganapalli, Babajan, Al-Rayes, Nuha, Awan, Zuhier Ahmed, Alsulaimany, Faten A., Alamri, Abdulhakeem S., Elango, Ramu, Malik, Md Zubbair, Shaik, Noor A.
Publicat a Comput Biol Med (2021)

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

per 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.
Publicat a Saudi J Biol Sci (2020)

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

per 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.
Publicat a Front Med (Lausanne) (2021)

Expanded Somatic Mutation Spectrum of MED12 Gene in Uterine Leiomyomas of Saudi Arabian Women

per Ajabnoor, Ghada M. A., Mohammed, Nesma Amin, Banaganapalli, Babajan, Abdullah, Layla Saleh, Bondagji, Ola Nabeel, Mansouri, Nisma, Sahly, Nora Naif, Vaidyanathan, Venkatesh, Bondagji, Nabeel, Elango, Ramu, Shaik, Noor Ahmad
Publicat a Front Genet (2018)

Exploring celiac disease candidate pathways by global gene expression profiling and gene network cluster analysis

per Banaganapalli, Babajan, Mansour, Haifa, Mohammed, Arif, Alharthi, Arwa Mastoor, Aljuaid, Nada Mohammed, Nasser, Khalidah Khalid, Ahmad, Aftab, Saadah, Omar I., Al-Aama, Jumana Yousuf, Elango, Ramu, Shaik, Noor Ahmad
Publicat a Sci Rep (2020)

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

per 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
Publicat a PLoS One (2019)

Association of Four Missense SNPs with Preeclampsia in Saudi Women

per Aljuaid, Nada Mohammed, Muharram, Ebtesam Ibrahim, Loqtum, Nouf Nasser, Al-Amoudi, Reem Mohammed, AlMahdi, Hadiah Bassam, Salama, Mohammed Assem, Banaganapalli, Babajan, Shaik, Noor Ahmad, Elango, Ramu, Bondagji, Nabeel Salem
Publicat a Saudi J Med Med Sci (2020)

Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families

per Saadah, Omar I., Banaganapalli, Babajan, Kamal, Naglaa M., Sahly, Ahmed N., Alsufyani, Hadeel A., Mohammed, Arif, Ahmad, Aftab, Nasser, Khalidah Khalid, Al-Aama, Jumana Y., Shaik, Noor Ahmad, Elango, Ramu
Publicat a Front Pediatr (2021)

TagSNP approach for HLA risk allele genotyping of Saudi celiac disease patients: effectiveness and pitfalls

per Baaqeel, Reham H., Banaganapalli, Babajan, Al Mahdi, Hadiah Bassam, Salama, Mohammed A., Alhussaini, Bakr H., Alaifan, Meshari A., Bin-Taleb, Yagoub, Shaik, Noor Ahmad, Al-Aama, Jumana Yousuf, Elango, Ramu, Saadah, Omar I.
Publicat a Biosci Rep (2021)

Dissecting the Role of NF-κb Protein Family and Its Regulators in Rheumatoid Arthritis Using Weighted Gene Co-Expression Network

per Sabir, Jamal S. M., El Omri, Abdelfatteh, Banaganapalli, Babajan, Al-Shaeri, Majed A., Alkenani, Naser A., Sabir, Mumdooh J., Hajrah, Nahid H., Zrelli, Houda, Ciesla, Lukasz, Nasser, Khalidah K., Elango, Ramu, Shaik, Noor Ahmad, Khan, Muhummadh
Publicat a Front Genet (2019)

Replication of GWAS Coding SNPs Implicates MMEL1 as a Potential Susceptibility Locus among Saudi Arabian Celiac Disease Patients

per Saadah, Omar I., Shaik, Noor Ahmad, Banaganapalli, Babajan, Salama, Mohammed A., Al-Harthi, Sameer E., Wang, Jun, Shawoosh, Harbi A., Alghamdi, Sharifa A., Bin-Taleb, Yagoub Y., Alhussaini, Bakr H., Elango, Ramu, Al-Aama, Jumana Y.
Publicat a Dis Markers (2015)

ACE insertion/deletion genetic polymorphism, serum ACE levels and high dietary salt intake influence the risk of obesity development among the Saudi adult population

per Sabir, Jamal SM, Omri, Abdelfatteh El, Ali Khan, Imran, Banaganapalli, Babajan, Hajrah, Nahid H, Zrelli, Houda, Omar, Abdulkader M Shaikh, Alharbi, Mona G, Alhebshi, Alawiah M, Jansen, Robert K, Altaf, Abdulmalik, Shaik, Noor Ahmad, Khan, Muhummadh
Publicat a J Renin Angiotensin Aldosterone Syst (2019)

Whole exome sequencing of a consanguineous family identifies the possible modifying effect of a globally rare AK5 allelic variant in celiac disease development among Saudi patients

per Al-Aama, Jumana Yousuf, Shaik, Noor Ahmad, Banaganapalli, Babajan, Salama, Mohammed A., Rashidi, Omran, Sahly, Ahmed N., Mohsen, Mohammed O., Shawoosh, Harbi A., Shalabi, Hebah Ahmad, Edreesi, Mohammad Al, Alharthi, Sameer E., Wang, Jun, Elango, Ramu, Saadah, Omar I.
Publicat a PLoS One (2017)