Molecular modelling and dynamic simulations of sequestosome 1 (SQSTM1) missense mutations linked to Paget disease of bone
Shaik, Noor Ahmad, Nasser, Khalidah K., Alruwaili, Muteb Muidh, Alallasi, Sami Raja, Elango, Ramu, Banaganapalli, Babajan
Published in Journal of biomolecular structure & dynamics (24.05.2021)
Published in Journal of biomolecular structure & dynamics (24.05.2021)
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Journal Article
Identification of miRNA–mRNA–TFs regulatory network and crucial pathways involved in asthma through advanced systems biology approaches
Shaik, Noor Ahmad, Nasser, Khalidah, Mohammed, Arif, Mujalli, Abdulrahman, Obaid, Ahmad A, El-Harouni, Ashraf A, Elango, Ramu, Banaganapalli, Babajan
Published in PloS one (20.10.2022)
Published in PloS one (20.10.2022)
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Journal Article
Identification of a de novo LRP1 mutation in a Saudi family with Tetralogy of Fallot
Alrayes, Nuha, Mallah, Bayan A, Issa, Noha M., Banaganapalli, Babajan, Ahmad Shaik, Noor, Nasser, Khalidah K., Alshehri, Bandar Ali, Bhuiyan, Zahurul A., Bdier, Amnah Y., Al-Aama, Jumana Y.
Published in Gene (30.01.2023)
Published in Gene (30.01.2023)
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Journal Article
Exploring celiac disease candidate pathways by global gene expression profiling and gene network cluster analysis
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
Published in Scientific reports (01.10.2020)
Published in Scientific reports (01.10.2020)
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Journal Article
Molecular insights into the coding region mutations of low‐density lipoprotein receptor adaptor protein 1 (LDLRAP1) linked to familial hypercholesterolemia
Shaik, Noor A., Al‐Qahtani, Faten, Nasser, Khalidah, Jamil, Kaiser, Alrayes, Nuha Mohammad, Elango, Ramu, Awan, Zuhier Ahmed, Banaganapalli, Babajan
Published in The journal of gene medicine (01.06.2020)
Published in The journal of gene medicine (01.06.2020)
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Journal Article
Molecular differential analysis of uterine leiomyomas and leiomyosarcomas through weighted gene network and pathway tracing approaches
Sahly, Nora Naif, Banaganapalli, Babajan, Sahly, Ahmed N., Aligiraigri, Ali H., Nasser, Khalidah K., Shinawi, Thoraia, Mohammed, Arif, Alamri, Abdulhakeem S., Bondagji, Nabeel, Elango, Ramu, Shaik, Noor Ahmad
Published in Systems biology in reproductive medicine (04.05.2021)
Published in Systems biology in reproductive medicine (04.05.2021)
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Journal Article
Dissecting the Role of NF-κb Protein Family and Its Regulators in Rheumatoid Arthritis Using Weighted Gene Co-Expression Network
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
Published in Frontiers in genetics (20.11.2019)
Published in Frontiers in genetics (20.11.2019)
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Journal Article
Computational Protein Phenotype Characterization of IL10RA Mutations Causative to Early Onset Inflammatory Bowel Disease (IBD)
Al-Abbasi, Fahad A, Mohammed, Kaleemuddin, Sadath, Saida, Banaganapalli, Babajan, Nasser, Khalidah, Shaik, Noor A
Published in Frontiers in genetics (27.04.2018)
Published in Frontiers in genetics (27.04.2018)
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Journal Article
Quality of life in children with Down syndrome and its association with parent and child demographic characteristics: Parent‐reported measures
Alrayes, Nuha, Issa, Noha M., Alghubayshi, Omar Y., Al‐Amaa, Jumana Y., Alsabban, Ashwaq Hassan, Al Shaer, Dalal Sameer, Alyoubi, Reem Abdullah, Nasser, Khalidah K., Alkhiary, Yaser M.
Published in Molecular genetics & genomic medicine (01.01.2024)
Published in Molecular genetics & genomic medicine (01.01.2024)
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Journal Article
Novel MYO1D Missense Variant Identified Through Whole Exome Sequencing and Computational Biology Analysis Expands the Spectrum of Causal Genes of Laterality Defects
Alsafwani, Rabab Said, Nasser, Khalidah K., Shinawi, Thoraia, Banaganapalli, Babajan, ElSokary, Hanan Abdelhalim, Zaher, Zhaher F., Shaik, Noor Ahmad, Abdelmohsen, Gaser, Al-Aama, Jumana Yousuf, Shapiro, Adam J., O. Al-Radi, Osman, Elango, Ramu, Alahmadi, Turki
Published in Frontiers in medicine (13.09.2021)
Published in Frontiers in medicine (13.09.2021)
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Journal Article
Bioinformatics insights into the genes and pathways on severe COVID-19 pathology in patients with comorbidities
Mujalli, Abdulrahman, Alghamdi, Kawthar Saad, Nasser, Khalidah Khalid, Al-Rayes, Nuha, Banaganapalli, Babajan, Shaik, Noor Ahmad, Elango, Ramu
Published in Frontiers in physiology (14.12.2022)
Published in Frontiers in physiology (14.12.2022)
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Journal Article
Exome sequencing and metabolomic analysis of a chronic kidney disease and hearing loss patient family revealed RMND1 mutation induced sphingolipid metabolism defects
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.
Published in Saudi journal of biological sciences (01.01.2020)
Published in Saudi journal of biological sciences (01.01.2020)
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Journal Article
A comparative mRNA- and miRNA transcriptomics reveals novel molecular signatures associated with metastatic prostate cancers
Shinawi, Thoraia, Nasser, Khalidah Khalid, Moradi, Fatima Amanullah, Mujalli, Abdulrahman, Albaqami, Walaa F., Almukadi, Haifa S., Elango, Ramu, Shaik, Noor Ahmad, Banaganapalli, Babajan
Published in Frontiers in genetics (16.11.2022)
Published in Frontiers in genetics (16.11.2022)
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Journal Article
Genome-Wide Association Study-Guided Exome Rare Variant Burden Analysis Identifies IL1R1 and CD3E as Potential Autoimmunity Risk Genes for Celiac Disease
Mansour, Haifa, Banaganapalli, Babajan, Nasser, Khalidah Khalid, Al-Aama, Jumana Yousuf, Shaik, Noor Ahmad, Saadah, Omar Ibrahim, Elango, Ramu
Published in Frontiers in pediatrics (14.02.2022)
Published in Frontiers in pediatrics (14.02.2022)
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Journal Article
Whole exome sequencing of a Saudi family and systems biology analysis identifies CPED1 as a putative causative gene to Celiac Disease
Bokhari, Hifaa A., Shaik, Noor Ahmad, Banaganapalli, Babajan, Nasser, Khalidah Khalid, Ageel, Hossain Ibrahim, Al Shamrani, Ali Saad, Rashidi, Omran M., Al Ghubayshi, Omar Yaseen, Shaik, Jilani, Ahmad, Aftab, Alrayes, Nuha Mohammad, Al-Aama, Jumana Yousuf, Elango, Ramu, Saadah, Omar Ibrahim
Published in Saudi journal of biological sciences (01.06.2020)
Published in Saudi journal of biological sciences (01.06.2020)
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Journal Article
Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families
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
Published in Frontiers in pediatrics (26.04.2021)
Published in Frontiers in pediatrics (26.04.2021)
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Journal Article
Molecular profiling of lamellar ichthyosis pathogenic missense mutations on the structural and stability aspects of TGM1 protein
Nasser, Khalidah Khalid, Banaganapalli, Babajan, Shinawi, Thoraia, Elango, Ramu, Shaik, Noor Ahmad
Published in Journal of biomolecular structure & dynamics (22.09.2021)
Published in Journal of biomolecular structure & dynamics (22.09.2021)
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Journal Article
Identification of miRNA–mRNA–TFs regulatory network and crucial pathways involved in asthma through advanced systems biology approaches
Noor Ahmad Shaik, Khalidah Nasser, Arif Mohammed, Abdulrahman Mujalli, Ahmad A. Obaid, Ashraf A. El‐Harouni, Ramu Elango, Babajan Banaganapalli
Published in PloS one (01.01.2022)
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Published in PloS one (01.01.2022)
Journal Article