Showing 1 - 8 results of 8 for search 'Noor Ahmad Shaik', query time: 0.06s Refine Results
  1. 1
    Exome Analysis Identifies a Novel Compound Heterozygous Alteration in TGM1 Gene Leading to Lamellar Ichthyosis in a Child From Saudi Arabia: Case Presentation

    Exome Analysis Identifies a Novel Compound Heterozygous Alteration in TGM1 Gene Leading to Lamellar Ichthyosis in a Child From Saudi Arabia: Case Presentation by Sami Raja Alallasi, Amal A. Kokandi, Babajan Banagnapali, Babajan Banagnapali, Noor Ahmad Shaik, Noor Ahmad Shaik, Bandar Ali Al-Shehri, Nuha Mohammad Alrayes, Jumana Yousuf Al-Aama, Jumana Yousuf Al-Aama, Musharraf Jelani, Musharraf Jelani

    Published 2019
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  2. 2
    Genome-Wide Association Study-Guided Exome Rare Variant Burden Analysis Identifies IL1R1 and CD3E as Potential Autoimmunity Risk Genes for Celiac Disease

    Genome-Wide Association Study-Guided Exome Rare Variant Burden Analysis Identifies IL1R1 and CD3E as Potential Autoimmunity Risk Genes for Celiac Disease by Haifa Mansour, Haifa Mansour, Babajan Banaganapalli, Babajan Banaganapalli, Khalidah Khalid Nasser, Khalidah Khalid Nasser, Khalidah Khalid Nasser, Jumana Yousuf Al-Aama, Jumana Yousuf Al-Aama, Noor Ahmad Shaik, Noor Ahmad Shaik, Omar Ibrahim Saadah, Omar Ibrahim Saadah, Ramu Elango, Ramu Elango

    Published 2022
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  3. 3
    Granulomatous hepatitis in a Saudi child with defect: a case report and literature review

    Granulomatous hepatitis in a Saudi child with defect: a case report and literature review by Meshari A. Alaifan, Ohood Abusharifah, Rana Yagoub Bokhary, Babajan Banaganapalli, Noor Ahmad Shaik, Naglaa M. Kamal, Omar I. Saadah

    Published 2022
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  4. 4
    Exploring somatic mutations in BRAF, KRAS, and NRAS as therapeutic targets in Saudi colorectal cancer patients through massive parallel sequencing and variant classification

    Exploring somatic mutations in BRAF, KRAS, and NRAS as therapeutic targets in Saudi colorectal cancer patients through massive parallel sequencing and variant classification by Thamer Abdulhamid Aljuhani, Thamer Abdulhamid Aljuhani, Noor Ahmad Shaik, Noor Ahmad Shaik, Rahaf Talal Alqawas, Rana Y. Bokhary, Mahmood Al-Mutadares, Hadiah Bassam Al Mahdi, Nuha Al-Rayes, Ashraf AbdulRahman El-Harouni, Ramu Elango, Ramu Elango, Babajan Banaganapalli, Babajan Banaganapalli, Zuhier Ahmad Awan

    Published 2024
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  5. 5
    Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families

    Identification of a Rare Exon 19 Skipping Mutation in ALMS1 Gene in Alström Syndrome Patients From Two Unrelated Saudi Families by Omar I. Saadah, Omar I. Saadah, Babajan Banaganapalli, Babajan Banaganapalli, Naglaa M. Kamal, Naglaa M. Kamal, Ahmed N. Sahly, Ahmed N. Sahly, Hadeel A. Alsufyani, Arif Mohammed, Aftab Ahmad, Khalidah Khalid Nasser, Khalidah Khalid Nasser, Jumana Y. Al-Aama, Jumana Y. Al-Aama, Noor Ahmad Shaik, Noor Ahmad Shaik, Ramu Elango, Ramu Elango

    Published 2021
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  6. 6
    Exome Sequencing Identifies the Extremely Rare ITGAV and FN1 Variants in Early Onset Inflammatory Bowel Disease Patients

    Exome Sequencing Identifies the Extremely Rare ITGAV and FN1 Variants in Early Onset Inflammatory Bowel Disease Patients by Huda Husain Al-Numan, Huda Husain Al-Numan, Rana Mohammed Jan, Rana Mohammed Jan, Najla bint Saud Al-Saud, Omran M. Rashidi, Nuha Mohammad Alrayes, Hadeel A. Alsufyani, Abdulrahman Mujalli, Abdulrahman Mujalli, Noor Ahmad Shaik, Noor Ahmad Shaik, Mahmoud Hisham Mosli, Mahmoud Hisham Mosli, Ramu Elango, Ramu Elango, Omar I. Saadah, Omar I. Saadah, Babajan Banaganapalli, Babajan Banaganapalli

    Published 2022
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  7. 7
    Evaluation of gestational diabetes mellitus risk in South Indian women based on MTHFR (C677T) and FVL (G1691A) mutations

    Evaluation of gestational diabetes mellitus risk in South Indian women based on MTHFR (C677T) and FVL (G1691A) mutations by Imran Ali Khan, Imran Ali Khan, Imran Ali Khan, Noor Ahmad Shaik, Vasundara eKamineni, Parveen eJahan, Qurratulain eHasan, Qurratulain eHasan, Pragna eRao

    Published 2015
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  8. 8
    Complex Inheritance of Rare Missense Variants in PAK2, TAP2, and PLCL1 Genes in a Consanguineous Arab Family With Multiple Autoimmune Diseases Including Celiac Disease

    Complex Inheritance of Rare Missense Variants in PAK2, TAP2, and PLCL1 Genes in a Consanguineous Arab Family With Multiple Autoimmune Diseases Including Celiac Disease by Arwa Mastoor Alharthi, Arwa Mastoor Alharthi, Babajan Banaganapalli, Babajan Banaganapalli, Sabah M. Hassan, Sabah M. Hassan, Omran Rashidi, Bandar Ali Al-Shehri, Meshari A. Alaifan, Meshari A. Alaifan, Bakr H. Alhussaini, Bakr H. Alhussaini, Hadeel A. Alsufyani, Kawthar Saad Alghamdi, Khalda Khalid Nasser, Khalda Khalid Nasser, Khalda Khalid Nasser, Yagoub Bin-Taleb, Ramu Elango, Ramu Elango, Noor Ahmad Shaik, Noor Ahmad Shaik, Omar I. Saadah, Omar I. Saadah

    Published 2022
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