Mohammed A Al Balwi (Mohammed Al-Balwi, Mohammed A Albalwi, Mohammed A AlBalwi, Mohammed Ali Al Balwi, Mohammed Al Balwi, Mohammad A Al Balwi, Mohammed AlBalwi)

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 12

Top Venues

Scientific reports

Molecular genetics & genomic medicine

Avicenna journal of medicine

Journal of personalized medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Aysha Alshahrani, Zainah Abuoliat, Awad Saad Alshahrani, Mohammed A Al Balwi
Prevalence of Associated Endocrine Diseases in Patients with Neurofibromatosis Type 1. Avicenna journal of medicine 12 (1) (2022)
Mamoon Rashid, Abdulrahman I Alasiri, Mohammed A Al Balwi, Aziza Alkhaldi, Ahmed Alsuhaibani, Abdulrahman Alsultan, Talal Alharbi, Lamya Alomair, Bader Almuzzaini
Identification of CSF3R Mutations in B-Lineage Acute Lymphoblastic Leukemia Using Comprehensive Cancer Panel and Next-Generation Sequencing. Genes 12 (9) (2021)
Bader Almuzzaini, Jahad Alghamdi, Alhanouf Alomani, Saleh Alghamdi, Abdullah A Alsharm, Saeed Alshieban, Ahood Sayed, Abdulmohsen G Alhejaily, Feda S Aljaser, Manal Abudawood, Faisal Almajed, Abdulhadi Samman, Mohammed A Al Balwi, Mohammad Azhar Aziz
Identification of Novel Mutations in Colorectal Cancer Patients Using AmpliSeq Comprehensive Cancer Panel. Journal of personalized medicine 11 (6) (2021)
Maha Al Ammari, Mohammed A Al Balwi, Khizra Sultana, Ibrahim B Alabdulkareem, Bader Almuzzaini, Nada S Almakhlafi, Mohammed Aldrees, Jahad Alghamdi
The effect of the VKORC1 promoter variant on warfarin responsiveness in the Saudi WArfarin Pharmacogenetic (SWAP) cohort. Scientific reports 10 (1) (2020)
Yazeid Alhaidan, Martin Jakob Larsen, Anders Jørgen Schou, Maria H Stenlid, Mohammed A Al Balwi, Henrik Thybo Christesen, Klaus Brusgaard
Exome sequencing revealed DNA variants in NCOR1, IGF2BP1, SGLT2 and NEK11 as potential novel causes of ketotic hypoglycemia in children. Scientific reports 10 (1) (2020)
Bader Almuzzaini, Nasser S Alatwi, Saif Alsaif, Mohammed A Al Balwi
A novel interstitial deletion of chromosome 2q21.1-q23.3: Case report and literature review. Molecular genetics & genomic medicine 8 (4) (2020)
Aida Maria Bertoli-Avella, Christian Beetz, Najim Ameziane, Maria Eugenia Rocha, Pilar Guatibonza, Catarina Pereira, María Calvo, Natalia Herrera-Ordonez, Monica Segura-Castel, Dan Diego-Alvarez, Michal Zawada, Krishna K Kandaswamy, Martin Werber, Omid Paknia, Susan Zielske, Dimitar Ugrinovski, Gitte Warnack, Kapil Kampe, Marius-Ionuț Iurașcu, Claudia Cozma, Florian Vogel, Amal M Alhashem, Jozef Hertecant, Aisha M Al-Shamsi, Abdulrahman Faiz Alswaid, Wafaa Eyaid, Fuad Al Mutairi, Ahmed Alfares, Mohammed A Al Balwi, Majid Alfadhel, Nouriya Abbas Al-Sannaa, Willie Reardon, Yasemin Alanay, Arndt Rolfs, Peter Bauer
Successful application of genome sequencing in a diagnostic setting: 1007 index cases from a clinically heterogeneous cohort. European journal of human genetics : EJHG 29 (1) (2020)
Yaseen M Arabi, Dunia Jawdat, Abderrezak Bouchama, Hani Tamim, Waleed Tamimi, Mohammed A Al Balwi, Hasan M Al-Dorzi, Musharaf Sadat, Lara Afesh, Mashan L Abdullah, Walid Mashaqbeh, Maram Sakhija, Mohamed A Hussein, Adila ElObeid, Abdulaziz Al-Dawood
Permissive underfeeding, cytokine profiles and outcomes in critically ill patients. PloS one 14 (1) (2019)
Yaseen M Arabi, Mohammed A Al Balwi, Ali H Hajeer, Dunia Jawdat, Musharaf Sadat, Hasan M Al-Dorzi, Hani Tamim, Lara Afesh, Walid Mashaqbeh, Haitham Alkadi, Deemah Alwadaani, G K UdayaRaja, Ibrahim B Al Abdulkareem, Abdulaziz Al-Dawood
Differential Gene Expression in Peripheral White Blood Cells with Permissive Underfeeding and Standard Feeding in Critically Ill Patients: A Descriptive Sub-study of the PermiT Randomized Controlled Trial. Scientific reports 8 (1) (2018)
Mohammad M Al-Qattan, Ali Hadadi, Abdullah M Al-Thunayan, Ahmed A Eldali, Mohammed A Al Balwi
Upper limb muscle overgrowth with hypoplasia of the index finger: a new over-growth syndrome caused by the somatic PIK3CA mutation c.3140A>G. BMC medical genetics 19 (1) (2018)
Saud Alsahli, Stefan T Arold, Ahmed Alfares, Bader Alhaddad, Mohammed A Al Balwi, Erik-Jan Kamsteeg, Waleed Al-Twaijri, Majid Alfadhel
KIF16B is a candidate gene for a novel autosomal-recessive intellectual disability syndrome. American journal of medical genetics. Part A 176 (7) (2018)
Saif AlSaif, Ma Bella Ponferrada, Khalid AlKhairy, Khalil AlTawil, Adel Sallam, Ibrahim Ahmed, Mohammed Khawaji, Khalid AlHathlol, Beverly Baylon, Ahmed AlSuhaibani, Mohammed A Al Balwi
Screening for glucose-6-phosphate dehydrogenase deficiency in neonates: a comparison between cord and peripheral blood samples. BMC pediatrics 17 (1) (2017)

Mohammed A Al Balwi.css-eqlu8i{font-size:small;padding-left:4px;} (Mohammed Al-Balwi, Mohammed A Albalwi, Mohammed A AlBalwi, Mohammed Ali Al Balwi, Mohammed Al Balwi, Mohammad A Al Balwi, Mohammed AlBalwi)

Publication Activity (10 Years)

Top Topics

Top Venues

Mohammed A Al Balwi (Mohammed Al-Balwi, Mohammed A Albalwi, Mohammed A AlBalwi, Mohammed Ali Al Balwi, Mohammed Al Balwi, Mohammad A Al Balwi, Mohammed AlBalwi)