Deep learning-based identification of esophageal cancer subtypes through analysis of high-resolution histopathology images.

Autor: Aalam SW; Department of Computer Science, Islamic University of Science and Technology, Awantipora, India., Ahanger AB; Department of Computer Science, Islamic University of Science and Technology, Awantipora, India., Masoodi TA; Human Immunology Department, Research Branch, Sidra Medicine, Doha, Qatar., Bhat AA; Department of Human Genetics-Precision Medicine in Diabetes, Obesity and Cancer Program, Sidra Medicine, Doha, Qatar., Akil ASA; Department of Human Genetics-Precision Medicine in Diabetes, Obesity and Cancer Program, Sidra Medicine, Doha, Qatar., Khan MA; DigiBiomics Inc, Mississauga, ON, Canada., Assad A; Department of Computer Science and Engineering, Islamic University of Science and Technology, Awantipora, India., Macha MA; Watson-Crick Centre for Molecular Medicine, Islamic University of Science and Technology, Awantipora, India., Bhat MR; Department of Computer Science, Islamic University of Science and Technology, Awantipora, India.

Publikováno v: Frontiers in molecular biosciences [Front Mol Biosci] 2024 Mar 19; Vol. 11, pp. 1346242. Date of Electronic Publication: 2024 Mar 19 (Print Publication: 2024).

Structural prediction, whole exome sequencing and molecular dynamics simulation confirms p.G118D somatic mutation of PIK3CA as functionally important in breast cancer patients.

Autor: Masoodi TA; Department of Biotechnology, K L University, Guntur, Andhra Pradesh, India; Department of Biotechnology, Hyderabad Science Society, Hyderabad, 500004, India. Electronic address: tahamasoodi@gmail.com., Shaik NA; Department of Biotechnology, Hyderabad Science Society, Hyderabad, 500004, India; Department of Genetic Medicine, Princess Al-Jawhara Al-Brahim Centre of Excellene in Research of Hereditary Disorders, Faculty of Medicine, King Abdulaziz University, Jeddah, Saudi Arabia. Electronic address: nshaik@kau.edu.sa., Burhan S; Department of Oncology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, India., Hasan Q; Department of Biotechnology, Hyderabad Science Society, Hyderabad, 500004, India., Shafi G; iNDX Technology, Cupertino, United States., Talluri VR; Department of Biotechnology, K L University, Guntur, Andhra Pradesh, India; Prof. TNA Innovation Center, Varsha Bioscience and Technology India Private Limited, Telangana, India. Electronic address: tvrao_bt@kluniversity.in.

Publikováno v: Computational biology and chemistry [Comput Biol Chem] 2019 Jun; Vol. 80, pp. 472-479. Date of Electronic Publication: 2019 May 29.

Exome sequencing identifies novel NTRK1 mutations in patients with HSAN-IV phenotype.

Autor: Altassan R; Department of Medical Genetics, King Faisal Specialist Hospital and Center Hospital, Riyadh, Saudi Arabia., Saud HA; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Masoodi TA; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Dosssari HA; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Khalifa O; Department of Medical Genetics, King Faisal Specialist Hospital and Center Hospital, Riyadh, Saudi Arabia.; Department of Pediatrics, Faculty of Medicine, Ain Shams University, Cairo, Egypt., Al-Zaidan H; Department of Medical Genetics, King Faisal Specialist Hospital and Center Hospital, Riyadh, Saudi Arabia.; College of Medicine, Al-Faisal University, Riyadh, Saudi Arabia., Sakati N; Department of Medical Genetics, King Faisal Specialist Hospital and Center Hospital, Riyadh, Saudi Arabia., Rhabeeni Z; Department of Medical Genetics, King Faisal Specialist Hospital and Center Hospital, Riyadh, Saudi Arabia., Al-Hassnan Z; Department of Medical Genetics, King Faisal Specialist Hospital and Center Hospital, Riyadh, Saudi Arabia.; College of Medicine, Al-Faisal University, Riyadh, Saudi Arabia., Binamer Y; College of Medicine, Al-Faisal University, Riyadh, Saudi Arabia.; Department of Dermatology, King Faisal Specialist., Alhashemi N; Department of Pediatrics, Royal hospital, Muscat, Oman., Wade W; Department of Orthopedics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Al-Zayed Z; Department of Orthopedics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Al-Sayed M; Department of Medical Genetics, King Faisal Specialist Hospital and Center Hospital, Riyadh, Saudi Arabia., Al-Muhaizea MA; Department of Neurology, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Meyer B; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Al-Owain M; Department of Medical Genetics, King Faisal Specialist Hospital and Center Hospital, Riyadh, Saudi Arabia.; College of Medicine, Al-Faisal University, Riyadh, Saudi Arabia., Wakil SM; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

Publikováno v: American journal of medical genetics. Part A [Am J Med Genet A] 2017 Apr; Vol. 173 (4), pp. 1009-1016.

Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus.

Autor: Alazami AM; Developmental Genetics Unit, King Faisal Specialist Hospital and Research Center, MBC-03 PO BOX 3354, Riyadh 11211, Saudi Arabia., Hijazi H, Al-Dosari MS, Shaheen R, Hashem A, Aldahmesh MA, Mohamed JY, Kentab A, Salih MA, Awaji A, Masoodi TA, Alkuraya FS

Publikováno v: Journal of medical genetics [J Med Genet] 2013 Jul; Vol. 50 (7), pp. 425-30. Date of Electronic Publication: 2013 Apr 25.

Mutation in MPDZ causes severe congenital hydrocephalus.

Autor: Al-Dosari MS; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Al-Owain M, Tulbah M, Kurdi W, Adly N, Al-Hemidan A, Masoodi TA, Albash B, Alkuraya FS

Publikováno v: Journal of medical genetics [J Med Genet] 2013 Jan; Vol. 50 (1), pp. 54-8.