Taurodontism in maxillary and mandibular molars using cone beam computed tomography in a dental center in Saudi Arabia

Autor: Ali Mohammed Alkhayrat, Shankargouda Patil, Abdullah Saeed Wasli, Saranya Varadarajan, Hemant Ramesh Chourasia, Hassan Mohammed Mahnashi, Mohammed Jebril Kamly, Ahmad H. Jabali

Publikováno v: Annals of Saudi Medicine, Vol 41, Iss 4, Pp 232-237 (2021)
Annals of Saudi Medicine

BACKGROUND: Taurodontism is a dental anomaly characterized by altered crown root ratio that is often diagnosed by radiographic evaluation. A three-dimensional cone beam computed tomography (CBCT) can aid in the diagnosis and treatment of taurodontic

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd7002876a98220c7b28de6a388fa6e8
https://www.annsaudimed.net/doi/full/10.5144/0256-4947.2021.232

The morbid genome of ciliopathies: an update

Autor: Maha Tulba, Amal Alhashem, Ali Howaidi, Tarfa Alshidi, Sawsan R. Nowilaty, Abdullah Alfaifi, Mais Hashem, Mohammad Shagrani, Mustafa A. Salih, Rubina Khan, Dalal K. Bubshait, Maged H. Hussein, Essam Al Sabban, Maisoon Almugbel, Ranad Shaheen, Hisham Alkuraya, Nour Ewida, Mohammad A. Al Muhaizea, Eman Alobeid, Zuhair Rahbeeni, Jameel M. Alghamdi, Niema Ibrahim, Yasser Sabr, Sameera Sogaty, Elham Al-Mardawi, Neama Meriki, Khalid Alhazmi, Mona M. Alenazi, Mohammed Zain Seidahmed, Heba Morsy, Ebtesam M. Abdalla, Mohammed Mahnashi, Abrar K. Alsalamah, Fowzan S. Alkuraya, Ahmed Alfares, Hamad Al-Zaidan, Afaf Alsagheir, Alya Qari, Firdous Abdulwahab, Hanan E. Shamseldin, Mohammed Al–Owain

Publikováno v: Genetics in medicine : official journal of the American College of Medical Genetics. 22(6)

Ciliopathies are highly heterogeneous clinical disorders of the primary cilium. We aim to characterize a large cohort of ciliopathies phenotypically and molecularly. Detailed phenotypic and genomic analysis of patients with ciliopathies, and function

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae441c96c55811650969eb16c5de2048
https://pubmed.ncbi.nlm.nih.gov/35394428

Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population

Autor: Malak Alghamdi, Susan Alhumaidi, Saeed Altala, Mirna Assoum, Aziza Chedrawi, Moeen Al-Sayed, Hisham Aldhalaan, Suzan A AlKhater, M. Abouelhoda, Turki Alshareef, Maha Alotaibi, Khalid S. Alqadi, Alya Alkaff, Syed Ahmed, Musad Abu Khaled, Suad Al Yamani, Bassem Albeirouti, Ali Al-Mehaidib, Walaa Alshuaibi, Nawal Makhseed, Ghada M H Abdel-Salam, Ewa Goljan, Zuhair Rahbeeni, Maisoon Almugbel, Shaza Makki, Ranad Albar, Fuad Al Mutairi, Khalid Alsaleem, Hanaa Banjar, Fahad A. Bashiri, Abdulaziz Bin Manee, Mona Alsaleh, Marwan Shaheen, Mohammed Fawzy, Sami Wali, Fahad Almohareb, Hisham Alkuraya, Shakir Bahzad, Ayman Shawli, Wesam Kurdi, Wajeeh Aldekhail, Somaya Alzelaye, Rand Arnaout, Abdullah Alsonbul, Sami Al-Hajjar, Saeed Hassan, Sameena Khan, Mohammed AlBalwi, Khalid Awartani, Sulaiman M. Al-Mayouf, Amal Alhashem, Hamoud Al-Mousa, Abdulaziz Alsemari, Hadeel Elbardisy, Mohamed El-Kalioby, Edward Cupler, Bandar Al-Saud, Hadeel Alghamdi, Isam Salih, Saadeh Sermin, Fahad Alsohaibaini, Shapar Nahrir, Hibah Alruwaili, Hamad Al-Zaidan, Nada Alsahan, Abdullah Alfaifi, Dalal K. Bubshait, Mohammed Nasr, Ahmed Alnahari, Ameen Tajuddin, Maged H. Hussein, Muddathir H Hamad, Asma Akilan, Afaf Alsagheir, Dorota Monies, Shamsad Shahrukh, Emadia Alaki, Tariq Abalkhail, Ahmed Sahly, Hamsa T. Tayeb, Badi Alenazi, Fowzan S. Alkuraya, Mohammed Al-Owain, Mohammed Abanemai, Ali Al-Ahmari, Maha Faden, Neama Meriki, Amal Alqasmi, Talal A. Basha, Hatem Murad, Hanna Akleh, Nabil Moghrabi, Asma I. Tahir, Abdulhadi Altalhi, Amal Jaafar, Ola Jarrad, Salah Baz, Abdullah Tamim, Ibraheem F. Abosoudah, Shazia Subhani, Manal Badawi, Raashida Sulaiman, Essam Al-Sabban, Brian F. Meyer, Talal Algoufi, Alya Qari, Mohammed Mahnashi, Hasan Al-Dhekri, Saeed Bohlega, Rafiullah Rafiullah, Naif A.M. Almontashiri, Mustafa A. Salih, Shahrukh K. Hashmi, Ibrahim Ghemlas, Zeeshan Shah, Abdullah Alashwal, Ehab Tous

Publikováno v: The American Journal of Human Genetics. 105:879

We report the results of clinical exome sequencing (CES) on >2,200 previously unpublished Saudi families as a first-tier test. The predominance of autosomal-recessive causes allowed us to make several key observations. We highlight 155 genes that we

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0365855d2d5af752e8f99d9baffcda1e
https://doi.org/10.1016/j.ajhg.2019.09.019