Exome sequencing unravels genetic variants associated with chronic kidney disease in Saudi Arabian patients

Authors: Al‐Hamed, Mohamed H., Hussein, Maged H., Shah, Yaser, Al‐Mojalli, Hamad, Alsabban, Essam, Alshareef, Turki, Altayyar, Ali, Elshouny, Samir, Ali, Wafaa, Abduljabbar, Mai, AlOtaibi, Afaf, AlShammasi, Amal, Akili, Rana, Abouelhoda, Mohamed, Sayer, John A., Dasouki, Majed J., Imtiaz, Faiqa

Source: Human mutation. 43(12):e24-e37

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100168379671.0x000001&indx=1&recIds=ETOCvdc_100168379671.0x000001

Genetic Diagnosis in Consanguineous Families With Kidney Disease by Homozygosity Mapping Coupled With Whole-Exome Sequencing

Authors: Al-Romaih, Khaldoun I., Genovese, Giulio, Al-Mojalli, Hamad, Al-Othman, Saleh, Al-Manea, Hadeel, Al-Suleiman, Mohammed, Al-Jondubi, Mohammed, Atallah, Nourah, Al-Rodayyan, Maha, Weins, Astrid, Pollak, Martin R., Adra, Chaker N.

Source: In American Journal of Kidney Diseases 2011 58(2):186-195

Novel mutations underlying nephrogenic diabetes insipidus in Arab families

Authors: Carroll, Pamela, Al-Mojalli, Hamad, Al-Abbad, Abbas, Al-Hassoun, Ibrahim, Al-Hamed, Mohamed, Al-Amr, Rana, Butt, Abdul Islam, Meyer, Brian Francis ^*

Source: In Genetics in Medicine July 2006 8(7):443-447

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Renal Failure Associated with APECED and Terminal 4q Deletion: Evidence of Autoimmune Nephropathy.

Authors: Al-Owain, Mohammed, Kaya, Namik, Al-Zaidan, Hamad, Hussain, Ibrahim Bin, Al-Manea, Hadeel, Al-Hindi, Hindi, Kennedy, Shelley, Iqbal, M. Anwar, Al-Mojalli, Hamad, Al-Bakheet, Albandary, Puel, Anne, Casanova, Jean-Laurent, Al-Muhsen, Saleh

Source: Clinical & Developmental Immunology; 2010, p1-7, 7p, 2 Color Photographs, 1 Chart, 1 Graph

Subject Terms: KIDNEY failure, INTELLECTUAL disabilities, PARATHYROID gland diseases, CHRONIC kidney failure, GENETICS

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