Fowzan S Alkuraya, MD
Fowzan S Alkuraya, MD
Professor of Human Genetics, Alfaisal University and KFSHRC, Riyadh, Saudi Arabia
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Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families
AM Alazami, N Patel, HE Shamseldin, S Anazi, MS Al-Dosari, F Alzahrani, ...
Cell reports 10 (2), 148-161, 2015
Loss-of-function variant in DNASE1L3 causes a familial form of systemic lupus erythematosus
SM Al-Mayouf, A Sunker, R Abdwani, SA Abrawi, F Almurshedi, ...
Nature genetics 43 (12), 1186-1188, 2011
International cooperation to enable the diagnosis of all rare genetic diseases
KM Boycott, A Rath, JX Chong, T Hartley, FS Alkuraya, G Baynam, ...
The American Journal of Human Genetics 100 (5), 695-705, 2017
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery
EM Scott, A Halees, Y Itan, EG Spencer, Y He, MA Azab, SB Gabriel, ...
Nature genetics 48 (9), 1071-1076, 2016
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism
M Horikoshi, H Yaghootkar, DO Mook-Kanamori, U Sovio, HR Taal, ...
Nature genetics 45 (1), 76-82, 2013
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
C Redin, H Brand, RL Collins, T Kammin, E Mitchell, JC Hodge, ...
Nature genetics 49 (1), 36-45, 2017
Autozygome-guided exome sequencing in retinal dystrophy patients reveals pathogenetic mutations and novel candidate disease genes
L Abu-Safieh, M Alrashed, S Anazi, H Alkuraya, AO Khan, M Al-Owain, ...
Genome research 23 (2), 236-247, 2013
LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency
A Alangari, A Alsultan, N Adly, MJ Massaad, IS Kiani, A Aljebreen, ...
Journal of Allergy and Clinical Immunology 130 (2), 481-488. e2, 2012
Mutations in lectin complement pathway genes COLEC11 and MASP1 cause 3MC syndrome
C Rooryck, A Diaz-Font, DPS Osborn, E Chabchoub, ...
Nature genetics 43 (3), 197-203, 2011
SUMO1 haploinsufficiency leads to cleft lip and palate
FS Alkuraya, I Saadi, JJ Lund, A Turbe-Doan, CC Morton, RL Maas
Science 313 (5794), 1751-1751, 2006
Mutations in CCNO result in congenital mucociliary clearance disorder with reduced generation of multiple motile cilia
J Wallmeier, DA Al-Mutairi, CT Chen, NT Loges, P Pennekamp, ...
Nature genetics 46 (6), 646-651, 2014
The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes
D Monies, M Abouelhoda, M AlSayed, Z Alhassnan, M Alotaibi, H Kayyali, ...
Human genetics 136, 921-939, 2017
Treatment of retinitis pigmentosa due to MERTK mutations by ocular subretinal injection of adeno-associated virus gene vector: results of a phase I trial
NG Ghazi, EB Abboud, SR Nowilaty, H Alkuraya, A Alhommadi, H Cai, ...
Human genetics 135, 327-343, 2016
Homozygous mutations in ADAMTS10 and ADAMTS17 cause lenticular myopia, ectopia lentis, glaucoma, spherophakia, and short stature
J Morales, L Al-Sharif, DS Khalil, JMA Shinwari, P Bavi, RA Al-Mahrouqi, ...
The American Journal of Human Genetics 85 (5), 558-568, 2009
An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes
G Wheway, M Schmidts, DA Mans, K Szymanska, TMT Nguyen, H Racher, ...
Nature cell biology 17 (8), 1074-1087, 2015
Human mutations in NDE1 cause extreme microcephaly with lissencephaly
FS Alkuraya, X Cai, C Emery, GH Mochida, MS Al-Dosari, JM Felie, ...
The American Journal of Human Genetics 88 (5), 536-547, 2011
Lessons learned from large-scale, first-tier clinical exome sequencing in a highly consanguineous population
D Monies, M Abouelhoda, M Assoum, N Moghrabi, R Rafiullah, ...
The American Journal of Human Genetics 104 (6), 1182-1201, 2019
CPAP promotes timely cilium disassembly to maintain neural progenitor pool
E Gabriel, A Wason, A Ramani, LM Gooi, P Keller, A Pozniakovsky, ...
The EMBO journal 35 (8), 803-819, 2016
Clinical genomics expands the morbid genome of intellectual disability and offers a high diagnostic yield
S Anazi, S Maddirevula, E Faqeih, H Alsedairy, F Alzahrani, ...
Molecular psychiatry 22 (4), 615-624, 2017
Mutations in the RNA granule component TDRD7 cause cataract and glaucoma
SA Lachke, FS Alkuraya, SC Kneeland, T Ohn, A Aboukhalil, GR Howell, ...
Science 331 (6024), 1571-1576, 2011
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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