Anna Rajab
Overview
Explore the profile of Anna Rajab including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
48
Citations
1731
Followers
0
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Reversade B, Escande-Beillard N, Dimopoulou A, Fischer B, Chng S, Li Y, et al.
Nat Genet
. 2022 Jan;
54(2):213.
PMID: 35064218
No abstract available.
2.
Courtland J, Bradshaw T, Waitt G, Soderblom E, Ho T, Rajab A, et al.
Elife
. 2021 Mar;
10.
PMID: 33749590
Mutation of the Wiskott-Aldrich syndrome protein and SCAR homology (WASH) complex subunit, SWIP, is implicated in human intellectual disability, but the cellular etiology of this association is unknown. We identify...
3.
Vatsyayan A, Sharma P, Gupta S, Sandhu S, Venu S, Sharma V, et al.
PLoS One
. 2021 Jan;
16(1):e0244567.
PMID: 33439861
The Arab population encompasses over 420 million people characterized by genetic admixture and a consequent rich genetic diversity. A number of genetic diseases have been reported for the first time...
4.
Coulter M, Musaev D, DeGennaro E, Zhang X, Henke K, James K, et al.
Genet Med
. 2020 Feb;
22(6):1040-1050.
PMID: 32103185
Purpose: The exocyst complex is a conserved protein complex that mediates fusion of intracellular vesicles to the plasma membrane and is implicated in processes including cell polarity, cell migration, ciliogenesis,...
5.
Rehman A, Najafi M, Kambouris M, Al-Gazali L, Makrythanasis P, Rad A, et al.
Hum Mutat
. 2018 Dec;
40(3):267-280.
PMID: 30520571
Next-generation sequencing (NGS) has been instrumental in solving the genetic basis of rare inherited diseases, especially neurodevelopmental syndromes. However, functional workup is essential for precise phenotype definition and to understand...
6.
Zollo M, Ahmed M, Ferrucci V, Salpietro V, Asadzadeh F, Carotenuto M, et al.
Brain
. 2017 Mar;
140(4):940-952.
PMID: 28334956
PRUNE is a member of the DHH (Asp-His-His) phosphoesterase protein superfamily of molecules important for cell motility, and implicated in cancer progression. Here we investigated multiple families from Oman, India,...
7.
Ouyang Q, Nakayama T, Baytas O, Davidson S, Yang C, Schmidt M, et al.
Proc Natl Acad Sci U S A
. 2016 Sep;
113(38):E5598-607.
PMID: 27601654
Mutations that cause neurological phenotypes are highly informative with regard to mechanisms governing human brain function and disease. We report autosomal recessive mutations in the enzyme glutamate pyruvate transaminase 2...
8.
Al-Alawi I, Goud T, Al-Harasi S, Rajab A
Reprod Biomed Online
. 2015 Dec;
32(2):162-9.
PMID: 26706459
The aim of this study was to evaluate cytogenetic findings in Omani patients who had been referred for suspicion of sex chromosome abnormalities that resulted in different clinical disorders. Furthermore,...
9.
Rajab A, Hamza N, Al Harasi S, Al Lawati F, Gibbons U, Al Alawi I, et al.
F1000Res
. 2015 Nov;
4:891.
PMID: 26594346
The Sultanate of Oman is a rapidly developing Muslim country with well-organized government-funded health care services, and expanding medical genetic facilities. The preservation of tribal structures within the Omani population...
10.
Goud T, Al Salmani K, Al Harasi S, Al Musalhi M, Wasifuddin S, Rajab A
Asian Pac J Cancer Prev
. 2015 Oct;
16(16):7343-50.
PMID: 26514535
Genetic changes associated with acute lymphoblastic leukemia (ALL) provide very important diagnostic and prognostic information with a direct impact on patient management. Detection of chromosome abnormalities by conventional cytogenetics combined...