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Taghrid Aloraini
Taghrid Aloraini
Genetic counsellor
Verified email at NGHA.MED.SA
Title
Cited by
Cited by
Year
Whole-genome sequencing offers additional but limited clinical utility compared with reanalysis of whole-exome sequencing
A Alfares, T Aloraini, A Alissa, A Al Qudsi, A Alahmad, F Al Mutairi, ...
Genetics in Medicine 20 (11), 1328-1333, 2018
1542018
EMC10 homozygous variant identified in a family with global developmental delay, mild intellectual disability, and speech delay
M Umair, M Ballow, A Asiri, Y Alyafee, A Al Tuwaijri, KM Alhamoudi, ...
Clinical Genetics 98 (6), 555-561, 2020
302020
Biallelic variants in COPB1 cause a novel, severe intellectual disability syndrome with cataracts and variable microcephaly
WL Macken, A Godwin, G Wheway, K Stals, L Nazlamova, S Ellard, ...
Genome Medicine 13, 1-19, 2021
292021
What is the right sequencing approach? Solo VS extended family analysis in consanguineous populations
A Alfares, L Alsubaie, T Aloraini, A Alaskar, A Althagafi, A Alahmad, ...
BMC medical genomics 13, 1-8, 2020
152020
DeepSVP: integration of genotype and phenotype for structural variant prioritization using deep learning
A Althagafi, L Alsubaie, N Kathiresan, K Mineta, T Aloraini, F Al Mutairi, ...
Bioinformatics 38 (6), 1677-1684, 2022
122022
Common disease-associated gene variants in a Saudi Arabian population
M Aleissa, T Aloraini, LF Alsubaie, M Hassoun, G Abdulrahman, A Swaid, ...
Annals of Saudi Medicine 42 (1), 29-35, 2022
122022
Genomic testing and counseling: the contribution of next‐generation sequencing to epilepsy genetics
L Alsubaie, T Aloraini, M Amoudi, A Swaid, W Eyiad, F Al Mutairi, ...
Annals of human genetics 84 (6), 431-436, 2020
82020
The diagnostic yield of CGH and WES in neurodevelopmental disorders
RS Alotibi, NS Sannan, M AlEissa, MG Aldriwesh, A Al Tuwaijri, MA Akiel, ...
Frontiers in Pediatrics 11, 1133789, 2023
72023
The rate of secondary genomic findings in the Saudi population
T Aloraini, L Alsubaie, S Alasker, A Al Muitiri, A Alswaid, W Eyiad, ...
American Journal of Medical Genetics Part A 188 (1), 83-88, 2022
72022
Genetic carrier screening for disorders included in newborn screening in the Saudi population
M Al Eissa, T Aloraini, L Alsubaie, A Alswaid, W Eyiad, F Al Mutairi, ...
Journal of Biochemical and Clinical Genetics 4 (2), 70-70, 2021
42021
subaie LA, Alissa A, Qudsi AA, Alahmad A, et al. Whole-genome sequencing offers additional but limited clinical utility compared with reanalysis of whole-exome sequencing
A Alfares, T Aloraini
Genet Med 20 (11), 1328-33, 2018
42018
Attitudes of geneticists and patients toward incidental findings in Saudi Arabia
T Aloraini, A Abdulrahim, GA Karbani
IRB 37, 17, 2019
32019
Prospect of genetic disorders in Saudi Arabia
AS Alqahtani, RS Alotibi, T Aloraini, F Almsned, Y Alassali, A Alfares, ...
Frontiers in Genetics 14, 1243518, 2023
22023
MEFV c.2230G>T p.(Ala744Ser) rs61732874 previously misclassified as pathogenic variant due to lack of a population specific database
L Alsubaie, R Alkhalaf, T Aloraini, M Amoudi, A Swaid, F Al Mutairi, ...
Annals of Human Genetics 84 (5), 370-379, 2020
22020
Reclassifying variations of unknown significance in diseases affecting Saudi Arabia’s population reveal new associations
MM Al Eissa, RS Alotibi, B Alhaddad, T Aloraini, MS Samman, A AlAsiri, ...
Frontiers in Genetics 14, 1250317, 2023
12023
The variant artificial intelligence easy scoring (VARIES) system
T Aloraini, A Aljouie, R Alniwaider, W Alharbi, L Alsubaie, W AlTuraif, ...
Computers in Biology and Medicine 145, 105492, 2022
12022
Supplementary testing after negative or inconclusive exome sequencing results
B AlMaarik, T Aloraini, R Paclejan, M Balwi, L Alsubaie, A Alswaid, ...
Journal of Biochemical and Clinical Genetics 6 (1), 1-1, 2023
2023
Genetic impact of non-consanguineous marriages in Saudi Arabia.
M Alyahya, T Aloraini, Y Al-Harbi, L Alsubaie, A Alswaid, W Eyaid, ...
Journal of Biochemical and Clinical Genetics 5 (2), 37-37, 2022
2022
Novel mutation of the FHL1 gene associated with congenital myopathy and early respiratory muscles involvement: a case report
R Almutairi, S Alrashidi, M Umair, M Alshalan, L Alsubaie, T Aloraini, ...
Journal of Biochemical and Clinical Genetics 3 (1), 45-45, 2020
2020
Comparison between the attitudes of genetics professionals and patients towards incidental findings from whole-genome or whole-exome sequencing
TM Aloraini, A Gari, G AlKarbani
EUROPEAN JOURNAL OF HUMAN GENETICS 27, 674-674, 2019
2019
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