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Al Turki, Saeed
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1

Consensus Recommendations for the Diagnosis, Biomarker Test..:

Mahrous, Mervat ; Omar Jebriel, Abdalla ; Allehebi, Ahmed...
Cureus.  , 2023
Link: https://doi.org/10.7759/..
 
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2

Development and Validation of ScriptTaq COVID PCR: An In-Ho..:

AbuObead, Dana Abdalghani ; Alhomsi, Tasnim Khalid ; Zhra, Mahmoud...
Current Issues in Molecular Biology.  44 (2022)  12 - p. 6117-6131 , 2022
Link: https://doi.org/10.3390/..
 
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3

The genomic history of the Middle East:

Almarri, Mohamed A. ; Haber, Marc ; Lootah, Reem A....
Cell.  184 (2021)  18 - p. 4612-4625.e14 , 2021
Link: https://doi.org/10.1016/..
 
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4

Low-frequency variation in TP53 has large effects on head c..:

Haworth, Simon ; Shapland, Chin Yang ; Hayward, Caroline...
Nature Communications.  10 (2019)  1 - p. , 2019
Link: https://doi.org/10.1038/..
 
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5

Isolated Bone Marrow Non–Langerhans Cell Histiocytosis Prec..:

Al Mugairi, Areej ; Al Turki, Saeed ; Salama, Hind...
American Journal of Clinical Pathology.  151 (2019)  6 - p. 638-646 , 2019
Link: https://doi.org/10.1093/..
 
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6

Exome sequencing identifies rare variants in multiple genes..:

D'Alessandro, Lisa C.A. ; Al Turki, Saeed ; Manickaraj, Ashok Kumar...
Genetics in Medicine.  18 (2016)  2 - p. 189-198 , 2016
Link: https://doi.org/10.1038/..
 
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7

Timing, rates and spectra of human germline mutation:

UK10K Consortium ; Rahbari, Raheleh ; Wuster, Arthur...
Nature Genetics.  48 (2015)  2 - p. 126-133 , 2015
Link: https://doi.org/10.1038/..
 
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8

Improved imputation of low-frequency and rare variants usin..:

Huang, Jie ; Howie, Bryan ; McCarthy, Shane...
Nature Communications.  6 (2015)  1 - p. , 2015
Link: https://doi.org/10.1038/..
 
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9

Recessive nephrocerebellar syndrome on the Galloway-Mowat s..:

Jinks, Robert N. ; Puffenberger, Erik G. ; Baple, Emma...
Brain.  138 (2015)  8 - p. 2173-2190 , 2015
Link: https://doi.org/10.1093/..
 
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10

Rare Variants in NR2F2 Cause Congenital Heart Defects in Hu..:

Al Turki, Saeed ; Manickaraj, Ashok K. ; Mercer, Catherine L....
The American Journal of Human Genetics.  94 (2014)  4 - p. 574-585 , 2014
Link: https://doi.org/10.1016/..
 
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11

Using population data for assessing next-generation sequenc..:

Houniet, Darren T. ; Rahman, Thahira J. ; Al Turki, Saeed...
Bioinformatics.  31 (2014)  1 - p. 56-61 , 2014
Link: https://doi.org/10.1093/..
 
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12

High throughput exome coverage of clinically relevant cardi..:

Manase, Dorin ; D'Alessandro, Lisa CA ; Manickaraj, Ashok Kumar...
BMC Medical Genomics.  7 (2014)  1 - p. , 2014
Link: https://doi.org/10.1186/..
 
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13

Recessive HYDIN Mutations Cause Primary Ciliary Dyskinesia ..:

Olbrich, Heike ; Schmidts, Miriam ; Werner, Claudius...
The American Journal of Human Genetics.  91 (2012)  4 - p. 672-684 , 2012
Link: https://doi.org/10.1016/..
 
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14

Early Diagnosis of Werner's Syndrome Using Exome-Wide Seque..:

Semple, Robert K. ; Barroso, Inês ; O'Rahilly, Stephen...
Frontiers in Endocrinology.  2 (2011)  - p. , 2011
Link: https://doi.org/10.3389/..
 
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15

Using large sequencing data sets to refine intragenic disea..:

Amr, Sami S. ; Al Turki, Saeed H. ; Lebo, Matthew...
Genetics in Medicine.  19 (2017)  5 - p. 496-504 , 2017
Link: https://doi.org/10.1038/..
 
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