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Al Tala, Saeed
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1

Beyond the exome: utility of long-read whole genome sequenc..:

AlAbdi, Lama ; Shamseldin, Hanan E. ; Khouj, Ebtissal...
Genome Medicine.  15 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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2

Mutations of the histone linker H1–4 in neurodevelopmental ..:

Tremblay, Martine W ; Green, Matthew V ; Goldstein, Benjamin M...
Human Molecular Genetics.  31 (2021)  9 - p. 1430-1442 , 2021
Link: https://doi.org/10.1093/..
 
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3

The landscape of early infantile epileptic encephalopathy i..:

Nashabat, Marwan ; Al Qahtani, Xena S. ; Almakdob, Salwa...
Seizure.  69 (2019)  - p. 154-172 , 2019
Link: https://doi.org/10.1016/..
 
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4

Genomic and phenotypic delineation of congenital microcepha..:

Shaheen, Ranad ; Maddirevula, Sateesh ; Ewida, Nour...
Genetics in Medicine.  21 (2019)  3 - p. 545-552 , 2019
Link: https://doi.org/10.1038/..
 
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5

The many faces of peroxisomal disorders: Lessons from a lar..:

Alshenaifi, Jumanah ; Ewida, Nour ; Anazi, Shams...
Clinical Genetics.  95 (2018)  2 - p. 310-319 , 2018
Link: https://doi.org/10.1111/..
 
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6

Further Delineation of the Clinical Phenotype of Cerebellar..:

Alsahli, Saud ; Alrifai, Muhammad Talal ; Al Tala, Saeed..
Journal of Central Nervous System Disease.  10 (2018)  - p. 117957351875968 , 2018
Link: https://doi.org/10.1177/..
 
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7

Correction to: Expanding the genetic heterogeneity of intel..:

Anazi, Shams ; Maddirevula, Sateesh ; Salpietro, Vincenzo...
Human Genetics.  137 (2017)  1 - p. 105-109 , 2017
Link: https://doi.org/10.1007/..
 
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8

Expanding the genetic heterogeneity of intellectual disabil..:

Anazi, Shams ; Maddirevula, Sateesh ; Salpietro, Vincenzo...
Human Genetics.  136 (2017)  11-12 - p. 1419-1429 , 2017
Link: https://doi.org/10.1007/..
 
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9

Joint laxity in homozygotes for severe POU1F1 mutations:

Shamseldin, Hanan E. ; Maddirevula, Sateesh ; Nabil, Amira...
American Journal of Medical Genetics Part A.  170 (2016)  12 - p. 3356-3358 , 2016
Link: https://doi.org/10.1002/..
 
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10

Characterizing the morbid genome of ciliopathies:

Ciliopathy WorkingGroup ; Shaheen, Ranad ; Szymanska, Katarzyna...
Genome Biology.  17 (2016)  1 - p. , 2016
Link: https://doi.org/10.1186/..
 
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11

Accelerating Novel Candidate Gene Discovery in Neurogenetic..:

Alazami, Anas M. ; Patel, Nisha ; Shamseldin, Hanan E....
Cell Reports.  10 (2015)  2 - p. 148-161 , 2015
Link: https://doi.org/10.1016/..
 
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12

A child with dilated cardiomyopathy and homozygous splice s..:

Alsubhi, Afaf ; Aldarwish, Manar ; Agrawal, Pankaj B....
Molecular Genetics and Metabolism Reports.  38 (2024)  - p. 101027 , 2024
Link: https://doi.org/10.1016/..
 
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13

Biallelic pathogenic variants inCOX11are associated with an..:

Rius, Rocio ; Bennett, Neal K. ; Bhattacharya, Kaustuv...
Human Mutation.  43 (2022)  12 - p. 1970-1978 , 2022
Link: https://doi.org/10.1002/..
 
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14

Autozygome and high throughput confirmation of disease gene..:

Maddirevula, Sateesh ; Alzahrani, Fatema ; Al-Owain, Mohammed...
Genetics in Medicine.  21 (2019)  3 - p. 736-742 , 2019
Link: https://doi.org/10.1038/..
 
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15

Experimental and modeling study of the surface tension and ..:

Khosharay, Shahin ; Talebi, Mehrnoosh ; Saeed, Tala Akbari.
Journal of Molecular Liquids.  249 (2018)  - p. 245-253 , 2018
Link: https://doi.org/10.1016/..
 
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