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Shaheen, Ranad
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1

The morbid genome of ciliopathies: an update:

Shamseldin, Hanan E. ; Shaheen, Ranad ; Ewida, Nour...
Genetics in Medicine.  24 (2022)  4 - p. 966 , 2022
Link: https://doi.org/10.1016/..
 
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2

Hypomorphic GINS3 variants alter DNA replication and cause ..:

McQuaid, Mary E. ; Ahmed, Kashif ; Tran, Stephanie...
JCI Insight.  7 (2022)  10 - p. , 2022
Link: https://doi.org/10.1172/..
 
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3

Transcriptome of CD8+ tumor-infiltrating T cells: a link be..:

Saleh, Reem ; Sasidharan Nair, Varun ; Murshed, Khaled...
Cancer Immunology, Immunotherapy.  70 (2021)  9 - p. 2625-2638 , 2021
Link: https://doi.org/10.1007/..
 
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4

Correction to: Transcriptome of CD8+ tumor-infiltrating T c..:

Saleh, Reem ; Nair, Varun Sasidharan ; Murshed, Khaled...
Cancer Immunology, Immunotherapy.  70 (2021)  9 - p. 2639-2640 , 2021
Link: https://doi.org/10.1007/..
 
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5

Mutations in phospholipase C eta-1 (PLCH1) are associated w..:

Drissi, Ichrak ; Fletcher, Emily ; Shaheen, Ranad...
Journal of Medical Genetics.  59 (2021)  4 - p. 358-365 , 2021
Link: https://doi.org/10.1136/..
 
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6

Complement C5a and Clinical Markers as Predictors of COVID-..:

Cyprian, Farhan S. ; Suleman, Muhammad ; Abdelhafez, Ibrahim...
Frontiers in Immunology.  12 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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7

The morbid genome of ciliopathies: an update:

Shamseldin, Hanan E. ; Shaheen, Ranad ; Ewida, Nour...
Genetics in Medicine.  22 (2020)  6 - p. 1051-1060 , 2020
Link: https://doi.org/10.1038/..
 
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8

YIF1B mutations cause a post-natal neurodevelopmental syndr..:

Diaz, Jorge ; Gérard, Xavier ; Emerit, Michel-Boris...
Brain.  143 (2020)  10 - p. 2911-2928 , 2020
Link: https://doi.org/10.1093/..
 
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9

Biallelic Mutations in Tetratricopeptide Repeat Domain 26 (..:

Shaheen, Ranad ; Alsahli, Saud ; Ewida, Nour...
Hepatology.  71 (2020)  6 - p. 2067-2079 , 2020
Link: https://doi.org/10.1002/..
 
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10

PUS7 mutations impair pseudouridylation in humans and cause..:

Shaheen, Ranad ; Tasak, Monika ; Maddirevula, Sateesh...
Human Genetics.  138 (2019)  3 - p. 231-239 , 2019
Link: https://doi.org/10.1007/..
 
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11

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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12

Biallelic variants inCTU2cause DREAM‐PL syndrome and impair..:

Shaheen, Ranad ; Mark, Paul ; Prevost, Christopher T....
Human Mutation.  40 (2019)  11 - p. 2108-2120 , 2019
Link: https://doi.org/10.1002/..
 
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13

Biallelic novel missense HHAT variant causes syndromic micr..:

Abdel‐Salam, Ghada M. H. ; Mazen, Inas ; Eid, Maha...
American Journal of Medical Genetics Part A.  179 (2019)  6 - p. 1053-1057 , 2019
Link: https://doi.org/10.1002/..
 
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14

Correction: Corrigendum: Autozygosity reveals recessive mut..:

Monies, Dorota ; Maddirevula, Sateesh ; Kurdi, Wesam...
Genetics in Medicine.  20 (2018)  3 - p. 380 , 2018
Link: https://doi.org/10.1038/..
 
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15

GWAS signals revisited using human knockouts:

Maddirevula, Sateesh ; AlZahrani, Fatema ; Anazi, Shams...
Genetics in Medicine.  20 (2018)  1 - p. 64-68 , 2018
Link: https://doi.org/10.1038/..
 
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