Publications by authors named "Abdullah Tamim"

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Assessment of Aflatoxin B1 Contamination in Feed and Aflatoxin M1 in Camel Milk Under Different Feeding Systems.
Dughaim Al-Ahmari, Abdullah Al-Tamim, Abdulmohsen Al-Jardan, Mohammed Almutairi, Abdulhakeem Alzahrani

Foodborne Pathog Dis· November 2025

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ADAT3 variants disrupt the activity of the ADAT tRNA deaminase complex and impair neuronal migration.
Jordi Del-Pozo-Rodriguez, Peggy Tilly, Romain Lecat, Hugo Rolando Vaca, Laureline Mosser, Abdullah Tamim

Brain· September 2025

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The protective effect of Saudi Arabian bee honey against excessive weight gain and obesity-related parameters in rats fed a high-fat diet.
Abdullah Al Tamim, Ghedeir M Alshammari, Abu ElGasim A Yagoub, Ali Saleh, Mohammed A Mohammed

Front Nutr· September 2025

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Bi-allelic UGGT1 variants cause a congenital disorder of glycosylation.
Zain Dardas, Laura Harrold, Daniel G Calame, Claire G Salter, Takashi Kikuma, Abdullah Tamim

Am J Hum Genet· May 2025

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An assessment of the prevalence of Aflatoxin M1 level in milk and milk powder based on high performance liquid chromatography and dietary risk assessment.
Yaser Almasoud, Manar Alwelaie, Zeyad Aldosari, Sarah Alotaibi, Abdullah Alsayari, Abdullah Al Tamim

Toxicol Rep· December 2024

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Occurrence of total aflatoxins (B1, B2, G1, G2) in commercial peanut and peanut butter from the Saudi market in the period from 2015 to 2020.
Abdullah Al Tamim, Rawan Alharbi, Zeyad Aldosari, Yaser Almasoud, Abdullah A Al Sayari

Toxicol Rep· December 2024

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Neurodevelopmental disorders associated variants in disrupt the activity of the ADAT2/ADAT3 tRNA deaminase complex and impair neuronal migration.
Jordi Del-Pozo-Rodriguez, Peggy Tilly, Romain Lecat, Hugo Rolando Vaca, Laureline Mosser, Abdullah Tamim

medRxiv· November 2024

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Biallelic ZBTB11 Variants: A Neurodevelopmental Condition with Progressive Complex Movement Disorders.
Juan Darío Ortigoza-Escobar, Mina Zamani, Nathalie Dorison, Saeid Sadeghian, Reza Azizimalamiri, Abdullah Tamim

Mov Disord· September 2024

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Genotype-phenotype correlations in RHOBTB2-associated neurodevelopmental disorders.
Franziska Langhammer, Reza Maroofian, Rueda Badar, Anne Gregor, Michelle Rochman, Abdullah M Tamim

Genet Med· August 2023

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Efficacy and Safety of Perampanel in Children with Drug-Resistant Focal-Onset Seizures: A Retrospective Review.
Ahmed Elmardenly, Zekra Aljehani, Abdullah Tamim, Anas Alyazidi, Osama Muthaffar

Children (Basel)· June 2023

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In silico screening of some compounds derived from the desert medicinal plant Rhazya stricta for the potential treatment of COVID-19.
Nabih A Baeshen, Abdulaziz O Albeshri, Naseebh N Baeshen, Roba Attar, Alaa Karkashan, Abdullah Al Tamim

Sci Rep· July 2022

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The efficacy of non-fasting ketogenic diet protocol in the management of intractable epilepsy in pediatric patients: a single center study from Saudi Arabia.
Hayat Alameen Ali, Osama Muthaffar, Nahla AlKarim, Husam Kayyali, Ahmed Elmardenly, Abdullah Tamim

J Int Med Res· March 2022

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Biallelic Loss-of-Function Variants Cause a Wide Phenotypic Spectrum from Leigh/Leigh-Like Syndrome to Isolated Optic Atrophy.
Francesca Magrinelli, Elisa Cali, Vinícius Lopes Braga, Uluç Yis, Hoda Tomoum, Abdullah Tamim

Mov Disord Clin Pract· February 2022

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Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy.
Holger Hengel, Célia Bosso-Lefèvre, George Grady, Emmanuelle Szenker-Ravi, Hankun Li, Abdullah M Tamim

Nat Commun· January 2020

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Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.
Dorota Monies, Mohammed Abouelhoda, Mirna Assoum, Nabil Moghrabi, Rafiullah Rafiullah, Abdullah Tamim

Am J Hum Genet· October 2019

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Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population.
Dorota Monies, Mohammed Abouelhoda, Mirna Assoum, Nabil Moghrabi, Rafiullah Rafiullah, Abdullah Tamim

Am J Hum Genet· June 2019

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The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes.
Dorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed, Zuhair Alhassnan, Maha Alotaibi, Abdullah Tamim

Hum Genet· August 2017

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