Publications by authors named "Manar Samman"

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Revisiting the molecular landscape of Rosai-Dorfman disease: insights from whole exome sequencing of Saudi patients.
Sarah Binhassan, Manar Samman, Yazeed Al-Sheikh, Wafaa Alshakweer, Tahani Alhalouli

Front Oncol· May 2025

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A rare presentation of BCR-ABL1 and RUNX1-MECOM rearrangement in a pediatric patient with acute myeloid leukemia.
Ragdah M Alamri, Maryam Alanazi, Rajeh K AlRajeh, Suha A Tashkandi, Azizah F Alswayyed, Manar A Samman

Clin Case Rep· May 2024

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Reclassifying variations of unknown significance in diseases affecting Saudi Arabia's population reveal new associations.
Mariam M Al Eissa, Raniah S Alotibi, Bader Alhaddad, Taghrid Aloraini, Manar S Samman

Front Genet· November 2023

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Fatal intracranial haemorrhage in acute promyelocytic leukemia patients with short isoform of PML-RARα: Review of molecular and radiological data.
Manal Abudawood, Hanan Alorini, Manar A Samman, Salman M Bashir, Azizah AlSwayed

Saudi J Biol Sci· July 2023

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Favorable outcome of short isoform and mutation in a patient with several adverse prognostic markers: A case report.
Mohammed A Bafail, Rahaf AlTahan, Manar A Samman, Suha A Tashkandi, Ibraheem H Motabi

Clin Case Rep· July 2023

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Clinical characterization and further confirmation of the autosomal recessive SLC12A2 disease.
Monis Bilal Shamsi, Mohamed Saleh, Makki Almuntashri, Essa Alharby, Manar Samman

J Hum Genet· July 2021

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Progressive Ataxia and Neurologic Regression in -Associated Bare Lymphocyte Syndrome.
Essa Alharby, Mona Obaid, Mohammed A O Elamin, Makki Almuntashri, Ismail Bakhsh, Manar Samman

Neurol Genet· June 2021

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New paradigms of USP53 disease: normal GGT cholestasis, BRIC, cholangiopathy, and responsiveness to rifampicin.
Hamoud Alhebbi, Abdul Ali Peer-Zada, Abdulrahman A Al-Hussaini, Sara Algubaisi, Awad Albassami, Manar A Samman

J Hum Genet· February 2021

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A GRM7 mutation associated with developmental delay reduces mGlu7 expression and produces neurological phenotypes.
Nicole M Fisher, Aqeela AlHashim, Aditi B Buch, Hana Badivuku, Manar M Samman

JCI Insight· February 2021

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Clinical, molecular, and biochemical delineation of asparagine synthetase deficiency in Saudi cohort.
Essa Alharby, Eissa A Faqeih, Mohammed Saleh, Seham Alameer, Makki Almuntashri, Manar A Samman

Genet Med· December 2020

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Further delineation of METTL23-associated intellectual disability.
Mohammed Almannai, Osama Obaid, Eissa Faqeih, Ali Alasmari, Manar M Samman

Am J Med Genet A· April 2020

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A null mutation in MICU2 causes abnormal mitochondrial calcium homeostasis and a severe neurodevelopmental disorder.
Hanan E Shamseldin, Ali Alasmari, Mohammed A Salih, Manar M Samman, Shahid A Mian

Brain· November 2017

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A novel genomic signature reclassifies an oral cancer subtype.
Manar Samman, Henry M Wood, Caroline Conway, Lucy Stead, Catherine Daly

Int J Cancer· November 2015

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Stratifying tumour subtypes based on copy number alteration profiles using next-generation sequence data.
Arief Gusnanto, Peter Tcherveniakov, Farag Shuweihdi, Manar Samman, Pamela Rabbitts

Bioinformatics· August 2015

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Next-generation sequencing analysis for detecting human papillomavirus in oral verrucous carcinoma.
Manar Samman, Henry Wood, Caroline Conway, Stefano Berri, Monica Pentenero

Oral Surg Oral Med Oral Pathol Oral Radiol· July 2014

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