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Author Details

Malak Abedalthagafi
Emory School of Medicine
2008
97
27
PMIDPaper TitleJournal TitlePublished Year
37306523Investigating the prevalence of pathogenic variants in Saudi Arabian patients with familial cancer using a multigene next generation sequencing panel.Oncotarget2023
37942402Ameloblastic Fibrosarcoma of the Jaw: Case Report, Genetic Profiling, and Literature Review.Case Rep Oncol2023
37609176Analytical code sharing practices in biomedical research.bioRxiv2023
37932837Fabrication of a three-dimensional bone marrow niche-like acute myeloid Leukemia disease model by an automated and controlled process using a robotic multicellular bioprinting system.Biomater Res2023
37761360The Genomic Landscape of Colorectal Cancer in the Saudi Arabian Population Using a Comprehensive Genomic Panel.Diagnostics (Basel)2023
37291798Rigorous benchmarking of T-cell receptor repertoire profiling methods for cancer RNA sequencing.Brief Bioinform2023
34508644A molecularly integrated grade for meningioma.Neuro Oncol2022
35699213Periocular Pigmented Basal Cell Carcinomas: Clinicopathologic Features and Mutational Profile.Ophthalmic Plast Reconstr Surg2022
35396471Unlocking capacities of genomics for the COVID-19 response and future pandemics.Nat Methods2022
36507516Clinicopathologic and genomic characterizations of brain metastases using a comprehensive genomic panel.Front Med (Lausanne)2022
36327219Exome-wide association study to identify rare variants influencing COVID-19 outcomes: Results from the Host Genetics Initiative.PLoS Genet2022
36263431Editorial: Women in science: Genetics.Front Genet2022
36290872Papillary Tumor of the Pineal Region Rare Pediatric CNS Tumor Case Series Treated in King Fahad Medical City (KFMC).Curr Oncol2022
36221028Commentary: Von Hippel-Lindau disease: A clinical and scientific review.Eur J Hum Genet2022
34978705Correlation between ABO Blood Group Phenotype and the Risk of COVID-19 Infection and Severity of Disease in a Saudi Arabian Cohort.J Epidemiol Glob Health2022
35064222Index case identification and outcomes of cascade testing in high-risk breast and colorectal cancer predisposition genes.Eur J Hum Genet2022
34931541Expression of Programmed Cell Death-L1 (PD-L1) Protein and Mismatch Repair Mutations in Orbital Tumours-a Pilot Study.Eur J Ophthalmol2022
34929414Association of KIR gene polymorphisms with COVID-19 disease.Clin Immunol2022
34764042The Saudi Critical Care Society practice guidelines on the management of COVID-19 in the ICU: Therapy section.J Infect Public Health2022
33216206Primary mismatch repair deficient IDH-mutant astrocytoma (PMMRDIA) is a distinct type with a poor prognosis.Acta Neuropathol2021
33492612Immune profiling of pituitary tumors reveals variations in immune infiltration and checkpoint molecule expression.Pituitary2021
33868589Landscape of somatic mutations in breast cancer: new opportunities for targeted therapies in Saudi Arabian patients.Oncotarget2021
33931704Epigenomics and immunotherapeutic advances in pediatric brain tumors.NPJ Precis Oncol2021
33858487Improving the completeness of public metadata accompanying omics studies.Genome Biol2021
34899845The History and Challenges of Women in Genetics: A Focus on Non-Western Women.Front Genet2021
34673814The clinico-pathologic profile of primary and recurrent orbital/periorbital plexiform neurofibromas (OPPN).PLoS One2021
34805593Fabrication of a Lateral Flow Assay for Rapid In-Field Detection of COVID-19 Antibodies Using Additive Manufacturing Printing Technologies.Int J Bioprint2021
34043590Rare loss-of-function variants in type I IFN immunity genes are not associated with severe COVID-19.J Clin Invest2021
34002093Diversity in immunogenomics: the value and the challenge.Nat Methods2021
33948451Unlocking capacities of viral genomics for the COVID-19 pandemic response.ArXiv2021
34367989Editorial: Genomics and Epigenomics of Cancer Immunotherapy: Challenges and Clinical Implications.Front Oncol2021
32265819Methylation Profiling of Medulloblastoma in a Clinical Setting Permits Sub-classification and Reveals New Outcome Predictions.Front Neurol2020
33492804Immunophenotype of Vestibular Schwannomas.Otol Neurotol2020
31970090Recent Advances in Meningioma Immunogenetics.Front Oncol2020
31995621Clinical management and genomic profiling of pediatric low-grade gliomas in Saudi Arabia.PLoS One2020
31669704Telomerase reverse transcriptase promoter mutations in cancers derived from multiple organ sites among middle eastern population.Genomics2020
32025336Familial/inherited cancer syndrome: a focus on the highly consanguineous Arab population.NPJ Genom Med2020
33192972Genomic Profiling of Circulating Tumor DNA From Cerebrospinal Fluid to Guide Clinical Decision Making for Patients With Primary and Metastatic Brain Tumors.Front Neurol2020
33398295Failure to replicate the association of rare loss-of-function variants in type I IFN immunity genes with severe COVID-19.medRxiv2020
32822689iSCAN: An RT-LAMP-coupled CRISPR-Cas12 module for rapid, sensitive detection of SARS-CoV-2.Virus Res2020
32923892Regression of <i>ETV6-NTRK3</i> Infantile Glioblastoma After First-Line Treatment With Larotrectinib.JCO Precis Oncol2020
32472748Position paper: Challenges and specific strategies for constitutional mismatch repair deficiency syndrome in low-resource settings.Pediatr Blood Cancer2020
32461667Cell-based analysis of CAD variants identifies individuals likely to benefit from uridine therapy.Genet Med2020
30844719Precision medicine of monogenic disorders: Lessons learned from the Saudi human genome.Front Biosci (Landmark Ed)2019
31565188New insights into the genomic landscape of meningiomas identified FGFR3 in a subset of patients with favorable prognoses.Oncotarget2019
29343221A case of molecularly profiled extraneural medulloblastoma metastases in a child.BMC Med Genet2018
32094946As a Saudi woman scientist, I'm tired of negative stereotypes.Nature2018
30082692A Jordanian biologist redefines success for women in science.Nature2018
30104292Durable Response to Nivolumab in a Pediatric Patient with Refractory Glioblastoma and Constitutional Biallelic Mismatch Repair Deficiency.Oncologist2018
29852761Craniopharyngioma: a roadmap for scientific translation.Neurosurg Focus2018
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Collaborators

Ian F Dunn
Co-authored papers 25
Sandro Santagata
Co-authored papers 23
Wenya Linda Bi
Co-authored papers 23
Rameen Beroukhim
Co-authored papers 16
Shakti H Ramkissoon
Co-authored papers 13
Keith L Ligon
Co-authored papers 12
Azra H Ligon
Co-authored papers 10
Patrick Y Wen
Co-authored papers 9
Serghei Mangul
School of Pharmacy, University of Southern California
Co-authored papers 9
Amal Almutairi
King Fahad Medical City and King Abdulaziz City for Science and Technology
Co-authored papers 8
Priscilla K Brastianos
Co-authored papers 7
Paul Van Hummelen
Co-authored papers 6
Aaron R Thorner
Co-authored papers 6
Salam Massadeh
National Centre for Genomic Technologies
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Saleh A Alqahtani
King Faisal Specialist Hospital & Research Centre
Co-authored papers 5
Gavin P Dunn
Washington University School of Medicine
Co-authored papers 5
Yaseen M Arabi
King Saud bin Abdulaziz Medical City for Science and Technology
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Manal Alaamery
National Centre for Genomic Technologies
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Lori A Ramkissoon
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David N Louis
Co-authored papers 4
Matthew Ducar
Co-authored papers 4
William J Gibson
Co-authored papers 4
Steven E Schumacher
Co-authored papers 4
Peleg M Horowitz
Co-authored papers 4
Mathieu Bourgey
McGill University
Co-authored papers 3
Guillaume Bourque
Institute for the Advanced Study of Human Biology (ASHBi), Kyoto University
Co-authored papers 3
Scott L Carter
Co-authored papers 3
Vincent Mooser
McGill University
Co-authored papers 3
David B Goldstein
Institute for Genomic Medicine, Columbia University Irving Medical Center
Co-authored papers 3
Gundula Povysil
Institute for Genomic Medicine, Columbia University Medical Center
Co-authored papers 3
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