Get started
Author

Faten Moassass

Observed names: F. Moassass, FATEN MOASSASS
ORCID: 0009-0000-8457-1780
Observed ORCID: 0009-0000-8457-1780
OpenAlex ID: A5071012592
Influence of CYP1A1, GST polymorphisms and susceptibility risk of chronic myeloid leukemia in Syrian population
2014 · Walid Al-Achkar, Ghassan Azeiz, et al. · Medical Oncology · 29
Association of Methylenetetrahydrofolate Reductase C677T and A1298C Gene Polymorphisms With Recurrent Pregnancy Loss in Syrian Women
2017 · Walid Al-Achkar, Abdulsamad Wafa, et al. · Reproductive Sciences · 28
Cytogenetic abnormalities and Y-chromosome microdeletions in infertile Syrian males
2012 · WALID AL-ACHKAR, ABDULSAMAD WAFA, et al. · Biomedical Reports · 22
PDF
Correlation of p210 BCR-ABL transcript variants with clinical, parameters and disease outcome in 45 chronic myeloid leukemia patients.
2016 · Walid Al-Achkar, Faten Moassass, et al. · PubMed · 20
Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl
2010 · Walid Al Achkar, Abdulsamad Wafa, et al. · Molecular Cytogenetics · 15
PDF
Acute promyelocytic leukemia with the translocation t(15;17)(q22;q21) associated with t(1;2)(q42~43;q11.2~12): a case report
2016 · Abdulsamad Wafa, Faten Moassass, et al. · Journal of Medical Case Reports · 13
PDF
A chronic myeloid leukemia case with a unique variant Philadelphia translocation: t(9;22;21)(q34;q11;p12)
2012 · WALID AL-ACHKAR, ABDULSAMAD WAFA, et al. · Oncology Letters · 12
PDF
Novel complex translocation involving 5 different chromosomes in a chronic myeloid leukemia with Philadelphia chromosome: a case report
2009 · Walid Al Achkar, Abdulsamad Wafa, et al. · Molecular Cytogenetics · 12
PDF
Detailed analysis of an idic(Y)(q11.21) in a mosaic karyotype
2012 · WALID AL-ACHKAR, ABDULSAMAD WAFA, et al. · Molecular Medicine Reports · 10
PDF
A rare case of chronic myeloid leukemia with secondary chromosomal changes including partial trisomy 17q21 to 17qter and partial monosomy of 16p13.3
2010 · Walid Al Achkar, Abdulsamad Wafa, et al. · Molecular Cytogenetics · 10
PDF
Investigation of the mtDNA mutations in Syrian families with non-syndromic sensorineural hearing loss
2018 · Faten Moassass, Bassel Al-Halabi, et al. · International Journal of Pediatric Otorhinolaryngology · 9
First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss
2016 · Walid AL-Achkar, Bassel AL-Halabi, et al. · International Journal of Pediatric Otorhinolaryngology · 9
A novel dic (17;18) (p13.1;q11.2) with loss of TP53 and BCR/ABL rearrangement in an Imatinib resistant chronic myeloid leukemia
2012 · Walid Al-achkar, Abdulsamad Wafa, et al. · Molecular Cytogenetics · 9
PDF
Evaluating the clinical significance of FLT3 mutation status in Syrian newly diagnosed acute myeloid leukemia patients with normal karyotype
2022 · Yahia Moualla, Faten Moassass, et al. · Heliyon · 8
Down syndrome associated childhood myeloid leukemia with yet unreported acquired chromosomal abnormalities and a new potential adverse marker: dup(1)(q25q44)
2018 · Faten Moassass, Abdulsamad Wafa, et al. · Molecular Cytogenetics · 8
PDF
A high complex karyotype involving eleven chromosomes including three novel chromosomal aberrations and monoallelic loss of TP53 in case of follicular lymphoma transformed into B-cell lymphoblastic leukemia
2016 · Abdulsamad Wafa, Faten Moassass, et al. · Molecular Cytogenetics · 8
PDF
Hyperdiploidy associated with T315I mutation in BCR-ABL kinase domain in an accelerated phase-chronic myeloid leukemia case
2014 · Walid Al-Achkar, Faten Moassass, et al. · Molecular Cytogenetics · 7
PDF
Multiple copies of BCR-ABL fusion gene on two isodicentric Philadelphia chromosomes in an imatinib mesylate-resistant chronic myeloid leukemia patient
2013 · WALID AL-ACHKAR, ABDULSAMAD WAFA, et al. · Oncology Letters · 7
PDF
Frequency of FLT3 Internal Tandem Duplications in Adult Syrian Patients with Acute Myeloid Leukemia and Normal Karyotype
2021 · Ismael Al-Arbeed, Abdulsamad Wafa, et al. · Asian Pacific Journal of Cancer Prevention · 6
PDF
De novo adult acute myeloid leukemia with two new mutations in juxtatransmembrane domain of the FLT3 gene: a case report
2021 · Ismael F. Alarbeed, Abdulsamad Wafa, et al. · Journal of Medical Case Reports · 6
PDF
Prognostic Relevance of DNMT3A, FLT3 and NPM1 Mutations in Syrian Acute Myeloid Leukemia Patients
2022 · Yahia Moualla, Faten Moassass, et al. · Asian Pacific Journal of Cancer Prevention · 5
PDF
Glutathione S-transferase T1, M1 and P1 gene polymorphisms and susceptibility to colorectal cancer, a Syrian population study
2019 · Walid Al-Achkar, Faten Moassass, et al. · Gene Reports · 5
Effect of Glutathione S-transferase mu 1 ( GSTM1 ) gene polymorphism on chronic myeloid leukemia risk and Imatinib treatment response
2017 · Walid Al-Achkar, Faten Moassass, et al. · Meta Gene · 5
An adult B-cell precursor acute lymphoblastic leukemia with multiple secondary cytogenetic aberrations
2014 · Walid AL-Achkar, Abdulsamad Wafa, et al. · Molecular Cytogenetics · 4
PDF
Two Novel Mutations of the NPM1 Gene in Syrian Adult Patients with Acute Myeloid Leukemia and Normal Karyotype
2021 · Ismael Alarbeed, Abdulsamad Wafa, et al. · Asian Pacific Journal of Cancer Prevention · 3
PDF
Works count: 37
Citation count: 279
H-index: 10
I10-index: 10
Year
Topic
Type