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Author Details

Yassmine Akkari
Association for Molecular Pathology
1999
46
22
PMIDPaper TitleJournal TitlePublished Year
36524989Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG).Genet Med2023
37378664Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG).Genet Med2023
36417763Optical genome mapping in acute myeloid leukemia: a multicenter evaluation.Blood Adv2023
35167654Guiding the global evolution of cytogenetic testing for hematologic malignancies.Blood2022
35802949A novel heptasomy 21 associated with complete loss of heterozygosity and loss of function RUNX1 mutation in acute myeloid leukemia.Cancer Genet2022
35771717Characterization of unusual iAMP21 B-lymphoblastic leukemia (iAMP21-ALL) from the Mayo Clinic and Children's Oncology Group.Genes Chromosomes Cancer2022
35506873Apparent coexistence of <i>ETV6::RUNX1</i> and <i>KMT2A::MLLT3</i> fusions due to a nonproductive <i>KMT2A</i> rearrangement in B-ALL.Leuk Lymphoma2022
36063163Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).Genet Med2022
35101336Standards for the classification of pathogenicity of somatic variants in cancer (oncogenicity): Joint recommendations of Clinical Genome Resource (ClinGen), Cancer Genomics Consortium (CGC), and Variant Interpretation for Cancer Consortium (VICC).Genet Med2022
34907337Correction to: Recommendations for future extensions to the HGNC gene fusion nomenclature.Leukemia2022
35304347Molecular Pathology Education: A Suggested Framework for Primary Care Resident Training in Genomic Medicine: A Report of the Association for Molecular Pathology Training and Education Committee.J Mol Diagn2022
32886736Conventional Cytogenetic Analysis of Hematologic Neoplasms: A 20-Year Review of Proficiency Test Results From the College of American Pathologists/American College of Medical Genetics and Genomics Cytogenetics Committee.Arch Pathol Lab Med2021
34764425Recommendations for future extensions to the HGNC gene fusion nomenclature.Leukemia2021
34429303Mechanisms of targeted therapy resistance in a pediatric glioma driven by <i>ETV6-NTRK3</i> fusion.Cold Spring Harb Mol Case Stud2021
34131312Chromosomal microarray analysis, including constitutional and neoplastic disease applications, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG).Genet Med2021
32302940Evidence-based review of genomic aberrations in B-lymphoblastic leukemia/lymphoma: Report from the cancer genomics consortium working group for lymphoblastic leukemia.Cancer Genet2020
30554721GGC Repeat Expansion and Exon 1 Methylation of XYLT1 Is a Common Pathogenic Variant in Baratela-Scott Syndrome.Am J Hum Genet2019
31160354Implementation of cancer next-generation sequencing testing in a community hospital.Cold Spring Harb Mol Case Stud2019
29754767Preconception Carrier Screening by Genome Sequencing: Results from the Clinical Laboratory.Am J Hum Genet2018
30455898A case for expanding carrier testing to include actionable X-linked disorders.Clin Case Rep2018
28726804Diagnostic cytogenetic testing following positive noninvasive prenatal screening results: a clinical laboratory practice resource of the American College of Medical Genetics and Genomics (ACMG).Genet Med2017
27181684Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium.Am J Hum Genet2016
27392081Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium.Am J Hum Genet2016
21626672Fanconi anemia-like presentation in an infant with constitutional deletion of 21q including the RUNX1 gene.Am J Med Genet A2011
19738377Topo IIIalpha and BLM act within the Fanconi anemia pathway in response to DNA-crosslinking agents.Cytogenet Genome Res2009
18180189Mammalian SNM1 is required for genome stability.Mol Genet Metab2008
18758156Loss of homologous recombination or non-homologous end-joining leads to radial formation following DNA interstrand crosslink damage.Cytogenet Genome Res2008
18672388ERCC1 is required for FANCD2 focus formation.Mol Genet Metab2008
16382135Fanconi anemia proteins are required to prevent accumulation of replication-associated DNA double-strand breaks.Mol Cell Biol2006
16855632Aberrant stabilization of c-Myc protein in some lymphoblastic leukemias.Leukemia2006
16919896CRELD2: gene mapping, alternate splicing, and comparative genomic identification of the promoter region.Gene2006
16982743Cytogenetic instability in ovarian epithelial cells from women at risk of ovarian cancer.Cancer Res2006
16397136Natural gene therapy in monozygotic twins with Fanconi anemia.Blood2006
16429406Novel inactivating mutations of FANCC in Brazilian patients with Fanconi anemia.Hum Mutat2006
16216560In vivo genetic selection of renal proximal tubules.Mol Ther2006
15665282Heterozygosity for p53 (Trp53+/-) accelerates epithelial tumor formation in fanconi anemia complementation group D2 (Fancd2) knockout mice.Cancer Res2005
16135554Fancd2 functions in a double strand break repair pathway that is distinct from non-homologous end joining.Hum Mol Genet2005
15849801Y chromosome heterochromatin of differing lengths in two cell populations of the same individual.Prenat Diagn2005
15084315Interstrand crosslink-induced radials form between non-homologous chromosomes, but are absent in sex chromosomes.DNA Repair (Amst)2004
15195088Myelomonocytic cells are sufficient for therapeutic cell fusion in liver.Nat Med2004
15345865Fanconi Anemia: A Decade of Discoveries.J Assoc Genet Technol2004
12665832Cell fusion is the principal source of bone-marrow-derived hepatocytes.Nature2003
12967657siRNA depletion of BRCA1, but not BRCA2, causes increased genome instability in Fanconi anemia cells.DNA Repair (Amst)2003
11749045The 4N cell cycle delay in Fanconi anemia reflects growth arrest in late S phase.Mol Genet Metab2001
11027296DNA replication is required To elicit cellular responses to psoralen-induced DNA interstrand cross-links.Mol Cell Biol2000
15216894Gamma-tubulin at ten: progress and prospects.Cell Struct Funct1999
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Mayo Clinic
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Co-authored papers 5
University of Washington Medical Center
Co-authored papers 4
Illumina Inc.
Co-authored papers 4
Baylor College of Medicine
Co-authored papers 4
Oregon Health & Science University (OHSU)
Co-authored papers 4
Iowa State University, Mayo Clinic, Nationwide Children's Hospital, The Ohio State University College of Medicine, University of Iowa, Washington University in Saint Louis
Co-authored papers 4
The University of Texas MD Anderson Cancer Center
Co-authored papers 4
Children's Hospital of Philadelphia
Co-authored papers 3
Dana-Farber Cancer Institute
Co-authored papers 3
Knight Cancer Institute, Oregon Health and Science University
Co-authored papers 3
University of Washington
Co-authored papers 3
University of Washington
Co-authored papers 3
German Cancer Research Center (DKFZ) and National Center for Tumor Diseases (NCT)
Co-authored papers 2
Institute for Health Metrics and Evaluation, University of Washington
Co-authored papers 2
Washington University
Co-authored papers 2
Harvard Medical School, Brigham and Women's Hospital
Co-authored papers 2
McDonnell Genome Institute, Washington University in St Louis School of Medicine
Co-authored papers 2
Genomic Medicine Institute, Cleveland Clinic Lerner Research Institute
Co-authored papers 2
Washington University
Co-authored papers 2
German Cancer Consortium and German Cancer Research Center
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Oregon Health and Science University
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University of Alabama at Birmingham
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Washington University School of Medicine
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Baylor College of Medicine
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Children's Hospital of Philadelphia, University of Pennsylvania
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University of California San Francisco
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Memorial Sloan Kettering Cancer Center
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Indiana University School of Medicine
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