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Yassmine M. N. Akkari · SciRah

Researcher profile · Semantic Scholar

Yassmine M. N. Akkari

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Yassmine M. N. Akkari — researcher profile on SciRah

h-index: 18
Works: 88
Citations: 5,635

Most-cited papers

The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Myeloid and Histiocytic/Dendritic Neoplasms
J. Khoury, É. Solary, O. Abla, Yassmine M. N. Akkari +58 more
2022Leukemia3,840 citations Open access
Semantic Scholar
Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium.
L. Amendola, G. Jarvik, M. Leo, H. Mclaughlin +28 more
2016American Journal of Human Genetics341 citations Open access
Semantic Scholar
Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium.
L. Amendola, G. Jarvik, M. Leo, H. Mclaughlin +28 more
2016American Journal of Human Genetics299 citations Open access
Semantic Scholar
Standards 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)
P. Horák, M. Griffith, Arpad M. Danos, B. Pitel +43 more
2022Genetics in Medicine232 citations Open access
Semantic Scholar
Noninvasive 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).
J. Dungan, S. Klugman, S. Darilek, Jennifer R. Malinowski +4 more
2022Genetics in Medicine197 citations Open access
Semantic Scholar
Optical genome mapping in acute myeloid leukemia: a multicenter evaluation
B. Levy, L. Baughn, Yassmine M. N. Akkari, S. Chartrand +14 more
2022Blood Advances106 citations Open access
Semantic Scholar
GGC Repeat Expansion and Exon 1 Methylation of XYLT1 Is a Common Pathogenic Variant in Baratela-Scott Syndrome.
Amy Lacroix, D. Stabley, Rebecca Sahraoui, M. Adam +19 more
2019American Journal of Human Genetics96 citations Open access
Semantic Scholar
Guiding the global evolution of cytogenetic testing for hematologic malignancies
Yassmine M. N. Akkari, L. Baughn, A. Dubuc, Adam C. Smith +14 more
2022Blood79 citations Open access
Semantic Scholar
Erratum: Performance of ACMG-AMP Variant-Interpretation Guidelines among Nine Laboratories in the Clinical Sequencing Exploratory Research Consortium (American Journal of Human Genetics (2016) 98(6) (1067–1076) (S0002929716300593) (10.1016/j.ajhg.2016.03.024))
L. Amendola, G. Jarvik, M. Leo, H. Mclaughlin +28 more
201674 citations Open access
Semantic Scholar
Diagnostic cytogenetic testing following positive noninvasive prenatal screening results: a clinical laboratory practice resource of the American College of Medical Genetics and Genomics (ACMG)
A. Cherry, Yassmine M. N. Akkari, Kimberly M Barr, H. Kearney +4 more
2017Genetics in Medicine49 citations Open access
Semantic Scholar
Chromosomal microarray analysis, including constitutional and neoplastic disease applications, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG)
Li-Na Shao, Yassmine M. N. Akkari, L. Cooley, David T. Miller +3 more
2021Genetics in Medicine48 citations Open access
Semantic Scholar
Preconception Carrier Screening by Genome Sequencing: Results from the Clinical Laboratory.
S. Punj, Yassmine M. N. Akkari, Jennifer Huang, Fei Yang +18 more
2018American Journal of Human Genetics47 citations Open access
Semantic Scholar
Noninvasive 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).
J. Dungan, S. Klugman, S. Darilek, Jennifer R. Malinowski +4 more
2023Genetics in Medicine41 citations
Semantic Scholar
Standards 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).
P. Horák, M. Griffith, Arpad M. Danos, B. Pitel +43 more
2022Genetics in Medicine23 citations Open access
Semantic Scholar
Evidence-based review of genomic aberrations in B-lymphoblastic leukemia/lymphoma: Report from the cancer genomics consortium working group for lymphoblastic leukemia.
Yassmine M. N. Akkari, H. Bruyèrè, R. T. Hagelstrom, R. Kanagal-Shamanna +11 more
2020Cancer Genetics22 citations
Semantic Scholar
Implementation of cancer next-generation sequencing testing in a community hospital
Yassmine M. N. Akkari, Tamara D. Smith, Jennifer Westfall, Stacie L. Lupo
2019Cold Spring Harbor molecular case studies22 citations Open access
Semantic Scholar
Characterization of Unusual iAMP21 B-lymphoblastic leukemia (iAMP21-ALL) from the Mayo Clinic and Children’s Oncology Group
Alaa Koleilat, J. Smadbeck, Cinthya Zepeda, C. Williamson +12 more
2022Genes, Chromosomes and Cancer20 citations Open access
Semantic Scholar
Post-zygotic rescue of meiotic errors causes brain mosaicism and focal epilepsy
Katherine E. Miller, Adithe Rivaldi, Noriyuki Shinagawa, Sahibjot Sran +30 more
2023Nature Genetics19 citations Open access
Semantic Scholar
Exploring current challenges in the technologist workforce of clinical genomics laboratories
Yassmine M. N. Akkari, S. Dobin, R. Best, Marco L. Leung
2023Genetics in medicine open14 citations Open access
Semantic Scholar
Section E6.1-6.6 of the American College of Medical Genetics and Genomics (ACMG) Technical Laboratory Standards: Cytogenomic studies of acquired chromosomal abnormalities in neoplastic blood, bone marrow, and lymph nodes.
Yassmine M. N. Akkari, L. Baughn, Annette S Kim, Ender Karaca +3 more
2024Genetics in Medicine13 citations Open access
Semantic Scholar
Clinical Cytogenetics: Current Practices and Beyond.
Mariam T. Mathew, Melanie Babcock, Y. Hou, Jesse M Hunter +4 more
2024The Journal of Applied Laboratory Medicine13 citations
Semantic Scholar
Molecular 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.
M. Arcila, Anthony N. Snow, Yassmine M. N. Akkari, D. Chabot-Richards +2 more
2022Journal of Molecular Diagnostics11 citations Open access
Semantic Scholar
Mechanisms of targeted therapy resistance in a pediatric glioma driven by ETV6-NTRK3 fusion
Clare Keddy, Tanaya L. Neff, J. Huan, J. Nickerson +11 more
2021Cold Spring Harbor molecular case studies11 citations Open access
Semantic Scholar
Apparent coexistence of ETV6::RUNX1 and KMT2A::MLLT3 fusions due to a nonproductive KMT2A rearrangement in B-ALL
M. Gagnon, J. Smadbeck, Neeraj Sharma, P. Blackburn +13 more
2022Leukemia and Lymphoma8 citations Open access
Semantic Scholar
Balanced chromosomal rearrangements offer insights into coding and noncoding genomic features associated with developmental disorders
Chelsea Lowther, M. Mehrjouy, Ryan L. Collins, M. Bak +151 more
2022medRxiv8 citations Open access
Semantic Scholar
Points to consider for the reporting of variants of uncertain significance in germline genetic and genomic testing: A statement of the American College of Medical Genetics and Genomics (ACMG).
Chloe E. Mighton, A. Abu-El-Haija, Vimla Aggarwal, Yassmine M. N. Akkari +12 more
2026Genetics in Medicine7 citations Open access
Semantic Scholar
Clinically significant findings in a decade‐long retrospective study of prenatal chromosomal microarray testing
Joy O. Olayiwola, Mohammad Marhabaie, D. Koboldt, T. Matthews +15 more
2024Molecular Genetics & Genomic Medicine5 citations Open access
Semantic Scholar
Conventional 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.
Daniel P. Larson, Yassmine M. N. Akkari, D. Van Dyke, G. Raca +13 more
2020Archives of Pathology & Laboratory Medicine5 citations Open access
Semantic Scholar
Points to consider for the next-generation-sequencing-based detection of copy-number abnormalities (CNAs) and balanced chromosomal rearrangements in neoplastic disorders: A statement of the American College of Medical Genetics and Genomics (ACMG).
K. Schieffer, C. Hawkins, Nan Jiang, Ross L. Levine +5 more
2026Genetics in Medicine4 citations
Semantic Scholar
Section E6.7-6.12 of the American College of Medical Genetics and Genomics (ACMG) Technical Laboratory Standards: Cytogenomic studies of acquired chromosomal abnormalities in solid tumors.
A. Church, Yassmine M. N. Akkari, K. Deeb, R. Kolhe +4 more
2024Genetics in Medicine4 citations Open access
Semantic Scholar
International Society for Prenatal Diagnosis 2024 Debate 3—Cytogenetics Is a Dinosaur and Should Be Replaced by Molecular Technologies
Yassmine M. N. Akkari, M. Talkowski, Amy M Breman
2025Prenatal Diagnosis3 citations Open access
Semantic Scholar
Genomic Reporting Practices Across 5 Molecular Disciplines: A Study From the College of American Pathologists.
Larissa V. Furtado, Annette S Kim, A. Moyer, J. Moncur +8 more
2024Archives of Pathology & Laboratory Medicine2 citations Open access
Semantic Scholar
Recommendations for future extensions to the HGNC gene fusion nomenclature
A. Wagner, Yassmine M. N. Akkari, Marilyn M. Li, A. Roy +2 more
2021Leukemia2 citations Open access
Semantic Scholar
Chromosome instability syndromes
Yassmine M. N. Akkari
20172 citations
Semantic Scholar
O09: Prevalence of germline variants in cancer predisposition genes in patients with pediatric solid tumors using paired tumor-normal exome sequencing
Ying-Chen Claire Hou, K. Parbhoo, Benjamin Kelly, Grant E. Lammi +17 more
2025Genetics in Medicine Open1 citations Open access
Semantic Scholar
Optical Genome Mapping in Prenatal Diagnosis: Democratizing Comprehensive Cytogenomic Testing.
Mariam T. Mathew, Yassmine M. N. Akkari
2024Clinical Chemistry1 citations
Semantic Scholar
A LINE-1 mediated deletion resulting in germline retinoblastoma predisposition
Erica L Macke, Anthony R. Miller, Eileen Stonerock, Randal S. Olshefski +6 more
2023Neuro-Oncology Advances1 citations Open access
Semantic Scholar
19. Evidence-based review of genomic aberrations in T-ALL: Strategy and progress of CGC T-ALL Working Group
Yassmine M. N. Akkari, Linda Baugn, H. Bruyèrè, Tanner Hagelstrom +5 more
2018Cancer Genetics1 citations
Semantic Scholar
Practice Guidelines for Genetic/Genomic Testing in Pediatric B-Lineage Acute Lymphoblastic Leukemia (B-ALL): A Cancer Genomics Consortium (CGC) Workgroup
Yassmine M. N. Akkari, L. Baughn, R. T. Hagelstrom, M. Hiemenz +3 more
20171 citations
Semantic Scholar
O13: Prevalence of cancer predisposition variants in a pediatric pineoblastoma cohort
Fang Fang, K. Parbhoo, V. Jayaraman, D. Corsmeier +18 more
2026Genetics in Medicine Open0 citations Open access
Semantic Scholar
EWSR1 Fusion Driven Pediatric B-Acute Lymphoblastic Leukemia: Diagnosis and Review of Literature
Molly S. Talman, Ashwani K Yenamandra, Yassmine M. N. Akkari, Karen D Tsuchiya +3 more
2026Pediatric and Developmental Pathology0 citations Open access
Semantic Scholar
Abstract 1508: A large-scale resource of standardized pediatric somatic cancer variant classifications
Alex H. Wagner, K. Kuzma, K. Schieffer, W. Goar +23 more
2026Cancer Research0 citations
Semantic Scholar
The 2023 clinical laboratory genetics workforce in the United States: trends, challenges, and evolving practices
Cinthya Zepeda-Mendoza, Rhonda West, Yassmine M. N. Akkari, Erica F. Andersen +5 more
2026Human Genetics0 citations
Semantic Scholar
27. Development of standards for the assessment of gene fusion oncogenicity
Karen Tsuchiya, W. Goar, Yassmine M. N. Akkari, Julia A Bridge +10 more
2025Cancer Genetics0 citations
Semantic Scholar
30. Enhancing data standardization and structure to improve clinical variant classification
W. Goar, K. Kuzma, Michael McCarrick, Kathryn Stahl +21 more
2025Cancer Genetics0 citations
Semantic Scholar
ETMR-03. Unique Case of Pontine CNS tumor with BCOR internal tandem duplication (ITD) in an Infant
Cierra M Brandt, Diana L. Thomas, Yassmine M. N. Akkari, Karen D Tsuchiya +9 more
2025Neuro-Oncology Pediatrics0 citations Open access
Semantic Scholar
80. Integrating expert knowledge for somatic variant interpretation: Achievements and future directions of ClinGen somatic
J. Saliba, Arpad M. Danos, K. Krysiak, Adam C. Coffman +24 more
2025Cancer Genetics0 citations Open access
Semantic Scholar
7. Application of expert panel-derived oncogenicity guidelines in BCR::ABL1-like B-lymphoblastic leukemia/lymphoma
Mark G. Evans, K. Krysiak, J. Saliba, C. Kesserwan +35 more
2025Cancer Genetics0 citations
Semantic Scholar
8. Systematic curation of defining and supportive diagnostic variants to enhance genomic diagnostics in pediatric oncology
Morteza Seifi, Laura B. Corson, Dianne E. Sylvester, J. Saliba +14 more
2025Cancer Genetics0 citations
Semantic Scholar
22: A case of partial trisomy 13 not detected on prenatal cfDNA screen
Laura Bryant, Mari Mori, Bimal P. Chaudhari, Michael Zinmeister +16 more
2025Genetics in Medicine Open0 citations Open access
Semantic Scholar

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