Works matching AU Akkari, Yassmine

Results: 20
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    Optical Genome Mapping (OGM) Identifies Multiple Structural Variants in a Case With Atypical Phelan‐McDermid Syndrome.

    Published in:
    American Journal of Medical Genetics. Part A, 2025, v. 197, n. 3, p. 1, doi. 10.1002/ajmg.a.63929
    By:
    • Macke, Erica L.;
    • Miller, Anthony R.;
    • Colwell, Caitlyn M.;
    • Gonzalez, Maria Hernandez;
    • Hunter, Jesse;
    • Venkata, Lakshmi Prakruthi Rao;
    • Walker, Lauren;
    • Wheeler, Gregory;
    • Wilson, Richard K.;
    • Mardis, Elaine R.;
    • Miller, Katherine E.;
    • Mathew, Mariam T.;
    • Chaudhari, Bimal P.;
    • Akkari, Yassmine
    Publication type:
    Article
    3

    Integration of Optical Genome Mapping in the Cytogenomic and Molecular Work‐Up of Hematological Malignancies: Expert Recommendations From the International Consortium for Optical Genome Mapping.

    Published in:
    American Journal of Hematology, 2025, v. 100, n. 6, p. 1029, doi. 10.1002/ajh.27688
    By:
    • Kanagal‐Shamanna, Rashmi;
    • Puiggros, Anna;
    • Granada, Isabel;
    • Raca, Gordana;
    • Rack, Katrina;
    • Mallo, Mar;
    • Dewaele, Barbara;
    • Smith, Adam C.;
    • Akkari, Yassmine;
    • Levy, Brynn;
    • Hasserjian, Robert P.;
    • Cisneros, Adela;
    • Salido, Marta;
    • Garcia‐Manero, Guillermo;
    • Yang, Hui;
    • Iqbal, M. Anwar;
    • Kolhe, Ravindra;
    • Solé, Francesc;
    • Espinet, Blanca
    Publication type:
    Article
    4

    Clinical Cytogenetics: Current Practices and Beyond.

    Published in:
    Journal of Applied Laboratory Medicine, 2024, v. 9, n. 1, p. 61, doi. 10.1093/jalm/jfad086
    By:
    • Mathew, Mariam T;
    • Babcock, Melanie;
    • Hou, Ying-Chen Claire;
    • Hunter, Jesse M;
    • Leung, Marco L;
    • Mei, Hui;
    • Schieffer, Kathleen;
    • Akkari, Yassmine
    Publication type:
    Article
    5

    Apparent coexistence of ETV6::RUNX1 and KMT2A::MLLT3 fusions due to a nonproductive KMT2A rearrangement in B-ALL.

    Published in:
    Leukemia & Lymphoma, 2022, v. 63, n. 9, p. 2243, doi. 10.1080/10428194.2022.2064991
    By:
    • Gagnon, Marie-France;
    • Smadbeck, James B.;
    • Sharma, Neeraj;
    • Blackburn, Patrick R.;
    • Demasi Benevides, Jonna;
    • Akkari, Yassmine M. N.;
    • Jaroscak, Jennifer J.;
    • Znoyko, Iya;
    • Wolff, Daynna J.;
    • Schandl, Cynthia A.;
    • Meyer, Reid;
    • Greipp, Patricia T.;
    • Xu, Xinjie;
    • Hoppman, Nicole L.;
    • Ketterling, Rhett P.;
    • Peterson, Jess F.;
    • Baughn, Linda B.
    Publication type:
    Article
    6

    Mechanisms of targeted therapy resistance in a pediatric glioma driven by ETV6-NTRK3 fusion.

    Published in:
    Cold Spring Harbor Molecular Case Studies, 2021, v. 7, n. 5, p. 1, doi. 10.1101/mcs.a006109
    By:
    • Keddy, Clare;
    • Neff, Tanaya;
    • Huan, Jianya;
    • Nickerson, Joshua P.;
    • Beach, Catherine Z.;
    • Akkari, Yassmine;
    • Jianling Ji;
    • Moore, Stephen;
    • Nazemi, Kellie J.;
    • Corless, Christopher L.;
    • Beadling, Carol;
    • Woltjer, Randy;
    • Yoon-Jae Cho;
    • Wood, Matthew D.;
    • Davare, Monika A.
    Publication type:
    Article
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    In Vivo Genetic Selection of Renal Proximal Tubules.

    Published in:
    Molecular Therapy, 2006, v. 13, n. 1, p. 49, doi. 10.1016/j.ymthe.2005.09.004
    By:
    • Held, Patrice K.;
    • Al-Dhalimy, Muhsen;
    • Willenbring, Holger;
    • Akkari, Yassmine;
    • Jiang, Shuguang;
    • Torimaru, Yumi;
    • Olson, Susan;
    • Fleming, William H.;
    • Finegold, Milton;
    • Grompe, Markus
    Publication type:
    Article
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    Characterization of unusual iAMP21 B‐lymphoblastic leukemia (iAMP21‐ALL) from the Mayo Clinic and Children's Oncology Group.

    Published in:
    Genes, Chromosomes & Cancer, 2022, v. 61, n. 12, p. 710, doi. 10.1002/gcc.23084
    By:
    • Koleilat, Alaa;
    • Smadbeck, James B.;
    • Zepeda‐Mendoza, Cinthya J.;
    • Williamson, Cynthia M.;
    • Pitel, Beth A.;
    • Golden, Crystal L.;
    • Xu, Xinjie;
    • Greipp, Patricia T.;
    • Ketterling, Rhett P.;
    • Hoppman, Nicole L.;
    • Peterson, Jess F.;
    • Harrison, Christine J.;
    • Akkari, Yassmine M. N.;
    • Tsuchiya, Karen D.;
    • Shago, Mary;
    • Baughn, Linda B.
    Publication type:
    Article
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    A case for expanding carrier testing to include actionable X‐linked disorders.

    Published in:
    2018
    By:
    • Rope, Alan F.;
    • Kauffman, Tia L.;
    • Himes, Pat;
    • Amendola, Laura M.;
    • Punj, Sumit;
    • Akkari, Yassmine;
    • Potter, Amiee;
    • Davis, James V.;
    • Schneider, Jennifer L.;
    • Reiss, Jacob A.;
    • Gilmore, Mari J.;
    • McMullen, Carmit K.;
    • Nickerson, Deborah A.;
    • Richards, C. Sue;
    • Jarvik, Gail P.;
    • Wilfond, Benjamin S.;
    • Goddard, Katrina A. B.
    Publication type:
    Case Study
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    Fanconi Anemia Proteins Are Required To Prevent Accumulation of Replication-Associated DNA Double-Strand Breaks.

    Published in:
    Molecular & Cellular Biology, 2006, v. 26, n. 2, p. 4, doi. 10.1128/MCB.26.2.425-437.2006
    By:
    • Sobeck, Alexandra;
    • Stone, Stacie;
    • Costanzo, Vincenzo;
    • De Graaf, Bendert;
    • Reuter, Tanja;
    • De Winter, Johan;
    • Wallisch, Michael;
    • Akkari, Yassmine;
    • Olson, Susan;
    • Weidong Wang;
    • Joenje, Hans;
    • Christian, Jan L.;
    • Lupardus, Patrick J.;
    • Cimprich, Karlene A.;
    • Gautier, Jean;
    • Hoatlin, Maureen E.
    Publication type:
    Article
    19

    Clinically significant findings in a decade‐long retrospective study of prenatal chromosomal microarray testing.

    Published in:
    Molecular Genetics & Genomic Medicine, 2024, v. 12, n. 3, p. 1, doi. 10.1002/mgg3.2349
    By:
    • Olayiwola, Joie O.;
    • Marhabaie, Mohammad;
    • Koboldt, Daniel;
    • Matthews, Theodora;
    • Siemon, Amy;
    • Mouhlas, Danielle;
    • Porter, Taylor;
    • Kyle, George;
    • Myers, Cortlandt;
    • Mei, Hui;
    • Hou, Ying‐Chen Claire;
    • Babcock, Melanie;
    • Hunter, Jesse;
    • Schieffer, Kathleen M.;
    • Akkari, Yassmine;
    • Reshmi, Shalini;
    • Cottrell, Catherine;
    • Mathew, Mariam T.;
    • Leung, Marco L.
    Publication type:
    Article
    20

    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.

    Published in:
    Archives of Pathology & Laboratory Medicine, 2021, v. 145, n. 2, p. 176, doi. 10.5858/arpa.2020-0089-CP
    By:
    • Larson, Daniel P.;
    • Akkari, Yassmine M.;
    • Van Dyke, Daniel L.;
    • Raca, Gordana;
    • Gardner, Juli-Anne;
    • Rehder, Catherine W.;
    • Kaiser-Rogers, Kathleen A.;
    • Eagle, Penny;
    • Yuhas, Jason A.;
    • Jun Gu;
    • Toydemir, Reha M.;
    • Kearney, Hutton;
    • Conlin, Laura K.;
    • Guilin Tang;
    • Dolan, Michelle M.;
    • Ketterling, Rhett P.;
    • Peterson, Jess F.
    Publication type:
    Article