Works by Levy, Brynn

Results: 51
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    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
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    A framework for the clinical implementation of optical genome mapping in hematologic malignancies.

    Published in:
    American Journal of Hematology, 2024, v. 99, n. 4, p. 642, doi. 10.1002/ajh.27175
    By:
    • Levy, Brynn;
    • Kanagal‐Shamanna, Rashmi;
    • Sahajpal, Nikhil S.;
    • Neveling, Kornelia;
    • Rack, Katrina;
    • Dewaele, Barbara;
    • Olde Weghuis, Daniel;
    • Stevens‐Kroef, Marian;
    • Puiggros, Anna;
    • Mallo, Mar;
    • Clifford, Benjamin;
    • Mantere, Tuomo;
    • Hoischen, Alexander;
    • Espinet, Blanca;
    • Kolhe, Ravindra;
    • Solé, Francesc;
    • Raca, Gordana;
    • Smith, Adam C.
    Publication type:
    Article
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    Activation of the DNA damage checkpoint and genomic instability in human precancerous lesions.

    Published in:
    Nature, 2005, v. 434, n. 7035, p. 907, doi. 10.1038/nature03485
    By:
    • Gorgoulis, Vassilis G.;
    • Vassiliou, Leandros-Vassilios F.;
    • Karakaidos, Panagiotis;
    • Zacharatos, Panayotis;
    • Kotsinas, Athanassios;
    • Liloglou, Triantafillos;
    • Venere, Monica;
    • DiTullio, Richard A.;
    • Kastrinakis, Nikolaos G.;
    • Levy, Brynn;
    • Kletsas, Dimitris;
    • Yoneta, Akihiro;
    • Herlyn, Meenhard;
    • Kittas, Christos;
    • Halazonetis, Thanos D.
    Publication type:
    Article
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    Mutations in the Cholesterol Transporter Gene <i>ABCA5</i> Are Associated with Excessive Hair Overgrowth.

    Published in:
    PLoS Genetics, 2014, v. 10, n. 5, p. 1, doi. 10.1371/journal.pgen.1004333
    By:
    • DeStefano, Gina M.;
    • Kurban, Mazen;
    • Anyane-Yeboa, Kwame;
    • Dall'Armi, Claudia;
    • Di Paolo, Gilbert;
    • Feenstra, Heather;
    • Silverberg, Nanette;
    • Rohena, Luis;
    • López-Cepeda, Larissa D.;
    • Jobanputra, Vaidehi;
    • Fantauzzo, Katherine A.;
    • Kiuru, Maija;
    • Tadin-Strapps, Marija;
    • Sobrino, Antonio;
    • Vitebsky, Anna;
    • Warburton, Dorothy;
    • Levy, Brynn;
    • Salas-Alanis, Julio C.;
    • Christiano, Angela M.
    Publication type:
    Article
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    Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome.

    Published in:
    2017
    By:
    • Burnett, Lisa C.;
    • LeDuc, Charles A.;
    • Sulsona, Carlos R.;
    • Pauli, Daniel;
    • Rausch, Richard;
    • Eddiry, Sanaa;
    • Carli, Jayne F. Martin;
    • Morabito, Michael V.;
    • Skowronski, Allcja A.;
    • Hubner, Gabriela;
    • Zimmer, Matthew;
    • Liheng Wang;
    • Day, Robert;
    • Levy, Brynn;
    • Fennoy, llene;
    • Dubern, Beatrice;
    • Poitou, Christine;
    • Clement, Karine;
    • Butler, Merlin G.;
    • Rosenbaum, Michael
    Publication type:
    journal article
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    Genomic imbalances in pediatric patients with chronic kidney disease.

    Published in:
    Journal of Clinical Investigation, 2015, v. 125, n. 5, p. 2171, doi. 10.1172/JCI80877
    By:
    • Verbitsky, Miguel;
    • Sanna-Cherchi, Simone;
    • Fasel, David A.;
    • Levy, Brynn;
    • Kiryluk, Krzysztof;
    • Wuttke, Matthias;
    • Abraham, Alison G.;
    • Kaskel, Frederick;
    • Köttgen, Anna;
    • Warady, Bradley A.;
    • Furth, Susan L.;
    • Wong, Craig S.;
    • Gharavi, Ali G.
    Publication type:
    Article
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    Conventional Cytogenetic Analysis of Constitutional Abnormalities: 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, 2025, v. 149, n. 3, p. 211, doi. 10.5858/arpa.2024-0048-CP
    By:
    • Boles, Brittney;
    • Gardner, Juli-Anne;
    • Rehder, Catherine W.;
    • Levy, Brynn;
    • Velagaleti, Gopalrao V.;
    • Toydemir, Reha M.;
    • Sukov, William R.;
    • Larson, Daniel P.;
    • Cao, Yang;
    • Mixon, Christopher;
    • Vanderscheldon, Rachel K.;
    • Zou, Ying S.;
    • Astbury, Caroline;
    • Tsuchiya, Karen D.;
    • Peterson, Jess F.
    Publication type:
    Article
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    High‐resolution genomic alterations in Barrett's metaplasia of patients who progress to esophageal dysplasia and adenocarcinoma.

    Published in:
    International Journal of Cancer, 2019, v. 145, n. 10, p. 2754, doi. 10.1002/ijc.32351
    By:
    • Sepulveda, Jorge L.;
    • Komissarova, Elena V.;
    • Kongkarnka, Sarawut;
    • Friedman, Richard A.;
    • Davison, Jon M.;
    • Levy, Brynn;
    • Bryk, Diana;
    • Jobanputra, Vaidehi;
    • Del Portillo, Armando;
    • Falk, Gary W.;
    • Sonett, Joshua R.;
    • Lightdale, Charles J.;
    • Abrams, Julian A.;
    • Wang, Timothy C.;
    • Sepulveda, Antonia R.
    Publication type:
    Article
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    Germline mosacism in Shprintzen-Goldberg syndrome.

    Published in:
    American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 7, p. 1574, doi. 10.1002/ajmg.a.35388
    By:
    • Shanske, Alan L.;
    • Goodrich, James T.;
    • Ala-Kokko, Leena;
    • Baker, Stuart;
    • Frederick, Barbara;
    • Levy, Brynn
    Publication type:
    Article
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    Duplication of the ZIC2 gene is not associated with holoprosencephaly.

    Published in:
    American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 1, p. 103, doi. 10.1002/ajmg.a.34375
    By:
    • Jobanputra, Vaidehi;
    • Burke, Alanna;
    • Kwame, Anyane-Yeboa;
    • Shanmugham, Anita;
    • Shirazi, Maryam;
    • Brown, Stephen;
    • Warburton, Peter E.;
    • Levy, Brynn;
    • Warburton, Dorothy
    Publication type:
    Article
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    Glut1 deficiency syndrome and erythrocyte glucose uptake assay.

    Published in:
    Annals of Neurology, 2011, v. 70, n. 6, p. 996, doi. 10.1002/ana.22640
    By:
    • Yang, Hong;
    • Wang, Dong;
    • Engelstad, Kristin;
    • Bagay, Leslie;
    • Wei, Ying;
    • Rotstein, Michael;
    • Aggarwal, Vimla;
    • Levy, Brynn;
    • Ma, Lijiang;
    • Chung, Wendy K.;
    • De Vivo, Darryl C.
    Publication type:
    Article
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    Study protocol: childhood outcomes of fetal genomic variants: the PrenatAL Microarray (PALM) cohort study.

    Published in:
    BMC Pediatrics, 2021, v. 21, n. 1, p. 1, doi. 10.1186/s12887-021-02809-7
    By:
    • Hui, Lisa;
    • Pynaker, Cecilia;
    • Kennedy, Joanne;
    • Lewis, Sharon;
    • Amor, David J.;
    • Walker, Susan P.;
    • Halliday, Jane;
    • On behalf of the PALM cohort study group;
    • Norris, Fiona;
    • Gugasyan, Lucy;
    • Regan, Matt;
    • Vasudevan, Anand;
    • Fawcett, Susan;
    • McGillivray, George;
    • Graetz, Melissa;
    • Said, Joanne;
    • Begg, Lisa;
    • Wapner, Ron;
    • Levy, Brynn
    Publication type:
    Article
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    Conventional Cytogenetic Analysis of Solid Tumor Abnormalities: A 25-Year Review of Proficiency Test Results from the College of American Pathologists/American College of Medical Genetics and Genomics Cytogenetics Committee.

    Published in:
    Genes, 2024, v. 15, n. 12, p. 1612, doi. 10.3390/genes15121612
    By:
    • Vanderscheldon, Rachel K.;
    • Sukov, William R.;
    • Gardner, Juli-Anne;
    • Rehder, Catherine W.;
    • Levy, Brynn;
    • Velagaleti, Gopalrao V.;
    • Toydemir, Reha M.;
    • Tang, Guilin;
    • Boles, Brittany;
    • Cao, Yang;
    • Mixon, Christopher;
    • Zou, Ying S.;
    • Astbury, Caroline;
    • Tsuchiya, Karen D.;
    • Peterson, Jess F.
    Publication type:
    Article
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    Identification of novel genomic imbalances in Saudi patients with congenital heart disease.

    Published in:
    Molecular Cytogenetics (17558166), 2018, v. 11, p. 1, doi. 10.1186/s13039-018-0356-6
    By:
    • Al-Hassnan, Zuhair N.;
    • Albawardi, Waad;
    • Almutairi, Faten;
    • AlMass, Rawan;
    • AlBakheet, Albandary;
    • Mustafa, Osama M.;
    • AlQuait, Laila;
    • Shinwari, Zarghuna M. A.;
    • Wakil, Salma;
    • Salih, Mustafa A.;
    • Al-Fayyadh, Majid;
    • Hassan, Saeed M.;
    • Aljoufan, Mansour;
    • Al-Nakhli, Osima;
    • Levy, Brynn;
    • AlMaarik, Balsam;
    • Al-Hakami, Hana A.;
    • Alsagob, Maysoon;
    • Colak, Dilek;
    • Kaya, Namik
    Publication type:
    Article