Array‐based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardationHow to cite this article: Lennon PA, Cooper ML, Curtis MA, Lim C, Ou Z, Patel A, Cheung SW, Bacino CA. 2006. Array‐based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation. Am J Med Genet Part A 140A:1156–1163.

Autor: Lennon, P.A., Cooper, M.L., Curtis, M.A., Lim, C., Ou, Z., Patel, A., Cheung, S.W., Bacino, C.A.

Publikováno v: American Journal of Medical Genetics. Part A; June 2006, Vol. 140 Issue: 11 p1156-1163, 8p

Optical genome mapping in acute myeloid leukemia: a multicenter evaluation.

Autor: Levy B; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY., Baughn LB; Division of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN., Akkari Y; Steve and Cindy Rasmussen Institute for Genomic Medicine, Nationwide Children's Hospital, Columbus, OH., Chartrand S; Department of Biochemistry and Molecular Biology, Penn State College of Medicine, Hershey, PA., LaBarge B; Department of Otolaryngology, Penn State College of Medicine, Hershey, PA., Claxton D; Department of Hematology and Oncology, Department of Medicine, Penn State College of Medicine, Hershey, PA., Lennon PA; PathGroup, Nashville, TN., Cujar C; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY., Kolhe R; Department of Pathology, Medical College of Georgia at Augusta University, Augusta, GA., Kroeger K; Cytogenetics Laboratory, Seattle Cancer Care Alliance, Seattle, WA., Pitel B; Division of Laboratory Genetics and Genomics, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN., Sahajpal N; Department of Pathology, Medical College of Georgia at Augusta University, Augusta, GA., Sathanoori M; PathGroup, Nashville, TN., Vlad G; Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY., Zhang L; Department of Biochemistry and Molecular Biology, Penn State College of Medicine, Hershey, PA., Fang M; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA., Kanagal-Shamanna R; Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX., Broach JR; Department of Biochemistry and Molecular Biology, Penn State College of Medicine, Hershey, PA.

Publikováno v: Blood advances [Blood Adv] 2023 Apr 11; Vol. 7 (7), pp. 1297-1307.

Assessing copy number aberrations and copy neutral loss of heterozygosity across the genome as best practice: An evidence based review of clinical utility from the cancer genomics consortium (CGC) working group for myelodysplastic syndrome, myelodysplastic/myeloproliferative and myeloproliferative neoplasms.

Autor: Kanagal-Shamanna R; Department of Hematopathology, The University of Texas M.D. Anderson Cancer Center, Houston TX, USA. Electronic address: rkanagal@mdanderson.org., Hodge JC; Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, USA; Department of Pediatrics, University of California Los Angeles, Los Angeles, CA, USA; Department of Pathology and Laboratory Medicine, Cedars-Sinai Medical Center, Los Angeles, CA, USA., Tucker T; Department of Pathology and Laboratory Medicine, Cancer Genetics Laboratory, British Columbia Cancer Agency, Vancouver, BC Canada., Shetty S; Department of Pathology, UHCMC, University Hospitals and Case Western Reserve University, Cleveland, OH, USA., Yenamandra A; Department of Pathology, Microbiology and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA., Dixon-McIver A; IGENZ, Auckland, New Zealand., Bryke C; Department of Pathology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA., Huxley E; West Midlands Regional Genetics Laboratory, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK., Lennon PA; PathGroup, Nashville TN, USA., Raca G; Department of Pathology and Laboratory Medicine, Children's Hospital of Los Angeles, Los Angeles, CA, USA., Xu X; ARUP Laboratories, University of Utah, Salt Lake City, UT, USA., Jeffries S; West Midlands Regional Genetics Laboratory, Birmingham Women's and Children's NHS Foundation Trust, Birmingham, UK., Quintero-Rivera F; Department of Pathology and Laboratory Medicine, UCLA Clinical Genomics Center, University of California Los Angeles, Los Angeles, CA, USA., Greipp PT; Department of Laboratory Medicine and Pathology, Genomics Laboratory, Mayo Clinic, Rochester, MN, USA., Slovak ML; TriCore Reference Laboratories, University of New Mexico, Albuquerque, NM, USA., Iqbal MA; University of Rochester Medical Center, Rochester, NY, USA., Fang M; Fred Hutchinson Cancer Research Center and University of Washington, Seattle, WA, USA. Electronic address: mfang@seattlecca.org.

Publikováno v: Cancer genetics [Cancer Genet] 2018 Dec; Vol. 228-229, pp. 197-217. Date of Electronic Publication: 2018 Oct 10.

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Chromosomal microarray provides enhanced targetable gene aberration detection when paired with next generation sequencing panel in profiling lung and colorectal tumors.

Autor: Mukherjee S; PathGroup, Nashville, TN, USA., Ma Z; PathGroup, Nashville, TN, USA., Wheeler S; PathGroup, Nashville, TN, USA., Sathanoori M; PathGroup, Nashville, TN, USA., Coldren C; PathGroup, Nashville, TN, USA., Prescott JL; PathGroup, Nashville, TN, USA., Kozyr N; Akesogen, Norcross, GA, USA., Bouzyk M; Akesogen, Norcross, GA, USA., Correll M; GenoSpace, Cambridge, MA, USA., Ho H; PathGroup, Nashville, TN, USA., Chandra PK; PathGroup, Nashville, TN, USA., Lennon PA; PathGroup, Nashville, TN, USA. Electronic address: palennon@pathgroup.com.

Publikováno v: Cancer genetics [Cancer Genet] 2016 Apr; Vol. 209 (4), pp. 119-29. Date of Electronic Publication: 2016 Jan 06.