Publications by authors named "Linda D Cooley"

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Successful classification of clinical pediatric leukemia genetic subtypes via structural variant detection using HiFi long-read sequencing.
Lisa A Lansdon, Byunggil Yoo, Ayse Keskus, Irina Pushel, Chengpeng Bi, Linda D Cooley

medRxiv· November 2024

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ROS1 Alterations as a Potential Driver of Gliomas in Infant, Pediatric, and Adult Patients.
David M Meredith, Linda D Cooley, Adrian Dubuc, Jennifer Morrissette, Robyn T Sussman

Mod Pathol· November 2023

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Integrated genetic profiling of archival pediatric high-grade glial tumors and reassessment with 2021 WHO classification of paediatric CNS tumours.
Linda D Cooley, Lisa A Lansdon, Kris Laurence, John C Herriges, Lei Zhang

Cancer Genet· June 2023

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Chromosomal microarray analysis, including constitutional and neoplastic disease applications, 2021 revision: a technical standard of the American College of Medical Genetics and Genomics (ACMG).
Lina Shao, Yassmine Akkari, Linda D Cooley, David T Miller, Bryce A Seifert

Genet Med· October 2021

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Factors Affecting Migration to GRCh38 in Laboratories Performing Clinical Next-Generation Sequencing.
Lisa A Lansdon, Maxime Cadieux-Dion, Byunggil Yoo, Neil Miller, Ana S A Cohen, Linda D Cooley

J Mol Diagn· May 2021

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Clinical Validation of Somatic Mutation Detection by the OncoScan CNV Plus Assay.
Scott C Smith, Midhat S Farooqi, Melissa A Gener, Kevin Ginn, Julie M Joyce, Linda D Cooley

J Mol Diagn· January 2021

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Near haploidization is a genomic hallmark which defines a molecular subgroup of giant cell glioblastoma.
Tiffany G Baker, Jay Alden, Adrian M Dubuc, Cynthia T Welsh, Iya Znoyko, Linda D Cooley

Neurooncol Adv· November 2020

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Application of 2016 WHO classification in the diagnosis of paediatric high-grade -negative mature B-cell lymphoma with Burkitt-like morphological features.
Lei Zhang, Laura E Brown, Laurel M Bowen, Laura C McCarthy, Linda D Cooley

J Clin Pathol· September 2020

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Occurrence and characterization of medulloblastoma in a patient with Curry-Jones syndrome.
Binu Porath, Sana Farooki, Melissa Gener, Shivarajan Manickavasagam Amudhavalli, Lauren Grote, Linda D Cooley

Clin Genet· April 2020

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CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders.
Elena A Repnikova, Dmitry A Lyalin, Kimberly McDonald, Caroline Astbury, Emily Hansen-Kiss, Linda D Cooley

Eur J Med Genet· January 2020

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Neuroblastoma in Adolescents and Children Older than 10 Years: Unusual Clinicopathologic and Biologic Features.
Laura C McCarthy, Katherine Chastain, Terrie G Flatt, Eugenio Taboada, Robert Garola, Linda D Cooley

J Pediatr Hematol Oncol· November 2019

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Technical laboratory standards for interpretation and reporting of acquired copy-number abnormalities and copy-neutral loss of heterozygosity in neoplastic disorders: a joint consensus recommendation from the American College of Medical Genetics and Genomics (ACMG) and the Cancer Genomics Consortium (CGC).
Fady M Mikhail, Jaclyn A Biegel, Linda D Cooley, Adrian M Dubuc, Betsy Hirsch

Genet Med· September 2019

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Cuplike nuclear morphology is highly associated with deletion in pediatric precursor B-cell ALL.
Weijie Li, Linda D Cooley, Keith J August, Aida I Richardson, Lei Shao

Blood· July 2019

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Maintaining a methods database to optimize solid tumor tissue culture: Review of a 15-year database from a single institution.
Scott C Smith, Lisa M Warren, Linda D Cooley

Cancer Genet· April 2019

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Juvenile myelomonocytic leukemia with t(3;5)(q25;q35), Auer rods and marked myelodysplasia.
Weijie Li, Linda D Cooley, Keith August

Pathol Res Pract· June 2018

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Unusual infant eosinophilia: myeloid neoplasm with FGFR1 abnormality.
Weijie Li, Linda D Cooley

Blood· September 2016

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Clinical detection of deletion structural variants in whole-genome sequences.
Aaron C Noll, Neil A Miller, Laurie D Smith, Byunggil Yoo, Stephanie Fiedler, Linda D Cooley

NPJ Genom Med· August 2016

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Section E6.1-6.4 of the ACMG technical standards and guidelines: chromosome studies of neoplastic blood and bone marrow-acquired chromosomal abnormalities.
Fady M Mikhail, Nyla A Heerema, Kathleen W Rao, Rachel D Burnside, Athena M Cherry, Linda D Cooley

Genet Med· June 2016

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Section E6.5-6.8 of the ACMG technical standards and guidelines: chromosome studies of lymph node and solid tumor-acquired chromosomal abnormalities.
Linda D Cooley, Cynthia C Morton, Warren G Sanger, Debra F Saxe, Fady M Mikhail

Genet Med· June 2016

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MMP21 is mutated in human heterotaxy and is required for normal left-right asymmetry in vertebrates.
Anne Guimier, George C Gabriel, Fanny Bajolle, Michael Tsang, Hui Liu, Linda D Cooley

Nat Genet· November 2015

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Spitzoid melanoma in a child with Li-Fraumeni syndrome.
Ramya Kollipara, Linda D Cooley, Kimberly A Horii, Maxine L Hetherington, Philip E Leboit

Pediatr Dev Pathol· May 2014

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A Newborn with Genital Ambiguity, 45,X/46,XY Mosaicism, a Jumping Chromosome Y, and Congenital Adrenal Hyperplasia.
Lei Zhang, Linda D Cooley, Sonal R Chandratre, Atif Ahmed, Jill D Jacobson

Case Rep Endocrinol· November 2013

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American College of Medical Genetics and Genomics technical standards and guidelines: microarray analysis for chromosome abnormalities in neoplastic disorders.
Linda D Cooley, Matthew Lebo, Marilyn M Li, Marilyn L Slovak, Daynna J Wolff

Genet Med· June 2013

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Higher dose imatinib for children with de novo chronic phase chronic myelogenous leukemia: a report from the Children's Oncology Group.
Martin A Champagne, Cecilia H Fu, Myron Chang, Helen Chen, Robert B Gerbing, Linda D Cooley

Pediatr Blood Cancer· July 2011

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An interstitial 15q11-q14 deletion: expanded Prader-Willi syndrome phenotype.
Merlin G Butler, Douglas C Bittel, Nataliya Kibiryeva, Linda D Cooley, Shihui Yu

Am J Med Genet A· February 2010

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