Publications by authors named "Philip D Cotter"

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Mosaicism for Autosomal Trisomies: A Comprehensive Analysis of 1266 Published Cases Focusing on Maternal Age and Reproductive History.
Natalia V Kovaleva, Philip D Cotter

Genes (Basel)· June 2024

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Evolution of biomarker research in autoimmunity conditions for health professionals and clinical practice.
Arthur Silverstein, Anton Dudaev, Maria Studneva, John Aitken, Sofya Blokh, Philip D Cotter

Prog Mol Biol Transl Sci· August 2022

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Factors affecting clinical manifestation of chromosomal imbalance in carriers of segmental autosomal mosaicism: differential impact of gender.
Natalia V Kovaleva, Philip D Cotter

J Appl Genet· May 2022

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Analytical performance evaluation of a commercial next generation sequencing liquid biopsy platform using plasma ctDNA, reference standards, and synthetic serial dilution samples derived from normal plasma.
Suman Verma, Mathew W Moore, Rebecca Ringler, Abhisek Ghosal, Kyle Horvath, Philip D Cotter

BMC Cancer· October 2020

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Multiparametric liquid biopsy analysis in metastatic prostate cancer.
Emmanuelle Hodara, Gareth Morrison, Alexander Cunha, Daniel Zainfeld, Tong Xu, Philip D Cotter

JCI Insight· March 2019

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Reference Size Matching, Whole-Genome Amplification, and Fluorescent Labeling as a Method for Chromosomal Microarray Analysis of Clinically Actionable Copy Number Alterations in Formalin-Fixed, Paraffin-Embedded Tumor Tissue.
Shelly R Gunn, Shailin Govender, Cynthe L Sims, Aditi Khurana, Samuel Koo, Philip D Cotter

J Mol Diagn· May 2018

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Mosaicism for structural non-centromeric autosomal rearrangement in prenatal diagnoses: evidence for sex-specific selection against chromosomal abnormalities.
Natalia V Kovaleva, Philip D Cotter

Mol Cytogenet· December 2017

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Mosaicism for structural non-centromeric autosomal rearrangements in disease-defined carriers: sex differences in the rearrangements profile and maternal age distributions.
Natalia V Kovaleva, Philip D Cotter

Mol Cytogenet· May 2017

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Somatic/gonadal mosaicism for structural autosomal rearrangements: female predominance among carriers of gonadal mosaicism for unbalanced rearrangements.
Natalia V Kovaleva, Philip D Cotter

Mol Cytogenet· January 2016

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Genomic Rearrangements of PTEN in Prostate Cancer.
Sopheap Phin, Mathew W Moore, Philip D Cotter

Front Oncol· September 2013

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Supernumerary marker chromosomes derived from chromosome 6: cytogenetic, molecular cytogenetic, and array CGH characterization.
Bing Huang, Phyllis Pearle, Katherine A Rauen, Philip D Cotter

Am J Med Genet A· July 2012

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Challenges in the codevelopment of companion diagnostics.
Mathew W Moore, Deepti Babu, Philip D Cotter

Per Med· July 2012

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Ovarian dysgenesis associated with an unbalanced X;6 translocation: first characterisation of reproductive anatomy and cytogenetic evaluation in partial trisomy 6 with breakpoints at Xq22 and 6p23.
Eric Scott Sills, Philip D Cotter, Kevin D Marron, Lyuda V Shkrobot, Harriet M A Walsh

Mol Med Rep· January 2012

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FISH-based determination of HER2 status in circulating tumor cells isolated with the microfluidic CEE™ platform.
Julie Ann Mayer, Tam Pham, Karina L Wong, Jayne Scoggin, Edgar V Sales, Philip D Cotter

Cancer Genet· November 2011

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Inversion and deletion of 16q22 defined by array CGH, FISH, and RT-PCR in a patient with AML.
Angelika J Dawson, Shibani Bal, Barry McTavish, Michelle Tomiuk, Ingo Schroedter, Philip D Cotter

Cancer Genet· June 2011

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Tissue-limited mosaicism for monosomy 13.
Mahin Golabi, Aaron W James, William V Good, Philip D Cotter

Am J Med Genet A· October 2010

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Clefting in trisomy 9p patients: genotype-phenotype correlation using microarray comparative genomic hybridization.
Angie Jelin, Hazel Perry, Jacob Hogue, Snehlata Oberoi, Philip D Cotter

J Craniofac Surg· September 2010

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Cervical intraepithelial neoplasia and aneusomy of TERC: assessment of liquid-based cytological preparations.
Reena Ramsaroop, Paul Oei, Daniel Ng, Nirup Kumar, Philip D Cotter

Diagn Cytopathol· June 2009

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Inv dup del(4)(:p13-->p16.3::p16.3-->qter) in a girl without typical manifestations of Wolf-Hirschhorn syndrome.
Giorgio A Paskulin, Mariluce Riegel, Philip D Cotter, Andrea Kiss, Rafael F M Rosa

Am J Med Genet A· June 2009

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Gardner-Silengo-Wachtel or genito-palato-cadiac syndrome with associated autosomal aneuploidy.
Mahin Golabi, Aaron W James, Nina Desai, Katherine Culver, Philip D Cotter

Am J Med Genet A· February 2009

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Whole-genome scanning by array comparative genomic hybridization as a clinical tool for risk assessment in chronic lymphocytic leukemia.
Shelly R Gunn, Mansoor S Mohammed, Mercedes E Gorre, Philip D Cotter, Jaeweon Kim

J Mol Diagn· September 2008

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Report of a child with a complete de novo 17p duplication localized to the terminal region of the long arm of chromosome 17.
Giorgio A Paskulin, Paulo R G Zen, Rafael F M Rosa, Rosana C Manique, Philip D Cotter

Am J Med Genet A· June 2007

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Detection of single clone deletions using array CGH: identification of submicroscopic deletions in the 22q11.2 deletion syndrome as a model system.
Taku A Tokuyasu, Philip D Cotter, Richard Segraves, Jeffrey Harris, Melissa E Elder

Am J Med Genet A· May 2007

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Double aneuploidy (48,XXY,+21): molecular analysis demonstrates a maternal origin.
Ian A Glass, Lei Li, Philip D Cotter

Eur J Med Genet· September 2006

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Molecular cytogenetic characterization of human papillomavirus16-transformed foreskin keratinocyte cell line 16-MT.
Eva M McGhee, Philip D Cotter, Jingly F Weier, Jennifer W Berline, Mary A Turner

Cancer Genet Cytogenet· July 2006

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