Cargando…

Early Breast Cancer Evolution by Autosomal Broad Copy Number Alterations

The availability of comprehensive genomic datasets across patient populations enables the application of novel methods for reconstructing tumor evolution within individual patients. To this end, we propose studying autosomal broad copy number alterations (CNAs) as a framework to better understand ea...

Descripción completa

Detalles Bibliográficos
Autores principales:	Larsen, Joseph R., Kuhn, Peter, Hicks, James B.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2022
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8896957/ https://www.ncbi.nlm.nih.gov/pubmed/35252434 http://dx.doi.org/10.1155/2022/9332922

Ejemplares similares

Prognostic Value of Copy Number Alteration Burden in Early-Stage Breast Cancer and the Construction of an 11-Gene Copy Number Alteration Model
por: Wang, Dingyuan, et al.
Publicado: (2022)

Recurrent copy number alterations in young women with breast cancer
por: Chi, Chen, et al.
Publicado: (2018)

Sweepstake evolution revealed by population-genetic analysis of copy-number alterations in single genomes of breast cancer
por: Kato, Mamoru, et al.
Publicado: (2017)

Functional Copy-Number Alterations in Cancer
por: Taylor, Barry S., et al.
Publicado: (2008)

Copy-number-variation and copy-number-alteration region detection by cumulative plots
por: Li, Wentian, et al.
Publicado: (2009)

Signatures of copy number alterations in human cancer
por: Steele, Christopher D., et al.
Publicado: (2022)

Analysis of copy number variations of the autosomal genome in 156 patients with azoospermia
por: Liu, Yongjie, et al.
Publicado: (2022)

Short somatic alterations at the site of copy number variation in breast cancer
por: Murakami, Fumi, et al.
Publicado: (2020)

Chromosomal copy number alterations for associations of ductal carcinoma in situ with invasive breast cancer
por: Afghahi, Anosheh, et al.
Publicado: (2015)

Convergent Evolution of Copy Number Alterations in Multi-Centric Hepatocellular Carcinoma
por: Lackner, Carolin, et al.
Publicado: (2019)

Copy number evolution with weighted aberrations in cancer
por: Zeira, Ron, et al.
Publicado: (2020)

Simultaneous Copy Number Alteration and Single-Nucleotide Variation Analysis in Matched Aqueous Humor and Tumor Samples in Children with Retinoblastoma
por: Schmidt, Michael J., et al.
Publicado: (2023)

Pan-cancer patterns of somatic copy-number alteration
por: Zack, Travis I., et al.
Publicado: (2013)

Coping with cancer genes altered by copy number
por: Wolf, Natalie K., et al.
Publicado: (2015)

Genomic copy number alterations as biomarkers for triple negative pregnancy-associated breast cancer
por: Suelmann, B. B. M., et al.
Publicado: (2022)

Punctuated Copy Number Evolution and Clonal Stasis in Triple-Negative Breast Cancer
por: Gao, Ruli, et al.
Publicado: (2016)

Male-Biased Autosomal Effect of 16p13.11 Copy Number Variation in Neurodevelopmental Disorders
por: Tropeano, Maria, et al.
Publicado: (2013)

Association Analysis of Somatic Copy Number Alteration Burden With Breast Cancer Survival
por: Zhang, Linfan, et al.
Publicado: (2018)

Copy number alterations associated with clinical features in an underrepresented population with breast cancer
por: Rodrigues‐Peres, Raquel M., et al.
Publicado: (2019)

Germline DNA copy number variation in familial and early-onset breast cancer
por: Krepischi, Ana CV, et al.
Publicado: (2012)

Copy Number Alterations and Methylation in Ewing's Sarcoma
por: Jahromi, Mona S., et al.
Publicado: (2011)

Determining Frequent Patterns of Copy Number Alterations in Cancer
por: Rapaport, Franck, et al.
Publicado: (2010)

Histotype-specific copy-number alterations in ovarian cancer
por: Huang, Ruby YunJu, et al.
Publicado: (2012)

Copy number alteration of neuropeptides and receptors in multiple cancers
por: Zhao, Min, et al.
Publicado: (2017)

The repertoire of copy number alteration signatures in human cancer
por: Tao, Ziyu, et al.
Publicado: (2023)

Selective Genomic Copy Number Imbalances and Probability of Recurrence in Early-Stage Breast Cancer
por: Thompson, Patricia A., et al.
Publicado: (2011)

Comparison of the Agilent, ROMA/NimbleGen and Illumina platforms for classification of copy number alterations in human breast tumors
por: Baumbusch, LO, et al.
Publicado: (2008)

Initial Clinical Experience with NIPT for Rare Autosomal Aneuploidies and Large Copy Number Variations
por: Harasim, Thomas, et al.
Publicado: (2022)

Comprehensive identification and characterization of somatic copy number alterations in triple-negative breast cancer
por: Li, Zaibing, et al.
Publicado: (2019)

Subtype-specific expression of MELK is partly due to copy number alterations in breast cancer
por: Hardeman, Ashley A., et al.
Publicado: (2022)

Copy Number Variation in Inflammatory Breast Cancer
por: Hazra, Aditi, et al.
Publicado: (2023)

BIRC5 Genomic Copy Number Variation in Early-Onset Breast Cancer
por: Ghaffari, Kimia, et al.
Publicado: (2016)

Adaptive Copy Number Evolution in Malaria Parasites
por: Nair, Shalini, et al.
Publicado: (2008)

Complexity and algorithms for copy-number evolution problems
por: El-Kebir, Mohammed, et al.
Publicado: (2017)

A zero-agnostic model for copy number evolution in cancer
por: Schmidt, Henri, et al.
Publicado: (2023)

A zero-agnostic model for copy number evolution in cancer
por: Schmidt, Henri, et al.
Publicado: (2023)

Recurrent Chromosomal Copy Number Alterations in Sporadic Chordomas
por: Le, Long Phi, et al.
Publicado: (2011)

Copy Number Alterations as Novel Biomarkers and Therapeutic Targets in Colorectal Cancer
por: Tan, Elaine S., et al.
Publicado: (2022)

Copy number variation and genomic alterations in health and disease
por: Patrinos, George P, et al.
Publicado: (2009)

The landscape of somatic copy-number alteration across human cancers
por: Beroukhim, Rameen, et al.
Publicado: (2010)

Cannot write session to /tmp/vufind_sessions/sess_rmav391lc7nc8bog13li72edhd