Whole-genome analysis of Nigerian patients with breast cancer reveals ethnic-driven somatic evolution and distinct genomic subtypes
Authors
Ansari-Pour, N.Zheng, Y.
Yoshimatsu, T. F.
Sanni, A.
Ajani, M.
Reynier, J. B.
Tapinos, Avraam
Pitt, J. J.
Dentro, S.
Woodard, A.
Rajagopal, P. S.
Fitzgerald, D.
Gruber, Andreas J
Odetunde, A.
Popoola, A.
Falusi, A. G.
Babalola, C. P.
Ogundiran, T.
Ibrahim, N.
Barretina, J.
Van Loo, P.
Chen, M.
White, K. P.
Ojengbede, O.
Obafunwa, J.
Huo, D.
Wedge, David C
Olopade, O. I.
Affiliation
Big Data Institute, Nuffield Department of Medicine, University of Oxford, Oxford, OX3 7LF, UK.Issue Date
2021
Metadata
Show full item recordCitation
Ansari-Pour N, Zheng Y, Yoshimatsu TF, Sanni A, Ajani M, Reynier J-B, et al. Whole-genome analysis of Nigerian patients with breast cancer reveals ethnic-driven somatic evolution and distinct genomic subtypes Vol. 12, Nature Communications. Springer Science and Business Media LLC; 2021.Journal
Nature CommunicationsDOI
10.1038/s41467-021-27079-wPubMed ID
34836952Type
Articleae974a485f413a2113503eed53cd6c53
10.1038/s41467-021-27079-w
Scopus Count
Collections
Related articles
- Comparison of Breast Cancer Molecular Features and Survival by African and European Ancestry in The Cancer Genome Atlas.
- Authors: Huo D, Hu H, Rhie SK, Gamazon ER, Cherniack AD, Liu J, Yoshimatsu TF, Pitt JJ, Hoadley KA, Troester M, Ru Y, Lichtenberg T, Sturtz LA, Shelley CS, Benz CC, Mills GB, Laird PW, Shriver CD, Perou CM, Olopade OI
- Issue date: 2017 Dec 1
- Characterization of Nigerian breast cancer reveals prevalent homologous recombination deficiency and aggressive molecular features.
- Authors: Pitt JJ, Riester M, Zheng Y, Yoshimatsu TF, Sanni A, Oluwasola O, Veloso A, Labrot E, Wang S, Odetunde A, Ademola A, Okedere B, Mahan S, Leary R, Macomber M, Ajani M, Johnson RS, Fitzgerald D, Grundstad AJ, Tuteja JH, Khramtsova G, Zhang J, Sveen E, Hwang B, Clayton W, Nkwodimmah C, Famooto B, Obasi E, Aderoju V, Oludara M, Omodele F, Akinyele O, Adeoye A, Ogundiran T, Babalola C, MacIsaac K, Popoola A, Morrissey MP, Chen LS, Wang J, Olopade CO, Falusi AG, Winckler W, Haase K, Van Loo P, Obafunwa J, Papoutsakis D, Ojengbede O, Weber B, Ibrahim N, White KP, Huo D, Olopade OI, Barretina J
- Issue date: 2018 Oct 16
- Novel insights into breast cancer copy number genetic heterogeneity revealed by single-cell genome sequencing.
- Authors: Baslan T, Kendall J, Volyanskyy K, McNamara K, Cox H, D'Italia S, Ambrosio F, Riggs M, Rodgers L, Leotta A, Song J, Mao Y, Wu J, Shah R, Gularte-Mérida R, Chadalavada K, Nanjangud G, Varadan V, Gordon A, Curtis C, Krasnitz A, Dimitrova N, Harris L, Wigler M, Hicks J
- Issue date: 2020 May 13
- Somatic mutations of triple-negative breast cancer: a comparison between Black and White women.
- Authors: Omilian AR, Wei L, Hong CC, Bandera EV, Liu S, Khoury T, Ambrosone CB, Yao S
- Issue date: 2020 Jul
- Whole-genome sequencing reveals clinically relevant insights into the aetiology of familial breast cancers.
- Authors: Nones K, Johnson J, Newell F, Patch AM, Thorne H, Kazakoff SH, de Luca XM, Parsons MT, Ferguson K, Reid LE, McCart Reed AE, Srihari S, Lakis V, Davidson AL, Mukhopadhyay P, Holmes O, Xu Q, Wood S, Leonard C, Kathleen Cuningham Foundation Consortium for Research into Familial Aspects of Breast Cancer (kConFab)., Australian Breast Cancer Tissue Bank (ABCTB)., Brisbane Breast Bank (BBB)., Beesley J, Harris JM, Barnes D, Degasperi A, Ragan MA, Spurdle AB, Khanna KK, Lakhani SR, Pearson JV, Nik-Zainal S, Chenevix-Trench G, Waddell N, Simpson PT
- Issue date: 2019 Jul 1