Uncovering the contribution of moderate-penetrance susceptibility genes to breast cancer by whole-exome sequencing and targeted enrichment sequencing of candidate genes in women of European ancestry

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Location: Deutsche Nationalbibliothek Frankfurt am Main

Extent: Online-Ressource

Language: Englisch

Bibliographic citation: In: Cancers (2022) 14:14, 3363. https://doi.org/10.3390/cancers14143363

Event: Veröffentlichung

(where): Würzburg

(who): Universität Würzburg

(when): 2023

Creator: Dumont, Martine
Weber-Lassalle, Nana
Joly-Beauparlant, Charles
Ernst, Corinna
Droit, Arnaud
Feng, Bing-Jian
Dubois, Stéphane
Collin-Deschesnes, Annie-Claude
Soucy, Penny
Vallée, Maxime
Fournier, Frédéric
Lemaçon, Audrey
Adank, Muriel A.
Allen, Jamie
Altmüller, Janine
Arnold, Norbert
Ausems, Margreet G. E. M.
Berutti, Riccardo
Bolla, Manjeet K.
Bull, Shelley
Carvalho, Sara
Cornelissen, Sten
Dufault, Michael R.
Dunning, Alison M.
Engel, Christoph
Gehrig, Andrea
Geurts-Giele, Willemina R. R.
Gieger, Christian
Green, Jessica
Hackmann, Karl
Helmy, Mohamed
Hentschel, Julia
Hogervorst, Frans B. L.
Hollestelle, Antoinette
Hooning, Maartje J.
Horváth, Judit
Ikram, M. Arfan
Kaulfuß, Silke
Keeman, Renske
Kuang, Da
Luccarini, Craig
Maier, Wolfgang
Martens, John W. M.
Niederacher, Dieter
Nürnberg, Peter
Ott, Claus-Eric
Peters, Annette
Pharoah, Paul D. P.
Ramirez, Alfredo
Ramser, Juliane
Riedel-Heller, Steffi Gerlinde
Schmidt, Gunnar
Shah, Mitul
Scherer, Martin
Stäbler, Antje
Strom, Tim M.
Sutter, Christian
Thiele, Holger
van Asperen, Christi J.
van der Kolk, Lizet
van der Luijt, Rob B.
Volk, Alexander E.
Wagner, Michael
Waisfisz, Quinten
Wang, Qin
Wang-Gohrke, Shan
Weber, Bernhard H. F.
Devilee, Peter
Tavtigian, Sean
Bader, Gary D.
Meindl, Alfons
Goldgar, David E.
Andrulis, Irene L.
Schmutzler, Rita
Easton, Douglas F.
Schmidt, Marjanka K.
Hahnen, Eric
Simard, Jacques

DOI: 10.3390/cancers14143363

URN: urn:nbn:de:bvb:20-opus-281768

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:57 AM CEST

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Associated

Dumont, Martine
Weber-Lassalle, Nana
Joly-Beauparlant, Charles
Ernst, Corinna
Droit, Arnaud
Feng, Bing-Jian
Dubois, Stéphane
Collin-Deschesnes, Annie-Claude
Soucy, Penny
Vallée, Maxime
Fournier, Frédéric
Lemaçon, Audrey
Adank, Muriel A.
Allen, Jamie
Altmüller, Janine
Arnold, Norbert
Ausems, Margreet G. E. M.
Berutti, Riccardo
Bolla, Manjeet K.
Bull, Shelley
Carvalho, Sara
Cornelissen, Sten
Dufault, Michael R.
Dunning, Alison M.
Engel, Christoph
Gehrig, Andrea
Geurts-Giele, Willemina R. R.
Gieger, Christian
Green, Jessica
Hackmann, Karl
Helmy, Mohamed
Hentschel, Julia
Hogervorst, Frans B. L.
Hollestelle, Antoinette
Hooning, Maartje J.
Horváth, Judit
Ikram, M. Arfan
Kaulfuß, Silke
Keeman, Renske
Kuang, Da
Luccarini, Craig
Maier, Wolfgang
Martens, John W. M.
Niederacher, Dieter
Nürnberg, Peter
Ott, Claus-Eric
Peters, Annette
Pharoah, Paul D. P.
Ramirez, Alfredo
Ramser, Juliane
Riedel-Heller, Steffi Gerlinde
Schmidt, Gunnar
Shah, Mitul
Scherer, Martin
Stäbler, Antje
Strom, Tim M.
Sutter, Christian
Thiele, Holger
van Asperen, Christi J.
van der Kolk, Lizet
van der Luijt, Rob B.
Volk, Alexander E.
Wagner, Michael
Waisfisz, Quinten
Wang, Qin
Wang-Gohrke, Shan
Weber, Bernhard H. F.
Devilee, Peter
Tavtigian, Sean
Bader, Gary D.
Meindl, Alfons
Goldgar, David E.
Andrulis, Irene L.
Schmutzler, Rita
Easton, Douglas F.
Schmidt, Marjanka K.
Hahnen, Eric
Simard, Jacques
Universität Würzburg

Time of origin

2023

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Uncovering the contribution of moderate-penetrance susceptibility genes to breast cancer by whole-exome sequencing and targeted enrichment sequencing of candidate genes in women of European ancestry

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Other Objects (12)

Whole-exome sequencing reveals candidate high-risk susceptibility genes for endometriosis

Early exploration of two candidate breast cancer susceptibility genes identified by whole-exome sequencing

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Sequencing genes in silico using single nucleotide polymorphisms

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Whole-exome sequencing reveals candidate high-risk susceptibility genes for endometriosis

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Genes to therapy: a comprehensive literature review of whole-exome sequencing in neurology and neurosurgery

Diagnosis of fusion genes using targeted RNA sequencing

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Phase-defined complete sequencing of the HLA genes by next-generation sequencing

Whole-exome sequencing study identifies rare variants and genes associated with intraocular pressure and glaucoma

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Identification of breast cancer susceptibility genes using whole exome sequencing

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