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Triple-Negative Breast Cancer Risk Genes Identified by Multigene Hereditary Cancer Panel Testing
Triple-Negative Breast Cancer Risk Genes Identified by Multigene Hereditary Cancer Panel Testing
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Triple-Negative Breast Cancer Risk Genes Identified by Multigene Hereditary Cancer Panel Testing

Shimelis, Hermela ; LaDuca, Holly ; Hu, Chunling ; Hart, Steven N ; Na, Jie ; Thomas, Abigail ; Akinhanmi, Margaret ; Moore, Raymond M ; Brauch, Hiltrud ; Cox, Angela ; Eccles, Diana M ; Ewart-Toland, Amanda ; Fasching, Peter A ; Fostira, Florentia ; Garber, Judy ; Godwin, Andrew K ; Konstantopoulou, Irene ; Nevanlinna, Heli ; Sharma, Priyanka ; Yannoukakos, Drakoulis ; Yao, Song ; Feng, Bing-Jian ; Tippin Davis, Brigette ; Lilyquist, Jenna ; Pesaran, Tina ; Goldgar, David E ; Polley, Eric C ; Dolinsky, Jill S ; Couch, Fergus J

JNCI : Journal of the National Cancer Institute, 2018-08, Vol.110 (8), p.855-862 [Periódico revisado por pares]

United States: Oxford University Press

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2
Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer
Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer
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Inherited mutations in 17 breast cancer susceptibility genes among a large triple-negative breast cancer cohort unselected for family history of breast cancer

Couch, Fergus J ; Hart, Steven N ; Sharma, Priyanka ; Toland, Amanda Ewart ; Wang, Xianshu ; Miron, Penelope ; Olson, Janet E ; Godwin, Andrew K ; Pankratz, V Shane ; Olswold, Curtis ; Slettedahl, Seth ; Hallberg, Emily ; Guidugli, Lucia ; Davila, Jaime I ; Beckmann, Matthias W ; Janni, Wolfgang ; Rack, Brigitte ; Ekici, Arif B ; Slamon, Dennis J ; Konstantopoulou, Irene ; Fostira, Florentia ; Vratimos, Athanassios ; Fountzilas, George ; Pelttari, Liisa M ; Tapper, William J ; Durcan, Lorraine ; Cross, Simon S ; Pilarski, Robert ; Shapiro, Charles L ; Klemp, Jennifer ; Yao, Song ; Garber, Judy ; Cox, Angela ; Brauch, Hiltrud ; Ambrosone, Christine ; Nevanlinna, Heli ; Yannoukakos, Drakoulis ; Slager, Susan L ; Vachon, Celine M ; Eccles, Diana M ; Fasching, Peter A

Journal of clinical oncology, 2015-02, Vol.33 (4), p.304-311 [Periódico revisado por pares]

United States: American Society of Clinical Oncology

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3
Metaplastic carcinoma of the breast: Prognosis and response to systemic treatment in metastatic disease
Metaplastic carcinoma of the breast: Prognosis and response to systemic treatment in metastatic disease
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Metaplastic carcinoma of the breast: Prognosis and response to systemic treatment in metastatic disease

Takala, Sari ; Heikkilä, Päivi ; Nevanlinna, Heli ; Blomqvist, Carl ; Mattson, Johanna

The breast journal, 2019-05, Vol.25 (3), p.418-424 [Periódico revisado por pares]

United States: Wiley Subscription Services, Inc

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4
Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer
Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer
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Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer

Kiiski, Johanna I. ; Pelttari, Liisa M. ; Khan, Sofia ; Freysteinsdottir, Edda S. ; Reynisdottir, Inga ; Hart, Steven N. ; Shimelis, Hermela ; Vilske, Sara ; Kallioniemi, Anne ; Schleutker, Johanna ; Leminen, Arto ; Bützow, Ralf ; Blomqvist, Carl ; Barkardottir, Rosa B. ; Couch, Fergus J. ; Aittomäki, Kristiina ; Nevanlinna, Heli

Proceedings of the National Academy of Sciences - PNAS, 2014-10, Vol.111 (42), p.15172-15177 [Periódico revisado por pares]

United States: National Academy of Sciences

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5
Subtyping of breast cancer by immunohistochemistry to investigate a relationship between subtype and short and long term survival: a collaborative analysis of data for 10,159 cases from 12 studies
Subtyping of breast cancer by immunohistochemistry to investigate a relationship between subtype and short and long term survival: a collaborative analysis of data for 10,159 cases from 12 studies
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Subtyping of breast cancer by immunohistochemistry to investigate a relationship between subtype and short and long term survival: a collaborative analysis of data for 10,159 cases from 12 studies

Blows, Fiona M ; Driver, Kristy E ; Schmidt, Marjanka K ; Broeks, Annegien ; van Leeuwen, Flora E ; Wesseling, Jelle ; Cheang, Maggie C ; Gelmon, Karen ; Nielsen, Torsten O ; Blomqvist, Carl ; Heikkilä, Päivi ; Heikkinen, Tuomas ; Nevanlinna, Heli ; Akslen, Lars A ; Bégin, Louis R ; Foulkes, William D ; Couch, Fergus J ; Wang, Xianshu ; Cafourek, Vicky ; Olson, Janet E ; Baglietto, Laura ; Giles, Graham G ; Severi, Gianluca ; McLean, Catriona A ; Southey, Melissa C ; Rakha, Emad ; Green, Andrew R ; Ellis, Ian O ; Sherman, Mark E ; Lissowska, Jolanta ; Anderson, William F ; Cox, Angela ; Cross, Simon S ; Reed, Malcolm W R ; Provenzano, Elena ; Dawson, Sarah-Jane ; Dunning, Alison M ; Humphreys, Manjeet ; Easton, Douglas F ; García-Closas, Montserrat ; Caldas, Carlos ; Pharoah, Paul D ; Huntsman, David Marincola, Francesco M.

PLoS medicine, 2010-05, Vol.7 (5), p.e1000279-e1000279 [Periódico revisado por pares]

United States: Public Library of Science

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6
SNPs in lncRNA Regions and Breast Cancer Risk
SNPs in lncRNA Regions and Breast Cancer Risk
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SNPs in lncRNA Regions and Breast Cancer Risk

Suvanto, Maija ; Beesley, Jonathan ; Blomqvist, Carl ; Chenevix-Trench, Georgia ; Khan, Sofia ; Nevanlinna, Heli

Frontiers in genetics, 2020-06, Vol.11, p.550-550 [Periódico revisado por pares]

Frontiers Media S.A

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7
Pathogenic Variant Spectrum in Breast Cancer Risk Genes in Finnish Patients
Pathogenic Variant Spectrum in Breast Cancer Risk Genes in Finnish Patients
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Pathogenic Variant Spectrum in Breast Cancer Risk Genes in Finnish Patients

Nurmi, Anna K ; Suvanto, Maija ; Dennis, Joe ; Aittomäki, Kristiina ; Blomqvist, Carl ; Nevanlinna, Heli

Cancers, 2022-12, Vol.14 (24), p.6158 [Periódico revisado por pares]

Switzerland: MDPI AG

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8
CHEK2 c.1100delC mutation is associated with an increased risk for male breast cancer in Finnish patient population
CHEK2 c.1100delC mutation is associated with an increased risk for male breast cancer in Finnish patient population
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CHEK2 c.1100delC mutation is associated with an increased risk for male breast cancer in Finnish patient population

Hallamies, Sanna ; Pelttari, Liisa M ; Poikonen-Saksela, Paula ; Jekunen, Antti ; Jukkola-Vuorinen, Arja ; Auvinen, Päivi ; Blomqvist, Carl ; Aittomäki, Kristiina ; Mattson, Johanna ; Nevanlinna, Heli

BMC cancer, 2017-09, Vol.17 (1), p.620-620, Article 620 [Periódico revisado por pares]

England: BioMed Central Ltd

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9
Constitutional mosaicism for a BRCA2 mutation as a cause of early-onset breast cancer
Constitutional mosaicism for a BRCA2 mutation as a cause of early-onset breast cancer
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Constitutional mosaicism for a BRCA2 mutation as a cause of early-onset breast cancer

Alhopuro, Pia ; Vainionpää, Reetta ; Anttonen, Anna-Kaisa ; Aittomäki, Kristiina ; Nevanlinna, Heli ; Pöyhönen, Minna

Familial cancer, 2020-10, Vol.19 (4), p.307-310 [Periódico revisado por pares]

Dordrecht: Springer Netherlands

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10
A search for modifying genetic factors in CHEK2:c.1100delC breast cancer patients
A search for modifying genetic factors in CHEK2:c.1100delC breast cancer patients
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A search for modifying genetic factors in CHEK2:c.1100delC breast cancer patients

Wendt, Camilla ; Muranen, Taru A. ; Mielikäinen, Lotta ; Thutkawkorapin, Jessada ; Blomqvist, Carl ; Jiao, Xiang ; Ehrencrona, Hans ; Tham, Emma ; Arver, Brita ; Melin, Beatrice ; Kuchinskaya, Ekaterina ; Stenmark Askmalm, Marie ; Paulsson-Karlsson, Ylva ; Einbeigi, Zakaria ; von Wachenfeldt Väppling, Anna ; Kalso, Eija ; Tasmuth, Tiina ; Kallioniemi, Anne ; Aittomäki, Kristiina ; Nevanlinna, Heli ; Borg, Åke ; Lindblom, Annika

Scientific reports, 2021-07, Vol.11 (1), p.14763-14763, Article 14763 [Periódico revisado por pares]

London: Nature Publishing Group

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