Other short opinions/comments on moderate/low cancer genetic risk markers in medical practice and the article Genetic contribution to all cancers: the first demonstration using the...

Por Aittomäki, Kristiina
Publicado em 2008

Evaluation of <it>SHOX </it>copy number variations in patients with Müllerian aplasia

Por Jokimaa Varpu, Halttunen Mervi, Sandbacka Maria, Aittomäki Kristiina, Laivuori Hannele
Publicado em 2011-08-01

Evaluation of SHOX copy number variations in patients with Müllerian aplasia

Por Sandbacka, Maria, Halttunen, Mervi, Jokimaa, Varpu, Aittomäki, Kristiina, Laivuori, Hannele
Publicado em 2011

A 4-bp Deletion in the Birt-Hogg-Dubé Gene (FLCN) Causes Dominantly Inherited Spontaneous Pneumothorax

Por Painter, Jodie N., Tapanainen, Hanna, Somer, Mirja, Tukiainen, Pentti, Aittomäki, Kristiina
Publicado em 2005

Histopathological features of breast tumours in BRCA1, BRCA2 and mutation-negative breast cancer families

Por Eerola, Hannaleena, Heikkilä, Päivi, Tamminen, Anitta, Aittomäki, Kristiina, Blomqvist, Carl, Nevanlinna, Heli
Publicado em 2005

Relationship of patients' age to histopathological features of breast tumours in BRCA1 and BRCA2 and mutation-negative breast cancer families

Por Eerola, Hannaleena, Heikkilä, Päivi, Tamminen, Anitta, Aittomäki, Kristiina, Blomqvist, Carl, Nevanlinna, Heli
Publicado em 2005

Comprehensive analysis of NuMA variation in breast cancer

Por Kilpivaara, Outi, Rantanen, Matias, Tamminen, Anitta, Aittomäki, Kristiina, Blomqvist, Carl, Nevanlinna, Heli
Publicado em 2008

RAD51, XRCC3, and XRCC2 mutation screening in Finnish breast cancer families

Por Pelttari, Liisa M, Kiiski, Johanna I, Ranta, Salla, Vilske, Sara, Blomqvist, Carl, Aittomäki, Kristiina, Nevanlinna, Heli
Publicado no Springerplus (2015)

Chorionic Gonadotropin Beta gene variants are associated with recurrent miscarriage in two European populations

Por Rull, Kristiina, Nagirnaja, Liina, Ulander, Veli-Matti, Kelgo, Piret, Margus, Tõnu, Kaare, Milja, Aittomäki, Kristiina, Laan, Maris
Publicado em 2008

TBX6, LHX1 and copy number variations in the complex genetics of Müllerian aplasia

Por Sandbacka, Maria, Laivuori, Hannele, Freitas, Érika, Halttunen, Mervi, Jokimaa, Varpu, Morin-Papunen, Laure, Rosenberg, Carla, Aittomäki, Kristiina
Publicado em 2013

Basal cytokeratins in breast tumours among BRCA1, BRCA2 and mutation-negative breast cancer families

Por Eerola, Hannaleena, Heinonen, Mira, Heikkilä, Päivi, Kilpivaara, Outi, Tamminen, Anitta, Aittomäki, Kristiina, Blomqvist, Carl, Ristimäki, Ari, Nevanlinna, Heli
Publicado em 2008

Polymorphism at 19q13.41 predicts breast cancer survival specifically after endocrine therapy

Por Khan, Sofia, Fagerholm, Rainer, Rafiq, Sajjad, Tapper, William, Aittomäki, Kristiina, Liu, Jianjun, Blomqvist, Carl, Eccles, Diana, Nevanlinna, Heli
Publicado no Clin Cancer Res (2015)

Variants on the promoter region of PTEN affect breast cancer progression and patient survival

Por Heikkinen, Tuomas, Greco, Dario, Pelttari, Liisa M, Tommiska, Johanna, Vahteristo, Pia, Heikkilä, Päivi, Blomqvist, Carl, Aittomäki, Kristiina, Nevanlinna, Heli
Publicado em 2011

CDC73 Intragenic Deletion in Familial Primary Hyperparathyroidism Associated With Parathyroid Carcinoma

Por Korpi-Hyövälti, Eeva, Cranston, Treena, Ryhänen, Eeva, Arola, Johanna, Aittomäki, Kristiina, Sane, Timo, Thakker, Rajesh V., Schalin-Jäntti, Camilla
Publicado em 2014

Hereditary leiomyomatosis and renal cell cancer (HLRCC). Renal cancer risk, surveillance and treatment

Por Menko, Fred H., Maher, Eamonn, Schmidt, Laura S., Middelton, Lindsay A., Aittomäki, Kristiina, Tomlinson, Ian, Richard, Stéphane, Linehan, W. Marston
Publicado no Fam Cancer (2014)

Ingraft chimerism in lung transplantation - a study in a porcine model of obliterative bronchiolitis

Por Päiväniemi, Outi E, Musilova, Petra, Raivio, Peter M, Maasilta, Paula K, Alho, Hanni S, Rubes, Jiri, Aittomäki, Kristiina, Salminen, Ulla-Stina
Publicado em 2011

Breast tumors from CHEK2 1100delC-mutation carriers: genomic landscape and clinical implications

Por Muranen, Taru A, Greco, Dario, Fagerholm, Rainer, Kilpivaara, Outi, Kämpjärvi, Kati, Aittomäki, Kristiina, Blomqvist, Carl, Heikkilä, Päivi, Borg, Åke, Nevanlinna, Heli
Publicado em 2011

ATM variants and cancer risk in breast cancer patients from Southern Finland

Por Tommiska, Johanna, Jansen, Laila, Kilpivaara, Outi, Edvardsen, Hege, Kristensen, Vessela, Tamminen, Anitta, Aittomäki, Kristiina, Blomqvist, Carl, Børresen-Dale, Anne-Lise, Nevanlinna, Heli
Publicado em 2006

Polygenic risk score is associated with increased disease risk in 52 Finnish breast cancer families

Por Muranen, Taru A., Mavaddat, Nasim, Khan, Sofia, Fagerholm, Rainer, Pelttari, Liisa, Lee, Andrew, Aittomäki, Kristiina, Blomqvist, Carl, Easton, Douglas F., Nevanlinna, Heli
Publicado no Breast Cancer Res Treat (2016)

Familial Cutaneous Leiomyomatosis Is a Two-Hit Condition Associated with Renal Cell Cancer of Characteristic Histopathology

Por Kiuru, Maija, Launonen, Virpi, Hietala, Marja, Aittomäki, Kristiina, Vierimaa, Outi, Salovaara, Reijo, Arola, Johanna, Pukkala, Eero, Sistonen, Pertti, Herva, Riitta, Aaltonen, Lauri A.
Publicado em 2001