Therese Törngren

Research EngineerFormer name: Therese Sandberg

Research engineer, Research project participant, Research support

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  1. 2019
  2. Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification

    Michael T Parsons, Emma Tudini, Hongyan Li, Eric Hahnen, Barbara Wappenschmidt, Lidia Feliubadaló, Cora M Aalfs, Simona Agata, Kristiina Aittomäki, Elisa Alducci, María Concepción Alonso-Cerezo, Norbert Arnold, Bernd Auber, Rachel Austin, Jacopo Azzollini, Judith Balmaña, Elena Barbieri, Claus R Bartram, Ana Blanco, Britta Blümcke & 31 others, Sandra Bonache, Bernardo Bonanni, Åke Borg, Beatrice Bortesi, Joan Brunet, Carla Bruzzone, Karolin Bucksch, Giulia Cagnoli, Trinidad Caldés, Almuth Caliebe, Maria A Caligo, Mariarosaria Calvello, Gabriele L Capone, Sandrine M Caputo, Ileana Carnevali, Estela Carrasco, Virginie Caux-Moncoutier, Pietro Cavalli, Giulia Cini, Edward M Clarke, Paola Concolino, Elisa J Cops, Laura Cortesi, Fergus J Couch, Esther Darder, Miguel de la Hoya, Michael Dean, Hans Ehrencrona, Anders Kvist, Therese Törngren & KConFab Investigators KConFab Investigators, 2019, In: Human Mutation. p. 1557-1578

    Research output: Contribution to journalArticle

  3. 2018
  4. Gene-panel testing of breast and ovarian cancer patients identifies a recurrent RAD51C duplication

    L. M. Pelttari, H. Shimelis, H. Toiminen, A. Kvist, T. Törngren, A. Borg, C. Blomqvist, R. Bützow, F. Couch, K. Aittomäki & H. Nevanlinna, 2018, In: Clinical Genetics. 93, 3, p. 595-602

    Research output: Contribution to journalArticle

  5. Individuals with FANCM biallelic mutations do not develop Fanconi anemia, but show risk for breast cancer, chemotherapy toxicity and may display chromosome fragility

    Irene Catucci, Ana Osorio, Brita Arver, Guido Neidhardt, Massimo Bogliolo, Federica Zanardi, Mirko Riboni, Simone Minardi, Roser Pujol, Jacopo Azzollini, Bernard Peissel, Siranoush Manoukian, Giovanna De Vecchi, Stefano Casola, Jan Hauke, Lisa Richters, Kerstin Rhiem, Rita K Schmutzler, Karin Wallander, Therese Törngren & 8 others, Åke Borg, Paolo Radice, Jordi Surrallés, Eric Hahnen, Hans Ehrencrona, Anders Kvist, Javier Benitez & Paolo Peterlongo, 2018, In: Genetics in Medicine. 20, p. 452–457 6 p.

    Research output: Contribution to journalArticle

  6. 2017
  7. Mutational and putative neoantigen load predict clinical benefit of adoptive T cell therapy in melanoma

    Martin Lauss, Marco Donia, Katja Harbst, Rikke Andersen, Shamik Mitra, Frida Rosengren, Maryem Salim, Johan Vallon-Christersson, Therese Törngren, Anders Kvist, Markus Ringnér, Inge Marie Svane & Göran Jönsson, 2017 Dec 1, In: Nature Communications. 8, 1, 1738.

    Research output: Contribution to journalArticle

  8. Expanding the genotype–phenotype spectrum in hereditary colorectal cancer by gene panel testing

    Anna Rohlin, Eva Rambech, Anders Kvist, Therese Törngren, Frida Eiengård, Ulf Lundstam, Theofanis Zagoras, Samuel Gebre-Medhin, Åke Borg, Jan Björk, Mef Nilbert & Margareta Nordling, 2017 Apr, In: Familial Cancer. 16, 2, p. 195-203

    Research output: Contribution to journalArticle

  9. Cytohesin 1 regulates homing and engraftment of human hematopoietic stem and progenitor cells

    Justyna Rak, Katie Foster, Kasia Potrzebowska, Mehrnaz Safaee Talkhoncheh, Natsumi Miharada, Karolina Komorowska, Therese Torngren, Anders Kvist, Åke Borg, Lena Svensson, Dominique Bonnet & Jonas Larsson, 2017 Feb 23, In: Blood. 129, 8, p. 950-958 9 p.

    Research output: Contribution to journalArticle

  10. 2016
  11. 2015
  12. Aberrant recombination and repair during immunoglobulin class switching in BRCA1-deficient human B cells.

    Andrea Björkman, Per Qvist, Likun Du, Margarita Bartish, Apostolos Zaravinos, Konstantinos Georgiou, Anders D Børglum, Richard A Gatti, Therese Törngren & Qiang Pan-Hammarström, 2015, In: Proceedings of the National Academy of Sciences. 112, 7, p. 2157-2162

    Research output: Contribution to journalArticle

  13. 2014
  14. 2013
  15. COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration

    Melissa C. Southey, Daniel J. Park, Tu Nguyen-Dumont, Ian Campbell, Ella Thompson, Alison H. Trainer, Georgia Chenevix-Trench, Jacques Simard, Martine Dumont, Penny Soucy, Mads Thomassen, Lars Jonson, Inge S. Pedersen, Thomas V. O. Hansen, Heli Nevanlinna, Sofia Khan, Olga Sinilnikova, Sylvie Mazoyer, Fabienne Lesueur, Francesca Damiola & 37 others, Rita Schmutzler, Alfons Meindl, Eric Hahnen, Michael R. Dufault, Tl Chris Chan, Ava Kwong, Rosa Barkardottir, Paolo Radice, Paolo Peterlongo, Peter Devilee, Florentine Hilbers, Javier Benitez, Anders Kvist, Therese Törngren, Douglas Easton, David Hunter, Sara Lindstrom, Peter Kraft, Wei Zheng, Yu-Tang Gao, Jirong Long, Susan Ramus, Bing-Jian Feng, Rey N. Weitzel, Katherine Nathanson, Kenneth Offit, Vijai Joseph, Mark Robson, Kasmintan Schrader, San Ming Wang, Yeong C. Kim, Henry Lynch, Carrie Snyder, Sean Tavtigian, Susan Neuhausen, Fergus J. Couch & David E. Goldgar, 2013, In: Breast Cancer Research. 15, 3

    Research output: Contribution to journalLetter

  16. 2012
  17. Molecular profiling reveals low- and high-grade forms of primary melanoma

    Katja Harbst, Johan Staaf, Martin Lauss, Anna Karlsson, Anna Måsbäck, Iva Johansson, Pär-Ola Bendahl, Johan Vallon-Christersson, Therese Törngren, Henrik Ekedahl, Jurgen Geisler, Mattias Höglund, Markus Ringnér, Lotta Lundgren, Karin Jirström, Håkan Olsson, Christian Ingvar, Åke Borg, Hensin Tsao & Göran B Jönsson, 2012, In: Clinical Cancer Research. 18, 15, p. 4026-4036

    Research output: Contribution to journalArticle

  18. 2011
  19. Androgen receptor htSNPs in relation to androgen levels and OC use in young women from high-risk breast cancer families.

    Maria Hietala, Maria Henningson, Therese Törngren, Håkan Olsson & Helena Jernström, 2011, In: Molecular Genetics and Metabolism. 102, p. 82-90

    Research output: Contribution to journalArticle

  20. IGF1 htSNPs in relation to IGF-1 levels in young women from high-risk breast cancer families: implications for early-onset breast cancer

    Maria Henningson, Maria Hietala, Therese Törngren, Håkan Olsson & Helena Jernström, 2011, In: Familial Cancer. 10, 2, p. 173-185

    Research output: Contribution to journalArticle

  21. 2010
  22. Characterization of BRCA1 and BRCA2 deleterious mutations and variants of unknown clinical significance in unilateral and bilateral breast cancer: the WECARE study.

    Åke Borg, Robert W Haile, Kathleen E Malone, Marinela Capanu, Ahn Diep, Therese Törngren, Sharon Teraoka, Colin B Begg, Duncan C Thomas, Patrick Concannon, Lene Mellemkjaer, Leslie Bernstein, Lina Tellhed, Shanyan Xue, Eric R Olson, Xiaolin Liang, Jessica Dolle, Anne-Lise Børresen-Dale & Jonine L Bernstein, 2010, In: Human Mutation. 31, p. E1200-E1240

    Research output: Contribution to journalArticle

  23. Genetic variants on chromosome 5p12 are associated with risk of breast cancer in African American women: the Black Women's Health Study

    Kerryn W. Reding, Jonine L. Bernstein, Bryan M. Langholz, Leslie Bernstein, Robert W. Haile, Colin B. Begg, Charles F. Lynch, Patrick Concannon, Åke Borg, Sharon N. Teraoka, Therese Törngren, Anh Diep, Shanyan Xue, Lisbeth Bertelsen, Xiaolin Liang, Anne S. Reiner, Marinela Capanu & Kathleen E. Malone, 2010, In: Breast Cancer Research and Treatment. 123, 2, p. 491-498

    Research output: Contribution to journalArticle

  24. Oral contraceptives and postmenopausal hormones and risk of contralateral breast cancer among BRCA1 and BRCA2 mutation carriers and noncarriers: the WECARE Study

    Jane C. Figueiredo, Robert W. Haile, Leslie Bernstein, Kathleen E. Malone, Joan Largent, Bryan Langholz, Charles F. Lynch, Lisbeth Bertelsen, Marinela Capanu, Patrick Concannon, Åke Borg, Anne-Lise Borresen-Dale, Anh Diep, Sharon Teraoka, Therese Törngren, Shanyan Xue & Jonine L. Bernstein, 2010, In: Breast Cancer Research and Treatment. 120, 1, p. 175-183

    Research output: Contribution to journalArticle

  25. Reproductive factors and risk of contralateral breast cancer by BRCA1 and BRCA2 mutation status: results from the WECARE study

    Jenny N. Poynter, Bryan Langholz, Joan Largent, Lene Mellemkjaer, Leslie Bernstein, Kathleen E. Malone, Charles F. Lynch, Åke Borg, Patrick Concannon, Sharon N. Teraoka, Shanyan Xue, Anh T. Diep, Therese Törngren, Colin B. Begg, Marinela Capanu, Robert W. Haile & Jonine L. Bernstein, 2010, In: Cancer Causes and Control. 21, 6, p. 839-846

    Research output: Contribution to journalArticle

  26. 2007
  27. Absence of the common IGF1 19 CA-repeat allele is more common among BRCA1 mutation carriers than among non-carriers from BRCA1 families.

    Maria Henningson, Erika Bågeman, Therese Törngren, Åke Borg, Håkan Olsson & Helena Jernström, 2007, In: Familial Cancer. 6, 4, p. 445-452

    Research output: Contribution to journalArticle

  28. Genomic profiling of malignant melanoma using tiling-resolution arrayCGH.

    Göran B Jönsson, C Dahl, Johan Staaf, Therese Törngren, Pär-Ola Bendahl, Markus Ringnér, P Guldberg & Åke Borg, 2007, In: Oncogene. 26, 32, p. 4738-4748

    Research output: Contribution to journalArticle

  29. 2006
  30. 2005
  31. Mapping of a novel ocular and cutaneous malignant melanoma susceptibility locus to chromosome 9q21.32.

    Göran B Jönsson, Pär-Ola Bendahl, Therese Törngren, Azra Kurbasic, Johan Staaf, Lone Sunde, Dorthe G Crüger, Christian Ingvar, Håkan Olsson & Åke Borg, 2005, In: Journal of the National Cancer Institute. 97, 18, p. 1377-1382

    Research output: Contribution to journalArticle

  32. 2004
  33. Melanoma and nonmelanoma skin cancer in patients with multiple tumours-evidence for new syndromes in a population-based study.

    Kari Nielsen, Christian Ingvar, Anna Måsbäck, Johan Westerdahl, Åke Borg, Therese Törngren, Nils Jonsson, J Nagel & Håkan Olsson, 2004, In: British Journal of Dermatology. 150, 3, p. 531-536

    Research output: Contribution to journalArticle

  34. 2003
  35. BRCA1 and BRCA2 mutation analysis in breast-ovarian cancer families from northeastern Poland

    Magdalena Perkowska, Izabela BroZek, Barbara Wysocka, Karin Haraldsson, Therese Törngren, Ulla Johansson, Gunilla Sellberg, Åke Borg & Janusz Limon, 2003, In: Human Mutation. 21, 5, p. 553-554

    Research output: Contribution to journalArticle

  36. 2002
  37. A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes

    E Rozenblum, P Vahteristo, Therese Törngren, JT Bergthorsson, K Syrjakoski, D Weaver, Karin Haraldsson, HK Johannsdottir, P Vehmanen, S Nigam, N Golberger, C Robbins, E Pak, A Dutra, E Gillander, DA Stephan, J Bailey-Wilson, SHH Juo, T Kainu, A Arason & 4 others, RB Barkardottir, H Nevanlinna, Åke Borg & OP Kallioniemi, 2002, In: Human Genetics. 110, 2, p. 111-121

    Research output: Contribution to journalArticle

  38. Clinical and histopathological features of malignant melanoma in germline CDKN2A mutation families

    Anna Måsbäck, Håkan Olsson, Johan Westerdahl, Therese Törngren, Åke Borg, Nils Jonsson & Christian Ingvar, 2002, In: Melanoma Research. 12, 6, p. 549-557

    Research output: Contribution to journalArticle

  39. 2001
  40. Haplotype analysis and age estimation of the 113insR CDKN2A founder mutation in Swedish melanoma families

    Jamileh Hashemi, Pär-Ola Bendahl, Therese Törngren, Anton Platz, Stig Linder, Ulrika Stierner, Håkan Olsson, Christian Ingvar, Johan Hansson & Åke Borg, 2001, In: Genes, Chromosomes and Cancer. 31, 2, p. 107-116

    Research output: Contribution to journalArticle

  41. 2000
  42. Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus

    T Kainu, S H Juo, R Desper, A A Schaffer, E Gillanders, E Rozenblum, D Freas-Lutz, D Weaver, D Stephan, J Bailey-Wilson, O P Kallioniemi, M Tirkkonen, K Syrjakoski, T Kuukasjarvi, P Koivisto, R Karhu, K Holli, A Arason, G Johannesdottir, Jon Thor Bergthorsson & 15 others, Hrefna Johannsdottir, Valgardur Egilsson, Rosa Björk Barkardottir, Oskar Johannsson, Karin Haraldsson, Therese Törngren, Eva Holmberg, Henrik Henrik Grönberg, Håkan Olsson, Åke Borg, Paula Vehmanen, Hannaleena Eerola, Päivi Heikkilä, Seppo Pyrhönen & Heli Nevanlinna, 2000, In: Proceedings of the National Academy of Sciences. 97, 17, p. 9603-9608

    Research output: Contribution to journalArticle

  43. 1999