Exonic trinucleotide repeat expansions in ZFHX3 cause spinocerebellar ataxia type 4: A poly-glycine disease

Authors: Wallenius, Joel, Kafantari, Efthymia, Jhaveri, Emma, Gorcenco, Sorina, Ameur, Adam, Karremo, Christin, Dobloug, Sigurd, Karrman, Kristina, de Koning, Tom, Ilinca, Andreea, Landqvist Waldö, Maria, Arvidsson, Andreas, Persson, Staffan, Englund, Elisabet, Ehrencrona, Hans, Puschmann, Andreas

Source: In The American Journal of Human Genetics 4 January 2024 111(1):82-95

Trailblazing precision medicine in Europe: A joint view by Genomic Medicine Sweden and the Centers for Personalized Medicine, ZPM, in Germany

Authors: Lindstrand, Anna, Wedell, Anna, Gisselsson, David, Melén, Erik, Helenius, Gisela, Ehrencrona, Hans, Engstrand, Lars, Palmqvist, Lars, Levin, Lars-Åke, Lovmar, Lovisa, Landström, Maréne, Hallbeck, Martin, Wadelius, Mia, Sikora, Per, Beer, Ambros J., Illert, Anna L., Budczies, Jan, Nikolaou, Konstantin, Kohlbacher, Oliver, Horak, Peter, Kuhn, Peter, Schroeder, Christopher, Boerries, Melanie, Lassmann, Silke, Gaidzik, Verena I., Stenzinger, Albrecht ^*, Edsjö, Anders ^**, Ploeger, Carolin, Friedman, Mikaela, Fröhling, Stefan, Wirta, Valtteri, Seufferlein, Thomas, Botling, Johan, Duyster, Justus, Akhras, Michael, Thimme, Robert, Fioretos, Thoas, Bitzer, Michael, Cavelier, Lucia, Schirmacher, Peter, Malek, Nisar, Rosenquist, Richard

Source: In Seminars in Cancer Biology September 2022 84:242-254

Extended genetic diagnostics for children with profound sensorineural hearing loss by implementing massive parallel sequencing. Diagnostic outcome, family experience and clinical implementation

Authors: Elander, Johanna, Ullmark, Tove, Ehrencrona, Hans, Jonson, Tord, Piccinelli, Paul, Samuelsson, Sofie, Löwgren, Karolina, Falkenius-Schmidt, Karolina, Ehinger, Johannes, Stenfeldt, Karin, Värendh, Maria

Source: In International Journal of Pediatric Otorhinolaryngology August 2022 159

Direct letters to relatives at risk of hereditary cancer—study protocol for a multi-center randomized controlled trial of healthcare-assisted versus family-mediated risk disclosure at Swedish cancer genetics clinics (DIRECT-study).

Authors: Hawranek, Carolina¹ (AUTHOR), Ehrencrona, Hans² (AUTHOR), Öfverholm, Anna³ (AUTHOR), Hellquist, Barbro Numan¹ (AUTHOR), Rosén, Anna¹ (AUTHOR) anna.rosen@umu.se

Source: Trials. 12/17/2023, Vol. 24 Issue 1, p1-15. 15p.

Subject Terms: *CANCER genetics, *CLINICS, *RANDOMIZED controlled trials, *DISEASE risk factors, *DISCLOSURE, *HEREDITARY cancer syndromes

Variations in the Referral Pattern for Genetic Counseling of Patients with Early-Onset Breast Cancer : A Population-Based Study in Southern Sweden

Authors: Augustinsson, Annelie, Ellberg, Carolina, Kristoffersson, Ulf, Olsson, Håkan, Ehrencrona, Hans

Source: Public Health Genomics, 2020 Jan 01. 23(3/4), 100-109.

Access URL: https://www.jstor.org/stable/27013214

Discontinuation of tyrosine kinase inhibitor therapy in chronic myeloid leukaemia (EURO-SKI): a prespecified interim analysis of a prospective, multicentre, non-randomised, trial

Authors: Ossenkoppele, Gert, Pagoni, Maria N., Söderlund, Stina, Escoffre-Barbe, Martine, Etienne, Gabriel, Dengler, Jolanta, Huguet, Francoise, von Bubnoff, Nikolas, Klamova, Hana, Faber, Edgar, Guilhot, Francois, Lotfi, Kourosh, Rea, Delphine, Brümmendorf, Tim H., de Greef, Gorgine E., Stenke, Leif, Nicolini, Franck E., Legros, Laurence, Burchert, Andreas, Voglova, Jaroslava, Charbonnier, Aude, Gyan, Emmanuel, Kunzmann, Volker, Westerweel, Peter E., Saussele, Susanne, Richter, Johan, Guilhot, Joelle, Gruber, Franz X, Hjorth-Hansen, Henrik, Almeida, Antonio, Janssen, Jeroen J W M, Mayer, Jiri, Koskenvesa, Perttu, Panayiotidis, Panayiotis, Olsson-Strömberg, Ulla, Martinez-Lopez, Joaquin, Rousselot, Philippe, Vestergaard, Hanne, Ehrencrona, Hans, Kairisto, Veli, Machová Poláková, Katerina, Müller, Martin C, Mustjoki, Satu, Berger, Marc G, Fabarius, Alice, Hofmann, Wolf-Karsten, Hochhaus, Andreas, Pfirrmann, Markus, Mahon, Francois-Xavier

Source: In The Lancet Oncology June 2018 19(6):747-757

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

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

Source: In Genetics in Medicine April 2018 20(4):452-457

Genetic counselling legislation and practice in cancer in EU Member States.

Authors: McCrary, J Matt, Valckenborgh, Els Van, Poirel, Hélène A, Putter, Robin de, Rooij, Jeroen van, Horgan, Denis, Dierks, Marie-Luise, Antonova, Olga, Brunet, Joan, Chirita-Emandi, Adela, Colas, Chrystelle, Dalmas, Miriam, Ehrencrona, Hans, Grima, Claire, Janavičius, Ramūnas, Klink, Barbara, Koczok, Katalin, Krajc, Mateja, Lace, Baiba, Leitsalu, Liis

Source: European Journal of Public Health; Aug2024, Vol. 34 Issue 4, p666-675, 10p

Subject Terms: GENETIC counseling laws, TUMOR genetics, HEALTH insurance reimbursement, RESEARCH funding, INTERVIEWING, GENETIC variation, RESEARCH methodology, GENETIC counselors, DATA analysis software, LABOR supply

Company/Entity: EUROPEAN Union

Retrospective genetic testing (Traceback) in women with early-onset breast cancer after revised national guidelines: a clinical implementation study.

Authors: Augustinsson, Annelie, Loman, Niklas, Ehrencrona, Hans

Source: Breast Cancer Research & Treatment; Jun2024, Vol. 205 Issue 3, p599-607, 9p

European Stop Tyrosine Kinase Inhibitor Trial (EURO-SKI) in Chronic Myeloid Leukemia: Final Analysis and Novel Prognostic Factors for Treatment-Free Remission.

Authors: Mahon, Francois-Xavier¹ (AUTHOR) francois-xavier.mahon@u-bordeaux.fr, Pfirrmann, Markus² (AUTHOR), Dulucq, Stéphanie^3,4 (AUTHOR), Hochhaus, Andreas⁵ (AUTHOR), Panayiotidis, Panayiotis⁶ (AUTHOR), Almeida, Antonio⁷ (AUTHOR), Mayer, Jiri⁸ (AUTHOR), Hjorth-Hansen, Henrik⁹ (AUTHOR), Janssen, Jeroen J.W.M.¹⁰ (AUTHOR), Mustjoki, Satu^11,12 (AUTHOR), Martinez-Lopez, Joaquin¹³ (AUTHOR), Vestergaard, Hanne¹⁴ (AUTHOR), Ehrencrona, Hans^15,16 (AUTHOR), Machová Poláková, Katerina¹⁷ (AUTHOR), Olsson-Strömberg, Ulla¹⁸ (AUTHOR), Ossenkoppele, Gert¹⁰ (AUTHOR), Berger, Marc G.¹⁹ (AUTHOR), Etienne, Gabriel^4,20 (AUTHOR), Dengler, Jolanta^21,22 (AUTHOR), Brümmendorf, Tim H.^23,24 (AUTHOR)

Source: Journal of Clinical Oncology. 2024 Supplement 16, Vol. 42, p1875-1880. 11p.

No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer

Authors: Hollestelle, Antoinette, van der Baan, Frederieke H., Berchuck, Andrew, Johnatty, Sharon E., Aben, Katja K., Agnarsson, Bjarni A., Aittomäki, Kristiina, Alducci, Elisa, Andrulis, Irene L., Anton-Culver, Hoda, Antonenkova, Natalia N., Antoniou, Antonis C., Apicella, Carmel, Arndt, Volker, Arnold, Norbert, Arun, Banu K., Arver, Brita, Ashworth, Alan, Baglietto, Laura, Balleine, Rosemary, Bandera, Elisa V., Barrowdale, Daniel, Bean, Yukie T., Beckmann, Lars, Beckmann, Matthias W., Benitez, Javier, Berger, Andreas, Berger, Raanan, Beuselinck, Benoit, Bisogna, Maria, Bjorge, Line, Blomqvist, Carl, Bogdanova, Natalia V., Bojesen, Anders, Bojesen, Stig E., Bolla, Manjeet K., Bonanni, Bernardo, Brand, Judith S., Brauch, Hiltrud, Brenner, Hermann, Brinton, Louise, Brooks-Wilson, Angela, Bruinsma, Fiona, Brunet, Joan, Brüning, Thomas, Budzilowska, Agnieszka, Bunker, Clareann H., Burwinkel, Barbara, Butzow, Ralf, Buys, Saundra S., Caligo, Maria A., Campbell, Ian, Carter, Jonathan, Chang-Claude, Jenny, Chanock, Stephen J., Claes, Kathleen B.M., Collée, J. Margriet, Cook, Linda S., Couch, Fergus J., Cox, Angela, Cramer, Daniel, Cross, Simon S., Cunningham, Julie M., Cybulski, Cezary, Czene, Kamila, Damiola, Francesca, Dansonka-Mieszkowska, Agnieszka, Darabi, Hatef, de la Hoya, Miguel, deFazio, Anna, Dennis, Joseph, Devilee, Peter, Dicks, Ed M., Diez, Orland, Doherty, Jennifer A., Domchek, Susan M., Dorfling, Cecilia M., Dörk, Thilo, Silva, Isabel Dos Santos, du Bois, Andreas, Dumont, Martine, Dunning, Alison M., Duran, Mercedes, Easton, Douglas F., Eccles, Diana, Edwards, Robert P., Ehrencrona, Hans, Ejlertsen, Bent, Ekici, Arif B., Ellis, Steve D., Engel, Christoph, Eriksson, Mikael, Fasching, Peter A., Feliubadalo, Lidia, Figueroa, Jonine, Flesch-Janys, Dieter, Fletcher, Olivia, Fontaine, Annette, Fortuzzi, Stefano, Fostira, Florentia, Fridley, Brooke L., Friebel, Tara, Friedman, Eitan, Friel, Grace, Frost, Debra, Garber, Judy, García-Closas, Montserrat, Gayther, Simon A., Gentry-Maharaj, Aleksandra, Gerdes, Anne-Marie, Giles, Graham G., Glasspool, Rosalind, Glendon, Gord, Godwin, Andrew K., Goodman, Marc T., Gore, Martin, Greene, Mark H., Grip, Mervi, Gronwald, Jacek, Gschwantler Kaulich, Daphne, Guénel, Pascal, Guzman, Starr R., Haeberle, Lothar, Haiman, Christopher A., Hall, Per, Halverson, Sandra L., Hamann, Ute, Hansen, Thomas V.O., Harter, Philipp, Hartikainen, Jaana M., Healey, Sue, Hein, Alexander, Heitz, Florian, Henderson, Brian E., Herzog, Josef, T Hildebrandt, Michelle A., Høgdall, Claus K., Høgdall, Estrid, Hogervorst, Frans B.L., Hopper, John L., Humphreys, Keith, Huzarski, Tomasz, Imyanitov, Evgeny N., Isaacs, Claudine, Jakubowska, Anna, Janavicius, Ramunas, Jaworska, Katarzyna, Jensen, Allan, Jensen, Uffe Birk, Johnson, Nichola, Jukkola-Vuorinen, Arja, Kabisch, Maria, Karlan, Beth Y., Kataja, Vesa, Kauff, Noah, Kelemen, Linda E., Kerin, Michael J., Kiemeney, Lambertus A., Kjaer, Susanne K., Knight, Julia A., Knol-Bout, Jacoba P., Konstantopoulou, Irene, Kosma, Veli-Matti, Krakstad, Camilla, Kristensen, Vessela, Kuchenbaecker, Karoline B., Kupryjanczyk, Jolanta, Laitman, Yael, Lambrechts, Diether, Lambrechts, Sandrina, Larson, Melissa C., Lasa, Adriana, Laurent-Puig, Pierre, Lazaro, Conxi, Le, Nhu D., Le Marchand, Loic, Leminen, Arto, Lester, Jenny, Levine, Douglas A., Li, Jingmei, Liang, Dong, Lindblom, Annika, Lindor, Noralane, Lissowska, Jolanta, Long, Jirong, Lu, Karen H., Lubinski, Jan, Lundvall, Lene, Lurie, Galina, Mai, Phuong L., Mannermaa, Arto, Margolin, Sara, Mariette, Frederique, Marme, Frederik, Martens, John W.M., Massuger, Leon F.A.G., Maugard, Christine, Mazoyer, Sylvie, McGuffog, Lesley, McGuire, Valerie, McLean, Catriona, McNeish, Iain, Meindl, Alfons, Menegaux, Florence, Menéndez, Primitiva, Menkiszak, Janusz, Menon, Usha, Mensenkamp, Arjen R., Miller, Nicola, Milne, Roger L., Modugno, Francesmary, Montagna, Marco, Moysich, Kirsten B., Müller, Heiko, Mulligan, Anna Marie, Muranen, Taru A., Narod, Steven A., Nathanson, Katherine L., Ness, Roberta B., Neuhausen, Susan L., Nevanlinna, Heli, Neven, Patrick, Nielsen, Finn C., Nielsen, Sune F., Nordestgaard, Børge G., Nussbaum, Robert L., Odunsi, Kunle, Offit, Kenneth, Olah, Edith, Olopade, Olufunmilayo I., Olson, Janet E., Olson, Sara H., Oosterwijk, Jan C., Orlow, Irene, Orr, Nick, Orsulic, Sandra, Osorio, Ana, Ottini, Laura, Paul, James, Pearce, Celeste L., Pedersen, Inge Sokilde, Peissel, Bernard, Pejovic, Tanja, Pelttari, Liisa M., Perkins, Jo, Permuth-Wey, Jenny, Peterlongo, Paolo, Peto, Julian, Phelan, Catherine M., Phillips, Kelly-Anne, Piedmonte, Marion, Pike, Malcolm C., Platte, Radka, Plisiecka-Halasa, Joanna, Poole, Elizabeth M., Poppe, Bruce, Pylkäs, Katri, Radice, Paolo, Ramus, Susan J., Rebbeck, Timothy R., Reed, Malcolm W.R., Rennert, Gad, Risch, Harvey A., Robson, Mark, Rodriguez, Gustavo C., Romero, Atocha, Rossing, Mary Anne, Rothstein, Joseph H., Rudolph, Anja, Runnebaum, Ingo, Salani, Ritu, Salvesen, Helga B., Sawyer, Elinor J., Schildkraut, Joellen M., Schmidt, Marjanka K., Schmutzler, Rita K., Schneeweiss, Andreas, Schoemaker, Minouk J., Schrauder, Michael G., Schumacher, Fredrick, Schwaab, Ira, Scuvera, Giulietta, Sellers, Thomas A., Severi, Gianluca, Seynaeve, Caroline M., Shah, Mitul, Shrubsole, Martha, Siddiqui, Nadeem, Sieh, Weiva, Simard, Jacques, Singer, Christian F., Sinilnikova, Olga M., Smeets, Dominiek, Sohn, Christof, Soller, Maria, Song, Honglin, Soucy, Penny, Southey, Melissa C., Stegmaier, Christa, Stoppa-Lyonnet, Dominique, Sucheston, Lara, Swerdlow, Anthony, Tangen, Ingvild L., Tea, Muy-Kheng, Teixeira, Manuel R., Terry, Kathryn L., Terry, Mary Beth, Thomassen, Mads, Thompson, Pamela J., Tihomirova, Laima, Tischkowitz, Marc, Toland, Amanda Ewart, Tollenaar, Rob A.E.M., Tomlinson, Ian, Torres, Diana, Truong, Thérèse, Tsimiklis, Helen, Tung, Nadine, Tworoger, Shelley S., Tyrer, Jonathan P., Vachon, Celine M., Van 't Veer, Laura J., van Altena, Anne M., Van Asperen, C.J., van den Berg, David, van den Ouweland, Ans M.W., van Doorn, Helena C., Van Nieuwenhuysen, Els, van Rensburg, Elizabeth J., Vergote, Ignace, Verhoef, Senno, Vierkant, Robert A., Vijai, Joseph, Vitonis, Allison F., von Wachenfeldt, Anna, Walsh, Christine, Wang, Qin, Wang-Gohrke, Shan, Wappenschmidt, Barbara, Weischer, Maren, Weitzel, Jeffrey N., Weltens, Caroline, Wentzensen, Nicolas, Whittemore, Alice S., Wilkens, Lynne R., Winqvist, Robert, Wu, Anna H., Wu, Xifeng, Yang, Hannah P., Zaffaroni, Daniela, Pilar Zamora, M., Zheng, Wei, Ziogas, Argyrios, Chenevix-Trench, Georgia, Pharoah, Paul D.P., Rookus, Matti A., Hooning, Maartje J., Goode, Ellen L.

Source: In Gynecologic Oncology May 2016 141(2):386-401

Clinical and genetic analyses of a Swedish patient series diagnosed with ataxia.

Authors: Gorcenco, Sorina, Kafantari, Efthymia, Wallenius, Joel, Karremo, Christin, Alinder, Erik, Dobloug, Sigurd, Landqvist Waldö, Maria, Englund, Elisabet, Ehrencrona, Hans, Wictorin, Klas, Karrman, Kristina, Puschmann, Andreas

Source: Journal of Neurology; Jan2024, Vol. 271 Issue 1, p526-542, 17p

Subject Terms: FRIEDREICH'S ataxia, MEDICAL genetics, WHOLE genome sequencing, ATAXIA, GENETIC variation

Presence of FLT3-ITD and high BAALC expression are independent prognostic markers in childhood acute myeloid leukemia

Authors: Staffas, Anna ^*, Kanduri, Meena ^*, Hovland, Randi, Rosenquist, Richard, Ommen, Hans Beier, Abrahamsson, Jonas, Forestier, Erik, Jahnukainen, Kirsi, Jónsson, Ólafur G., Zeller, Bernward, Palle, Josefine, Lönnerholm, Gudmar, Hasle, Henrik, Palmqvist, Lars, Ehrencrona, Hans

Source: In Blood 24 November 2011 118(22):5905-5913

Combination of pegylated IFN-α2b with imatinib increases molecular response rates in patients with low- or intermediate-risk chronic myeloid leukemia

Authors: Simonsson, Bengt, Gedde-Dahl, Tobias, Markevärn, Berit, Remes, Kari, Stentoft, Jesper, Almqvist, Anders, Björeman, Mats, Flogegård, Max, Koskenvesa, Perttu, Lindblom, Anders, Malm, Claes, Mustjoki, Satu, Myhr-Eriksson, Kristina, Ohm, Lotta, Räsänen, Anu, Sinisalo, Marjatta, Själander, Anders, Strömberg, Ulla, Bjerrum, Ole Weiss, Ehrencrona, Hans, Gruber, Franz, Kairisto, Veli, Olsson, Karin, Sandin, Fredrik, Nagler, Arnon, Nielsen, Johan Lanng, Hjorth-Hansen, Henrik, Porkka, Kimmo

Source: In Blood 22 September 2011 118(12):3228-3235

Extended genetic analysis and tumor characteristics in over 4600 women with suspected hereditary breast and ovarian cancer.

Authors: Öfverholm, Anna, Törngren, Therese, Rosén, Anna, Arver, Brita, Einbeigi, Zakaria, Haraldsson, Karin, Ståhlbom, Anne Kinhult, Kuchinskaya, Ekaterina, Lindblom, Annika, Melin, Beatrice, Paulsson-Karlsson, Ylva, Stenmark-Askmalm, Marie, Tham, Emma, von Wachenfeldt, Anna, Kvist, Anders, Borg, Åke, Ehrencrona, Hans

Source: BMC Cancer; 8/10/2023, Vol. 23 Issue 1, p1-12, 12p

Subject Terms: HEREDITARY cancer syndromes, OVARIAN cancer, BRCA genes, BREAST cancer, TRIPLE-negative breast cancer, CANCER genes, GENETIC testing, MEDICAL registries, TRAUMA registries

Geographic Terms: SWEDEN

Establishment of the first World Health Organization International Genetic Reference Panel for quantitation of BCR-ABL mRNA

Authors: White, Helen E., Matejtschuk, Paul, Rigsby, Peter, Gabert, Jean, Lin, Feng, Lynn Wang, Y., Branford, Susan, Müller, Martin C., Beaufils, Nathalie, Beillard, Emmanuel, Colomer, Dolors, Dvorakova, Dana, Ehrencrona, Hans, Goh, Hyun-Gyung, El Housni, Hakim, Jones, Dan, Kairisto, Veli, Kamel-Reid, Suzanne, Kim, Dong-Wook, Langabeer, Stephen, Ma, Edmond S.K., Press, Richard D., Romeo, Giuliana, Wang, Lihui, Zoi, Katerina, Hughes, Timothy, Saglio, Giuseppe, Hochhaus, Andreas, Goldman, John M., Metcalfe, Paul ^*, Cross, Nicholas C.P. ^*

Source: In Blood 25 November 2010 116(22):e111-e117

Comparison of imatinib 400 mg and 800 mg daily in the front-line treatment of high-risk, Philadelphia-positive chronic myeloid leukemia: a European LeukemiaNet Study

Authors: Baccarani, Michele, Rosti, Gianantonio, Castagnetti, Fausto, Haznedaroglu, Ibrahim, Porkka, Kimmo, Abruzzese, Elisabetta, Alimena, Giuliana, Ehrencrona, Hans, Hjorth-Hansen, Henrik, Kairisto, Veli, Levato, Luciano, Martinelli, Giovanni, Nagler, Arnon, Lanng Nielsen, Johan, Ozbek, Ugur, Palandri, Francesca, Palmieri, Fausto, Pane, Fabrizio, Rege-Cambrin, Giovanna, Russo, Domenico, Specchia, Giorgina, Testoni, Nicoletta, Weiss-Bjerrum, Ole, Saglio, Giuseppe, Simonsson, Bengt

Source: In Blood 7 May 2009 113(19):4497-4504

Molecular characteristics of breast tumors in patients screened for germline predisposition from a population-based observational study.

Authors: Nacer, Deborah F., Vallon-Christersson, Johan, Nordborg, Nicklas, Ehrencrona, Hans, Kvist, Anders, Borg, Åke, Staaf, Johan

Source: Genome Medicine; 4/14/2023, Vol. 15 Issue 1, p1-20, 20p

Subject Terms: BREAST, BREAST tumors, MEDICAL screening, TRIPLE-negative breast cancer, GENETIC testing, GERM cells

Geographic Terms: SWEDEN

Building a precision medicine infrastructure at a national level: The Swedish experience.

Authors: Edsjö, Anders, Lindstrand, Anna, Gisselsson, David, Mölling, Paula, Friedman, Mikaela, Cavelier, Lucia, Johansson, Maria, Ehrencrona, Hans, Fagerqvist, Therese, Strid, Tobias, Lovmar, Lovisa, Jacobsson, Bo, Johansson, Åsa, Engstrand, Lars, Wheelock, Craig E., Sikora, Per, Wirta, Valtteri, Fioretos, Thoas, Rosenquist, Richard

Source: Cambridge Prisms: Precision Medicine; 2023, Vol. 1, p1-16, 16p

Subject Terms: INDIVIDUALIZED medicine, COMMUNICABLE diseases, PHARMACOGENOMICS, RARE diseases, GRAND strategy (Political science), EXPERTISE

Geographic Terms: SWEDEN

Genetic testing in women with early-onset breast cancer: a Traceback pilot study.

Authors: Augustinsson, Annelie, Nilsson, Martin P., Ellberg, Carolina, Kristoffersson, Ulf, Olsson, Håkan, Ehrencrona, Hans

Source: Breast Cancer Research & Treatment; Nov2021, Vol. 190 Issue 2, p307-315, 9p