Clinical Cancer Genetic Service in Sweden

por Kristoffersson, Ulf
Publicado 1999

From Mendel to Medical Genetics

por Kristoffersson, Ulf, Macek, Milan
Publicado 2017

A century of Hereditas: from local publication to international journal

por Tunlid, Anna, Kristoffersson, Ulf, Åström, Fredrik
Publicado 2020

Correction to: A century of Hereditas: from local publication to international journal

por Tunlid, Anna, Kristoffersson, Ulf, Åström, Fredrik
Publicado 2021

Broad phenotypic spectrum in familial adenomatous polyposis; from early onset and severe phenotypes to late onset of attenuated polyposis with the first manifestation at age 72

por Nilbert, Mef, Kristoffersson, Ulf, Ericsson, Mats, Johannsson, Oskar, Rambech, Eva, Mangell, Peter
Publicado 2008

Long-term prognosis of early-onset breast cancer in a population-based cohort with a known BRCA1/2 mutation status

por Nilsson, Martin P., Hartman, Linda, Idvall, Ingrid, Kristoffersson, Ulf, Johannsson, Oskar T., Loman, Niklas
Publicado 2014

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

por Augustinsson, Annelie, Nilsson, Martin P., Ellberg, Carolina, Kristoffersson, Ulf, Olsson, Håkan, Ehrencrona, Hans
Publicado 2021

Efficacy versus effectiveness of clinical genetic testing criteria for BRCA1 and BRCA2 hereditary mutations in incident breast cancer

por Nilsson, Martin P., Winter, Christof, Kristoffersson, Ulf, Rehn, Martin, Larsson, Christer, Saal, Lao H., Loman, Niklas
Publicado 2017

BRCAsearch: written pre-test information and BRCA1/2 germline mutation testing in unselected patients with newly diagnosed breast cancer

por Nilsson, Martin P., Törngren, Therese, Henriksson, Karin, Kristoffersson, Ulf, Kvist, Anders, Silfverberg, Barbro, Borg, Åke, Loman, Niklas
Publicado 2017

High risk of in-breast tumor recurrence after BRCA1/2-associated breast cancer

por Nilsson, Martin P., Hartman, Linda, Kristoffersson, Ulf, Johannsson, Oskar T., Borg, Åke, Henriksson, Karin, Lanke, Elsa, Olsson, Håkan, Loman, Niklas
Publicado 2014

Updated Stroke Gene Panels: Rapid evolution of knowledge on monogenic causes of stroke

por Ilinca, Andreea, Puschmann, Andreas, Putaala, Jukka, de Leeuw, Frank Erik, Cole, John, Kittner, Stephen, Kristoffersson, Ulf, Lindgren, Arne G.
Publicado 2022

Germline mutations in BRCA1 and BRCA2 incidentally revealed in a biobank research study: experiences from re-contacting mutation carriers and relatives

por Nilsson, Martin P., Emmertz, Monica, Kristoffersson, Ulf, Borg, Åke, Larsson, Christer, Rehn, Martin, Winter, Christof, Saal, Lao H., Brandberg, Yvonne, Loman, Niklas
Publicado 2017

Prevalence of germline pathogenic variants in 22 cancer susceptibility genes in Swedish pediatric cancer patients

por von Stedingk, Kristoffer, Stjernfelt, Karl-Johan, Kvist, Anders, Wahlström, Cecilia, Kristoffersson, Ulf, Stenmark-Askmalm, Marie, Wiebe, Thomas, Hjorth, Lars, Koster, Jan, Olsson, Håkan, Øra, Ingrid
Publicado 2021

General practitioner management of genetic aspects of a cardiac disease: a scenario-based study to anticipate providers’ practices

por Challen, Kirsty, Harris, Hilary, Kristoffersson, Ulf, Nippert, Irmgard, Schmidtke, Joerg, Ten Kate, Leo P., Benjamin, Caroline, Anionwu, Elizabeth, Plass, Anne-Marie, Julian-Reynier, Claire, Harris, Rodney
Publicado 2010

Reflecting on Earlier Experiences with Unsolicited Findings: Points to Consider for Next-Generation Sequencing and Informed Consent in Diagnostics

por Rigter, Tessel, Henneman, Lidewij, Kristoffersson, Ulf, Hall, Alison, Yntema, Helger G, Borry, Pascal, Tönnies, Holger, Waisfisz, Quinten, Elting, Mariet W, Dondorp, Wybo J, Cornel, Martina C
Publicado 2013

Community genetics. Its definition 2010

por ten Kate, Leo P., Al-Gazali, Lihadh, Anand, Sonia, Bittles, Alan, Cassiman, Jean-Jacques, Christianson, Arnold, Cornel, Martina C., Hamamy, Hanan, Kääriäinen, Helena, Kristoffersson, Ulf, Marais, David, Penchaszadeh, Victor B., Rahman, Proton, Schmidtke, Jörg
Publicado 2010

Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness

por Severin, Franziska, Borry, Pascal, Cornel, Martina C, Daniels, Norman, Fellmann, Florence, Victoria Hodgson, Shirley, Howard, Heidi C, John, Jürgen, Kääriäinen, Helena, Kayserili, Hülya, Kent, Alastair, Koerber, Florian, Kristoffersson, Ulf, Kroese, Mark, Lewis, Celine, Marckmann, Georg, Meyer, Peter, Pfeufer, Arne, Schmidtke, Jörg, Skirton, Heather, Tranebjærg, Lisbeth, Rogowski, Wolf H
Publicado 2015

Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers

por Walker, Logan C, Fredericksen, Zachary S, Wang, Xianshu, Tarrell, Robert, Pankratz, Vernon S, Lindor, Noralane M, Beesley, Jonathan, Healey, Sue, Chen, Xiaoqing, Stoppa-Lyonnet, Dominique, Tirapo, Carole, Giraud, Sophie, Mazoyer, Sylvie, Muller, Danièle, Fricker, Jean-Pierre, Delnatte, Capucine, Schmutzler, Rita K, Wappenschmidt, Barbara, Engel, Christoph, Schönbuchner, Ines, Deissler, Helmut, Meindl, Alfons, Hogervorst, Frans B, Verheus, Martijn, Hooning, Maartje J, van den Ouweland, Ans MW, Nelen, Marcel R, Ausems, Margreet GEM, Aalfs, Cora M, van Asperen, Christi J, Devilee, Peter, Gerrits, Monique M, Waisfisz, Quinten, Szabo, Csilla I, Easton, Douglas F, Peock, Susan, Cook, Margaret, Oliver, Clare T, Frost, Debra, Harrington, Patricia, Evans, D Gareth, Lalloo, Fiona, Eeles, Ros, Izatt, Louise, Chu, Carol, Davidson, Rosemarie, Eccles, Diana, Ong, Kai-Ren, Cook, Jackie, Rebbeck, Tim, Nathanson, Katherine L, Domchek, Susan M, Singer, Christian F, Gschwantler-Kaulich, Daphne, Dressler, Anne-Catharina, Pfeiler, Georg, Godwin, Andrew K, Heikkinen, Tuomas, Nevanlinna, Heli, Agnarsson, Bjarni A, Caligo, Maria Adelaide, Olsson, Håkan, Kristoffersson, Ulf, Liljegren, Annelie, Arver, Brita, Karlsson, Per, Melin, Beatrice, Sinilnikova, Olga M, McGuffog, Lesley, Antoniou, Antonis C, Chenevix-Trench, Georgia, Spurdle, Amanda B, Couch, Fergus J
Publicado 2010