Ulf Kristoffersson

Ulf Kristoffersson

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Ulf Kristoffersson

Publications by authors named "Ulf Kristoffersson"

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56Publications

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A stroke gene panel for whole-exome sequencing.

Eur J Hum Genet 2019 02 24;27(2):317-324. Epub 2018 Oct 24.

Department of Clinical Sciences Lund, Neurology, Lund University, Lund, Sweden.

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http://www.nature.com/articles/s41431-018-0274-4
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http://dx.doi.org/10.1038/s41431-018-0274-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6336868PMC
February 2019

Accuracy of self-reported family history of cancer, mutation status and tumor characteristics in patients with early onset breast cancer.

Acta Oncol 2018 May 22;57(5):595-603. Epub 2017 Nov 22.

a Department of Clinical Sciences in Lund, Oncology and Pathology , Lund University , Lund , Sweden.

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http://dx.doi.org/10.1080/0284186X.2017.1404635DOI Listing
May 2018

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

Breast Cancer Res Treat 2018 Feb 21;168(1):117-126. Epub 2017 Nov 21.

Division of Oncology and Pathology, Department of Clinical Sciences, Lund University, Lund, Sweden.

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http://dx.doi.org/10.1007/s10549-017-4584-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5847037PMC
February 2018

Utvidgad anlagsbärartestning kan bredda fosterdiagnostiken - Recessiva sjukdomsanlag kan kartläggas hos friska personer inför planerad graviditet.

Lakartidningen 2018 02 1;115. Epub 2018 Feb 1.

Clinical genetics - LAboratory medicine Lund, Sweden Clinical genetics - LAboratory medicine Lund, Sweden.

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February 2018

From Mendel to Medical Genetics.

Eur J Hum Genet 2017 12;25(s2):S53-S59

Charles University and Motol University Hospital, Prague, Czech Republic.

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http://dx.doi.org/10.1038/ejhg.2017.157DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5763265PMC
December 2017

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

Eur J Hum Genet 2015 Jun 24;23(6):729-35. Epub 2014 Sep 24.

1] Institute for Health Economics and Health Care Management, Helmholtz Zentrum München, German Research Center for Environmental Health (GmbH), Neuherberg, Germany [2] Institute and Outpatient Clinic for Occupational, Social and Environmental Medicine, Clinical Center, Ludwig Maximilians University, Munich, Germany.

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http://dx.doi.org/10.1038/ejhg.2014.190DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795066PMC
June 2015

Developing a framework for implementation of genetic services: learning from examples of testing for monogenic forms of common diseases.

J Community Genet 2014 Oct 4;5(4):337-47. Epub 2014 Jun 4.

Department of Clinical Genetics, EMGO Institute for Health and Care Research, VU University Medical Center (BS7, D450), PO Box 7057, 1007, Amsterdam, The Netherlands.

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http://dx.doi.org/10.1007/s12687-014-0189-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4159469PMC
October 2014

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

Breast Cancer Res Treat 2014 Oct 4;147(3):571-8. Epub 2014 Sep 4.

Department of Oncology, Skåne University Hospital, Clinical Sciences, Lund University, Lund, Sweden,

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http://dx.doi.org/10.1007/s10549-014-3115-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174291PMC
October 2014

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

Breast Cancer Res Treat 2014 Feb 30;144(1):133-42. Epub 2014 Jan 30.

Department of Oncology, Skåne University Hospital, Clinical Sciences, Lund University, S-221 85, Lund, Sweden,

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http://dx.doi.org/10.1007/s10549-014-2842-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3924030PMC
February 2014

Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnostics.

Hum Mutat 2013 Oct 16;34(10):1322-8. Epub 2013 Jul 16.

Department of Clinical Genetics, Section of Community Genetics and the EMGO Institute for Health and Care Research, VU University Medical Center, Amsterdam, The Netherlands.

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http://dx.doi.org/10.1002/humu.22370DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4285964PMC
October 2013

Genetics and democracy-what is the issue?

J Community Genet 2013 Apr 25;4(2):181-8. Epub 2012 Jul 25.

Department of Arts and Cultural Sciences, Ethnology, Lund University, Biskopsgatan 7, 223 62, Lund, Sweden,

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http://dx.doi.org/10.1007/s12687-012-0109-xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3666837PMC
April 2013

A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers.

Authors:
Yuan C Ding Lesley McGuffog Sue Healey Eitan Friedman Yael Laitman Shani- Paluch-Shimon Bella Kaufman Annelie Liljegren Annika Lindblom Håkan Olsson Ulf Kristoffersson Marie Stenmark-Askmalm Beatrice Melin Susan M Domchek Katherine L Nathanson Timothy R Rebbeck Anna Jakubowska Jan Lubinski Katarzyna Jaworska Katarzyna Durda Jacek Gronwald Tomasz Huzarski Cezary Cybulski Tomasz Byrski Ana Osorio Teresa Ramóny Cajal Alexandra V Stavropoulou Javier Benítez Ute Hamann Matti Rookus Cora M Aalfs Judith L de Lange Hanne E J Meijers-Heijboer Jan C Oosterwijk Christi J van Asperen Encarna B Gómez García Nicoline Hoogerbrugge Agnes Jager Rob B van der Luijt Douglas F Easton Susan Peock Debra Frost Steve D Ellis Radka Platte Elena Fineberg D Gareth Evans Fiona Lalloo Louise Izatt Ros Eeles Julian Adlard Rosemarie Davidson Diana Eccles Trevor Cole Jackie Cook Carole Brewer Marc Tischkowitz Andrew K Godwin Harsh Pathak Dominique Stoppa-Lyonnet Olga M Sinilnikova Sylvie Mazoyer Laure Barjhoux Mélanie Léoné Marion Gauthier-Villars Virginie Caux-Moncoutier Antoine de Pauw Agnès Hardouin Pascaline Berthet Hélène Dreyfus Sandra Fert Ferrer Marie-Agnès Collonge-Rame Johanna Sokolowska Saundra Buys Mary Daly Alex Miron Mary Beth Terry Wendy Chung Esther M John Melissa Southey David Goldgar Christian F Singer Muy-Kheng Maria Tea Daphne Gschwantler-Kaulich Anneliese Fink-Retter Thomas V O Hansen Bent Ejlertsen Oskar T Johannsson Kenneth Offit Kara Sarrel Mia M Gaudet Joseph Vijai Mark Robson Marion R Piedmonte Lesley Andrews David Cohn Leslie R DeMars Paul DiSilvestro Gustavo Rodriguez Amanda Ewart Toland Marco Montagna Simona Agata Evgeny Imyanitov Claudine Isaacs Ramunas Janavicius Conxi Lazaro Ignacio Blanco Susan J Ramus Lara Sucheston Beth Y Karlan Jenny Gross Patricia A Ganz Mary S Beattie Rita K Schmutzler Barbara Wappenschmidt Alfons Meindl Norbert Arnold Dieter Niederacher Sabine Preisler-Adams Dorotehea Gadzicki Raymonda Varon-Mateeva Helmut Deissler Andrea Gehrig Christian Sutter Karin Kast Heli Nevanlinna Kristiina Aittomäki Jacques Simard Amanda B Spurdle Jonathan Beesley Xiaoqing Chen Gail E Tomlinson Jeffrey Weitzel Judy E Garber Olufunmilayo I Olopade Wendy S Rubinstein Nadine Tung Joanne L Blum Steven A Narod Sean Brummel Daniel L Gillen Noralane Lindor Zachary Fredericksen Vernon S Pankratz Fergus J Couch Paolo Radice Paolo Peterlongo Mark H Greene Jennifer T Loud Phuong L Mai Irene L Andrulis Gord Glendon Hilmi Ozcelik Anne-Marie Gerdes Mads Thomassen Uffe Birk Jensen Anne-Bine Skytte Maria A Caligo Andrew Lee Georgia Chenevix-Trench Antonis C Antoniou Susan L Neuhausen

Cancer Epidemiol Biomarkers Prev 2012 Aug 22;21(8):1362-70. Epub 2012 Jun 22.

Department of Population Sciences, Beckman Research Institute of City of Hope, Duarte, California 91010, USA.

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http://dx.doi.org/10.1158/1055-9965.EPI-12-0229DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3415567PMC
August 2012

Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers.

Authors:
Susan J Ramus Antonis C Antoniou Karoline B Kuchenbaecker Penny Soucy Jonathan Beesley Xiaoqing Chen Lesley McGuffog Olga M Sinilnikova Sue Healey Daniel Barrowdale Andrew Lee Mads Thomassen Anne-Marie Gerdes Torben A Kruse Uffe Birk Jensen Anne-Bine Skytte Maria A Caligo Annelie Liljegren Annika Lindblom Håkan Olsson Ulf Kristoffersson Marie Stenmark-Askmalm Beatrice Melin Susan M Domchek Katherine L Nathanson Timothy R Rebbeck Anna Jakubowska Jan Lubinski Katarzyna Jaworska Katarzyna Durda Elżbieta Złowocka Jacek Gronwald Tomasz Huzarski Tomasz Byrski Cezary Cybulski Aleksandra Toloczko-Grabarek Ana Osorio Javier Benitez Mercedes Duran Maria-Isabel Tejada Ute Hamann Matti Rookus Flora E van Leeuwen Cora M Aalfs Hanne E J Meijers-Heijboer Christi J van Asperen K E P van Roozendaal Nicoline Hoogerbrugge J Margriet Collée Mieke Kriege Rob B van der Luijt Susan Peock Debra Frost Steve D Ellis Radka Platte Elena Fineberg D Gareth Evans Fiona Lalloo Chris Jacobs Ros Eeles Julian Adlard Rosemarie Davidson Diana Eccles Trevor Cole Jackie Cook Joan Paterson Fiona Douglas Carole Brewer Shirley Hodgson Patrick J Morrison Lisa Walker Mary E Porteous M John Kennedy Harsh Pathak Andrew K Godwin Dominique Stoppa-Lyonnet Virginie Caux-Moncoutier Antoine de Pauw Marion Gauthier-Villars Sylvie Mazoyer Mélanie Léoné Alain Calender Christine Lasset Valérie Bonadona Agnès Hardouin Pascaline Berthet Yves-Jean Bignon Nancy Uhrhammer Laurence Faivre Catherine Loustalot Saundra Buys Mary Daly Alex Miron Mary Beth Terry Wendy K Chung Esther M John Melissa Southey David Goldgar Christian F Singer Muy-Kheng Tea Georg Pfeiler Anneliese Fink-Retter Thomas v O Hansen Bent Ejlertsen Oskar Th Johannsson Kenneth Offit Tomas Kirchhoff Mia M Gaudet Joseph Vijai Mark Robson Marion Piedmonte Kelly-Anne Phillips Linda Van Le James S Hoffman Amanda Ewart Toland Marco Montagna Silvia Tognazzo Evgeny Imyanitov Claudine Issacs Ramunas Janavicius Conxi Lazaro Iganacio Blanco Eva Tornero Matilde Navarro Kirsten B Moysich Beth Y Karlan Jenny Gross Edith Olah Tibor Vaszko Soo-Hwang Teo Patricia A Ganz Mary S Beattie Cecelia M Dorfling Elizabeth J van Rensburg Orland Diez Ava Kwong Rita K Schmutzler Barbara Wappenschmidt Christoph Engel Alfons Meindl Nina Ditsch Norbert Arnold Simone Heidemann Dieter Niederacher Sabine Preisler-Adams Dorotehea Gadzicki Raymonda Varon-Mateeva Helmut Deissler Andrea Gehrig Christian Sutter Karin Kast Britta Fiebig Dieter Schäfer Trinidad Caldes Miguel de la Hoya Heli Nevanlinna Kristiina Aittomäki Marie Plante Amanda B Spurdle Susan L Neuhausen Yuan Chun Ding Xianshu Wang Noralane Lindor Zachary Fredericksen V Shane Pankratz Paolo Peterlongo Siranoush Manoukian Bernard Peissel Daniela Zaffaroni Bernardo Bonanni Loris Bernard Riccardo Dolcetti Laura Papi Laura Ottini Paolo Radice Mark H Greene Phuong L Mai Irene L Andrulis Gord Glendon Hilmi Ozcelik Paul D P Pharoah Simon A Gayther Jacques Simard Douglas F Easton Fergus J Couch Georgia Chenevix-Trench

Hum Mutat 2012 Apr 14;33(4):690-702. Epub 2012 Feb 14.

Department of Preventive Medicine, Keck School of Medicine, University of Southern California, California, USA.

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http://dx.doi.org/10.1002/humu.22025DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458423PMC
April 2012

Definitions of genetic testing in European legal documents.

J Community Genet 2012 Apr 26;3(2):125-41. Epub 2012 Jan 26.

Institute for Molecular and Cell Biology (IBMC), University of Porto, R. Campo Alegre 823, 4150-180, Porto, Portugal.

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http://dx.doi.org/10.1007/s12687-012-0077-1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312943PMC
April 2012

Editorial: genetics and democracy.

J Community Genet 2012 Apr 9;3(2):57-9. Epub 2012 Mar 9.

Department of Political Science, Lund University, Lund, Sweden.

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http://link.springer.com/10.1007/s12687-012-0088-y
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http://dx.doi.org/10.1007/s12687-012-0088-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3312945PMC
April 2012

Increased incidence of childhood, prostate and breast cancers in relatives of childhood cancer patients.

Fam Cancer 2012 Mar;11(1):145-55

Department of Oncology, Clinical Sciences, Lund University, Barngatan 2B, 22185, Lund, Sweden.

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http://dx.doi.org/10.1007/s10689-011-9493-3DOI Listing
March 2012

Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer.

JAMA 2012 Jan;307(4):382-90

Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1001/jama.2012.20DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3727895PMC
January 2012

Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation.

Eur J Med Genet 2011 Jul-Aug;54(4):e383-8. Epub 2011 Mar 21.

Wilhelm Johannsen Centre for Functional Genome Research, Department of Cellular and Molecular Medicine, University of Copenhagen, Copenhagen N, Denmark.

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https://linkinghub.elsevier.com/retrieve/pii/S17697212110004
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http://dx.doi.org/10.1016/j.ejmg.2011.03.008DOI Listing
October 2011

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

Breast Cancer Res 2010 29;12(6):R102. Epub 2010 Nov 29.

Division of Genetics and Population Health, Queensland Institute of Medical Research, Brisbane, Australia.

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http://dx.doi.org/10.1186/bcr2785DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3046447PMC
September 2011

Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers.

Authors:
Susan J Ramus Christiana Kartsonaki Simon A Gayther Paul D P Pharoah Olga M Sinilnikova Jonathan Beesley Xiaoqing Chen Lesley McGuffog Sue Healey Fergus J Couch Xianshu Wang Zachary Fredericksen Paolo Peterlongo Siranoush Manoukian Bernard Peissel Daniela Zaffaroni Gaia Roversi Monica Barile Alessandra Viel Anna Allavena Laura Ottini Laura Papi Viviana Gismondi Fabio Capra Paolo Radice Mark H Greene Phuong L Mai Irene L Andrulis Gord Glendon Hilmi Ozcelik Mads Thomassen Anne-Marie Gerdes Torben A Kruse Dorthe Cruger Uffe Birk Jensen Maria Adelaide Caligo Håkan Olsson Ulf Kristoffersson Annika Lindblom Brita Arver Per Karlsson Marie Stenmark Askmalm Ake Borg Susan L Neuhausen Yuan Chun Ding Katherine L Nathanson Susan M Domchek Anna Jakubowska Jan Lubiński Tomasz Huzarski Tomasz Byrski Jacek Gronwald Bohdan Górski Cezary Cybulski Tadeusz Dębniak Ana Osorio Mercedes Durán Maria-Isabel Tejada Javier Benítez Ute Hamann Matti A Rookus Senno Verhoef Madeleine A Tilanus-Linthorst Maaike P Vreeswijk Danielle Bodmer Margreet G E M Ausems Theo A van Os Christi J Asperen Marinus J Blok Hanne E J Meijers-Heijboer Susan Peock Margaret Cook Clare Oliver Debra Frost Alison M Dunning D Gareth Evans Ros Eeles Gabriella Pichert Trevor Cole Shirley Hodgson Carole Brewer Patrick J Morrison Mary Porteous M John Kennedy Mark T Rogers Lucy E Side Alan Donaldson Helen Gregory Andrew Godwin Dominique Stoppa-Lyonnet Virginie Moncoutier Laurent Castera Sylvie Mazoyer Laure Barjhoux Valérie Bonadona Dominique Leroux Laurence Faivre Rosette Lidereau Catherine Nogues Yves-Jean Bignon Fabienne Prieur Marie-Agnès Collonge-Rame Laurence Venat-Bouvet Sandra Fert-Ferrer Alex Miron Saundra S Buys John L Hopper Mary B Daly Esther M John Mary Beth Terry David Goldgar Thomas v O Hansen Lars Jønson Bent Ejlertsen Bjarni A Agnarsson Kenneth Offit Tomas Kirchhoff Joseph Vijai Ana V C Dutra-Clarke Jennifer A Przybylo Marco Montagna Cinzia Casella Evgeny N Imyanitov Ramunas Janavicius Ignacio Blanco Conxi Lázaro Kirsten B Moysich Beth Y Karlan Jenny Gross Mary S Beattie Rita Schmutzler Barbara Wappenschmidt Alfons Meindl Ina Ruehl Britta Fiebig Christian Sutter Norbert Arnold Helmut Deissler Raymonda Varon-Mateeva Karin Kast Dieter Niederacher Dorothea Gadzicki Trinidad Caldes Miguel de la Hoya Heli Nevanlinna Kristiina Aittomäki Jacques Simard Penny Soucy Amanda B Spurdle Helene Holland Georgia Chenevix-Trench Douglas F Easton Antonis C Antoniou

J Natl Cancer Inst 2011 Jan 17;103(2):105-16. Epub 2010 Dec 17.

Department of Gynaecological Oncology, UCL EGA Institute for Women's Health, University College London, London, UK.

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http://dx.doi.org/10.1093/jnci/djq494DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3107565PMC
January 2011

Association of the variants CASP8 D302H and CASP10 V410I with breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers.

Cancer Epidemiol Biomarkers Prev 2010 Nov 26;19(11):2859-68. Epub 2010 Oct 26.

Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Leipzig, Germany.

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http://dx.doi.org/10.1158/1055-9965.EPI-10-0517DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3077716PMC
November 2010

Scope of definitions of genetic testing: evidence from a EuroGentest survey.

J Community Genet 2010 Mar 16;1(1):29-35. Epub 2010 Mar 16.

UnIGENe and CGPP, IBMC-Institute for Molecular and Cell Biology, University of Porto, R. Campo Alegre 823, 4150-180, Porto, Portugal.

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http://dx.doi.org/10.1007/s12687-010-0004-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185974PMC
March 2010

[Hereditary risk of sudden cardiac death--genetic investigation of the family].

Lakartidningen 2009 Apr 7-21;106(15-16):1089-93

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June 2009

Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes.

Fam Cancer 2008 15;7(4):331-7. Epub 2008 May 15.

Department of Oncology, Institution of Clinical Sciences, Lund University, Lund University Hospital, Lund, 22185, Sweden.

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http://dx.doi.org/10.1007/s10689-008-9195-7DOI Listing
January 2009

Regulations and practices of genetic counselling in 38 European countries: the perspective of national representatives.

Eur J Hum Genet 2008 Oct 14;16(10):1208-16. Epub 2008 May 14.

Department of Medical Genetics, University of Turku, Turku, Finland.

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http://dx.doi.org/10.1038/ejhg.2008.93DOI Listing
October 2008

Regulatory issues for genetic testing in clinical practice.

Mol Biotechnol 2008 Sep 13;40(1):113-7. Epub 2008 Feb 13.

Department of Clinical Genetics, University Hospital, SE-221 85, Lund, Sweden.

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http://dx.doi.org/10.1007/s12033-008-9041-zDOI Listing
September 2008

Ischaemic stroke in hypertensive patients is associated with variations in the PDE4D genome region.

Eur J Hum Genet 2008 Sep 9;16(9):1117-25. Epub 2008 Apr 9.

Department of Clinical Sciences, Lund, Neurology, Lund University Hospital, Lund, Sweden.

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http://dx.doi.org/10.1038/ejhg.2008.62DOI Listing
September 2008

What is ideal genetic counselling? A survey of current international guidelines.

Eur J Hum Genet 2008 Apr 16;16(4):445-52. Epub 2008 Jan 16.

Department of Medical Genetics, University of Turku, Turku, Finland.

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http://dx.doi.org/10.1038/sj.ejhg.5201983DOI Listing
April 2008

EuroGentest: DNA-based testing for heritable disorders in Europe.

Community Genet 2008 17;11(2):75-120. Epub 2008 Jan 17.

Department of Human Genetics, Hannover Medical School, Hannover, Germany.

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http://dx.doi.org/10.1159/000111984DOI Listing
March 2008

Cytogenetic Guidelines and Quality Assurance: a common European framework for quality assessment for constitutional and acquired cytogenetic investigations.

Eur J Hum Genet 2007 May 14;15(5):525-7. Epub 2007 Mar 14.

UKNEQAS for Clinical Cytogenetics, Women's Centre, John Radcliffe Hospital, Oxford, OX3 9DU, UK.

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http://dx.doi.org/10.1038/sj.ejhg.5201809DOI Listing
May 2007

Education in medical genetics for non-genetic health care providers in Sweden.

Community Genet 2006 ;9(4):240-5

Department of Clinical Genetics, University Hospital, Lund, Sweden.

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https://www.karger.com/Article/FullText/94472
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http://dx.doi.org/10.1159/000094472DOI Listing
February 2007

The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer.

Gynecol Oncol 2006 May 19;101(2):238-43. Epub 2005 Dec 19.

Department of Oncology, Institute of Clinical Sciences, Lund University Hospital, SE-221 85 Lund, Sweden.

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http://dx.doi.org/10.1016/j.ygyno.2005.10.029DOI Listing
May 2006

[New discoveries about the fragile X syndrome complicate genetic counseling. More symptoms than earlier known caused by the disease gene].

Lakartidningen 2005 Oct 31-Nov 6;102(44):3232-4, 3236

Universitetssjukhuset i Lund.

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December 2005

[New knowledge of inheritance and heredity and new aspects of heart disease].

Lakartidningen 2005 Mar 14-20;102(11):826-7

Genetiska kliniken, Universitetssjukhuset i Lund.

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April 2005

The need for oncogenetic counselling. Ten years' experience of a regional oncogenetic clinic.

Acta Oncol 2004 ;43(7):637-49

South Swedish Tumour Registry, University Hospital, Lund, Sweden.

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http://dx.doi.org/10.1080/02841860410018520DOI Listing
February 2005

Regulation of genetic testing in clinical practice.

Methods Mol Med 2004 ;92:369-75

Department of Clinical Genetics, University Hospital, Lund, Sweden.

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April 2004

[An ethical dilemma: pharmacogenetic tests can yield unwanted information].

Lakartidningen 2003 Jun;100(25):2241-2

Genetiska kliniken, Universitetssjukhuset, Lund.

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June 2003