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- 2024
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Mark
Retrospective genetic testing (Traceback) in women with early-onset breast cancer after revised national guidelines : a clinical implementation study
2024) In Breast Cancer Research and Treatment(
- Contribution to journal › Article
- 2023
-
Mark
Validation of immunofluorescence analysis of blood smears in patients with inherited platelet disorders
(
- Contribution to journal › Article
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Mark
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
(
- Contribution to journal › Article
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Mark
Extended genetic analysis and tumor characteristics in over 4600 women with suspected hereditary breast and ovarian cancer
(
- Contribution to journal › Article
- 2022
-
Mark
Merged testing for colorectal cancer syndromes and re-evaluation of genetic variants improve diagnostic yield : Results from a nationwide prospective cohort
(
- Contribution to journal › Article
- 2021
-
Mark
Breast cancer in young women. Aspects of heredity and contralateral disease.
2021) In Lund University, Faculty of Medicine Doctoral Dissertation Series(
- Thesis › Doctoral thesis (compilation)
-
Mark
Genetic testing in women with early-onset breast cancer : a Traceback pilot study
(
- Contribution to journal › Article
- 2020
-
Mark
Parental anxiety after 5 years of participation in a longitudinal study of children at high risk of type 1 diabetes
(
- Contribution to journal › Article
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Mark
Transparency, consent and trust in the use of customers' data by an online genetic testing company : an Exploratory survey among 23andMe users
(
- Contribution to journal › Article
- 2019
-
Mark
Genetic counselling and testing of susceptibility genes for therapeutic decision-making in breast cancer—an European consensus statement and expert recommendations
(
- Contribution to journal › Article
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Mark
Idiopathic ventricular fibrillation – Long term prognosis in relation to clinical findings and ECG patterns in a Swedish cohort
(
- Contribution to journal › Article
- 2018
-
Mark
BRCAsearch : written pre-test information and BRCA1/2 germline mutation testing in unselected patients with newly diagnosed breast cancer
(
- Contribution to journal › Article
-
Mark
Enrichment of rare copy number variation in children with developmental language disorder
(
- Contribution to journal › Article
-
Mark
Multigene panel testing beyond BRCA1/2 in breast/ovarian cancer Spanish families and clinical actionability of findings
(
- Contribution to journal › Article
- 2017
-
Mark
Efficacy versus effectiveness of clinical genetic testing criteria for BRCA1 and BRCA2 hereditary mutations in incident breast cancer
(
- Contribution to journal › Article
-
Mark
Current ethical and legal issues in health-related direct-to-consumer genetic testing
(
- Contribution to journal › Scientific review
- 2015
-
Mark
Risk Screening, Testing, and Diagnosis : Ethical Aspects
2015) p.698-705(
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2014
-
Mark
Laboratory aspects of von Willebrand disease : test repertoire and options for activity assays and genetic analysis
(
- Contribution to journal › Scientific review
-
Mark
CDKN2A-mutation hos en familie med arveligt malignt melanom
(
- Contribution to journal › Article
-
Mark
Science and Regulation. Changes on the horizon for consumer genomics in the EU
(
- Contribution to journal › Article
-
Mark
Is There a Right Time to Know? : The Right Not to Know and Genetic Testing in Children
(
- Contribution to journal › Article
- 2012
-
Mark
Perceptions of genetic research and testing among members of families with an increased risk of malignant melanoma
(
- Contribution to journal › Article
-
Mark
Difficult Questions and Ambivalent Answers on Genetic Testing
(
- Contribution to journal › Article
- 2011
-
Mark
Tentative (id)entities: On technopolitical cultures and the experiencing of genetic testing
(
- Contribution to journal › Article
-
Mark
Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities Background Document to the ESHG recommendations on genetic testing and common disorders
(
- Contribution to journal › Article
-
Mark
High-resolution genomic screening in mantle cell lymphoma--specific changes correlate with genomic complexity, the proliferation signature and survival.
(
- Contribution to journal › Article
- 2009
-
Mark
Selection criteria for genetic assessment of patients with familial melanoma
(
- Contribution to journal › Scientific review
- 2008
-
Mark
Regulations and practices of genetic counselling in 38 European countries: the perspective of national representatives
(
- Contribution to journal › Article
-
Mark
What is ideal genetic counselling? A survey of current international guidelines
(
- Contribution to journal › Article
-
Mark
EuroGentest: DNA-based testing for heritable disorders in Europe
(
- Contribution to journal › Article
-
Mark
The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions
(
- Contribution to journal › Article
- 2007
-
Mark
Some ethical issues raised by personalized nutrition
(
- Contribution to journal › Article
-
Mark
...han fick det bättre i himmelen
(
- Contribution to journal › Article
- 2005
-
Mark
Genetic testing for maturity onset diabetes of the young: uptake, attitudes and comparison with hereditary non-polyposis colorectal cancer
(
- Contribution to journal › Article
-
Mark
Association of oestrogen receptor alpha gene polymorphisms with postmenopausal bone loss, bone mass, and quantitative ultrasound properties of bone
(
- Contribution to journal › Article
- 2004
-
Mark
External quality assessment for mutation detection in the BRCA1 and BRCA2 genes: EMQN's experience of 3 years
(
- Contribution to journal › Article
-
Mark
Inherited predisposition to early onset lung cancer according to histological type
(
- Contribution to journal › Article
-
Mark
Familial risk of urological cancers : data for clinical counseling
(
- Contribution to journal › Article
- 2003
-
Mark
Provision of genetic services in Europe: current practices and issues
(
- Contribution to journal › Article
- 2001
-
Mark
Family history of breast and ovarian cancers and BRCA1 and BRCA2 mutations in a population-based series of early-onset breast cancer
(
- Contribution to journal › Article
-
Mark
Predictive genetic screening and clinical findings in multiple endocrine neoplasia type I families
(
- Contribution to journal › Article
-
Mark
COL1A1 Sp1 polymorphism predicts perimenopausal and early postmenopausal spinal bone loss
(
- Contribution to journal › Article
- 2000
-
Mark
Risk perception, screening practice and interest in genetic testing among unaffected men in families with hereditary prostate cancer
(
- Contribution to journal › Article
- 1999
-
Mark
hMLH1, hMSH2 and hMSH6 mutations in hereditary non-polyposis colorectal cancer families from southern Sweden
(
- Contribution to journal › Article
-
Mark
Guidelines for follow-up of women at high risk for inherited breast cancer : consensus statement from the Biomed 2 Demonstration Programme on Inherited Breast Cancer
(
- Contribution to journal › Article
- 1998
-
Mark
Keimbahnmutationen im MEN1-Gen : Basis für prädiktives genetisches Screening und klinisches Management von MEN1-Familien
(
- Contribution to journal › Article
- 1996
-
Mark
Genetic predisposition to breast cancer
(
- Contribution to journal › Article