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- 2024
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Mark
Pregnancy Planning and Genetic Testing: Exploring Advantages, and Challenges
(
- Contribution to journal › Scientific review
- 2023
-
Mark
Updated Stroke Gene Panels : Rapid evolution of knowledge on monogenic causes of stroke
(
- Contribution to journal › Article
- 2021
-
Mark
Genetic testing in women with early-onset breast cancer : a Traceback pilot study
(
- Contribution to journal › Article
-
Mark
Rare diseases : past achievements and future prospects
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Prevalence of germline pathogenic variants in 22 cancer susceptibility genes in Swedish pediatric cancer patients
(
- Contribution to journal › Article
- 2020
-
Mark
Increased cancer risk in families with pediatric cancer is associated with gender, age, diagnosis, and degree of relation to the child
2020) In Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 29(11). p.2171-2179(
- Contribution to journal › Article
-
Mark
Variations in the Referral Pattern for Genetic Counseling of Patients with Early-Onset Breast Cancer : A Population-Based Study in Southern Sweden
(
- Contribution to journal › Article
-
Mark
Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke
(
- Contribution to journal › Article
-
Mark
A century of Hereditas : from local publication to international journal
(
- Contribution to journal › Article
- 2019
-
Mark
A stroke gene panel for whole-exome sequencing
(
- Contribution to journal › Article
-
Mark
Att inte debattera är inte ett alternativ
2019) In Svenska Dagbladet, Stockholm(
- Contribution to specialist publication or newspaper › Newspaper article
-
Mark
Vi måste ta ställning till den nya gentekniken
2019) In Svenska Dagbladet, Stockholm(
- Contribution to specialist publication or newspaper › Newspaper article
- 2018
-
Mark
Utvidgad anlagsbärartestning kan bredda fosterdiagnostiken - Recessiva sjukdomsanlag kan kartläggas hos friska personer inför planerad graviditet
(
- Contribution to journal › Debate/Note/Editorial
-
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
Accuracy of self-reported family history of cancer, mutation status and tumor characteristics in patients with early onset breast cancer
(
- Contribution to journal › Article
-
Mark
Germline mutations in BRCA1 and BRCA2 incidentally revealed in a biobank research study : experiences from re-contacting mutation carriers and relatives
(
- 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
From Mendel to Medical Genetics
(
- Contribution to journal › Scientific review
- 2016
-
Mark
An update of a classical textbook.
(
- Contribution to journal › Review (Book/Film/Exhibition/etc.)
-
Mark
Familial aggregation of stroke amongst young patients in Lund Stroke Register.
(
- Contribution to journal › Article
-
Mark
Targeted sequencing of BRCA1 and BRCA2 across a large unselected breast cancer cohort suggests that one-third of mutations are somatic
(
- Contribution to journal › Article
-
Mark
Cancer in first-degree relatives of women with early-onset breast cancer: a comparison of self-reported and cancer registry data
(
- Contribution to journal › Published meeting abstract
- 2015
-
Mark
Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness.
(
- Contribution to journal › Article
-
Mark
Increasing age at first full-time pregnancy correlates to use of oral contraceptives before age 20 in women with a family history of breast cancer
2015) 106th Annual Meeting of the American Association for Cancer Research(
- Contribution to conference › Abstract
- 2014
-
Mark
Long-term prognosis of early-onset breast cancer in a population-based cohort with a known BRCA1/2 mutation status.
(
- Contribution to journal › Article
-
Mark
High risk of in-breast tumor recurrence after BRCA1/2-associated breast cancer.
(
- Contribution to journal › Article
- 2013
-
Mark
Are 25 SNPs from the CARDIoGRAM study associated with ischaemic stroke?
(
- Contribution to journal › Article
- 2012
-
Mark
A Nonsynonymous Polymorphism in IRS1 Modifies Risk of Developing Breast and Ovarian Cancers in BRCA1 and Ovarian Cancer in BRCA2 Mutation Carriers
(
- Contribution to journal › Article
-
Mark
Increased incidence of childhood, prostate and breast cancers in relatives of childhood cancer patients.
(
- Contribution to journal › Article
-
Mark
Genetics and democracy-what is the issue?
2012) In Journal of Community Genetics(
- Contribution to journal › Article
-
Mark
Editorial: Genetics and Democracy
(
- Contribution to journal › Letter
-
Mark
A large-sample assessment of possible association between ischaemic stroke and rs12188950 in the PDE4D gene.
(
- Contribution to journal › Article
-
Mark
Prevalence of germline TP53 mutations and history of Li-Fraumeni syndrome in families with childhood adrenocortical tumors, choroid plexus tumors, and rhabdomyosarcoma: A population-based survey.
(
- Contribution to journal › Article
-
Mark
Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers
(
- Contribution to journal › Article
-
Mark
Association Between BRCA1 and BRCA2 Mutations and Survival in Women With Invasive Epithelial Ovarian Cancer
(
- Contribution to journal › Article
- 2011
-
Mark
Biparental inheritance of chromosomal abnormalities in male twins with non-syndromic mental retardation
(
- 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
Genetic Variation at 9p22.2 and Ovarian Cancer Risk for BRCA1 and BRCA2 Mutation Carriers.
(
- Contribution to journal › Article
- 2010
-
Mark
Genetic Screening in Europe
(
- Contribution to journal › Article
-
Mark
Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers
(
- Contribution to journal › Article
-
Mark
Association of the Variants CASP8 D302H and CASP10 V410I with Breast and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers.
2010) In Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 19. p.2859-2868(
- Contribution to journal › Article
- 2009
-
Mark
Educational priorities and current involvement in genetic practice: a survey of midwives in the Netherlands, UK and Sweden
(
- Contribution to journal › Article
-
Mark
Testing the Children: Do Non-Genetic Health-Care Providers Differ in Their Decision to Advise Genetic Presymptomatic Testing on Minors? A Cross-Sectional Study in Five Countries in the European Union
(
- Contribution to journal › Article
- 2008
-
Mark
Regulations and practices of genetic counselling in 38 European countries: the perspective of national representatives
(
- Contribution to journal › Article
-
Mark
Genetics in clinical practice: general practitioners' educational priorities in European countries
(
- 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
Assessing educational priorities in genetics for general practitioners and specialists in five countries: factor structure of the Genetic-Educational Priorities (Gen-EP) scale
(
- Contribution to journal › Article
-
Mark
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
(
- Contribution to journal › Article
-
Mark
Higher occurrence of childhood cancer in families with germline mutations in BRCA2, MMR and CDKN2A genes.
(
- Contribution to journal › Article
-
Mark
Ischaemic stroke in hypertensive patients is associated with variations in the PDE4D genome region.
(
- Contribution to journal › Article
-
Mark
Regulatory Issues for Genetic Testing in Clinical Practice.
(
- Contribution to journal › Article
- 2007
-
Mark
Cytogenetic Guidelines and Quality Assurance: a common European framework for quality assessment for constitutional and acquired cytogenetic investigations
(
- Contribution to journal › Article
-
Mark
A hypothesis-generating search for new genetic breast cancer syndromes - a national study in 803 Swedish families
(
- Contribution to journal › Article
-
Mark
Report of an international survey of molecular genetic testing laboratories
(
- Contribution to journal › Article
-
Mark
Brister i genetisk kunskap i vården?
2007) p.109-109(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Etisk argumentation och klinisk verklighet kan med fördel förenas.
(
- Contribution to journal › Article
- 2006
-
Mark
Education in medical genetics for non-genetic health care providers in sweden.
(
- Contribution to journal › Article
-
Mark
Handy book on cancer genetics risk assessment
(
- Contribution to journal › Review (Book/Film/Exhibition/etc.)
-
Mark
The contribution of the hereditary nonpolyposis colorectal cancer syndrome to the development of ovarian cancer.
(
- Contribution to journal › Article
-
Mark
Genetic education for non-geneticist health professionals
(
- Contribution to journal › Article
-
Mark
Hemizygosity for chromosome 2q14.2-q22.1 spanning the GLI2 and PROC genes associated with growth hormone deficiency, polydactyly, deep vein thrombosis and urogenital abnormalities
(
- Contribution to journal › Letter
-
Mark
ECA Permanent working group for cytogenetics and society: Cytogenetic guidelines and quality assurance. A common framework for quality assessment for constitutional and acquired cytogenetic investigations
(
- Contribution to journal › Article
- 2005
-
Mark
Prevalence of Stroke and Vascular Risk Factors among First-Degree Relatives of Stroke Patients and Control Subjects.
(
- Contribution to journal › Article
-
Mark
Genetic education and nongenetic health professionals: Educational providers and curricula in Europe.
(
- Contribution to journal › Article
-
Mark
Ny kunskap om arv och ärftlighet ger nya aspekter på hjärtsjukdom
(
- Contribution to journal › Article
-
Mark
Book review: Genetic predisposition of cancer, 2nd ed.
(
- Contribution to journal › Review (Book/Film/Exhibition/etc.)
-
Mark
Nya rön om fragil X-syndromet komplicerar genetisk vägledning. Sjukdomsgenen orsakar fler symtom än vad som tidigare varit känt
(
- Contribution to journal › Article
- 2004
-
Mark
A new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length.
(
- Contribution to journal › Article
-
Mark
An excess of chromosome 1 breakpoints in male infertility.
(
- Contribution to journal › Article
-
Mark
One in 10 ovarian cancer patients carry germ line BRCA1 or BRCA2 mutations : results of a prospective study in Southern Sweden
(
- Contribution to journal › Article
-
Mark
External quality assessment for mutation detection in the BRCA1 and BRCA2 genes: EMQN's experience of 3 years
(
- Contribution to journal › Article
-
Mark
Genetisk rådgivning och fosterdiagnostik.
2004) p.56-56(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
The need for oncogenetic counselling - Ten years' experience of a regional oncogenetic clinic
(
- Contribution to journal › Article
-
Mark
Regulation of genetic testing in clinical practice
(
- Chapter in Book/Report/Conference proceeding › Book chapter
- 2003
-
Mark
Population genetic screening programmes: technical, social, and ethical issues.
(
- Contribution to journal › Article
-
Mark
Provision of genetic services in Europe: current practices and issues
(
- Contribution to journal › Article
-
Mark
Provision of genetic service in Europe: current practices and issues.
(
- Contribution to journal › Article
-
Mark
Data storage and DNA banking for biomedical research: technical, social and ethical issues.
(
- Contribution to journal › Article
-
Mark
Ring Y chromosome in an azoospermic male with short stature: additional evidence for a distinct ring Y syndrome in non-mosaic patients?
(
- Contribution to journal › Letter
-
Mark
Genetic information and testing insurance and employment: technical, social, and ethical issues.
(
- Contribution to journal › Article
-
Mark
Statens medicinsk-etiska råd. Genetisk screening - om hälsa och ärftlig sjukdomsrisk. Etiska vägmärken 11. (rec)
(
- Contribution to journal › Article
-
Mark
Medicinsk genetik – en introduktion.
2003)(
- Book/Report › Book
-
Mark
Book review: P.J. Morrison, S.V. Hodgson, N.E. Haites (eds): Familial breast cancer: genetics, screening and managementCambridge University Press, 2002, 401 pp, hardcover (ISBN 0-521-80373-X) pound 65.00.
(
- Contribution to journal › Article
-
Mark
Ett etiskt dilemma: Farmakogenetiskt test kan ge oönskad information [An ethical dilemma: pharmacogenetic tests can yield unwanted information]
(
- Contribution to journal › Article
-
Mark
Gendiagnostik vid sjukdom – och innan den bryter ut
2003) p.31-31(
- Chapter in Book/Report/Conference proceeding › Book chapter
-
Mark
Lundensisk allvarshumor
(
- Contribution to journal › Review (Book/Film/Exhibition/etc.)
- 2002
-
Mark
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism-jaw tumor syndrome
(
- Contribution to journal › Article
- 2001
-
Mark
Issues in Human GenEthics
(
- Contribution to journal › Article
-
Mark
Functional analysis of BRCA1 C-terminal missense mutations identified in breast and ovarian cancer families
(
- Contribution to journal › Article
-
Mark
Essential genetics education for non-genetics health professionals (EC Project GenEd)
(
- Contribution to journal › Article
-
Mark
Identification of human candidate genes for male infertility by digital differential display
(
- Contribution to journal › Article
-
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
- 2000
-
Mark
Naturvetare och kulturforskare kan överbrygga ämnesgränser
(
- Contribution to journal › Article
-
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
Prognostic implications of cytogenetic aberrations in diffuse large B-cell lymphomas
(
- Contribution to journal › Article
-
Mark
Incidence of malignant tumours in relatives of BRCA1 and BRCA2 germline mutation carriers
(
- Contribution to journal › Article
-
Mark
CAG repeat length in the androgen receptor gene is related to age at diagnosis of prostate cancer and response to endocrine therapy, but not to prostate cancer risk
(
- Contribution to journal › Article
-
Mark
Familial and hereditary prostate cancer in southern Sweden. A population-based case-control study
(
- Contribution to journal › Article
- 1998
-
Mark
Clinical course of early onset prostate cancer with special reference to family history as a prognostic factor
(
- Contribution to journal › Article
-
Mark
Forskningsframsteg om hereditär prostatacancer. Riskfamiljer bör kartläggas och erbjudas screening
(
- Contribution to journal › Article
- 1997
-
Mark
Moderate frequency of BRCA1 and BRCA2 germ-line mutations in Scandinavian familial breast cancer
(
- Contribution to journal › Article
-
Mark
The risk of malignant tumours in first-degree relatives of men with early onset prostate cancer : a population-based cohort study
(
- Contribution to journal › Article
-
Mark
Sons of men with prostate cancer : their attitudes regarding possible inheritance of prostate cancer, screening, and genetic testing
(
- Contribution to journal › Article
-
Mark
Hypereosinophilic syndrome in a child mosaic for a congenital triplication of the short arm of chromosome 8
(
- Contribution to journal › Article
- 1996
-
Mark
Chromosome aberrations in prophylactic mastectomies from women belonging to breast cancer families
(
- Contribution to journal › Article
- 1993
-
Mark
Clinical impact of breakpoint position within M-bcr in chronic myeloid leukemia
(
- Contribution to journal › Article
-
Mark
Piebaldism in a mentally retarded girl with rare deletion of the long arm of chromosome 4
(
- Contribution to journal › Article
- 1990
-
Mark
Bone marrow karyotypes in 94 children with acute leukemia
(
- Contribution to journal › Article
-
Mark
Remarkably long survival of a patient with Ph1-positive chronic myeloid leukemia and 5' bcr rearrangement
(
- Contribution to journal › Article
-
Mark
Deletion of 14q in non‐Hodgkin's lymphoma
(
- Contribution to journal › Article
- 1989
-
Mark
Relation between occupational exposure to organic solvents and chromosome aberrations in non‐Hodgkin's lymphoma
(
- Contribution to journal › Article
-
Mark
No abnormal C‐band polymorphism in lung cancer patients
(
- Contribution to journal › Article
- 1988
-
Mark
Normal frequency of structural chromosome aberrations in fibroblasts from patients with non‐Hodgkin's lymphoma
(
- Contribution to journal › Article
-
Mark
Do clonal chromosome abnormalities prognosticate early relapse in hodgkin's disease?
(
- Contribution to journal › Letter
-
Mark
Breakprone chromosome bands in fibroblasts from patients with non‐Hodgkin's lymphoma do not coincide with bands involved in primary rearrangements in non‐Hodgkin's lymphomas
(
- Contribution to journal › Article
-
Mark
Trisomy 5 and t(5;14)(q11;q32) as the sole abnormalities in two different clones from a centroblastic non-Hodgkin's lymphoma
(
- Contribution to journal › Article
- 1987
-
Mark
A new specific chromosomal rearrangement, t(8;16) (p11;p13), in acute monocytic leukaemia
(
- Contribution to journal › Article
-
Mark
New structural chromosomal rearrangements in congenital leukemia
(
- Contribution to journal › Article
-
Mark
CYTOGENETIC STUDIES IN HODGKIN'S DISEASE
(
- Contribution to journal › Article
-
Mark
RELATIONSHIP BETWEEN CYTOGENETIC FINDINGS AND HISTOPATHOLOGY IN NON‐HODGKIN LYMPHOMA
(
- Contribution to journal › Article
-
Mark
Prognostic implication of cytogenetic findings in 106 patients with non-Hodgkin lymphoma
(
- Contribution to journal › Article
- 1986
-
Mark
Reciprocal translocation (11;19)(q23;p13) in congenital acute lymphoblastic leukemia
(
- Contribution to journal › Article
-
Mark
High resolution banding analysis of the reciprocal translocation t(6;9) in acute nonlymphocytic leukemia
(
- Contribution to journal › Article
-
Mark
Proliferative activity and number of clonal chromosome aberrations in non‐Hodgkin's lymphomas
(
- Contribution to journal › Article
-
Mark
Cytogenetic studies in non‐Hodgkin lymphomas ‐ Results from surgical biopsies
(
- Contribution to journal › Article
-
Mark
Near-haploidy in a case of plasmocytoma
(
- Contribution to journal › Article
- 1985
-
Mark
C‐band polymorphism in non‐Hodgkin lymphoma
(
- Contribution to journal › Article
-
Mark
C-band heteromorphism in breast cancer patients
(
- Contribution to journal › Article
-
Mark
Cytogenetic studies in non‐Hodgkin lymphomas‐Results from fineneedle aspiration samples
(
- Contribution to journal › Article
- 1984
-
Mark
First-trimester diagnosis on chorionic villi obtained by direct vision technique
(
- Contribution to journal › Article
-
Mark
Hypophyseal tumor and gynecomastia preceding bilateral breast cancer development in a man
(
- Contribution to journal › Article
- 1983
-
Mark
Diagnostisk korionbiopsi vid Lasarettet i Lund
(
- Contribution to journal › Article
- 1981
-
Mark
Fine needle aspiration biopsy: A useful tool in tumor cytogenetics with special reference to malignant lymphomas
(
- Contribution to journal › Article