1 – 142 of 142
- show: 250
- |
- sort: year (new to old)
Close
Embed this list
<iframe src=" "
width=" "
height=" "
allowtransparency="true"
frameborder="0">
</iframe>
- 2024
-
Mark
A genome-wide association study of social trust in 33,882 Danish blood donors
(
- Contribution to journal › Article
- 2023
-
Mark
Aggregation tests identify new gene associations with breast cancer in populations with diverse ancestry
(
- Contribution to journal › Article
-
Mark
Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study
(
- Contribution to journal › Article
-
Mark
Extended genetic analysis and tumor characteristics in over 4600 women with suspected hereditary breast and ovarian cancer
(
- Contribution to journal › Article
-
Mark
European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation
(
- Contribution to journal › Article
-
Mark
A large meta-analysis identifies genes associated with anterior uveitis
(
- Contribution to journal › Article
-
Mark
How Well do Polygenic Risk Scores Identify Men at High Risk for Prostate Cancer? Systematic Review and Meta-Analysis
(
- Contribution to journal › Article
-
Mark
Genetic insights into resting heart rate and its role in cardiovascular disease
(
- Contribution to journal › Article
-
Mark
Association of the CHEK2 c.1100delC variant, radiotherapy, and systemic treatment with contralateral breast cancer risk and breast cancer-specific survival
(
- Contribution to journal › Article
-
Mark
Associations of height, body mass index, and weight gain with breast cancer risk in carriers of a pathogenic variant in BRCA1 or BRCA2 : the BRCA1 and BRCA2 Cohort Consortium
(
- Contribution to journal › Article
-
Mark
A genome-wide gene-environment interaction study of breast cancer risk for women of European ancestry
(
- Contribution to journal › Article
-
Mark
The EAT-Lancet diet, genetic susceptibility and risk of atrial fibrillation in a population-based cohort
(
- Contribution to journal › Article
- 2022
-
Mark
Rare coding variants in 35 genes associate with circulating lipid levels—A multi-ancestry analysis of 170,000 exomes
(
- Contribution to journal › Article
-
Mark
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis
(
- Contribution to journal › Article
-
Mark
Genome-wide interaction analysis identified low-frequency variants with sex disparity in lung cancer risk
(
- Contribution to journal › Article
-
Mark
Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers
(
- Contribution to journal › Article
-
Mark
Breast cancer risks associated with missense variants in breast cancer susceptibility genes
(
- Contribution to journal › Article
-
Mark
Polygenic risk modeling for prediction of epithelial ovarian cancer risk
(
- Contribution to journal › Article
-
Mark
Colorectal cancer risk in association with colorectal cancer as a second malignancy in relatives : a nationwide cohort study
(
- Contribution to journal › Article
-
Mark
Genome-wide association study identifies Sjögren's risk loci with functional implications in immune and glandular cells
(
- Contribution to journal › Article
-
Mark
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation
(
- Contribution to journal › Article
-
Mark
Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence from the COURAGE-PD Consortium
(
- Contribution to journal › Article
-
Mark
Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer
(
- Contribution to journal › Article
- 2021
-
Mark
Systems biology analysis of human genomes points to key pathways conferring spina bifida risk
(
- Contribution to journal › Article
-
Mark
Translating polygenic risk scores for clinical use by estimating the confidence bounds of risk prediction
(
- Contribution to journal › Article
-
Mark
Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes
(
- Contribution to journal › Article
-
Mark
The predictive ability of the 313 variant–based polygenic risk score for contralateral breast cancer risk prediction in women of European ancestry with a heterozygous BRCA1 or BRCA2 pathogenic variant
(
- Contribution to journal › Article
-
Mark
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture
(
- Contribution to journal › Article
-
Mark
A search for modifying genetic factors in CHEK2:c.1100delC breast cancer patients
(
- Contribution to journal › Article
- 2020
-
Mark
The Rare IL22RA2 Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1, -2 and -3 and Is Associated with Risk for Multiple Sclerosis
(
- Contribution to journal › Article
-
Mark
Recurrent Fusions Between YAP1 and KMT2A in Morphologically Distinct Neoplasms Within the Spectrum of Low-grade Fibromyxoid Sarcoma and Sclerosing Epithelioid Fibrosarcoma
(
- Contribution to journal › Article
-
Mark
Association of TIM-1 (T-Cell Immunoglobulin and Mucin Domain 1) With Incidence of Stroke
(
- Contribution to journal › Article
-
Mark
Copy number variants (CNVs) : a powerful tool for iPSC-based modelling of ASD
(
- Contribution to journal › Scientific review
- 2018
-
Mark
Polygenic Risk Score for Coronary Heart Disease Modifies the Elevated Risk by Cigarette Smoking for Disease Incidence
(
- Contribution to journal › Article
-
Mark
A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes
(
- 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
-
Mark
Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways
(
- Contribution to journal › Article
- 2017
-
Mark
A sibling based design to quantify genetic and shared environmental effects of venous thromboembolism in Sweden
(
- Contribution to journal › Article
-
Mark
A low-frequency inactivating AKT2 variant enriched in the finnish population is associated with fasting insulin levels and type 2 diabetes risk
(
- Contribution to journal › Article
-
Mark
Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease
(
- Contribution to journal › Article
-
Mark
Association Between Early-Life Antibiotic Use and the Risk of Islet or Celiac Disease Autoimmunity
(
- Contribution to journal › Article
-
Mark
Polymorphisms in ADH1B and ALDH2 genes associated with the increased risk of gastric cancer in West Bengal, India
(
- Contribution to journal › Article
- 2016
-
Mark
Genetic variants in CETP increase risk of intracerebral hemorrhage
(
- Contribution to journal › Article
-
Mark
The genetic architecture of type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function
(
- Contribution to journal › Article
- 2015
-
Mark
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
(
- Contribution to journal › Article
-
Mark
Polymorphisms in DCDC2 and S100B associate with developmental dyslexia
(
- Contribution to journal › Article
-
Mark
Risk of childhood asthma is associated with CpG-site polymorphisms, regional DNA methylation and mRNA levels at the GSDMB/ORMDL3 locus
(
- Contribution to journal › Article
-
Mark
Association between MAPT haplotype and memory function in patients with Parkinson's disease and healthy aging individuals
(
- Contribution to journal › Article
-
Mark
miR-155, identified as anti-metastatic by global miRNA profiling of a metastasis model, inhibits cancer cell extravasation and colonization in vivo and causes significant signaling alterations
(
- Contribution to journal › Article
-
Mark
Cell-specific effects in different immune subsets associated with SOCS1 genotypes in multiple sclerosis
(
- Contribution to journal › Article
-
Mark
Large-scale assessment of polyglutamine repeat expansions in Parkinson disease
(
- Contribution to journal › Article
- 2014
-
Mark
Inherited variation in the PARP1 gene and survival from melanoma
(
- Contribution to journal › Article
-
Mark
Associations of hormone replacement therapy and oral contraceptives with risk of colorectal cancer defined by clinicopathological factors, beta-catenin alterations, expression of cyclin D1, p53, and microsatellite-instability
(
- Contribution to journal › Article
-
Mark
CDKN2A-mutation hos en familie med arveligt malignt melanom
(
- Contribution to journal › Article
-
Mark
Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes
2014) In Proceedings of the National Academy of Sciences of the United States of America 111(36). p.32-13127(
- Contribution to journal › Article
-
Mark
Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers
(
- Contribution to journal › Article
-
Mark
Protective effect of LRRK2 p.R1398H on risk of Parkinson's disease is independent of MAPT and SNCA variants
(
- Contribution to journal › Article
- 2013
-
Mark
Gene × physical activity interactions in obesity: combined analysis of 111,421 individuals of European ancestry. : combined analysis of 111,421 individuals of European ancestry
(
- Contribution to journal › Article
- 2012
-
Mark
Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers
(
- Contribution to journal › Article
-
Mark
Effects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers
(
- 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
Large-scale replication and heterogeneity in Parkinson disease genetic loci
(
- Contribution to journal › Article
-
Mark
Closing the case of APOE in multiple sclerosis : no association with disease risk in over 29 000 subjects
(
- Contribution to journal › Article
-
Mark
ANKRD55 and DHCR7 are novel multiple sclerosis risk loci
(
- Contribution to journal › Article
- 2011
-
Mark
Common Genetic Variation at BARD1 Is Not Associated with Breast Cancer Risk in BRCA1 or BRCA2 Mutation Carriers
(
- Contribution to journal › Article
-
Mark
Interplay between BRCA1 and RHAMM Regulates Epithelial Apicobasal Polarization and May Influence Risk of Breast Cancer
(
- Contribution to journal › Article
-
Mark
Exploring the link between MORF4L1 and risk of breast cancer
(
- Contribution to journal › Article
-
Mark
Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2
(
- Contribution to journal › Article
-
Mark
Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers
(
- Contribution to journal › Article
-
Mark
Polymorphic variation in the androgen receptor gene : association with risk of testicular germ cell cancer and metastatic disease
(
- Contribution to journal › Article
-
Mark
Targeted inhibition of mitochondrial Hsp90 suppresses localised and metastatic prostate cancer growth in a genetic mouse model of disease
(
- Contribution to journal › Article
-
Mark
Network analysis of skin tumor progression identifies a rewired genetic architecture affecting inflammation and tumor susceptibility
(
- Contribution to journal › Article
-
Mark
Pathway-based analysis of a melanoma genome-wide association study : analysis of genes related to tumour-immunosuppression
(
- Contribution to journal › Article
-
Mark
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma
(
- Contribution to journal › Article
-
Mark
Single nucleotide polymorphism (SNP) analysis demonstrates a significant association of tumour necrosis factor-alpha (TNFA) with primary immune thrombocytopenia among Caucasian adults
(
- Contribution to journal › Article
-
Mark
A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease
(
- Contribution to journal › Article
-
Mark
Exonic DNA sequencing of ERBB4 in bipolar disorder
(
- Contribution to journal › Article
- 2010
-
Mark
Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers : implications for risk prediction
(
- Contribution to journal › Article
-
Mark
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population
(
- Contribution to journal › Article
-
Mark
Variation in CDKN2A at 9p21.3 influences childhood acute lymphoblastic leukemia risk
(
- Contribution to journal › Article
-
Mark
Verification of the susceptibility loci on 7p12.2, 10q21.2, and 14q11.2 in precursor B-cell acute lymphoblastic leukemia of childhood
(
- Contribution to journal › Article
-
Mark
Association between vitamin D receptor gene polymorphisms, falls, balance and muscle power : results from two independent studies (APOSS and OPUS)
(
- Contribution to journal › Article
-
Mark
Aberrant DNA methylation links cancer susceptibility locus 15q25.1 to apoptotic regulation and lung cancer
(
- Contribution to journal › Article
-
Mark
Specific genomic aberrations in primary colorectal cancer are associated with liver metastases
(
- Contribution to journal › Article
- 2009
-
Mark
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers
(
- Contribution to journal › Article
-
Mark
Familial risks for amyotrophic lateral sclerosis and autoimmune diseases
(
- Contribution to journal › Article
-
Mark
Risk for multiple sclerosis in relatives and spouses of patients diagnosed with autoimmune and related conditions
(
- Contribution to journal › Article
- 2008
-
Mark
Vra4 congenic rats with allelic differences in the class II transactivator gene display altered susceptibility to experimental autoimmune encephalomyelitis
(
- Contribution to journal › Article
-
Mark
Familial risks for chronic obstructive pulmonary disease among siblings based on hospitalisations in Sweden
(
- Contribution to journal › Article
-
Mark
Do inflammatory bowel disease and cancer share susceptibility : a family study
(
- Contribution to journal › Letter
-
Mark
Shared familial risk factors between cancer and RA patients
(
- Contribution to journal › Letter
-
Mark
Familial risks for common diseases : etiologic clues and guidance to gene identification
(
- Contribution to journal › Scientific review
-
Mark
The Environmental Determinants of Diabetes in the Young (TEDDY) Study
(
- Contribution to journal › Article
- 2007
-
Mark
Nature's choice of genes controlling chronic inflammation.
2007) Symposium on Immunotherapy 2020 - Visions and Trends for Targeting Inflammatory Disease 4. p.1-15(
- Chapter in Book/Report/Conference proceeding › Paper in conference proceeding
-
Mark
The axon reaction : identifying the genes that make a difference
(
- Contribution to journal › Article
-
Mark
Incidence and familial risks in pituitary adenoma and associated tumors
(
- Contribution to journal › Article
-
Mark
Risks for familial and contralateral breast cancer interact multiplicatively and cause a high risk
(
- Contribution to journal › Article
-
Mark
Familial risks for asthma among twins and other siblings based on hospitalizations in Sweden
(
- Contribution to journal › Article
-
Mark
Familial risks for nerve, nerve root and plexus disorders in siblings based on hospitalisations in Sweden
(
- Contribution to journal › Article
-
Mark
Detection of oncogenic viruses SV40, BKV, JCV, HCMV, HPV and p53 codon 72 polymorphism in lung carcinoma
(
- Contribution to journal › Article
- 2006
-
Mark
Constitutional downregulation of SEMA5A expression in autism
(
- Contribution to journal › Article
-
Mark
Re: "Familial risk of multiple sclerosis: a nationwide cohort study"
(
- Contribution to journal › Letter
-
Mark
Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes : the GENOMOS study
(
- Contribution to journal › Article
- 2005
-
Mark
Familial risk for lung cancer by histology and age of onset : evidence for recessive inheritance
(
- Contribution to journal › Article
-
Mark
Familial multiple primary lung cancers : a population-based analysis from Sweden
(
- Contribution to journal › Article
- 2004
-
Mark
Fetal programmering av ohälsa i vuxen ålder - arv eller miljö?
(
- Contribution to journal › Article
-
Mark
BRCA1 och BRCA2 har nått kliniken. Tioårigt fynd av genmutation ger nu möjlighet förebygga ärftlig bröstcan
(
- Contribution to journal › Article
-
Mark
Familial risk in testicular cancer as a clue to a heritable and environmental aetiology
(
- Contribution to journal › Article
-
Mark
Familial risk of cancer : data for clinical counseling and cancer genetics
(
- Contribution to journal › Article
-
Mark
Familial aggregation of Hodgkin lymphoma and related tumors
(
- Contribution to journal › Article
-
Mark
Susceptibility to Paget's disease of bone is influenced by a common polymorphic variant of osteoprotegerin
(
- Contribution to journal › Article
-
Mark
Association of the Pro12Ala and C1431T variants of PPARG and their haplotypes with susceptibility to Type 2 diabetes
(
- Contribution to journal › Article
-
Mark
Differential genetic effects of ESR1 gene polymorphisms on osteoporosis outcomes
(
- Contribution to journal › Article
- 2003
-
Mark
Subsequent primary malignancies after endometrial carcinoma and ovarian carcinoma
(
- Contribution to journal › Article
-
Mark
Familial and second lung cancers : a nation-wide epidemiologic study from Sweden
(
- Contribution to journal › Article
-
Mark
Familial risk of cancer by site and histopathology
(
- Contribution to journal › Article
- 2002
-
Mark
Identification of susceptibility genes for experimental autoimmune encephalomyelitis that overcome the effect of protective alleles at the eae2 locus.
(
- Contribution to journal › Article
-
Mark
Contribution of known and unknown susceptibility genes to early-onset diabetes in scandinavia: evidence for heterogeneity.
(
- Contribution to journal › Article
-
Mark
Thrifty genotypes and phenotypes in the pathogenesis of early-onset obesity.
(
- Contribution to journal › Letter
-
Mark
Viktigt att upptäcka ärftliga fall av kolorektal- och endometriecancer. Mutationer hos »HNPCC-individer» kan orsaka flera tumörsjukdomar
(
- Contribution to journal › Article
-
Mark
Många vägar leder till artros. Kunskapen om riskfaktorer och sjukdomsmekanismer ökar snabbt
(
- Contribution to journal › Article
-
Mark
Risk of invasive cervical cancer associated with polymorphic HLA DR/DQ haplotypes.
(
- Contribution to journal › Article
-
Mark
HLA-DQ genotypes in classic type 1 diabetes and in latent autoimmune diabetes of the adult.
(
- Contribution to journal › Article
- 2001
-
Mark
Familial carcinoid tumors and subsequent cancers : a nation-wide epidemiologic study from Sweden
(
- Contribution to journal › Article
-
Mark
Parental cancer as a risk factor for brain tumors (Sweden)
(
- Contribution to journal › Article
-
Mark
Increased cancer risk in the offspring of women with colorectal carcinoma. A Swedish Register-Based Cohort Study
(
- Contribution to journal › Debate/Note/Editorial
-
Mark
Association between COLIA1 Sp1 alleles and femoral neck geometry
(
- Contribution to journal › Article
-
Mark
Prediction of osteoporotic fractures by bone densitometry and COLIA1 genotyping : a prospective, population-based study in men and women
(
- Contribution to journal › Article
-
Mark
COL1A1 Sp1 polymorphism predicts perimenopausal and early postmenopausal spinal bone loss
(
- Contribution to journal › Article
-
Mark
Primär hyperparatyreoidism vanligt hos postmenopausala kvinnor. Identifiering av genetiska riskfaktorer kan ge individanpassad behandling
(
- Contribution to specialist publication or newspaper › Specialist publication article
- 2000
-
Mark
Cytogenetic heterogeneity and clonal evolution in synchronous bilateral breast carcinomas and their lymph node metastases from a male patient without any detectable BRCA2 germline mutation
(
- Contribution to journal › Article
-
Mark
Tumour biology of a breast cancer at least partly reflects the biology of the tissue/epithelial cell of origin at the time of initiation - a hypothesis
(
- Contribution to journal › Article
-
Mark
Familial breast and ovarian cancer : a Swedish population-based register study
(
- 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
-
Mark
Susceptibility to osteoporotic fracture is determined by allelic variation at the Sp1 site, rather than other polymorphic sites at the COL1A1 locus
(
- Contribution to journal › Article
- 1999
-
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
-
Mark
Kommersialiseringen av gener--patent på bröstcancergener pilotfall. Sverige får inte stå vid sidan om utvecklingen
(
- Contribution to journal › Article
-
Mark
Familial and hereditary prostate cancer in southern Sweden. A population-based case-control study
(
- Contribution to journal › Article
-
Mark
Thrombophilia as a multigenic disease
(
- Contribution to journal › Article
- 1997
-
Mark
Activated protein C resistance due to a common factor V gene mutation is a major risk factor for venous thrombosis
(
- Contribution to journal › Article
- 1996
-
Mark
Genetic predisposition to breast cancer
(
- Contribution to journal › Article