Joyce Carlson
Titel
Leg Läkare
Organisation
046-173855
0768 871018
Joyce [dot] Carlson [at] med [dot] lu [dot] se
Publikationer (hämtat ur Lunds universitets publikationsdatabas)
författare
- 2013
- 2012
- A Common Missense Variant in the ATP Receptor P2X7 Is Associated with Reduced Risk of Cardiovascular Events.
- Design of recombinant antibody microarrays for urinary proteomics.
- Semi-automated quantification of methylmalonic acid in human serum by LC-MS/MS
- Use of class I and class II HLA loci for predicting age at onset of type 1 diabetes in multiple populations
- 2011
- A candidate CpG SNP approach identifies a breast cancer associated ESR1-SNP.
- A new PCR-SSP method for HLA DR-DQ risk assessment for celiac disease.
- Extraction, quantitation, and evaluation of function DNA from various sample types.
- Genetic variants in serum and glucocortocoid regulated kinase 1, a regulator of the epithelial sodium channel, are associated with ischaemic stroke.
- Multiple Loci in the HLA Complex Are Associated with Addison's Disease.
- Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome
- 2010
- HLA Class I and Genetic Susceptibility to Type 1 Diabetes Results From the Type 1 Diabetes Genetics Consortium
- HLA DPA1, DPB1 Alleles and Haplotypes Contribute to the Risk Associated With Type 1 Diabetes Analysis of the Type 1 Diabetes Genetics Consortium Families
- HLA genotyping in the international Type 1 Diabetes Genetics Consortium
- Plasma Folate Concentrations Are Positively Associated with Risk of Estrogen Receptor {beta} Negative Breast Cancer in a Swedish Nested Case Control Study.
- 2009
- A modified general primer PCR system for sensitive detection of multiple types of oncogenic Human Papillomavirus.
- A new automated human leukocyte antigen genotyping strategy to identify DR-DQ risk alleles for celiac disease and type 1 diabetes mellitus.
- Clinical, Immunological, and Genetic Features of Autoimmune Primary Adrenal Insufficiency: Observations from a Norwegian Registry.
- Common Genetic Variants on Chromosome 9p21 Confers Risk of Ischemic Stroke A Large-Scale Genetic Association Study
- Folate intake, methylenetetrahydrofolate reductase polymorphisms, and breast cancer risk in women from the Malmö Diet and Cancer cohort.
- Increased breast cancer risk at high plasma folate concentrations among women with the MTHFR 677T allele.
- Modified General Primer PCR System for Sensitive Detection of Multiple Types of Oncogenic Human Papillomavirus
- Polymorphism in the oxytocin promoter region in patients with lactase non-persistence is not related to symptoms.
- The Protective Association of High Plasma Enterolactone with Breast Cancer Is Reasonably Robust in Women with Polymorphisms in the Estrogen Receptor alpha and beta Genes
- Validation of a new plasma cystatin C-based formula and the Modification of Diet in Renal Disease creatinine-based formula for determination of glomerular filtration rate
- Validity of maternal genotypes in DNA from archival pregnancy serum samples.
- 2008
- HLA DR-DQ haplotypes and genotypes and type 1 diabetes risk: Analysis of the Type 1 Diabetes Genetics Consortium families
- High throughput genotyping of oncogenic human papilloma viruses using MALDI-TOF mass spectrometry.
- Multiplex detection of human herpesviruses from archival specimens by using matrix-assisted laser desorption ionization-time of flight mass spectrometry.
- 2007
- Assessing Quality and Functionality of DNA from Fresh and Archival Dried Blood Spots and Recommendations for Quality Control Guidelines.
- Biobanking and biorepositiories: looking to the future.
- Ethical framework for previously collected biobank samples
- Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
- Multiplex detection of all Herpes viruses from archival specimens using MALDI-TOF Mass spectrometry.
- Prediction of relative glomerular filtration rate in adults: New improved equations based on Swedish Caucasians and standardized plasma-creatinine assays.
- Variation in GYS1 Interacts with Exercise and Gender to Predict Cardiovascular Mortality.
- 2006
- 24-hour Ambulatory Blood Pressure is Linked to Chromosome 18q21-22 and Genetic Variation of NEDD4L Associates with Cross-Sectional and Longitudinal Blood Pressure in Swedes.
- A risk haplotype including TNFA-308A in the promoter region of the gene for TNF-a influences the risk of inhibitor development in patients with hemophilia A.
- Polymorphisms in the TNFA gene and the risk of inhibitor development in patients with hemophilia A.
- Should donors be authorized to give broad consent to future biobank research?
- Standardization of p-creatinine assays and use of lean body mass allow improved prediction of calculated GFR in adults with a new equation.
- 2005
- Comparison of archival plasma and formalin-fixed paraffin-embedded tissue for genotyping in hepatocellular carcinoma.
- Genetic variance of SGK-1 is associated with blood pressure, blood pressure change over time and strength of the insulin-diastolic blood pressure relationship.
- Type 1 Diabetes: Evidence for susceptibility loci from four genome-wide linkage scans in 1,435 multiplex families.
- {alpha}1-Antitrypsin Deficiency in 26-Year-Old Subjects: Lung, Liver, and Protease/Protease Inhibitor Studies.
- 2002
- 2001
- 1999
- 1997
- 1990
