perinnöllinen alttius

name

• perinnöllinen alttius

Works about perinnöllinen alttius

• A study on genetic mutations involving mitochondrial disorders :
• Brain responses to speech sounds in infants and children with and without familial risk for dyslexia
• BRCA/Fanconi anemia pathway genes in hereditary predisposition to breast cancer
• Catechol-O-methyltransferase and pain in rodents and humans
• DNA damage response gene mutations and inherited susceptibility to breast cancer
• Early adversity, psychosis risk and brain response to faces
• Etiological pathways of osteoarthritis
• Familial adenomatous polyposis :
• Genetic background and antenatal risk factors of bronchopulmonary dysplasia
• Genetic background of spontaneous preterm birth and lung diseases in preterm infants : studies of potential susceptibility genes and polymorphisms
• Genetic causes and risk factors associated with phenotypes occurring in mitochondrial disorders
• Genetic predisposition to breast and ovarian cancer :
• Genetic predisposition to spontaneous preterm birth : approaches to identify susceptibility genes
• Genetic risk factors for hereditary prostate cancer in Finland : from targeted analysis of susceptibility loci to genome-wide copy number variation study
• Genetic risk profiles for coronary heart disease
• Genetic studies on susceptibility genes in osteoarthritis
• Genetic susceptibility factors for prostate cancer at chromosomal region 11q13.5
• Genetic susceptibility to asbestos and tobacco smoke related non-malignant pleuropulmonary changes
• Genetic susceptibility to childhood bronchiolitis
• Genetic variants predisposing to prognosis in pulmonary sarcoidosis
• Genetics of breast and ovarian cancer predisposition with a focus on RAD51C and RAD51D genes
• Genetics of multiple sclerosis
• Genome-wide associations and computational search for the genetic risk factors for diabetic nephropathy
• Germline predisposition to childhood acute lymphoblastic leukemia and bone marrow failure, and mitochondrial DNA variants in leukemia
• Hereditary predisposition to breast cancer : with a focus on AATF, MRG15, PALB2, and three Fanconi anaemia genes
• Histological characteristics and gene expression profiling of Dupuytren's disease
• Human pluripotent stem cells and CRISPR-Cas9 genome editing to model diabetes
• Identification of novel tumor predisposition families and underlying genetic defects
• In quest of genetic susceptibility to disorders manifesting in fractures : assessing the significance of genetic factors in femoral neck stress fractures and childhood non-OI primary osteoporosis
• Interplay of genetic and environmental triggers in intestinal inflammation : genetics and transcriptomics in celiac disease and inflammatory bowel disease
• Iskiasoireyhtymään liittyvät perinnölliset tekijät : perimänlaajuinen tutkimus neljässä suuressa väestöotoksessa
• Molecular and functional characterization of ABRAXAS and PALB2 genes in hereditary breast cancer predisposition
• New insights into the genetic basis of colorectal cancer
• Obesity, physical activity and cardiorespiratory fitness in young adulthood : studies in Finnish twins
• On the genetics of intracranial aneurysms and on growth factor induced angiogenesis in the murine brain
• PALB2 and RAP80 genes in hereditary breast cancer predisposition
• Perinatal factors as predictors of brain damage and neurodevelopmental outcome :
• Periytyvän rintasyöpäalttiusmutaation (BRCA1/2) kantajamiesten hypoteettinen perinnöllisyysneuvontamalli
• Rare genetic variants and complex diseases : a bayesian approach
• Role of the RNF8, UBC13, MMS2 and RAD51C DNA damage response genes and rare copy number variants in hereditary predisposition to breast cancer
• Skeletal and extra-skeletal characteristics of WNT1 osteoporosis
• Studies on causes of multiple sclerosis : from genes to transcriptome
• Studies on the genetics of heart failure
• Systems and mechanistic understanding of genetic predisposition to prostate cancer
• Syöpäsolun tarina
• The development of immune responses and gut microbiota in children at genetic risk of type 1 diabetes
• The search for genetic factors in hand osteoarthritis
• The search for susceptibility genes in lumbar disc degeneration : focus on young individuals
• Tupakka- ja nikotiiniriippuvuus
• Type 1 family history and gad autoantibodies in subjects without diabetes and patients with type 2 diabetes
• Variation of the PALB2 and PTEN genes and eIF4E protein expression as prognostic factors in breast cancer
• Yksilöllisten alttiustekijöiden merkitys rakennustyöntekijöiden vaikean asbestoosin ja emfyseeman synnyssä :