Genetic analyses of muscular Search for familial combined hyperlipidemia Molecular genetics of autism spectrum Molecular genetics of schizophrenia and dystrophies in Finland susceptibility genes disorders in the Finnish population comorbid and related traits Molecular genetics of Positional cloning of Positional cloning of Finnish genes of hypertension the CLN5 gene the GRACILE syndrome Identication of multiple sclerosis the INCL-gene Human lysosomal. Aspartylglucosaminidase: susceptibility genes in Finnish structure, function and intracellular targeting The age of the mutations in Molecular and cell biology of infantile population Molecular defect in the infantile Molecular genetics of Meckel syndrome the Finnish disease heritage: (CLN1) and variant late infantile (CLN5) neuronal ceroid lipofuscinosis Intracellular maturation of a genealogical and linkage neuronal ceroid lipofuscinoses Search for susceptibility genes aspartylglucosaminidase disequilibrium study in autism spectrum disorders Molecular pathogenesis of Molecular genetics of familial schizophrenia and PLO-SL (polycystic Monogenic model for autoimmune diseases: familial amyloidosis, molecular basis of autoimmune polyendocrinopathy – Finnish type lipomembranous osteodysplasia with Molecular genetics of Molecular pathogenesis of sclerosing leukoencephalopathy) candidiasis – ectodermal dystrophy (APECED) Genetics of schizophrenia: Marfan syndrome the late infantile neuronal the 1q42 locus in Finnish families Aspartylglucosaminuria: ceroid lipofuscinosis (LINCL) molecular pathogenesis and in vitro Genetic mapping of the loci for A link between the autoimmune correction of the enzyme defect Molecular genetics of APECED a monogenic and a multifactorial regulator gene (AIRE) and peripheral Search for genetic variants (Autoimmune PolyEndocrinopathy neuropsychiatric disorder: From disease gene to molecular self-tolerance conferring the susceptibility to Molecular genetics of Candidiasis Ectocermal Dystrophy) PLO-SL and familial bipolar disorder pathogenesis: APECED obesity and related metabolic traits multiple sclerosis Defective genes behind PLOSL: Mouse aspartylglucosaminidase molecular and neuropathological Molecular genetics of bipolar Fibrillin defects in Marfan syndrome: Scoring human genomic SNPs and mutations: characteristics of the disease Mutations of mitochondrial DNA Impact on DNA diagnosis and gene and mouse model for Multiplexed primer extension with manifolds disorder and related traits in human disease molecular pathogenesis aspartylglucosaminuria and microarrays as solid-support Identication of gene variations Investigations on molecular The human type II collagen gene Molecular genetics of on chromosome 17 associated with and cartilage diseases Autosomal dominant progressive aspects of lethal congenital Aspartylglucosaminuria (AGU): type I brillinopathies multiple sclerosis contacture syndrome lysosomal targeting of AGA, external ophthalmoplegia (adPEO): Prognosis of acute porphyrias and a tale of two genomes the cellular consequences of Molecular genetics of infantile Molecular pathogenesis of Identication of the Meckel molecular genetics of acute mutations and an attempt intermittent porphyria in Finland onset spinocerebellar ataxia salla disease syndrome gene (MKS1) at gene therapy Familial amyloidosis of the Finnish type (FAF) - Exposes a novel ciliopathy Molecular genetics of consequences of amyloidosis-associated Molecular genetics of tibial muscular Marfan syndrome mutation for gelsolin processing and function dystrophy (TMD) and a novel distal Search for susceptibility genes Aspartylglucosaminuria: myopathy disease pathogenesis, developmental in schizophrenia DNA analysis in forensic science: expression and regulation of The search for genes predisposing Characterization of aspartylglucosaminidase application of the polymerase chain the aspartylglucosaminidase gene to obesity activation and aspartylglucosaminuria Candidate gene studies on reaction (PCR) to the identication of mutations cardiovascular traits individuals Search for gene loci predisposing to Free sialic acid storage diseases: Pathogenic mechanisms of polycystic Molecular genetics of multiple sclerosis in the Finnish CLN5 – from mutation to defective population same gene – dierent mutations protein and clinical phenotype lipomembranous osteodysplasia with aspartylglucosaminuria sclerosing leukoencephalopathy (PLOSL) Hypervariable regions of human The identication and characterization Searching for genes predisposing of the hydrolethalus syndrome gene, Molecular background of genome in identication of individuals to common dyslipidemias common dyslipidemias and malignant cell clones HYLS on 11q24 Human 1-aspartamido-N- Search for genetic variants acetylglucosamine amidohydrolase Molecular genetics of in uencing human height lactase persistence Molecular distinction of neuronal Novel multiple sclerosis predisposing ceroid-lipofuscinoses: assignment of genetic variants outside the HLA region separate gene loci for infantile and juvenile forms Genetics of cardiovascular disease: a candidate gene study of USF1. DNA-ngerprinting in acute leukemia Genetic heterogeneity in autism spectrum Type III procollagen N-proteinase. disorders in a population Isolate. Purication of the enzyme and the cleavage Leena Peltonen-Palotie process in type VII of the Ehlers-Danlos Molecular genetics of schizophrenia and related syndrome intermediate phenotypes in a founder population.