Virtual International Authority File


Leena Peltonen-Palotie suomalainen geenitutkuja, professori ja akateemikko Wikidata

Peltonen, Leena National Library of Israel Library of Congress/NACO

Leena Peltonen-Palotie ISNI

VIAF ID: 73254321 (Personal)


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Title Sources
ABCB6 (MTABC3) excluded as the causative gene for the growth retardation syndrome with aminoaciduria, cholestasis, iron overload, and lactacidosis Wikidata
Aire deficient mice develop multiple features of APECED phenotype and show altered immune response Wikidata
Aire regulates negative selection of organ-specific T cells Wikidata
An association analysis of murine anxiety genes in humans implicates novel candidate genes for anxiety disorders Wikidata
Biological, clinical and population relevance of 95 loci for blood lipids Wikidata
Childhood adversities are associated with shorter telomere length at adult age both in individuals with an anxiety disorder and controls Wikidata
Common genetic determinants of vitamin D insufficiency: a genome-wide association study Wikidata
Common missense variant in the glucokinase regulatory protein gene is associated with increased plasma triglyceride and C-reactive protein but lower fasting glucose concentrations Wikidata
A common variant of HMGA2 is associated with adult and childhood height in the general population Wikidata
Common variants at 30 loci contribute to polygenic dyslipidemia Wikidata
Common variants conferring risk of schizophrenia Wikidata
DAP12/TREM2 deficiency results in impaired osteoclast differentiation and osteoporotic features Wikidata
Data on characterizing the gene expression patterns of neuronal ceroid lipofuscinosis genes: CLN1, CLN2, CLN3, CLN5 and their association to interneuron and neurotransmission markers: Parvalbumin and Somatostatin. Wikidata
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21. Wikidata
Dissolution testing of acetylsalicylic acid by a channel flow method-correlation to USP basket and intrinsic dissolution methods Wikidata
Evaluation of HapMap data in six populations of European descent. Wikidata
Evidence of still-ongoing convergence evolution of the lactase persistence T-13910 alleles in humans Wikidata
Family-based association study of DYX1C1 variants in autism Wikidata
The federated database--a basis for biobank-based post-genome studies, integrating phenome and genome data from 600,000 twin pairs in Europe. Wikidata
Genes and schizophrenia: beyond schizophrenia: the role of DISC1 in major mental illness Wikidata
Genetic architecture of circulating lipid levels Wikidata
Genetic determinants of height growth assessed longitudinally from infancy to adulthood in the northern Finland birth cohort 1966 Wikidata
Genetic Loci associated with C-reactive protein levels and risk of coronary heart disease Wikidata
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis Wikidata
Genetic structure of Europeans: a view from the North-East Wikidata
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk Wikidata
Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder Wikidata
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population Wikidata
A genome-wide association scan on estrogen receptor-negative breast cancer Wikidata
A genome-wide association search for type 2 diabetes genes in African Americans Wikidata
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. Wikidata
Genome-wide association study identifies multiple loci influencing human serum metabolite levels Wikidata
Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region Wikidata
The genome-wide patterns of variation expose significant substructure in a founder population Wikidata
Genome-wide screen for metabolic syndrome susceptibility Loci reveals strong lipid gene contribution but no evidence for common genetic basis for clustering of metabolic syndrome traits Wikidata
A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27 Wikidata
Global transcript profiles of fat in monozygotic twins discordant for BMI: pathways behind acquired obesity Wikidata
GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L Wikidata
Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects Wikidata
A high-density association screen of 155 ion transport genes for involvement with common migraine Wikidata
High-Resolution Physical and Transcriptional Mapping of the Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy Locus on Chromosome 21q22.3 by FISH Wikidata
Hundreds of variants clustered in genomic loci and biological pathways affect human height Wikidata
Hydrolethalus syndrome is caused by a missense mutation in a novel gene HYLS1 Wikidata
Identification of a variant associated with adult-type hypolactasia Wikidata
Identification of CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle Wikidata
Identification of ten loci associated with height highlights new biological pathways in human growth Wikidata
Independent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk culture Wikidata
Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and Twinky Wikidata
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility. Wikidata
Interaction of early environment, gender and genes of monoamine neurotransmission in the aetiology of depression in a large population-based Finnish birth cohort Wikidata
Isolated populations and complex disease gene identification Wikidata
Large recurrent microdeletions associated with schizophrenia Wikidata
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes Wikidata
Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study Wikidata
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations Wikidata
Mice with Ppt1Deltaex4 mutation replicate the INCL phenotype and show an inflammation-associated loss of interneurons Wikidata
Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases Wikidata
A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging Wikidata
The mouse ortholog of the neuronal ceroid lipofuscinosis CLN5 gene encodes a soluble lysosomal glycoprotein expressed in the developing brain Wikidata
Multiple common variants for celiac disease influencing immune gene expression Wikidata
Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD. Wikidata
Mutations in mRNA export mediator GLE1 result in a fetal motoneuron disease Wikidata
Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotype Wikidata
Neuronal ceroid lipofuscinoses are connected at molecular level: interaction of CLN5 protein with CLN2 and CLN3 Wikidata
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk Wikidata
OSBPL10, a novel candidate gene for high triglyceride trait in dyslipidemic Finnish subjects, regulates cellular lipid metabolism. Wikidata
Population-prevalent desmosomal mutations predisposing to arrhythmogenic right ventricular cardiomyopathy Wikidata
A population-specific HTR2B stop codon predisposes to severe impulsivity Wikidata
Replication of association between working memory and Reelin, a potential modifier gene in schizophrenia Wikidata
The role of the CD58 locus in multiple sclerosis Wikidata
Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families Wikidata
Sialin expression in the CNS implicates extralysosomal function in neurons Wikidata
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans Wikidata
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation Wikidata
The SLC6A14 gene shows evidence of association with obesity Wikidata
Stabilizing Agents for Drug Nanocrystals: Effect on Bioavailability Wikidata
Story of my roots, 2004: National Library of Israel Library of Congress/NACO
Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titin Wikidata
Understanding Critical Quality Attributes for Nanocrystals from Preparation to Delivery Wikidata
Unraveling the molecular pathogenesis of free sialic acid storage disorders: altered targeting of mutant sialin Wikidata
Use of genome-wide expression data to mine the "Gray Zone" of GWA studies leads to novel candidate obesity genes Wikidata
USF1 deficiency activates brown adipose tissue and improves cardiometabolic health Wikidata
Variants in MTNR1B influence fasting glucose levels. Wikidata

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