Virtual International Authority File


Leena Peltonen-Palotie suomalainen geenitutkuja, professori ja akateemikko Wikidata

Leena Peltonen-Palotie ISNI

Peltonen, Leena Library of Congress/NACO

VIAF ID: 73254321 (Personal)


ISNI: 0000  0000  3683  7620 

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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
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
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
Evidence of still-ongoing convergence evolution of the lactase persistence T-13910 alleles in humans 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
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Wikidata
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution Wikidata
Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region Wikidata
A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27 Wikidata
GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L Wikidata
A high-density association screen of 155 ion transport genes for involvement with common migraine 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 CC2D2A as a Meckel syndrome gene adds an important piece to the ciliopathy puzzle Wikidata
Independent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk culture Wikidata
Isolated populations and complex disease gene identification Wikidata
Large recurrent microdeletions associated with schizophrenia Wikidata
Meta-analysis of 28,141 individuals identifies common variants within five new loci that influence uric acid concentrations Wikidata
Multiple common variants for celiac disease influencing immune gene expression 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
OSBPL10, a novel candidate gene for high triglyceride trait in dyslipidemic Finnish subjects, regulates cellular lipid metabolism 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
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
Story of my roots, 2004: 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
Use of genome-wide expression data to mine the "Gray Zone" of GWA studies leads to novel candidate obesity genes Wikidata
Variants in MTNR1B influence fasting glucose levels Wikidata

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