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LCCS: A Lethal Motoneuron Disease of the Fetus Maps to Chromosome 9 q34.
- Published in:
- Annals of the New York Academy of Sciences, 1998, v. 857, n. 1, p. 260, doi. 10.1111/j.1749-6632.1998.tb10127.x
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- Article
Variation in the selenoprotein S gene locus is associated with coronary heart disease and ischemic stroke in two independent Finnish cohorts.
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- Human Genetics, 2007, v. 122, n. 3/4, p. 355, doi. 10.1007/s00439-007-0402-7
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- Article
Prevalence of dichromate sensitivity.
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- Contact Dermatitis (01051873), 1983, v. 9, n. 3, p. 190, doi. 10.1111/j.1600-0536.1983.tb04356.x
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- Article
Comparison of A1-test and Finn chamber test.
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- Contact Dermatitis (01051873), 1981, v. 7, n. 4, p. 192, doi. 10.1111/j.1600-0536.1981.tb04041.x
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- Article
Nickel sensitivity in the general population.
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- Contact Dermatitis (01051873), 1979, v. 5, n. 1, p. 27, doi. 10.1111/j.1600-0536.1979.tb05531.x
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- Publication type:
- Article
Electrospray Encapsulation of Hydrophilic and Hydrophobic Drugs in Poly( L-lactic acid) Nanoparticles.
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- Small, 2009, v. 5, n. 15, p. 1791, doi. 10.1002/smll.200801907
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- Article
Primate-specific evolution of noncoding element insertion into PLA2G4C and human preterm birth.
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- BMC Medical Genomics, 2010, v. 3, p. 62, doi. 10.1186/1755-8794-3-62
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- Article
Genetics of Healthy Aging in Europe.
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- Annals of the New York Academy of Sciences, 2007, v. 1100, p. 21, doi. 10.1196/annals.1395.003
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- Article
The impact of newly identified loci on coronary heart disease, stroke and total mortality in the MORGAM prospective cohorts.
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- Genetic Epidemiology, 2009, v. 33, n. 3, p. 237, doi. 10.1002/gepi.20374
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- Article
Angiotensin-converting enzyme genotypes in the high- and low-risk area for coronary heart disease in Finland.
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- Genetic Epidemiology, 1995, v. 12, n. 4, p. 391, doi. 10.1002/gepi.1370120407
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- Article
3D Printing of Drug Nanocrystals for Film Formulations.
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- Molecules, 2021, v. 26, n. 13, p. 3941, doi. 10.3390/molecules26133941
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- Article
Understanding Critical Quality Attributes for Nanocrystals from Preparation to Delivery.
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- Molecules, 2015, v. 20, n. 12, p. 22286, doi. 10.3390/molecules201219851
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- Article
Mother’s Genome or Maternally-Inherited Genes Acting in the Fetus Influence Gestational Age in Familial Preterm Birth.
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- Human Heredity, 2009, v. 68, n. 3, p. 209, doi. 10.1159/000224641
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- Article
Positional Cloning of Disease Genes: Advantages of Genetic Isolates.
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- Human Heredity, 2000, v. 50, n. 1, p. 66, doi. 10.1159/000022892
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- Article
DNA Profiling in a Genetically Isolated Population Using Three Hypervariable DNA Markers.
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- Human Heredity, 1992, v. 42, n. 6, p. 372, doi. 10.1159/000154100
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- Article
Classical twin studies and beyond.
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- Nature Reviews Genetics, 2002, v. 3, n. 11, p. 872, doi. 10.1038/nrg932
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- Article
USE OF POPULATION ISOLATES FOR MAPPING COMPLEX TRAITS.
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- Nature Reviews Genetics, 2000, v. 1, n. 3, p. 182, doi. 10.1038/35042049
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- Article
Circadian Clock-Related Polymorphisms in Seasonal Affective Disorder and their Relevance to Diurnal Preference.
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- Neuropsychopharmacology, 2003, v. 28, n. 4, p. 734, doi. 10.1038/sj.npp.1300121
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- Article
Phenotype mining in CNV carriers from a population cohort†.
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- Human Molecular Genetics, 2011, v. 20, n. 13, p. 2686
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- Article
Association of serum cotinine level with a cluster of three nicotinic acetylcholine receptor genes (CHRNA3/CHRNA5/CHRNB4) on chromosome 15.
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- Human Molecular Genetics, 2009, v. 18, n. 20, p. 4007, doi. 10.1093/hmg/ddp322
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- Article
Linkage and linkage disequilibrium scan for autism loci in an extended pedigree from Finland.
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- Human Molecular Genetics, 2009, v. 18, n. 15, p. 2912, doi. 10.1093/hmg/ddp229
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- Article
Common variants in the region around Osterix are associated with bone mineral density and growth in childhood.
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- Human Molecular Genetics, 2009, v. 18, n. 8, p. 1510, doi. 10.1093/hmg/ddp052
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- Article
Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments.
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- Human Molecular Genetics, 2007, v. 16, n. 20, p. 3517, doi. 10.1093/hmg/ddm207
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- Article
Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.
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- Human Molecular Genetics, 2007, v. 16, n. 5, p. 453, doi. 10.1093/hmg/ddl462
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- Article
Cross-species analyses implicate Lipin 1 involvement in human glucose metabolism.
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- Human Molecular Genetics, 2006, v. 15, n. 3, p. 377, doi. 10.1093/hmg/ddi448
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- Article
Lessons from studying monogenic disease for common disease.
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- Human Molecular Genetics, 2006, v. 15, n. suppl_1, p. R67, doi. 10.1093/hmg/ddl060
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- Article
Lessons from studying monogenic disease for common disease.
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- Human Molecular Genetics, 2006, v. 15, n. 1, p. r67, doi. 10.1093/hmg/ddl060
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- Article
Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and Twinky.
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- Human Molecular Genetics, 2005, v. 14, n. 20, p. 2981, doi. 10.1093/hmg/ddi328
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- Article
USF1 and dyslipidemias: converging evidence for a functional intronic variant.
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- Human Molecular Genetics, 2005, v. 14, n. 17, p. 2595, doi. 10.1093/hmg/ddi294
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- Article
Hydrolethalus syndrome is caused by a missense mutation in a novel gene HYLS1.
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- Human Molecular Genetics, 2005, v. 14, n. 11, p. 1475, doi. 10.1093/hmg/ddi157
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- Article
A mouse model for Finnish variant late infantile neuronal ceroid lipofuscinosis, CLN5, reveals neuropathology associated with early aging.
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- Human Molecular Genetics, 2004, v. 13, n. 23, p. 2893, doi. 10.1093/hmg/ddh312
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- Article
Search for cognitive trait components of schizophrenia reveals a locus for verbal learning and memory on 4q and for visual working memory on 2q.
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- Human Molecular Genetics, 2004, v. 13, n. 16, p. 1693, doi. 10.1093/hmg/ddh184
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- Article
Haplotype transmission analysis provides evidence of association for DISC1 to schizophrenia and suggests sex-dependent effects.
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- Human Molecular Genetics, 2003, v. 12, n. 23, p. 3151, doi. 10.1093/hmg/ddg341
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- Article
Molecular defect of RAPADILINO syndrome expands the phenotype spectrum of RECQL diseases.
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- Human Molecular Genetics, 2003, v. 12, n. 21, p. 2837, doi. 10.1093/hmg/ddg306
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- Article
Genetic Loci Associated With C-Reactive Protein Levels and Risk of Coronary Heart Disease.
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- JAMA: Journal of the American Medical Association, 2009, v. 302, n. 1, p. 37, doi. 10.1001/jama.2009.954
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- Article
Several cooperating binding sites mediate the interaction of a lysosomal enzyme with phosphotransferase.
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- EMBO Journal, 1997, v. 16, n. 22, p. 6684, doi. 10.1093/emboj/16.22.6684
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- Article
Brain gene expression profiles of Cln1 and Cln5 deficient mice unravels common molecular pathways underlying neuronal degeneration in NCL diseases.
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- BMC Genomics, 2008, v. 9, p. 1, doi. 10.1186/1471-2164-9-146
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- Article
Association analysis of the AIRE and insulin genes in Finnish type 1 diabetic patients.
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- Immunogenetics, 2006, v. 58, n. 5/6, p. 331, doi. 10.1007/s00251-006-0088-3
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- Article
A population-specific HTR2B stop codon predisposes to severe impulsivity.
- Published in:
- 2011
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- Correction notice
A population-specific HTR2B stop codon predisposes to severe impulsivity.
- Published in:
- Nature, 2010, v. 468, n. 7327, p. 1061, doi. 10.1038/nature09629
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- Article
Integrating common and rare genetic variation in diverse human populations.
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- Nature, 2010, v. 467, n. 7311, p. 52, doi. 10.1038/nature09298
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- Article
Marfan Database (second edition): software and database for the analysis of mutations in the human FBN1 gene.
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- Nucleic Acids Research, 1997, v. 25, n. 1, p. 147, doi. 10.1093/nar/25.1.147
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- Article
Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland.
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- European Journal of Human Genetics, 2011, v. 19, n. 7, p. 776, doi. 10.1038/ejhg.2011.23
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- Publication type:
- Article
NordicDB: a Nordic pool and portal for genome-wide control data.
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- European Journal of Human Genetics, 2010, v. 18, n. 12, p. 1322, doi. 10.1038/ejhg.2010.112
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- Article
MYO9B polymorphisms in multiple sclerosis.
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- European Journal of Human Genetics, 2009, v. 17, n. 6, p. 840, doi. 10.1038/ejhg.2008.251
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- Article
Genome-wide linkage screen for stature and body mass index in 3.032 families: evidence for sex- and population-specific genetic effects.
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- European Journal of Human Genetics, 2009, v. 17, n. 2, p. 258, doi. 10.1038/ejhg.2008.152
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- Publication type:
- Article
Genome-wide search for QTLs for apolipoprotein A-I level in elderly Swedish DZ twins: evidence of female-specific locus on 15q11–13.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1103, doi. 10.1038/ejhg.2008.50
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- Article
Evaluation of HapMap data in six populations of European descent.
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- European Journal of Human Genetics, 2008, v. 16, n. 9, p. 1142, doi. 10.1038/ejhg.2008.77
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- Article
Within-family outliers: segregating alleles or environmental effects? A linkage analysis of height from 5815 sibling pairs.
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- European Journal of Human Genetics, 2008, v. 16, n. 4, p. 516, doi. 10.1038/sj.ejhg.5201992
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- Article
The federated database – a basis for biobank-based post-genome studies, integrating phenome and genome data from 600 000 twin pairs in Europe.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 7, p. 718, doi. 10.1038/sj.ejhg.5201850
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- Article