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Worldwide increase in incidence of Type I diabetes : the analysis of the data on published incidence trends

Diabetologia, 1999-12, Vol.42 (12), p.1395-1403

1999

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Archaeological Artefact Database of Finland (AADA)

Scientific data, 2024-07, Vol.11 (1), p.815-11, Article 815

2024

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A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions

Molecular psychiatry, 2015-02, Vol.20 (2), p.275-282

2015

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Clinical and laboratory characteristics of Finnish lupus erythematosus patients with cutaneous manifestations

Lupus, 2008-04, Vol.17 (4), p.337-347

2008

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An empirical comparison of case-control and trio based study designs in high throughput association mapping

Journal of medical genetics, 2006-07, Vol.43 (7), p.617-624

2006

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Genome scan on Swedish Alzheimer's disease families

Molecular psychiatry, 2006-02, Vol.11 (2), p.182-186

2006

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Analysis of Complement C3 Gene Reveals Susceptibility to Severe Preeclampsia

Frontiers in immunology, 2017-05, Vol.8, p.589-589

2017

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Clinical associations of the risk alleles of HLA-cw6 and CCHCR1WWCC in psoriasis

Acta dermato-venereologica, 2007, Vol.87 (2), p.127-134

2007

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A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

Human molecular genetics, 2007-03, Vol.16 (6), p.667-677

2007

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Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene

Human genetics, 2004-04, Vol.114 (5), p.510-516

2004

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Genetic background and the risk of otitis media

International journal of pediatric otorhinolaryngology, 2012-01, Vol.76 (1), p.41-44

2012

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SNP Variations in the 7q33 Region Containing DGKI are Associated with Dyslexia in the Finnish and German Populations

Behavior genetics, 2011, Vol.41 (1), p.134-140

2011

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Bayesian Association Mapping for Quantitative Traits in a Mixture of Two Populations

Genetic epidemiology, 2001, Vol.21 (S1), p.S692-S699

2001

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Analysis of 9p24 and 11p12-13 regions in autism spectrum disorders: rs1340513 in the JMJD2C gene is associated with ASDs in Finnish sample

Psychiatric genetics, 2010-06, Vol.20 (3), p.102-108

2010

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Association analysis for quantitative traits by data mining: QHPM

Annals of human genetics, 2002-11, Vol.66 (5‐6), p.419-429

2002

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Interleukin‐8 promoter polymorphism is associated with the initial repose to bevacizumab in AMD treatment

Acta ophthalmologica (Oxford, England), 2013-08, Vol.91 (s252), p.0-0

2013

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Association analysis for quantitative traits by data mining: QHPM

Annals of human genetics, 2002-11, Vol.66 (5-6), p.419-429

2002

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Mining Associations Between Genetic Markers, Phenotypes, and Covariates

Genetic epidemiology, 2001, Vol.21 (S1), p.S588-S593

2001

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A novel low-penetrance locus for familial glioma at 15q23-q26.3

Cancer research (Chicago, Ill.), 2002-07, Vol.62 (13), p.3798-3802

2002

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The effects of interleukin‐8, VEGF and CFH polymorphisms on the long‐term response to bevacizumab therapy in exudative age‐related macular degeneration

Acta ophthalmologica (Oxford, England), 2013-08, Vol.91 (s252), p.0-0

2013

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Data Mining Applied to Linkage Disequilibrium Mapping

American journal of human genetics, 2000-07, Vol.67 (1), p.133-145

2000

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Haplotype associations define target regions for susceptibility loci in systemic lupus erythematosus

European journal of human genetics : EJHG, 2004-06, Vol.12 (6), p.489-494

2004

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A bayesian markov chain monte carlo approach to map disease genes in simulated GAW11 data

Genetic epidemiology, 1999, Vol.17 (S1), p.S743-S748

1999

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Estimation of Transmission Probabilities in Families Ascertained through a Proband with Variable Age-at-Onset Disease: Application to the HLA A, B and DR Loci in Finnish Families with Type 1 Diabetes

Human heredity, 2000-09, Vol.50 (5), p.308-317

2000

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Neonatal anthropometric measurements and risk of childhood-onset type 1 diabetes. DiMe Study Group

Diabetes care, 1999-12, Vol.22 (12), p.2092-2094

1999

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Worldwide increase in incidence of Type I diabetes : the analysis of the data on published incidence trends

Archaeological Artefact Database of Finland (AADA)

A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions

Clinical and laboratory characteristics of Finnish lupus erythematosus patients with cutaneous manifestations

An empirical comparison of case-control and trio based study designs in high throughput association mapping

Genome scan on Swedish Alzheimer's disease families

Analysis of Complement C3 Gene Reveals Susceptibility to Severe Preeclampsia

Clinical associations of the risk alleles of HLA-cw6 and CCHCR1WWCC in psoriasis

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene

Genetic background and the risk of otitis media

SNP Variations in the 7q33 Region Containing DGKI are Associated with Dyslexia in the Finnish and German Populations

Bayesian Association Mapping for Quantitative Traits in a Mixture of Two Populations

Analysis of 9p24 and 11p12-13 regions in autism spectrum disorders: rs1340513 in the JMJD2C gene is associated with ASDs in Finnish sample

Association analysis for quantitative traits by data mining: QHPM

Interleukin‐8 promoter polymorphism is associated with the initial repose to bevacizumab in AMD treatment

Association analysis for quantitative traits by data mining: QHPM

Mining Associations Between Genetic Markers, Phenotypes, and Covariates

A novel low-penetrance locus for familial glioma at 15q23-q26.3

The effects of interleukin‐8, VEGF and CFH polymorphisms on the long‐term response to bevacizumab therapy in exudative age‐related macular degeneration

Data Mining Applied to Linkage Disequilibrium Mapping

Haplotype associations define target regions for susceptibility loci in systemic lupus erythematosus

A bayesian markov chain monte carlo approach to map disease genes in simulated GAW11 data

Estimation of Transmission Probabilities in Families Ascertained through a Proband with Variable Age-at-Onset Disease: Application to the HLA A, B and DR Loci in Finnish Families with Type 1 Diabetes

Neonatal anthropometric measurements and risk of childhood-onset type 1 diabetes. DiMe Study Group

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