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Author Details
Full Name
P??ivi Onkamo
Affiliation
University of Turku
ORCID
Career Start Year
1999
Papers
47
H Index
21
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
36513080
Genetic admixture and language shift in the medieval Volga-Oka interfluve.
Curr Biol
2023
35393601
Emergence and intensification of dairying in the Caucasus and Eurasian steppes.
Nat Ecol Evol
2022
34618559
Ten millennia of hepatitis B virus evolution.
Science
2021
32315354
Buried in water, burdened by nature-Resilience carried the Iron Age people through Fimbulvinter.
PLoS One
2020
32795443
Ancient Bacterial Genomes Reveal a High Diversity of Treponema pallidum Strains in Early Modern Europe.
Curr Biol
2020
31729399
Human mitochondrial DNA lineages in Iron-Age Fennoscandia suggest incipient admixture and eastern introduction of farming-related maternal ancestry.
Sci Rep
2019
30479341
Ancient Fennoscandian genomes reveal origin and spread of Siberian ancestry in Europe.
Nat Commun
2018
28733587
Identification and analysis of mtDNA genomes attributed to Finns reveal long-stagnant demographic trends obscured in the total diversity.
Sci Rep
2017
28611769
Analysis of Complement <i>C3</i> Gene Reveals Susceptibility to Severe Preeclampsia.
Front Immunol
2017
26909693
Creative Activities in Music--A Genome-Wide Linkage Analysis.
PLoS One
2016
28004803
Convergent evidence for the molecular basis of musical traits.
Sci Rep
2016
24614497
A genome-wide linkage and association study of musical aptitude identifies loci containing genes related to inner ear development and neurocognitive functions.
Mol Psychiatry
2015
26132657
Vestiges of an Ancient Border in the Contemporary Genetic Diversity of North-Eastern Europe.
PLoS One
2015
26154559
The genetic variant rs4073 Aâ¿¿T of the Interleukin-8 promoter region is associated with the earlier onset of exudative age-related macular degeneration.
Acta Ophthalmol
2015
25707602
Association and Promoter Analysis of AVPR1A in Finnish Autism Families.
Autism Res
2015
22998103
Correlation between components of newly diagnosed exudative age-related macular degeneration lesion and focal retinal sensitivity.
Acta Ophthalmol
2014
25080345
Neolithic dairy farming at the extreme of agriculture in northern Europe.
Proc Biol Sci
2014
23584701
Interleukin 8 promoter polymorphism predicts the initial response to bevacizumab treatment for exudative age-related macular degeneration.
Retina
2013
22018929
Genetic background and the risk of otitis media.
Int J Pediatr Otorhinolaryngol
2012
22380611
Mutations of complement lectin pathway genes MBL2 and MASP2 associated with placental malaria.
Malar J
2012
21203819
SNP variations in the 7q33 region containing DGKI are associated with dyslexia in the Finnish and German populations.
Behav Genet
2011
21307861
Association of the arginine vasopressin receptor 1A (AVPR1A) haplotypes with listening to music.
J Hum Genet
2011
20410850
Analysis of 9p24 and 11p12-13 regions in autism spectrum disorders: rs1340513 in the JMJD2C gene is associated with ASDs in Finnish sample.
Psychiatr Genet
2010
20122735
Screening of DNA-variants in the properdin gene (CFP) in age-related macular degeneration (AMD).
Mol Immunol
2010
19461995
Musical aptitude is associated with AVPR1A-haplotypes.
PLoS One
2009
19999660
[Identification of susceptibility genes for age-related macular degeneration--a success story of molecular genetics].
Duodecim
2009
19997561
Identification of MAMDC1 as a candidate susceptibility gene for systemic lupus erythematosus (SLE).
PLoS One
2009
19343041
Association of LOXL1 gene with Finnish exfoliation syndrome patients.
J Hum Genet
2009
18413417
Clinical and laboratory characteristics of Finnish lupus erythematosus patients with cutaneous manifestations.
Lupus
2008
19048105
Multifactor effects and evidence of potential interaction between complement factor H Y402H and LOC387715 A69S in age-related macular degeneration.
PLoS One
2008
17340018
Clinical associations of the risk alleles of HLA-Cw6 and CCHCR1*WWCC in psoriasis.
Acta Derm Venereol
2007
17309879
A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia.
Hum Mol Genet
2007
16288313
Genome scan on Swedish Alzheimer's disease families.
Mol Psychiatry
2006
16595078
A survey of data mining methods for linkage disequilibrium mapping.
Hum Genomics
2006
16258007
An empirical comparison of case-control and trio based study designs in high throughput association mapping.
J Med Genet
2006
15054392
Haplotype associations define target regions for susceptibility loci in systemic lupus erythematosus.
Eur J Hum Genet
2004
15007729
Fine mapping of the 2p11 dyslexia locus and exclusion of TACR1 as a candidate gene.
Hum Genet
2004
15059244
Increasing incidence of Type 1 diabetes--role for genes?
BMC Genet
2004
12097292
A novel low-penetrance locus for familial glioma at 15q23-q26.3.
Cancer Res
2002
12485474
Association analysis for quantitative traits by data mining: QHPM.
Ann Hum Genet
2002
11793743
Mining associations between genetic markers, phenotypes, and covariates.
Genet Epidemiol
2001
11793763
Bayesian association mapping for quantitative traits in a mixture of two populations.
Genet Epidemiol
2001
10878475
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. The DiMe Study Group.
Hum Hered
2000
10848493
Data mining applied to linkage disequilibrium mapping.
Am J Hum Genet
2000
10597524
A Bayesian Markov chain Monte Carlo approach to map disease genes in simulated GAW11 data.
Genet Epidemiol
1999
10587856
Neonatal anthropometric measurements and risk of childhood-onset type 1 diabetes. DiMe Study Group.
Diabetes Care
1999
10651256
Worldwide increase in incidence of Type I diabetes--the analysis of the data on published incidence trends.
Diabetologia
1999
1 - 47 of 47
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