Preussner A, Leinonen J, Riikonen J, Pirinen M, Tukiainen T
Eur J Hum Genet. 2024; 33(1):89-97.
PMID: 39465313
PMC: 11711460.
DOI: 10.1038/s41431-024-01707-7.
Kivisild T, Saag L, Hui R, Biagini S, Pankratov V, DAtanasio E
Am J Hum Genet. 2021; 108(9):1792-1806.
PMID: 34411538
PMC: 8456179.
DOI: 10.1016/j.ajhg.2021.07.012.
Wiesen B, Hafren L, Einarsdottir E, Kere J, Mattila P, Santos-Cortez R
Genet Test Mol Biomarkers. 2019; 23(11):823-827.
PMID: 31693456
PMC: 6857544.
DOI: 10.1089/gtmb.2019.0135.
Lokki A, Daly E, Triebwasser M, Kurki M, Roberson E, Happola P
Hypertension. 2017; 70(2):365-371.
PMID: 28652462
PMC: 5535812.
DOI: 10.1161/HYPERTENSIONAHA.117.09406.
Lim R, Silver A, Silver M, Borroto C, Spurrier B, Petrossian T
Genet Med. 2015; 18(2):174-9.
PMID: 25880441
DOI: 10.1038/gim.2015.52.
Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland.
Wang S, Agarwala V, Flannick J, Chiang C, Altshuler D, Hirschhorn J
Am J Hum Genet. 2014; 94(5):710-20.
PMID: 24768551
PMC: 4067550.
DOI: 10.1016/j.ajhg.2014.03.019.
Increased Female MS Incidence and Differences in Gender-Specific Risk in Medium- and High-Risk Regions in Finland from 1981-2010.
Holmberg M, Murtonen A, Elovaara I, Sumelahti M
Mult Scler Int. 2013; 2013:182516.
PMID: 24324888
PMC: 3844161.
DOI: 10.1155/2013/182516.
Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging.
Surakka I, Kristiansson K, Anttila V, Inouye M, Barnes C, Moutsianas L
Genome Res. 2010; 20(10):1344-51.
PMID: 20810666
PMC: 2945183.
DOI: 10.1101/gr.106534.110.
NordicDB: a Nordic pool and portal for genome-wide control data.
Leu M, Humphreys K, Surakka I, Rehnberg E, Muilu J, Rosenstrom P
Eur J Hum Genet. 2010; 18(12):1322-6.
PMID: 20664631
PMC: 3002853.
DOI: 10.1038/ejhg.2010.112.
Reduced-volume and low-volume typing of Y-chromosomal SNPs to obtain Finnish Y-chromosomal compound haplotypes.
Heinrich M, Braun T, Sanger T, Saukko P, Lutz-Bonengel S, Schmidt U
Int J Legal Med. 2009; 123(5):413-8.
PMID: 19711091
DOI: 10.1007/s00414-009-0358-3.
Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in Northern Europe.
Salmela E, Lappalainen T, Fransson I, Andersen P, Dahlman-Wright K, Fiebig A
PLoS One. 2008; 3(10):e3519.
PMID: 18949038
PMC: 2567036.
DOI: 10.1371/journal.pone.0003519.
Subpopulation difference scanning: a strategy for exclusion mapping of susceptibility genes.
Salmela E, Taskinen O, Seppanen J, Sistonen P, Daly M, Lahermo P
J Med Genet. 2006; 43(7):590-7.
PMID: 16443857
PMC: 2564554.
DOI: 10.1136/jmg.2005.038414.
Different effects of a CD14 gene polymorphism on disease outcome in patients with alcoholic liver disease and chronic hepatitis C infection.
Meiler C, Muhlbauer M, Johann M, Hartmann A, Schnabl B, Wodarz N
World J Gastroenterol. 2005; 11(38):6031-7.
PMID: 16273620
PMC: 4436730.
DOI: 10.3748/wjg.v11.i38.6031.
A developmental behavior-genetic perspective on alcoholism risk.
Rose R
Alcohol Health Res World. 2005; 22(2):131-43.
PMID: 15706788
PMC: 6761808.
The western and eastern roots of the Saami--the story of genetic "outliers" told by mitochondrial DNA and Y chromosomes.
Tambets K, Rootsi S, Kivisild T, Help H, Serk P, Loogvali E
Am J Hum Genet. 2004; 74(4):661-82.
PMID: 15024688
PMC: 1181943.
DOI: 10.1086/383203.
Finnish Disease Heritage II: population prehistory and genetic roots of Finns.
Norio R
Hum Genet. 2003; 112(5-6):457-69.
PMID: 12627296
DOI: 10.1007/s00439-002-0876-2.
Finnish Disease Heritage I: characteristics, causes, background.
Norio R
Hum Genet. 2003; 112(5-6):441-56.
PMID: 12627295
DOI: 10.1007/s00439-002-0875-3.
The effect of population history on the lengths of ancestral chromosome segments.
Chapman N, Thompson E
Genetics. 2002; 162(1):449-58.
PMID: 12242253
PMC: 1462250.
DOI: 10.1093/genetics/162.1.449.
[Demographic reproduction and genetic transmission in the north-east of the province of Quebec (18th-20th centuries)].
Bouchard G, Laberge C, Scriver C
Eur J Popul. 1988; 4(1):39-67.
PMID: 12158994
DOI: 10.1007/BF01797106.
A coalescent model of ancestry for a rare allele.
Graham J, Thompson E
Genetics. 2000; 156(1):375-84.
PMID: 10978301
PMC: 1461240.
DOI: 10.1093/genetics/156.1.375.