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Items: 1 to 20 of 81

1.

Fine-Scale Genetic Structure in Finland.

Kerminen S, Havulinna AS, Hellenthal G, Martin AR, Sarin AP, Perola M, Palotie A, Salomaa V, Daly MJ, Ripatti S, Pirinen M.

G3 (Bethesda). 2017 Oct 5;7(10):3459-3468. doi: 10.1534/g3.117.300217.

2.

Genome-wide association study of bronchopulmonary dysplasia: a potential role for variants near the CRP gene.

Mahlman M, Karjalainen MK, Huusko JM, Andersson S, Kari MA, Tammela OKT, Sankilampi U, Lehtonen L, Marttila RH, Bassler D, Poets CF, Lacaze-Masmonteil T, Danan C, Delacourt C, Palotie A, Muglia LJ, Lavoie PM, Hadchouel A, Rämet M, Hallman M.

Sci Rep. 2017 Aug 24;7(1):9271. doi: 10.1038/s41598-017-08977-w.

3.

The prevalence of diseases caused by lysosome-related genes in a cohort of undiagnosed patients.

Vairo FP, Boczek NJ, Cousin MA, Kaiwar C, Blackburn PR, Conboy E, Lanpher BC, Gavrilova RH, Pichurin PN, Lazaridis KN, Babovic-Vuksanovic D, Klee EW.

Mol Genet Metab Rep. 2017 Aug 11;13:46-51. doi: 10.1016/j.ymgmr.2017.08.001. eCollection 2017 Dec.

4.

Genetics in an isolated population like Finland: a different basis for genomic medicine?

Kääriäinen H, Muilu J, Perola M, Kristiansson K.

J Community Genet. 2017 Oct;8(4):319-326. doi: 10.1007/s12687-017-0318-4. Epub 2017 Jul 20.

5.

A population-specific reference panel empowers genetic studies of Anabaptist populations.

Hou L, Kember RL, Roach JC, O'Connell JR, Craig DW, Bucan M, Scott WK, Pericak-Vance M, Haines JL, Crawford MH, Shuldiner AR, McMahon FJ.

Sci Rep. 2017 Jul 20;7(1):6079. doi: 10.1038/s41598-017-05445-3. Erratum in: Sci Rep. 2018 Apr 25;8(1):6771.

6.

Whole-genome view of the consequences of a population bottleneck using 2926 genome sequences from Finland and United Kingdom.

Chheda H, Palta P, Pirinen M, McCarthy S, Walter K, Koskinen S, Salomaa V, Daly M, Durbin R, Palotie A, Aittokallio T, Ripatti S.

Eur J Hum Genet. 2017 Apr;25(4):477-484. doi: 10.1038/ejhg.2016.205. Epub 2017 Feb 1.

7.

The impact of recent population history on the deleterious mutation load in humans and close evolutionary relatives.

Simons YB, Sella G.

Curr Opin Genet Dev. 2016 Dec;41:150-158. doi: 10.1016/j.gde.2016.09.006. Epub 2016 Oct 13. Review.

8.

Exome sequencing in pooled DNA samples to identify maternal pre-eclampsia risk variants.

Kaartokallio T, Wang J, Heinonen S, Kajantie E, Kivinen K, Pouta A, Gerdhem P, Jiao H, Kere J, Laivuori H.

Sci Rep. 2016 Jul 7;6:29085. doi: 10.1038/srep29085.

9.

Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland.

Trotta L, Hautala T, Hämäläinen S, Syrjänen J, Viskari H, Almusa H, Lepisto M, Kaustio M, Porkka K, Palotie A, Seppänen M, Saarela J.

Eur J Hum Genet. 2016 Oct;24(10):1473-8. doi: 10.1038/ejhg.2016.37. Epub 2016 May 4.

10.

The (in)famous GWAS P-value threshold revisited and updated for low-frequency variants.

Fadista J, Manning AK, Florez JC, Groop L.

Eur J Hum Genet. 2016 Aug;24(8):1202-5. doi: 10.1038/ejhg.2015.269. Epub 2016 Jan 6.

11.

Abnormal wiring of the connectome in adults with high-functioning autism spectrum disorder.

Roine U, Roine T, Salmi J, Nieminen-von Wendt T, Tani P, Leppämäki S, Rintahaka P, Caeyenberghs K, Leemans A, Sams M.

Mol Autism. 2015 Dec 15;6:65. doi: 10.1186/s13229-015-0058-4. eCollection 2015.

12.

Impulsive alcohol-related risk-behavior and emotional dysregulation among individuals with a serotonin 2B receptor stop codon.

Tikkanen R, Tiihonen J, Rautiainen MR, Paunio T, Bevilacqua L, Panarsky R, Goldman D, Virkkunen M.

Transl Psychiatry. 2015 Nov 17;5:e681. doi: 10.1038/tp.2015.170.

13.

Predisposition to Childhood Otitis Media and Genetic Polymorphisms within the Toll-Like Receptor 4 (TLR4) Locus.

Hafrén L, Einarsdottir E, Kentala E, Hammarén-Malmi S, Bhutta MF, MacArthur CJ, Wilmot B, Casselbrant M, Conley YP, Weeks DE, Mandel EM, Vaarala O, Kallio A, Melin M, Nieminen JK, Leinonen E, Kere J, Mattila PS.

PLoS One. 2015 Jul 15;10(7):e0132551. doi: 10.1371/journal.pone.0132551. eCollection 2015.

14.

GENLIB: an R package for the analysis of genealogical data.

Gauvin H, Lefebvre JF, Moreau C, Lavoie EM, Labuda D, Vézina H, Roy-Gagnon MH.

BMC Bioinformatics. 2015 May 15;16:160. doi: 10.1186/s12859-015-0581-5.

15.

Genetic causal beliefs about morbidity: associations with health behaviors and health outcome beliefs about behavior changes between 1982-2002 in the Finnish population.

Haukkala A, Konttinen H, Hankonen N, Perola M, Kääriäinen H, Salomaa V.

BMC Public Health. 2015 Apr 17;15:389. doi: 10.1186/s12889-015-1657-x.

16.

Constrained spherical deconvolution-based tractography and tract-based spatial statistics show abnormal microstructural organization in Asperger syndrome.

Roine U, Salmi J, Roine T, Wendt TN, Leppämäki S, Rintahaka P, Tani P, Leemans A, Sams M.

Mol Autism. 2015 Jan 16;6:4. doi: 10.1186/2040-2392-6-4. eCollection 2015.

17.

How evolutionary principles improve the understanding of human health and disease.

Gluckman PD, Low FM, Buklijas T, Hanson MA, Beedle AS.

Evol Appl. 2011 Mar;4(2):249-63. doi: 10.1111/j.1752-4571.2010.00164.x.

18.

Evolutionary principles and their practical application.

Hendry AP, Kinnison MT, Heino M, Day T, Smith TB, Fitt G, Bergstrom CT, Oakeshott J, Jørgensen PS, Zalucki MP, Gilchrist G, Southerton S, Sih A, Strauss S, Denison RF, Carroll SP.

Evol Appl. 2011 Mar;4(2):159-83. doi: 10.1111/j.1752-4571.2010.00165.x.

19.

Population distribution and ancestry of the cancer protective MDM2 SNP285 (rs117039649).

Knappskog S, Gansmo LB, Dibirova K, Metspalu A, Cybulski C, Peterlongo P, Aaltonen L, Vatten L, Romundstad P, Hveem K, Devilee P, Evans GD, Lin D, Van Camp G, Manolopoulos VG, Osorio A, Milani L, Ozcelik T, Zalloua P, Mouzaya F, Bliznetz E, Balanovska E, Pocheshkova E, Kučinskas V, Atramentova L, Nymadawa P, Titov K, Lavryashina M, Yusupov Y, Bogdanova N, Koshel S, Zamora J, Wedge DC, Charlesworth D, Dörk T, Balanovsky O, Lønning PE.

Oncotarget. 2014 Sep 30;5(18):8223-34.

20.

Exome sequencing identifies FANCM as a susceptibility gene for triple-negative breast cancer.

Kiiski JI, Pelttari LM, Khan S, Freysteinsdottir ES, Reynisdottir I, Hart SN, Shimelis H, Vilske S, Kallioniemi A, Schleutker J, Leminen A, Bützow R, Blomqvist C, Barkardottir RB, Couch FJ, Aittomäki K, Nevanlinna H.

Proc Natl Acad Sci U S A. 2014 Oct 21;111(42):15172-7. doi: 10.1073/pnas.1407909111. Epub 2014 Oct 6.

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