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Items: 1 to 20 of 23

1.

Genetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropy.

Byars SG, Huang QQ, Gray LA, Bakshi A, Ripatti S, Abraham G, Stearns SC, Inouye M.

PLoS Genet. 2017 Jun 22;13(6):e1006328. doi: 10.1371/journal.pgen.1006328. eCollection 2017 Jun.

2.

The impact of rare and low-frequency genetic variants in common disease.

Bomba L, Walter K, Soranzo N.

Genome Biol. 2017 Apr 27;18(1):77. doi: 10.1186/s13059-017-1212-4. Review.

3.

Genome-Wide Meta-Analysis of Sciatica in Finnish Population.

Lemmelä S, Solovieva S, Shiri R, Benner C, Heliövaara M, Kettunen J, Anttila V, Ripatti S, Perola M, Seppälä I, Juonala M, Kähönen M, Salomaa V, Viikari J, Raitakari OT, Lehtimäki T, Palotie A, Viikari-Juntura E, Husgafvel-Pursiainen K.

PLoS One. 2016 Oct 20;11(10):e0163877. doi: 10.1371/journal.pone.0163877. eCollection 2016.

4.

Combined hybridization capture and shotgun sequencing for ancient DNA analysis of extinct wild and domestic dromedary camel.

Mohandesan E, Speller CF, Peters J, Uerpmann HP, Uerpmann M, De Cupere B, Hofreiter M, Burger PA.

Mol Ecol Resour. 2017 Mar;17(2):300-313. doi: 10.1111/1755-0998.12551. Epub 2016 Aug 1.

5.

Genomic study of the Ket: a Paleo-Eskimo-related ethnic group with significant ancient North Eurasian ancestry.

Flegontov P, Changmai P, Zidkova A, Logacheva MD, Altınışık NE, Flegontova O, Gelfand MS, Gerasimov ES, Khrameeva EE, Konovalova OP, Neretina T, Nikolsky YV, Starostin G, Stepanova VV, Travinsky IV, Tříska M, Tříska P, Tatarinova TV.

Sci Rep. 2016 Feb 11;6:20768. doi: 10.1038/srep20768.

6.

Impact of imputation methods on the amount of genetic variation captured by a single-nucleotide polymorphism panel in soybeans.

Xavier A, Muir WM, Rainey KM.

BMC Bioinformatics. 2016 Feb 2;17:55. doi: 10.1186/s12859-016-0899-7.

7.

Choosing Subsamples for Sequencing Studies by Minimizing the Average Distance to the Closest Leaf.

Kang JT, Zhang P, Zöllner S, Rosenberg NA.

Genetics. 2015 Oct;201(2):499-511. doi: 10.1534/genetics.115.176909. Epub 2015 Aug 24.

8.

The European Genome-phenome Archive of human data consented for biomedical research.

Lappalainen I, Almeida-King J, Kumanduri V, Senf A, Spalding JD, Ur-Rehman S, Saunders G, Kandasamy J, Caccamo M, Leinonen R, Vaughan B, Laurent T, Rowland F, Marin-Garcia P, Barker J, Jokinen P, Torres AC, de Argila JR, Llobet OM, Medina I, Puy MS, Alberich M, de la Torre S, Navarro A, Paschall J, Flicek P.

Nat Genet. 2015 Jul;47(7):692-5. doi: 10.1038/ng.3312. No abstract available.

9.

Derived immune and ancestral pigmentation alleles in a 7,000-year-old Mesolithic European.

Olalde I, Allentoft ME, Sánchez-Quinto F, Santpere G, Chiang CW, DeGiorgio M, Prado-Martinez J, Rodríguez JA, Rasmussen S, Quilez J, Ramírez O, Marigorta UM, Fernández-Callejo M, Prada ME, Encinas JM, Nielsen R, Netea MG, Novembre J, Sturm RA, Sabeti P, Marquès-Bonet T, Navarro A, Willerslev E, Lalueza-Fox C.

Nature. 2014 Mar 13;507(7491):225-8. doi: 10.1038/nature12960. Epub 2014 Jan 26.

10.

Upper Palaeolithic Siberian genome reveals dual ancestry of Native Americans.

Raghavan M, Skoglund P, Graf KE, Metspalu M, Albrechtsen A, Moltke I, Rasmussen S, Stafford TW Jr, Orlando L, Metspalu E, Karmin M, Tambets K, Rootsi S, Mägi R, Campos PF, Balanovska E, Balanovsky O, Khusnutdinova E, Litvinov S, Osipova LP, Fedorova SA, Voevoda MI, DeGiorgio M, Sicheritz-Ponten T, Brunak S, Demeshchenko S, Kivisild T, Villems R, Nielsen R, Jakobsson M, Willerslev E.

Nature. 2014 Jan 2;505(7481):87-91. doi: 10.1038/nature12736. Epub 2013 Nov 20.

11.

Local exome sequences facilitate imputation of less common variants and increase power of genome wide association studies.

Joshi PK, Prendergast J, Fraser RM, Huffman JE, Vitart V, Hayward C, McQuillan R, Glodzik D, Polašek O, Hastie ND, Rudan I, Campbell H, Wright AF, Haley CS, Wilson JF, Navarro P.

PLoS One. 2013 Jul 16;8(7):e68604. doi: 10.1371/journal.pone.0068604. Print 2013.

12.

Genome-wide association study on detailed profiles of smoking behavior and nicotine dependence in a twin sample.

Loukola A, Wedenoja J, Keskitalo-Vuokko K, Broms U, Korhonen T, Ripatti S, Sarin AP, Pitkäniemi J, He L, Häppölä A, Heikkilä K, Chou YL, Pergadia ML, Heath AC, Montgomery GW, Martin NG, Madden PA, Kaprio J.

Mol Psychiatry. 2014 May;19(5):615-24. doi: 10.1038/mp.2013.72. Epub 2013 Jun 11.

13.

Genetic variants and their interactions in disease risk prediction - machine learning and network perspectives.

Okser S, Pahikkala T, Aittokallio T.

BioData Min. 2013 Mar 1;6(1):5. doi: 10.1186/1756-0381-6-5.

14.

Anisotropic isolation by distance: the main orientations of human genetic differentiation.

Jay F, Sjödin P, Jakobsson M, Blum MG.

Mol Biol Evol. 2013 Mar;30(3):513-25. doi: 10.1093/molbev/mss259. Epub 2012 Nov 20.

15.

Genotype imputation in a coalescent model with infinitely-many-sites mutation.

Huang L, Buzbas EO, Rosenberg NA.

Theor Popul Biol. 2013 Aug;87:62-74. doi: 10.1016/j.tpb.2012.09.006. Epub 2012 Oct 16.

16.

Utilizing extended pedigree information for discovery and confirmation of copy number variable regions among Mexican Americans.

Blackburn A, Göring HH, Dean A, Carless MA, Dyer T, Kumar S, Fowler S, Curran JE, Almasy L, Mahaney M, Comuzzie A, Duggirala R, Blangero J, Lehman DM.

Eur J Hum Genet. 2013 Apr;21(4):404-9. doi: 10.1038/ejhg.2012.188. Epub 2012 Aug 22.

17.

Intracranial aneurysm risk locus 5q23.2 is associated with elevated systolic blood pressure.

Gaál EI, Salo P, Kristiansson K, Rehnström K, Kettunen J, Sarin AP, Niemelä M, Jula A, Raitakari OT, Lehtimäki T, Eriksson JG, Widen E, Günel M, Kurki M, von und Zu Fraunberg M, Jääskeläinen JE, Hernesniemi J, Järvelin MR, Pouta A; International Consortium for Blood Pressure Genome-Wide Association Studies, Newton-Cheh C, Salomaa V, Palotie A, Perola M.

PLoS Genet. 2012;8(3):e1002563. doi: 10.1371/journal.pgen.1002563. Epub 2012 Mar 15.

18.

A common variant near the KCNJ2 gene is associated with T-peak to T-end interval.

Marjamaa A, Oikarinen L, Porthan K, Ripatti S, Peloso G, Noseworthy PA, Viitasalo M, Nieminen MS, Toivonen L, Kontula K, Peltonen L, Havulinna AS, Jula A, O'Donnell CJ, Newton-Cheh C, Perola M, Salomaa V.

Heart Rhythm. 2012 Jul;9(7):1099-103. doi: 10.1016/j.hrthm.2012.02.019. Epub 2012 Feb 15.

19.

Genome-wide association study identifies multiple loci influencing human serum metabolite levels.

Kettunen J, Tukiainen T, Sarin AP, Ortega-Alonso A, Tikkanen E, Lyytikäinen LP, Kangas AJ, Soininen P, Würtz P, Silander K, Dick DM, Rose RJ, Savolainen MJ, Viikari J, Kähönen M, Lehtimäki T, Pietiläinen KH, Inouye M, McCarthy MI, Jula A, Eriksson J, Raitakari OT, Salomaa V, Kaprio J, Järvelin MR, Peltonen L, Perola M, Freimer NB, Ala-Korpela M, Palotie A, Ripatti S.

Nat Genet. 2012 Jan 29;44(3):269-76. doi: 10.1038/ng.1073.

20.

Bayesian variable selection in searching for additive and dominant effects in genome-wide data.

Peltola T, Marttinen P, Jula A, Salomaa V, Perola M, Vehtari A.

PLoS One. 2012;7(1):e29115. doi: 10.1371/journal.pone.0029115. Epub 2012 Jan 3.

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