Similar articles for PMID: 24768551

Year	Number of Results
2000	1
2009	1
2010	5
2011	4
2012	5
2013	13
2014	17
2015	16
2016	17
2017	14
2018	6
2019	12
2020	6
2021	4
2022	5
2023	2
2024	0

1

Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland.

Wang SR, Agarwala V, Flannick J, Chiang CW, Altshuler D; GoT2D Consortium; Hirschhorn JN. Wang SR, et al. Am J Hum Genet. 2014 May 1;94(5):710-20. doi: 10.1016/j.ajhg.2014.03.019. Epub 2014 Apr 24. Am J Hum Genet. 2014. PMID: 24768551 Free PMC article.

2

Distribution and medical impact of loss-of-function variants in the Finnish founder population.

Lim ET, Würtz P, Havulinna AS, Palta P, Tukiainen T, Rehnström K, Esko T, Mägi R, Inouye M, Lappalainen T, Chan Y, Salem RM, Lek M, Flannick J, Sim X, Manning A, Ladenvall C, Bumpstead S, Hämäläinen E, Aalto K, Maksimow M, Salmi M, Blankenberg S, Ardissino D, Shah S, Horne B, McPherson R, Hovingh GK, Reilly MP, Watkins H, Goel A, Farrall M, Girelli D, Reiner AP, Stitziel NO, Kathiresan S, Gabriel S, Barrett JC, Lehtimäki T, Laakso M, Groop L, Kaprio J, Perola M, McCarthy MI, Boehnke M, Altshuler DM, Lindgren CM, Hirschhorn JN, Metspalu A, Freimer NB, Zeller T, Jalkanen S, Koskinen S, Raitakari O, Durbin R, MacArthur DG, Salomaa V, Ripatti S, Daly MJ, Palotie A; Sequencing Initiative Suomi (SISu) Project. Lim ET, et al. PLoS Genet. 2014 Jul 31;10(7):e1004494. doi: 10.1371/journal.pgen.1004494. eCollection 2014 Jul. PLoS Genet. 2014. PMID: 25078778 Free PMC article.

3

A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits.

Fan R, Chiu CY, Jung J, Weeks DE, Wilson AF, Bailey-Wilson JE, Amos CI, Chen Z, Mills JL, Xiong M. Fan R, et al. Genet Epidemiol. 2016 Dec;40(8):702-721. doi: 10.1002/gepi.21984. Epub 2016 Jul 4. Genet Epidemiol. 2016. PMID: 27374056 Free PMC article.

4

Exome sequencing of Finnish isolates enhances rare-variant association power.

Locke AE, Steinberg KM, Chiang CWK, Service SK, Havulinna AS, Stell L, Pirinen M, Abel HJ, Chiang CC, Fulton RS, Jackson AU, Kang CJ, Kanchi KL, Koboldt DC, Larson DE, Nelson J, Nicholas TJ, Pietilä A, Ramensky V, Ray D, Scott LJ, Stringham HM, Vangipurapu J, Welch R, Yajnik P, Yin X, Eriksson JG, Ala-Korpela M, Järvelin MR, Männikkö M, Laivuori H; FinnGen Project; Dutcher SK, Stitziel NO, Wilson RK, Hall IM, Sabatti C, Palotie A, Salomaa V, Laakso M, Ripatti S, Boehnke M, Freimer NB. Locke AE, et al. Nature. 2019 Aug;572(7769):323-328. doi: 10.1038/s41586-019-1457-z. Epub 2019 Jul 31. Nature. 2019. PMID: 31367044 Free PMC article.

5

Population genetic simulation study of power in association testing across genetic architectures and study designs.

Tong DMH, Hernandez RD. Tong DMH, et al. Genet Epidemiol. 2020 Jan;44(1):90-103. doi: 10.1002/gepi.22264. Epub 2019 Oct 6. Genet Epidemiol. 2020. PMID: 31587362 Free PMC article.

6

The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease.

Moutsianas L, Agarwala V, Fuchsberger C, Flannick J, Rivas MA, Gaulton KJ, Albers PK; GoT2D Consortium; McVean G, Boehnke M, Altshuler D, McCarthy MI. Moutsianas L, et al. PLoS Genet. 2015 Apr 23;11(4):e1005165. doi: 10.1371/journal.pgen.1005165. eCollection 2015 Apr. PLoS Genet. 2015. PMID: 25906071 Free PMC article.

7

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. Trotta L, et al. Eur J Hum Genet. 2016 Oct;24(10):1473-8. doi: 10.1038/ejhg.2016.37. Epub 2016 May 4. Eur J Hum Genet. 2016. PMID: 27142677 Free PMC article.

8

A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing.

Chiu CY, Jung J, Wang Y, Weeks DE, Wilson AF, Bailey-Wilson JE, Amos CI, Mills JL, Boehnke M, Xiong M, Fan R. Chiu CY, et al. Genet Epidemiol. 2017 Jan;41(1):18-34. doi: 10.1002/gepi.22014. Epub 2016 Dec 5. Genet Epidemiol. 2017. PMID: 27917525 Free PMC article.

9

Generalization of Rare Variant Association Tests for Longitudinal Family Studies.

Chien LC, Hsu FC, Bowden DW, Chiu YF. Chien LC, et al. Genet Epidemiol. 2016 Feb;40(2):101-12. doi: 10.1002/gepi.21951. Epub 2016 Jan 18. Genet Epidemiol. 2016. PMID: 26783077

10

Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland.

Järvelä I, Määttä T, Acharya A, Leppälä J, Jhangiani SN, Arvio M, Siren A, Kankuri-Tammilehto M, Kokkonen H, Palomäki M, Varilo T, Fang M, Hadley TD, Jolly A, Linnankivi T, Paetau R, Saarela A, Kälviäinen R, Olme J, Nouel-Saied LM, Cornejo-Sanchez DM, Llaci L, Lupski JR, Posey JE, Leal SM, Schrauwen I. Järvelä I, et al. Hum Genet. 2021 Jul;140(7):1011-1029. doi: 10.1007/s00439-021-02268-1. Epub 2021 Mar 12. Hum Genet. 2021. PMID: 33710394 Free PMC article.

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