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Items: 1 to 20 of 120


Polygenic Influence on Educational Attainment: New evidence from The National Longitudinal Study of Adolescent to Adult Health.

Domingue BW, Belsky D, Conley D, Harris KM, Boardman JD.

AERA Open. 2015 Jul-Sep;1(3):1-13. doi: 10.1177/2332858415599972. Epub 2015 Aug 19.


Identifying Pleiotropic Genes in Genome-Wide Association Studies for Multivariate Phenotypes with Mixed Measurement Scales.

Yang JJ, Williams LK, Buu A.

PLoS One. 2017 Jan 12;12(1):e0169893. doi: 10.1371/journal.pone.0169893. eCollection 2017.


Genetic factors influencing risk to orofacial clefts: today's challenges and tomorrow's opportunities.

Beaty TH, Marazita ML, Leslie EJ.

F1000Res. 2016 Nov 30;5:2800. eCollection 2016. Review.


Assessing transmission ratio distortion in extended families: a comparison of analysis methods.

Bhatnagar SR, Greenwood CM, Labbe A.

BMC Proc. 2016 Oct 18;10(Suppl 7):197-202. eCollection 2016.


Previous GWAS hits in relation to young-onset breast cancer.

Shi M, O'Brien KM, Sandler DP, Taylor JA, Zaykin DV, Weinberg CR.

Breast Cancer Res Treat. 2017 Jan;161(2):333-344. doi: 10.1007/s10549-016-4053-z. Epub 2016 Nov 15.


Novel genetic risk variants for pediatric celiac disease.

Balasopoulou A, Stanković B, Panagiotara A, Nikčevic G, Peters BA, John A, Mendrinou E, Stratopoulos A, Legaki AI, Stathakopoulou V, Tsolia A, Govaris N, Govari S, Zagoriti Z, Poulas K, Kanariou M, Constantinidou N, Krini M, Spanou K, Radlovic N, Ali BR, Borg J, Drmanac R, Chrousos G, Pavlovic S, Roma E, Zukic B, Patrinos GP, Katsila T.

Hum Genomics. 2016 Oct 24;10(1):34.


Associations between homocysteine metabolism related SNPs and carotid intima-media thickness: a Chinese sib pair study.

Sun K, Song J, Liu K, Fang K, Wang L, Wang X, Li J, Tang X, Wu Y, Qin X, Wu T, Gao P, Chen D, Hu Y.

J Thromb Thrombolysis. 2017 Apr;43(3):401-410. doi: 10.1007/s11239-016-1449-x.


Increasing Generality and Power of Rare-Variant Tests by Utilizing Extended Pedigrees.

Sul JH, Cade BE, Cho MH, Qiao D, Silverman EK, Redline S, Sunyaev S.

Am J Hum Genet. 2016 Oct 6;99(4):846-859. doi: 10.1016/j.ajhg.2016.08.015. Epub 2016 Sep 22.


Family-based approaches: design, imputation, analysis, and beyond.

Wijsman EM.

BMC Genet. 2016 Feb 3;17 Suppl 2:9. doi: 10.1186/s12863-015-0318-5.


Disease and Polygenic Architecture: Avoid Trio Design and Appropriately Account for Unscreened Control Subjects for Common Disease.

Peyrot WJ, Boomsma DI, Penninx BW, Wray NR.

Am J Hum Genet. 2016 Feb 4;98(2):382-91. doi: 10.1016/j.ajhg.2015.12.017.


A computational method for genotype calling in family-based sequencing data.

Chang LC, Li B, Fang Z, Vrieze S, McGue M, Iacono WG, Tseng GC, Chen W.

BMC Bioinformatics. 2016 Jan 16;17:37. doi: 10.1186/s12859-016-0880-5.


The Norwegian preeclampsia family cohort study: a new resource for investigating genetic aspects and heritability of preeclampsia and related phenotypes.

Roten LT, Thomsen LC, Gundersen AS, Fenstad MH, Odland ML, Strand KM, Solberg P, Tappert C, Araya E, Bærheim G, Lyslo I, Tollaksen K, Bjørge L, Austgulen R.

BMC Pregnancy Childbirth. 2015 Dec 1;15:319. doi: 10.1186/s12884-015-0754-2.


Estimating genetic effect sizes under joint disease-endophenotype models in presence of gene-environment interactions.

Bureau A, Croteau J, Couture C, Vohl MC, Bouchard C, Pérusse L.

Front Genet. 2015 Jul 28;6:248. doi: 10.3389/fgene.2015.00248. eCollection 2015.


Novel evidence of association with nonsyndromic cleft lip with or without cleft palate was shown for single nucleotide polymorphisms in FOXF2 gene in an Asian population.

Bu L, Chen Q, Wang H, Zhang T, Hetmanski JB, Schwender H, Parker M, Chou YH, Yeow V, Chong SS, Zhang B, Jabs EW, Scott AF, Beaty TH.

Birth Defects Res A Clin Mol Teratol. 2015 Oct;103(10):857-62. doi: 10.1002/bdra.23413. Epub 2015 Aug 17.


Using Network Methodology to Infer Population Substructure.

Prokopenko D, Hecker J, Silverman E, Nöthen MM, Schmid M, Lange C, Loehlein Fier H.

PLoS One. 2015 Jun 22;10(6):e0130708. doi: 10.1371/journal.pone.0130708. eCollection 2015.


Identification of cancer predisposition variants in apparently healthy individuals using a next-generation sequencing-based family genomics approach.

Karageorgos I, Mizzi C, Giannopoulou E, Pavlidis C, Peters BA, Zagoriti Z, Stenson PD, Mitropoulos K, Borg J, Kalofonos HP, Drmanac R, Stubbs A, van der Spek P, Cooper DN, Katsila T, Patrinos GP.

Hum Genomics. 2015 Jun 20;9:12. doi: 10.1186/s40246-015-0034-2.


Robust and Powerful Affected Sibpair Test for Rare Variant Association.

Lin KH, Zöllner S.

Genet Epidemiol. 2015 Jul;39(5):325-33. doi: 10.1002/gepi.21903. Epub 2015 May 13.


A re-formulation of generalized linear mixed models to fit family data in genetic association studies.

Wang T, He P, Ahn KW, Wang X, Ghosh S, Laud P.

Front Genet. 2015 Mar 31;6:120. doi: 10.3389/fgene.2015.00120. eCollection 2015.


Genetic linkage analysis in the age of whole-genome sequencing.

Ott J, Wang J, Leal SM.

Nat Rev Genet. 2015 May;16(5):275-84. doi: 10.1038/nrg3908. Epub 2015 Mar 31. Review.


A powerful nonparametric statistical framework for family-based association analyses.

Li M, He Z, Schaid DJ, Cleves MA, Nick TG, Lu Q.

Genetics. 2015 May;200(1):69-78. doi: 10.1534/genetics.115.175174. Epub 2015 Mar 5.

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