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Results: 1 to 20 of 82

Cited In for PubMed (Select 1493912)


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.


Adaptive combination of P-values for family-based association testing with sequence data.

Lin WY.

PLoS One. 2014 Dec 26;9(12):e115971. doi: 10.1371/journal.pone.0115971. eCollection 2014.


Testing genetic association with rare and common variants in family data.

Chen H, Malzahn D, Balliu B, Li C, Bailey JN.

Genet Epidemiol. 2014 Sep;38 Suppl 1:S37-43. doi: 10.1002/gepi.21823.


PSEUDOMARKER 2.0: efficient computation of likelihoods using NOMAD.

Gertz EM, Hiekkalinna T, Digabel SL, Audet C, Terwilliger JD, Schäffer AA.

BMC Bioinformatics. 2014 Feb 17;15:47. doi: 10.1186/1471-2105-15-47.


Rare-variant extensions of the transmission disequilibrium test: application to autism exome sequence data.

He Z, O'Roak BJ, Smith JD, Wang G, Hooker S, Santos-Cortez RL, Li B, Kan M, Krumm N, Nickerson DA, Shendure J, Eichler EE, Leal SM.

Am J Hum Genet. 2014 Jan 2;94(1):33-46. doi: 10.1016/j.ajhg.2013.11.021. Epub 2013 Dec 19.


Catecholaminergic gene variants: contribution in ADHD and associated comorbid attributes in the eastern Indian probands.

Ghosh P, Sarkar K, Bhaduri N, Ray A, Sarkar K, Sinha S, Mukhopadhyay K.

Biomed Res Int. 2013;2013:918410. doi: 10.1155/2013/918410. Epub 2013 Sep 19.


Sequence kernel association test for quantitative traits in family samples.

Chen H, Meigs JB, Dupuis J.

Genet Epidemiol. 2013 Feb;37(2):196-204. doi: 10.1002/gepi.21703. Epub 2012 Dec 26.


On the validity of the likelihood ratio test and consistency of resulting parameter estimates in joint linkage and linkage disequilibrium analysis under improperly specified parametric models.

Hiekkalinna T, Göring HH, Terwilliger JD.

Ann Hum Genet. 2012 Jan;76(1):63-73. doi: 10.1111/j.1469-1809.2011.00683.x. Epub 2011 Nov 14.


Pseudosibship methods in the case-parents design.

Yu Z, Deng L.

Stat Med. 2011 Nov 30;30(27):3236-51. doi: 10.1002/sim.4397. Epub 2011 Sep 23.


On the statistical properties of family-based association tests in datasets containing both pedigrees and unrelated case-control samples.

Hiekkalinna T, Göring HH, Lambert B, Weiss KM, Norrgrann P, Schäffer AA, Terwilliger JD.

Eur J Hum Genet. 2012 Feb;20(2):217-23. doi: 10.1038/ejhg.2011.173. Epub 2011 Sep 21.


PSEUDOMARKER: a powerful program for joint linkage and/or linkage disequilibrium analysis on mixtures of singletons and related individuals.

Hiekkalinna T, Schäffer AA, Lambert B, Norrgrann P, Göring HH, Terwilliger JD.

Hum Hered. 2011;71(4):256-66. doi: 10.1159/000329467. Epub 2011 Jul 28.


William Allan Award Address: On the role and soul of a statistical geneticist.

Ott J.

Am J Hum Genet. 2011 Mar 11;88(3):264-8. No abstract available.


Haplotype association analyses in resources of mixed structure using Monte Carlo testing.

Abo R, Wong J, Thomas A, Camp NJ.

BMC Bioinformatics. 2010 Dec 9;11:592. doi: 10.1186/1471-2105-11-592.


Meta-analysis of genome-wide association studies of attention-deficit/hyperactivity disorder.

Neale BM, Medland SE, Ripke S, Asherson P, Franke B, Lesch KP, Faraone SV, Nguyen TT, Schäfer H, Holmans P, Daly M, Steinhausen HC, Freitag C, Reif A, Renner TJ, Romanos M, Romanos J, Walitza S, Warnke A, Meyer J, Palmason H, Buitelaar J, Vasquez AA, Lambregts-Rommelse N, Gill M, Anney RJ, Langely K, O'Donovan M, Williams N, Owen M, Thapar A, Kent L, Sergeant J, Roeyers H, Mick E, Biederman J, Doyle A, Smalley S, Loo S, Hakonarson H, Elia J, Todorov A, Miranda A, Mulas F, Ebstein RP, Rothenberger A, Banaschewski T, Oades RD, Sonuga-Barke E, McGough J, Nisenbaum L, Middleton F, Hu X, Nelson S; Psychiatric GWAS Consortium: ADHD Subgroup.

J Am Acad Child Adolesc Psychiatry. 2010 Sep;49(9):884-97. doi: 10.1016/j.jaac.2010.06.008. Epub 2010 Aug 1.


Dopamine D4 receptors modulate brain metabolic activity in the prefrontal cortex and cerebellum at rest and in response to methylphenidate.

Michaelides M, Pascau J, Gispert JD, Delis F, Grandy DK, Wang GJ, Desco M, Rubinstein M, Volkow ND, Thanos PK.

Eur J Neurosci. 2010 Aug;32(4):668-76. doi: 10.1111/j.1460-9568.2010.07319.x. Epub 2010 Jul 16.


Overview of techniques to account for confounding due to population stratification and cryptic relatedness in genomic data association analyses.

Sillanpää MJ.

Heredity (Edinb). 2011 Apr;106(4):511-9. doi: 10.1038/hdy.2010.91. Epub 2010 Jul 14. Review.


Unbiased and locally efficient estimation of genetic effect on quantitative trait in the presence of population admixture.

Wang Y, Yang Q, Rabinowitz D.

Biometrics. 2011 Jun;67(2):331-43. doi: 10.1111/j.1541-0420.2010.01454.x. Epub 2010 Jun 16.


A preliminary report of the dopamine receptor D(4) and the dopamine transporter 1 gene polymorphism and its association with attention deficit hyperactivity disorder.

Niederhofer H, Menzel F, Göbel K, Hackenberg B, Richter R, Walter MH, Gross C, Huber M, Pycha R, Menzel HJ.

Neuropsychiatr Dis Treat. 2008 Aug;4(4):701-5.


The trace amine associated receptor (TAAR6) gene is not associated with schizophrenia in the Irish Case-Control Study of Schizophrenia (ICCSS) sample.

Vladimirov VI, Maher BS, Wormley B, O'Neill FA, Walsh D, Kendler KS, Riley BP.

Schizophr Res. 2009 Feb;107(2-3):249-54. doi: 10.1016/j.schres.2008.09.030. Epub 2008 Oct 30.


Assessing genuine parents-offspring trios for genetic association studies.

Teo YY, Fry AE, Sanjoaquin MA, Pederson B, Small KS, Rockett KA, Kwiatkowski DP, Clark TG.

Hum Hered. 2009;67(1):26-37. doi: 10.1159/000164396. Epub 2008 Oct 17.

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