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Items: 1 to 50 of 110

1.

Summary statistic analyses can mistake confounding bias for heritability.

Holmes JB, Speed D, Balding DJ.

Genet Epidemiol. 2019 Sep 20. doi: 10.1002/gepi.22259. [Epub ahead of print]

PMID:
31541496
2.

A general framework for moment-based analysis of genetic data.

Speed MS, Balding DJ, Hobolth A.

J Math Biol. 2019 May;78(6):1727-1769. doi: 10.1007/s00285-018-01325-0. Epub 2019 Jan 28.

PMID:
30734077
3.

SumHer better estimates the SNP heritability of complex traits from summary statistics.

Speed D, Balding DJ.

Nat Genet. 2019 Feb;51(2):277-284. doi: 10.1038/s41588-018-0279-5. Epub 2018 Dec 3.

4.

How many individuals share a mitochondrial genome?

Andersen MM, Balding DJ.

PLoS Genet. 2018 Nov 1;14(11):e1007774. doi: 10.1371/journal.pgen.1007774. eCollection 2018 Nov.

5.

Y-profile evidence: Close paternal relatives and mixtures.

Andersen MM, Balding DJ.

Forensic Sci Int Genet. 2019 Jan;38:48-53. doi: 10.1016/j.fsigen.2018.10.004. Epub 2018 Oct 10.

PMID:
30340211
6.

Evaluating DNA evidence in a genetically complex population.

Hessab T, Aranha RS, Moura-Neto RS, Balding DJ, Schrago CG.

Forensic Sci Int Genet. 2018 Sep;36:141-147. doi: 10.1016/j.fsigen.2018.06.019. Epub 2018 Jun 28.

PMID:
29990826
7.

How convincing is a matching Y-chromosome profile?

Andersen MM, Balding DJ.

PLoS Genet. 2017 Nov 3;13(11):e1007028. doi: 10.1371/journal.pgen.1007028. eCollection 2017 Nov.

8.

Optimizing genomic medicine in epilepsy through a gene-customized approach to missense variant interpretation.

Traynelis J, Silk M, Wang Q, Berkovic SF, Liu L, Ascher DB, Balding DJ, Petrovski S.

Genome Res. 2017 Oct;27(10):1715-1729. doi: 10.1101/gr.226589.117. Epub 2017 Sep 1.

9.

Reevaluation of SNP heritability in complex human traits.

Speed D, Cai N; UCLEB Consortium, Johnson MR, Nejentsev S, Balding DJ.

Nat Genet. 2017 Jul;49(7):986-992. doi: 10.1038/ng.3865. Epub 2017 May 22.

10.

GWAlpha: genome-wide estimation of additive effects (alpha) based on trait quantile distribution from pool-sequencing experiments.

Fournier-Level A, Robin C, Balding DJ.

Bioinformatics. 2017 Apr 15;33(8):1246-1247. doi: 10.1093/bioinformatics/btw805.

PMID:
28003266
11.

Erratum to 'Encoding of low-quality DNA profiles as genotype probability matrices for improved profile comparisons, relatedness evalation and database searches'. Forensic Science International: Genetics (2016) 227-239.

Ryan K, Williams DG, Balding DJ.

Forensic Sci Int Genet. 2017 Mar;27:189-190. doi: 10.1016/j.fsigen.2016.11.003. Epub 2016 Dec 9. No abstract available.

PMID:
27940064
12.

A comment on the PCAST report: Skip the "match"/"non-match" stage.

Morrison GS, Kaye DH, Balding DJ, Taylor D, Dawid P, Aitken CGG, Gittelson S, Zadora G, Robertson B, Willis S, Pope S, Neil M, Martire KA, Hepler A, Gill RD, Jamieson A, de Zoete J, Ostrum RB, Caliebe A.

Forensic Sci Int. 2017 Mar;272:e7-e9. doi: 10.1016/j.forsciint.2016.10.018. Epub 2016 Oct 26.

PMID:
27817943
13.

Encoding of low-quality DNA profiles as genotype probability matrices for improved profile comparisons, relatedness evaluation and database searches.

Ryan K, Williams DG, Balding DJ.

Forensic Sci Int Genet. 2016 Nov;25:227-239. doi: 10.1016/j.fsigen.2016.09.004. Epub 2016 Sep 21. Erratum in: Forensic Sci Int Genet. 2017 Mar;27:189-190.

PMID:
27768939
14.

Increased Population Risk of AIP-Related Acromegaly and Gigantism in Ireland.

Radian S, Diekmann Y, Gabrovska P, Holland B, Bradley L, Wallace H, Stals K, Bussell AM, McGurren K, Cuesta M, Ryan AW, Herincs M, Hernández-Ramírez LC, Holland A, Samuels J, Aflorei ED, Barry S, Dénes J, Pernicova I, Stiles CE, Trivellin G, McCloskey R, Ajzensztejn M, Abid N, Akker SA, Mercado M, Cohen M, Thakker RV, Baldeweg S, Barkan A, Musat M, Levy M, Orme SM, Unterländer M, Burger J, Kumar AV, Ellard S, McPartlin J, McManus R, Linden GJ, Atkinson B, Balding DJ, Agha A, Thompson CJ, Hunter SJ, Thomas MG, Morrison PJ, Korbonits M.

Hum Mutat. 2017 Jan;38(1):78-85. doi: 10.1002/humu.23121. Epub 2016 Oct 4.

15.

Evaluation of low-template DNA profiles using peak heights.

Steele CD, Greenhalgh M, Balding DJ.

Stat Appl Genet Mol Biol. 2016 Oct 1;15(5):431-445. doi: 10.1515/sagmb-2016-0038.

PMID:
27416618
16.

Worldwide F(ST) estimates relative to five continental-scale populations.

Steele CD, Court DS, Balding DJ.

Ann Hum Genet. 2014 Nov;78(6):468-77. doi: 10.1111/ahg.12081.

17.

Integrating dynamic mixed-effect modelling and penalized regression to explore genetic association with pharmacokinetics.

Bertrand J, De Iorio M, Balding DJ.

Pharmacogenet Genomics. 2015 May;25(5):231-8. doi: 10.1097/FPC.0000000000000127.

18.

The genomic and phenotypic diversity of Schizosaccharomyces pombe.

Jeffares DC, Rallis C, Rieux A, Speed D, Převorovský M, Mourier T, Marsellach FX, Iqbal Z, Lau W, Cheng TM, Pracana R, Mülleder M, Lawson JL, Chessel A, Bala S, Hellenthal G, O'Fallon B, Keane T, Simpson JT, Bischof L, Tomiczek B, Bitton DA, Sideri T, Codlin S, Hellberg JE, van Trigt L, Jeffery L, Li JJ, Atkinson S, Thodberg M, Febrer M, McLay K, Drou N, Brown W, Hayles J, Carazo Salas RE, Ralser M, Maniatis N, Balding DJ, Balloux F, Durbin R, Bähler J.

Nat Genet. 2015 Mar;47(3):235-41. doi: 10.1038/ng.3215. Epub 2015 Feb 9.

19.

Bayesian models for syndrome- and gene-specific probabilities of novel variant pathogenicity.

Ruklisa D, Ware JS, Walsh R, Balding DJ, Cook SA.

Genome Med. 2015 Jan 28;7(1):5. doi: 10.1186/s13073-014-0120-4. eCollection 2015.

20.

Choice of population database for forensic DNA profile analysis.

Steele CD, Balding DJ.

Sci Justice. 2014 Dec;54(6):487-93. doi: 10.1016/j.scijus.2014.10.004. Epub 2014 Nov 7.

21.

Relatedness in the post-genomic era: is it still useful?

Speed D, Balding DJ.

Nat Rev Genet. 2015 Jan;16(1):33-44. doi: 10.1038/nrg3821. Epub 2014 Nov 18. Review.

PMID:
25404112
22.

Multiple quantitative trait analysis using bayesian networks.

Scutari M, Howell P, Balding DJ, Mackay I.

Genetics. 2014 Sep;198(1):129-37. doi: 10.1534/genetics.114.165704.

23.

Verifying likelihoods for low template DNA profiles using multiple replicates.

Steele CD, Greenhalgh M, Balding DJ.

Forensic Sci Int Genet. 2014 Nov;13:82-9. doi: 10.1016/j.fsigen.2014.06.018. Epub 2014 Jul 10.

24.

Describing the genetic architecture of epilepsy through heritability analysis.

Speed D, O'Brien TJ, Palotie A, Shkura K, Marson AG, Balding DJ, Johnson MR.

Brain. 2014 Oct;137(Pt 10):2680-9. doi: 10.1093/brain/awu206. Epub 2014 Jul 26.

25.

MultiBLUP: improved SNP-based prediction for complex traits.

Speed D, Balding DJ.

Genome Res. 2014 Sep;24(9):1550-7. doi: 10.1101/gr.169375.113. Epub 2014 Jun 24.

26.

Storytelling and story testing in domestication.

Gerbault P, Allaby RG, Boivin N, Rudzinski A, Grimaldi IM, Pires JC, Climer Vigueira C, Dobney K, Gremillion KJ, Barton L, Arroyo-Kalin M, Purugganan MD, Rubio de Casas R, Bollongino R, Burger J, Fuller DQ, Bradley DG, Balding DJ, Richerson PJ, Gilbert MT, Larson G, Thomas MG.

Proc Natl Acad Sci U S A. 2014 Apr 29;111(17):6159-64. doi: 10.1073/pnas.1400425111. Epub 2014 Apr 21.

27.

Interaction between gas cooking and GSTM1 null genotype in bronchial responsiveness: results from the European Community Respiratory Health Survey.

Amaral AF, Ramasamy A, Castro-Giner F, Minelli C, Accordini S, Sørheim IC, Pin I, Kogevinas M, Jõgi R, Balding DJ, Norbäck D, Verlato G, Olivieri M, Probst-Hensch N, Janson C, Zock JP, Heinrich J, Jarvis DL.

Thorax. 2014 Jun;69(6):558-64. doi: 10.1136/thoraxjnl-2013-204574. Epub 2014 Mar 10.

28.

Response to Lee et al.: SNP-based heritability analysis with dense data.

Speed D, Hemani G, Johnson MR, Balding DJ.

Am J Hum Genet. 2013 Dec 5;93(6):1155-7. doi: 10.1016/j.ajhg.2013.10.016. No abstract available.

29.

Dysregulation of complement system and CD4+ T cell activation pathways implicated in allergic response.

Couto Alves A, Bruhn S, Ramasamy A, Wang H, Holloway JW, Hartikainen AL, Jarvelin MR, Benson M, Balding DJ, Coin LJ.

PLoS One. 2013 Oct 8;8(10):e74821. doi: 10.1371/journal.pone.0074821. eCollection 2013.

30.

Evaluation of mixed-source, low-template DNA profiles in forensic science.

Balding DJ.

Proc Natl Acad Sci U S A. 2013 Jul 23;110(30):12241-6. doi: 10.1073/pnas.1219739110. Epub 2013 Jul 1.

31.

Genetic screening for Niemann-Pick disease type C in adults with neurological and psychiatric symptoms: findings from the ZOOM study.

Bauer P, Balding DJ, Klünemann HH, Linden DE, Ory DS, Pineda M, Priller J, Sedel F, Muller A, Chadha-Boreham H, Welford RW, Strasser DS, Patterson MC.

Hum Mol Genet. 2013 Nov 1;22(21):4349-56. doi: 10.1093/hmg/ddt284. Epub 2013 Jun 16.

32.

Multiple single nucleotide polymorphism analysis using penalized regression in nonlinear mixed-effect pharmacokinetic models.

Bertrand J, Balding DJ.

Pharmacogenet Genomics. 2013 Mar;23(3):167-74. doi: 10.1097/FPC.0b013e32835dd22c.

PMID:
23337849
33.

Improved heritability estimation from genome-wide SNPs.

Speed D, Hemani G, Johnson MR, Balding DJ.

Am J Hum Genet. 2012 Dec 7;91(6):1011-21. doi: 10.1016/j.ajhg.2012.10.010.

34.

Understanding complex traits: from farmers to pharmas.

Speed D, Balding DJ.

Genome Med. 2012 Jul 27;4(7):59. doi: 10.1186/gm360. eCollection 2012.

35.

Decision-making in familial database searching: KI alone or not alone?

Balding DJ, Krawczak M, Buckleton JS, Curran JM.

Forensic Sci Int Genet. 2013 Jan;7(1):52-4. doi: 10.1016/j.fsigen.2012.06.001. Epub 2012 Jun 29.

PMID:
22749791
36.

Ethiopian genetic diversity reveals linguistic stratification and complex influences on the Ethiopian gene pool.

Pagani L, Kivisild T, Tarekegn A, Ekong R, Plaster C, Gallego Romero I, Ayub Q, Mehdi SQ, Thomas MG, Luiselli D, Bekele E, Bradman N, Balding DJ, Tyler-Smith C.

Am J Hum Genet. 2012 Jul 13;91(1):83-96. doi: 10.1016/j.ajhg.2012.05.015. Epub 2012 Jun 21.

37.

Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.

Mead S, Uphill J, Beck J, Poulter M, Campbell T, Lowe J, Adamson G, Hummerich H, Klopp N, Rückert IM, Wichmann HE, Azazi D, Plagnol V, Pako WH, Whitfield J, Alpers MP, Whittaker J, Balding DJ, Zerr I, Kretzschmar H, Collinge J.

Hum Mol Genet. 2012 Apr 15;21(8):1897-906. doi: 10.1093/hmg/ddr607. Epub 2011 Dec 30.

38.

A genome-wide meta-analysis of genetic variants associated with allergic rhinitis and grass sensitization and their interaction with birth order.

Ramasamy A, Curjuric I, Coin LJ, Kumar A, McArdle WL, Imboden M, Leynaert B, Kogevinas M, Schmid-Grendelmeier P, Pekkanen J, Wjst M, Bircher AJ, Sovio U, Rochat T, Hartikainen AL, Balding DJ, Jarvelin MR, Probst-Hensch N, Strachan DP, Jarvis DL.

J Allergy Clin Immunol. 2011 Nov;128(5):996-1005. doi: 10.1016/j.jaci.2011.08.030.

PMID:
22036096
39.

Using penalised logistic regression to fine map HLA variants for rheumatoid arthritis.

Vignal CM, Bansal AT, Balding DJ.

Ann Hum Genet. 2011 Nov;75(6):655-64. doi: 10.1111/j.1469-1809.2011.00670.x. Epub 2011 Sep 1.

40.

Admixture provides new insights into recombination.

O'Reilly PF, Balding DJ.

Nat Genet. 2011 Aug 29;43(9):819-20. doi: 10.1038/ng.918. No abstract available.

PMID:
21874032
41.

Epigenome-wide association studies for common human diseases.

Rakyan VK, Down TA, Balding DJ, Beck S.

Nat Rev Genet. 2011 Jul 12;12(8):529-41. doi: 10.1038/nrg3000. Review.

42.

AIP mutation in pituitary adenomas in the 18th century and today.

Chahal HS, Stals K, Unterländer M, Balding DJ, Thomas MG, Kumar AV, Besser GM, Atkinson AB, Morrison PJ, Howlett TA, Levy MJ, Orme SM, Akker SA, Abel RL, Grossman AB, Burger J, Ellard S, Korbonits M.

N Engl J Med. 2011 Jan 6;364(1):43-50. doi: 10.1056/NEJMoa1008020.

43.

Genome-wide association mapping to candidate polymorphism resolution in the unsequenced barley genome.

Cockram J, White J, Zuluaga DL, Smith D, Comadran J, Macaulay M, Luo Z, Kearsey MJ, Werner P, Harrap D, Tapsell C, Liu H, Hedley PE, Stein N, Schulte D, Steuernagel B, Marshall DF, Thomas WT, Ramsay L, Mackay I, Balding DJ; AGOUEB Consortium, Waugh R, O'Sullivan DM.

Proc Natl Acad Sci U S A. 2010 Dec 14;107(50):21611-6. doi: 10.1073/pnas.1010179107. Epub 2010 Nov 29.

44.

On optimal selection of summary statistics for approximate Bayesian computation.

Nunes MA, Balding DJ.

Stat Appl Genet Mol Biol. 2010;9:Article34. doi: 10.2202/1544-6115.1576. Epub 2010 Sep 6.

PMID:
20887273
45.

A genome-wide association study of the metabolic syndrome in Indian Asian men.

Zabaneh D, Balding DJ.

PLoS One. 2010 Aug 4;5(8):e11961. doi: 10.1371/journal.pone.0011961.

46.

A genome-wide association study of neuroticism in a population-based sample.

Calboli FC, Tozzi F, Galwey NW, Antoniades A, Mooser V, Preisig M, Vollenweider P, Waterworth D, Waeber G, Johnson MR, Muglia P, Balding DJ.

PLoS One. 2010 Jul 9;5(7):e11504. doi: 10.1371/journal.pone.0011504.

47.

cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVs.

Coin LJ, Asher JE, Walters RG, Moustafa JS, de Smith AJ, Sladek R, Balding DJ, Froguel P, Blakemore AI.

Nat Methods. 2010 Jul;7(7):541-6. doi: 10.1038/nmeth.1466. Epub 2010 May 30.

PMID:
20512141
48.

Inferring combined CNV/SNP haplotypes from genotype data.

Su SY, Asher JE, Jarvelin MR, Froguel P, Blakemore AI, Balding DJ, Coin LJ.

Bioinformatics. 2010 Jun 1;26(11):1437-45. doi: 10.1093/bioinformatics/btq157. Epub 2010 Apr 20.

49.

Interpreting low template DNA profiles.

Balding DJ, Buckleton J.

Forensic Sci Int Genet. 2009 Dec;4(1):1-10. doi: 10.1016/j.fsigen.2009.03.003. Epub 2009 May 2.

PMID:
19948328
50.

Heritability and genetic correlations of insulin resistance and component phenotypes in Asian Indian families using a multivariate analysis.

Zabaneh D, Chambers JC, Elliott P, Scott J, Balding DJ, Kooner JS.

Diabetologia. 2009 Dec;52(12):2585-9. doi: 10.1007/s00125-009-1504-7. Epub 2009 Sep 10.

PMID:
19763535

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