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Items: 18

1.

Genetics of the human face: Identification of large-effect single gene variants.

Crouch DJM, Winney B, Koppen WP, Christmas WJ, Hutnik K, Day T, Meena D, Boumertit A, Hysi P, Nessa A, Spector TD, Kittler J, Bodmer WF.

Proc Natl Acad Sci U S A. 2018 Jan 23;115(4):E676-E685. doi: 10.1073/pnas.1708207114. Epub 2018 Jan 4.

PMID:
29301965
2.

Large-scale recent expansion of European patrilineages shown by population resequencing.

Batini C, Hallast P, Zadik D, Delser PM, Benazzo A, Ghirotto S, Arroyo-Pardo E, Cavalleri GL, de Knijff P, Dupuy BM, Eriksen HA, King TE, López de Munain A, López-Parra AM, Loutradis A, Milasin J, Novelletto A, Pamjav H, Sajantila A, Tolun A, Winney B, Jobling MA.

Nat Commun. 2015 May 19;6:7152. doi: 10.1038/ncomms8152.

3.

The fine-scale genetic structure of the British population.

Leslie S, Winney B, Hellenthal G, Davison D, Boumertit A, Day T, Hutnik K, Royrvik EC, Cunliffe B; Wellcome Trust Case Control Consortium 2; International Multiple Sclerosis Genetics Consortium, Lawson DJ, Falush D, Freeman C, Pirinen M, Myers S, Robinson M, Donnelly P, Bodmer W.

Nature. 2015 Mar 19;519(7543):309-314. doi: 10.1038/nature14230.

4.

The Y-chromosome tree bursts into leaf: 13,000 high-confidence SNPs covering the majority of known clades.

Hallast P, Batini C, Zadik D, Maisano Delser P, Wetton JH, Arroyo-Pardo E, Cavalleri GL, de Knijff P, Destro Bisol G, Dupuy BM, Eriksen HA, Jorde LB, King TE, Larmuseau MH, López de Munain A, López-Parra AM, Loutradis A, Milasin J, Novelletto A, Pamjav H, Sajantila A, Schempp W, Sears M, Tolun A, Tyler-Smith C, Van Geystelen A, Watkins S, Winney B, Jobling MA.

Mol Biol Evol. 2015 Mar;32(3):661-73. doi: 10.1093/molbev/msu327. Epub 2014 Dec 2.

5.

Associations of HLA alleles with specific language impairment.

Nudel R, Simpson NH, Baird G, O'Hare A, Conti-Ramsden G, Bolton PF, Hennessy ER; SLI Consortium, Monaco AP, Knight JC, Winney B, Fisher SE, Newbury DF.

J Neurodev Disord. 2014 Jan 17;6(1):1. doi: 10.1186/1866-1955-6-1.

6.

Human telomeres that carry an integrated copy of human herpesvirus 6 are often short and unstable, facilitating release of the viral genome from the chromosome.

Huang Y, Hidalgo-Bravo A, Zhang E, Cotton VE, Mendez-Bermudez A, Wig G, Medina-Calzada Z, Neumann R, Jeffreys AJ, Winney B, Wilson JF, Clark DA, Dyer MJ, Royle NJ.

Nucleic Acids Res. 2014 Jan;42(1):315-27. doi: 10.1093/nar/gkt840. Epub 2013 Sep 19.

7.

Role of rare variants in undetermined multiple adenomatous polyposis and early-onset colorectal cancer.

Lefevre JH, Bonilla C, Colas C, Winney B, Johnstone E, Tonks S, Day T, Hutnik K, Boumertit A, Soubrier F, Midgley R, Kerr D, Parc Y, Bodmer WF.

J Hum Genet. 2012 Nov 26;57(11):709-716. doi: 10.1038/jhg.2012.99. Epub 2012 Aug 9.

8.

The peopling of Europe and the cautionary tale of Y chromosome lineage R-M269.

Busby GB, Brisighelli F, Sánchez-Diz P, Ramos-Luis E, Martinez-Cadenas C, Thomas MG, Bradley DG, Gusmão L, Winney B, Bodmer W, Vennemann M, Coia V, Scarnicci F, Tofanelli S, Vona G, Ploski R, Vecchiotti C, Zemunik T, Rudan I, Karachanak S, Toncheva D, Anagnostou P, Ferri G, Rapone C, Hervig T, Moen T, Wilson JF, Capelli C.

Proc Biol Sci. 2012 Mar 7;279(1730):884-92. doi: 10.1098/rspb.2011.1044. Epub 2011 Aug 24.

9.

People of the British Isles: preliminary analysis of genotypes and surnames in a UK-control population.

Winney B, Boumertit A, Day T, Davison D, Echeta C, Evseeva I, Hutnik K, Leslie S, Nicodemus K, Royrvik EC, Tonks S, Yang X, Cheshire J, Longley P, Mateos P, Groom A, Relton C, Bishop DT, Black K, Northwood E, Parkinson L, Frayling TM, Steele A, Sampson JR, King T, Dixon R, Middleton D, Jennings B, Bowden R, Donnelly P, Bodmer W.

Eur J Hum Genet. 2012 Feb;20(2):203-10. doi: 10.1038/ejhg.2011.127. Epub 2011 Aug 10.

10.

Cyclin D1 rare variants in UK multiple adenoma and early-onset colorectal cancer patients.

Bonilla C, Lefèvre JH, Winney B, Johnstone E, Tonks S, Colas C, Day T, Hutnik K, Boumertit A, Midgley R, Kerr D, Parc Y, Bodmer WF.

J Hum Genet. 2011 Jan;56(1):58-63. doi: 10.1038/jhg.2010.144. Epub 2010 Nov 25.

11.

Mutations in the AXIN1 gene in advanced prostate cancer.

Yardy GW, Bicknell DC, Wilding JL, Bartlett S, Liu Y, Winney B, Turner GD, Brewster SF, Bodmer WF.

Eur Urol. 2009 Sep;56(3):486-94. doi: 10.1016/j.eururo.2008.05.029. Epub 2008 May 23.

PMID:
18514389
12.

Genetic evidence for female-biased dispersal and gene flow in a polygynous primate.

Hammond RL, Handley LJ, Winney BJ, Bruford MW, Perrin N.

Proc Biol Sci. 2006 Feb 22;273(1585):479-84.

13.

Rare variant hypothesis for multifactorial inheritance: susceptibility to colorectal adenomas as a model.

Fearnhead NS, Winney B, Bodmer WF.

Cell Cycle. 2005 Apr;4(4):521-5. Epub 2005 Apr 7. Review.

PMID:
15753653
14.

Multiple rare variants in different genes account for multifactorial inherited susceptibility to colorectal adenomas.

Fearnhead NS, Wilding JL, Winney B, Tonks S, Bartlett S, Bicknell DC, Tomlinson IP, Mortensen NJ, Bodmer WF.

Proc Natl Acad Sci U S A. 2004 Nov 9;101(45):15992-7. Epub 2004 Nov 1.

15.

Crossing the Red Sea: phylogeography of the hamadryas baboon, Papio hamadryas hamadryas.

Winney BJ, Hammond RL, Macasero W, Flores B, Boug A, Biquand V, Biquand S, Bruford MW.

Mol Ecol. 2004 Sep;13(9):2819-27.

PMID:
15315692
16.

The subspecific origin of the inland breeding colonies of the cormorant Phalacrocorax carbo in Britain.

Winney BJ, Litton CD, Parkin DT, Feare CJ.

Heredity (Edinb). 2001 Jan;86(Pt 1):45-53.

PMID:
11298814
17.

State certification standards and reciprocity for teachers of the hearing impaired.

Moulton RD, Roth RA, Winney B.

Am Ann Deaf. 1983 Aug;128(4):490-8. No abstract available.

PMID:
6637723
18.

Lamar pilot school survey.

Richardson D, Winney B.

Am Ann Deaf. 1974 Dec;119(6):736-9. No abstract available.

PMID:
4440621

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