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Items: 30


Finland's failure to deliver key healthcare reforms provides valuable lessons for other countries.

Whibley A.

Acta Paediatr. 2019 Jul;108(7):1187-1189. doi: 10.1111/apa.14817. Epub 2019 May 22. No abstract available.


Genome structure and evolution of Antirrhinum majus L.

Li M, Zhang D, Gao Q, Luo Y, Zhang H, Ma B, Chen C, Whibley A, Zhang Y, Cao Y, Li Q, Guo H, Li J, Song Y, Zhang Y, Copsey L, Li Y, Li X, Qi M, Wang J, Chen Y, Wang D, Zhao J, Liu G, Wu B, Yu L, Xu C, Li J, Zhao S, Zhang Y, Hu S, Liang C, Yin Y, Coen E, Xue Y.

Nat Plants. 2019 Feb;5(2):174-183. doi: 10.1038/s41477-018-0349-9. Epub 2019 Jan 28.


Selection and gene flow shape genomic islands that control floral guides.

Tavares H, Whibley A, Field DL, Bradley D, Couchman M, Copsey L, Elleouet J, Burrus M, Andalo C, Li M, Li Q, Xue Y, Rebocho AB, Barton NH, Coen E.

Proc Natl Acad Sci U S A. 2018 Oct 23;115(43):11006-11011. doi: 10.1073/pnas.1801832115. Epub 2018 Oct 8.


Supergene Evolution Triggered by the Introgression of a Chromosomal Inversion.

Jay P, Whibley A, Frézal L, Rodríguez de Cara MÁ, Nowell RW, Mallet J, Dasmahapatra KK, Joron M.

Curr Biol. 2018 Jun 4;28(11):1839-1845.e3. doi: 10.1016/j.cub.2018.04.072. Epub 2018 May 24.


Evolution of flower color pattern through selection on regulatory small RNAs.

Bradley D, Xu P, Mohorianu II, Whibley A, Field D, Tavares H, Couchman M, Copsey L, Carpenter R, Li M, Li Q, Xue Y, Dalmay T, Coen E.

Science. 2017 Nov 17;358(6365):925-928. doi: 10.1126/science.aao3526.


Genetic architecture and balancing selection: the life and death of differentiated variants.

Llaurens V, Whibley A, Joron M.

Mol Ecol. 2017 May;26(9):2430-2448. doi: 10.1111/mec.14051. Epub 2017 Mar 6. Review.


Selection of Valid Reference Genes for Reverse Transcription Quantitative PCR Analysis in Heliconius numata (Lepidoptera: Nymphalidae).

Piron Prunier F, Chouteau M, Whibley A, Joron M, Llaurens V.

J Insect Sci. 2016 Jun 7;16(1). pii: 50. doi: 10.1093/jisesa/iew034. Print 2016.


The gene cortex controls mimicry and crypsis in butterflies and moths.

Nadeau NJ, Pardo-Diaz C, Whibley A, Supple MA, Saenko SV, Wallbank RW, Wu GC, Maroja L, Ferguson L, Hanly JJ, Hines H, Salazar C, Merrill RM, Dowling AJ, ffrench-Constant RH, Llaurens V, Joron M, McMillan WO, Jiggins CD.

Nature. 2016 Jun 2;534(7605):106-10. doi: 10.1038/nature17961.


Conservatism and novelty in the genetic architecture of adaptation in Heliconius butterflies.

Huber B, Whibley A, Poul YL, Navarro N, Martin A, Baxter S, Shah A, Gilles B, Wirth T, McMillan WO, Joron M.

Heredity (Edinb). 2015 May;114(5):515-24. doi: 10.1038/hdy.2015.22. Epub 2015 Mar 25.


Evolution of dominance mechanisms at a butterfly mimicry supergene.

Le Poul Y, Whibley A, Chouteau M, Prunier F, Llaurens V, Joron M.

Nat Commun. 2014 Nov 27;5:5644. doi: 10.1038/ncomms6644.


Whole-genome re-sequencing of non-model organisms: lessons from unmapped reads.

Gouin A, Legeai F, Nouhaud P, Whibley A, Simon JC, Lemaitre C.

Heredity (Edinb). 2015 May;114(5):494-501. doi: 10.1038/hdy.2014.85. Epub 2014 Oct 1.


Wing shape variation associated with mimicry in butterflies.

Jones RT, Le Poul Y, Whibley AC, Mérot C, ffrench-Constant RH, Joron M.

Evolution. 2013 Aug;67(8):2323-34. doi: 10.1111/evo.12114. Epub 2013 Apr 24.


Fecal immunochemical tests compared with guaiac fecal occult blood tests for population-based colorectal cancer screening.

Rabeneck L, Rumble RB, Thompson F, Mills M, Oleschuk C, Whibley A, Messersmith H, Lewis N.

Can J Gastroenterol. 2012 Mar;26(3):131-47. Review.


Predictors of re-participation in faecal occult blood test- based screening for colorectal cancer.

Cole SR, Gregory T, Whibley A, Ward P, Turnbull D, Wilson C, Flight I, Esterman A, Young GP.

Asian Pac J Cancer Prev. 2012;13(12):5989-94.


Genomic islands of divergence in hybridizing Heliconius butterflies identified by large-scale targeted sequencing.

Nadeau NJ, Whibley A, Jones RT, Davey JW, Dasmahapatra KK, Baxter SW, Quail MA, Joron M, ffrench-Constant RH, Blaxter ML, Mallet J, Jiggins CD.

Philos Trans R Soc Lond B Biol Sci. 2012 Feb 5;367(1587):343-53. doi: 10.1098/rstb.2011.0198.


Chromosomal rearrangements maintain a polymorphic supergene controlling butterfly mimicry.

Joron M, Frezal L, Jones RT, Chamberlain NL, Lee SF, Haag CR, Whibley A, Becuwe M, Baxter SW, Ferguson L, Wilkinson PA, Salazar C, Davidson C, Clark R, Quail MA, Beasley H, Glithero R, Lloyd C, Sims S, Jones MC, Rogers J, Jiggins CD, ffrench-Constant RH.

Nature. 2011 Aug 14;477(7363):203-6. doi: 10.1038/nature10341.


Disruption at the PTCHD1 Locus on Xp22.11 in Autism spectrum disorder and intellectual disability.

Noor A, Whibley A, Marshall CR, Gianakopoulos PJ, Piton A, Carson AR, Orlic-Milacic M, Lionel AC, Sato D, Pinto D, Drmic I, Noakes C, Senman L, Zhang X, Mo R, Gauthier J, Crosbie J, Pagnamenta AT, Munson J, Estes AM, Fiebig A, Franke A, Schreiber S, Stewart AF, Roberts R, McPherson R, Guter SJ, Cook EH Jr, Dawson G, Schellenberg GD, Battaglia A, Maestrini E; Autism Genome Project Consortium, Jeng L, Hutchison T, Rajcan-Separovic E, Chudley AE, Lewis SM, Liu X, Holden JJ, Fernandez B, Zwaigenbaum L, Bryson SE, Roberts W, Szatmari P, Gallagher L, Stratton MR, Gecz J, Brady AF, Schwartz CE, Schachar RJ, Monaco AP, Rouleau GA, Hui CC, Lucy Raymond F, Scherer SW, Vincent JB.

Sci Transl Med. 2010 Sep 15;2(49):49ra68. doi: 10.1126/scitranslmed.3001267.


Stripes, sex and sparrows: what processes underlie heteromorphic chromosome evolution?

Joron M, Whibley A.

Heredity (Edinb). 2011 Apr;106(4):531-2. doi: 10.1038/hdy.2010.106. Epub 2010 Aug 18. No abstract available.


Fine-scale survey of X chromosome copy number variants and indels underlying intellectual disability.

Whibley AC, Plagnol V, Tarpey PS, Abidi F, Fullston T, Choma MK, Boucher CA, Shepherd L, Willatt L, Parkin G, Smith R, Futreal PA, Shaw M, Boyle J, Licata A, Skinner C, Stevenson RE, Turner G, Field M, Hackett A, Schwartz CE, Gecz J, Stratton MR, Raymond FL.

Am J Hum Genet. 2010 Aug 13;87(2):173-88. doi: 10.1016/j.ajhg.2010.06.017. Epub 2010 Jul 22.


Deletion of MAOA and MAOB in a male patient causes severe developmental delay, intermittent hypotonia and stereotypical hand movements.

Whibley A, Urquhart J, Dore J, Willatt L, Parkin G, Gaunt L, Black G, Donnai D, Raymond FL.

Eur J Hum Genet. 2010 Oct;18(10):1095-9. doi: 10.1038/ejhg.2010.41. Epub 2010 May 19.


Endorsement by the primary care practitioner consistently improves participation in screening for colorectal cancer: a longitudinal analysis.

Zajac IT, Whibley AH, Cole SR, Byrne D, Guy J, Morcom J, Young GP.

J Med Screen. 2010;17(1):19-24. doi: 10.1258/jms.2010.009101. Erratum in: J Med Screen. 2010 Jun;17(2):106.


Recurrent deletion of ZNF630 at Xp11.23 is not associated with mental retardation.

Lugtenberg D, Zangrande-Vieira L, Kirchhoff M, Whibley AC, Oudakker AR, Kjaergaard S, Vianna-Morgante AM, Kleefstra T, Ruiter M, Jehee FS, Ullmann R, Schwartz CE, Stratton M, Raymond FL, Veltman JA, Vrijenhoek T, Pfundt R, Schuurs-Hoeijmakers JH, Hehir-Kwa JY, Froyen G, Chelly J, Ropers HH, Moraine C, Gècz J, Knijnenburg J, Kant SG, Hamel BC, Rosenberg C, van Bokhoven H, de Brouwer AP.

Am J Med Genet A. 2010 Mar;152A(3):638-45. doi: 10.1002/ajmg.a.33292.


Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaks.

Kerzendorfer C, Whibley A, Carpenter G, Outwin E, Chiang SC, Turner G, Schwartz C, El-Khamisy S, Raymond FL, O'Driscoll M.

Hum Mol Genet. 2010 Apr 1;19(7):1324-34. doi: 10.1093/hmg/ddq008. Epub 2010 Jan 11.


CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes.

Hackett A, Tarpey PS, Licata A, Cox J, Whibley A, Boyle J, Rogers C, Grigg J, Partington M, Stevenson RE, Tolmie J, Yates JR, Turner G, Wilson M, Futreal AP, Corbett M, Shaw M, Gecz J, Raymond FL, Stratton MR, Schwartz CE, Abidi FE.

Eur J Hum Genet. 2010 May;18(5):544-52. doi: 10.1038/ejhg.2009.220. Epub 2009 Dec 23. Erratum in: Eur J Hum Genet. 2010 May;18(5):552.


A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.

Tarpey PS, Smith R, Pleasance E, Whibley A, Edkins S, Hardy C, O'Meara S, Latimer C, Dicks E, Menzies A, Stephens P, Blow M, Greenman C, Xue Y, Tyler-Smith C, Thompson D, Gray K, Andrews J, Barthorpe S, Buck G, Cole J, Dunmore R, Jones D, Maddison M, Mironenko T, Turner R, Turrell K, Varian J, West S, Widaa S, Wray P, Teague J, Butler A, Jenkinson A, Jia M, Richardson D, Shepherd R, Wooster R, Tejada MI, Martinez F, Carvill G, Goliath R, de Brouwer AP, van Bokhoven H, Van Esch H, Chelly J, Raynaud M, Ropers HH, Abidi FE, Srivastava AK, Cox J, Luo Y, Mallya U, Moon J, Parnau J, Mohammed S, Tolmie JL, Shoubridge C, Corbett M, Gardner A, Haan E, Rujirabanjerd S, Shaw M, Vandeleur L, Fullston T, Easton DF, Boyle J, Partington M, Hackett A, Field M, Skinner C, Stevenson RE, Bobrow M, Turner G, Schwartz CE, Gecz J, Raymond FL, Futreal PA, Stratton MR.

Nat Genet. 2009 May;41(5):535-43. doi: 10.1038/ng.367. Epub 2009 Apr 19.


Lessons learnt from large-scale exon re-sequencing of the X chromosome.

Raymond FL, Whibley A, Stratton MR, Gecz J.

Hum Mol Genet. 2009 Apr 15;18(R1):R60-4. doi: 10.1093/hmg/ddp071. Review.


SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome.

Gilfillan GD, Selmer KK, Roxrud I, Smith R, Kyllerman M, Eiklid K, Kroken M, Mattingsdal M, Egeland T, Stenmark H, Sjøholm H, Server A, Samuelsson L, Christianson A, Tarpey P, Whibley A, Stratton MR, Futreal PA, Teague J, Edkins S, Gecz J, Turner G, Raymond FL, Schwartz C, Stevenson RE, Undlien DE, Strømme P.

Am J Hum Genet. 2008 Apr;82(4):1003-10. doi: 10.1016/j.ajhg.2008.01.013. Epub 2008 Mar 13.


Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation.

Froyen G, Corbett M, Vandewalle J, Jarvela I, Lawrence O, Meldrum C, Bauters M, Govaerts K, Vandeleur L, Van Esch H, Chelly J, Sanlaville D, van Bokhoven H, Ropers HH, Laumonnier F, Ranieri E, Schwartz CE, Abidi F, Tarpey PS, Futreal PA, Whibley A, Raymond FL, Stratton MR, Fryns JP, Scott R, Peippo M, Sipponen M, Partington M, Mowat D, Field M, Hackett A, Marynen P, Turner G, Gécz J.

Am J Hum Genet. 2008 Feb;82(2):432-43. doi: 10.1016/j.ajhg.2007.11.002. Epub 2008 Jan 24.


Evolutionary paths underlying flower color variation in Antirrhinum.

Whibley AC, Langlade NB, Andalo C, Hanna AI, Bangham A, Thébaud C, Coen E.

Science. 2006 Aug 18;313(5789):963-6.



Whibley A, Baxter C.

Curr Biol. 2004 Apr 6;14(7):R260-1. No abstract available.

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