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Annabel Whibley
Annabel Whibley
Bioinformatician at Bragato Research Institute and Honorary Academic, University of Auckland
Verified email at auckland.ac.nz
Title
Cited by
Cited by
Year
Butterfly genome reveals promiscuous exchange of mimicry adaptations among species
Nature 487 (7405), 94-98, 2012
11762012
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation
PS Tarpey, R Smith, E Pleasance, A Whibley, S Edkins, C Hardy, ...
Nature genetics 41 (5), 535-543, 2009
6762009
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation
PS Tarpey, R Smith, E Pleasance, A Whibley, S Edkins, C Hardy, ...
Nature genetics 41 (5), 535-543, 2009
6762009
Chromosomal rearrangements maintain a polymorphic supergene controlling butterfly mimicry
M Joron, L Frezal, RT Jones, NL Chamberlain, SF Lee, CR Haag, ...
Nature 477 (7363), 203-206, 2011
5582011
Genomic islands of divergence in hybridizing Heliconius butterflies identified by large-scale targeted sequencing
NJ Nadeau, A Whibley, RT Jones, JW Davey, KK Dasmahapatra, ...
Philosophical Transactions of the Royal Society B: Biological Sciences 367 …, 2012
3402012
SLC9A6 mutations cause X-linked mental retardation, microcephaly, epilepsy, and ataxia, a phenotype mimicking Angelman syndrome
GD Gilfillan, KK Selmer, I Roxrud, R Smith, M Kyllerman, K Eiklid, ...
The American Journal of Human Genetics 82 (4), 1003-1010, 2008
2522008
The gene cortex controls mimicry and crypsis in butterflies and moths
NJ Nadeau, C Pardo-Diaz, A Whibley, MA Supple, SV Saenko, ...
Nature 534 (7605), 106-110, 2016
2452016
Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability
A Noor, A Whibley, CR Marshall, PJ Gianakopoulos, A Piton, AR Carson, ...
Science translational medicine 2 (49), 49ra68-49ra68, 2010
2452010
Submicroscopic duplications of the hydroxysteroid dehydrogenase HSD17B10 and the E3 ubiquitin ligase HUWE1 are associated with mental retardation
G Froyen, M Corbett, J Vandewalle, I Jarvela, O Lawrence, C Meldrum, ...
The American Journal of Human Genetics 82 (2), 432-443, 2008
2432008
Evolutionary paths underlying flower color variation in Antirrhinum
AC Whibley, NB Langlade, C Andalo, AI Hanna, A Bangham, C Thébaud, ...
Science 313 (5789), 963-966, 2006
1932006
Fine-scale survey of X chromosome copy number variants and indels underlying intellectual disability
AC Whibley, V Plagnol, PS Tarpey, F Abidi, T Fullston, MK Choma, ...
The American Journal of Human Genetics 87 (2), 173-188, 2010
1412010
Supergene evolution triggered by the introgression of a chromosomal inversion
P Jay, A Whibley, L Frézal, MÁR de Cara, RW Nowell, J Mallet, ...
Current Biology 28 (11), 1839-1845. e3, 2018
1392018
Genetic architecture and balancing selection: the life and death of differentiated variants
V Llaurens, A Whibley, M Joron
Molecular ecology 26 (9), 2430-2448, 2017
1372017
CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes
A Hackett, PS Tarpey, A Licata, J Cox, A Whibley, J Boyle, C Rogers, ...
European Journal of Human Genetics 18 (5), 544-552, 2010
1302010
CASK mutations are frequent in males and cause X-linked nystagmus and variable XLMR phenotypes
A Hackett, PS Tarpey, A Licata, J Cox, A Whibley, J Boyle, C Rogers, ...
European Journal of Human Genetics 18 (5), 544-552, 2010
1302010
Mutation load at a mimicry supergene sheds new light on the evolution of inversion polymorphisms
P Jay, M Chouteau, A Whibley, H Bastide, H Parrinello, V Llaurens, ...
Nature genetics 53 (3), 288-293, 2021
1032021
Genome structure and evolution of Antirrhinum majus L
M Li, D Zhang, Q Gao, Y Luo, H Zhang, B Ma, C Chen, A Whibley, ...
Nature Plants 5 (2), 174-183, 2019
882019
Evolution of dominance mechanisms at a butterfly mimicry supergene
Y Le Poul, A Whibley, M Chouteau, F Prunier, V Llaurens, M Joron
Nature communications 5 (1), 5644, 2014
862014
Selection and gene flow shape genomic islands that control floral guides
H Tavares, A Whibley, DL Field, D Bradley, M Couchman, L Copsey, ...
Proceedings of the National Academy of Sciences 115 (43), 11006-11011, 2018
752018
Mutations in Cullin 4B result in a human syndrome associated with increased camptothecin-induced topoisomerase I-dependent DNA breaks
C Kerzendorfer, A Whibley, G Carpenter, E Outwin, SC Chiang, G Turner, ...
Human molecular genetics 19 (7), 1324-1334, 2010
732010
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