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Carole Charlier
Carole Charlier
GIGA, university of Liège
Dirección de correo verificada de uliege.be
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A mutation creating a potential illegitimate microRNA target site in the myostatin gene affects muscularity in sheep
A Clop, F Marcq, H Takeda, D Pirottin, X Tordoir, B Bibé, J Bouix, ...
Nature genetics 38 (7), 813-818, 2006
16052006
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
NA Singh, C Charlier, D Stauffer, BR DuPont, RJ Leach, R Melis, ...
Nature genetics 18 (1), 25-29, 1998
14461998
A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
C Charlier, NA Singh, SG Ryan, TB Lewis, BE Reus, RJ Leach, M Leppert
Nature genetics 18 (1), 53-55, 1998
11691998
RNAi-mediated allelic trans-interaction at the imprinted Rtl1/Peg11 locus
E Davis, F Caiment, X Tordoir, J Cavaillé, A Ferguson-Smith, N Cockett, ...
Current Biology 15 (8), 743-749, 2005
4152005
Highly effective SNP-based association mapping and management of recessive defects in livestock
C Charlier, W Coppieters, F Rollin, D Desmecht, JS Agerholm, ...
Nature genetics 40 (4), 449-454, 2008
3662008
KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum
NA Singh, P Westenskow, C Charlier, C Pappas, J Leslie, J Dillon, ...
Brain 126 (12), 2726-2737, 2003
3392003
Harnessing genomic information for livestock improvement
M Georges, C Charlier, B Hayes
Nature Reviews Genetics 20 (3), 135-156, 2019
2942019
The mh gene causing double-muscling in cattle maps to bovine Chromosome 2
C Charlier, W Coppieters, F Farnir, L Grobet, PL Leroy, C Michaux, M Mni, ...
Mammalian Genome 6, 788-792, 1995
2731995
Human–ovine comparative sequencing of a 250-kb imprinted domain encompassing the callipyge (clpg) locus and identification of six imprinted transcripts: DLK1, DAT, GTL2, PEG11 …
C Charlier, K Segers, D Wagenaar, L Karim, S Berghmans, O Jaillon, ...
Genome research 11 (5), 850-862, 2001
2522001
A locus for febrile seizures (FEB3) maps to chromosome 2q23‐24
A Peiffer, J Thompson, C Charlier, B Otterud, T Varvil, C Pappas, ...
Annals of Neurology: Official Journal of the American Neurological …, 1999
2281999
The callipyge mutation enhances the expression of coregulated imprinted genes in cis without affecting their imprinting status
C Charlier, K Segers, L Karim, T Shay, G Gyapay, N Cockett, M Georges
Nature genetics 27 (4), 367-369, 2001
2092001
A 660-Kb deletion with antagonistic effects on fertility and milk production segregates at high frequency in Nordic Red cattle: additional evidence for the common occurrence of …
NK Kadri, G Sahana, C Charlier, T Iso-Touru, B Guldbrandtsen, L Karim, ...
PLoS genetics 10 (1), e1004049, 2014
1952014
The callipyge locus: evidence for the trans interaction of reciprocally imprinted genes
M Georges, C Charlier, N Cockett
Trends in Genetics 19 (5), 248-252, 2003
1872003
Serial translocation by means of circular intermediates underlies colour sidedness in cattle
K Durkin, W Coppieters, C Drögemüller, N Ahariz, N Cambisano, T Druet, ...
Nature 482 (7383), 81-84, 2012
1792012
Patrocles: a database of polymorphic miRNA-mediated gene regulation in vertebrates
S Hiard, C Charlier, W Coppieters, M Georges, D Baurain
Nucleic acids research 38 (suppl_1), D640-D651, 2010
1672010
Polymorphic miRNA-mediated gene regulation: contribution to phenotypic variation and disease
M Georges, W Coppieters, C Charlier
Current opinion in genetics & development 17 (3), 166-176, 2007
1662007
Ectopic expression of DLK1 protein in skeletal muscle of padumnal heterozygotes causes the callipyge phenotype
E Davis, CH Jensen, HD Schroder, F Farnir, T Shay-Hadfield, A Kliem, ...
Current Biology 14 (20), 1858-1862, 2004
1602004
Comparative sequence analysis of the imprinted Dlk1–Gtl2 locus in three mammalian species reveals highly conserved genomic elements and refines comparison with the Igf2–H19 region
M Paulsen, S Takada, NA Youngson, M Benchaib, C Charlier, K Segers, ...
Genome Research 11 (12), 2085-2094, 2001
1542001
Genetic Variants in REC8, RNF212, and PRDM9 Influence Male Recombination in Cattle
C Sandor, W Li, W Coppieters, T Druet, C Charlier, M Georges
PLoS genetics 8 (7), e1002854, 2012
1502012
Mosaicism of Solid Gold supports the causality of a noncoding A-to-G transition in the determinism of the callipyge phenotype
M Smit, K Segers, LG Carrascosa, T Shay, F Baraldi, G Gyapay, ...
Genetics 163 (1), 453-456, 2003
1492003
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