Louis Lefebvre
Louis Lefebvre
Associate Professor, Medical Genetics, University of British Columbia
Verified email at ubc.ca - Homepage
Cited by
Cited by
Abnormal maternal behaviour and growth retardation associated with loss of the imprinted gene Mest
L Lefebvre, S Viville, SC Barton, F Ishino, EB Keverne, MA Surani
Nature genetics 20 (2), 163-169, 1998
Embryonic germ cells induce epigenetic reprogramming of somatic nucleus in hybrid cells
M Tada, T Tada, L Lefebvre, SC Barton, MA Surani
The EMBO journal 16 (21), 6510-6520, 1997
Androgenetic/biparental mosaicism causes placental mesenchymal dysplasia
KA Kaiser-Rogers, DE Mcfadden, CA Livasy, J Dansereau, R Jiang, ...
Journal of medical genetics 43 (2), 187-192, 2006
Setdb1 is required for germline development and silencing of H3K9me3-marked endogenous retroviruses in primordial germ cells
S Liu, J Brind’Amour, MM Karimi, K Shirane, A Bogutz, L Lefebvre, ...
Genes & development 28 (18), 2041-2055, 2014
Genomic structure and parent-of-origin-specific methylation of Peg1
L Lefebvre, S Viville, SC Barton, F Ishino, MA Surani
Human molecular genetics 6 (11), 1907-1915, 1997
Maternal DNA methylation regulates early trophoblast development
MR Branco, M King, V Perez-Garcia, AB Bogutz, M Caley, E Fineberg, ...
Developmental cell 36 (2), 152-163, 2016
Human placental-specific epipolymorphism and its association with adverse pregnancy outcomes
RKC Yuen, L Avila, MS Peñaherrera, P von Dadelszen, L Lefebvre, ...
PloS one 4 (10), e7389, 2009
Developmental regulation of somatic imprints
RM John, L Lefebvre
Differentiation 81 (5), 270-280, 2011
Partial loss of Ascl2 function affects all three layers of the mature placenta and causes intrauterine growth restriction
R Oh-McGinnis, AB Bogutz, L Lefebvre
Developmental biology 351 (2), 277-286, 2011
SETD2 regulates the maternal epigenome, genomic imprinting and embryonic development
Q Xu, Y Xiang, Q Wang, L Wang, J Brind’Amour, AB Bogutz, Y Zhang, ...
Nature genetics 51 (5), 844-856, 2019
The ANB1 locus of Saccharomyces cerevisiae encodes the protein synthesis initiation factor eIF-4D.
KD Mehta, D Leung, L Lefebvre, M Smith
Journal of Biological Chemistry 265 (15), 8802-8807, 1990
Selection for transgene homozygosity in embryonic stem cells results in extensive loss of heterozygosity.
L Lefebvre, N Dionne, J Karaskova, JA Squire, A Nagy
Nature genetics 27 (3), 257-258, 2001
Beckwith–Wiedemann and Silver–Russell syndromes: opposite developmental imbalances in imprinted regulators of placental function and embryonic growth
KJ Jacob, WP Robinson, L Lefebvre
Clinical genetics 84 (4), 326-334, 2013
Loss‐of‐imprinting of Peg1 in mouse interspecies hybrids is correlated with altered growth
W Shi, L Lefebvre, Y Yu, S Otto, A Krella, A Orth, R Fundele
genesis 39 (1), 65-72, 2004
LTR retrotransposons transcribed in oocytes drive species-specific and heritable changes in DNA methylation
J Brind’Amour, H Kobayashi, JR Albert, K Shirane, A Sakashita, A Kamio, ...
Nature communications 9 (1), 1-14, 2018
The placental imprintome and imprinted gene function in the trophoblast glycogen cell lineage
L Lefebvre
Reproductive biomedicine online 25 (1), 44-57, 2012
Tissue-specific alternative polyadenylation at the imprinted gene Mest regulates allelic usage at Copg2
JL MacIsaac, AB Bogutz, AS Morrissy, L Lefebvre
Nucleic acids research 40 (4), 1523-1535, 2012
Impact of flanking chromosomal sequences on localization and silencing by the human non-coding RNA XIST
AD Kelsey, C Yang, D Leung, J Minks, T Dixon-McDougall, SEL Baldry, ...
Genome biology 16 (1), 1-16, 2015
An extended domain of Kcnq1ot1 silencing revealed by an imprinted fluorescent reporter
MJ Jones, AB Bogutz, L Lefebvre
Molecular and cellular biology 31 (14), 2827-2837, 2011
Mutational and functional analysis of dominant SPT2 (SIN1) suppressor alleles in Saccharomyces cerevisiae.
L Lefebvre, M Smith
Molecular and cellular biology 13 (9), 5393-5407, 1993
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