3t-seq: automatic gene expression analysis of single-copy genes, transposable elements, and tRNAs from RNA-seq data.

Tabaro F, Boulard M

Briefings in bioinformatics, 2024

doi:10.1093/bib/bbae467.

Trim66's paternal deficiency causes intrauterine overgrowth.

Mielnicka M, Tabaro F, Sureka R, Acurzio B, Paoletti R, Scavizzi F, Raspa M, Crevenna AH, Lapouge K, Remans K, Boulard M

Life science alliance, 2024

doi:10.26508/lsa.202302512.

Long interspersed nuclear elements safeguard neural progenitors from precocious differentiation.

Toda T, Bedrosian TA, Schafer ST, Cuoco MS, Linker SB, Ghassemzadeh S, Mitchell L, Whiteley JT, Novaresi N, McDonald AH, Gallina IS, Yoon H, Hester ME, Pena M, Lim C, Suljic E, AlFatah Mansour A, Boulard M, Parylak SL, Gage FH

Cell reports, 2024

doi:10.1016/j.celrep.2024.113774.

Germinal center output is sustained by HELLS-dependent DNA-methylation-maintenance in B cells.

Cousu C, Mulot E, De Smet A, Formichetti S, Lecoeuche D, Ren J, Muegge K, Boulard M, Weill JC, Reynaud CA, Storck S

Nature communications, 2023

doi:10.1038/s41467-023-41317-3.

Methylation-directed glycosylation of chromatin factors represses retrotransposon promoters.

Boulard M, Rucli S, Edwards JR, Bestor TH

Proceedings of the National Academy of Sciences of the United States of America, 2020

doi:10.1073/pnas.1912074117.

BAH domains and a histone-like motif in DNA methyltransferase 1 (DNMT1) regulate de novo and maintenance methylation in vivo.

Yarychkivska O, Shahabuddin Z, Comfort N, Boulard M, Bestor TH

The Journal of biological chemistry, 2018

doi:10.1074/jbc.RA118.004612.

DNA methylation and DNA methyltransferases.

Edwards JR, Yarychkivska O, Boulard M, Bestor TH

Epigenetics & chromatin, 2017

doi:10.1186/s13072-017-0130-8.

Abnormal X chromosome inactivation and sex-specific gene dysregulation after ablation of FBXL10

Boulard M, Edwards JR, Bestor TH

Epigenetics & chromatin, 2016

doi:10.1186/s13072-016-0069-1.

Notes on the role of dynamic DNA methylation in mammalian development

Bestor TH, Edwards JR, Boulard M

Proceedings of the National Academy of Sciences of the United States of America, 2015

doi:10.1073/pnas.1415301111.

FBXL10 protects Polycomb-bound genes from hypermethylation

Boulard M, Edwards JR, Bestor TH

Nature genetics, 2015

doi:10.1038/ng.3272.

Histone variant macroH2A1 deletion in mice causes female-specific steatosis

Boulard M, Storck S, Cong R, Pinto R, Delage H, Bouvet P

Epigenetics & chromatin, 2010

doi:10.1186/1756-8935-3-8.

The incorporation of the novel histone variant H2AL2 confers unusual structural and functional properties of the nucleosome

Syed SH, Boulard M, Shukla MS, Gautier T, Travers A, Bednar J, Faivre-Moskalenko C, Dimitrov S, Angelov D

Nucleic acids research, 2009

doi:10.1093/nar/gkp473.

Germline mutation in RNASEL predicts increased risk of head and neck, uterine cervix and breast cancer

Madsen BE, Ramos EM, Boulard M, Duda K, Overgaard J, Nordsmark M, Wiuf C, Hansen LL

PloS one, 2008

doi:10.1371/journal.pone.0002492.

Histone variant nucleosomes: structure, function and implication in disease

Boulard M, Bouvet P, Kundu TK, Dimitrov S

Sub-cellular biochemistry, 2007

doi:10.1007/1-4020-5466-1_4.

The NH2 tail of the novel histone variant H2BFWT exhibits properties distinct from conventional H2B with respect to the assembly of mitotic chromosomes

Boulard M, Gautier T, Mbele GO, Gerson W, Hamiche A, Angelov D, Bouvet P, Dimitrov S

Molecular and cellular biology, 2006

doi:10.1128/MCB.26.4.1518-1526.2006.

Control of the vascular endothelial growth factor internal ribosome entry site (IRES) activity and translation initiation by alternatively spliced coding sequences

Bornes S, Boulard M, Hieblot C, Zanibellato C, Iacovoni JS, Prats H, Touriol C

The Journal of biological chemistry, 2004

doi:10.1074/jbc.M308410200.