Christophe Caloustian - Search Results

Year	Number of Results
2002	1
2004	1
2006	1
2012	1
2015	1
2019	1
2023	1
2024	0

1

Characterisation of gut microbiota composition in patients with axial spondyloarthritis and its modulation by TNF inhibitor treatment.

Vallier M, Segurens B, Larsonneur E, Meyer V, Ferreira S, Caloustian C, Deleuze JF, Dougados M, Chamaillard M, Miceli-Richard C. Vallier M, et al. Among authors: caloustian c. RMD Open. 2023 Mar;9(1):e002794. doi: 10.1136/rmdopen-2022-002794. RMD Open. 2023. PMID: 36963782 Free PMC article.

2

Molecular haplotyping at high throughput.

Tost J, Brandt O, Boussicault F, Derbala D, Caloustian C, Lechner D, Gut IG. Tost J, et al. Among authors: caloustian c. Nucleic Acids Res. 2002 Oct 1;30(19):e96. doi: 10.1093/nar/gnf095. Nucleic Acids Res. 2002. PMID: 12364613 Free PMC article.

3

A new titinopathy: Childhood-juvenile onset Emery-Dreifuss-like phenotype without cardiomyopathy.

De Cid R, Ben Yaou R, Roudaut C, Charton K, Baulande S, Leturcq F, Romero NB, Malfatti E, Beuvin M, Vihola A, Criqui A, Nelson I, Nectoux J, Ben Aim L, Caloustian C, Olaso R, Udd B, Bonne G, Eymard B, Richard I. De Cid R, et al. Among authors: caloustian c. Neurology. 2015 Dec 15;85(24):2126-35. doi: 10.1212/WNL.0000000000002200. Epub 2015 Nov 18. Neurology. 2015. PMID: 26581302 Free PMC article.

4

A novel nonsense variant in SUPT20H gene associated with Rheumatoid Arthritis identified by Whole Exome Sequencing of multiplex families.

Veyssiere M, Perea J, Michou L, Boland A, Caloustian C, Olaso R, Deleuze JF, Cornelis F, Petit-Teixeira E, Chaudru V. Veyssiere M, et al. Among authors: caloustian c. PLoS One. 2019 Mar 7;14(3):e0213387. doi: 10.1371/journal.pone.0213387. eCollection 2019. PLoS One. 2019. PMID: 30845214 Free PMC article.

5

Nested core collections maximizing genetic diversity in Arabidopsis thaliana.

McKhann HI, Camilleri C, Bérard A, Bataillon T, David JL, Reboud X, Le Corre V, Caloustian C, Gut IG, Brunel D. McKhann HI, et al. Among authors: caloustian c. Plant J. 2004 Apr;38(1):193-202. doi: 10.1111/j.1365-313X.2004.02034.x. Plant J. 2004. PMID: 15053772 Free article.

6

SRPX2 mutations in disorders of language cortex and cognition.

Roll P, Rudolf G, Pereira S, Royer B, Scheffer IE, Massacrier A, Valenti MP, Roeckel-Trevisiol N, Jamali S, Beclin C, Seegmuller C, Metz-Lutz MN, Lemainque A, Delepine M, Caloustian C, de Saint Martin A, Bruneau N, Depétris D, Mattéi MG, Flori E, Robaglia-Schlupp A, Lévy N, Neubauer BA, Ravid R, Marescaux C, Berkovic SF, Hirsch E, Lathrop M, Cau P, Szepetowski P. Roll P, et al. Among authors: caloustian c. Hum Mol Genet. 2006 Apr 1;15(7):1195-207. doi: 10.1093/hmg/ddl035. Epub 2006 Feb 23. Hum Mol Genet. 2006. PMID: 16497722

7

Sequence variants and haplotype analysis of cat ERBB2 gene: a survey on spontaneous cat mammary neoplastic and non-neoplastic lesions.

Santos S, Bastos E, Baptista CS, Sá D, Caloustian C, Guedes-Pinto H, Gärtner F, Gut IG, Chaves R. Santos S, et al. Among authors: caloustian c. Int J Mol Sci. 2012;13(3):2783-2800. doi: 10.3390/ijms13032783. Epub 2012 Mar 2. Int J Mol Sci. 2012. PMID: 22489125 Free PMC article.

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