Bahram S - Search Results

1

Bahram S, Carapito R, Gourraud PA, Charron D. Bahram S, et al. Hum Immunol. 2016 Nov;77(11):1005-1007. doi: 10.1016/j.humimm.2016.10.016. Hum Immunol. 2016. PMID: 27881245

2

A new mutation in the C-SH2 domain of PTPN11 causes Noonan syndrome with multiple giant cell lesions.

Carapito R, Paul N, Untrau M, Ott L, Corradini N, Poignant S, Geffroy L, Caldagues E, Heymann MF, Cassagnau E, Isidor B, Bahram S. Carapito R, et al. Among authors: bahram s. J Hum Genet. 2014 Jan;59(1):57-9. doi: 10.1038/jhg.2013.118. Epub 2013 Nov 14. J Hum Genet. 2014. PMID: 24225993

3

High diversity of MIC genes in non-human primates.

Meyer A, Carapito R, Ott L, Radosavljevic M, Georgel P, Adams EJ, Parham P, Bontrop RE, Blancher A, Bahram S. Meyer A, et al. Among authors: bahram s. Immunogenetics. 2014 Oct;66(9-10):581-7. doi: 10.1007/s00251-014-0791-4. Epub 2014 Jul 31. Immunogenetics. 2014. PMID: 25073428

4

Eosinophilic myositis as first manifestation in a patient with type 2 myotonic dystrophy CCTG expansion mutation and rheumatoid arthritis.

Meyer A, Lannes B, Carapito R, Bahram S, Echaniz-Laguna A, Geny B, Sibilia J, Gottenberg JE. Meyer A, et al. Among authors: bahram s. Neuromuscul Disord. 2015 Feb;25(2):149-52. doi: 10.1016/j.nmd.2014.09.009. Epub 2014 Sep 28. Neuromuscul Disord. 2015. PMID: 25443993

5

A de novo ADCY5 mutation causes early-onset autosomal dominant chorea and dystonia.

Carapito R, Paul N, Untrau M, Le Gentil M, Ott L, Alsaleh G, Jochem P, Radosavljevic M, Le Caignec C, David A, Damier P, Isidor B, Bahram S. Carapito R, et al. Among authors: bahram s. Mov Disord. 2015 Mar;30(3):423-7. doi: 10.1002/mds.26115. Epub 2014 Dec 27. Mov Disord. 2015. PMID: 25545163

6

On the genetics of the Silk Route: association analysis of HLA, IL10, and IL23R-IL12RB2 regions with Behçet's disease in an Iranian population.

Carapito R, Shahram F, Michel S, Le Gentil M, Radosavljevic M, Meguro A, Abdollahi BS, Inoko H, Ota M, Davatchi F, Bahram S. Carapito R, et al. Among authors: bahram s. Immunogenetics. 2015 Jun;67(5-6):289-93. doi: 10.1007/s00251-015-0841-6. Epub 2015 May 5. Immunogenetics. 2015. PMID: 25940109

7

Genetics, genomics, and evolutionary biology of NKG2D ligands.

Carapito R, Bahram S. Carapito R, et al. Among authors: bahram s. Immunol Rev. 2015 Sep;267(1):88-116. doi: 10.1111/imr.12328. Immunol Rev. 2015. PMID: 26284473 Review.

8

Next-Generation Sequencing of the HLA locus: Methods and impacts on HLA typing, population genetics and disease association studies.

Carapito R, Radosavljevic M, Bahram S. Carapito R, et al. Among authors: bahram s. Hum Immunol. 2016 Nov;77(11):1016-1023. doi: 10.1016/j.humimm.2016.04.002. Epub 2016 Apr 5. Hum Immunol. 2016. PMID: 27060029 Review.

9

Protein-altering MYH3 variants are associated with a spectrum of phenotypes extending to spondylocarpotarsal synostosis syndrome.

Carapito R, Goldenberg A, Paul N, Pichot A, David A, Hamel A, Dumant-Forest C, Leroux J, Ory B, Isidor B, Bahram S. Carapito R, et al. Among authors: bahram s. Eur J Hum Genet. 2016 Dec;24(12):1746-1751. doi: 10.1038/ejhg.2016.84. Epub 2016 Jul 6. Eur J Hum Genet. 2016. PMID: 27381093 Free PMC article.

10

Matching for the nonconventional MHC-I MICA gene significantly reduces the incidence of acute and chronic GVHD.

Carapito R, Jung N, Kwemou M, Untrau M, Michel S, Pichot A, Giacometti G, Macquin C, Ilias W, Morlon A, Kotova I, Apostolova P, Schmitt-Graeff A, Cesbron A, Gagne K, Oudshoorn M, van der Holt B, Labalette M, Spierings E, Picard C, Loiseau P, Tamouza R, Toubert A, Parissiadis A, Dubois V, Lafarge X, Maumy-Bertrand M, Bertrand F, Vago L, Ciceri F, Paillard C, Querol S, Sierra J, Fleischhauer K, Nagler A, Labopin M, Inoko H, von dem Borne PA, Kuball J, Ota M, Katsuyama Y, Michallet M, Lioure B, Peffault de Latour R, Blaise D, Cornelissen JJ, Yakoub-Agha I, Claas F, Moreau P, Milpied N, Charron D, Mohty M, Zeiser R, Socié G, Bahram S. Carapito R, et al. Among authors: bahram s. Blood. 2016 Oct 13;128(15):1979-1986. doi: 10.1182/blood-2016-05-719070. Epub 2016 Aug 22. Blood. 2016. PMID: 27549307 Free PMC article. Clinical Trial.

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