Pinson S - Search Results

1

Genome profiling of chronic myelomonocytic leukemia: frequent alterations of RAS and RUNX1 genes.

Gelsi-Boyer V, Trouplin V, Adélaïde J, Aceto N, Remy V, Pinson S, Houdayer C, Arnoulet C, Sainty D, Bentires-Alj M, Olschwang S, Vey N, Mozziconacci MJ, Birnbaum D, Chaffanet M. Gelsi-Boyer V, et al. Among authors: pinson s. BMC Cancer. 2008 Oct 16;8:299. doi: 10.1186/1471-2407-8-299. BMC Cancer. 2008. PMID: 18925961 Free PMC article.

2

Very early prophylactic thyroid surgery for infants with a mutation of the RET proto-oncogene at codon 634: evaluation of the implementation of international guidelines for MEN type 2 in a single centre.

Piolat C, Dyon JF, Sturm N, Pinson S, Bost M, Jouk PS, Plantaz D, Chabre O. Piolat C, et al. Among authors: pinson s. Clin Endocrinol (Oxf). 2006 Jul;65(1):118-24. doi: 10.1111/j.1365-2265.2006.02559.x. Clin Endocrinol (Oxf). 2006. PMID: 16817830

3

Non-C282Y familial iron overload: evidence for locus heterogeneity in haemochromatosis.

Pinson S, Yaouanq J, Jouanolle AM, Turlin B, Plauchu H. Pinson S, et al. J Med Genet. 1998 Nov;35(11):954-6. doi: 10.1136/jmg.35.11.954. J Med Genet. 1998. PMID: 9832046 Free PMC article.

4

Polymorphisms in RET and its coreceptors and ligands as genetic modifiers of multiple endocrine neoplasia type 2A.

Lesueur F, Cebrian A, Robledo M, Niccoli-Sire P, Svensson KA, Pinson S, Leyland J, Whittaker J, Pharoah PD, Ponder BA. Lesueur F, et al. Among authors: pinson s. Cancer Res. 2006 Jan 15;66(2):1177-80. doi: 10.1158/0008-5472.CAN-05-2995. Cancer Res. 2006. PMID: 16424056

5

[Cardiogenetics in the year 2000].

Pinson S, Guichard C, Lenoir D, el Zein L, Nizard P, Bozio A, Bouvagnet P. Pinson S, et al. Arch Mal Coeur Vaiss. 2000 May;93(5):595-611. Arch Mal Coeur Vaiss. 2000. PMID: 10858858 Review. French.

6

Does the RET variant G691S influence the features of sporadic medullary thyroid carcinoma?

Cardot-Bauters C, Leteurtre E, Leclerc L, Vantyghem MC, Do Cao C, Wemeau JL, d'Herbomez M, Carnaille B, Barbu V, Pinson S, Pigny P; Groupe d'Etude des Tumeurs Endocrines (GTE). Cardot-Bauters C, et al. Among authors: pinson s. Clin Endocrinol (Oxf). 2008 Sep;69(3):506-10. doi: 10.1111/j.1365-2265.2008.03230.x. Epub 2008 Mar 10. Clin Endocrinol (Oxf). 2008. PMID: 18331611

7

The UMD-APC database, a model of nation-wide knowledge base: update with data from 3,581 variations.

Grandval P, Blayau M, Buisine MP, Coulet F, Maugard C, Pinson S, Remenieras A, Tinat J, Uhrhammer N, Béroud C, Olschwang S. Grandval P, et al. Among authors: pinson s. Hum Mutat. 2014 May;35(5):532-6. doi: 10.1002/humu.22539. Epub 2014 Apr 7. Hum Mutat. 2014. PMID: 24599579

8

Genomic variations integrated database for MUTYH-associated adenomatous polyposis.

Grandval P, Fabre AJ, Gaildrat P, Baert-Desurmont S, Blayau M, Buisine MP, Coulet F, Maugard C, Pinson S, Remenieras A, Rouleau E, Uhrhammer N, Beroud C, Olschwang S. Grandval P, et al. Among authors: pinson s. J Med Genet. 2015 Jan;52(1):25-7. doi: 10.1136/jmedgenet-2014-102752. Epub 2014 Nov 3. J Med Genet. 2015. PMID: 25368107 No abstract available.

9

Novel biallelic mutations in MSH6 and PMS2 genes: gene conversion as a likely cause of PMS2 gene inactivation.

Auclair J, Leroux D, Desseigne F, Lasset C, Saurin JC, Joly MO, Pinson S, Xu XL, Montmain G, Ruano E, Navarro C, Puisieux A, Wang Q. Auclair J, et al. Among authors: pinson s. Hum Mutat. 2007 Nov;28(11):1084-90. doi: 10.1002/humu.20569. Hum Mutat. 2007. PMID: 17557300

10

NF1 single and multi-exons copy number variations in neurofibromatosis type 1.

Imbard A, Pasmant E, Sabbagh A, Luscan A, Soares M, Goussard P, Blanché H, Laurendeau I, Ferkal S, Vidaud M, Pinson S, Bellanne-Chantelot C, Vidaud D, Wolkenstein P; members of the NF France Network; Parfait B. Imbard A, et al. Among authors: pinson s. J Hum Genet. 2015 Apr;60(4):221-4. doi: 10.1038/jhg.2015.6. Epub 2015 Jan 29. J Hum Genet. 2015. PMID: 25631097

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