Sobol H - Search Results

1

Molecular characterization by array comparative genomic hybridization and DNA sequencing of 194 desmoid tumors.

Salas S, Chibon F, Noguchi T, Terrier P, Ranchere-Vince D, Lagarde P, Benard J, Forget S, Blanchard C, Dômont J, Bonvalot S, Guillou L, Leroux A, Mechine-Neuville A, Schöffski P, Laë M, Collin F, Verola O, Carbonnelle A, Vescovo L, Bui B, Brouste V, Sobol H, Aurias A, Coindre JM. Salas S, et al. Among authors: sobol h. Genes Chromosomes Cancer. 2010 Jun;49(6):560-8. doi: 10.1002/gcc.20766. Genes Chromosomes Cancer. 2010. PMID: 20232483

2

About sequence quality: impact on clinical applications.

Noguchi T, Bourdon V, Sobol H. Noguchi T, et al. Among authors: sobol h. Genet Test Mol Biomarkers. 2014 May;18(5):299-305. doi: 10.1089/gtmb.2013.0435. Epub 2014 Mar 12. Genet Test Mol Biomarkers. 2014. PMID: 24620857

3

Genome-wide search for loss of heterozygosity in Burkitt lymphoma cell lines.

Sobol H, Benziane A, Kerangueven F, Yin L, Noguchi T, Pauly S, Eisinger F, Longy M, Romeo G, Lenoir G, Birnbaum D. Sobol H, et al. Genes Chromosomes Cancer. 2002 Feb;33(2):217-24. doi: 10.1002/gcc.10022. Genes Chromosomes Cancer. 2002. PMID: 11793449

4

Patterns of loss of heterozygosity at loci from chromosome arm 13q suggests a possible involvement of BRCA2 in sporadic breast tumors.

Kerangueven F, Allione F, Noguchi T, Adélaïde J, Sobol H, Jacquemier J, Birnbaum D. Kerangueven F, et al. Among authors: sobol h. Genes Chromosomes Cancer. 1995 Aug;13(4):291-4. doi: 10.1002/gcc.2870130410. Genes Chromosomes Cancer. 1995. PMID: 7547638

5

BARD1 homozygous deletion, a possible alternative to BRCA1 mutation in basal breast cancer.

Sabatier R, Adélaïde J, Finetti P, Ferrari A, Huiart L, Sobol H, Chaffanet M, Birnbaum D, Bertucci F. Sabatier R, et al. Among authors: sobol h. Genes Chromosomes Cancer. 2010 Dec;49(12):1143-51. doi: 10.1002/gcc.20822. Genes Chromosomes Cancer. 2010. PMID: 20842729

6

SMARCB1/INI1 germline mutations contribute to 10% of sporadic schwannomatosis.

Rousseau G, Noguchi T, Bourdon V, Sobol H, Olschwang S. Rousseau G, et al. Among authors: sobol h. BMC Neurol. 2011 Jan 24;11:9. doi: 10.1186/1471-2377-11-9. BMC Neurol. 2011. PMID: 21255467 Free PMC article.

7

Quantitative PCR high-resolution melting (qPCR-HRM) curve analysis, a new approach to simultaneously screen point mutations and large rearrangements: application to MLH1 germline mutations in Lynch syndrome.

Rouleau E, Lefol C, Bourdon V, Coulet F, Noguchi T, Soubrier F, Bièche I, Olschwang S, Sobol H, Lidereau R. Rouleau E, et al. Among authors: sobol h. Hum Mutat. 2009 Jun;30(6):867-75. doi: 10.1002/humu.20947. Hum Mutat. 2009. PMID: 19224586

8

Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAP.

Lagarde A, Rouleau E, Ferrari A, Noguchi T, Qiu J, Briaux A, Bourdon V, Rémy V, Gaildrat P, Adélaïde J, Birnbaum D, Lidereau R, Sobol H, Olschwang S. Lagarde A, et al. Among authors: sobol h. J Med Genet. 2010 Oct;47(10):721-2. doi: 10.1136/jmg.2010.078964. Epub 2010 Aug 3. J Med Genet. 2010. PMID: 20685668 Free article.

9

Loss of heterozygosity at loci from chromosome arm 22Q in human sporadic breast carcinomas.

Allione F, Eisinger F, Parc P, Noguchi T, Sobol H, Birnbaum D. Allione F, et al. Among authors: sobol h. Int J Cancer. 1998 Jan 19;75(2):181-6. doi: 10.1002/(sici)1097-0215(19980119)75:2<181::aid-ijc3>3.0.co;2-q. Int J Cancer. 1998. PMID: 9462705 Free article.

10

Genome-wide search for loss of heterozygosity shows extensive genetic diversity of human breast carcinomas.

Kerangueven F, Noguchi T, Coulier F, Allione F, Wargniez V, Simony-Lafontaine J, Longy M, Jacquemier J, Sobol H, Eisinger F, Birnbaum D. Kerangueven F, et al. Among authors: sobol h. Cancer Res. 1997 Dec 15;57(24):5469-74. Cancer Res. 1997. PMID: 9407952

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