Chiara Conte - Search Results

Year	Number of Results
2002	2
2007	1
2008	8
2009	1
2011	1
2019	1
2020	1
2021	1
2022	0

1

Breast cancer in West Africa: molecular analysis of BRCA genes in early-onset breast cancer patients in Burkina Faso.

Biancolella M, Ouédraogo NLM, Zongo N, Zohoncon TM, Testa B, Rizzacasa B, Latini A, Conte C, Compaore TR, Ouedraogo CMR, Traore SS, Simpore J, Novelli G. Biancolella M, et al. Among authors: conte c. Hum Genomics. 2021 Oct 30;15(1):65. doi: 10.1186/s40246-021-00365-w. Hum Genomics. 2021. PMID: 34717758 Free PMC article.

2

Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience.

Mannucci L, Luciano S, Salehi LB, Gigante L, Conte C, Longo G, Ferradini V, Piumelli N, Brancati F, Ruvolo G, Novelli G, Sangiuolo F. Mannucci L, et al. Among authors: conte c. Clin Chim Acta. 2020 Feb;501:154-164. doi: 10.1016/j.cca.2019.10.037. Epub 2019 Nov 12. Clin Chim Acta. 2020. PMID: 31730815

3

Gene symbol: ED1. Disease: X-linked anhidrotic ectodermal dysplasia.

Conte C. Conte C. Hum Genet. 2008 Feb;123(1):104. Hum Genet. 2008. PMID: 18386319 No abstract available.

4

Novel mutations of TCOF1 gene in European patients with Treacher Collins syndrome.

Conte C, D'Apice MR, Rinaldi F, Gambardella S, Sangiuolo F, Novelli G. Conte C, et al. BMC Med Genet. 2011 Sep 27;12:125. doi: 10.1186/1471-2350-12-125. BMC Med Genet. 2011. PMID: 21951868 Free PMC article.

5

Screening of EDA1 gene in X-linked anhidrotic ectodermal dysplasia using DHPLC: identification of 14 novel mutations in Italian patients.

Conte C, Gambardella S, Bulli C, Rinaldi F, Di Marino D, Falconi M, Bramanti P, Desideri A, Novelli G. Conte C, et al. Genet Test. 2008 Sep;12(3):437-42. doi: 10.1089/gte.2008.0020. Genet Test. 2008. PMID: 18666859

6

Mutational analysis of Peroxiredoxin IV: exclusion of a positional candidate for multinodular goitre.

Giardina E, Capon F, D'Apice MR, Amati F, Arturi F, Filetti S, Bonifazi E, Pucci S, Conte C, Novelli G. Giardina E, et al. Among authors: conte c. BMC Med Genet. 2002 Jul 23;3:5. doi: 10.1186/1471-2350-3-5. Epub 2002 Jul 23. BMC Med Genet. 2002. PMID: 12135533 Free PMC article.

7

Familial medullary thyroid carcinoma: clinical variability and low aggressiveness associated with RET mutation at codon 804.

Lombardo F, Baudin E, Chiefari E, Arturi F, Bardet S, Caillou B, Conte C, Dallapiccola B, Giuffrida D, Bidart JM, Schlumberger M, Filetti S. Lombardo F, et al. Among authors: conte c. J Clin Endocrinol Metab. 2002 Apr;87(4):1674-80. doi: 10.1210/jcem.87.4.8403. J Clin Endocrinol Metab. 2002. PMID: 11932300

8

Prenatal diagnosis of Cockayne syndrome type A based on the identification of two novel mutations in the ERCC8 gene.

Conte C, D'Apice MR, Botta A, Sangiuolo F, Novelli G. Conte C, et al. Genet Test Mol Biomarkers. 2009 Feb;13(1):127-31. doi: 10.1089/gtmb.2008.0092. Genet Test Mol Biomarkers. 2009. PMID: 19309286

9

Gene symbol: EDA. Disease: Ectodermal dysplasia.

Conte C. Conte C. Hum Genet. 2008 Jun;123(5):548. Hum Genet. 2008. PMID: 20960637 No abstract available.

10

Gene symbol: EDA. Disease: Ectodermal dysplasia.

Conte C. Conte C. Hum Genet. 2008 Jun;123(5):548. Hum Genet. 2008. PMID: 20960636 No abstract available.

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