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Mickael Guedj

Explore the profile of Mickael Guedj including associated specialties, affiliations and a list of published articles. Areas
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Articles 54
Citations 2378
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Recent Articles
21.
Attarian S, Vallat J, Magy L, Funalot B, Gonnaud P, Lacour A, et al.
Orphanet J Rare Dis . 2014 Dec; 9:199. PMID: 25519680
Background: Charcot-Marie-Tooth type 1A disease (CMT1A) is a rare orphan inherited neuropathy caused by an autosomal dominant duplication of a gene encoding for the structural myelin protein PMP22, which induces...
22.
Chumakov I, Milet A, Cholet N, Primas G, Boucard A, Pereira Y, et al.
Orphanet J Rare Dis . 2014 Dec; 9:201. PMID: 25491744
Charcot-Marie-Tooth disease type 1A (CMT1A) is the most common inherited sensory and motor peripheral neuropathy. It is caused by PMP22 overexpression which leads to defects of peripheral myelination, loss of...
23.
Ibarrola-Villava M, Kumar R, Nagore E, Benfodda M, Guedj M, Gazal S, et al.
Int J Cancer . 2014 Oct; 136(9):2109-19. PMID: 25303718
Multifactorial predisposition to melanoma includes genes involved in pigmentation, immunity and DNA repair. Nonetheless, missing heritability in melanoma is still important. We studied the role of 335 candidate SNPs in...
24.
Bonora E, Rizzato C, Diquigiovanni C, Oudot-Mellakh T, Campa D, Vargiolu M, et al.
Int J Cancer . 2013 Oct; 134(9):2098-107. PMID: 24127282
Thyroid cancer is the most common endocrine malignancy and nonmedullary thyroid carcinoma (NMTC) represents 90% of all cases. NMTC risk in first-degree relatives of affected cases is elevated fivefold to...
25.
Bonnet F, Guedj M, Jones N, Sfar S, Brouste V, Elarouci N, et al.
BMC Med Genomics . 2012 Nov; 5:54. PMID: 23186559
Background: Despite entering complete remission after primary treatment, a substantial proportion of patients with early stage breast cancer will develop metastases. Prediction of such an outcome remains challenging despite the...
26.
Bouaziz M, Paccard C, Guedj M, Ambroise C
PLoS One . 2012 Oct; 7(10):e45685. PMID: 23077494
Inferring the structure of populations has many applications for genetic research. In addition to providing information for evolutionary studies, it can be used to account for the bias induced by...
27.
Dillies M, Rau A, Aubert J, Hennequet-Antier C, Jeanmougin M, Servant N, et al.
Brief Bioinform . 2012 Sep; 14(6):671-83. PMID: 22988256
During the last 3 years, a number of approaches for the normalization of RNA sequencing data have emerged in the literature, differing both in the type of bias adjustment and...
28.
Koumakis E, Wipff J, Dieude P, Ruiz B, Bouaziz M, Revillod L, et al.
Ann Rheum Dis . 2012 Aug; 71(11):1900-3. PMID: 22896741
Introduction: Systemic sclerosis (SSc)-related pulmonary arterial hypertension (PAH) has emerged as a major mortality prognostic factor. Mutations of transforming growth factor beta (TGFβ) receptor genes strongly contribute to idiopathic and...
29.
Bouaziz M, Jeanmougin M, Guedj M
Methods Mol Biol . 2012 Jun; 888:213-33. PMID: 22665284
Recent advances in Molecular Biology and improvements in microarray and sequencing technologies have led biologists toward high-throughput genomic studies. These studies aim at finding associations between genetic markers and a...
30.
Ibarrola-Villava M, Hu H, Guedj M, Fernandez L, Descamps V, Basset-Seguin N, et al.
Eur J Cancer . 2012 Apr; 48(14):2183-91. PMID: 22464347
Background And Methods: Seven genetic biomarkers previously associated with melanoma were analysed in a meta-analysis conducted in three South European populations: five red hair colour (RHC) MC1R alleles, one SLC45A2...