Guylène Bertrand

PTHR1 mutations associated with Ollier disease result in receptor loss of function

Alain Couvineau, Vinciane Wouters, Guylène Bertrand et al. · Human Molecular Genetics · 2008 · 122 citations · Full text

<i>PRKAR1A</i>and<i>PDE4D</i>Mutations Cause Acrodysostosis but Two Distinct Syndromes with or without GPCR-Signaling Hormone Resistance

Agnès Linglart, Helena Fryssira, Olaf Hiort et al. · The Journal of Clinical Endocrinology & Metabolism · 2012 · 108 citations · Full text

Dominant-Negative <i>GCMB</i> Mutations Cause an Autosomal Dominant Form of Hypoparathyroidism

Michael Mannstadt, Guylène Bertrand, Mihaela Mureşan et al. · The Journal of Clinical Endocrinology & Metabolism · 2008 · 99 citations · Full text

Allele variations in the OCA2 gene (pink-eyed-dilution locus) are associated with genetic susceptibility to melanoma

Anne‐Sophie Jannot, Roubila Meziani, Guylène Bertrand et al. · European Journal of Human Genetics · 2005 · 99 citations · Full text

Allelic Variant, Oca2 Gene, Somatic Variant +11

Absence of microsatellite instability in transitional cell carcinoma of the bladder

Christine Bonnal, V. Ravery, Mariane Toublanc et al. · Urology · 2000 · 61 citations

Urology, Transitional Cell Carcinoma, Tumor Heterogeneity +7