Consensus statement on management of intersex disorders PA Lee, CP Houk, SF Ahmed, IA Hughes, ... Pediatrics 118 (2), e488-e500, 2006 | 1442 | 2006 |
Clinical features and prognostic factors of listeriosis: the MONALISA national prospective cohort study C Charlier, É Perrodeau, A Leclercq, B Cazenave, B Pilmis, B Henry, ... The Lancet Infectious Diseases 17 (5), 510-519, 2017 | 515 | 2017 |
Evaluation of gonadal function in 107 intersex patients by means of serum antimullerian hormone measurement RA Rey, C Belville, C Nihoul-Fékété, L Michel-Calemard, MG Forest, ... The Journal of Clinical Endocrinology & Metabolism 84 (2), 627-631, 1999 | 316 | 1999 |
Congenital adrenal hyperplasia due to point mutations in the type II 3β–hydroxysteroid dehydrogenase gene E Rhéaume, J Simard, Y Morel, F Mebarki, M Zachmann, MG Forest, ... Nature genetics 1 (4), 239-245, 1992 | 278 | 1992 |
Clinical and molecular characterization of a cohort of 161 unrelated women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency and 330 family members M Bidet, C Bellanné-Chantelot, MB Galand-Portier, V Tardy, L Billaud, ... The Journal of Clinical Endocrinology & Metabolism 94 (5), 1570-1578, 2009 | 249 | 2009 |
Fertility in women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency M Bidet, C Bellanne-Chantelot, MB Galand-Portier, JL Golmard, V Tardy, ... The Journal of Clinical Endocrinology & Metabolism 95 (3), 1182-1190, 2010 | 248 | 2010 |
Clinical and molecular genetics of congenital adrenal hyperplasia due to 21-hydroxylase deficiency Y Morel, WL Miller Advances in human genetics, 1-68, 1991 | 239 | 1991 |
Aerosol administration of a recombinant adenovirus expressing CFTR to cystic fibrosis patients: a phase I clinical trial G Bellon, L Michel-Calemard, D Thouvenot, V Jagneaux, F Poitevin, ... Human gene therapy 8 (1), 15-25, 1997 | 218 | 1997 |
Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development S Benko, CT Gordon, D Mallet, R Sreenivasan, C Thauvin-Robinet, ... Journal of medical genetics 48 (12), 825-830, 2011 | 213 | 2011 |
Summary of consensus statement on intersex disorders and their management CP Houk, IA Hughes, SF Ahmed, PA Lee, ... Pediatrics 118 (2), 753-757, 2006 | 209 | 2006 |
Phenotype-genotype correlation in 56 women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency C Deneux, V Tardy, A Dib, E Mornet, L Billaud, D Charron, Y Morel, ... The Journal of Clinical Endocrinology & Metabolism 86 (1), 207-213, 2001 | 200 | 2001 |
Prenatal diagnosis and treatment of 21-hydroxylase deficiency MG Forest, M David, Y Morel The Journal of steroid biochemistry and molecular biology 45 (1-3), 75-82, 1993 | 192 | 1993 |
Transcript encoded on the opposite strand of the human steroid 21-hydroxylase/complement component C4 gene locus. Y Morel, J Bristow, SE Gitelman, WL Miller Proceedings of the National Academy of Sciences 86 (17), 6582-6586, 1989 | 192 | 1989 |
Postnatal changes of T, LH, and FSH in 46, XY infants with mutations in the AR gene C Bouvattier, JC Carel, C Lecointre, A David, C Sultan, AM Bertrand, ... The Journal of Clinical Endocrinology & Metabolism 87 (1), 29-32, 2002 | 187 | 2002 |
Influence of SHBG Gene Pentanucleotide TAAAA Repeat and D327N Polymorphism on Serum Sex Hormone-Binding Globulin Concentration in Hirsute Women P Cousin, L Calemard-Michel, H Lejeune, G Raverot, N Yessaad, ... The Journal of Clinical Endocrinology & Metabolism 89 (2), 917-924, 2004 | 171 | 2004 |
Molecular biology and genetics of the 3β-hydroxysteroid dehydrogenase/Δ5-Δ4 isomerase gene family. J Simard, F Durocher, F Mebarki, C Turgeon, R Sanchez, Y Labrie, ... | 164 | 1996 |
Aetiological diagnosis of male sex ambiguity: a collaborative study Y Morel, R Rey, C Teinturier, M Nicolino, L Michel-Calemard, ... European journal of pediatrics 161, 49-59, 2002 | 163 | 2002 |
Anti-müllerian hormone in children with androgen insensitivity R Rey, F Mebarki, MG Forest, I Mowszowicz, RL Cate, Y Morel, ... The Journal of Clinical Endocrinology & Metabolism 79 (4), 960-964, 1994 | 157 | 1994 |
The molecular genetics of 21-hydroxylase deficiency WL Miller, Y Morel Annual review of genetics 23 (1), 371-393, 1989 | 151 | 1989 |
Long Term Treatment of Male and Female Precocious Puberty by Periodic Administration of a Long-Acting Preparation of D-Trp6-Luteinizing Hormone-Releasing … M Roger, JL Chaussain, P Berlier, M Bost, P CANLORBE, M Colle, ... The Journal of Clinical Endocrinology & Metabolism 62 (4), 670-677, 1986 | 151 | 1986 |