| Sexual precocity after immigration from developing countries to Belgium: evidence of previous exposure to organochlorine pesticides M Krstevska‐Konstantinova, C Charlier, M Craen, M Du Caju, C Heinrichs, ... Apmis 109 (S103), S135-S143, 2001 | 368 | 2001 |
| 11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic … I Netchine, S Rossignol, MN Dufourg, S Azzi, A Rousseau, L Perin, ... The Journal of Clinical Endocrinology & Metabolism 92 (8), 3148-3154, 2007 | 317 | 2007 |
| Congenital hypothyroidism: A 2020–2021 consensus guidelines update—an ENDO-European reference network initiative endorsed by the European society for pediatric endocrinology … P Van Trotsenburg, A Stoupa, J Léger, T Rohrer, C Peters, L Fugazzola, ... Thyroid 31 (3), 387-419, 2021 | 316 | 2021 |
| Familial congenital hypothyroidism due to inactivating mutation of the thyrotropin receptor causing profound hypoplasia of the thyroid gland. MJ Abramowicz, L Duprez, J Parma, G Vassart, C Heinrichs The Journal of clinical investigation 99 (12), 3018-3024, 1997 | 307 | 1997 |
| Multilocus methylation analysis in a large cohort of 11p15-related foetal growth disorders (Russell Silver and Beckwith Wiedemann syndromes) reveals simultaneous loss of … S Azzi, S Rossignol, V Steunou, T Sas, N Thibaud, F Danton, M Le Jule, ... Human molecular genetics 18 (24), 4724-4733, 2009 | 256 | 2009 |
| Phenotypical, biological, and molecular heterogeneity of 5α-reductase deficiency: an extensive international experience of 55 patients L Maimoun, P Philibert, B Cammas, F Audran, P Bouchard, P Fenichel, ... The Journal of Clinical Endocrinology & Metabolism 96 (2), 296-307, 2011 | 234 | 2011 |
| Autosomal dominant transmission of congenital thyroid hypoplasia due to loss-of-function mutation of PAX8 C Vilain, C Rydlewski, L Duprez, C Heinrichs, M Abramowicz, P Malvaux, ... The Journal of Clinical Endocrinology & Metabolism 86 (1), 234-238, 2001 | 211 | 2001 |
| Discordance of monozygotic twins for thyroid dysgenesis: implications for screening and for molecular pathophysiology R Perry, C Heinrichs, P Bourdoux, K Khoury, F Szöts, JH Dussault, ... The Journal of Clinical Endocrinology & Metabolism 87 (9), 4072-4077, 2002 | 185 | 2002 |
| Linkage of the gene for the triple A syndrome to chromosome 12q13 near the type II keratin gene cluster A Weber, TF Wienker, M Jung, D Easton, HJ Dean, C Heinrichs, A Reis, ... Human molecular genetics 5 (12), 2061-2066, 1996 | 183 | 1996 |
| Trends in age at diagnosis of Turner syndrome G Massa, F Verlinde, J De Schepper, M Thomas, JP Bourguignon, ... Archives of disease in childhood 90 (3), 267-268, 2005 | 159 | 2005 |
| Neurological aspects of hyperinsulinism–hyperammonaemia syndrome N Bahi‐Buisson, E Roze, C Dionisi, F Escande, V Valayannopoulos, ... Developmental medicine & child neurology 50 (12), 945-949, 2008 | 138 | 2008 |
| Longitudinal study of behavioral and affective patterns in girls with central precocious puberty during long‐acting triptorelin therapy D Xhrouet‐Heinrichs, K Lagrou, C Heinrichs, M Craen, L Dooms, ... Acta Paediatrica 86 (8), 808-815, 1997 | 124 | 1997 |
| High-dose growth hormone treatment of short children born small for gestational age F De Zegher, M Maes, SE Gargosky, C Heinrichs, MV Du Caju, G Thiry, ... The Journal of Clinical Endocrinology & Metabolism 81 (5), 1887-1892, 1996 | 120 | 1996 |
| Prevalence and demographic features of childhood growth hormone deficiency in Belgium during the period 1986-2001 M Thomas, G Massa, M Craen, F de Zegher, JP Bourguignon, C Heinrichs, ... European journal of endocrinology 151 (1), 67-72, 2004 | 112 | 2004 |
| Effects of human growth hormone therapy on melanocytic naevi JP Bourguignon, C Ernould, JE Arrese, C Franchimont, GE Piérard, ... The Lancet 341 (8859), 1505-1506, 1993 | 111 | 1993 |
| PRKAR1A and PDE4D Mutations Cause Acrodysostosis but Two Distinct Syndromes with or without GPCR-Signaling Hormone Resistance A Linglart, H Fryssira, O Hiort, PM Holterhus, G Perez de Nanclares, ... The Journal of Clinical Endocrinology & Metabolism 97 (12), E2328-E2338, 2012 | 108 | 2012 |
| FGFR1 mutations cause Hartsfield syndrome, the unique association of holoprosencephaly and ectrodactyly N Simonis, I Migeotte, N Lambert, C Perazzolo, DC de Silva, B Dimitrov, ... Journal of medical genetics 50 (9), 585-592, 2013 | 96 | 2013 |
| Dexamethasone increases growth hormone receptor messenger ribonucleic acid levels in liver and growth plate C Heinrichs, JA Yanovski, AH Roth, YM Yu, HM Domene, K Yano, ... Endocrinology 135 (3), 1113-1118, 1994 | 94 | 1994 |
| Growth-promoting effect of growth hormone and low dose ethinyl estradiol in girls with Turner's syndrome M Vanderschueren-Lodeweyckx, G Massa, M Maes, M CRAEN, ... The Journal of Clinical Endocrinology & Metabolism 70 (1), 122-126, 1990 | 93 | 1990 |
| Early, discontinuous, high dose growth hormone treatment to normalize height and weight of short children born small for gestational age: results over 6 years F De Zegher, MVL Du Caju, C Heinrichs, M Maes, J De Schepper, ... The Journal of Clinical Endocrinology & Metabolism 84 (5), 1558-1561, 1999 | 87 | 1999 |
