| Consensus statement on the diagnosis and treatment of children with idiopathic short stature: a summary of the Growth Hormone Research Society, the Lawson Wilkins Pediatric … P Cohen, AD Rogol, CL Deal, P Saenger, EO Reiter, JL Ross, ... The Journal of Clinical Endocrinology & Metabolism 93 (11), 4210-4217, 2008 | 877* | 2008 |
| Child health, developmental plasticity, and epigenetic programming Z Hochberg, R Feil, M Constancia, M Fraga, C Junien, JC Carel, ... Endocrine reviews 32 (2), 159-224, 2011 | 795 | 2011 |
| Parental genomic imprinting of the human IGF2 gene N Giannoukakis, C Deal, J Paquette, CG Goodyer, C Polychronakos Nature genetics 4 (1), 98-101, 1993 | 523 | 1993 |
| Growth Hormone Research Society workshop summary: consensus guidelines for recombinant human growth hormone therapy in Prader-Willi syndrome CL Deal, M Tony, C Höybye, DB Allen, M Tauber, JS Christiansen, ... The Journal of Clinical Endocrinology & Metabolism 98 (6), E1072-E1087, 2013 | 339 | 2013 |
| GrowthHormone Research Society workshop summary: consensus guidelines for recombinant human growth hormone therapy in Prader-Willi syndrome. CL Deal, M Tony, C Höybye, DB Allen, M Tauber, JS Christiansen, ... J Clin Endocrinol Metab. 2013 Jun;98(6):E1072-87. doi: 10.1210/jc.2012-3888 …, 2013 | 339 | 2013 |
| Tracing the origins of “fetal origins” of adult diseases: programming by oxidative stress? ZC Luo, WD Fraser, P Julien, CL Deal, F Audibert, GN Smith, X Xiong, ... Medical hypotheses 66 (1), 38-44, 2006 | 315 | 2006 |
| A novel mechanism for isolated central hypothyroidism: inactivating mutations in the thyrotropin-releasing hormone receptor gene R Collu, JQ Tang, J Castagné, G Lagacé, N Masson, C Huot, C Deal, ... The Journal of Clinical Endocrinology & Metabolism 82 (5), 1561-1565, 1997 | 294 | 1997 |
| Functional polymorphism in the parental imprinting of the human IGF2R gene YQ Xu, CG Goodyer, C Deal, C Polychronakos Biochemical and biophysical research communications 197 (2), 747-754, 1993 | 269 | 1993 |
| Novel Promoter Polymorphism in Insulin-Like Growth Factor-Binding Protein-3: Correlation with Serum Levels and Interaction with Known Regulators1 C Deal, J Ma, F Wilkin, J Paquette, F Rozen, B Ge, T Hudson, M Stampfer, ... The Journal of Clinical Endocrinology & Metabolism 86 (3), 1274-1280, 2001 | 266 | 2001 |
| Outcome of severe congenital hypothyroidism: closing the developmental gap with early high dose levothyroxine treatment. JM Dubuis, J Glorieux, F Richer, CL Deal, JH Dussault, G Van Vliet The Journal of Clinical Endocrinology & Metabolism 81 (1), 222-227, 1996 | 254 | 1996 |
| Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International Perspective PF Collett-Solberg, G Ambler, PF Backeljauw, M Bidlingmaier, BMK Biller, ... Hormone Research in Paediatrics 92 (1), 1-14, 2019 | 252 | 2019 |
| GH safety workshop position paper: a critical appraisal of recombinant human GH therapy in children and adults DB Allen, P Backeljauw, M Bidlingmaier, BMK Biller, M Boguszewski, ... European Journal of Endocrinology 174 (2), P1-P9, 2016 | 233 | 2016 |
| Pituitary blastoma: a pathognomonic feature of germ-line DICER1 mutations L De Kock, N Sabbaghian, F Plourde, A Srivastava, E Weber, ... Acta neuropathologica 128, 111-122, 2014 | 230 | 2014 |
| Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency AM Pulichino, S Vallette-Kasic, C Couture, Y Gauthier, T Brue, M David, ... Genes & development 17 (6), 711-716, 2003 | 222 | 2003 |
| Genetic and nongenetic factors associated with variation of plasma levels of insulin-like growth factor-I and insulin-like growth factor-binding protein-3 in healthy … H Jernström, C Deal, F Wilkin, W Chu, Y Tao, N Majeed, T Hudson, ... Cancer Epidemiology Biomarkers & Prevention 10 (4), 377-384, 2001 | 220 | 2001 |
| Primary adrenal insufficiency in children: twenty years experience at the Sainte-Justine Hospital, Montreal R Perry, O Kecha, J Paquette, C Huot, G Van Vliet, C Deal The Journal of Clinical Endocrinology & Metabolism 90 (6), 3243-3250, 2005 | 211 | 2005 |
| Mutations in origin recognition complex gene ORC4 cause Meier-Gorlin syndrome DL Guernsey, M Matsuoka, H Jiang, S Evans, C Macgillivray, ... Nature genetics 43 (4), 360-364, 2011 | 183 | 2011 |
| Apparent congenital athyreosis contrasting with normal plasma thyroglobulin levels and associated with inactivating mutations in the thyrotropin receptor gene: are athyreosis … N Gagne, J Parma, C Deal, G Vassart, G Van Vliet The Journal of Clinical Endocrinology & Metabolism 83 (5), 1771-1775, 1998 | 180 | 1998 |
| Severe autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy in an adolescent girl with a novel AIRE mutation: response to immunosuppressive therapy L Ward, J Paquette, E Seidman, C Huot, F Alvarez, P Crock, E Delvin, ... The Journal of Clinical Endocrinology & Metabolism 84 (3), 844-852, 1999 | 174 | 1999 |
| The INS 5′ variable number of tandem repeats is associated with IGF2 expression in humans J Paquette, N Giannoukakis, C Polychronakos, P Vafiadis, C Deal Journal of Biological Chemistry 273 (23), 14158-14164, 1998 | 172 | 1998 |
Jean PaquetteMontreal Heart InstituteVerified email at inflammgen.org
