MadeleineHarbisonMD

PubMed

• 2 citations
  Silver Russell syndrome in a preterm girl with 8q12.1 deletion encompassing PLAG1.
  Jose Ramón Fernández-Fructuoso, Cristina De la Torre-Sandoval, Madeleine D. Harbison, Sandra Chantot-Bastaraud, Karen Temple, Jose María Lloreda-García, Maria Olmo-San...> ;Clinical Dysmorphology. 2021 Oct 1
• 4 citations
  Silver-Russell Syndrome
  Howard M. Saal, Madeleine D. Harbison, Irène Netchine> ;Headache: The Journal of Head and Face Pain. 2019 Oct 21
• 24 citations
  Transcriptional Profiling at the DLK1/MEG3 Domain Explains Clinical Overlap Between Imprinting Disorders
  Walid Abi Habib, Frédéric Brioude, Salah Azzi, Sylvie Rossignol, Agnès Linglart, Marie-Laure Sobrier, Eloise Giabicani, Virginie Steunou, Madeleine D. Harbison, Yves L...> ;Science Advances. 2019 Feb 1
• 37 citations
  Chromosome 14q32.2 Imprinted Region Disruption as an Alternative Molecular Diagnosis of Silver-Russell Syndrome.
  Sophie Geoffron, Walid Abi Habib, Sandra Chantot-Bastaraud, Béatrice Dubern, Virginie Steunou, Salah Azzi, Alexandra Afenjar, Tiffanny Busa, Ana Pinheiro Machado Canto...> ;The Journal of Clinical Endocrinology and Metabolism. 2018 Jul 1
• 35 citations
  Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p15.5 duplications with associated phenotypes and putative functional consequences.
  Solveig Heide, Sandra Chantot-Bastaraud, Boris Keren, Madeleine D. Harbison, Salah Azzi, Sylvie Rossignol, Caroline Michot, Marilyn Lackmy-Port Lys, Bénédicte Demeer, ...> ;Journal of Medical Genetics. 2018 Jan 5
• 1 citations
  The Importance of Collaboration in Advancing Understanding of Rare Disorders: US/EU Joint Initiative on Silver-Russell Syndrome.
  Jennifer Salem, Irène Netchine, Madeleine D. Harbison> ;Pediatric Endocrinology Reviews. 2017 Nov 1
• 89 citations
  Genetic disruption of the oncogenic HMGA2 – PLAG1 – IGF2 pathway causes fetal growth restriction
  Walid Abi Habib, Frédéric Brioude, Thomas Edouard, James T. Bennett, Anne Lienhardt-Roussie, Frédérique Tixier, Jennifer Salem, Tony Yuen, Salah Azzi, Yves Le Bouc, Ma...> ;Genetics in Medicine. 2018 Feb 1
• 9 citations
  Effect of Cyproheptadine on Weight and Growth Velocity in Children With Silver-Russell Syndrome.
  A. Lemoine, Madeleine D. Harbison, Jennifer Salem, Patrick Tounian, Irene Netchine, Béatrice Dubern> ;Journal of Pediatric Gastroenterology and Nutrition. 2017 Aug 1
• 8 citations
  Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction
  Sandra Chantot-Bastaraud, Svea Stratmann, Frédéric Brioude, Matthias Begemann, Miriam Elbracht, Luitgard Graul-Neumann, Madeleine D. Harbison, Irène Netchine, Thomas E...> ;Molecular Cytogenetics. 2017 Jul 25
• 24 citations
  11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver-Russell Syndrome.
  Walid Abi Habib, Frédéric Brioude, Salah Azzi, Jennifer Salem, Cristina Das Neves, Claire Personnier, Sandra Chantot-Bastaraud, Boris Keren, Yves Le Bouc, Madeleine D....> ;Human Mutation. 2017 Jan 1
• 277 citations
  Diagnosis and management of Silver–Russell syndrome: first international consensus statement
  Emma Wakeling, Frédéric Brioude, Oluwakemi Lokulo-Sodipe, Susan M. O’Connell, Jennifer Salem, Jet Bliek, Ana Pinheiro Machado Canton, Krystyna H. Chrzanowska, Justin H...> ;Nature Reviews. Endocrinology. 2017 Feb 1
• 10 citations
  A rare CYP21A2 mutation in a congenital adrenal hyperplasia kindred displaying genotype-phenotype nonconcordance.
  Ahmed Khattab, Tony Yuen, Sultan Al-Malki, Mabel Yau, Diya Kazmi, Li Sun, Madeleine D. Harbison, Shozeb Haider, Mone Zaidi, Maria I. New> ;Annals of the New York Academy of Sciences. 2016 Jan 1
• 144 citations
  A prospective study validating a clinical scoring system and demonstrating phenotypical-genotypical correlations in Silver-Russell syndrome
  Salah Azzi, Jennifer Salem, Nathalie Thibaud, Sandra Chantot-Bastaraud, Eli Lieber, Irène Netchine, Madeleine D. Harbison> ;Journal of Medical Genetics. 2015 May 7
• 32 citations
  Complex Tissue‐Specific Epigenotypes in Russell–Silver Syndrome Associated with 11p15 ICR1 Hypomethylation
  Salah Azzi, Annick Blaise, Virginie Steunou, Madeleine D. Harbison, Jennifer Salem, Frédéric Brioude, Sylvie Rossignol, Walid Abi Habib, Nathalie Thibaud, Cristina Das...> ;Human Mutation. 2014 Oct 1
• Limb lengthening in children with Russell-Silver syndrome: a comparison to other etiologies.
  Goldman, V.,McCoy, T. H.,Harbison, M. D.,Fragomen, A. T.,Rozbruch, S. R.> ;J Child Orthop. 2014 Jan 17
• 37 citations
  Final Adult Height in Children with Congenital Adrenal Hyperplasia Treated with Growth Hormone
  Karen Lin-Su, Madeleine D. Harbison, Oksana Lekarev, Maria G. Vogiatzi, Maria I. New> ;The Journal of Clinical Endocrinology and Metabolism. 2011 Mar 30
• 3 citations
  Growth hormone treatment in children with congenital adrenal hyperplasia.
  Madeleine D. Harbison, Karen Lin-Su, Maria I. New> ;Advances in Experimental Medicine and Biology. 2011 Jan 1
• 23 citations
  Aortic distensibility and dilation in Turner's syndrome.
  Jayendra Sharma, Deborah M. Friedman, Swati Dave-Sharma, Madeleine D. Harbison> ;Cardiology in the Young. 2009 Dec 1
• 9 citations
  Predictors of first-year growth response to a fixed-dose growth hormone treatment in children born small for gestational age: results of an open-label, multicenter tri...
  Robert Rapaport, Paul Saenger, Michael Wajnrajch, Bruce A. Boston, Mauri Carakushansky, Steven D. Chernausek, Pamela A. Clark, Jay Cohen, Deborah Counts, Patricia A. D...> ;Journal of Pediatric Endocrinology & Metabolism. 2008 Jan 1
• 59 citations
  Treatment with Growth Hormone and Luteinizing Hormone Releasing Hormone Analog Improves Final Adult Height in Children with Congenital Adrenal Hyperplasia
  Karen Lin-Su, Maria G. Vogiatzi, Ian Marshall, Madeleine D. Harbison, Maria C. Macapagal, Brian P. Betensky, Susan Tansil, Maria I. New> ;The Journal of Clinical Endocrinology and Metabolism. 2005 Jun 1
• 18 citations
  Haplotype analysis of the growth hormone releasing hormone receptor locus in three apparently unrelated kindreds from the indian subcontinent with the identical mutati...
  Michael P. Wajnrajch, Joseph M. Gertner, Alisa S. Sokoloff, Irina Ten, Madeleine D. Harbison, Irene Netchine, Hiralal G. Maheshwari, David Goldstein, Serge Amselem, Ge...> ;American Journal of Medical Genetics. Part A. 2003 Jul 1
• 70 citations
  Growth hormone therapy alone or in combination with gonadotropin-releasing hormone analog therapy to improve the height deficit in children with congenital adrenal hyp...
  Jose Bernardo Quintos, Maria G. Vogiatzi, Madeleine D. Harbison, Maria I. New> ;The Journal of Clinical Endocrinology and Metabolism. 2001 Apr 1
• 55 citations
  Osteoporosis: an unusual presentation of childhood Crohn's disease.
  Marie S. Thearle, Mary Horlick, J. P. Bilezikian, J. Levy, Joseph M. Gertner, Lenore S. Levine, Madeleine D. Harbison, Walter E. Berdon, S E Oberfield> ;The Journal of Clinical Endocrinology and Metabolism. 2000 Jun 1
• 3 citations
  Profile of the pediatric endocrine clinic at New York-Presbyterian Hospital, New York Weill Cornell Center.
  Maria I. New, Jihad S. Obeid, Robert C. Wilson, Monina S. Cabrera, Amanda Goseco, Maria C. Macapagal, Ian Marshall, Saroj Nimkarn, Jose Bernardo Quintos, Svetlana Ten,...> ;The Journal of Clinical Endocrinology and Metabolism. 1999 Dec 1
• 140 citations
  Examination of genotype and phenotype relationships in 14 patients with apparent mineralocorticoid excess.
  Swati Dave-Sharma, Robert C. Wilson, Madeleine D. Harbison, Ron S. Newfield, Maryam Razzaghy Azar, Zygmunt S. Krozowski, John W. Funder, Cedric H. L. Shackleton, H. Le...> ;The Journal of Clinical Endocrinology and Metabolism. 1998 Jul 1
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Journal Articles

• Chromosome 14q322 imprinted region disruption as an alternative molecular diagnosis of Silver-Russell Syndrome  
  Geoffron S, Abi Habib W, Chantot-Bastaraud S, Dubern B, Steunou V, Azzi S, Afenjar A, Busa T, Canton AP, Chalouhi C, Dufourg MN, Esteva B, Fradin M, Genevi�ve D, Heide..., J Clin Endocrinol Metab, 1/1/2018
• Chromosomal rearrangements in the 11p15 imprinted region: 17 new 11p155 duplications with associated phenotypes and putative functional consequences  
  Heide S, Chantot-Bastaraud S, Keren B, Harbison MD, Azzi S, Rossignol S, Michot C, Lackmy-Port Lys M, Demeer B, Heinrichs C, Newfield RS, Sarda P, Van Maldergem L, Tri..., J Med Genet, 1/1/2018
• Effect of Cyproheptadine on Weight and Growth Velocity in Children With Silver-Russell Syndrome  
  Lemoine A, Harbison MD, Salem J, Tounian P, Netchine I, Dubern B, J Pediatr Gastroenterol Nutr, 1/1/2018
• Genetic disruption of the oncogenic HMGA2-PLAG1-IGF2 pathway causes fetal growth restriction  
  Abi Habib W, Brioude F, Edouard T, Bennett JT, Lienhardt-Roussie A, Tixier F, Salem J, Yuen T, Azzi S, Le Bouc Y, Harbison MD, Netchine I, Genet Med, 1/1/2018
• Formation of upd(7)mat by trisomic rescue: SNP array typing provides new insights in chromosomal nondisjunction  
  Chantot-Bastaraud Sandra, Stratmann Svea, Brioude Frederic, Begernann Matthias, Elbracht, Miriam, Graul-Meumann Luitguard, Harbison, Madeleine, Netchine Irene, Eggerma..., Molecular Cytogenetics, 1/25/2017
• 11p15 ICR1 Partial Deletions Associated with IGF2/H19 DMR Hypomethylation and Silver-Russell Syndrome  
  Abi Habib W, Brioude F, Azzi S, Salem J, Das Neves C, Personnier C, Chantot-Bastaraud S, Keren B, Le Bouc Y, Harbison MD, Netchine I, Hum Mutat, 1/1/2017
• A rare CYP21A2 mutation in a congenital adrenal hyperplasia kindred displaying genotype-phenotype nonconcordance  
  Khattab A, Yuen T, Al-Malki S, Yau M, Kazmi D, Sun L, Harbison M, Haider S, Zaidi M, New MI, Ann N Y Acad Sci, 1/20/2015
• A prospective study validating a clinical scoring system and demonstrating phenotypical-genotypical correlations in Silver-Russell syndrome  
  Azzi S, Salem J, Thibaud N, Chantot-Bastaraud S, Lieber E, Netchine I, Harbison MD, J Med Genet, 1/1/2015
• Complex tissue-specific epigenotypes in Russell-Silver Syndrome associated with 11p15 ICR1 hypomethylation  
  Azzi S, Blaise A, Steunou V, Harbison MD, Salem J, Brioude F, Rossignol S, Habib WA, Thibaud N, Neves CD, Jule ML, Brachet C, Heinrichs C, Bouc YL, Netchine I, Hum Mutat, 1/1/2014
• Prospective safety surveillance of GH-deficient adults: comparison of GH-treated vs untreated patients  
  Hartman ML, Xu R, Crowe BJ, Robison LL, Erfurth EM, Kleinberg DL, Zimmermann AG, Woodmansee WW, Cutler GB Jr, Chipman JJ, Melmed S; International HypoCCS Advisory Board, J Clin Endocrinol Metab, 1/1/2013
• Iatrogenic Creutzfeldt-Jakob disease from commercial cadaveric human growth hormone  
  Appleby BS, Lu M, Bizzi A, Phillips MD, Berri SM, Harbison MD, Schonberger LB, Emerg Infect Dis, 1/1/2013
• Growth hormone treatment in children with congenital adrenal hyperplasia  
  Harbison MD, Lin-Su K, New MI, Adv Exp Med Biol, 1/1/2011
• Occurrence of impaired fasting glucose in GH-deficient adults receiving GH replacement compared with untreated subjects  
  Woodmansee WW, Hartman ML, Lamberts SW, Zagar AJ, Clemmons DR; International HypoCCS Advisory Board, Clin Endocrinol (Oxf), 1/1/2010
• Aortic distensibility and dilation in Turner's syndrome  
  Sharma J, Friedman D, Dave-Sharma S, Harbison M, Cardiol Young, 1/27/2009
• Predictors of first-year growth response to a fixed-dose growth hormone treatment in children born small for gestational age: results of an open-label, multicenter tri...  
  Rapaport R, Saenger P, Wajnrajch MP; Pfizer SGA Collaborative Study Group, J Pediatr Endocrinol Metab, 1/1/2008
• Meier-Gorlin syndrome: report of eight additional cases and review  
  Bongers EM, Opitz JM, Fryer A, Sarda P, Hennekam RC, Hall BD, Superneau DW, Harbison M, Poss A, van Bokhoven H, Hamel BC, Knoers NV, Am J Med Genet, 1/1/2001
• Thoracolumbar accessory penis: etiology, diagnosis, and management  
  Ostad M, Mininberg DT, Harbison M, Magid MS, Urology, 1/1/1999
• Complete testicular feminization caused by an amino-terminal truncation of the androgen receptor with downstream initiation  
  Zoppi S, Wilson CM, Harbison MD, Griffin JE, Wilson JD, McPhaul MJ, Marcelli M, J Clin Invest, 1/1/1993
• Multiple serum protein abnormalities in carbohydrate-deficient glycoprotein syndrome: pathognomonic finding of two-dimensional electrophoresis?  
  Harrison HH, Miller KL, Harbison MD, Slonim AE, Clin Chem, 1/1/1992
• Ileal adenomas after colectomy in nine patients with adenomatous polyposis coli/Gardner's syndrome  
  Hamilton SR, Bussey HJ, Mendelsohn G, Diamond MP, Pavlides G, Hutcheon D, Harbison M, Shermeta D, Morson BC, Yardley JH, Gastroenterology, 1/1/1979
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