Keywords
Last Name
Institution

Bruce D. Gelb

TitleDIRECTOR Child Health and Development Institute
InstitutionMount Sinai
Address5th Avenue
New York NY 12323
    Other Positions
    TitlePROFESSOR
    InstitutionMount Sinai
    DepartmentCardiology

    TitlePROFESSOR
    InstitutionMount Sinai
    DepartmentGenetics and Genomic Sciences


     Bibliographic 
     selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
    List All   |   Timeline
    1. Cornwall JW, Green RS, Nielsen JC, Gelb BD. Frequency of aortic dilation in noonan syndrome. Am J Cardiol. 2014 Jan 15; 113(2):368-71.
      View in: PubMed
    2. Carey AS, Liang L, Edwards J, Brandt T, Mei H, Sharp AJ, Hsu DT, Newburger JW, Ohye RG, Chung WK, Russell MW, Rosenfeld JA, Shaffer LG, Parides MK, Edelmann L, Gelb BD. Effect of copy number variants on outcomes for infants with single ventricle heart defects. Circ Cardiovasc Genet. 2013 Oct; 6(5):444-51.
      View in: PubMed
    3. Subramanian S, Di Pierro V, Shah H, Jayaprakash AD, Weisberger I, Shim J, George A, Gelb BD, Sachidanandam R. MiST: a new approach to variant detection in deep sequencing datasets. Nucleic Acids Res. 2013 Sep; 41(16):e154.
      View in: PubMed
    4. Yoon SR, Choi SK, Eboreime J, Gelb BD, Calabrese P, Arnheim N. Age-dependent germline mosaicism of the most common noonan syndrome mutation shows the signature of germline selection. Am J Hum Genet. 2013 Jun 6; 92(6):917-26.
      View in: PubMed
    5. Zaidi S, Choi M, Wakimoto H, Ma L, Jiang J, Overton JD, Romano-Adesman A, Bjornson RD, Breitbart RE, Brown KK, Carriero NJ, Cheung YH, Deanfield J, DePalma S, Fakhro KA, Glessner J, Hakonarson H, Italia MJ, Kaltman JR, Kaski J, Kim R, Kline JK, Lee T, Leipzig J, Lopez A, Mane SM, Mitchell LE, Newburger JW, Parfenov M, Pe'er I, Porter G, Roberts AE, Sachidanandam R, Sanders SJ, Seiden HS, State MW, Subramanian S, Tikhonova IR, Wang W, Warburton D, White PS, Williams IA, Zhao H, Seidman JG, Brueckner M, Chung WK, Gelb BD, Goldmuntz E, Seidman CE, Lifton RP. De novo mutations in histone-modifying genes in congenital heart disease. Nature. 2013 Jun 13; 498(7453):220-3.
      View in: PubMed
    6. Lacro RV, Guey LT, Dietz HC, Pearson GD, Yetman AT, Gelb BD, Loeys BL, Benson DW, Bradley TJ, De Backer J, Forbus GA, Klein GL, Lai WW, Levine JC, Lewin MB, Markham LW, Paridon SM, Pierpont ME, Radojewski E, Selamet Tierney ES, Sharkey AM, Wechsler SB, Mahony L. Characteristics of children and young adults with Marfan syndrome and aortic root dilation in a randomized trial comparing atenolol and losartan therapy. Am Heart J. 2013 May; 165(5):828-835.e3.
      View in: PubMed
    7. Lawrence EJ, Nguyen K, Morris SA, Hollinger I, Graham DA, Jenkins KJ, Bodian C, Lin HM, Gelb BD, Mittnacht AJ. Economic and safety implications of introducing fast tracking in congenital heart surgery. Circ Cardiovasc Qual Outcomes. 2013 Mar 1; 6(2):201-7.
      View in: PubMed
    8. Fahed AC, Gelb BD, Seidman JG, Seidman CE. Genetics of congenital heart disease: the glass half empty. Circ Res. 2013 Feb 15; 112(4):707-20.
      View in: PubMed
    9. The Congenital Heart Disease Genetic Network Study: rationale, design, and early results. Circ Res. 2013 Feb 15; 112(4):698-706.
      View in: PubMed
    10. Roberts AE, Allanson JE, Tartaglia M, Gelb BD. Noonan syndrome. Lancet. 2013 Jan 26; 381(9863):333-42.
      View in: PubMed
    11. Sala V, Gallo S, Leo C, Gatti S, Gelb BD, Crepaldi T. Signaling to cardiac hypertrophy: insights from human and mouse RASopathies. Mol Med. 2012; 18:938-47.
      View in: PubMed
    12. Lee DF, Su J, Ang YS, Carvajal-Vergara X, Mulero-Navarro S, Pereira CF, Gingold J, Wang HL, Zhao R, Sevilla A, Darr H, Williamson AJ, Chang B, Niu X, Aguilo F, Flores ER, Sher YP, Hung MC, Whetton AD, Gelb BD, Moore KA, Snoeck HW, Ma'ayan A, Schaniel C, Lemischka IR. Regulation of embryonic and induced pluripotency by aurora kinase-p53 signaling. Cell Stem Cell. 2012 Aug 3; 11(2):179-94.
      View in: PubMed
    13. Babaoglu K, Oruç M, Günlemez A, Gelb BD. Char syndrome, a familial form of patent ductus arteriosus, with a new finding: hypoplasia [corrected] of the 3rd finger. Anadolu Kardiyol Derg. 2012 Sep; 12(6):523-4.
      View in: PubMed
    14. Martinelli S, Nardozza AP, Delle Vigne S, Sabetta G, Torreri P, Bocchinfuso G, Flex E, Venanzi S, Palleschi A, Gelb BD, Cesareni G, Stella L, Castagnoli L, Tartaglia M. Counteracting effects operating on Src homology 2 domain-containing protein-tyrosine phosphatase 2 (SHP2) function drive selection of the recurrent Y62D and Y63C substitutions in Noonan syndrome. J Biol Chem. 2012 Aug 3; 287(32):27066-77.
      View in: PubMed
    15. Gelb BD, Seidman CE. The Good SHP2 Association: a porthole into the genetics of congenital heart disease. Circ Cardiovasc Genet. 2012 Jun; 5(3):271-3.
      View in: PubMed
    16. Southard AE, Edelmann LJ, Gelb BD. Role of copy number variants in structural birth defects. Pediatrics. 2012 Apr; 129(4):755-63.
      View in: PubMed
    17. Downing J, Birtar D, Chambers L, Gelb B, Drake R, Kiman R. Children's palliative care: a global concern. Int J Palliat Nurs. 2012 Mar; 18(3):109-14.
      View in: PubMed
    18. Caputo V, Cianetti L, Niceta M, Carta C, Ciolfi A, Bocchinfuso G, Carrani E, Dentici ML, Biamino E, Belligni E, Garavelli L, Boccone L, Melis D, Andria G, Gelb BD, Stella L, Silengo M, Dallapiccola B, Tartaglia M. A restricted spectrum of mutations in the SMAD4 tumor-suppressor gene underlies Myhre syndrome. Am J Hum Genet. 2012 Jan 13; 90(1):161-9.
      View in: PubMed
    19. Sun J, Sukhova GK, Zhang J, Chen H, Sjöberg S, Libby P, Xia M, Xiong N, Gelb BD, Shi GP. Cathepsin K deficiency reduces elastase perfusion-induced abdominal aortic aneurysms in mice. Arterioscler Thromb Vasc Biol. 2012 Jan; 32(1):15-23.
      View in: PubMed
    20. Josowitz R, Carvajal-Vergara X, Lemischka IR, Gelb BD. Induced pluripotent stem cell-derived cardiomyocytes as models for genetic cardiovascular disorders. Curr Opin Cardiol. 2011 May; 26(3):223-9.
      View in: PubMed
    21. Lepri F, De Luca A, Stella L, Rossi C, Baldassarre G, Pantaleoni F, Cordeddu V, Williams BJ, Dentici ML, Caputo V, Venanzi S, Bonaguro M, Kavamura I, Faienza MF, Pilotta A, Stanzial F, Faravelli F, Gabrielli O, Marino B, Neri G, Silengo MC, Ferrero GB, Torrrente I, Selicorni A, Mazzanti L, Digilio MC, Zampino G, Dallapiccola B, Gelb BD, Tartaglia M. SOS1 mutations in Noonan syndrome: molecular spectrum, structural insights on pathogenic effects, and genotype-phenotype correlations. Hum Mutat. 2011 Jul; 32(7):760-72.
      View in: PubMed
    22. Dhandapany PS, Fabris F, Tonk R, Illaste A, Karakikes I, Sorourian M, Sheng J, Hajjar RJ, Tartaglia M, Sobie EA, Lebeche D, Gelb BD. Cyclosporine attenuates cardiomyocyte hypertrophy induced by RAF1 mutants in Noonan and LEOPARD syndromes. J Mol Cell Cardiol. 2011 Jul; 51(1):4-15.
      View in: PubMed
    23. Gelb BD, Tartaglia M. RAS signaling pathway mutations and hypertrophic cardiomyopathy: getting into and out of the thick of it. J Clin Invest. 2011 Mar; 121(3):844-7.
      View in: PubMed
    24. Tartaglia M, Gelb BD, Zenker M. Noonan syndrome and clinically related disorders. Best Pract Res Clin Endocrinol Metab. 2011 Feb; 25(1):161-79.
      View in: PubMed
    25. Tartaglia M, Gelb BD. Disorders of dysregulated signal traffic through the RAS-MAPK pathway: phenotypic spectrum and molecular mechanisms. Ann N Y Acad Sci. 2010 Dec; 1214:99-121.
      View in: PubMed
    26. Romano AA, Allanson JE, Dahlgren J, Gelb BD, Hall B, Pierpont ME, Roberts AE, Robinson W, Takemoto CM, Noonan JA. Noonan syndrome: clinical features, diagnosis, and management guidelines. Pediatrics. 2010 Oct; 126(4):746-59.
      View in: PubMed
    27. Au AC, Hernandez PA, Lieber E, Nadroo AM, Shen YM, Kelley KA, Gelb BD, Diaz GA. Protein tyrosine phosphatase PTPN14 is a regulator of lymphatic function and choanal development in humans. Am J Hum Genet. 2010 Sep 10; 87(3):436-44.
      View in: PubMed
    28. Martinelli S, De Luca A, Stellacci E, Rossi C, Checquolo S, Lepri F, Caputo V, Silvano M, Buscherini F, Consoli F, Ferrara G, Digilio MC, Cavaliere ML, van Hagen JM, Zampino G, van der Burgt I, Ferrero GB, Mazzanti L, Screpanti I, Yntema HG, Nillesen WM, Savarirayan R, Zenker M, Dallapiccola B, Gelb BD, Tartaglia M. Heterozygous germline mutations in the CBL tumor-suppressor gene cause a Noonan syndrome-like phenotype. Am J Hum Genet. 2010 Aug 13; 87(2):250-7.
      View in: PubMed
    29. Vagefi PA, Klein I, Gelb B, Hameed B, Moff SL, Simko JP, Fix OK, Eilers H, Feiner JR, Ascher NL, Freise CE, Bass NM. Emergent orthotopic liver transplantation for hemorrhage from a giant cavernous hepatic hemangioma: case report and review. J Gastrointest Surg. 2011 Jan; 15(1):209-14.
      View in: PubMed
    30. Carvajal-Vergara X, Sevilla A, D'Souza SL, Ang YS, Schaniel C, Lee DF, Yang L, Kaplan AD, Adler ED, Rozov R, Ge Y, Cohen N, Edelmann LJ, Chang B, Waghray A, Su J, Pardo S, Lichtenbelt KD, Tartaglia M, Gelb BD, Lemischka IR. Patient-specific induced pluripotent stem-cell-derived models of LEOPARD syndrome. Nature. 2010 Jun 10; 465(7299):808-12.
      View in: PubMed
    31. Bauer RC, Laney AO, Smith R, Gerfen J, Morrissette JJ, Woyciechowski S, Garbarini J, Loomes KM, Krantz ID, Urban Z, Gelb BD, Goldmuntz E, Spinner NB. Jagged1 (JAG1) mutations in patients with tetralogy of Fallot or pulmonic stenosis. Hum Mutat. 2010 May; 31(5):594-601.
      View in: PubMed
    32. Stoller JZ, Huang L, Tan CC, Huang F, Zhou DD, Yang J, Gelb BD, Epstein JA. Ash2l interacts with Tbx1 and is required during early embryogenesis. Exp Biol Med (Maywood). 2010 May; 235(5):569-76.
      View in: PubMed
    33. Tartaglia M, Zampino G, Gelb BD. Noonan syndrome: clinical aspects and molecular pathogenesis. Mol Syndromol. 2010 Feb; 1(1):2-26.
      View in: PubMed
    34. Rauen KA, Schoyer L, McCormick F, Lin AE, Allanson JE, Stevenson DA, Gripp KW, Neri G, Carey JC, Legius E, Tartaglia M, Schubbert S, Roberts AE, Gelb BD, Shannon K, Gutmann DH, McMahon M, Guerra C, Fagin JA, Yu B, Aoki Y, Neel BG, Balmain A, Drake RR, Nolan GP, Zenker M, Bollag G, Sebolt-Leopold J, Gibbs JB, Silva AJ, Patton EE, Viskochil DH, Kieran MW, Korf BR, Hagerman RJ, Packer RJ, Melese T. Proceedings from the 2009 genetic syndromes of the Ras/MAPK pathway: From bedside to bench and back. Am J Med Genet A. 2010 Jan; 152A(1):4-24.
      View in: PubMed
    35. Tan CC, Walsh MJ, Gelb BD. Fgfr3 is a transcriptional target of Ap2delta and Ash2l-containing histone methyltransferase complexes. PLoS One. 2009; 4(12):e8535.
      View in: PubMed
    36. Cirstea IC, Kutsche K, Dvorsky R, Gremer L, Carta C, Horn D, Roberts AE, Lepri F, Merbitz-Zahradnik T, König R, Kratz CP, Pantaleoni F, Dentici ML, Joshi VA, Kucherlapati RS, Mazzanti L, Mundlos S, Patton MA, Silengo MC, Rossi C, Zampino G, Digilio C, Stuppia L, Seemanova E, Pennacchio LA, Gelb BD, Dallapiccola B, Wittinghofer A, Ahmadian MR, Tartaglia M, Zenker M. A restricted spectrum of NRAS mutations causes Noonan syndrome. Nat Genet. 2010 Jan; 42(1):27-9.
      View in: PubMed
    37. Gelb B, Feng S. Management of the liver transplant patient. Expert Rev Gastroenterol Hepatol. 2009 Dec; 3(6):631-47.
      View in: PubMed
    38. Pagani MR, Oishi K, Gelb BD, Zhong Y. The phosphatase SHP2 regulates the spacing effect for long-term memory induction. Cell. 2009 Oct 2; 139(1):186-98.
      View in: PubMed
    39. Cordeddu V, Di Schiavi E, Pennacchio LA, Ma'ayan A, Sarkozy A, Fodale V, Cecchetti S, Cardinale A, Martin J, Schackwitz W, Lipzen A, Zampino G, Mazzanti L, Digilio MC, Martinelli S, Flex E, Lepri F, Bartholdi D, Kutsche K, Ferrero GB, Anichini C, Selicorni A, Rossi C, Tenconi R, Zenker M, Merlo D, Dallapiccola B, Iyengar R, Bazzicalupo P, Gelb BD, Tartaglia M. Mutation of SHOC2 promotes aberrant protein N-myristoylation and causes Noonan-like syndrome with loose anagen hair. Nat Genet. 2009 Sep; 41(9):1022-6.
      View in: PubMed
    40. Sarkozy A, Carta C, Moretti S, Zampino G, Digilio MC, Pantaleoni F, Scioletti AP, Esposito G, Cordeddu V, Lepri F, Petrangeli V, Dentici ML, Mancini GM, Selicorni A, Rossi C, Mazzanti L, Marino B, Ferrero GB, Silengo MC, Memo L, Stanzial F, Faravelli F, Stuppia L, Puxeddu E, Gelb BD, Dallapiccola B, Tartaglia M. Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum. Hum Mutat. 2009 Apr; 30(4):695-702.
      View in: PubMed
    41. Boskey AL, Gelb BD, Pourmand E, Kudrashov V, Doty SB, Spevak L, Schaffler MB. Ablation of cathepsin k activity in the young mouse causes hypermineralization of long bone and growth plates. Calcif Tissue Int. 2009 Mar; 84(3):229-39.
      View in: PubMed
    42. Oishi K, Zhang H, Gault WJ, Wang CJ, Tan CC, Kim IK, Ying H, Rahman T, Pica N, Tartaglia M, Mlodzik M, Gelb BD. Phosphatase-defective LEOPARD syndrome mutations in PTPN11 gene have gain-of-function effects during Drosophila development. Hum Mol Genet. 2009 Jan 1; 18(1):193-201.
      View in: PubMed
    43. Yang M, Sun J, Zhang T, Liu J, Zhang J, Shi MA, Darakhshan F, Guerre-Millo M, Clement K, Gelb BD, Dolgnov G, Shi GP. Deficiency and inhibition of cathepsin K reduce body weight gain and increase glucose metabolism in mice. Arterioscler Thromb Vasc Biol. 2008 Dec; 28(12):2202-8.
      View in: PubMed
    44. Lee KA, Williams B, Roza K, Ferguson H, David K, Eddleman K, Stone J, Edelmann L, Richard G, Gelb BD, Kornreich R. PTPN11 analysis for the prenatal diagnosis of Noonan syndrome in fetuses with abnormal ultrasound findings. Clin Genet. 2009 Feb; 75(2):190-4.
      View in: PubMed
    45. Tan CC, Sindhu KV, Li S, Nishio H, Stoller JZ, Oishi K, Puttreddy S, Lee TJ, Epstein JA, Walsh MJ, Gelb BD. Transcription factor Ap2delta associates with Ash2l and ALR, a trithorax family histone methyltransferase, to activate Hoxc8 transcription. Proc Natl Acad Sci U S A. 2008 May 27; 105(21):7472-7.
      View in: PubMed
    46. Martinelli S, Torreri P, Tinti M, Stella L, Bocchinfuso G, Flex E, Grottesi A, Ceccarini M, Palleschi A, Cesareni G, Castagnoli L, Petrucci TC, Gelb BD, Tartaglia M. Diverse driving forces underlie the invariant occurrence of the T42A, E139D, I282V and T468M SHP2 amino acid substitutions causing Noonan and LEOPARD syndromes. Hum Mol Genet. 2008 Jul 1; 17(13):2018-29.
      View in: PubMed
    47. Flex E, Petrangeli V, Stella L, Chiaretti S, Hornakova T, Knoops L, Ariola C, Fodale V, Clappier E, Paoloni F, Martinelli S, Fragale A, Sanchez M, Tavolaro S, Messina M, Cazzaniga G, Camera A, Pizzolo G, Tornesello A, Vignetti M, Battistini A, Cavé H, Gelb BD, Renauld JC, Biondi A, Constantinescu SN, Foà R, Tartaglia M. Somatically acquired JAK1 mutations in adult acute lymphoblastic leukemia. J Exp Med. 2008 Apr 14; 205(4):751-8.
      View in: PubMed
    48. Profitlich LE, Weismann CG, Srivastava S, Gelb BD, Nguyen K, Joashi U. Multiple thoracic aortic aneurysms after mediastinitis in an infant after repair of coarctation of the aorta. J Thorac Cardiovasc Surg. 2008 Feb; 135(2):444-5, 445.e1.
      View in: PubMed
    49. Pandit B, Sarkozy A, Pennacchio LA, Carta C, Oishi K, Martinelli S, Pogna EA, Schackwitz W, Ustaszewska A, Landstrom A, Bos JM, Ommen SR, Esposito G, Lepri F, Faul C, Mundel P, López Siguero JP, Tenconi R, Selicorni A, Rossi C, Mazzanti L, Torrente I, Marino B, Digilio MC, Zampino G, Ackerman MJ, Dallapiccola B, Tartaglia M, Gelb BD. Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy. Nat Genet. 2007 Aug; 39(8):1007-12.
      View in: PubMed
    50. Pierpont ME, Basson CT, Benson DW, Gelb BD, Giglia TM, Goldmuntz E, McGee G, Sable CA, Srivastava D, Webb CL. Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics. Circulation. 2007 Jun 12; 115(23):3015-38.
      View in: PubMed
    51. Weismann CG, Gelb BD. The genetics of congenital heart disease: a review of recent developments. Curr Opin Cardiol. 2007 May; 22(3):200-6.
      View in: PubMed
    52. Zampino G, Pantaleoni F, Carta C, Cobellis G, Vasta I, Neri C, Pogna EA, De Feo E, Delogu A, Sarkozy A, Atzeri F, Selicorni A, Rauen KA, Cytrynbaum CS, Weksberg R, Dallapiccola B, Ballabio A, Gelb BD, Neri G, Tartaglia M. Diversity, parental germline origin, and phenotypic spectrum of de novo HRAS missense changes in Costello syndrome. Hum Mutat. 2007 Mar; 28(3):265-72.
      View in: PubMed
    53. Xue J, Zhou D, Yao H, Gavrialov O, McConnell MJ, Gelb BD, Haddad GG. Novel functional interaction between Na+/H+ exchanger 1 and tyrosine phosphatase SHP-2. Am J Physiol Regul Integr Comp Physiol. 2007 Jun; 292(6):R2406-16.
      View in: PubMed
    54. Tartaglia M, Pennacchio LA, Zhao C, Yadav KK, Fodale V, Sarkozy A, Pandit B, Oishi K, Martinelli S, Schackwitz W, Ustaszewska A, Martin J, Bristow J, Carta C, Lepri F, Neri C, Vasta I, Gibson K, Curry CJ, Siguero JP, Digilio MC, Zampino G, Dallapiccola B, Bar-Sagi D, Gelb BD. Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome. Nat Genet. 2007 Jan; 39(1):75-9.
      View in: PubMed
    55. Ramaswamy P, Lytrivi ID, Nguyen K, Gelb BD. Neonatal Marfan syndrome : in utero presentation with aortic and pulmonary artery dilatation and successful repair of an acute flail mitral valve leaflet in infancy. Pediatr Cardiol. 2006 Nov-Dec; 27(6):763-5.
      View in: PubMed
    56. Gelb BD, Tartaglia M. Noonan syndrome and related disorders: dysregulated RAS-mitogen activated protein kinase signal transduction. Hum Mol Genet. 2006 Oct 15; 15 Spec No 2:R220-6.
      View in: PubMed
    57. Khan SA, Gelb BD, Nguyen KH. Evaluation of pulmonary artery banding in the setting of ventricular septal defects and severely elevated pulmonary vascular resistance. Congenit Heart Dis. 2006 Sep; 1(5):244-50.
      View in: PubMed
    58. Gelb BD. Marfan's syndrome and related disorders--more tightly connected than we thought. N Engl J Med. 2006 Aug 24; 355(8):841-4.
      View in: PubMed
    59. Sniekers M, Foulon V, Mannaerts GP, Van Maldergem L, Mandel H, Gelb BD, Casteels M, Van Veldhoven PP. Thiamine pyrophosphate: an essential cofactor for the alpha-oxidation in mammals--implications for thiamine deficiencies? Cell Mol Life Sci. 2006 Jul; 63(13):1553-63.
      View in: PubMed
    60. Li CY, Jepsen KJ, Majeska RJ, Zhang J, Ni R, Gelb BD, Schaffler MB. Mice lacking cathepsin K maintain bone remodeling but develop bone fragility despite high bone mass. J Bone Miner Res. 2006 Jun; 21(6):865-75.
      View in: PubMed
    61. Carta C, Pantaleoni F, Bocchinfuso G, Stella L, Vasta I, Sarkozy A, Digilio C, Palleschi A, Pizzuti A, Grammatico P, Zampino G, Dallapiccola B, Gelb BD, Tartaglia M. Germline missense mutations affecting KRAS Isoform B are associated with a severe Noonan syndrome phenotype. Am J Hum Genet. 2006 Jul; 79(1):129-35.
      View in: PubMed
    62. Oishi K, Gaengel K, Krishnamoorthy S, Kamiya K, Kim IK, Ying H, Weber U, Perkins LA, Tartaglia M, Mlodzik M, Pick L, Gelb BD. Transgenic Drosophila models of Noonan syndrome causing PTPN11 gain-of-function mutations. Hum Mol Genet. 2006 Feb 15; 15(4):543-53.
      View in: PubMed
    63. Tartaglia M, Martinelli S, Stella L, Bocchinfuso G, Flex E, Cordeddu V, Zampino G, Burgt Iv, Palleschi A, Petrucci TC, Sorcini M, Schoch C, Foa R, Emanuel PD, Gelb BD. Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease. Am J Hum Genet. 2006 Feb; 78(2):279-90.
      View in: PubMed
    64. Shemesh E, Annunziato RA, Shneider BL, Newcorn JH, Warshaw JK, Dugan CA, Gelb BD, Kerkar N, Yehuda R, Emre S. Parents and clinicians underestimate distress and depression in children who had a transplant. Pediatr Transplant. 2005 Oct; 9(5):673-9.
      View in: PubMed
    65. Bertola DR, Pereira AC, Passetti F, de Oliveira PS, Messiaen L, Gelb BD, Kim CA, Krieger JE. Neurofibromatosis-Noonan syndrome: molecular evidence of the concurrence of both disorders in a patient. Am J Med Genet A. 2005 Jul 30; 136(3):242-5.
      View in: PubMed
    66. Weismann CG, Hager A, Kaemmerer H, Maslen CL, Morris CD, Schranz D, Kreuder J, Gelb BD. PTPN11 mutations play a minor role in isolated congenital heart disease. Am J Med Genet A. 2005 Jul 15; 136(2):146-51.
      View in: PubMed
    67. Kratz CP, Niemeyer CM, Castleberry RP, Cetin M, Bergsträsser E, Emanuel PD, Hasle H, Kardos G, Klein C, Kojima S, Stary J, Trebo M, Zecca M, Gelb BD, Tartaglia M, Loh ML. The mutational spectrum of PTPN11 in juvenile myelomonocytic leukemia and Noonan syndrome/myeloproliferative disease. Blood. 2005 Sep 15; 106(6):2183-5.
      View in: PubMed
    68. Shemesh E, Newcorn JH, Rockmore L, Shneider BL, Emre S, Gelb BD, Rapaport R, Noone SA, Annunziato R, Schmeidler J, Yehuda R. Comparison of parent and child reports of emotional trauma symptoms in pediatric outpatient settings. Pediatrics. 2005 May; 115(5):e582-9.
      View in: PubMed
    69. Tartaglia M, Gelb BD. Germ-line and somatic PTPN11 mutations in human disease. Eur J Med Genet. 2005 Apr-Jun; 48(2):81-96.
      View in: PubMed
    70. Lee JS, Tartaglia M, Gelb BD, Fridrich K, Sachs S, Stratakis CA, Muenke M, Robey PG, Collins MT, Slavotinek A. Phenotypic and genotypic characterisation of Noonan-like/multiple giant cell lesion syndrome. J Med Genet. 2005 Feb; 42(2):e11.
      View in: PubMed
    71. Tartaglia M, Gelb BD. Noonan syndrome and related disorders: genetics and pathogenesis. Annu Rev Genomics Hum Genet. 2005; 6:45-68.
      View in: PubMed
    72. Tartaglia M, Cordeddu V, Chang H, Shaw A, Kalidas K, Crosby A, Patton MA, Sorcini M, van der Burgt I, Jeffery S, Gelb BD. Paternal germline origin and sex-ratio distortion in transmission of PTPN11 mutations in Noonan syndrome. Am J Hum Genet. 2004 Sep; 75(3):492-7.
      View in: PubMed
    73. Fratzl-Zelman N, Valenta A, Roschger P, Nader A, Gelb BD, Fratzl P, Klaushofer K. Decreased bone turnover and deterioration of bone structure in two cases of pycnodysostosis. J Clin Endocrinol Metab. 2004 Apr; 89(4):1538-47.
      View in: PubMed
    74. Fragale A, Tartaglia M, Wu J, Gelb BD. Noonan syndrome-associated SHP2/PTPN11 mutants cause EGF-dependent prolonged GAB1 binding and sustained ERK2/MAPK1 activation. Hum Mutat. 2004 Mar; 23(3):267-77.
      View in: PubMed
    75. Gelb BD. Genetic basis of congenital heart disease. Curr Opin Cardiol. 2004 Mar; 19(2):110-5.
      View in: PubMed
    76. Tartaglia M, Martinelli S, Cazzaniga G, Cordeddu V, Iavarone I, Spinelli M, Palmi C, Carta C, Pession A, Aricò M, Masera G, Basso G, Sorcini M, Gelb BD, Biondi A. Genetic evidence for lineage-related and differentiation stage-related contribution of somatic PTPN11 mutations to leukemogenesis in childhood acute leukemia. Blood. 2004 Jul 15; 104(2):307-13.
      View in: PubMed
    77. Oishi K, Barchi M, Au AC, Gelb BD, Diaz GA. Male infertility due to germ cell apoptosis in mice lacking the thiamin carrier, Tht1. A new insight into the critical role of thiamin in spermatogenesis. Dev Biol. 2004 Feb 15; 266(2):299-309.
      View in: PubMed
    78. O'Brien EK, d'Alençon C, Bonde G, Li W, Schoenebeck J, Allende ML, Gelb BD, Yelon D, Eisen JS, Cornell RA. Transcription factor Ap-2alpha is necessary for development of embryonic melanophores, autonomic neurons and pharyngeal skeleton in zebrafish. Dev Biol. 2004 Jan 1; 265(1):246-61.
      View in: PubMed
    79. Ravishankar C, Nafday S, Green RS, Kamenir S, Lorber R, Stacewicz-Sapuntzakis M, Bridges ND, Holzman IR, Gelb BD. A trial of vitamin A therapy to facilitate ductal closure in premature infants. J Pediatr. 2003 Nov; 143(5):644-8.
      View in: PubMed
    80. Everts V, Hou WS, Rialland X, Tigchelaar W, Saftig P, Brömme D, Gelb BD, Beertsen W. Cathepsin K deficiency in pycnodysostosis results in accumulation of non-digested phagocytosed collagen in fibroblasts. Calcif Tissue Int. 2003 Oct; 73(4):380-6.
      View in: PubMed
    81. Tartaglia M, Niemeyer CM, Fragale A, Song X, Buechner J, Jung A, Hählen K, Hasle H, Licht JD, Gelb BD. Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia. Nat Genet. 2003 Jun; 34(2):148-50.
      View in: PubMed
    82. Tartaglia M, Cotter PD, Zampino G, Gelb BD, Rauen KA. Exclusion of PTPN11 mutations in Costello syndrome: further evidence for distinct genetic etiologies for Noonan, cardio-facio-cutaneous and Costello syndromes. Clin Genet. 2003 May; 63(5):423-6.
      View in: PubMed
    83. Zhao F, Lufkin T, Gelb BD. Expression of Tfap2d, the gene encoding the transcription factor Ap-2 delta, during mouse embryogenesis. Gene Expr Patterns. 2003 May; 3(2):213-7.
      View in: PubMed
    84. Foulon V, Casteels M, Mannaerts GP, Gelb BD, Van Veldhoven PP. Thiamine pyrophosphate: an essential cofactor in the mammalian metabolism of 3-methyl-branched fatty acids--implications for thiamine deficiencies? Adv Exp Med Biol. 2003; 544:305-6.
      View in: PubMed
    85. Oishi K, Hofmann S, Diaz GA, Brown T, Manwani D, Ng L, Young R, Vlassara H, Ioannou YA, Forrest D, Gelb BD. Targeted disruption of Slc19a2, the gene encoding the high-affinity thiamin transporter Thtr-1, causes diabetes mellitus, sensorineural deafness and megaloblastosis in mice. Hum Mol Genet. 2002 Nov 1; 11(23):2951-60.
      View in: PubMed
    86. Parvari R, Hershkovitz E, Grossman N, Gorodischer R, Loeys B, Zecic A, Mortier G, Gregory S, Sharony R, Kambouris M, Sakati N, Meyer BF, Al Aqeel AI, Al Humaidan AK, Al Zanhrani F, Al Swaid A, Al Othman J, Diaz GA, Weiner R, Khan KT, Gordon R, Gelb BD. Mutation of TBCE causes hypoparathyroidism-retardation-dysmorphism and autosomal recessive Kenny-Caffey syndrome. Nat Genet. 2002 Nov; 32(3):448-52.
      View in: PubMed
    87. Ion A, Tartaglia M, Song X, Kalidas K, van der Burgt I, Shaw AC, Ming JE, Zampino G, Zackai EH, Dean JC, Somer M, Parenti G, Crosby AH, Patton MA, Gelb BD, Jeffery S. Absence of PTPN11 mutations in 28 cases of cardiofaciocutaneous (CFC) syndrome. Hum Genet. 2002 Oct; 111(4-5):421-7.
      View in: PubMed
    88. Li Z, Hou WS, Escalante-Torres CR, Gelb BD, Bromme D. Collagenase activity of cathepsin K depends on complex formation with chondroitin sulfate. J Biol Chem. 2002 Aug 9; 277(32):28669-76.
      View in: PubMed
    89. Tartaglia M, Kalidas K, Shaw A, Song X, Musat DL, van der Burgt I, Brunner HG, Bertola DR, Crosby A, Ion A, Kucherlapati RS, Jeffery S, Patton MA, Gelb BD. PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity. Am J Hum Genet. 2002 Jun; 70(6):1555-63.
      View in: PubMed
    90. Tartaglia M, Mehler EL, Goldberg R, Zampino G, Brunner HG, Kremer H, van der Burgt I, Crosby AH, Ion A, Jeffery S, Kalidas K, Patton MA, Kucherlapati RS, Gelb BD. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome. Nat Genet. 2001 Dec; 29(4):465-8.
      View in: PubMed
    91. Zhao F, Satoda M, Licht JD, Hayashizaki Y, Gelb BD. Cloning and characterization of a novel mouse AP-2 transcription factor, AP-2delta, with unique DNA binding and transactivation properties. J Biol Chem. 2001 Nov 2; 276(44):40755-60.
      View in: PubMed
    92. Zhao F, Weismann CG, Satoda M, Pierpont ME, Sweeney E, Thompson EM, Gelb BD. Novel TFAP2B mutations that cause Char syndrome provide a genotype-phenotype correlation. Am J Hum Genet. 2001 Oct; 69(4):695-703.
      View in: PubMed
    93. Oishi K, Hirai T, Gelb BD, Diaz GA. Slc19a2: cloning and characterization of the murine thiamin transporter cDNA and genomic sequence, the orthologue of the human TRMA gene. Mol Genet Metab. 2001 Jun; 73(2):149-59.
      View in: PubMed
    94. Gelb BD. Genetic basis of syndromes associated with congenital heart disease. Curr Opin Cardiol. 2001 May; 16(3):188-94.
      View in: PubMed
    95. Akolkar PN, Gulwani-Akolkar B, Lin XY, Zhou Z, Daly M, Katz S, Levine J, Present D, Gelb B, Desnick R, Mayer L, Silver J. The IBD1 locus for susceptibility to Crohn's disease has a greater impact in Ashkenazi Jews with early onset disease. Am J Gastroenterol. 2001 Apr; 96(4):1127-32.
      View in: PubMed
    96. Zhao R, Gao F, Wang Y, Diaz GA, Gelb BD, Goldman ID. Impact of the reduced folate carrier on the accumulation of active thiamin metabolites in murine leukemia cells. J Biol Chem. 2001 Jan 12; 276(2):1114-8.
      View in: PubMed
    97. Zannolli R, Mostardini R, Matera M, Pucci L, Gelb BD, Morgese G. Char syndrome: an additional family with polythelia, a new finding. Am J Med Genet. 2000 Nov 27; 95(3):201-3.
      View in: PubMed
    98. Gelb A, Gelb B. The neurologic illness of Eugene O'Neill. N Engl J Med. 2000 Sep 7; 343(10):741; author reply 742.
      View in: PubMed
    99. Sicherer SH, Furlong TJ, Maes HH, Desnick RJ, Sampson HA, Gelb BD. Genetics of peanut allergy: a twin study. J Allergy Clin Immunol. 2000 Jul; 106(1 Pt 1):53-6.
      View in: PubMed
    100. Satoda M, Zhao F, Diaz GA, Burn J, Goodship J, Davidson HR, Pierpont ME, Gelb BD. Mutations in TFAP2B cause Char syndrome, a familial form of patent ductus arteriosus. Nat Genet. 2000 May; 25(1):42-6.
      View in: PubMed
    101. Gorlin RJ, Gelb B, Diaz GA, Lofsness KG, Pittelkow MR, Fenyk JR. WHIM syndrome, an autosomal dominant disorder: clinical, hematological, and molecular studies. Am J Med Genet. 2000 Apr 24; 91(5):368-76.
      View in: PubMed
    102. Diaz GA, Gelb BD, Risch N, Nygaard TG, Frisch A, Cohen IJ, Miranda CS, Amaral O, Maire I, Poenaru L, Caillaud C, Weizberg M, Mistry P, Desnick RJ. Gaucher disease: the origins of the Ashkenazi Jewish N370S and 84GG acid beta-glucosidase mutations. Am J Hum Genet. 2000 Jun; 66(6):1821-32.
      View in: PubMed
    103. Gelb BD. Recent advances in the understanding of genetic causes of congenital heart defects. Front Biosci. 2000 Mar 1; 5:D321-33.
      View in: PubMed
    104. Martignetti JA, Gelb BD, Pierce H, Picci P, Desnick RJ. Malignant fibrous histiocytoma: inherited and sporadic forms have loss of heterozygosity at chromosome bands 9p21-22-evidence for a common genetic defect. Genes Chromosomes Cancer. 2000 Feb; 27(2):191-5.
      View in: PubMed
    105. Gelb BD, Zhang J, Sommer RJ, Wasserman JM, Reitman MJ, Willner JP. Familial patent ductus arteriosus and bicuspid aortic valve with hand anomalies: a novel heart-hand syndrome. Am J Med Genet. 1999 Nov 19; 87(2):175-9.
      View in: PubMed
    106. Zhou G, Chen Y, Zhou L, Thirunavukkarasu K, Hecht J, Chitayat D, Gelb BD, Pirinen S, Berry SA, Greenberg CR, Karsenty G, Lee B. CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasia. Hum Mol Genet. 1999 Nov; 8(12):2311-6.
      View in: PubMed
    107. Nishi Y, Atley L, Eyre DE, Edelson JG, Superti-Furga A, Yasuda T, Desnick RJ, Gelb BD. Determination of bone markers in pycnodysostosis: effects of cathepsin K deficiency on bone matrix degradation. J Bone Miner Res. 1999 Nov; 14(11):1902-8.
      View in: PubMed
    108. Diaz GA, Gelb BD, Ali F, Sakati N, Sanjad S, Meyer BF, Kambouris M. Sanjad-Sakati and autosomal recessive Kenny-Caffey syndromes are allelic: evidence for an ancestral founder mutation and locus refinement. Am J Med Genet. 1999 Jul 2; 85(1):48-52.
      View in: PubMed
    109. Diaz GA, Banikazemi M, Oishi K, Desnick RJ, Gelb BD. Mutations in a new gene encoding a thiamine transporter cause thiamine-responsive megaloblastic anaemia syndrome. Nat Genet. 1999 Jul; 22(3):309-12.
      View in: PubMed
    110. Satoda M, Pierpont ME, Diaz GA, Bornemeier RA, Gelb BD. Char syndrome, an inherited disorder with patent ductus arteriosus, maps to chromosome 6p12-p21. Circulation. 1999 Jun 15; 99(23):3036-42.
      View in: PubMed
    111. Hou WS, Brömme D, Zhao Y, Mehler E, Dushey C, Weinstein H, Miranda CS, Fraga C, Greig F, Carey J, Rimoin DL, Desnick RJ, Gelb BD. Characterization of novel cathepsin K mutations in the pro and mature polypeptide regions causing pycnodysostosis. J Clin Invest. 1999 Mar; 103(5):731-8.
      View in: PubMed
    112. Martignetti JA, Desnick RJ, Aliprandis E, Norton KI, Hardcastle P, Nade S, Gelb BD. Diaphyseal medullary stenosis with malignant fibrous histiocytoma: a hereditary bone dysplasia/cancer syndrome maps to 9p21-22. Am J Hum Genet. 1999 Mar; 64(3):801-7.
      View in: PubMed
    113. Banikazemi M, Diaz GA, Vossough P, Jalali M, Desnick RJ, Gelb BD. Localization of the thiamine-responsive megaloblastic anemia syndrome locus to a 1.4-cM region of 1q23. Mol Genet Metab. 1999 Mar; 66(3):193-8.
      View in: PubMed
    114. Aliprandis E, Harris J, Yoo B, Gelb BD, Martignetti JA. Isolation, characterization, and mapping of four novel polymorphic markers and an H3.3B pseudogene to chromosome 9p21-22. J Hum Genet. 1999; 44(5):348-9.
      View in: PubMed
    115. Herzberg GZ, Rossi AF, Courtney M, Gelb BD. The effects of HLA mismatching and immunosuppressive therapy on early rejection outcome in pediatric heart transplant recipients. J Heart Lung Transplant. 1998 Dec; 17(12):1195-200.
      View in: PubMed
    116. Montgomery RA, Geraghty MT, Bull E, Gelb BD, Johnson M, McIntosh I, Francomano CA, Dietz HC. Multiple molecular mechanisms underlying subdiagnostic variants of Marfan syndrome. Am J Hum Genet. 1998 Dec; 63(6):1703-11.
      View in: PubMed
    117. Diaz GA, Khan KT, Gelb BD. The autosomal recessive Kenny-Caffey syndrome locus maps to chromosome 1q42-q43. Genomics. 1998 Nov 15; 54(1):13-8.
      View in: PubMed
    118. Herzberg GZ, Rossi AF, Courtney M, Lansman SL, Gelb BD, Parness IA, Lai WW. Usefulness of tacrolimus versus cyclosporine after pediatric heart transplantation. Am J Cardiol. 1998 Aug 15; 82(4):541-3.
      View in: PubMed
    119. Gelb BD, Willner JP, Dunn TM, Kardon NB, Verloes A, Poncin J, Desnick RJ. Paternal uniparental disomy for chromosome 1 revealed by molecular analysis of a patient with pycnodysostosis. Am J Hum Genet. 1998 Apr; 62(4):848-54.
      View in: PubMed
    120. Rothstein MA, Gelb BD, Craig SG. Protecting genetic privacy by permitting employer access only to job-related employee medical information: analysis of a unique Minnesota law. Am J Law Med. 1998; 24(4):399-416.
      View in: PubMed
    121. Recto MR, Parness IA, Gelb BD, Lopez L, Lai WW. Clinical implications and possible association of malposition of the branch pulmonary arteries with DiGeorge syndrome and microdeletion of chromosomal region 22q11. Am J Cardiol. 1997 Dec 15; 80(12):1624-7.
      View in: PubMed
    122. Gelb BD. Molecular genetics of congenital heart disease. Curr Opin Cardiol. 1997 May; 12(3):321-8.
      View in: PubMed
    123. Gelb BD, Shi GP, Heller M, Weremowicz S, Morton C, Desnick RJ, Chapman HA. Structure and chromosomal assignment of the human cathepsin K gene. Genomics. 1997 Apr 15; 41(2):258-62.
      View in: PubMed
    124. Gelb BD, Zhang J, Cotter PD, Gershin IF, Desnick RJ. Physical mapping of the human connexin 40 (GJA5), flavin-containing monooxygenase 5, and natriuretic peptide receptor a genes on 1q21. Genomics. 1997 Feb 1; 39(3):409-11.
      View in: PubMed
    125. Levy B, Gershin IF, Desnick RJ, Babu A, Gelb BD, Hirschhorn K, Cotter PD. Characterization of a de novo unbalanced chromosome rearrangement by comparative genomic hybridization and fluorescence in situ hybridization. Cytogenet Cell Genet. 1997; 76(1-2):68-71.
      View in: PubMed
    126. Gelb BD, Jones MY. Promoting physician referral services. Prospective users are not necessarily the best advertising target. Mark Health Serv. 1997; 17(3):22-5.
      View in: PubMed
    127. Gelb BD, Moissoglu K, Zhang J, Martignetti JA, Brömme D, Desnick RJ. Cathepsin K: isolation and characterization of the murine cDNA and genomic sequence, the homologue of the human pycnodysostosis gene. Biochem Mol Med. 1996 Dec; 59(2):200-6.
      View in: PubMed
    128. Gelb BD, Shi GP, Chapman HA, Desnick RJ. Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiency. Science. 1996 Aug 30; 273(5279):1236-8.
      View in: PubMed
    129. Gelb BD, Spencer E, Obad S, Edelson GJ, Faure S, Weissenbach J, Desnick RJ. Pycnodysostosis: refined linkage and radiation hybrid analyses reduce the critical region to 2 cM at 1q21 and map two candidate genes. Hum Genet. 1996 Aug; 98(2):141-4.
      View in: PubMed
    130. Gelb BD, Cooper E, Shevell M, Desnick RJ. Genetic mapping of the cleidocranial dysplasia (CCD) locus on chromosome band 6p21 to include a microdeletion. Am J Med Genet. 1995 Aug 28; 58(2):200-5.
      View in: PubMed
    131. Gelb BD, Edelson JG, Desnick RJ. Linkage of pycnodysostosis to chromosome 1q21 by homozygosity mapping. Nat Genet. 1995 Jun; 10(2):235-7.
      View in: PubMed
    132. Kipel G, Rossi AF, Steinberg LG, Gelb B, Fiumecaldo F, Golinko RJ, Griepp RB. Malignant wide complex tachycardia after adenosine administration to a postoperative pediatric patient with congenital heart disease. Pediatr Cardiol. 1995 Jan-Feb; 16(1):36-7.
      View in: PubMed
    133. Gelb B, Johnson M. Word-of-mouth communication: causes and consequences. J Health Care Mark. 1995; 15(3):54-8.
      View in: PubMed
    134. Stanaland AJ, Gelb BD. Can prevention be marketed profitably? J Health Care Mark. 1995; 15(4):59-63.
      View in: PubMed
    135. Martin AB, Webber S, Fricker FJ, Jaffe R, Demmler G, Kearney D, Zhang YH, Bodurtha J, Gelb B, Ni J, et al. Acute myocarditis. Rapid diagnosis by PCR in children. Circulation. 1994 Jul; 90(1):330-9.
      View in: PubMed
    136. Pastores GM, Santorelli FM, Shanske S, Gelb BD, Fyfe B, Wolfe D, Willner JP. Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G). Am J Med Genet. 1994 Apr 15; 50(3):265-71.
      View in: PubMed
    137. Gelb BD, Boutwell WB, Cummings S. Using mass media communication for health promotion: results from a cancer center effort. Hosp Health Serv Adm. 1994; 39(3):283-93.
      View in: PubMed
    138. Gelb BD, Cowan S. Consequences of bad publicity: one example. Hosp Health Serv Adm. 1994; 39(4):435-49.
      View in: PubMed
    139. Gelb BD. Turning volunteers into patients--and vice versa. J Health Care Mark. 1994; 14(1):8-9.
      View in: PubMed
    140. Gelb BD. Sensory assistance to improve your hospital. J Health Care Mark. 1994; 14(2):6-7.
      View in: PubMed
    141. Gelb BD. Genomic structure of and a cardiac promoter for the mouse carnitine palmitoyltransferase II gene. Genomics. 1993 Dec; 18(3):651-5.
      View in: PubMed
    142. Towbin JA, Hejtmancik JF, Brink P, Gelb B, Zhu XM, Chamberlain JS, McCabe ER, Swift M. X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus. Circulation. 1993 Jun; 87(6):1854-65.
      View in: PubMed
    143. O'Laughlin MP, Bricker JT, Mullins CE, Cabalka AK, Gelb BD, Towbin JA. Transcatheter closure of residual atrial septal defect following cardiac transplantation. Cathet Cardiovasc Diagn. 1993 Feb; 28(2):162-3.
      View in: PubMed
    144. Martin AB, Bricker JT, Fishman M, Frazier OH, Price JK, Radovancevic B, Louis PT, Cabalka AK, Gelb BD, Towbin JA. Neurologic complications of heart transplantation in children. J Heart Lung Transplant. 1992 Sep-Oct; 11(5):933-42.
      View in: PubMed
    145. Gelb BD, Worley KC, Griffin LD, Adams V, Chinault AC, McCabe ER. Characterization of human genomic yeast artificial chromosome inserts containing hexokinase 1 coding information on chromosome 10. Biochem Med Metab Biol. 1992 Jun; 47(3):265-9.
      View in: PubMed
    146. Louis PT, Bricker JT, Frazier OH, Duncan M, Towbin JA, Gelb BD, Macris MA, Radovencavic B, Kearney D, Igo S, et al. Nonpulsatile total left ventricular support in pediatric patients. Crit Care Med. 1992 May; 20(5):704-7.
      View in: PubMed
    147. Gelb BD, Bryant JM. Designing health promotion programs by watching the market. J Health Care Mark. 1992 Mar; 12(1):65-70.
      View in: PubMed
    148. Griffin LD, Gelb BD, Adams V, McCabe ER. Developmental expression of hexokinase 1 in the rat. Biochim Biophys Acta. 1992 Feb 11; 1129(3):309-17.
      View in: PubMed
    149. Gelb BD, Adams V, Jones SN, Griffin LD, MacGregor GR, McCabe ER. Targeting of hexokinase 1 to liver and hepatoma mitochondria. Proc Natl Acad Sci U S A. 1992 Jan 1; 89(1):202-6.
      View in: PubMed
    150. Gelb BD, Gelb LM, Noey HE. Large employers and their coalitions: exploring a hospital constituency. Hosp Health Serv Adm. 1992; 37(2):259-68.
      View in: PubMed
    151. Gelb BD, Gaskins JN, Hendrickson JG, Iszard JE. Does greater usage of a health plan reduce satisfaction? J Health Care Mark. 1991 Dec; 11(4):68-74.
      View in: PubMed
    152. Griffin LD, Gelb BD, Wheeler DA, Davison D, Adams V, McCabe ER. Mammalian hexokinase 1: evolutionary conservation and structure to function analysis. Genomics. 1991 Dec; 11(4):1014-24.
      View in: PubMed
    153. Gelb BD, Denfield S, Friedman R, Garson AT, Price J, Bricker JT, Towbin JA. Pseudoconduction of atrial flutter of a recipient atrium. J Heart Lung Transplant. 1991 Nov-Dec; 10(6):1033-5.
      View in: PubMed
    154. Gelb BD, Towbin JA, McCabe ER, Sujansky E. San Luis Valley recombinant chromosome 8 and tetralogy of Fallot: a review of chromosome 8 anomalies and congenital heart disease. Am J Med Genet. 1991 Sep 15; 40(4):471-6.
      View in: PubMed
    155. Adams V, Griffin LD, Gelb BD, McCabe ER. Protein kinase activity of rat brain hexokinase. Biochem Biophys Res Commun. 1991 Jun 28; 177(3):1101-6.
      View in: PubMed
    156. Adams V, Griffin L, Towbin J, Gelb B, Worley K, McCabe ER. Porin interaction with hexokinase and glycerol kinase: metabolic microcompartmentation at the outer mitochondrial membrane. Biochem Med Metab Biol. 1991 Jun; 45(3):271-91.
      View in: PubMed
    157. Zentner RD, Gelb BD. Scenarios: a planning tool for health care organizations. Hosp Health Serv Adm. 1991; 36(2):211-22.
      View in: PubMed
    158. Gelb BD, O'Laughlin MP, Mullins CE. Prevalence of additional cardiovascular anomalies in patients referred for transcatheter closure of patent ductus arteriosus. J Am Coll Cardiol. 1990 Dec; 16(7):1680-6.
      View in: PubMed
    159. Gelb BD, Garson A. Noninvasive discrimination of right atrial ectopic tachycardia from sinus tachycardia in "dilated cardiomyopathy". Am Heart J. 1990 Oct; 120(4):886-91.
      View in: PubMed
    160. Gelb BD. Telephoned appointment-scheduling by a physician's office: does it work? J Health Care Mark. 1989 Dec; 9(4):61-3.
      View in: PubMed
    161. Gelb BD. When to advertise to consumers, and when not to. J Health Care Mark. 1988 Jun; 8(2):58-60.
      View in: PubMed
    162. Gelb BD. What university research can offer the health care marketer. J Health Care Mark. 1987 Dec; 7(4):41-4.
      View in: PubMed
    163. Gelb GM, Gelb BD. Physicians and hospital decision making: a two-stage technique for improvement. Hosp Health Serv Adm. 1987 May; 32(2):139-49.
      View in: PubMed
    164. Gelb BD. Preventive medicine and employee productivity. Harv Bus Rev. 1985 Mar-Apr; 63(2):12, 16.
      View in: PubMed
    165. Safirstein BH, Dhakhwa RB, Gelb B, Fontunato FD. Bronchodilator effects of oral salbutamol and theophylline-salbutamol combinations in chronic steroid-dependent asthmatics. J Med Soc N J. 1979 Dec; 76(13):892-4.
      View in: PubMed
    Gelb's Networks
    Click the "See All" links for more information and interactive visualizations!
    Concepts
    _
    Co-Authors
    _
    Similar People
    _
    Same Department
     
    Mount Sinai Profiles is managed by Conduits - The Institutes for Translational Sciences at Icahn School of Medicine, supported by the National Center for Research Resources and the National Center for Advancing Translational Sciences of the National Institutes of Health through Grant Number UL1TR000067