Bioresorbable airway splint created with a three-dimensional printer DA Zopf, SJ Hollister, ME Nelson, RG Ohye, GE Green New England Journal of Medicine 368 (21), 2043-2045, 2013 | 716 | 2013 |
Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness GE Green, DA Scott, JM McDonald, GG Woodworth, VC Sheffield, ... Jama 281 (23), 2211-2216, 1999 | 525 | 1999 |
Androgen receptors mediate hypertrophy in cardiac myocytes JD Marsh, MH Lehmann, RH Ritchie, JK Gwathmey, GE Green, ... Circulation 98 (3), 256-261, 1998 | 519 | 1998 |
Mitigation of tracheobronchomalacia with 3D-printed personalized medical devices in pediatric patients RJ Morrison, SJ Hollister, MF Niedner, MG Mahani, AH Park, DK Mehta, ... Science translational medicine 7 (285), 285ra64-285ra64, 2015 | 486 | 2015 |
Pendred syndrome, DFNB4, and PDS/SLC26A4 identification of eight novel mutations and possible genotype–phenotype correlations C Campbell, RA Cucci, S Prasad, GE Green, JB Edeal, CE Galer, ... Human mutation 17 (5), 403-411, 2001 | 384 | 2001 |
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13) WT McGuirt, SD Prasad, AJ Griffith, HPM Kunst, GE Green, KB Shpargel, ... Nature genetics 23 (4), 413-419, 1999 | 322 | 1999 |
Regulatory considerations in the design and manufacturing of implantable 3D‐printed medical devices RJ Morrison, KN Kashlan, CL Flanangan, JK Wright, GE Green, ... Clinical and translational science 8 (5), 594-600, 2015 | 279 | 2015 |
Atypical phenotypes associated with pathogenic CHD7 variants and a proposal for broadening CHARGE syndrome clinical diagnostic criteria CL Hale, AN Niederriter, GE Green, DM Martin American Journal of Medical Genetics Part A 170 (2), 344-354, 2016 | 153 | 2016 |
Computer aided–designed, 3-dimensionally printed porous tissue bioscaffolds for craniofacial soft tissue reconstruction DA Zopf, AG Mitsak, CL Flanagan, M Wheeler, GE Green, SJ Hollister Otolaryngology--Head and Neck Surgery 152 (1), 57-62, 2015 | 150 | 2015 |
Temporal bone histopathology in connexin 26–related hearing loss AI Jun, WT McGuirt, R Hinojosa, GE Green, N Fischel‐Ghodsian, ... The Laryngoscope 110 (2), 269-269, 2000 | 129 | 2000 |
Pathogenesis and treatment of juvenile onset recurrent respiratory papillomatosis GE Green, NM Bauman, RJH Smith Otolaryngologic Clinics of North America 33 (1), 187-207, 2000 | 127 | 2000 |
Linkage of otosclerosis to a third locus (OTSC3) on human chromosome 6p21. 3-22.3 W Chen, CA Campbell, GE Green, K Van Den Bogaert, C Komodikis, ... Journal of medical genetics 39 (7), 473-477, 2002 | 125 | 2002 |
Obesity and risk of peri-operative complications in children presenting for adenotonsillectomy OO Nafiu, GE Green, S Walton, M Morris, S Reddy, KK Tremper International journal of pediatric otorhinolaryngology 73 (1), 89-95, 2009 | 117 | 2009 |
Design control for clinical translation of 3D printed modular scaffolds SJ Hollister, CL Flanagan, DA Zopf, RJ Morrison, H Nasser, JJ Patel, ... Annals of biomedical engineering 43, 774-786, 2015 | 115 | 2015 |
Performance of cochlear implant recipients with GJB2‐related deafness GE Green, DA Scott, JM McDonald, HFB Teagle, BJ Tomblin, LJ Spencer, ... American journal of medical genetics 109 (3), 167-170, 2002 | 115 | 2002 |
Treatment of severe porcine tracheomalacia with a 3-dimensionally printed, bioresorbable, external airway splint DA Zopf, CL Flanagan, M Wheeler, SJ Hollister, GE Green JAMA Otolaryngology–Head & Neck Surgery 140 (1), 66-71, 2014 | 109 | 2014 |
A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome MJ Rieder, GE Green, SS Park, BD Stamper, CT Gordon, JM Johnson, ... The American Journal of Human Genetics 90 (5), 907-914, 2012 | 108 | 2012 |
Genetic testing for hereditary hearing loss: Connexin 26 (GJB2) allele variants and two novel deafness‐causing mutations (R32C and 645‐648delTAGA) S Prasad, RA Cucci, GE Green, RJH Smith Human mutation 16 (6), 502-508, 2000 | 108 | 2000 |
Digital music exposure reliably induces temporary threshold shift in normal-hearing human subjects CG Le Prell, S Dell, B Hensley, JW Hall III, KCM Campbell, PJ Antonelli, ... Ear and hearing 33 (6), e44-e58, 2012 | 101 | 2012 |
Syndromes of the first and second branchial arches, part 1: embryology and characteristic defects JM Johnson, G Moonis, GE Green, R Carmody, HN Burbank American journal of neuroradiology 32 (1), 14-19, 2011 | 94 | 2011 |