| Mutations in apoptosis-inducing factor cause X-linked recessive auditory neuropathy spectrum disorder L Zong, J Guan, M Ealy, Q Zhang, D Wang, H Wang, Y Zhao, Z Shen, ... Journal of medical genetics 52 (8), 523-531, 2015 | 129 | 2015 |
| The coding polymorphism T263I in TGF-β1 is associated with otosclerosis in two independent populations M Thys, I Schrauwen, K Vanderstraeten, K Janssens, N Dieltjens, ... Human molecular genetics 16 (17), 2021-2030, 2007 | 102 | 2007 |
| Otosclerosis M Ealy, RJH Smith Medical Genetics in the Clinical Practice of ORL 70, 122-129, 2011 | 91 | 2011 |
| A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis I Schrauwen, M Ealy, MJ Huentelman, M Thys, N Homer, ... The American Journal of Human Genetics 84 (3), 328-338, 2009 | 89 | 2009 |
| Association of bone morphogenetic proteins with otosclerosis I Schrauwen, M Thys, K Vanderstraeten, E Fransen, N Dieltjens, ... Journal of Bone and Mineral Research 23 (4), 507-516, 2008 | 86 | 2008 |
| The genetics of otosclerosis M Ealy, RJH Smith Hearing research 266 (1-2), 70-74, 2010 | 71 | 2010 |
| Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations I Schrauwen, M Ealy, E Fransen, K Vanderstraeten, M Thys, NC Meyer, ... Human genetics 127, 155-162, 2010 | 47 | 2010 |
| The prevalence of mitochondrial mutations associated with aminoglycoside‐induced sensorineural hearing loss in an NICU population M Ealy, KA Lynch, NC Meyer, RJH Smith The Laryngoscope 121 (6), 1184-1186, 2011 | 46 | 2011 |
| Detection of Rare Nonsynonymous Variants in TGFB1 in Otosclerosis Patients M Thys, I Schrauwen, K Vanderstraeten, N Dieltjens, E Fransen, M Ealy, ... Annals of human genetics 73 (2), 171-175, 2009 | 46 | 2009 |
| No evidence for association between the renin-angiotensin-aldosterone system and otosclerosis in a large Belgian-Dutch population I Schrauwen, M Thys, K Vanderstraeten, E Fransen, M Ealy, ... Otology & Neurotology 30 (8), 1079-1083, 2009 | 45 | 2009 |
| Gene expression analysis of human otosclerotic stapedial footplates M Ealy, W Chen, GY Ryu, JG Yoon, DB Welling, M Hansen, A Madan, ... Hearing research 240 (1-2), 80-86, 2008 | 34 | 2008 |
| COL1A1 association and otosclerosis: A meta‐analysis I Schrauwen, A Khalfallah, M Ealy, E Fransen, C Claes, A Huber, ... American Journal of Medical Genetics Part A 158 (5), 1066-1070, 2012 | 31 | 2012 |
| Genetic variants in RELN are associated with otosclerosis in a non‐European population from Tunisia A Khalfallah, I Schrauwen, M Mnaja, E Fransen, I Lahmar, M Ealy, ... Annals of human genetics 74 (5), 399-405, 2010 | 27 | 2010 |
| Rare variants in BMP2 and BMP4 found in otosclerosis patients reduce Smad signaling M Ealy, NC Meyer, JC Corchado, I Schrauwen, A Bress, M Pfister, ... Otology & Neurotology 35 (3), 395-400, 2014 | 19 | 2014 |
| Commentary on" Otosclerosis: thirty-year follow-up after surgery" M Ealy, I Schrauwen, G Van Camp Annals of Otology Rhinology and Laryngology-Including Supplements 120 (9), 615, 2011 | 4 | 2011 |
| Otosclerosis–identifying genetic contributions to a complex hearing disorder ML Ealy PhD thesis, University of Iowa, 2011 | 2 | 2011 |
| Exome capture and array comparative genomic hybridization of a monozygotic twin pair discordant for dense deposit disease JCCC Corchado, C Nishimura, C Meyer, KF Frees, MB Jones, YZ Zang, ... Molecular Immunology 14 (48), 1685, 2011 | | 2011 |
