| Human malformations and related anomalies RE Stevenson, JG Hall, DB Everman, BD Solomon Oxford University Press, 2015 | 75 | 2015 |
| Medical management of the surgical patient: a textbook of perioperative medicine MF Lubin, TF Dodson, NH Winawer Cambridge University Press, 2013 | 58 | 2013 |
| Augmented Hummelsheim procedure to treat complete abducens nerve palsy NL Couser, PD Lenhart, AK Hutchinson Journal of American Association for Pediatric Ophthalmology and Strabismus …, 2012 | 53 | 2012 |
| A randomized trial comparing the cost-effectiveness of 2 approaches for treating unilateral nasolacrimal duct obstruction Pediatric Eye Disease Investigator Group Archives of ophthalmology 130 (12), 1525-1533, 2012 | 51 | 2012 |
| Functional validation of novel compound heterozygous variants in B3GAT3 resulting in severe osteopenia and fractures: expanding the disease phenotype F Job, S Mizumoto, L Smith, N Couser, A Brazil, H Saal, M Patterson, ... BMC Medical Genetics 17, 1-8, 2016 | 34 | 2016 |
| The phenotype of multiple congenital anomalies‐hypotonia‐seizures syndrome 1: Report and review NL Couser, MM Masood, NT Strande, AKM Foreman, K Crooks, KE Weck, ... American Journal of Medical Genetics Part A 167 (9), 2176-2181, 2015 | 30 | 2015 |
| Mild achondroplasia/hypochondroplasia with acanthosis nigricans, normal development, and a p.Ser348Cys FGFR3 mutation NL Couser, CK Pande, CM Turcott, EB Spector, AS Aylsworth, CM Powell American Journal of Medical Genetics Part A 173 (4), 1097-1101, 2017 | 20 | 2017 |
| Botulinum toxin a treatment of consecutive esotropia in children NL Couser, SR Lambert Strabismus 20 (4), 158-161, 2012 | 18 | 2012 |
| Ocular findings in the 16p11. 2 microdeletion syndrome: a case report and literature review CS Stingl, C Jackson-Cook, NL Couser Case reports in pediatrics 2020 (1), 2031701, 2020 | 16 | 2020 |
| Ocular manifestations in the X-linked intellectual disability syndromes NL Couser, MM Masood, AS Aylsworth, RE Stevenson Ophthalmic genetics 38 (5), 401-412, 2017 | 13 | 2017 |
| Survey of practice patterns for the management of ophthalmic genetic disorders among AAPOS members: report by the AAPOS Genetic Eye Disease Task Force AV Drack, VM Utz, K Wang, DM Alcorn, BP Brooks, DM Costakos, ... Journal of American Association for Pediatric Ophthalmology and Strabismus …, 2019 | 12 | 2019 |
| Cleft palate and hypopituitarism in a patient with Noonan‐like syndrome with loose anagen hair‐1 NL Couser, D Keelean‐Fuller, ML Davenport, E Haverfield, MM Masood, ... American Journal of Medical Genetics Part A 176 (9), 2024-2027, 2018 | 12 | 2018 |
| The first cataract surgeons in the British Isles CT Leffler, SG Schwartz, E Peterson, NL Couser, AR Salman American journal of ophthalmology 230, 75-122, 2021 | 10 | 2021 |
| Ocular Manifestations of the NAA10‐Related Syndrome AS Gupta, HA Saif, JM Lent, NL Couser Case Reports in Genetics 2019 (1), 8492965, 2019 | 10 | 2019 |
| Homocysteinemia due to MTHFR deficiency in a young adult presenting with bilateral lens subluxations NL Couser, J McClure, MW Evans, NR Haines, SK Burden, J Muenzer Ophthalmic Genetics 38 (1), 91-94, 2017 | 10 | 2017 |
| Vision screening in the pediatrician’s office NL Couser, FQ Esmail, AK Hutchinson Open Journal of Ophthalmology 2 (2), 9-13, 2012 | 10 | 2012 |
| Oculodentodigital dysplasia: a case report and major review of the eye and ocular adnexa features of 295 reported cases V Kumar, NL Couser, A Pandya Case Reports in Ophthalmological Medicine 2020 (1), 6535974, 2020 | 8 | 2020 |
| The WHEELS Preschool Vision Screening Program’s initial outcomes for 12,402 children screened using the Plusoptix photoscreener NL Couser International scholarly research notices 2014 (1), 793546, 2014 | 8 | 2014 |
| The washington metropolitan pediatric vision screening quality control assessment NL Couser, J Smith-Marshall International Scholarly Research Notices 2011 (1), 801957, 2011 | 8 | 2011 |
| The history of Glaucoma CT Leffler Wayenborgh Publishing, 2020 | 7 | 2020 |
