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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1988 2
1991 1
1992 2
1993 1
1995 1
1997 2
1998 2
2000 3
2001 2
2002 3
2003 5
2004 1
2005 3
2006 2
2007 1
2008 1
2009 3
2010 1
2011 1
2012 4
2013 5
2014 3
2015 1
2016 4
2017 2
2018 1
2019 2
2020 1
2021 2
2022 1
2023 1
2024 1
2025 0

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60 results

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Page 1
Genetics and therapy for pediatric eye diseases.
Chen HY, Lehmann OJ, Swaroop A. Chen HY, et al. Among authors: lehmann oj. EBioMedicine. 2021 May;67:103360. doi: 10.1016/j.ebiom.2021.103360. Epub 2021 May 8. EBioMedicine. 2021. PMID: 33975254 Free PMC article. Review.
Fox's in development and disease.
Lehmann OJ, Sowden JC, Carlsson P, Jordan T, Bhattacharya SS. Lehmann OJ, et al. Trends Genet. 2003 Jun;19(6):339-44. doi: 10.1016/S0168-9525(03)00111-2. Trends Genet. 2003. PMID: 12801727 Review.
Changes at CMAJ.
Lehmann OJ. Lehmann OJ. CMAJ. 2016 Apr 5;188(6):449-450. doi: 10.1503/cmaj.1150094. CMAJ. 2016. PMID: 27044787 Free PMC article. No abstract available.
Ectopic retinal tacks.
Lehmann OJ, Canning CR. Lehmann OJ, et al. Eye (Lond). 1995;9 ( Pt 3):378-9. doi: 10.1038/eye.1995.77. Eye (Lond). 1995. PMID: 7556755 No abstract available.
The Axenfeld-Rieger Syndrome Gene FOXC1 Contributes to Left-Right Patterning.
Chrystal PW, French CR, Jean F, Havrylov S, van Baarle S, Peturson AM, Xu P, Crump JG, Pilgrim DB, Lehmann OJ, Waskiewicz AJ. Chrystal PW, et al. Among authors: lehmann oj. Genes (Basel). 2021 Jan 26;12(2):170. doi: 10.3390/genes12020170. Genes (Basel). 2021. PMID: 33530637 Free PMC article.
Genetic background-dependent role of Egr1 for eyelid development.
Oh J, Wang Y, Chen S, Li P, Du N, Yu ZX, Butcher D, Gebregiorgis T, Strachan E, Lehmann OJ, Brooks BP, Chan CC, Leonard WJ. Oh J, et al. Among authors: lehmann oj. Proc Natl Acad Sci U S A. 2017 Aug 22;114(34):E7131-E7139. doi: 10.1073/pnas.1705848114. Epub 2017 Aug 4. Proc Natl Acad Sci U S A. 2017. PMID: 28778995 Free PMC article.
Utility of whole-exome sequencing for those near the end of the diagnostic odyssey: time to address gaps in care.
Sawyer SL, Hartley T, Dyment DA, Beaulieu CL, Schwartzentruber J, Smith A, Bedford HM, Bernard G, Bernier FP, Brais B, Bulman DE, Warman Chardon J, Chitayat D, Deladoëy J, Fernandez BA, Frosk P, Geraghty MT, Gerull B, Gibson W, Gow RM, Graham GE, Green JS, Heon E, Horvath G, Innes AM, Jabado N, Kim RH, Koenekoop RK, Khan A, Lehmann OJ, Mendoza-Londono R, Michaud JL, Nikkel SM, Penney LS, Polychronakos C, Richer J, Rouleau GA, Samuels ME, Siu VM, Suchowersky O, Tarnopolsky MA, Yoon G, Zahir FR; FORGE Canada Consortium; Care4Rare Canada Consortium; Majewski J, Boycott KM. Sawyer SL, et al. Among authors: lehmann oj. Clin Genet. 2016 Mar;89(3):275-84. doi: 10.1111/cge.12654. Epub 2015 Sep 22. Clin Genet. 2016. PMID: 26283276 Free PMC article. Review.
BMP3 is a novel locus involved in the causality of ocular coloboma.
Fox SC, Widen SA, Asai-Coakwell M, Havrylov S, Benson M, Prichard LB, Baddam P, Graf D, Lehmann OJ, Waskiewicz AJ. Fox SC, et al. Among authors: lehmann oj. Hum Genet. 2022 Aug;141(8):1385-1407. doi: 10.1007/s00439-022-02430-3. Epub 2022 Jan 28. Hum Genet. 2022. PMID: 35089417
60 results