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

Year Number of Results
2007 3
2008 2
2009 1
2010 2
2012 2
2013 4
2014 4
2016 1
2017 5
2019 2
2020 1
2021 1
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28 results
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Page 1
Biallelic CPAMD8 Variants Are a Frequent Cause of Childhood and Juvenile Open-Angle Glaucoma.
Siggs OM, Souzeau E, Taranath DA, Dubowsky A, Chappell A, Zhou T, Javadiyan S, Nicholl J, Kearns LS, Staffieri SE, Narita A, Smith JEH, Pater J, Hewitt AW, Ruddle JB, Elder JE, Mackey DA, Burdon KP, Craig JE. Siggs OM, et al. Among authors: taranath da. Ophthalmology. 2020 Jun;127(6):758-766. doi: 10.1016/j.ophtha.2019.12.024. Epub 2020 Jan 7. Ophthalmology. 2020. PMID: 32085876
Prevalence of FOXC1 Variants in Individuals With a Suspected Diagnosis of Primary Congenital Glaucoma.
Siggs OM, Souzeau E, Pasutto F, Dubowsky A, Smith JEH, Taranath D, Pater J, Rait JL, Narita A, Mauri L, Del Longo A, Reis A, Chappell A, Kearns LS, Staffieri SE, Elder JE, Ruddle JB, Hewitt AW, Burdon KP, Mackey DA, Craig JE. Siggs OM, et al. Among authors: taranath d. JAMA Ophthalmol. 2019 Apr 1;137(4):348-355. doi: 10.1001/jamaophthalmol.2018.5646. JAMA Ophthalmol. 2019. PMID: 30653210 Free PMC article.
Spontaneously resolved infantile glaucoma.
Hsu TT, Cugati S, Craig JE, Taranath D, Hodson T. Hsu TT, et al. Among authors: taranath d. Clin Exp Ophthalmol. 2014 Nov;42(8):800-2. doi: 10.1111/ceo.12327. Epub 2014 Apr 15. Clin Exp Ophthalmol. 2014. PMID: 24641779 No abstract available.
Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants.
Souzeau E, Siggs OM, Zhou T, Galanopoulos A, Hodson T, Taranath D, Mills RA, Landers J, Pater J, Smith JE, Elder JE, Rait JL, Giles P, Phakey V, Staffieri SE, Kearns LS, Dubowsky A, Mackey DA, Hewitt AW, Ruddle JB, Burdon KP, Craig JE. Souzeau E, et al. Among authors: taranath d. Eur J Hum Genet. 2017 Jun;25(7):839-847. doi: 10.1038/ejhg.2017.59. Epub 2017 May 17. Eur J Hum Genet. 2017. PMID: 28513611 Free PMC article.
Glaucoma spectrum and age-related prevalence of individuals with FOXC1 and PITX2 variants.
Souzeau E, Siggs OM, Zhou T, Galanopoulos A, Hodson T, Taranath D, Mills RA, Landers J, Pater J, Smith JE, Elder JE, Rait JL, Giles P, Phakey V, Staffieri SE, Kearns LS, Dubowsky A, Mackey DA, Hewitt AW, Ruddle JB, Burdon KP, Craig JE. Souzeau E, et al. Among authors: taranath d. Eur J Hum Genet. 2017 Nov;25(11):1290. doi: 10.1038/ejhg.2017.147. Eur J Hum Genet. 2017. PMID: 29023440 Free PMC article.
Reply: To PMID 23084378.
Wang BZ, Taranath D. Wang BZ, et al. Among authors: taranath d. J AAPOS. 2013 Feb;17(1):116. doi: 10.1016/j.jaapos.2012.11.003. Epub 2013 Jan 23. J AAPOS. 2013. PMID: 23352723 No abstract available.
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