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

Year Number of Results
1972 1
1974 1
1975 3
1977 2
1978 2
1979 3
1980 4
1981 5
1982 3
1983 4
1984 6
1985 8
1986 13
1987 7
1988 10
1989 10
1990 9
1991 6
1992 6
1993 10
1994 9
1995 7
1996 14
1997 15
1998 9
1999 6
2000 5
2001 12
2002 9
2003 13
2004 11
2005 5
2006 9
2007 8
2008 14
2009 6
2010 15
2011 10
2012 9
2013 9
2014 8
2015 10
2016 6
2017 10
2018 5
2019 6
2020 2
2021 4
2022 11
2023 9
2024 7
2025 5

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362 results

Results by year

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Page 1
Diagnostic genome sequencing improves diagnostic yield: a prospective single-centre study in 1000 patients with inherited eye diseases.
Weisschuh N, Mazzola P, Zuleger T, Schaeferhoff K, Kühlewein L, Kortüm F, Witt D, Liebmann A, Falb R, Pohl L, Reith M, Stühn LG, Bertrand M, Müller A, Casadei N, Kelemen O, Kelbsch C, Kernstock C, Richter P, Sadler F, Demidov G, Schütz L, Admard J, Sturm M, Grasshoff U, Tonagel F, Heinrich T, Nasser F, Wissinger B, Ossowski S, Kohl S, Riess O, Stingl K, Haack TB. Weisschuh N, et al. Among authors: reith m. J Med Genet. 2024 Jan 19;61(2):186-195. doi: 10.1136/jmg-2023-109470. J Med Genet. 2024. PMID: 37734845 Free PMC article.
SLC6 transporter oligomerization.
Jayaraman K, Das AK, Luethi D, Szöllősi D, Schütz GJ, Reith MEA, Sitte HH, Stockner T. Jayaraman K, et al. Among authors: reith mea. J Neurochem. 2021 May;157(4):919-929. doi: 10.1111/jnc.15145. Epub 2020 Aug 28. J Neurochem. 2021. PMID: 32767560 Free PMC article. Review.
Molecular Mechanisms of Amphetamines.
Reith MEA, Gnegy ME. Reith MEA, et al. Handb Exp Pharmacol. 2020;258:265-297. doi: 10.1007/164_2019_251. Handb Exp Pharmacol. 2020. PMID: 31286212 Review.
Sequence-Defined Mikto-Arm Star-Shaped Macromolecules.
Reith MA, De Franceschi I, Soete M, Badi N, Aksakal R, Du Prez FE. Reith MA, et al. J Am Chem Soc. 2022 Apr 27;144(16):7236-7244. doi: 10.1021/jacs.2c00145. Epub 2022 Apr 15. J Am Chem Soc. 2022. PMID: 35426304
[Pharmacotherapy of ABCA4-associated Retinal Dystrophies].
Gerhardt M, Stingl K, Reith M. Gerhardt M, et al. Among authors: reith m. Klin Monbl Augenheilkd. 2025 Mar;242(3):205-212. doi: 10.1055/a-2533-1009. Epub 2025 Mar 24. Klin Monbl Augenheilkd. 2025. PMID: 40127654 Review. German.
Variants in CFAP410 cause a range of retinal and skeletal phenotypes.
Schmidt RE, Pohodich AE, Birch D, Jones K, Lam BL, Jung EH, Jain N, Georgiou M, Mahroo OA, Webster AR, Michaelides M, Bakall B, Iannaccone A, Vincent A, Parameswarappa DC, Heon E, Scholl HPN, Janeschitz-Kriegl L, Traboulsi EI, Zein W, Brooks BP, Cukras C, Hufnagel R, Aleman TS, Sylla MM, Tsang SH, Alabek M, Sahel J, Gorin MB, van Genderen MM, Stingl K, Reith M, Kohl S, Amaral RAS, Sallum JMF, Vincent AL, Hull S, Duncan JL, Hanson JVM, Tedeus M, Maggi J, Graf U, Koller S, Berger W, Gerth-Kahlert C, Marra M, Everett LA, Yang P, Pennesi ME. Schmidt RE, et al. Among authors: reith m. NPJ Genom Med. 2025 Apr 17;10(1):32. doi: 10.1038/s41525-025-00489-1. NPJ Genom Med. 2025. PMID: 40246852 Free PMC article.
Therapy with voretigene neparvovec. How to measure success?
Stingl K, Kempf M, Jung R, Kortüm F, Righetti G, Reith M, Dimopoulos S, Ott S, Kohl S, Stingl K. Stingl K, et al. Among authors: reith m. Prog Retin Eye Res. 2023 Jan;92:101115. doi: 10.1016/j.preteyeres.2022.101115. Epub 2022 Sep 10. Prog Retin Eye Res. 2023. PMID: 36096933 Free article. Review.
Characterising the refractive error in paediatric patients with congenital stationary night blindness: a multicentre study.
Igelman AD, White E, Tayyib A, Everett L, Vincent A, Heon E, Zeitz C, Michaelides M, Mahroo OA, Katta M, Webster A, Preising M, Lorenz B, Khateb S, Banin E, Sharon D, Luski S, Van Den Broeck F, Leroy BP, De Baere E, Walraedt S, Stingl K, Kuehlewein L, Kohl S, Reith M, Fulton A, Raghuram A, Meunier I, Dollfus H, Aleman TS, Bedoukian EC, O'Neil EC, Krauss E, Vincent A, Jordan C, Iannaccone A, Sen P, Sundaramurthy S, Nagasamy S, Balikova I, Casteels I, Borooah S, Yassin S, Nagiel A, Schwartz H, Zanlonghi X, Gottlob I, McLean RJ, Munier FL, Stephenson A, Sisk R, Koenekoop R, Wilson LB, Fredrick D, Choi D, Yang P, Pennesi ME. Igelman AD, et al. Among authors: reith m. Br J Ophthalmol. 2025 Jan 28;109(2):286-292. doi: 10.1136/bjo-2023-323747. Br J Ophthalmol. 2025. PMID: 39079892
The dopamine transporter gene SLC6A3: multidisease risks.
Reith MEA, Kortagere S, Wiers CE, Sun H, Kurian MA, Galli A, Volkow ND, Lin Z. Reith MEA, et al. Mol Psychiatry. 2022 Feb;27(2):1031-1046. doi: 10.1038/s41380-021-01341-5. Epub 2021 Oct 14. Mol Psychiatry. 2022. PMID: 34650206 Free PMC article.
362 results