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

Year Number of Results
1975 1
1976 1
1977 2
1980 1
1981 3
1984 2
1985 1
1986 2
1987 5
1988 2
1989 5
1990 2
1991 2
1992 1
1993 6
1994 1
1995 3
1996 3
1997 4
1998 4
1999 2
2000 5
2001 5
2002 6
2003 8
2004 8
2005 4
2006 3
2007 5
2008 6
2009 11
2010 8
2011 6
2012 5
2013 6
2014 2
2015 4
2016 7
2017 6
2018 7
2019 10
2020 18
2021 9
2022 4
Text availability
Article attribute
Article type
Publication date

Search Results

183 results
Results by year
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Page 1
Choroideremia.
MacDonald IM, Hume S, Zhai Y, Xu M. MacDonald IM, et al. 2003 Feb 21 [updated 2021 Mar 4]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2003 Feb 21 [updated 2021 Mar 4]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301511 Free Books & Documents. Review.
Bestrophinopathies.
MacDonald IM, Lee T, Lawrence J. MacDonald IM, et al. 2003 Sep 30 [updated 2020 Jul 16]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2003 Sep 30 [updated 2020 Jul 16]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301346 Free Books & Documents. Review.
Choroideremia.
Dimopoulos IS, Radziwon A, St Laurent CD, MacDonald IM. Dimopoulos IS, et al. Among authors: macdonald im. Curr Opin Ophthalmol. 2017 Sep;28(5):410-415. doi: 10.1097/ICU.0000000000000392. Curr Opin Ophthalmol. 2017. PMID: 28520608 Review.
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.
Khan M, Cornelis SS, Pozo-Valero MD, Whelan L, Runhart EH, Mishra K, Bults F, AlSwaiti Y, AlTalbishi A, De Baere E, Banfi S, Banin E, Bauwens M, Ben-Yosef T, Boon CJF, van den Born LI, Defoort S, Devos A, Dockery A, Dudakova L, Fakin A, Farrar GJ, Sallum JMF, Fujinami K, Gilissen C, Glavač D, Gorin MB, Greenberg J, Hayashi T, Hettinga YM, Hoischen A, Hoyng CB, Hufendiek K, Jägle H, Kamakari S, Karali M, Kellner U, Klaver CCW, Kousal B, Lamey TM, MacDonald IM, Matynia A, McLaren TL, Mena MD, Meunier I, Miller R, Newman H, Ntozini B, Oldak M, Pieterse M, Podhajcer OL, Puech B, Ramesar R, Rüther K, Salameh M, Salles MV, Sharon D, Simonelli F, Spital G, Steehouwer M, Szaflik JP, Thompson JA, Thuillier C, Tracewska AM, van Zweeden M, Vincent AL, Zanlonghi X, Liskova P, Stöhr H, Roach JN, Ayuso C, Roberts L, Weber BHF, Dhaenens CM, Cremers FPM. Khan M, et al. Among authors: macdonald im. Genet Med. 2020 Jul;22(7):1235-1246. doi: 10.1038/s41436-020-0787-4. Epub 2020 Apr 20. Genet Med. 2020. PMID: 32307445 Free article.
X-Linked Congenital Retinoschisis.
Sieving PA, MacDonald IM, Hoang S. Sieving PA, et al. Among authors: macdonald im. 2003 Oct 24 [updated 2020 Nov 5]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2003 Oct 24 [updated 2020 Nov 5]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301401 Free Books & Documents. Review.
X-Linked Congenital Stationary Night Blindness.
MacDonald IM, Hoang S, Tuupanen S. MacDonald IM, et al. 2008 Jan 16 [updated 2019 Jul 3]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2008 Jan 16 [updated 2019 Jul 3]. In: Adam MP, Everman DB, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301423 Free Books & Documents. Review.
RP1L1 and inherited photoreceptor disease: A review.
Noel NCL, MacDonald IM. Noel NCL, et al. Among authors: macdonald im. Surv Ophthalmol. 2020 Nov-Dec;65(6):725-739. doi: 10.1016/j.survophthal.2020.04.005. Epub 2020 Apr 30. Surv Ophthalmol. 2020. PMID: 32360662 Free article. Review.
Choroideremia gene testing.
MacDonald IM, Sereda C, McTaggart K, Mah D. MacDonald IM, et al. Expert Rev Mol Diagn. 2004 Jul;4(4):478-84. doi: 10.1586/14737159.4.4.478. Expert Rev Mol Diagn. 2004. PMID: 15225095 Review.
183 results