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

Year Number of Results
1959 1
1965 1
1967 1
1972 1
1974 1
1978 1
1979 4
1980 1
1981 3
1982 2
1983 5
1984 5
1985 10
1986 9
1987 5
1988 14
1989 15
1990 14
1991 17
1992 39
1993 20
1994 28
1995 28
1996 26
1997 16
1998 19
1999 12
2000 15
2001 10
2002 7
2003 11
2004 7
2005 14
2006 8
2007 6
2008 4
2009 6
2010 12
2011 11
2012 9
2013 13
2014 8
2015 7
2016 1
2017 4
2019 4
2020 4
2021 4
2022 3
2023 8
2024 1

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461 results

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Page 1
Genotyping and population characteristics of the China Kadoorie Biobank.
Walters RG, Millwood IY, Lin K, Schmidt Valle D, McDonnell P, Hacker A, Avery D, Edris A, Fry H, Cai N, Kretzschmar WW, Ansari MA, Lyons PA, Collins R, Donnelly P, Hill M, Peto R, Shen H, Jin X, Nie C, Xu X, Guo Y, Yu C, Lv J, Clarke RJ, Li L, Chen Z; China Kadoorie Biobank Collaborative Group. Walters RG, et al. Among authors: mcdonnell p. Cell Genom. 2023 Jul 20;3(8):100361. doi: 10.1016/j.xgen.2023.100361. eCollection 2023 Aug 9. Cell Genom. 2023. PMID: 37601966 Free PMC article.
Refractive surgery.
McDonnell PJ. McDonnell PJ. Br J Ophthalmol. 1999 Nov;83(11):1257-60. doi: 10.1136/bjo.83.11.1257. Br J Ophthalmol. 1999. PMID: 10535852 Free PMC article. Review. No abstract available.
Intrafamilial variability in SLC6A1-related neurodevelopmental disorders.
Kassabian B, Fenger CD, Willems M, Aledo-Serrano A, Linnankivi T, McDonnell PP, Lusk L, Jepsen BS, Bayat M, Kattentidt A, Vidal AA, Valero-Lopez G, Alarcon-Martinez H, Goodspeed K, van Slegtenhorst M, Barakat TS, Møller RS, Johannesen KM, Rubboli G. Kassabian B, et al. Among authors: mcdonnell pp. Front Neurosci. 2023 Jul 12;17:1219262. doi: 10.3389/fnins.2023.1219262. eCollection 2023. Front Neurosci. 2023. PMID: 37502687 Free PMC article.
Rotational autokeratoplasty.
McDonnell PJ, Falcon MG. McDonnell PJ, et al. Eye (Lond). 1989;3 ( Pt 5):576-80. doi: 10.1038/eye.1989.90. Eye (Lond). 1989. PMID: 2630334
Spontaneous pseudophakia.
Kirwan JF, Potamitis T, McDonnell PJ. Kirwan JF, et al. Among authors: mcdonnell pj. Eye (Lond). 1994;8 ( Pt 1):146. doi: 10.1038/eye.1994.31. Eye (Lond). 1994. PMID: 8013712 No abstract available.
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
Paul MS, Michener SL, Pan H, Chan H, Pfliger JM, Rosenfeld JA, Lerma VC, Tran A, Longley MA, Lewis RA, Weisz-Hubshman M, Bekheirnia MR, Bekheirnia N, Massingham L, Zech M, Wagner M, Engels H, Cremer K, Mangold E, Peters S, Trautmann J, Mester JL, Guillen Sacoto MJ, Person R, McDonnell PP, Cohen SR, Lusk L, Cohen ASA, Le Pichon JB, Pastinen T, Zhou D, Engleman K, Racine C, Faivre L, Moutton S, Denommé-Pichon AS, Koh HY, Poduri A, Bolton J, Knopp C, Julia Suh DS, Maier A, Toosi MB, Karimiani EG, Maroofian R, Schaefer GB, Ramakumaran V, Vasudevan P, Prasad C, Osmond M, Schuhmann S, Vasileiou G, Russ-Hall S, Scheffer IE, Carvill GL, Mefford H; Undiagnosed Diseases Network; Bacino CA, Lee BH, Chao HT. Paul MS, et al. Among authors: mcdonnell pp. Am J Hum Genet. 2024 Jan 4;111(1):96-118. doi: 10.1016/j.ajhg.2023.12.004. Am J Hum Genet. 2024. PMID: 38181735
461 results