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

Year Number of Results
1993 1
1994 1
1995 2
1996 4
1999 4
2000 3
2001 1
2002 3
2003 1
2004 1
2006 2
2007 2
2008 3
2009 1
2010 1
2013 2
2014 2
2015 1
2016 5
2017 6
2018 1
2020 3
2022 2
2024 0

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46 results

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Page 1
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease.
Holstege H, Hulsman M, Charbonnier C, Grenier-Boley B, Quenez O, Grozeva D, van Rooij JGJ, Sims R, Ahmad S, Amin N, Norsworthy PJ, Dols-Icardo O, Hummerich H, Kawalia A, Amouyel P, Beecham GW, Berr C, Bis JC, Boland A, Bossù P, Bouwman F, Bras J, Campion D, Cochran JN, Daniele A, Dartigues JF, Debette S, Deleuze JF, Denning N, DeStefano AL, Farrer LA, Fernández MV, Fox NC, Galimberti D, Genin E, Gille JJP, Le Guen Y, Guerreiro R, Haines JL, Holmes C, Ikram MA, Ikram MK, Jansen IE, Kraaij R, Lathrop M, Lemstra AW, Lleó A, Luckcuck L, Mannens MMAM, Marshall R, Martin ER, Masullo C, Mayeux R, Mecocci P, Meggy A, Mol MO, Morgan K, Myers RM, Nacmias B, Naj AC, Napolioni V, Pasquier F, Pastor P, Pericak-Vance MA, Raybould R, Redon R, Reinders MJT, Richard AC, Riedel-Heller SG, Rivadeneira F, Rousseau S, Ryan NS, Saad S, Sanchez-Juan P, Schellenberg GD, Scheltens P, Schott JM, Seripa D, Seshadri S, Sie D, Sistermans EA, Sorbi S, van Spaendonk R, Spalletta G, Tesi N, Tijms B, Uitterlinden AG, van der Lee SJ, Visser PJ, Wagner M, Wallon D, Wang LS, Zarea A, Clarimon J, van Swieten JC, Greicius MD, Yokoyama JS, Cruchaga C, Hardy J, Ramirez A, Mead S, van der Flier WM, van Duijn CM, W… See abstract for full author list ➔ Holstege H, et al. Among authors: norsworthy pj. Nat Genet. 2022 Dec;54(12):1786-1794. doi: 10.1038/s41588-022-01208-7. Epub 2022 Nov 21. Nat Genet. 2022. PMID: 36411364 Free PMC article.
Hepatitis C in Egypt - past, present, and future.
Elgharably A, Gomaa AI, Crossey MM, Norsworthy PJ, Waked I, Taylor-Robinson SD. Elgharably A, et al. Among authors: norsworthy pj. Int J Gen Med. 2016 Dec 20;10:1-6. doi: 10.2147/IJGM.S119301. eCollection 2017. Int J Gen Med. 2016. PMID: 28053553 Free PMC article. Review.
Complement components and their autoantibodies.
Norsworthy P, Davies KA. Norsworthy P, et al. Mol Biotechnol. 2003 Mar;23(3):259-70. doi: 10.1385/MB:23:3:259. Mol Biotechnol. 2003. PMID: 12665695 Review.
Hereditary C1q deficiency and systemic lupus erythematosus.
Bowness P, Davies KA, Norsworthy PJ, Athanassiou P, Taylor-Wiedeman J, Borysiewicz LK, Meyer PA, Walport MJ. Bowness P, et al. Among authors: norsworthy pj. QJM. 1994 Aug;87(8):455-64. QJM. 1994. PMID: 7922299 Review.
Increased brain-predicted aging in treated HIV disease.
Cole JH, Underwood J, Caan MW, De Francesco D, van Zoest RA, Leech R, Wit FW, Portegies P, Geurtsen GJ, Schmand BA, Schim van der Loeff MF, Franceschi C, Sabin CA, Majoie CB, Winston A, Reiss P, Sharp DJ; COBRA collaboration. Cole JH, et al. Neurology. 2017 Apr 4;88(14):1349-1357. doi: 10.1212/WNL.0000000000003790. Epub 2017 Mar 3. Neurology. 2017. PMID: 28258081 Free PMC article.
Malaria susceptibility and CD36 mutation.
Aitman TJ, Cooper LD, Norsworthy PJ, Wahid FN, Gray JK, Curtis BR, McKeigue PM, Kwiatkowski D, Greenwood BM, Snow RW, Hill AV, Scott J. Aitman TJ, et al. Among authors: norsworthy pj. Nature. 2000 Jun 29;405(6790):1015-6. doi: 10.1038/35016636. Nature. 2000. PMID: 10890433 No abstract available.
Immune complex processing in C1q-deficient mice.
Nash JT, Taylor PR, Botto M, Norsworthy PJ, Davies KA, Walport MJ. Nash JT, et al. Among authors: norsworthy pj. Clin Exp Immunol. 2001 Feb;123(2):196-202. doi: 10.1046/j.1365-2249.2001.01459.x. Clin Exp Immunol. 2001. PMID: 11207648 Free PMC article.
Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes.
Schramm C, Charbonnier C, Zaréa A, Lacour M, Wallon D; CNRMAJ collaborators; Boland A, Deleuze JF, Olaso R; ADES consortium; Alarcon F, Campion D, Nuel G, Nicolas G. Schramm C, et al. Genome Med. 2022 Jun 28;14(1):69. doi: 10.1186/s13073-022-01070-6. Genome Med. 2022. PMID: 35761418 Free PMC article.
46 results