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

Year Number of Results
1951 1
1986 1
1987 1
1988 1
1989 2
1990 1
1991 1
1995 2
1996 2
1997 9
1998 6
1999 1
2000 1
2001 4
2002 3
2003 2
2004 5
2005 5
2006 6
2007 3
2008 6
2009 4
2010 5
2011 3
2012 4
2013 1
2014 1
2015 1
2016 2
2017 1
2018 3
2019 3
2020 1
2021 1
2023 1
2024 0

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87 results

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Page 1
Analysis of shared heritability in common disorders of the brain.
Brainstorm Consortium; Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, Lee PH, Turley P, Grenier-Boley B, Chouraki V, Kamatani Y, Berr C, Letenneur L, Hannequin D, Amouyel P, Boland A, Deleuze JF, Duron E, Vardarajan BN, Reitz C, Goate AM, Huentelman MJ, Kamboh MI, Larson EB, Rogaeva E, St George-Hyslop P, Hakonarson H, Kukull WA, Farrer LA, Barnes LL, Beach TG, Demirci FY, Head E, Hulette CM, Jicha GA, Kauwe JSK, Kaye JA, Leverenz JB, Levey AI, Lieberman AP, Pankratz VS, Poon WW, Quinn JF, Saykin AJ, Schneider LS, Smith AG, Sonnen JA, Stern RA, Van Deerlin VM, Van Eldik LJ, Harold D, Russo G, Rubinsztein DC, Bayer A, Tsolaki M, Proitsi P, Fox NC, Hampel H, Owen MJ, Mead S, Passmore P, Morgan K, Nöthen MM, Rossor M, Lupton MK, Hoffmann P, Kornhuber J, Lawlor B, McQuillin A, Al-Chalabi A, Bis JC, Ruiz A, Boada M, Seshadri S, Beiser A, Rice K, van der Lee SJ, De Jager PL, Geschwind DH, Riemenschneider M, Riedel-Heller S, Rotter JI, Ransmayr G, Hyman BT, Cruchaga C, Alegret M, Winsvold B, Palta P, Farh KH, Cuenca-Leon E, Furlotte N, Kurth T, Ligthart L, Terwindt GM, Freilinge… See abstract for full author list ➔ Brainstorm Consortium, et al. Among authors: stroink h. Science. 2018 Jun 22;360(6395):eaap8757. doi: 10.1126/science.aap8757. Science. 2018. PMID: 29930110 Free PMC article.
Phakomatosis pigmentovascularis.
Van Gysel D, Oranje AP, Stroink H, Simonsz HJ. Van Gysel D, et al. Among authors: stroink h. Pediatr Dermatol. 1996 Jan-Feb;13(1):33-5. doi: 10.1111/j.1525-1470.1996.tb01184.x. Pediatr Dermatol. 1996. PMID: 8919522 Free article.
How confident are we of the diagnosis of epilepsy?
van Donselaar CA, Stroink H, Arts WF; Dutch Study Group of Epilepsy in Childhood. van Donselaar CA, et al. Among authors: stroink h. Epilepsia. 2006;47 Suppl 1:9-13. doi: 10.1111/j.1528-1167.2006.00653.x. Epilepsia. 2006. PMID: 17044819 Free article. Review.
[Tuberous sclerosis].
Stroink H, Oranje AP, Hoff M, Lindhout D, Willems MH, Fleury P. Stroink H, et al. Ned Tijdschr Geneeskd. 1990 Aug 11;134(32):1535-40. Ned Tijdschr Geneeskd. 1990. PMID: 2202910 Review. Dutch. No abstract available.
Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy.
Schijven D, Stevelink R, McCormack M, van Rheenen W, Luykx JJ, Koeleman BPC, Veldink JH; Project MinE ALS GWAS Consortium; International League Against Epilepsy Consortium on Complex Epilepsies. Schijven D, et al. Neurobiol Aging. 2020 Aug;92:153.e1-153.e5. doi: 10.1016/j.neurobiolaging.2020.04.011. Epub 2020 Apr 18. Neurobiol Aging. 2020. PMID: 32409253 Free PMC article.
Shared genetic basis between genetic generalized epilepsy and background electroencephalographic oscillations.
Stevelink R, Luykx JJ, Lin BD, Leu C, Lal D, Smith AW, Schijven D, Carpay JA, Rademaker K, Rodrigues Baldez RA, Devinsky O, Braun KPJ, Jansen FE, Smit DJA, Koeleman BPC; International League Against Epilepsy Consortium on Complex Epilepsies; Epi25 Collaborative. Stevelink R, et al. Epilepsia. 2021 Jul;62(7):1518-1527. doi: 10.1111/epi.16922. Epub 2021 May 18. Epilepsia. 2021. PMID: 34002374 Free PMC article.
87 results