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

Year Number of Results
1965 1
1973 1
1975 1
1978 1
1982 1
1986 1
1988 4
1989 2
1990 2
1991 5
1992 4
1993 3
1994 2
1995 3
1996 4
1997 2
1998 2
2000 4
2001 11
2002 11
2003 12
2004 9
2005 13
2006 12
2007 10
2008 20
2009 20
2010 20
2011 15
2012 16
2013 19
2014 17
2015 20
2016 24
2017 22
2018 18
2019 16
2020 21
2021 29
2022 21
2023 2
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373 results
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Page 1
Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism.
Chopra M, McEntagart M, Clayton-Smith J, Platzer K, Shukla A, Girisha KM, Kaur A, Kaur P, Pfundt R, Veenstra-Knol H, Mancini GMS, Cappuccio G, Brunetti-Pierri N, Kortüm F, Hempel M, Denecke J, Lehman A; CAUSES Study; Kleefstra T, Stuurman KE, Wilke M, Thompson ML, Bebin EM, Bijlsma EK, Hoffer MJV, Peeters-Scholte C, Slavotinek A, Weiss WA, Yip T, Hodoglugil U, Whittle A, diMonda J, Neira J, Yang S, Kirby A, Pinz H, Lechner R, Sleutels F, Helbig I, McKeown S, Helbig K, Willaert R, Juusola J, Semotok J, Hadonou M, Short J; Genomics England Research Consortium; Yachelevich N, Lala S, Fernández-Jaen A, Pelayo JP, Klöckner C, Kamphausen SB, Abou Jamra R, Arelin M, Innes AM, Niskakoski A, Amin S, Williams M, Evans J, Smithson S, Smedley D, de Burca A, Kini U, Delatycki MB, Gallacher L, Yeung A, Pais L, Field M, Martin E, Charles P, Courtin T, Keren B, Iascone M, Cereda A, Poke G, Abadie V, Chalouhi C, Parthasarathy P, Halliday BJ, Robertson SP, Lyonnet S, Amiel J, Gordon CT. Chopra M, et al. Among authors: wilke m. Am J Hum Genet. 2021 Jun 3;108(6):1138-1150. doi: 10.1016/j.ajhg.2021.04.007. Epub 2021 Apr 27. Am J Hum Genet. 2021. PMID: 33909992 Free PMC article.
International consensus recommendations on the diagnostic work-up for malformations of cortical development.
Oegema R, Barakat TS, Wilke M, Stouffs K, Amrom D, Aronica E, Bahi-Buisson N, Conti V, Fry AE, Geis T, Andres DG, Parrini E, Pogledic I, Said E, Soler D, Valor LM, Zaki MS, Mirzaa G, Dobyns WB, Reiner O, Guerrini R, Pilz DT, Hehr U, Leventer RJ, Jansen AC, Mancini GMS, Di Donato N. Oegema R, et al. Among authors: wilke m. Nat Rev Neurol. 2020 Nov;16(11):618-635. doi: 10.1038/s41582-020-0395-6. Epub 2020 Sep 7. Nat Rev Neurol. 2020. PMID: 32895508 Free PMC article. Review.
Reduced alpha amplitudes predict perceptual suppression.
Poland E, Bhonsle A, Steinmann I, Wilke M. Poland E, et al. Among authors: wilke m. Sci Rep. 2021 Jun 22;11(1):13040. doi: 10.1038/s41598-021-92404-8. Sci Rep. 2021. PMID: 34158567 Free PMC article.
[Current strategies against multi-drug resistant organisms].
Pletz MW, Eckmann C, Hagel S, Heppner HJ, Huber K, Kämmerer W, Schmitz FJ, Wilke M, Grabein B. Pletz MW, et al. Among authors: wilke m. Dtsch Med Wochenschr. 2015 Jun;140(13):975-81. doi: 10.1055/s-0041-102452. Epub 2015 Jun 26. Dtsch Med Wochenschr. 2015. PMID: 26115132 Review. German.
Combining brain perturbation and neuroimaging in non-human primates.
Klink PC, Aubry JF, Ferrera VP, Fox AS, Froudist-Walsh S, Jarraya B, Konofagou EE, Krauzlis RJ, Messinger A, Mitchell AS, Ortiz-Rios M, Oya H, Roberts AC, Roe AW, Rushworth MFS, Sallet J, Schmid MC, Schroeder CE, Tasserie J, Tsao DY, Uhrig L, Vanduffel W, Wilke M, Kagan I, Petkov CI. Klink PC, et al. Among authors: wilke m. Neuroimage. 2021 Jul 15;235:118017. doi: 10.1016/j.neuroimage.2021.118017. Epub 2021 Mar 29. Neuroimage. 2021. PMID: 33794355 Free article. Review.
Animal models of cystic fibrosis.
Scholte BJ, Davidson DJ, Wilke M, De Jonge HR. Scholte BJ, et al. Among authors: wilke m. J Cyst Fibros. 2004 Aug;3 Suppl 2:183-90. doi: 10.1016/j.jcf.2004.05.039. J Cyst Fibros. 2004. PMID: 15463956 Free article. Review.
Functional magnetic resonance imaging in pediatrics.
Wilke M, Holland SK, Myseros JS, Schmithorst VJ, Ball WS Jr. Wilke M, et al. Neuropediatrics. 2003 Jun;34(5):225-33. doi: 10.1055/s-2003-43260. Neuropediatrics. 2003. PMID: 14598227 Free PMC article. Review.
Expanding the phenotype of DNAJC30-associated Leigh syndrome.
Zawadzka M, Krygier M, Pawłowicz M, Wilke MVMB, Rutkowska K, Gueguen N, Desquiret-Dumas V, Klee EW, Schimmenti LA, Sławek J, Procaccio V, Płoski R, Mazurkiewicz-Bełdzińska M. Zawadzka M, et al. Among authors: wilke mvmb. Clin Genet. 2022 Nov;102(5):438-443. doi: 10.1111/cge.14196. Epub 2022 Jul 29. Clin Genet. 2022. PMID: 35861300
373 results