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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 9

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380 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.
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.
[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.
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.
Clinical application of advanced MR methods in children: points to consider.
Wilke M, Groeschel S, Lorenzen A, Rona S, Schuhmann MU, Ernemann U, Krägeloh-Mann I. Wilke M, et al. Ann Clin Transl Neurol. 2018 Sep 27;5(11):1434-1455. doi: 10.1002/acn3.658. eCollection 2018 Nov. Ann Clin Transl Neurol. 2018. PMID: 30480038 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
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.
380 results