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

Year Number of Results
1945 2
1946 1
1953 2
1967 2
1970 1
1971 2
1972 1
1973 4
1975 2
1977 2
1978 1
1979 1
1980 5
1981 3
1982 4
1983 4
1984 2
1985 5
1986 1
1987 3
1988 10
1989 9
1990 6
1991 6
1992 9
1993 9
1994 8
1995 17
1996 13
1997 13
1998 20
1999 12
2000 17
2001 19
2002 22
2003 24
2004 28
2005 36
2006 30
2007 31
2008 31
2009 30
2010 33
2011 34
2012 36
2013 53
2014 47
2015 49
2016 39
2017 37
2018 30
2019 27
2020 36
2021 35
2022 46
2023 47
2024 38
2025 43

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971 results

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Page 1
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology.
Oppermann H, Marcos-Grañeda E, Weiss LA, Gurnett CA, Jelsig AM, Vineke SH, Isidor B, Mercier S, Magnussen K, Zacher P, Hashim M, Pagnamenta AT, Race S, Srivastava S, Frazier Z, Maiwald R, Pergande M, Milani D, Rinelli M, Levy J, Krey I, Fontana P, Lonardo F, Riley S, Kretzer J, Rankin J, Reis LM, Semina EV, Reuter MS, Scherer SW, Iascone M, Weis D, Fagerberg CR, Brasch-Andersen C, Hansen LK, Kuechler A, Noble N, Gardham A, Tenney J, Rathore G, Beck-Woedl S, Haack TB, Pavlidou DC, Atallah I, Vodopiutz J, Janecke AR, Hsieh TC, Lesmann H, Klinkhammer H, Krawitz PM, Lemke JR, Jamra RA, Nieto M, Tümer Z, Platzer K. Oppermann H, et al. Among authors: reuter ms. Eur J Hum Genet. 2023 Nov;31(11):1251-1260. doi: 10.1038/s41431-023-01445-2. Epub 2023 Aug 30. Eur J Hum Genet. 2023. PMID: 37644171 Free PMC article.
Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental Disorders.
Reuter MS, Tawamie H, Buchert R, Hosny Gebril O, Froukh T, Thiel C, Uebe S, Ekici AB, Krumbiegel M, Zweier C, Hoyer J, Eberlein K, Bauer J, Scheller U, Strom TM, Hoffjan S, Abdelraouf ER, Meguid NA, Abboud A, Al Khateeb MA, Fakher M, Hamdan S, Ismael A, Muhammad S, Abdallah E, Sticht H, Wieczorek D, Reis A, Abou Jamra R. Reuter MS, et al. JAMA Psychiatry. 2017 Mar 1;74(3):293-299. doi: 10.1001/jamapsychiatry.2016.3798. JAMA Psychiatry. 2017. PMID: 28097321
An update on recent developments at JEB.
Reuter M. Reuter M. J Evol Biol. 2022 Jul;35(7):903-904. doi: 10.1111/jeb.14054. J Evol Biol. 2022. PMID: 35785455 Free article. No abstract available.
SuperSAGE.
Matsumura H, Ito A, Saitoh H, Winter P, Kahl G, Reuter M, Krüger DH, Terauchi R. Matsumura H, et al. Among authors: reuter m. Cell Microbiol. 2005 Jan;7(1):11-8. doi: 10.1111/j.1462-5822.2004.00478.x. Cell Microbiol. 2005. PMID: 15617519 Review.
Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus.
Scala M, Bradley CA, Howe JL, Trost B, Salazar NB, Shum C, Mendes M, Reuter MS, Anagnostou E, MacDonald JR, Ko SY, Frankland PW, Charlebois J, Elsabbagh M, Granger L, Anadiotis G, Pullano V, Brusco A, Keller R, Parisotto S, Pedro HF, Lusk L, McDonnell PP, Helbig I, Mullegama SV; Undiagnosed Diseases Network; Douine ED, Corona RI, Russell BE, Nelson SF, Graziano C, Schwab M, Simone L, Zara F, Scherer SW. Scala M, et al. Among authors: reuter ms. Am J Hum Genet. 2025 Jan 2;112(1):154-167. doi: 10.1016/j.ajhg.2024.11.003. Epub 2024 Dec 19. Am J Hum Genet. 2025. PMID: 39706195 Free PMC article.
Microglia and CD8+ T cell activation precede neuronal loss in a murine model of spastic paraplegia 15.
Frolov A, Huang H, Schütz D, Köhne M, Blank-Stein N, Osei-Sarpong C, Büttner M, Elmzzahi T, Khundadze M, Zahid M, Reuter M, Becker M, De Domenico E, Bonaguro L, Kallies A, Morrison H, Hübner CA, Händler K, Stumm R, Mass E, Beyer MD. Frolov A, et al. Among authors: reuter m. J Exp Med. 2025 Jul 7;222(7):e20232357. doi: 10.1084/jem.20232357. Epub 2025 Apr 23. J Exp Med. 2025. PMID: 40266307 Free PMC article.
Mid-space-independent deformable image registration.
Aganj I, Iglesias JE, Reuter M, Sabuncu MR, Fischl B. Aganj I, et al. Among authors: reuter m. Neuroimage. 2017 May 15;152:158-170. doi: 10.1016/j.neuroimage.2017.02.055. Epub 2017 Feb 24. Neuroimage. 2017. PMID: 28242316 Free PMC article.
971 results