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

Year Number of Results
1957 1
1958 3
1959 1
1960 2
1961 4
1965 1
1969 1
1970 3
1971 1
1972 1
1973 1
1974 3
1975 2
1976 4
1977 1
1978 9
1979 5
1980 2
1981 1
1982 6
1983 5
1984 6
1986 1
1988 1
1989 3
1990 4
1992 1
1993 2
1995 1
1996 1
2001 1
2005 1
2006 1
2007 1
2009 1
2010 2
2012 1
2013 2
2014 1
2016 2
2017 7
2018 7
2019 4
2020 2
2021 3
2022 4
Text availability
Article attribute
Article type
Publication date

Search Results

108 results
Results by year
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Page 1
SYT1-associated neurodevelopmental disorder: a case series.
Baker K, Gordon SL, Melland H, Bumbak F, Scott DJ, Jiang TJ, Owen D, Turner BJ, Boyd SG, Rossi M, Al-Raqad M, Elpeleg O, Peck D, Mancini GMS, Wilke M, Zollino M, Marangi G, Weigand H, Borggraefe I, Haack T, Stark Z, Sadedin S; Broad Center for Mendelian Genomics, Tan TY, Jiang Y, Gibbs RA, Ellingwood S, Amaral M, Kelley W, Kurian MA, Cousin MA, Raymond FL. Baker K, et al. Among authors: weigand h. Brain. 2018 Sep 1;141(9):2576-2591. doi: 10.1093/brain/awy209. Brain. 2018. PMID: 30107533 Free PMC article.
De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability.
Schalk A, Cousin MA, Dsouza NR, Challman TD, Wain KE, Powis Z, Minks K, Trimouille A, Lasseaux E, Lacombe D, Angelini C, Michaud V, Van-Gils J, Spataro N, Ruiz A, Gabau E, Stolerman E, Washington C, Louie R, Lanpher BC, Kemppainen JL, Innes M, Kooy F, Meuwissen M, Goldenberg A, Lecoquierre F, Vera G, Diderich KEM, Sheidley B, El Achkar CM, Park M, Hamdan FF, Michaud JL, Lewis AJ, Zweier C, Reis A, Wagner M, Weigand H, Journel H, Keren B, Passemard S, Mignot C, van Gassen K, Brilstra EH, Itzikowitz G, O'Heir E, Allen J, Donald KA, Korf BR, Skelton T, Thompson M, Robin NH, Rudy NL, Dobyns WB, Foss K, Zarate YA, Bosanko KA, Alembik Y, Durand B, Tran Mau-Them F, Ranza E, Blanc X, Antonarakis SE, McWalter K, Torti E, Millan F, Dameron A, Tokita M, Zimmermann MT, Klee EW, Piton A, Gerard B. Schalk A, et al. Among authors: weigand h. J Med Genet. 2021 Dec 15:jmedgenet-2021-107751. doi: 10.1136/jmedgenet-2021-107751. Online ahead of print. J Med Genet. 2021. PMID: 34930816 Free PMC article.
[Percutaneous nucleotomy].
Weigand H. Weigand H. Radiologe. 1993 Oct;33(10):581-4. Radiologe. 1993. PMID: 8234671 Review. German.
DNA barcode reference libraries for the monitoring of aquatic biota in Europe: Gap-analysis and recommendations for future work.
Weigand H, Beermann AJ, Čiampor F, Costa FO, Csabai Z, Duarte S, Geiger MF, Grabowski M, Rimet F, Rulik B, Strand M, Szucsich N, Weigand AM, Willassen E, Wyler SA, Bouchez A, Borja A, Čiamporová-Zaťovičová Z, Ferreira S, Dijkstra KB, Eisendle U, Freyhof J, Gadawski P, Graf W, Haegerbaeumer A, van der Hoorn BB, Japoshvili B, Keresztes L, Keskin E, Leese F, Macher JN, Mamos T, Paz G, Pešić V, Pfannkuchen DM, Pfannkuchen MA, Price BW, Rinkevich B, Teixeira MAL, Várbíró G, Ekrem T. Weigand H, et al. Sci Total Environ. 2019 Aug 15;678:499-524. doi: 10.1016/j.scitotenv.2019.04.247. Epub 2019 Apr 27. Sci Total Environ. 2019. PMID: 31077928 Free article. Review.
Nanoscale Near-Field Tomography of Surface States on (Bi0.5Sb0.5)2Te3.
Mooshammer F, Sandner F, Huber MA, Zizlsperger M, Weigand H, Plankl M, Weyrich C, Lanius M, Kampmeier J, Mussler G, Grützmacher D, Boland JL, Cocker TL, Huber R. Mooshammer F, et al. Among authors: weigand h. Nano Lett. 2018 Dec 12;18(12):7515-7523. doi: 10.1021/acs.nanolett.8b03008. Epub 2018 Nov 19. Nano Lett. 2018. PMID: 30419748
108 results