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

Year Number of Results
1983 1
1991 1
1993 1
2003 1
2004 2
2015 1
2016 4
2017 1
2018 3
2019 2
2020 3
2021 2
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19 results
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Page 1
Modulation of microRNA processing by 5-lipoxygenase.
Uebbing S, Kreiß M, Scholl F, Häfner AK, Sürün D, Garscha U, Werz O, Basavarajappa D, Samuelsson B, Rådmark O, Suess B, Steinhilber D. Uebbing S, et al. Among authors: kreiss m. FASEB J. 2021 Feb;35(2):e21193. doi: 10.1096/fj.202002108R. Epub 2020 Nov 17. FASEB J. 2021. PMID: 33205517
De Novo Duplication of 11p15 Associated With Congenital Diaphragmatic Hernia.
Dworschak GC, Engels H, Becker J, Soellner L, Eggermann T, Kipfmueller F, Müller A, Reutter H, Kreiß M. Dworschak GC, et al. Among authors: kreiss m. Front Pediatr. 2018 Apr 25;6:116. doi: 10.3389/fped.2018.00116. eCollection 2018. Front Pediatr. 2018. PMID: 29922638 Free PMC article.
Bi-allelic truncating mutations in VWA1 cause neuromyopathy.
Deschauer M, Hengel H, Rupprich K, Kreiß M, Schlotter-Weigel B, Grimmel M, Admard J, Schneider I, Alhaddad B, Gazou A, Sturm M, Vorgerd M, Balousha G, Balousha O, Falna M, Kirschke JS, Kornblum C, Jordan B, Kraya T, Strom TM, Weis J, Schöls L, Schara U, Zierz S, Riess O, Meitinger T, Haack TB. Deschauer M, et al. Among authors: kreiss m. Brain. 2021 Mar 3;144(2):574-583. doi: 10.1093/brain/awaa418. Brain. 2021. PMID: 33459760
Loss-of-function variants in HIVEP2 are a cause of intellectual disability.
Srivastava S, Engels H, Schanze I, Cremer K, Wieland T, Menzel M, Schubach M, Biskup S, Kreiß M, Endele S, Strom TM, Wieczorek D, Zenker M, Gupta S, Cohen J, Zink AM, Naidu S. Srivastava S, et al. Among authors: kreiss m. Eur J Hum Genet. 2016 Apr;24(4):556-61. doi: 10.1038/ejhg.2015.151. Epub 2015 Jul 8. Eur J Hum Genet. 2016. PMID: 26153216 Free PMC article.
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