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

Year Number of Results
1985 1
1986 1
1990 2
1992 1
1993 1
1994 4
1996 2
1997 5
1999 3
2000 1
2001 1
2002 3
2003 1
2004 4
2005 4
2006 3
2007 4
2008 5
2009 1
2010 1
2011 1
2013 3
2014 7
2015 5
2016 3
2017 1
2018 3
2019 2
2020 2
2021 8
2022 10
2023 5
2024 1

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91 results

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Page 1
Cutis marmorata telangiectatica congenita being caused by postzygotic GNA11 mutations.
Schuart C, Bassi A, Kapp F, Wieland I, Pagliazzi A, Losch H, Mazzatenta C, Bacci GM, Oranges T, Schanze D, Mohnike K, Nanda A, Fischer J, Zenker M, Happle R. Schuart C, et al. Among authors: wieland i. Eur J Med Genet. 2022 May;65(5):104472. doi: 10.1016/j.ejmg.2022.104472. Epub 2022 Mar 26. Eur J Med Genet. 2022. PMID: 35351629
Unusual phenotypes in patients with a pathogenic germline variant in DICER1.
Venger K, Elbracht M, Carlens J, Deutz P, Zeppernick F, Lassay L, Kratz C, Zenker M, Kim J, Stewart DR, Wieland I, Schultz KAP, Schwerk N, Kurth I, Kontny U. Venger K, et al. Among authors: wieland i. Fam Cancer. 2023 Oct;22(4):475-480. doi: 10.1007/s10689-021-00271-z. Epub 2021 Jul 31. Fam Cancer. 2023. PMID: 34331184 Free PMC article.
NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly.
Schanze I, Bunt J, Lim JWC, Schanze D, Dean RJ, Alders M, Blanchet P, Attié-Bitach T, Berland S, Boogert S, Boppudi S, Bridges CJ, Cho MT, Dobyns WB, Donnai D, Douglas J, Earl DL, Edwards TJ, Faivre L, Fregeau B, Genevieve D, Gérard M, Gatinois V, Holder-Espinasse M, Huth SF, Izumi K, Kerr B, Lacaze E, Lakeman P, Mahida S, Mirzaa GM, Morgan SM, Nowak C, Peeters H, Petit F, Pilz DT, Puechberty J, Reinstein E, Rivière JB, Santani AB, Schneider A, Sherr EH, Smith-Hicks C, Wieland I, Zackai E, Zhao X, Gronostajski RM, Zenker M, Richards LJ. Schanze I, et al. Among authors: wieland i. Am J Hum Genet. 2018 Nov 1;103(5):752-768. doi: 10.1016/j.ajhg.2018.10.006. Am J Hum Genet. 2018. PMID: 30388402 Free PMC article.
Achromatopsia-Visual Cortex Stability and Plasticity in the Absence of Functional Cones.
Molz B, Herbik A, Baseler HA, de Best P, Raz N, Gouws A, Ahmadi K, Lowndes R, McLean RJ, Gottlob I, Kohl S, Choritz L, Maguire J, Kanowski M, Käsmann-Kellner B, Wieland I, Banin E, Levin N, Morland AB, Hoffmann MB. Molz B, et al. Among authors: wieland i. Invest Ophthalmol Vis Sci. 2023 Oct 3;64(13):23. doi: 10.1167/iovs.64.13.23. Invest Ophthalmol Vis Sci. 2023. PMID: 37847226 Free PMC article.
Consensus Recommendations for Intramuscular COVID-19 Vaccination in Patients with Hemophilia.
Pfrepper C, Holstein K, Königs C, Heller C, Krause M, Olivieri M, Bidlingmaier C, Sigl-Kraetzig M, Wendisch J, Halimeh S, Horneff S, Richter H, Wieland I, Klamroth R, Oldenburg J, Tiede A; Hemophilia Board of the German, Austrian, Swiss Society on Thrombosis Hemostasis Research (GTH). Pfrepper C, et al. Among authors: wieland i. Hamostaseologie. 2021 Jun;41(3):190-196. doi: 10.1055/a-1401-2691. Epub 2021 Apr 15. Hamostaseologie. 2021. PMID: 33860513
Structural changes to primary visual cortex in the congenital absence of cone input in achromatopsia.
Molz B, Herbik A, Baseler HA, de Best PB, Vernon RW, Raz N, Gouws AD, Ahmadi K, Lowndes R, McLean RJ, Gottlob I, Kohl S, Choritz L, Maguire J, Kanowski M, Käsmann-Kellner B, Wieland I, Banin E, Levin N, Hoffmann MB, Morland AB. Molz B, et al. Among authors: wieland i. Neuroimage Clin. 2022;33:102925. doi: 10.1016/j.nicl.2021.102925. Epub 2021 Dec 21. Neuroimage Clin. 2022. PMID: 34959047 Free PMC article.
Possible New Strategies for the Treatment of Congenital Hyperinsulinism.
Sikimic J, Hoffmeister T, Gresch A, Kaiser J, Barthlen W, Wolke C, Wieland I, Lendeckel U, Krippeit-Drews P, Düfer M, Drews G. Sikimic J, et al. Among authors: wieland i. Front Endocrinol (Lausanne). 2020 Oct 27;11:545638. doi: 10.3389/fendo.2020.545638. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 33193079 Free PMC article.
91 results