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Year Number of Results
1985 1
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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 12
2023 5
2024 4

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95 results

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Page 1
Biallelic inactivation of the NF1 tumour suppressor gene in juvenile myelomonocytic leukaemia: Genetic evidence of driver function and implications for diagnostic workup.
Ramamoorthy S, Lebrecht D, Schanze D, Schanze I, Wieland I, Andrieux G, Metzger P, Hess M, Albert MH, Borkhardt A, Bresters D, Buechner J, Catala A, De Haas V, Dworzak M, Erlacher M, Hasle H, Jahnukainen K, Locatelli F, Masetti R, Stary J, Turkiewicz D, Vinci L, Wlodarski MW, Yoshimi A, Boerries M, Niemeyer CM, Zenker M, Flotho C. Ramamoorthy S, et al. Among authors: wieland i. Br J Haematol. 2024 Feb;204(2):595-605. doi: 10.1111/bjh.19190. Epub 2023 Nov 9. Br J Haematol. 2024. PMID: 37945316
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.
Assessment of gene-disease associations and recommendations for genetic testing for somatic variants in vascular anomalies by VASCERN-VASCA.
Revencu N, Eijkelenboom A, Bracquemart C, Alhopuro P, Armstrong J, Baselga E, Cesario C, Dentici ML, Eyries M, Frisk S, Karstensen HG, Gene-Olaciregui N, Kivirikko S, Lavarino C, Mero IL, Michiels R, Pisaneschi E, Schönewolf-Greulich B, Wieland I, Zenker M, Vikkula M. Revencu N, et al. Among authors: wieland i. Orphanet J Rare Dis. 2024 May 22;19(1):213. doi: 10.1186/s13023-024-03196-9. Orphanet J Rare Dis. 2024. PMID: 38778413 Free PMC article.
Bilateral lung transplantation for pediatric pulmonary arterial hypertension: perioperative management and one-year follow-up.
Jack T, Carlens J, Diekmann F, Hasan H, Chouvarine P, Schwerk N, Müller C, Wieland I, Tudorache I, Warnecke G, Avsar M, Horke A, Ius F, Bobylev D, Hansmann G. Jack T, et al. Among authors: wieland i. Front Cardiovasc Med. 2023 Jun 27;10:1193326. doi: 10.3389/fcvm.2023.1193326. eCollection 2023. Front Cardiovasc Med. 2023. PMID: 37441704 Free PMC article.
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.
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
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.
95 results