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Did you mean muiswinkel w[au] (47 results)?
GestaltMatcher facilitates rare disease matching using facial phenotype descriptors.
Hsieh TC, Bar-Haim A, Moosa S, Ehmke N, Gripp KW, Pantel JT, Danyel M, Mensah MA, Horn D, Rosnev S, Fleischer N, Bonini G, Hustinx A, Schmid A, Knaus A, Javanmardi B, Klinkhammer H, Lesmann H, Sivalingam S, Kamphans T, Meiswinkel W, Ebstein F, Krüger E, Küry S, Bézieau S, Schmidt A, Peters S, Engels H, Mangold E, Kreiß M, Cremer K, Perne C, Betz RC, Bender T, Grundmann-Hauser K, Haack TB, Wagner M, Brunet T, Bentzen HB, Averdunk L, Coetzer KC, Lyon GJ, Spielmann M, Schaaf CP, Mundlos S, Nöthen MM, Krawitz PM. Hsieh TC, et al. Among authors: meiswinkel w. Nat Genet. 2022 Mar;54(3):349-357. doi: 10.1038/s41588-021-01010-x. Epub 2022 Feb 10. Nat Genet. 2022. PMID: 35145301 Free PMC article.
GestaltMatcher Database - a FAIR database for medical imaging data of rare disorders.
Lesmann H, Lyon GJ, Caro P, Abdelrazek IM, Moosa S, Pantel JT, Hagen MT, Rosnev S, Kamphans T, Meiswinkel W, Li JM, Klinkhammer H, Hustinx A, Javanmardi B, Knaus A, Uwineza A, Knopp C, Marchi E, Elbracht M, Mattern L, Jamra RA, Velmans C, Strehlow V, Nabil A, Graziano C, Artem B, Schnabel F, Heuft L, Herrmann V, Höller M, Alaaeldin K, Jezela-Stanek A, Mohamed A, Lasa-Aranzasti A, Elmakkawy G, Safwat S, Ebstein F, Küry S, Arlt A, Marbach F, Netzer C, Kaptain S, Weiland H, Devriendt K, Gripp KW, Mücke M, Verloes A, Schaaf CP, Nellåker C, Solomon BD, Waikel R, Abdalla E, Nöthen MM, Krawitz PM, Hsieh TC. Lesmann H, et al. Among authors: meiswinkel w. medRxiv. 2023 Jun 10:2023.06.06.23290887. doi: 10.1101/2023.06.06.23290887. Preprint. medRxiv. 2023. PMID: 37503210 Free PMC article.