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Haas, Cordula; Alterauge, Amelie (2021). Genetische Verwandtschaftsanalyse an den Mumien aus Riesa. In: Stadtmuseum, Riesa; Ev.-Luth. Kirchgemeinde, Riesa (eds.) Geschichten über den Tod hinaus - die Grüfte in der Klosterkirche Riesa. Kasseler Studien zur Sepulkralkultur: Vol. 26 (pp. 102-109). Königsbrück: Via Regia Verlag
Alterauge, Amelie Sophie; Lösch, Sandra; Sulzer, Andrea; Gysi, Mario; Haas, Cordula (2021). Beyond simple kinship and identification. aDNA analyses from a 17th-19th century crypt in Germany. Forensic science international. Genetics, 53, p. 102498. Elsevier 10.1016/j.fsigen.2021.102498
Neubauer, Jacqueline; Wang, Zizun; Rougier, Jean-Sébastien; Abriel, Hugues; Rieubland, Claudine; Bartholdi, Deborah; Haas, Cordula; Medeiros-Domingo, Argelia (2019). Functional characterization of a novel SCN5A variant associated with long QT syndrome and sudden cardiac death. International journal of legal medicine, 133(6), pp. 1733-1742. Springer 10.1007/s00414-019-02141-x
Neubauer, Jacqueline; Rougier, Jean-Sébastien; Abriel, Hugues; Haas, Cordula (2018). Functional implications of a rare variant in the sodium channel β1B subunit () in a 5-month-old male sudden infant death syndrome case. HeartRhythm Case Reports, 4(5), pp. 187-190. Elsevier 10.1016/j.hrcr.2018.01.010
Asadollahi, Reza; Strauss, Justin E; Zenker, Martin; Beuing, Oliver; Edvardson, Simon; Elpeleg, Orly; Strom, Tim M; Joset, Pascal; Niedrist, Dunja; Otte, Christine; Oneda, Beatrice; Boonsawat, Paranchai; Azzarello-Burri, Silvia; Bartholdi, Deborah; Papik, Michael; Zweier, Markus; Haas, Cordula; Ekici, Arif B; Baumer, Alessandra; Boltshauser, Eugen; ... (2018). Clinical and experimental evidence suggest a link between KIF7 and C5orf42-related ciliopathies through Sonic Hedgehog signaling. European journal of human genetics, 26(2), pp. 197-209. Nature Publishing Group 10.1038/s41431-017-0019-9
Neubauer, Jaqueline; Lecca, MR; Russo, G; Bartsch, C; Medeiros Domingo, Argelia; Berger, Wolfgang; Haas, Cordula (2017). Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases. European journal of human genetics, 25(4), pp. 404-409. Nature Publishing Group 10.1038/ejhg.2016.199
Neubauer, Jaqueline; Haas, Cordula; Bartsch, Christine; Medeiros Domingo, Argelia; Berger, Wolfgang (2016). Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases. International journal of legal medicine, 130(4), pp. 1011-1021. Springer 10.1007/s00414-016-1317-4
Haeusler, Martin; Haas, Cordula; Lösch, Sandra; Hossein Moghaddam Horri, Negahnaz; Villa, Igor Maria; Walsh, Susan; Kayser, Manfred; Seiler, Roger; Ruehli, Frank; Janosa, Manuel; Papageorgopoulou, Christina (2016). Multidisciplinary Identification of the Controversial Freedom Fighter Jörg Jenatsch, Assassinated 1639 in Chur, Switzerland. PLoS ONE, 11(12), e0168014. Public Library of Science 10.1371/journal.pone.0168014
