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Veröffentlichungsdatum
Anzahl der Publikationen: 4
2024
Brugger, Markus; Lutz, Manuel; Müller-Nurasyid, Martina 
ORCID: https://orcid.org/0000-0003-3793-5910; Lichtner, Peter; Slater, Emily P.; Matthäi, Elvira; Bartsch, Detlef K. und Strauch, Konstantin
(2024):
Joint linkage and association analysis using GENEHUNTER-MODSCORE with an application to familial pancreatic cancer.
In: Human Heredity, Bd. 89, Nr. 1: S. 8-31
[PDF, 1MB]
ORCID: https://orcid.org/0000-0003-3793-5910; Lichtner, Peter; Slater, Emily P.; Matthäi, Elvira; Bartsch, Detlef K. und Strauch, Konstantin
(2024):
Joint linkage and association analysis using GENEHUNTER-MODSCORE with an application to familial pancreatic cancer.
In: Human Heredity, Bd. 89, Nr. 1: S. 8-31
[PDF, 1MB]
2021
Grosche, Sarah; Marenholz, Ingo; Esparza-Gordillo, Jorge; Arnau-Soler, Aleix; Pairo-Castineira, Erola; Rueschendorf, Franz; Ahluwalia, Tarunveer S.; Almqvist, Catarina; Arnold, Andreas; Baurecht, Hansjoerg; Bisgaard, Hans; Bonnelykke, Klaus; Brown, Sara J.; Bustamante, Mariona; Curtin, John A.; Custovic, Adnan; Dharmage, Shyamali C.; Esplugues, Ana; Falchi, Mario; Fernandez-Orth, Dietmar; Ferreira, Manuel A. R.; Franke, Andre; Gerdes, Sascha; Gieger, Christian; Hakonarson, Hakon; Holt, Patrick G.; Homuth, Georg; Hubner, Norbert; Hysi, Pirro G.; Jarvelin, Marjo-Riitta; Karlsson, Robert; Koppelman, Gerard H.; Lau, Susanne; Lutz, Manuel; Magnusson, Patrik K. E.; Marks, Guy B.; Mueller-Nurasyid, Martina; Noethen, Markus M.; Paternoster, Lavinia; Pennell, Craig E.; Peters, Annette; Rawlik, Konrad; Robertson, Colin F.; Rodriguez, Elke; Sebert, Sylvain; Simpson, Angela; Sleiman, Patrick M. A.; Standl, Marie; Stoelzl, Dora; Strauch, Konstantin; Szwajda, Agnieszka; Tenesa, Albert; Thompson, Philip J.; Ullemar, Vilhelmina; Visconti, Alessia; Vonk, Judith M.; Wang, Carol A.; Weidinger, Stephan; Wielscher, Matthias; Worth, Catherine L.; Xu, Chen-Jian und Lee, Young-Ae
(2021):
Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4.
In: Nature Communications, Bd. 12, Nr. 1, 6618
Slater, Emily P.; Wilke, Lisa M.; Boehm, Lutz Benedikt; Strauch, Konstantin; Lutz, Manuel; Gercke, Norman; Matthai, Elvira; Hemminki, Kari; Forsti, Asta; Schlesner, Matthias; Paramasivam, Nagarajan und Bartsch, Detlef K.
(2021):
Combinations of Low-Frequency Genetic Variants Might Predispose to Familial Pancreatic Cancer.
In: Journal of Personalized Medicine, Bd. 11, Nr. 7, 631
2018
Steinbeck, Gerhard; Sinner, Moritz F.; Lutz, Manuel; Müller-Nurasyid, Martina; Kaeaed, Stefan und Reinecke, Holger
(2018):
Incidence of complications related to catheter ablation of atrial fibrillation and atrial flutter: a nationwide in-hospital analysis of administrative data for Germany in 2014.
In: European Heart Journal, Bd. 39, Nr. 45: S. 4020-4029