![[höher]](/style/images/multi_up.png)
Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 3
2022
Ferguson, Amy Christina; Thrippleton, Sophie; Henshall, David; Whittaker, Ed; Conway, Bryan; MacLeod, Malcolm; Malik, Rainer; Rawlik, Konrad; Tenesa, Albert; Sudlow, Cathie und Rannikmae, Kristiina
(2022):
Frequency and Phenotype Associations of Rare Variants in 5 Monogenic Cerebral Small Vessel Disease Genes in 200,000 UK Biobank Participants.
In: Neurology - Genetics, Bd. 8, Nr. 5, e200015
Rannikmae, Kristiina; Rawlik, Konrad; Ferguson, Amy C.; Avramidis, Nikos; Jiang, Muchen; Pirastu, Nicola; Shen, Xia; Davidson, Emma; Woodfield, Rebecca; Malik, Rainer; Dichgans, Martin; Tenesa, Albert und Sudlow, Cathie
(2022):
Physician-Confirmed and Administrative Definitions of Stroke in UK Biobank Reflect the Same Underlying Genetic Trait.
In: Frontiers in Neurology, Bd. 12, 787107
[PDF, 2MB]
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