Rare variant analysis in eczema identifies exonic variants in DUSP1, NOTCH4 and SLC9A4

- Grosche, Sarah, Marenholz, Ingo, Bisgaard, Hans, Bønnelykke, Klaus, Brown, Sara J., Bustamante, Mariona, Curtin, John A., Custovic, Adnan, Dharmage, Shyamali C., Esplugues, Ana, Falchi, Mario, Fernandez-Orth, Dietmar, Esparza-Gordillo, Jorge, Ferreira, Manuel A. R., Franke, A, Gerdes, S, Gieger, C, Hakonarson, H, Holt, PG, Homuth, G, Hubner, N, Hysi, PG, Jarvelin, M-R, Arnau-Soler, Aleix, Karlsson, R, Koppelman, GH, Lau, S, Lutz, M, Magnusson, PKE, Marks, GB, Mueller-Nurasyid, M, Noethen, MM, Paternoster, L, Pennell, Craig E., Pairo-Castineira, Erola, Peters, A, Rawlik, K, Robertson, CF, Rodriguez, E, Sebert, S, Simpson, A, Sleiman, PMA, Standl, M, Stoelzl, D, Strauch, K, Rüschendorf, Franz, Szwajda, A, Tenesa, A, Thompson, PJ, Ullemar, V, Visconti, A, Vonk, JM, Wang, CA, Weidinger, S, Wielscher, M, Worth, CL, Ahluwalia, Tarunveer S., Xu, C-J, Lee, Y-A, Almqvist, Catarina, Arnold, Andreas, Baurecht, Hansjörg

The economic and health impact of rare diseases: a meta-analysis

- Sequeira, Ana Rita, Mentzakis, Emmanouil, Archangelidi, Olga, Paolucci, Francesco

A powerful team: the family physician advocating for patients with a rare disease

- Dudding-Byth, T.