Explaining chest x-ray pathologies in natural language von Kayser, M, Emde, C, Camburu, OM, Parsons, G, Papiez, B, Lukasiewicz, T

Lightweight visual question answering using scene graphs von Nuthalapati, SV, Chandradevan, R, Giunchiglia, E, Li, B, Kayser, M, Lukasiewicz, T, Yang, C

e-ViL: A dataset and benchmark for natural language explanations in vision-language tasks von Kayser, M, Camburu, O-M, Salewski, L, Emde, C, Do, V, Akata, Z, Lukasiewicz, T

Genome-wide significant risk genes for multiple sclerosis von Hoppenbrouwers, I, Aulchenko, Y, Janssens, C, Ramagopalan, S, Kayser, M, Ebers, G, Oostra, B, van Duijn, C, Hintzen, R

Genetic admixture history of Eastern Indonesia as revealed by y-chromosome and mitochondrial DNA analysis von Mona, S, Grunz, K, Brauer, S, Pakendorf, B, Castrì, L, Sudoyo, H, Marzuki, S, Barnes, R, Schmidtke, J, Stoneking, M, Kayser, M

Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis. von Hoppenbrouwers, I, Aulchenko, Y, Janssens, A, Ramagopalan, S, Broer, L, Kayser, M, Ebers, G, Oostra, B, van Duijn, C, Hintzen, R

Ancient genomes indicate population replacement in Early Neolithic Britain von Brace, S, Diekmann, Y, Booth, TJ, Van Dorp, L, Faltyskova, Z, Rohland, N, Mallick, S, Olalde, I, Ferry, M, Michel, M, Oppenheimer, J, Broomandkhoshbacht, N, Stewardson, K, Martiniano, R, Walsh, S, Kayser, M, Charlton, S, Hellenthal, G, Armit, I, Schulting, R, Craig, OE, Sheridan, A, Pearson, M, Stringer, C, Reich, D, Thomas, MG, Barnes, I

An objective comparison of detection and segmentation algorithms for artefacts in clinical endoscopy von Ali, S, Zhou, F, Braden, B, Bailey, A, Yang, S, Cheng, G, Zhang, P, Li, X, Kayser, M, Soberanis-Mukul, RD, Albarqouni, S, Wang, X, Wang, C, Watanabe, S, Oksuz, I, Ning, Q, Yang, S, Khan, MA, Gao, XW, Realdon, S, Loshchenov, M, Schnabel, JA, East, JE, Wagnieres, G, Loschenov, VB, Grisan, E, Daul, C, Blondel, W, Rittscher, J

Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways von Duffy, DL, Zhu, G, Li, X, Sanna, M, Iles, MM, Jacobs, LC, Evans, DM, Yazar, S, Beesley, J, Law, MH, Kraft, P, Visconti, A, Taylor, JC, Liu, F, Wright, MJ, Henders, AK, Bowdler, L, Glass, D, Ikram, MA, Uitterlinden, AG, Madden, PA, Heath, AC, Nelson, EC, Green, AC, Chanock, S, Barrett, JH, Brown, MA, Hayward, NK, Macgregor, S, Sturm, RA, Hewitt, AW, Kayser, M, Hunter, DJ, Newton Bishop, JA, Spector, TD, Montgomery, GW, Mackey, DA, Smith, GD, Nijsten, TE, Bishop, DT, Bataille, V, Falchi, M, Han, J, Martin, NG

Genome-wide association study in almost 195,000 individuals identifies 50 previously unidentified genetic loci for eye color von Simcoe, M, Valdes, A, Liu, F, Furlotte, NA, Evans, DM, Hemani, G, Ring, SM, Smith, GD, Duffy, DL, Zhu, G, Gordon, SD, Medland, SE, Vuckovic, D, Girotto, G, Sala, C, Catamo, E, Concas, MP, Brumat, M, Gasparini, P, Toniolo, D, Cocca, M, Robino, A, Yazar, S, Hewitt, A, Wu, W, Kraft, P, Hammond, CJ, Shi, Y, Chen, Y, Zeng, C, Klaver, CCW, Uitterlinden, AG, Ikram, MA, Hamer, MA, van Duijn, CM, Nijsten, T, Han, J, Mackey, DA, Martin, NG, Cheng, C-Y, 23andMe Research Team, International Visible Trait Genetics Consortium, Hinds, DA, Spector, TD, Kayser, M, Hysi, PG

PoPoolation: a toolbox for population genetic analysis of next generation sequencing data from pooled individuals von Kofler, R, Orozco-terWengel, P, De Maio, N, Pandey, R, Nolte, V, Futschik, A, Kosiol, C, Schlötterer, C

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