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

Lightweight visual question answering using scene graphs de réir 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 de réir Kayser, M, Camburu, O-M, Salewski, L, Emde, C, Do, V, Akata, Z, Lukasiewicz, T

Genome-wide significant risk genes for multiple sclerosis de réir 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 de réir 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. de réir 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 de réir 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 de réir 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 de réir 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 de réir 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 de réir Kofler, R, Orozco-terWengel, P, De Maio, N, Pandey, R, Nolte, V, Futschik, A, Kosiol, C, Schlötterer, C

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