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

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

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

Autres auteurs: “…Kayser, M…”