A genome-wide association study identifies an association between variants in EFCAB4B gene and periodontal disease in an Italian isolated population

by Bevilacqua, L., Gasparini, P., Lenarda, R.D, Navarra, C.O, Pirastu, N., Robino, A.
Published 2018

Novel caries loci in children and adults implicated by genome-wide analysis of families

by Crout, R.J, Feingold, E., Govil, M., Levy, S.M, Marazita, M.L, McNeil, D.W, Mukhopadhyay, N., Shaffer, J.R, Slayton, R.L, Vieira, A.R, Weeks, D.E, Weyant, R.J
Published 2018

Novel GREM1 variations in Sub-Saharan African patients with cleft lip and/or cleft palate

by Abdur-Rahman, L.O, Adeyemo, A.A, Adeyemo, W.L, Agbenorku, P., Aregbesola, B.S, Audu, R., Bello, S.A, Busch, T.D, Butali, A., Donkor, P., Eshete, M.A, Gowans, L.J.J, Marazita, M.L, Mossey, P.A, Murray, J.C, Obiri-Yeboah, S., Oginni, F.O, Ogunlewe, M.O, Olaitan, P.B, Onwuamah, C., Oseni, G., Oti, A.A, Owais, A., Plange-Rhule, G.
Published 2018

Integration of Murine and Human Studies for Mapping Periodontitis Susceptibility

by Berger, K., Botzman, M., de Groot, L.C.P.G.M, Divaris, K., Dommisch, H., Franke, A., Gat-Viks, I., Haddad, Y.H, Hoffmann, P., Iraqi, F.A, Kocher, T., Krone, B., Laudes, M., Lieb, W., Loos, B., Mott, R., Munz, M., Nashef, A., Offenbacher, S., Qabaja, R., Salaymeh, Y., Schaefer, A., Uitterlinden, A.G, van der Velde, N., Wellmann, J., Wiess, E.
Published 2018

Rare and Common Variants Conferring Risk of Tooth Agenesis

by Alonso, I., Audolfsson, G., Bjornsdottir, G., Dhamo, B., Feenstra, B., Geller, F., Gudbjartsson, D.F, Gudmundsson, L., Gustafsson, O., Howe, B.J, Ingason, A., Jonsson, L., Jonsson, R., Jonsson, T., Leslie, E.J, Magnusson, T.E, Marazita, M.L, Melbye, M., Moreno Uribe, L.M, Nawaz, M.S, Nohr, E.A, Oddsson, A., Olafsson, S., Ongkosuwito, E.M, Pinho, T., Rivadeneira, F., Santos, M., Stefansson, H., Stefansson, K., Steinberg, S., Thordarson, A., Unnsteinsdottir, U., Vucic, S., Walters, G.B, Wolvius, E.B, Zervas, M.
Published 2018

A systematic analysis of gene–gene interaction in multiple sclerosis

by Azencott, C.-A, Chatelain, C., Foucauld, H., Slim, L.
Published 2022

Genome-wide association and Mendelian randomization study of blood copper levels and 213 deep phenotypes in humans

by Bao, Y., Chen, X., Cheng, H., Feng, X., Ge, X., Huang, L., Li, L., Liu, C., Mo, Z., Wang, F., Yang, W., Yang, X.
Published 2022

mRNA microarray profiling identifies a novel circulating HTRA2 for detection of gastric cancer

by Chen, X., Cheng, Y., Li, X., Lv, C., Sun, G., Tang, W., Wu, F., Wu, L., Zhang, W.
Published 2021

Noise Exposure and Distortion Product Otoacoustic Emission Suprathreshold Amplitudes: A Genome-Wide Association Study

by Allayee, H., Bento, R.F, Crow, A.L, Friedman, R.A, Kasperbauer, G., Lavinsky, J., Mendonça, A., Wang, J.
Published 2021

The morphometry of left cuneus mediating the genetic regulation on working memory

by Fu, J., He, X., Li, W., Li, X., Liu, H., Qin, W., Xu, J., Ye, Z., Yu, C., Zhang, P.
Published 2021

Targeted resequencing showing novel common and rare genetic variants increases the risk of asthma in the Chinese Han population

by Cheng, Z., Deng, Y., Fang, S., Li, J., Li, Z., Liu, J., Luo, G., Luo, L., Mo, B., Shu, Y., Wang, Y., Wang, Z., Wei, J., Xiong, W., Yang, H., Yang, J., Yu, B., Zhang, X., Zhu, J.
Published 2021

Using the PhenX Toolkit to Select Standard Measurement Protocols for Your Research Study

by Cox, L.A, Engle, M.L, Haines, J., Hamilton, C.M, Hendershot, T., Hwang, S., Marazita, M.L, McCarty, C.A, Pan, H., Ramos, E.M
Published 2021

Genetic scores for adult subcortical volumes associate with subcortical volumes during infancy and childhood

by Ikram, M.A, Jansen, P.R, Labrecque, J.A, Lamballais, S., White, T.
Published 2021

Multidimensional chromatin profiling of zebrafish pancreas to uncover and investigate disease-relevant enhancers

by Acemel, R.D, Bessa, J., Bordeira-Carriço, R., Carneiro, F., Duque, M., Eufrásio, A., Ferreira, F.J, Firbas, P.N, Freitas, T., Galhardo, M., Goméz-Skarmeta, J.L, Marques, J., Ribeiro, D., Teixeira, J., Tena, J.J
Published 2022

Development and validation of polygenic risk scores for prediction of breast cancer and breast cancer subtypes in Chinese women

by Hao, Y., Hou, C., Li, J., Song, H., Xu, B., Yang, D.
Published 2022

Secure tumor classification by shallow neural network using homomorphic encryption

by Cheon, J.H, Cho, W., Choe, H., Hong, S., Park, J.H
Published 2022

Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels

by Ahmad, S., Beiser, A.S, Bis, J.C, Boerwinkle, E., Bouteloup, V., Chouraki, V., Cupples, L.A, Damotte, V., Debette, S., DeCarli, C.S, DeStefano, A.L, Djoussé, L., Dufouil, C., Fohner, A.E, Fornage, M., Franz, C.E, Ghanbari, M., Ikram, M.A, Kautz, T.F, Kremen, W.S, Lambert, J.-C, Launer, L.J, Logue, M., Longstreth, W.T, Lyons, M.J, Mishra, A., Mosley, T.H, Mukamal, K.J, Pase, M.P, Portilla Fernandez, E.C, Rissman, R.A, Sarnowski, C., Satizabal, C.L, Seshadri, S., Vasan, R.S, Yaqub, A.
Published 2022

gJLS2: an R package for generalized joint location and scale analysis in X-inclusive genome-wide association studies

by Deng, W.Q, Sun, L.
Published 2022

Genome-wide association study identifies SNP markers and putative candidate genes for terpene traits important for Leptocybe invasa resistance in Eucalyptus grandis

by Külheim, C., Mhoswa, L., Myburg, A.A, Naidoo, S., Slippers, B.
Published 2022

Genome-wide association studies dissect the genetic architecture of seed shape and size in common bean

by Chiorato, A.F, Gama, H.C, Garcia, A.A.F, Giordani, W., Vieira, M.L.C
Published 2022