Genome-wide association study and functional validation implicates JADE1 in tauopathy

by Andrews, S.J, Attems, J., Ayalon, G., Beach, T.G, Bhangale, T., Borukov, V.Y, Bowles, K.R, Cairns, N.J, Casella, A., Cherry, J.D, Cobos, I., Cohen, H.T, Corrada, M.M, Cortes, E.P, Crary, J.F, Dangoor, D.K, de Paiva Lopes, K., Dickson, D.W, Farrell, K., Fischer, P., Flanagan, M.E, Franklin, E.E, Frosch, M.P, Frost, B., Fulton-Howard, B., Gandy, S., Gearing, M., Glass, J., Goate, A., Gonzalez, E.M, Graham, R.R, Han, N., Haroutunian, V., Hefti, M.M, Hof, P.R, Humphrey, J., Hunkapiller, J., Hyman, B.T, Iida, M.A, Kapoor, M., Kawas, C.H, Keene, C.D, Kim, S.H, Kofler, J., Kovacs, G.G, Latimer, C.S, Lee, E.B, Lutz, M.I, Mao, Q., Marcora, E., McKee, A.C, McMillan, C.T, Mesulam, M.-M, Metcalf, J., Montine, T.J, Murray, M.E, Nelson, P.T, Novikova, G., Otero-Garcia, M., Perrin, R.J, Pham, T., Poon, W., Purohit, D.P, Raj, T., Renton, A.E, Richardson, T.E, Rissman, R.A, Salehi, B., Sano, M., Schneider, J.A, Shuldberg, S., Sissoko, C.T, Stein, T.D, Tang, W., Teich, A.F, Trojanowski, J.Q, Troncoso, J.C, Udine, E., Vialle, R.A, Vonsattel, J.-P, Walker, J.M, Walsh, H., Weintraub, S., White III, C.L, Whitney, K., Wolk, D.A, Woltjer, R.L, Wong, G., Yu, L.
Published 2022

Genome assembly of the JD17 soybean provides a new reference genome for comparative genomics

by Chen, N., Chen, S., Fan, W., Kudrna, D., Lee, S., Lei, L., Liu, J., Liu, M., Wang, X., Wing, R.A, Wu, H., Xu, Q., Yang, C., Yi, X., Zhang, B., Zhang, J., Zhang, M.
Published 2022

Grouping of genomic markers in populations with family structure

by Doschoris, M., Klosa, J., Wittenburg, D.
Published 2021

Systematic Pharmacogenomics Analysis of a Malay Whole Genome: Proof of Concept for Personalized Medicine

by Adam, A., Ahmed, A.Z, Hamzah, A.S, Hatta, F.H.M, Hoh, B.P, Ismail, M.I, Ismet, R.I, Janor, R.M, Joshi, K., Lee, L.S, Pasha, A., Patowary, A., Salleh, M.Z, Scaria, V., Sivasubbu, S., Teh, L.K, Yusoff, K.

Multi-ancestry genome-wide association study of asthma exacerbations

by Ampleford, E.J, Bahmer, T., Bleecker, E., Brinkman, P., Brusselle, G., Burchard, E.G, Canino, G., Celedón, J.C, Chew, F.T, Cloutier, M., Corcuera, P., Cruz, M.J, de Roos, E., Del Pozo, V., Eng, C., Espuela-Ortiz, A., Figueiredo, C., Forno, E., González-Barcala, F.-J, González-Pérez, R., Gorenjak, M., Granell, R., Hansen, G., Hashimoto, S., Hawcutt, D.B, Hawkins, G.A, Hernandez-Pacheco, N., Hernández-Pérez, J.M, Herrera-Luis, E., Jorgensen, A.L, Kabesch, M., Kopp, M.V, Korta-Murua, J., Lethem, R., Lorenzo-Diaz, F., Maitland-van der Zee, A.H, Marsico, A., Martin-Gonzalez, E., Melén, E., Meyers, D., Mukhopadhyay, S., Olaguibel, J.M, Ortega, V.E, Palmer, C.N, Perez-Garcia, J., Pino-Yanes, M., Pirmohamed, M., Plaza, V., Potočnik, U., Poza-Guedes, P., Quirce, S., Rabe, K.F, Rios, R., Rodriguez-Santana, J.R, Sardón, O., Sio, Y.Y, Terzikhan, N., Turner, S., U-BIOPRED Study Group, Vergara, E.E, Vijverberg, S.J, Villar, J., von Mutius, E., Yan, Q.
Published 2022

A genome-wide characterization of copy number variations in native populations of Peninsular Malaysia

by Fu, R., Hoh, B.-P, Mokhtar, S.S, Phipps, M.E, Xu, S.
Published 2018

Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1

by Bye, C.R, Cheng, F.-F, Garton, F.C, Giacomotto, J., Gusev, A., Henders, A.K, Henderson, R.D, Kabashi, E., Kiernan, M.C, Mathers, S., McCombe, P.A, McRae, A.F, Nabais, M.F, Needham, M., Ngo, S.T, Ophoff, R., Qi, T., Restuadi, R., Schultz, D., Steyn, F.J, Thompson, M.J, Turner, B.J, van den Berg, L.H, van Rheenen, W., Veldink, J.H, Wallace, L., Wray, N.R, Wu, Y., Zaitlen, N., Ziser, L.
Published 2022

Genome-wide variant-based study of genetic effects with the largest neuroanatomic coverage

by Bao, P., Chen, F., Fang, S., Gao, Y., Jiang, H., Li, H., Li, J., Li, Y., Liang, H., Liu, W., Luo, H.
Published 2021

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

Transcript annotation tool (TransAT): an R package for retrieving annotations for transcript-specific genetic variants

by Chattopadhyay, A., Lu, T.-P, Shih, C.-Y, Tien, Y.-W, Wu, C.-H
Published 2021

Wavelet Screening: a novel approach to analyzing GWAS data

by Denault, W.R.P, Gjessing, H.K, Jacobsson, B., Jugessur, A., Juodakis, J.
Published 2021

Whole-genome comparative analysis reveals genetic mechanisms of disease resistance and heat tolerance of tropical Bos indicus cattle breeds

by Bakyaraj, S., Jagadeesan, K., Mishra, A., Singaravadivelan, A., Sivakumar, T., Suresh, R., Vijayakumar, P.
Published 2022

Genome-wide association study identifies SNP markers and putative candidate genes for terpene...

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

A globally diverse reference alignment and panel for imputation of mitochondrial DNA variants

by Andrews, S.J, Easteal, S., for the Alzheimer's Disease Neuroimaging Initiative, Fulton-Howard, B., Goate, A., Jermiin, L.S, McInerney, T.W, Pa, J., Paliwal, D., Patel, H.R, Patterson, C., Swerdlow, R.H
Published 2021

Genetic analysis of over half a million people characterises C-reactive protein loci

by Alizadeh, B.Z, Bodinier, B., Chadeau-Hyam, M., Chasman, D.I, Dehghan, A., Elliott, P., Evangelou, E., Jarvelin, M.-R, Karhunen, V., Koskeridis, F., Ligthart, S., Pazoki, R., Said, S., Sattar, N., Tzoulaki, I., Võsa, U., Welsh, P.
Published 2022

RNA editing regulates lncRNA splicing in human early embryo development

by Ma, X., Qiu, J., Yan, J., Zeng, F.
Published 2021

Spatial rank-based multifactor dimensionality reduction to detect gene–gene interactions for multivariate phenotypes

by Jeong, H.-B, Lee, J.-H, Park, M., Park, T.
Published 2021

Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts

by Ahmadizar, F., Bielak, L.F, Blokstra, A., Boerwinkle, E., Bottinger, E.P, Chaker, L., Chen, Y., Chen, Y.-D.I, Cole, J.B, de Vries, P.S, DiCorpo, D., Dupuis, J., Faquih, T., Florez, J.C, Ghanbari, M., Goodarzi, M.O, Gudmundsdottir, V., Gudnason, V., Guo, X., Hasbani, N.R, Ibi, D., Ikram, M.A, Jukema, J.W, Kardia, S.L.R, Kavousi, M., LeClair, J., Leonard, H.L, Leong, A., Liu, C.-T, Loos, R.J.F, Manning, A.K, Meigs, J.B, Mercader, J.M, Mook-Kanamori, D., Morrison, A.C, Nadkarni, G.N, Nalls, M.A, Noordam, R., Pankow, J.S, Picavet, H.S.J, Preuss, M., Rotter, J.I, Sarnowski, C., Sattar, N., Simonsick, E.M, Smith, J.A, Trompet, S., Udler, M.S, Verschuren, W.M.M, Vissink, P., Willems van Dijk, K., Yao, J., Zhao, W.
Published 2022

Super-variants identification for brain connectivity

by Hu, J., Li, T., Wang, S., Zhang, H.
Published 2021

Methylation quantitative trait loci are largely consistent across disease states in Crohn's disease

by Conneely, K.N, Cutler, D.J, Denson, L.A, Gibson, G., Hyams, J.S, Katrinli, S., Kellermayer, R., Kilaru, V., Kugathasan, S., Okou, D.T, Prince, J., Smith, A.K, Somineni, H.K, Venkateswaran, S.
Published 2022