Pangenome-based genome inference allows efficient and accurate genotyping across a wide spectrum of variant classes

by Audano, P.A, Clarke, W.E, Dilthey, A.T, Ebert, P., Ebler, J., Eichler, E.E, Houwaart, T., Korbel, J.O, Mao, Y., Marschall, T., Rausch, T., Zody, M.C
Published 2022

Overcoming constraints on the detection of recessive selection in human genes from population frequency data

by Balick, D.J, Do, R., Jordan, D.M, Sunyaev, S.
Published 2022

Evolution of phenotypic fluctuation under host-parasite interactions

by Kaneko, K., Nishiura, N.
Published 2021

Reconstructing contact network structure and cross-immunity patterns from multiple infection histories

by Alizon, S., Selinger, C.
Published 2021

The genetic architecture of pediatric cardiomyopathy

by Aronow, B., Bansal, N., Bhatnagar, S., Canter, C.E, Chung, W.K, Colan, S.D, Dexheimer, P.J, Everitt, M.D, Fan, X., Hsu, D.T, Kantor, P.F, Lal, A.K, Lee, T.M, Lipshultz, S.E, Martin, L.J, Miller, E.M, Pahl, E., Pediatric Cardiomyopathy Registry Study Group, Rossano, J.W, Rusconi, P., Schubert, J.A, Shen, Y., Shi, L., Sridhar, A., Tariq, M., Towbin, J.A, Ware, S.M, Webber, S.A, Wilkinson, J.D
Published 2022

PharmGKB, an Integrated Resource of Pharmacogenomic Knowledge

by Gong, L., Klein, T.E, Whirl-Carrillo, M.
Published 2021

Detection of CYP2C19 genetic variants in Malaysian Orang Asli from massively parallel sequencing data

by Ahmad, A., Ang, G.Y, Aziz, T.A.T.A, Isa, K.M, Ismail, A.I, James, R.J, Khalid, M.I.H.A, Nor, F.M, Rahman, T.A, Salleh, H., Salleh, M.Z, Subramaniam, V., Teh, L.K, Yu, C.Y
Published 2016

A Genetic Variation in the Y Chromosome Among Modern Japanese Males Related to Several Physiological and Psychological Characteristics

by Ishii, K., Masuda, T., Matsunaga, M., Noguchi, Y., Ohtsubo, Y., Yamasue, H.
Published 2021

The role of frontostriatal systems in instructed reinforcement learning: Evidence from genetic and experimentally-induced variation

by Graves, K.N, Tardiff, N., Thompson-Schill, S.L
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

Machine learning approaches for the genomic prediction of rheumatoid arthritis and systemic lupus erythematosus

by Chen, H.-H, Chen, T.-S, Chen, Y.-J, Chen, Y.-M, Chou, S.-C, Chung, C.-W, Chung, Y.-F, Hsiao, T.-H, Huang, C.-J, Lin, C.-H, Yang, H.-I
Published 2021

A novel rare copy number variant of the ABCF1 gene identified among dengue fever patients from Peninsular Malaysia

by AbuBakar, S., Hoh, B.P, Mahiran, M., Nik Khairudin, N.Y, Rafidah Hanim, S., Sam, S.S, Umi, S.H
Published 2014

Association of ficolin-1 and ficolin-3 gene variation and pulmonary tuberculosis susceptibility in a Chinese population

by Li, H.-M, Li, Y., Lin, W.-H, Liu, X.-N, Ma, D.-C, Shen, D.-P, You, E.-Q, Zhang, X.-L
Published 2021

The role of BDNF exon I region methylation in the treatment of depression with sertraline and its clinical diagnostic value

by Cheng, J., Gao, S., Li, G., Sun, T., Xing, Y., Xu, G.
Published 2021

Novel population specific autosomal copy number variation and its functional analysis amongst Negritos from Peninsular Malaysia

by Lionel, A.C, Marshall, C.R, Mokhtar, S.S, Peng, H.B, Phipps, M.E, Scherer, S.W, Thiruvahindrapuram, B.
Published 2014