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

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

Application of high-throughput sequencing for hereditary thrombocytopenia in southwestern China

by Dou, Y., Guan, X., Guo, Y., Luo, M., Wen, X., Xian, Y., Yu, J., Zhang, L.
Published 2021

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

Somatic mutational profiles and germline polygenic risk scores in human cancer

by Alexandrov, L.B, Gusev, A., Heng, Y.J, Kraft, P., Liu, Y.
Published 2022

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

Dopaminergic genes are associated with both directed and random exploration

by Gershman, S.J, Tzovaras, B.G
Published 2018

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

Genetic analysis of 39 erythrocytosis and hereditary hemochromatosis-associated genes in the Slovenian family with idiopathic erythrocytosis

by Anžej Doma, S., Debeljak, N., Fink, M., Gašperšič, J., Količ, R., Kristan, A., Kunej, T., Pajič, T., Podgornik, H., Preložnik Zupan, I., Režen, T., Vuga, A., Žula, Š
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