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

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

Rare copy number variants identified suggest the regulating pathways in hypertension-related left ventricular hypertrophy

by Basir, F., Boon-Peng, H., Danuri, N., Jusoh, J.A.M, Majid, F., Marshall, C.R, Scherer, S.W, Thiruvahindrapuram, B., Yusoff, K.
Published 2016

Impact of cytotoxic T-lymphocyte-associated protein 4 codon 17 variant and expression on vitiligo risk

by Fawzy, M.S, Gouda, N.S, Toraih, E.A
Published 2021

A nonsynonymous polymorphism (rs117179004, T392M) of hyaluronidase 1 (HYAL1) is associated with increased risk of idiopathic pulmonary fibrosis in Southern Han Chinese

by Cheng, Z., Deng, Y., Fang, S., Ge, R., Li, J., Li, Z., Liu, J., Luo, G., Mo, B., Peng, Q., Shu, Y., Wang, X., Wang, Y., Wang, Z., Wei, G., Wei, J., Wu, M., Xiong, W., Xu, X., Yang, H., Yang, J., Yang, S., Zhang, X., Zhu, J.
Published 2021

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

Association between SP-A rs1965708 gene polymorphism and allergic rhinitis risk in Chinese population

by Hu, L., Wang, B., Yan, Z., Yin, X., Zhang, X.
Published 2021

A novel CD209 polymorphism is associated with rheumatoid arthritis patients in Taiwan

by Chan, H.-C, Li, R.-N, Lin, C.-H, Lin, Y.-Z, Wang, S.-C, Yen, J.-H
Published 2021

Association between the TAP1 gene polymorphisms and recurrent respiratory papillomatosis in patients from Western Mexico: A pilot study

by Araujo-Caballero, V., Cazarez-Navarro, G., Govea-Camacho, L.H, Hernandez-Cañaveral, I.I, Martinez-Lopez, E., Muñoz-Valle, J.F, Ortiz-Hernandez, E., Palomares-Marin, J., Rodriguez-Preciado, S.Y
Published 2021

Association of ISL1 polymorphisms and eosinophilic levels among otitis media patients

by Biswal, N.C, Kondyarpu, A., Panda, K.C, Ramchander, P.V, Ray, C.S
Published 2021

Association between aldehyde dehydrogenase 2 gene rs671 G>A polymorphism and alcoholic liver cirrhosis in southern Chinese Hakka population

by Huang, Q., Wu, H., Yu, Z., Zeng, D.
Published 2021

Association of ANGPTL3 polymorphisms with high-density lipoprotein cholesterol uptake capacity in patients with cardiovascular disease

by Aghasizadeh, M., Akbarpour, E., Assadian, P., Avan, A., Ferns, G.A, Ghayour-Mobarhan, M., Kazemi, T., Miri-Moghaddam, E., Nosrati, M., Saberi-Karimian, M., Safarian, H., Sahebkar, A.
Published 2021

Common variants of chemokine receptor gene CXCR3 and its ligands CXCL10 and CXCL11 associated with vascular permeability of dengue infection in peninsular Malaysia

by Benedict, L.H.S, Christopher, K.C.L, Hoh, B.P, Mahiran, M., Masliza, Z., Nik Khairudin, N.Y, Rafidah-Hanim, S., Sazaly, A.B, Umi-Shakina, H., Zaiharina, M.Z, Zuraihan, Z.
Published 2015

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

Altered gene expression of VEGF, IGFs and H19 lncRNA and epigenetic profile of H19-DMR region in endometrial tissues of women with endometriosis

by Amirchaghmaghi, E., Ghaedi, K., Ghaffari, F., Kamrani, S., Shahhoseini, M.
Published 2022

Association of vitamin D receptor polymorphisms with metabolic syndrome-related components: A cross-sectional study

by Gong, X., Jin, T., Lu, W., Wu, F., Zhou, J.
Published 2021

Impact of YTHDF1 gene polymorphisms on Wilms tumor susceptibility: A five-center case-control study

by Bian, J., Cheng, J., Hua, R.-X, Li, S., Lin, H., Liu, Y., Zhang, J., Zhou, H., Zhuo, Z.
Published 2021

Association of DYNC1H1 gene SNP/CNV with disease susceptibility, GCs efficacy, HRQOL, anxiety, and depression in Chinese SLE patients

by Cai, J., Chen, Y., Huang, H., Huang, S., Li, M., Li, Z., Liu, S., Lou, Q., Teng, Y., Wang, L., Wang, Y., Xu, Z., Yan, Z., Zhang, T., Zou, Y.
Published 2021

Relevance of HLA gene polymorphisms in Romanian patients with chronic renal insufficiency undergoing renal transplantation

by Constantinescu, I., Cristea, B.M, Mărunţelu, I., Omer, S., Preda, C.M
Published 2021

An SNP reducing SNORD105 and PPAN expression decreases the risk of hepatocellular carcinoma in a Chinese population

by Chen, X., Gao, Y., He, Y., Li, L., Qu, Y., Tan, R., Yang, Z., Yu, H., Zhang, Q.
Published 2021