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

CYP2D6 Genetic Polymorphisms and Phenotypes in Different Ethnicities of Malaysian Breast Cancer Patients

by Abdul Rahman, S., Chan, S.C, Chin, F.W, Noor Akmal, S., Rosli, R.
Published 2016

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

Mutational screening through comprehensive bioinformatics analysis to detect novel germline mutations in the APC gene in patients with familial adenomatous polyposis (FAP)

by Bagherian, H., Ghadamyari, F., Ghasemi, F., Heidari, M.M, Khatami, M., Merat, S., Rejali, L., Zeinali, S.
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

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

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 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

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

Methylenetetrahydrofolate reductase C677T gene polymorphism and the association with dyslipidemia in type 2 diabetic Palestinian patients

by Abu Sabha, M., Elqadi, M., Ereqat, S., Eweidat, K., Nasereddin, A., Sabarneh, A., Yagmour, A.
Published 2021

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