Australian Parkinson's Genetics Study (APGS): Pilot (n=1532)

by Bivol, S., Campos, A.I, Cross, S., Ferguson, M., Garcia-Marin, L.M, Gratten, J., Lind, P.A, Loesch, D.Z, Martin, N.G, Medland, S.E, Mellick, G.D, Mitchell, B.L, Mosley, P.E, Mulcahy, A., Parker, R., Poortvliet, P.C, Rentería, M.E, Scherzer, C.R, Visscher, P.M
Published 2022

Genetic risk score for ovarian cancer based on chromosomal-scale length variation

by Brody, J.P, Toh, C.
Published 2021

Sensitive period-regulating genetic pathways and exposure to adversity shape risk for depression

by Crawford, K.M, Davis, K.A, de Leeuw, C., Dunn, E.C, Hensch, T.K, Lussier, A.A, Major Depressive Disorder Working Group of the Psychiatric Genomics Consortium, Ramírez-Tapia, J.C, Smoller, J.W, Takesian, A.E, Wang, M.-J, Zhu, Y.
Published 2022

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

The genetic consequences of captive breeding, environmental change and human exploitation in the endangered peninsular pronghorn

by Gutiérrez-Rivera, J.N, Hoffman, J.I, Klimova, A., Sánchez-Sotomayor, V.
Published 2022

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

Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates

by Harley, J.B, Hawley, M., Jarvik, G.P, Karlson, E.W, Koch, C., Lebo, M.S, Leppig, K.A, Mahanta, L.M, Myers, M.F, Oza, A., Prows, C.A, Rehm, H.L, Vijay Kumar, P.K, Weiss, S.T, Williams, M.S, Yu, W., Zouk, H.
Published 2022

Stratifying the Presymptomatic Phase of Genetic Frontotemporal Dementia by Serum NfL and pNfH: A Longitudinal Multicentre Study

by Afonso, S., Almeida, M.R, Anderl-Straub, S., Andersson, C., Antonell, A., Archetti, S., Arighi, A., Balasa, M., Barandiaran, M., Bargalló, N., Barro, C., Bartha, R., Bender, B., Benussi, A., Benussi, L., Bessi, V., Binetti, G., Black, S., Bocchetta, M., Borrego-Ecija, S., Borroni, B., Bras, J., Bruffaerts, R., Butler, C.R, Cañada, M., Cantoni, V., Caroppo, P., Cash, D., Castelo-Branco, M., Convery, R., Cope, T., Danek, A., de Mendonça, A., Di Fede, G., Díez, A., Ducharme, S., Duro, D., Fenoglio, C., Ferrari, C., Ferreira, C.B, Finger, E., Fox, N., Freedman, M., Frisoni, G., Fumagalli, G., Gabilondo, A., Galimberti, D., Gasparotti, R., Gauthier, S., Gazzina, S., Genetic Frontotemporal dementia Initiative (GENFI), Gerhard, A., Ghidoni, R., Giaccone, G., Gorostidi, A., Graff, C., Greaves, C., Guerreiro, R., Heller, C., Hoegen, T., Indakoetxea, B., Jelic, V., Jiskoot, L., Karnath, H.-O, Keren, R., Kuhle, J., Laforce, R., Langheinrich, T., Leitão, M.J, Levin, J., Lladó, A., Lombardi, G., Loosli, S., Maruta, C., Masellis, M., Mead, S., Meeter, L., Miltenberger, G., Mitchell, S., Moore, K., Moreno, F., Nacmias, B., Nicholas, J., Öijerstedt, L., Olives, J., Otto, M., Ourselin, S., Padovani, A., Panman, J., Papma, J.M, Peakman, G., Pievani, M., Pijnenburg, Y., Polito, C., Premi, E., Prioni, S., Prix, C., Rademakers, R., Redaelli, V., Reich, S., Rittman, T., Rogaeva, E., Rohrer, J.D, Rosa-Neto, P., Rosser, M., Rossi, G., Rowe, J.B, Sanchez-Valle, R., Santana, I., Santiago, B., Scarpini, E., Schönecker, S., Seelaar, H., Semler, E., Shafei, R., Shoesmith, C., Sorbi, S., Synofzik, M., Tábuas-Pereira, M., Tagliavini, F., Tainta, M., Taipa, R., Tang-Wai, D., Tartaglia, M.C, Thomas, D.L, Thompson, P., Thonberg, H., Timberlake, C., Tiraboschi, P., Todd, E., Van Damme, P., van Minkelen, R., van Swieten, J.C, Vandenberghe, R., Vandenbulcke, M., Veldsman, M., Verdelho, A., Villanua, J., Warren, J., Wilke, C., Wlasich, E., Woollacott, I., Zetterberg, H., Zulaica, M.
Published 2022

Gene-Environment Interaction Analysis Incorporating Sex, Cardiometabolic Diseases, and Multiple Deprivation Index Reveals Novel Genetic Associations With COVID-19 Severity

by Lin, J., Manning, A.K, Marchek, C., Sevilla-Gonzalez, M.D.R, Tadess, B., Westerman, K.E
Published 2022

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

Hypothesizing in the Face of the Opioid Crisis Coupling Genetic Addiction Risk Severity (GARS...

by Badgaiyan, R.D, Bajaj, A., Baron, D., Blum, K., Bowirrat, A., Braverman, E.R, Elman, I., Giordano, J., Gold, M.S, Gomez, L.L, Gupta, A., Jalali, R., Modestino, E.J
Published 2022

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