Factors associated with participation by African Americans in a study of the genetics of glaucoma

by Addis, V., Lehman, A., Maguire, M., Mccoskey, M., Miller-Ellis, E., O’Brien, J., O’Keefe, L., Pan, W., Parikh, R., Salowe, R., Sankar, P.
Published 2019

Primary failure of eruption: Clinical and genetic findings in the mixed dentition

by Cafiero, C., D'Apolito, I., Frazier-Bowers, S.A, Grippaudo, C., Ricci, B.
Published 2018

Genetic analysis and prenatal diagnosis of 20 Chinese families with oculocutaneous albinism

by Li, H., Mao, Y., Tang, S., Xiang, Y., Xu, C., Xu, X., Xu, Y., Zhou, L.
Published 2021

Influence of genetic polymorphisms in genes of bone remodeling and angiogenesis process in the apical periodontitis

by Antunes, L.A.A, Antunes, L.S, da Silva, L.A.B, Küchler, E.C, Mazzi-Chaves, J.F, Petean, I.B.F, Salles, A.G, Segato, R.A.B, Soares, I.M.V, Sousa-Neto, M.D
Published 2018

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

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

Genetic differential susceptibility to the parent–child relationship quality and the life span development of compassion

by Cloninger, R., Dobewall, H., Hintsanen, M., Keltikangas-Järvinen, L., Lehtimäki, T., Lyytikäinen, L.-P, Raitakari, O.T, Saarinen, A., Zwir, I.
Published 2021

Recessive Genome-Wide Meta-analysis Illuminates Genetic Architecture of Type 2 Diabetes

by Bonàs-Guarch, S., Brandslund, I., Cole, J.B, Cortés-Sánchez, P., Florez, J.C, Grarup, N., Guindo-Martínez, M., Hansen, T., Huerta-Chagoya, A., Kaur, V., Kurki, M., Leong, A., Linneberg, A., Mercader, J.M, O'Connor, M.J, Pedersen, O., Rundsten, C.F, Schroeder, P., Torrents, D., Veerapen, K.
Published 2022

Clinical features and molecular genetic analysis in a Turkish family with oral white sponge nevus

by Ak, G., Cassidy, A.J, Çefle, K., Güllüoğlu, M.G, Koray, M., Kürklü, E., McLean, W.-H.-I, Öztürk, Ş, Palandüz, Ş, Tanyeri, H.
Published 2018

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

Genetic variability in exon 1 of the glucocorticoid receptor gene NR3C1 is associated with postoperative complications

by Bergman, E.A, Gråberg, T., Sjöholm, L.K, Strömmer, L., Wikström, A.-C, Winerdal, M., Winqvist, O.
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

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

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

Integration of Murine and Human Studies for Mapping Periodontitis Susceptibility

by Berger, K., Botzman, M., de Groot, L.C.P.G.M, Divaris, K., Dommisch, H., Franke, A., Gat-Viks, I., Haddad, Y.H, Hoffmann, P., Iraqi, F.A, Kocher, T., Krone, B., Laudes, M., Lieb, W., Loos, B., Mott, R., Munz, M., Nashef, A., Offenbacher, S., Qabaja, R., Salaymeh, Y., Schaefer, A., Uitterlinden, A.G, van der Velde, N., Wellmann, J., Wiess, E.
Published 2018

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