What can genetics tell us about the schizophrenia construct?

by Smoller, J.W
Published 2022

Genetic researches among Malaysian familial hypercholesterolaemic population

by Al-Khateeb, A.R, Al-Talib, H.
Published 2016

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

Inferred expression regulator activities suggest genes mediating cardiometabolic genetic signals

by Amundadottir, L.T, Chung, C.C, Collins, I., Connelly, K., Hoskins, J.W, O'Brien, A., Shi, J., Zhong, J.
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

Towards the Development, Maintenance, and Standardized Phenotypic Characterization of Single-Seed-Descent Genetic Resources for Common Bean

by Alseekh, S., Bellucci, E., Bitocchi, E., Cortinovis, G., Fernie, A.R, Gioia, T., Graner, A., Marsella, M., Neumann, K., Oppermann, M., Papa, R.
Published 2021

Biomedical Data Commons (BMDC) prioritizes B-lymphocyte non-coding genetic variants in Type 1 Diabetes

by Bhardwaj, P., Gaddam, S., Guha, R.V, Oro, A.E, Piekos, S.N, Radhakrishnan, P.
Published 2021

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

PharmGKB, an Integrated Resource of Pharmacogenomic Knowledge

by Gong, L., Klein, T.E, Whirl-Carrillo, M.
Published 2021

Genetic differences in the behavioral organization of binge eating, conditioned food reward, and compulsive-like eating in C57BL/6J and DBA/2J strains

by Babbs, R.K, Bryant, C.D, Kelliher, J.C, Luttik, K.P, Mulligan, M.K, Scotellaro, J.L
Published 2018

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

Translational research for improving the care of familial hypercholesterolemia: The “ten countries study” and beyond

by Arikketh, D., Ashavaid, T.F, Atiqah, N., Balasubramaniam, S., Chan, D.C, Chang, N.-T, Ding, P.Y, Do, T.C, Ellis, K.L, George, P., Gonzalez-Santos, L.B, Hagger, M.S, Han, K.H, Hardcastle, S.J, Hu, M., Ismail, Z.M, Jannes, C.E, Kassim, A.M, Khoo, K.L, Kwok, S., Lam, C.S, Lansberg, P.J, Lin, J., Livingston, M., Marais, A.D, Mehta, M., Miida, T., Muir, L., Nawawi, H.M, Pang, J., Park, J.E, Peng, H.B, Pereira, A.C, Rahman, T.H.A, Ramli, A.S, Rangarajan, N., Razak, S.A, Santos, R.D, Shyong Tai, E., Sijbrands, E.J, Soran, H., Su, T.-C, Sullivan, D.R, Tan, H.C, Tomlinson, B., Truong, T.H, Verma, I.C, Watts, G.F, Wu, X., Yamashita, S., Zhao, D.
Published 2016

Identification of Cytochrome b-245, beta-chain gene mutations, and clinical presentations in Iranian patients with X-linked chronic granulomatous disease

by Abolnezhadian, F., Ghadiri, A.A, Ghandil, P., Heydari, A., Saberi, A., Sadeghi-Shabestari, M., Shamsizadeh, A.
Published 2021

Sequence and functional analyses of Haemophilus spp. genomic islands

by Adegbola, R., Bentley, S., Crook, D.W, Dimopoulou, I.D, Elamin, A.R.E, Erwin, A., Ferguson, D.J.P, Harding, R.M, Harrison, A., Hood, D.W, Juhas, M., Mansfield, L., Mohd-Zain, Z., Munson, R.S, Power, P.M, Smith, A.

Noise Exposure and Distortion Product Otoacoustic Emission Suprathreshold Amplitudes: A Genome-Wide Association Study

by Allayee, H., Bento, R.F, Crow, A.L, Friedman, R.A, Kasperbauer, G., Lavinsky, J., Mendonça, A., Wang, J.
Published 2021

Super-variants identification for brain connectivity

by Hu, J., Li, T., Wang, S., Zhang, H.
Published 2021

Heterozygous familial hypercholesterolaemia in a pair of identical twins: A case report and updated review

by Al-Khateeb, A.M, Chua, Y.-A, Mohd Kasim, N.A, Mohd Nawawi, H., Mohd Nor, N.S
Published 2019

Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability Syndrome

by Alkhunaizi, E., Brandt, T., Chitayat, D.A, DeFilippo, C.P, Douglas, G.V, Dubbs, H.A, Elloumi, H.Z, Glassford, M.R, Graf, W.D, Hannibal, M.C, Héron, B., Kim, L.E, Marco, E.J, Mignot, C., Monaghan, K.G, Morrow, M.M, Myers, K.A, Parikh, S., Quinonez, S.C, Rajabi, F., Sarnat, H.B, Shankar, S.P, Shinawi, M.S, Steele, J.L, van de Kamp, J.J.P, Veerapandiyan, A., Waldman, A.T
Published 2022

Relative proteome quantification of alpha, beta, gamma and delta globin chains in early eluting peaks of Bio-Rad variant II® CE-HPLC of hemoglobin from healthy and beta-thalassemia...

by Abdullah, U.Y.H, Fakhruzzaman bin Noorizhab, M.N, Fucharoen, S., Ibrahim, H.M, Jassim, H.M, Kek, T.L, Salleh, M.Z, Wilairat, P., Zilfalil, B.A
Published 2019

A novel homozygous synonymous variant further expands the phenotypic spectrum of POLR3A-related pathologies

by Altmüller, J., Campbell, S.E, Gordon, L.B, Kubisch, C., Lessel, D., Rading, K., Thiele, H.
Published 2022