Hoh, Josephine

Complement factor H polymorphism in age-related macular degeneration

Klein, R. J., Zeiss, C., Chew, E. Y., Tsai, J.-Y., Sackler, R. S., Haynes, C., Henning, A. K., SanGiovanni, J. P., Mane, S. M., Mayne, S. T., et al. (2005) · Science

Retinal Diseases and TreatmentsComplement system in diseases

Cited by 4,492

Interaction Between the Serotonin Transporter Gene (5-HTTLPR), Stressful Life Events, and Risk of Depression: A Meta-analysis

Risch, N., Herrell, R., Lehner, T., Liang, K.-Y., Eaves, L., Hoh, J., Griem, A., Kovacs, M., Ott, J., & Merikangas, K. R. (2009) · JAMA

Neurotransmitter Receptor Influence on BehaviorGenetic Associations and Epidemiology

Cited by 1,655

Replicating genotype–phenotype associations

NCI-NHGRI Working Group on Replication in Association Studies, Chanock, S. J., Manolio, T., Boehnke, M., Boerwinkle, E., Hunter, D. J., Thomas, G., Hirschhorn, J. N., Abecasis, G., Altshuler, D., et al. (2007) · Nature

Genetic Associations and EpidemiologyMeta-analysis and systematic reviews

Cited by 1,352

HTRA1 Promoter Polymorphism in Wet Age-Related Macular Degeneration

DeWan, A., Liu, M., Hartman, S., Zhang, S. S.-M., Liu, D. T. L., Zhao, C., Tam, P. O. S., Chan, W. M., Lam, D. S. C., Snyder, M., et al. (2006) · Science

Retinal Diseases and TreatmentsGenetic Associations and Epidemiology

Cited by 876

A Variant of the HTRA1 Gene Increases Susceptibility to Age-Related Macular Degeneration

Yang, Z., Camp, N. J., Sun, H., Tong, Z., Gibbs, D., Cameron, D. J., Chen, H., Zhao, Y., Pearson, E., Li, X., et al. (2006) · Science

Retinal Diseases and TreatmentsRetinal Development and Disorders

Cited by 796

Genetic signatures of exceptional longevity in humans

Sebastiani, P., Solovieff, N., DeWan, A. T., Walsh, K. M., Puca, A., Hartley, S. W., Melista, E., Andersen, S., Dworkis, D. A., Wilk, J. B., et al. (2012) · PLoS ONE

Genetic Associations and EpidemiologyGenetics, Aging, and Longevity in Model Organisms

Cited by 464

Strong association of the Y402H variant in complement factor H at 1q32 with susceptibility to age-related macular degeneration

Zareparsi, S., Branham, K. E. H., Li, M., Shah, S., Klein, R. J., Ott, J., Hoh, J., Abecasis, G. R., & Swaroop, A. (2005) · The American Journal of Human Genetics

Retinal Diseases and TreatmentsComplement system in diseases

Cited by 371

Loss of HtrA1-induced attenuation of TGF-β signaling in fibroblasts might not be the main mechanism of CARASIL pathogenesis

Liu, J., Dong, F., & Hoh, J. (2015) · Proceedings of the National Academy of Sciences

Cerebrovascular and genetic disordersTGF-β signaling in diseases

Cited by 9

Systematically identifying genetic signatures including novel SNP-clusters, nonsense variants, frame-shift INDELs, and long STR expansions that potentially link to unknown phenotypes existing in dog breeds

Li, Z., Wang, Z., Chen, Z., Voegeli, H., Lichtman, J. H., Smith, P., Liu, J., DeWan, A. T., & Hoh, J. (2023) · BMC Genomics

Genetic and phenotypic traits in livestockHuman-Animal Interaction Studies

Cited by 2