Kushner, Steven A.

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

Mullins, N., Forstner, A. J., O’Connell, K. S., Coombes, B., Coleman, J. R. I., Qiao, Z., Als, T. D., Bigdeli, T. B., Børte, S., Bryois, J., et al. (2021) · Nature Genetics

Bipolar Disorder and TreatmentGenetic Associations and Epidemiology

Cited by 1,517

Neuronal competition and selection during memory formation

Han, J.-H., Kushner, S. A., Yiu, A. P., Cole, C. J., Matynia, A., Brown, R. A., Neve, R. L., Guzowski, J. F., Silva, A. J., & Josselyn, S. A. (2007) · Science

Memory and Neural MechanismsNeuroscience and Neuropharmacology Research

Cited by 682

Risk of Postpartum Relapse in Bipolar Disorder and Postpartum Psychosis: A Systematic Review and Meta-Analysis

Wesseloo, R., Kamperman, A. M., Munk-Olsen, T., Pop, V. J. M., Kushner, S. A., & Bergink, V. (2016) · American Journal of Psychiatry

Maternal Mental Health During Pregnancy and PostpartumBipolar Disorder and Treatment

Cited by 469

Activity-based protein profiling reveals off-target proteins of the FAAH inhibitor BIA 10-2474

van Esbroeck, A. C. M., Janssen, A. P. A., Cognetta, A. B., Ogasawara, D., Shpak, G., van der Kroeg, M., Kantae, V., Baggelaar, M. P., de Vrij, F. M. S., Deng, H., et al. (2017) · Science

Cannabis and Cannabinoid ResearchComputational Drug Discovery Methods

Cited by 332

Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome model

Silva-Santos, S., van Woerden, G. M., Bruinsma, C. F., Mientjes, E., Jolfaei, M. A., Distel, B., Kushner, S. A., & Elgersma, Y. (2015) · Journal of Clinical Investigation

Genetic Syndromes and ImprintingGenetics and Neurodevelopmental Disorders

Cited by 238

Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

Mullins, N., Kang, J., Campos, A. I., Coleman, J. R. I., Edwards, A. C., Galfalvy, H., Levey, D. F., Lori, A., Shabalin, A., Starnawska, A., et al. (2022) · Biological Psychiatry

Suicide and Self-Harm StudiesGenetic Associations and Epidemiology

Cited by 238

Treatment of Psychosis and Mania in the Postpartum Period

Bergink, V., Burgerhout, K. M., Koorengevel, K. M., Kamperman, A. M., Hoogendijk, W. J., Lambregtse-van den Berg, M. P., & Kushner, S. A. (2015) · American Journal of Psychiatry

Maternal Mental Health During Pregnancy and PostpartumElectroconvulsive Therapy Studies

Cited by 143

Novel genetic loci affecting facial shape variation in humans

Xiong, Z., Dankova, G., Howe, L. J., Lee, M. K., Hysi, P. G., de Jong, M. A., Zhu, G., Adhikari, K., Li, D., Li, Y., et al. (2019) · eLife

Genetic Associations and EpidemiologyMorphological variations and asymmetry

Cited by 92

Fragile X mice have robust mGluR5-dependent alterations of social behaviour in the Automated Tube Test

de Esch, C. E. F., van den Berg, W. E., Buijsen, R. A. M., Jaafar, I. A., Nieuwenhuizen-Bakker, I. M., Gasparini, F., Kushner, S. A., & Willemsen, R. (2015) · Neurobiology of Disease

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 45

Temporal and Region-Specific Requirements of αCaMKII in Spatial and Contextual Learning

Achterberg, K. G., Buitendijk, G. H. S., Kool, M. J., Goorden, S. M. I., Post, L., Slump, D. E., Silva, A. J., van Woerden, G. M., Kushner, S. A., & Elgersma, Y. (2014) · The Journal of Neuroscience

Memory and Neural MechanismsNeuroscience and Neuropharmacology Research

Cited by 44

The intellectual disability-associated CAMK2G p.Arg292Pro mutation acts as a pathogenic gain-of-function

Proietti Onori, M., Koopal, B., Everman, D. B., Worthington, J. D., Jones, J. R., Ploeg, M. A., Mientjes, E., van Bon, B. W., Kleefstra, T., Schulman, H., et al. (2018) · Human Mutation

Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases

Cited by 39

A rare missense variant in RCL1 segregates with depression in extended families.

Amin, N., de Vrij, F. M. S., Baghdadi, M., Brouwer, R. W. W., van Rooij, J. G. J., Jovanova, O., Uitterlinden, A. G., Hofman, A., Janssen, H. L. A., Darwish Murad, S., et al. (2018) · Molecular Psychiatry

Genetic Associations and EpidemiologyTreatment of Major Depression

Cited by 37

Second-tier trio exome sequencing after negative solo clinical exome sequencing: an efficient strategy to increase diagnostic yield and decipher molecular bases in undiagnosed developmental disorders

Tran Mau-Them, F., Moutton, S., Racine, C., Vitobello, A., Bruel, A.-L., Nambot, S., Kushner, S. A., de Vrij, F. M. S., Lehalle, D., Jean-Marçais, N., et al. (2020) · Human Genetics

Genomics and Rare DiseasesConnective tissue disorders research

Cited by 14