Strom, Tim M.
Institut für Humangenetik · Technical University of Munich
27 papers on CoChat
Most cited papers
- Verified
Functional identity of hypothalamic melanocortin neurons depends on Tbx3
Quarta, C., Fisette, A., Xu, Y., Colldén, G., Legutko, B., Tseng, Y.-T., Reim, A., Wierer, M., De Rosa, M. C., Klaus, V., et al. (2019) · Nature Metabolism
Regulation of Appetite and ObesityHypothalamic control of reproductive hormones
Cited by 54
- Verified
Variants in CPLX1 in two families with autosomal-recessive severe infantile myoclonic epilepsy and ID
Redler, S., Strom, T. M., Wieland, T., Cremer, K., Engels, H., Distelmaier, F., Schaper, J., Küchler, A., Lemke, J. R., Jeschke, S., et al. (2017) · European Journal of Human Genetics
Genetics and Neurodevelopmental DisordersEpilepsy research and treatment
Cited by 38
- Verified
Bi-allelic Variants in RALGAPA1 Cause Profound Neurodevelopmental Disability, Muscular Hypotonia, Infantile Spasms, and Feeding Abnormalities
Wagner, M., Skorobogatko, Y., Pode-Shakked, B., Powell, C. M., Alhaddad, B., Seibt, A., Barel, O., Heimer, G., Hoffmann, C., Demmer, L. A., et al. (2020) · The American Journal of Human Genetics
Genetics and Neurodevelopmental DisordersProtein Kinase Regulation and GTPase Signaling
Cited by 31
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