Wenzel, Wolfgang

Mutations in CHD7, Encoding a Chromatin-Remodeling Protein, Cause Idiopathic Hypogonadotropic Hypogonadism and Kallmann Syndrome

Kim, H.-G., Kurth, I., Lan, F., Meliciani, I., Wenzel, W., Eom, S. H., Kang, G. B., Rosenberger, G., Tekin, M., Ozata, M., et al. (2008) · The American Journal of Human Genetics

Congenital Ear and Nasal AnomaliesHypothalamic control of reproductive hormones

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WDR11, a WD protein that interacts with transcription factor EMX1, is mutated in idiopathic hypogonadotropic hypogonadism and Kallmann syndrome

Kim, H.-G., Ahn, J.-W., Kurth, I., Ullmann, R., Kim, H.-T., Kulharya, A., Ha, K.-S., Itokawa, Y., Meliciani, I., Wenzel, W., et al. (2010) · The American Journal of Human Genetics

Hypothalamic control of reproductive hormonesGenetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities

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GENIUS: An agentic AI framework for autonomous design and execution of simulation protocols

Soleymanibrojeni, M., Aydin, R., Guedes-Sobrinho, D., Dias, A. C., Piotrowski, M. J., Wenzel, W., & Rêgo, C. R. C. (2026) · Communications Materials

Machine Learning in Materials ScienceScientific Computing and Data Management

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