Horsthemke, Bernhard

Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization

Cavaillé, J., Buiting, K., Kiefmann, M., Lalande, M., Brannan, C. I., Horsthemke, B., Bachellerie, J.-P., Brosius, J., & Hüttenhofer, A. (2000) · Proceedings of the National Academy of Sciences

Genetic Syndromes and ImprintingRNA modifications and cancer

Cited by 601

Epimutations in Prader-Willi and Angelman Syndromes: A Molecular Study of 136 Patients with an Imprinting Defect

Buiting, K., Groß, S., Lich, C., Gillessen-Kaesbach, G., El-Maarri, O., & Horsthemke, B. (2003) · The American Journal of Human Genetics

Genetic Syndromes and ImprintingGenomic variations and chromosomal abnormalities

Cited by 372

A critical view on transgenerational epigenetic inheritance in humans

Horsthemke, B. (2018) · Nature Communications

Epigenetics and DNA MethylationBirth, Development, and Health

Cited by 349

Mechanisms of imprinting of the Prader-Willi/Angelman region

Horsthemke, B., & Wagstaff, J. (2008) · American Journal of Medical Genetics Part A

Genetic Syndromes and ImprintingEpigenetics and DNA Methylation

Cited by 320

C15orf2 and a novel noncoding transcript from the Prader–Willi/Angelman syndrome region show monoallelic expression in fetal brain

Buiting, K., Nazlican, H., Galetzka, D., Wawrzik, M., Groβ, S., & Horsthemke, B. (2007) · Genomics

Genetic Syndromes and ImprintingGenomics and Chromatin Dynamics

Cited by 61

Systematic analysis and prediction of genes associated with monogenic disorders on human chromosome X

Leitão, E., Schröder, C., Parenti, I., Dalle, C., Rastetter, A., Kühnel, T., Kuechler, A., Kaya, S., Gérard, B., Schaefer, E., et al. (2022) · Nature Communications

Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders

Cited by 47