Buiting, Karin

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

Prader–Willi syndrome and Angelman syndrome

Buiting, K. (2010) · American Journal of Medical Genetics Part C: Seminars in Medical Genetics

Genetic Syndromes and ImprintingGenomic variations and chromosomal abnormalities

Cited by 336

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