Nina S. Heiss

X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions

Nina S. Heiss, S. W. Knight, Tom Vulliamy et al. · Nature Genetics · 1998 · 944 citations

Genome Instability, Mendelian Disorder, Genetic Disorder +10

Genomic rearrangement in NEMO impairs NF-κB activation and is a cause of incontinentia pigmenti

Asma Smahi, Nina S. Heiss, Petra Kioschis et al. · Nature · 2000 · 736 citations

Transcriptional Regulation, Genetics, Genomic Mechanism +7

X-Linked Dyskeratosis Congenita Is Predominantly Caused by Missense Mutations in the DKC1 Gene

S. W. Knight, Nina S. Heiss, T. Vulliamy et al. · The American Journal of Human Genetics · 1999 · 260 citations · Full text

Missense Mutations, Dkc1 Gene, Mendelian Disorder +8

Unexplained aplastic anaemia, immunodeficiency, and cerebellar hypoplasia (Hoyeraal‐Hreidarsson syndrome) due to mutations in the dyskeratosis congenita gene, <i>DKC1</i>

S. W. Knight, Nina S. Heiss, Tom Vulliamy et al. · British Journal of Haematology · 1999 · 222 citations

Developmental Anomaly, Dyskeratosis Congenita Gene, Mendelian Disorder +15

Overlap of dyskeratosis congenita with the Hoyeraal-Hreidarsson syndrome

Reza Yaghmai, Arash Kimyai‐Asadi, Karoline Rostamiani et al. · The Journal of Pediatrics · 2000 · 74 citations