6 results for author:"Fossdal R." in Literature citations
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| No association between a common single nucleotide polymorphism, rs4141463, in the MACROD2 gene and autism spectrum disorder. Curran S., Bolton P., Rozsnyai K., Chiocchetti A., Klauck S.M., Duketis E., Poustka F., Schlitt S., Freitag C.M., Lee I. et al. Am. J. Med. Genet. B Neuropsychiatr. Genet. 156B:633-639(2011) · Mapped (1) |
| Common variants conferring risk of schizophrenia. Stefansson H., Ophoff R.A., Steinberg S., Andreassen O.A., Cichon S., Rujescu D., Werge T., Pietilainen O.P., Mors O., Mortensen P.B. et al. Nature 460:744-747(2009) · Mapped (34) |
| Disruption of the neurexin 1 gene is associated with schizophrenia. Rujescu D., Ingason A., Cichon S., Pietilainen O.P., Barnes M.R., Toulopoulou T., Picchioni M., Vassos E., Ettinger U., Bramon E. et al. Hum. Mol. Genet. 18:988-996(2009) · Mapped (8) |
| A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration). Fossdal R., Jonasson F., Kristjansdottir G.T., Kong A., Stefansson H., Gosh S., Gulcher J.R., Stefansson K. Hum. Mol. Genet. 13:975-981(2004) · UniProtKB (1) · Mapped (2) |
| Aberrant splicing in the PKD2 gene as a cause of polycystic kidney disease. Reynolds D.M., Hayashi T., Cai Y., Veldhuisen B., Watnick T.J., Lens X.M., Mochizuki T., Qian F., Maeda Y., Li L. et al. J. Am. Soc. Nephrol. 10:2342-2351(1999) · UniProtKB (1) |
| A spectrum of mutations in the second gene for autosomal dominant polycystic kidney disease (PKD2). Veldhuisen B., Saris J.J., de Haij S., Hayashi T., Reynolds D.M., Mochizuki T., Elles R., Fossdal R., Bogdanova N., van Dijk M.A. et al. Am. J. Hum. Genet. 61:547-555(1997) · UniProtKB (1) |