Corinne Pfister

Publications | Mémoires et thèses

La recherche avancée est accessible via Serval

Les publications peuvent être gérées en accédant à Serval via MyUnil


9 publications

2023 | 2019 | 2017 | 2014 | 2011 | 2010 | 2007 | 2000 |
2023
Epigenetic silencing of selected hypothalamic neuropeptides in narcolepsy with cataplexy.
Seifinejad A., Ramosaj M., Shan L., Li S., Possovre M.L., Pfister C., Fronczek R., Garrett-Sinha L.A., Frieser D., Honda M. et al., 2023/05/09. Proceedings of the National Academy of Sciences of the United States of America, 120 (19) pp. e2220911120. Peer-reviewed.
[URN][DOI][WoS][Pmid][serval:BIB_1008AC8B48C5]
2019
 
Kleine-Levin syndrome is associated with LMOD3 variants.
Al Shareef S.M., Basit S., Li S., Pfister C., Pradervand S., Lecendreux M., Mayer G., Dauvilliers Y., Salpietro V., Houlden H. et al., 2019/06. Journal of sleep research, 28 (3) pp. e12718. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_193D58CD77E1]
2017
 
Rare missense mutations in P2RY11 in narcolepsy with cataplexy.
Degn M., Dauvilliers Y., Dreisig K., Lopez R., Pfister C., Pradervand S., Rahbek Kornum B., Tafti M., 2017/06/01. Brain, 140 (6) pp. 1657-1668. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_31CF0EE2F0EA]
2014
 
DQB1 locus alone explains most of the risk and protection in narcolepsy with cataplexy in Europe.
Tafti M., Hor H., Dauvilliers Y., Lammers G.J., Overeem S., Mayer G., Javidi S., Iranzo A., Santamaria J., Peraita-Adrados R. et al., 2014. Sleep, 37 (1) pp. 19-25.
[DOI][WoS][Pmid][serval:BIB_0828CCB5A667]
2011
 
A missense mutation in myelin oligodendrocyte glycoprotein as a cause of familial narcolepsy with cataplexy.
Hor H., Bartesaghi L., Kutalik Z., Vicário J.L., de Andrés C., Pfister C., Lammers G.J., Guex N., Chrast R., Tafti M. et al., 2011. American Journal of Human Genetics, 89 (3) pp. 474-479.
[DOI][WoS][Pmid][serval:BIB_74EAE8242716]
2010
 
Elevated Tribbles homolog 2-specific antibody levels in narcolepsy patients.
Cvetkovic-Lopes V., Bayer L., Dorsaz S., Maret S., Pradervand S., Dauvilliers Y., Lecendreux M., Lammers G.J., Donjacour C.E., Du Pasquier R.A. et al., 2010. Journal of Clinical Investigation, 120 (3) pp. 713-719. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_6F1CF4DFB5CB]
 
Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy.
Hor H., Kutalik Z., Dauvilliers Y., Valsesia A., Lammers G.J., Donjacour C.E., Iranzo A., Santamaria J., Peraita Adrados R., Vicario J.L. et al., 2010. Nature Genetics, 42 (9) pp. 786-789.
[DOI][WoS][Pmid][serval:BIB_CFB40FFC4F99]
2007
 
Homer1a is a core brain molecular correlate of sleep loss.
Maret S., Dorsaz S., Gurcel L., Pradervand S., Petit B., Pfister C., Hagenbuchle O., O'Hara B.F., Franken P., Tafti M., 2007. Proceedings of the National Academy of Sciences of the United States of America, 104 (50) pp. 20090-20095. Peer-reviewed.
[DOI][WoS][Pmid][serval:BIB_1FDDFE432EBA]
2000
 
Activation of the amiloride-sensitive epithelial sodium channel by the serine protease mCAP1 expressed in a mouse cortical collecting duct cell line
Vuagniaux G., Vallet V., Jaeger N. F., Pfister C., Bens M., Farman N., Courtois-Coutry N., Vandewalle A., Rossier B. C., Hummler E., 2000/05. Journal of the American Society of Nephrology, 11 (5) pp. 828-34. Peer-reviewed.
[WoS][Pmid][serval:BIB_58082E4DD25F]
Partagez:
Unicentre - CH-1015 Lausanne
Suisse
Tél. +41 21 692 11 11
Canton de Vaud
Swiss University