Mooser, Vincent

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Number of items: 7.

Journal Article

Bhérer, Claude; Eveleigh, Robert; Trajanoska, Katerina; St-Cyr, Janick; Paccard, Antoine; Nadukkalam Ravindran, Praveen; Caron, Elizabeth; Bader Asbah, Nimara; McClelland, Peyton; Wei, Clare; Baumgartner, Iris; Schindewolf, Marc; Döring, Yvonne; Perley, Danielle; Lefebvre, François; Lepage, Pierre; Bourgey, Mathieu; Bourque, Guillaume; Ragoussis, Jiannis; Mooser, Vincent; ... (2024). A cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genome. NPJ genomic medicine, 9(8) Springer Nature 10.1038/s41525-024-00390-3

Hasse, Barbara; Tarr, Philip E; Marques-Vidal, Pedro; Waeber, Gerard; Preisig, Martin; Mooser, Vincent; Valeri, Fabio; Djalali, Sima; Rauch, Andri; Bernasconi, Enos; Calmy, Alexandra; Cavassini, Matthias; Vernazza, Pietro; Battegay, Manuel; Weber, Rainer; Senn, Oliver; Vollenweider, Peter; Ledergerber, Bruno; Aubert, V; Barth, J; ... (2015). Strong Impact of Smoking on Multimorbidity and Cardiovascular Risk Among Human Immunodeficiency Virus-Infected Individuals in Comparison With the General Population. Open Forum Infectious Diseases, 2(3), ofv108. Oxford University Press 10.1093/ofid/ofv108

Glaus, Jennifer; Vandeleur, Caroline L; von Känel, Roland; Lasserre, Aurélie M; Strippoli, Marie-Pierre F; Gholam-Rezaee, Mehdi; Castelao, Enrique; Marques-Vidal, Pedro; Bovet, Pascal; Merikangas, Kathleen; Mooser, Vincent; Waeber, Gérard; Vollenweider, Peter; Aubry, Jean-Michel; Preisig, Martin (2014). Associations between mood, anxiety or substance use disorders and inflammatory markers after adjustment for multiple covariates in a population-based study. Journal of psychiatric research, 58, pp. 36-45. Elsevier 10.1016/j.jpsychires.2014.07.012

Blum, Manuel R.; Collet, Tinh-Hai; Krebs, Danielle; Stettler, Christoph; Christ, Emanuel; Virgini, Vanessa; Sykiotis, Gerasimos; Frey, Peter; Reichenbach, Stephan; Boulat, Olivier; Mooser, Vincent; Jüni, Peter; Fiedler, Martin; Aujesky, Drahomir; Pitteloud, Nelly; Rodondi, Nicolas (2013). Subklinische Hypothyreose: Risiken, aktuelle Empfehlungen und randomisierte Studie in der Schweiz. Schweizerisches Medizin-Forum SMF / Swiss medical forum / Forum médical suisse FMS, 13(39), pp. 772-775. EMH Editores Medicorum Helveticorum

Bender, Nicole; Allemann, Noëmi; Marek, Diana; Vollenweider, Peter; Waeber, Gérard; Mooser, Vincent; Egger, Matthias; Bochud, Murielle (2011). Association between variants of the leptin receptor gene (LEPR) and overweight: a systematic review and an analysis of the CoLaus study. PLoS ONE, 6(10), e26157. Lawrence, Kans.: Public Library of Science 10.1371/journal.pone.0026157

Hor, Hyun; Kutalik, Zoltán; Dauvilliers, Yves; Valsesia, Armand; Lammers, Gert J; Donjacour, Claire E H M; Iranzo, Alex; Santamaria, Joan; Peraita Adrados, Rosa; Vicario, José L; Overeem, Sebastiaan; Arnulf, Isabelle; Theodorou, Ioannis; Jennum, Poul; Knudsen, Stine; Bassetti, Claudio; Mathis, Johannes; Lecendreux, Michel; Mayer, Geert; Geisler, Peter; ... (2010). Genome-wide association study identifies new HLA class II haplotypes strongly protective against narcolepsy. Nature genetics, 42(9), pp. 786-9. New York, N.Y.: Nature America 10.1038/ng.647

Working Paper

Bhérer, Claude; Eveleigh, Robert; Trajanoska, Katerina; St-Cry, Janick; Paccard, Antoine; Ravindran, Praveen Nadukkalam; Caron, Elizabeth; Asbah, Nimara Bader; Wei, Claire; Baumgartner, Iris; Schindewolf, Marc; Döring, Yvonne; Perley, Danielle; Lefebvre, François; Lepage, Pierre; Bourgey, Mathieu; Bourque, Guillaume; Ragoussis, Jiannis; Mooser, Vincent and Taliun, Daniel (2023). WEGS: a cost-effective sequencing method for genetic studies combining high-depth whole exome and low-depth whole genome (In Press) (bioRxiv). Cold Spring Harbor Laboratory 10.1101/2023.04.27.538531

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