Anzahl der Publikationen: 5
Zeitschriftenartikel
Torres, Guillermo G.; Nygaard, Marianne; Caliebe, Amke; Blanche, Helene; Hoffmann, Per; Flachsbart, Friederike; Schreiber, Stefan; Ellinghaus, David; Franke, Andre; Dose, Janina; Nebel, Almut; Strauch, Konstantin und Müller-Nurasyid, Martina
(2021):
Exome-wide association study identifies FN3KRP and PGP as new candidate longevity genes.
In: The Journals of Gerontology: Series A, Bd. 76, Nr. 5: S. 786-795
Torres, Guillermo G.; Nygaard, Marianne; Caliebe, Amke; Blanche, Helene; Chantalat, Sophie; Galan, Pilar; Lieb, Wolfgang; Christiansen, Lene; Deleuze, Jean-Francois; Christensen, Kaare; Strauch, Konstantin; Mueller-Nurasyid, Martina; Peters, Annette; Noethen, Markus M.; Hoffmann, Per; Flachsbart, Friederike; Schreiber, Stefan; Ellinghaus, David; Franke, Andre; Dose, Janina und Nebel, Almut
(2021):
Exome-Wide Association Study Identifies FN3KRP and PGP as New Candidate Longevity Genes.
In: Journals of Gerontology Series A-Biological Sciences and Medical Sciences, Bd. 76, Nr. 5: S. 786-795
Flachsbart, Friederike; Ellinghaus, David; Gentschew, Liljana; Heinsen, Femke-Anouska; Caliebe, Amke; Christiansen, Lene; Nygaard, Marianne; Christensen, Kaare; Blanche, Helene; Deleuze, Jean-Francois; Derbois, Celine; Galan, Pilar; Büning, Carsten; Brand, Stephan; Peters, Annette ORCID: https://orcid.org/0000-0001-6645-0985; Strauch, Konstantin; Müller-Nurasyid, Martina; Hoffmann, Per; Nöthen, Markus M.; Lieb, Wolfgang; Franke, Andre; Schreiber, Stefan und Nebel, Almut
(2016):
Immunochip analysis identifies association of the RAD50/IL13 region with human longevity.
In: Aging Cell, Bd. 15, Nr. 3: S. 585-588
[PDF, 187kB]
Hoffmann, Sandra; Clauss, Sebastian; Berger, Ina M.; Weiß, Birgit; Montalbano, Antonino; Röth, Ralph; Bucher, Madeline; Klier, Ina; Wakili, Reza; Seitz, Hervé; Schulze-Bahr, Eric; Katus, Hugo A.; Flachsbart, Friederike; Nebel, Almut; Guenther, Sabina P. W.; Bagaev, Erik; Rottbauer, Wolfgang; Kääb, Stefan; Just, Steffen und Rappold, Gudrun A.
(2016):
Coding and non-coding variants in the SHOX2 gene in patients with early-onset atrial fibrillation.
In: Basic Research in Cardiology, Bd. 111, Nr. 3, 36
Heid, Iris M.; Huth, Cornelia; Loos, Ruth J. F.; Kronenberg, Florian; Adamkova, Vera; Anand, Sonia S.; Ardlie, Kristin; Biebermann, Heike; Bjerregaard, Peter; Boeing, Heiner; Bouchard, Claude; Ciullo, Marina; Cooper, Jackie A.; Corella, Dolores; Dina, Christian; Engert, James C.; Fisher, Eva; Frances, Francesc; Froguel, Philippe; Hebebrand, Johannes; Hegele, Robert A.; Hinney, Anke; Hoehe, Margret R.; Hu, Frank B.; Hubacek, Jaroslav A.; Humphries, Steve E.; Hunt, Steven C.; Illig, Thomas; Jarvelin, Marjo-Riita; Kaakinen, Marika; Kollerits, Barbara; Krude, Heiko; Kumar, Jitender; Lange, Leslie A.; Langer, Birgit; Li, Shengxu; Luchner, Andreas; Lyon, Helen N.; Meyre, David; Mohlke, Karen L.; Mooser, Vincent; Nebel, Almut; Nguyen, Thuy Trang; Paulweber, Bernhard; Perusse, Louis; Qi, Lu; Rankinen, Tuomo; Rosskopf, Dieter; Schreiber, Stefan; Sengupta, Shantanu; Sorice, Rossella; Suk, Anita; Thorleifsson, Gudmar; Thorsteinsdottir, Unnur; Voelzke, Henry; Vimaleswaran, Karani S.; Wareham, Nicholas J.; Waterworth, Dawn; Yusuf, Salim; Lindgren, Cecilia; McCarthy, Mark I.; Lange, Christoph; Hirschhorn, Joel N.; Laird, Nan und Wichmann, Heinz-Erich
(Oktober 2009):
Meta-Analysis of the INSIG2 Association with Obesity Including 74,345 Individuals. Does Heterogeneity of Estimates Relate to Study Design?
In: PLOS Genetics
5(10), e1000694
[PDF, 297kB]
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