Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Bengt Fundín"'
Autor:
Jan Gehlen, Ann-Sophie Giel, Ricarda Köllges, Stephan L. Haas, Rong Zhang, Jiri Trcka, Ayse Ö. Sungur, Florian Renziehausen, Dorothea Bornholdt, Daphne Jung, Paul D. Hoyer, Agneta Nordenskjöld, Dick Tibboel, John Vlot, Manon C.W. Spaander, Robert Smigiel, Dariusz Patkowski, Nel Roeleveld, Iris ALM. van Rooij, Ivo de Blaauw, Alice Hölscher, Marcus Pauly, Andreas Leutner, Joerg Fuchs, Joel Niethammer, Maria-Theodora Melissari, Ekkehart Jenetzky, Nadine Zwink, Holger Thiele, Alina Christine Hilger, Timo Hess, Jessica Trautmann, Matthias Marks, Martin Baumgarten, Gaby Bläss, Mikael Landén, Bengt Fundin, Cynthia M. Bulik, Tracie Pennimpede, Michael Ludwig, Kerstin U. Ludwig, Elisabeth Mangold, Stefanie Heilmann-Heimbach, Susanne Moebus, Bernhard G. Herrmann, Kristina Alsabeah, Carmen M. Burgos, Helene E. Lilja, Sahar Azodi, Pernilla Stenström, Einar Arnbjörnsson, Barbora Frybova, Dariusz M. Lebensztejn, Wojciech Debek, Elwira Kolodziejczyk, Katarzyna Kozera, Jaroslaw Kierkus, Piotr Kaliciński, Marek Stefanowicz, Anna Socha-Banasiak, Michal Kolejwa, Anna Piaseczna-Piotrowska, Elzbieta Czkwianianc, Markus M. Nöthen, Phillip Grote, Michal Rygl, Konrad Reinshagen, Nicole Spychalski, Barbara Ludwikowski, Jochen Hubertus, Andreas Heydweiller, Benno Ure, Oliver J. Muensterer, Ophelia Aubert, Jan-Hendrik Gosemann, Martin Lacher, Petra Degenhardt, Thomas M. Boemers, Anna Mokrowiecka, Ewa Małecka-Panas, Markus Wöhr, Michael Knapp, Guido Seitz, Annelies de Klein, Grzegorz Oracz, Erwin Brosens, Heiko Reutter, Johannes Schumacher
Publikováno v:
HGG Advances, Vol 3, Iss 2, Pp 100093- (2022)
Summary: Esophageal atresia with or without tracheoesophageal fistula (EA/TEF) is the most common congenital malformation of the upper digestive tract. This study represents the first genome-wide association study (GWAS) to identify risk loci for EA/
Externí odkaz:
https://doaj.org/article/e9a5e2a8eb8e4559958fd4286f773ad1
Autor:
Abraham Reichenberg, Nancy L Pedersen, David Mataix-Cols, Matthew W Halvorsen, Bengt Fundín, Lambertus Klei, Cynthia M Bulik, Dorothy E. Grice, Kathryn Roeder, Christian Rück, B. Devlin, James J Crowley, Christina M. Hultman, Joseph D. Buxbaum, Mikael Landén, Sven Sandin, Elles de Schipper, Julia Boberg, Behrang Mahjani, Manuel Mattheisen
Publikováno v:
Mahjani, B, Klei, L, Mattheisen, M, Halvorsen, M W, Reichenberg, A, Roeder, K, Pedersen, N L, Boberg, J, de Schipper, E, Bulik, C M, Landén, M, Fundín, B, Mataix-Cols, D, Sandin, S, Hultman, C M, Crowley, J J, Buxbaum, J D, Rück, C, Devlin, B & Grice, D E 2022, ' The Genetic Architecture of Obsessive-Compulsive Disorder : Contribution of Liability to OCD From Alleles Across the Frequency Spectrum ', American Journal of Psychiatry, vol. 179, no. 3, pp. 216-225 . https://doi.org/10.1176/appi.ajp.2021.21010101
Am J Psychiatry
Am J Psychiatry
Objective: Obsessive-compulsive disorder (OCD) is known to be substantially heritable; however, the contribution of genetic variation across the allele frequency spectrum to this heritability remains uncertain. The authors used two new homogeneous co
Autor:
Ruyue Zhang, Andreas Birgegård, Bengt Fundín, Mikael Landén, Laura M. Thornton, Cynthia M. Bulik, Lisa Dinkler
Publikováno v:
European eating disorders review : the journal of the Eating Disorders Association. 30(5)
Among individuals with eating disorders (ED), those with co-occurring autism are often considered to have more severe presentations and poorer prognosis. However, previous findings have been contradictory and limited by small sample size and/or cross