Search Results

Contribution of rare and potentially functionally relevant sequence variants in schizophrenia risk-Locus Xq28,distal by Claus, Isabelle (Author) , Sivalingam, S. (Author) , Koller, A. C. (Author) , Weiß, A. (Author) , Mathey, C. M. (Author) , Sindermann, L. (Author) , Klein, D. (Author) , Henschel, L. (Author) , Ludwig, K. U. (Author) , Hoffmann, P. (Author) , Heimbach, A. (Author) , Heilmann-Heimbach, S. (Author) , Vedder, H. (Author) , Kammerer-Ciernioch, J. (Author) , Stürmer, T. (Author) , Streit, Fabian (Author) , Maaser-Hecker, A. (Author) , Nenadić, I. (Author) , Baune, B. T. (Author) , Hartmann, A. M. (Author) , Konte, B. (Author) , Giegling, I. (Author) , Heilbronner, U. (Author) , Wagner, M. (Author) , Philipsen, A. (Author) , Schmidt, B. (Author) , Rujescu, D. (Author) , Buness, A. (Author) , Schulze, T. G. (Author) , Rietschel, Marcella (Author) , Forstner, A. J. (Author) , Nöthen, M. M. (Author) , Degenhardt, F. (Author) ,

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Impact of the -1T>C single-nucleotide polymorphism of the CD40 gene on the development of endothelial dysfunction in a pro-diabetic microenvironment by Joshi, Pooja (Author) , Rehberg, Franziska (Author) , Rumig, Cordula (Author) , Kliemank, Elisabeth (Author) , Krenning, Guido (Author) , Kopf, Stefan (Author) , Hecker, Markus (Author) , Wagner, Andreas H. (Author) ,

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Potential association between PSCA rs2976395 functional variant and pancreatic cancer risk by Corradi, Chiara (Author) , Lencioni, Giulia (Author) , Felici, Alessio (Author) , Rizzato, Cosmeri (Author) , Gentiluomo, Manuel (Author) , Ermini, Stefano (Author) , Archibugi, Livia (Author) , Mickevicius, Antanas (Author) , Lucchesi, Maurizio (Author) , Malecka-Wojciesko, Ewa (Author) , Basso, Daniela (Author) , Arcidiacono, Paolo Giorgio (Author) , Petrone, Maria Chiara (Author) , Carrara, Silvia (Author) , Götz, Mara (Author) , Bunduc, Stefania (Author) , Holleczek, Bernd (Author) , Aoki, Mateus Nóbrega (Author) , Uzunoglu, Faik G. (Author) , Zanette, Dalila Lucíola (Author) , Mambrini, Andrea (Author) , Jamroziak, Krzysztof (Author) , Oliverius, Martin (Author) , Lovecek, Martin (Author) , Cavestro, Giulia Martina (Author) , Milanetto, Anna Caterina (Author) , Peduzzi, Giulia (Author) , Duchonova, Beatrice Mohelnikova (Author) , Izbicki, Jakob R. (Author) , Zalinkevicius, Rimantas (Author) , Hlavac, Viktor (Author) , van Eijck, Casper H. J. (Author) , Brenner, Hermann (Author) , Vanella, Giuseppe (Author) , Vokacova, Klara (Author) , Soucek, Pavel (Author) , Tavano, Francesca (Author) , Perri, Francesco (Author) , Capurso, Gabriele (Author) , Hussein, Tamás (Author) , Kiudelis, Mindaugas (Author) , Kupcinskas, Juozas (Author) , Busch, Olivier R. (Author) , Morelli, Luca (Author) , Theodoropoulos, George E. (Author) , Testoni, Sabrina Gloria Giulia (Author) , Adamonis, Kestutis (Author) , Neoptolemos, John P. (Author) , Gazouli, Maria (Author) , Pasquali, Claudio (Author) , Kormos, Zita (Author) , Skalicky, Pavel (Author) , Pezzilli, Raffaele (Author) , Sperti, Cosimo (Author) , Kauffmann, Emanuele (Author) , Büchler, Markus W. (Author) , Schöttker, Ben (Author) , Hegyi, Péter (Author) , Capretti, Giovanni (Author) , Lawlor, Rita T. (Author) , Canzian, Federico (Author) , Campa, Daniele (Author) ,

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The role of polymorphisms at the Interleukin-1, Interleukin-4, GATA-3 and Cyclooxygenase-2 genes in non-surgical periodontal therapy by Walther, Kay-Arne (Author) , Gonzales, José Roberto (Author) , Gröger, Sabine (Author) , Ehmke, Benjamin (Author) , Kaner, Dogan (Author) , Lorenz, Katrin (Author) , Eickholz, Peter (Author) , Kocher, Thomas (Author) , Kim, Ti-Sun (Author) , Schlagenhauf, Ulrich (Author) , Koch, Raphael (Author) , Meyle, Jörg (Author) ,

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FOXG1 syndrome: genotype–phenotype association in 83 patients with FOXG1 variants by Mitter, Diana (Author) , Pringsheim, Milka (Author) , Kaulisch, Marc (Author) , Plümacher, Kim Sarah (Author) , Schröder, Simone (Author) , Warthemann, Rita (Author) , Abou Jamra, Rami (Author) , Baethmann, Martina (Author) , Bast, Thomas (Author) , Büttel, Hans-Martin (Author) , Cohen, Julie S. (Author) , Conover, Elizabeth (Author) , Courage, Carolina (Author) , Eger, Angelika (Author) , Fatemi, Ali (Author) , Grebe, Theresa A. (Author) , Hauser, Natalie S. (Author) , Heinritz, Wolfram (Author) , Helbig, Katherine L. (Author) , Heruth, Marion (Author) , Huhle, Dagmar (Author) , Höft, Karen (Author) , Karch, Stephanie (Author) , Kluger, Gerhard (Author) , Korenke, Christoph (Author) , Lemke, Johannes R. (Author) , Lutz, Richard E. (Author) , Patzer, Steffi (Author) , Prehl, Isabelle (Author) , Hoertnagel, Konstanze (Author) , Ramsey, Keri (Author) , Rating, Tina (Author) , Rieß, Angelika (Author) , Rohena, Luis (Author) , Schimmel, Mareike (Author) , Westman, Rachel (Author) , Zech, Frank-Martin (Author) , Zoll, Barbara (Author) , Malzahn, Dörthe (Author) , Zirn, Birgit (Author) , Brockmann, Knut (Author) ,

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Deleterious single nucleotide polymorphisms of protein kinase R identified by the computational approach by Melzer, Anna Maria (Author) , Palanisamy, Navaneethan (Author) ,

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A genome-wide association study of corneal astigmatism: the CREAM Consortium by Shah, Rupal (Author) , Jonas, Jost B. (Author) ,

A variant of the CXCL11 gene may influence susceptibility to contact allergy, particularly in polysensitized patients by Westphal, Götz Alexander (Author) , Schäkel, Knut (Author) ,

CYP24A1 variant modifies the association between use of oestrogen plus progestogen therapy and colorectal cancer risk by Garcia-Albeniz, Xabier (Author) , Brenner, Hermann (Author) , Hoffmeister, Michael (Author) , Ulrich, Cornelia (Author) , Chang-Claude, Jenny (Author) ,

T-786C single nucleotide polymorphism of the endothelial nitric oxide synthase gene as a risk factor for endothelial dysfunction in polymyalgia rheumatica by Löffers, Christine (Author) , Heilig, Bernhard (Author) , Hecker, Markus (Author) ,

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An integrated map of genetic variation from 1,092 human genomes by McVean, Gil (Author) , Korbel, Jan Oliver (Author) ,

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Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci by Asselbergs, Folkert W. (Author) , Kleber, Marcus E. (Author) , März, Winfried (Author) ,

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The role of genetic breast cancer susceptibility variants as prognostic factors by Fasching, Peter Andreas (Author) , Chang-Claude, Jenny (Author) , Nickels, Stefan (Author) , Burwinkel, Barbara (Author) , Marmé, Frederik (Author) , Schneeweiss, Andreas (Author) , Sohn, Christof (Author) ,

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A polymorphism within the connective tissue growth factor (CTGF) gene has no effect on non-invasive markers of beta-cell area and risk of type 2 diabetes by Pivovarova-Ramich, Olga (Author) , Fisher, Eva (Author) , Dudziak, Katarzyna (Author) , Ilkavets, Iryna (Author) , Dooley, Steven (Author) , Slominsky, Petr (Author) , Limborska, Svetlana (Author) , Weickert, Martin O. (Author) , Spranger, Joachim (Author) , Fritsche, Andreas (Author) , Boeing, Heiner (Author) , Pfeiffer, Andreas F. H. (Author) , Rudovich, Natalia (Author) ,

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Risk variant for schizophrenia in the neurogranin gene impacts on hippocampus activation during contextual fear conditioning by Pohlack, Sebastian (Author) , Nees, Frauke (Author) , Ruttorf, Michaela (Author) , Witt, Stephanie (Author) , Nieratschker, Vanessa (Author) , Rietschel, Marcella (Author) , Flor, Herta (Author) ,

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Evaluation of SNPs in miR-146a, miR196a2 and miR-499 as low-penetrance alleles in German and Italian familial breast cancer cases by Catucci, Irene (Author) , Yang, Rongxi (Author) , Verderio, Paolo (Author) , Pizzamiglio, Sara (Author) , Heesen, Ludwig (Author) , Hemminki, Kari (Author) , Sutter, Christian (Author) , Wappenschmidt, Barbara (Author) , Rath, Michèlle Geneviève (Author) , Arnold, Norbert (Author) , Bugert, Peter (Author) , Niederacher, Dieter (Author) , Meindl, Alfons (Author) , Schmutzler, Rita K. (Author) , Bartram, Claus R. (Author) , Ficarazzi, Filomena (Author) , Tizzoni, Laura (Author) , Zaffaroni, Daniela (Author) , Manoukian, Siranoush (Author) , Barile, Monica (Author) , Pierotti, Marco A. (Author) , Radice, Paolo (Author) , Burwinkel, Barbara (Author) , Peterlongo, Paolo (Author) ,

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Two naturally occurring variants of the serotonin receptor gene HTR3C are associated with nausea in pregnancy by Goecke, Tamme W. (Author) , Ekici, Arif B. (Author) , Niesler, Beate (Author) , Loehberg, Christian R. (Author) , Hammer, Christian (Author) , Rappold, Gudrun (Author) , Schanze, Denny (Author) , Straub, Verica (Author) , Altmann, Hans-Harald (Author) , Strissel, Pamela (Author) , Strick, Reiner (Author) , Beckmann, Matthias W. (Author) , Fasching, Peter Andreas (Author) ,

Single-nucleotide polymorphisms in DNA-repair genes and cutaneous melanoma by Figl, Adina (Author) , Scherer, Dominique (Author) , Nagore, Eduardo (Author) , Lorenzo Bermejo, Justo (Author) , Botella-Estrada, Rafael (Author) , Gast, Andreas (Author) , Thirumaran, Ranjit Kumar (Author) , Planelles, Dolores (Author) , Hemminki, Kari (Author) , Schadendorf, Dirk (Author) , Kumar, Rajiv (Author) ,

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Complement in human diseases: lessons from complement deficiencies by Botto, Marina (Author) , Kirschfink, Michael (Author) , Macor, Paolo (Author) , Pickering, Matthew C. (Author) , Würzner, Reinhard (Author) , Tedesco, Francesco (Author) ,

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TIMP-2 gene polymorphism is associated with intracerebral hemorrhage by Reuter, Björn (Author) , Bugert, Peter (Author) , Stroick, Mark Gregor (Author) , Bukow, Simone (Author) , Griebe, Martin (Author) , Hennerici, Michael G. (Author) , Fatar, Marc (Author) ,

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