31. Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2. (December 2016) Authors: Degenhardt, Franziska; Heinemann, Barbara; Strohmaier, Jana; Pfohl, Marvin A.; Giegling, Ina; Hofmann, Andrea; Ludwig, Kerstin U.; Witt, Stephanie H.; Ludwig, Michael; Forstner, Andreas J.; Albus, Margot; Schwab, Sibylle G.; Borrmann-Hassenbach, Margitta; Lennertz, Leonard; Wagner, Michael; Hoffm... Journal: Psychiatric genetics Issue: Volume 26:Number 6(2016:Dec.) Page Start: 293 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
32. Immunochip analysis identifies association of the RAD50/IL13 region with human longevity. Issue 3 (22nd March 2016) Authors: Flachsbart, Friederike; Ellinghaus, David; Gentschew, Liljana; Heinsen, Femke‐Anouska; Caliebe, Amke; Christiansen, Lene; Nygaard, Marianne; Christensen, Kaare; Blanché, Hélène; Deleuze, Jean‐François; Derbois, Céline; Galan, Pilar; Büning, Carsten; Brand, Stephan; Peters, Anette; Strauch, Konsta... Journal: Aging cell Issue: Volume 15:Issue 3(2016) Page Start: 585 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
33. Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study. (28th June 2018) Authors: Kalman, Janos L; Papiol, Sergi; Forstner, Andreas J; Heilbronner, Urs; Degenhardt, Franziska; Strohmaier, Jana; Adli, Mazda; Adorjan, Kristina; Akula, Nirmala; Alda, Martin; Anderson‐Schmidt, Heike; Andlauer, Till FM; Anghelescu, Ion‐George; Ardau, Raffaella; Arias, Bárbara; Arolt, Volker; Aubry,... Journal: Bipolar disorders Issue: Volume 21:Number 1(2019) Page Start: 68 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
34. Investigation of the role of TCF4 rare sequence variants in schizophrenia. Issue 5 (22nd May 2015) Authors: Basmanav, F. Buket; Forstner, Andreas J.; Fier, Heide; Herms, Stefan; Meier, Sandra; Degenhardt, Franziska; Hoffmann, Per; Barth, Sandra; Fricker, Nadine; Strohmaier, Jana; Witt, Stephanie H.; Ludwig, Michael; Schmael, Christine; Moebus, Susanne; Maier, Wolfgang; Mössner, Rainald; Rujescu, Dan; R... Journal: American journal of medical genetics Issue: Volume 168:Issue 5(2015) Page Start: 354 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
35. Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.1212. Issue 3 (29th January 2013) Authors: Draaken, Markus; Mughal, Sadaf S.; Pennimpede, Tracie; Wolter, Stefanie; Wittler, Lars; Ebert, Anne‐Karoline; Rösch, Wolfgang; Stein, Raimund; Bartels, Enrika; Schmidt, Dominik; Boemers, Thomas M.; Schmiedeke, Eberhard; Hoffmann, Per; Moebus, Susanne; Herrmann, Bernhard G.; Nöthen, Markus M.; Reu... Journal: Birth defects research Issue: Volume 97:Issue 3(2013:Mar.) Page Start: 133 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
36. Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis cases. Issue 3 (27th November 2015) Authors: Spier, Isabel; Drichel, Dmitriy; Kerick, Martin; Kirfel, Jutta; Horpaopan, Sukanya; Laner, Andreas; Holzapfel, Stefanie; Peters, Sophia; Adam, Ronja; Zhao, Bixiao; Becker, Tim; Lifton, Richard P; Perner, Sven; Hoffmann, Per; Kristiansen, Glen; Timmermann, Bernd; Nöthen, Markus M; Holinski-Feder, ... Journal: Journal of medical genetics Issue: Volume 53:Issue 3(2016) Page Start: 172 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
37. Meta-analysis of genome-wide association studies of aggressive and chronic periodontitis identifies two novel risk loci. (January 2019) Authors: Munz, Matthias; Richter, Gesa; Loos, Bruno; Jepsen, Søren; Divaris, Kimon; Offenbacher, Steven; Teumer, Alexander; Holtfreter, Birte; Kocher, Thomas; Bruckmann, Corinna; Jockel-Schneider, Yvonne; Graetz, Christian; Ahmad, Ilyas; Staufenbiel, Ingmar; Velde, Nathalie; Uitterlinden, André; Groot, Li... Journal: European journal of human genetics Issue: Volume 27:Number 1(2019) Page Start: 102 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
38. No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy. (4th February 2019) Authors: Schulz, Herbert; Ruppert, Ann‐Kathrin; Zara, Federico; Madia, Francesca; Iacomino, Michele; S. Vari, Maria; Balagura, Ganna; Minetti, Carlo; Striano, Pasquale; Bianchi, Amedeo; Marini, Carla; Guerrini, Renzo; Weber, Yvonne G.; Becker, Felicitas; Lerche, Holger; Kapser, Claudia; Schankin, Christop... Journal: Epilepsia Issue: Volume 60:issue 5(2019) Page Start: e31 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
39. Nonsyndromic cleft lip with or without cleft palate: Increased burden of rare variants within Gremlin‐1, a component of the bone morphogenetic protein 4 pathway. Issue 6 (7th April 2014) Authors: Al Chawa, Taofik; Ludwig, Kerstin U.; Fier, Heide; Pötzsch, Bernd; Reich, Rudolf H.; Schmidt, Gül; Braumann, Bert; Daratsianos, Nikolaos; Böhmer, Anne C.; Schuencke, Hannah; Alblas, Margrieta; Fricker, Nadine; Hoffmann, Per; Knapp, Michael; Lange, Christoph; Nöthen, Markus M.; Mangold, Elisabeth Journal: Birth defects research Issue: Volume 100:Issue 6(2014:Jun.) Page Start: 493 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
40. Pathway-Specific Genetic Risk for Alzheimer's Disease Differentiates Regional Patterns of Cortical Atrophy in Older Adults. (9th August 2019) Authors: Caspers, Svenja; Röckner, Melanie E; Jockwitz, Christiane; Bittner, Nora; Teumer, Alexander; Herms, Stefan; Hoffmann, Per; Nöthen, Markus M; Moebus, Susanne; Amunts, Katrin; Cichon, Sven; Mühleisen, Thomas W Journal: Cerebral cortex Issue: Volume 30:Number 2(2020) Page Start: 801 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗