1. A Novel Method for Detecting Association Between DNA Methylation and Diseases Using Spatial Information. Issue 8 (22nd September 2014) Authors: Yip, Wai‐Ki; Fier, Heide; DeMeo, Dawn L.; Aryee, Martin; Laird, Nan; Lange, Christoph Journal: Genetic epidemiology Issue: Volume 38:Issue 8(2014) Page Start: 714 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. 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) ↗
3. 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) ↗