1. A novel ALDH5A1 mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family. Issue 8 (4th July 2013) Authors: Püttmann, Lucia; Stehr, Henning; Garshasbi, Masoud; Hu, Hao; Kahrizi, Kimia; Lipkowitz, Bettina; Jamali, Payman; Tzschach, Andreas; Najmabadi, Hossein; Ropers, Hans‐Hilger; Musante, Luciana; Kuss, Andreas W. Journal: American journal of medical genetics Issue: Volume 161:Issue 8(2013:Aug.) Page Start: 1915 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. BDNF: mRNA expression in urine cells of patients with chronic kidney disease and its role in kidney function. Issue 11 (21st August 2018) Authors: Endlich, Nicole; Lange, Tim; Kuhn, Jana; Klemm, Paul; Kotb, Ahmed M.; Siegerist, Florian; Kindt, Frances; Lindenmeyer, Maja T.; Cohen, Clemens D.; Kuss, Andreas W.; Nath, Neetika; Rettig, Rainer; Lendeckel, Uwe; Zimmermann, Uwe; Amann, Kerstin; Stracke, Sylvia; Endlich, Karlhans Journal: Journal of cellular and molecular medicine Issue: Volume 22:Issue 11(2018) Page Start: 5265 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Exome Sequencing Discloses Ionizing-radiation-induced DNA Variants in the Genome of Human Gingiva Fibroblasts. Issue 1 (July 2018) Authors: Nath, Neetika; Esche, Jennifer; Müller, Jessica; Jensen, Lars R.; Port, Matthias; Stanke, Mario; Kaderali, Lars; Scherthan, Harry; Kuss, Andreas W. Journal: Health physics Issue: Volume 115:Issue 1(2018:Jul.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Ionizing Radiation Alters the Transition/Transversion Ratio in the Exome of Human Gingiva Fibroblasts. Issue 1 (July 2020) Authors: Nath, Neetika; Hagenau, Lisa; Weiss, Stefan; Tzvetkova, Ana; Jensen, Lars R.; Kaderali, Lars; Port, Matthias; Scherthan, Harry; Kuss, Andreas W. Journal: Health physics Issue: Volume 119:Issue 1(2020) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Mutations of the aminoacyl‐tRNA‐synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability. Issue 6 (23rd March 2017) Authors: Musante, Luciana; Püttmann, Lucia; Kahrizi, Kimia; Garshasbi, Masoud; Hu, Hao; Stehr, Henning; Lipkowitz, Bettina; Otto, Sabine; Jensen, Lars R.; Tzschach, Andreas; Jamali, Payman; Wienker, Thomas; Najmabadi, Hossein; Ropers, Hans Hilger; Kuss, Andreas W. Journal: Human mutation Issue: Volume 38:Issue 6(2017) Page Start: 621 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Submicroscopic genomic rearrangements change gene expression in T‐cell large granular lymphocyte leukemia. (9th April 2014) Authors: Iżykowska, Katarzyna; Zawada, Mariola; Nowicka, Karina; Grabarczyk, Piotr; Kuss, Andreas W.; Weissmann, Robert; Busemann, Christoph; Ludwig, Wolf‐Dieter; Schmidt, Christian A.; Przybylski, Grzegorz K. Journal: European journal of haematology Issue: Volume 93:Number 2(2014:Aug.) Page Start: 143 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. The transcription factor Dach1 is essential for podocyte function. Issue 5 (2nd March 2018) Authors: Endlich, Nicole; Kliewe, Felix; Kindt, Frances; Schmidt, Katharina; Kotb, Ahmed M.; Artelt, Nadine; Lindenmeyer, Maja T.; Cohen, Clemens D.; Döring, Franziska; Kuss, Andreas W.; Amann, Kerstin; Moeller, Marcus J.; Kabgani, Nazanin; Blumenthal, Antje; Endlich, Karlhans Journal: Journal of cellular and molecular medicine Issue: Volume 22:Issue 5(2018) Page Start: 2656 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Transcriptome Alterations In X-Irradiated Human Gingiva Fibroblasts. Issue 2 (August 2016) Authors: Weissmann, Robert; Kacprowski, Tim; Peper, Michel; Esche, Jennifer; Jensen, Lars R.; van Diepen, Laura; Port, Matthias; Kuss, Andreas W.; Scherthan, Harry Journal: Health physics Issue: Volume 111:Issue 2(2016:Aug.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. West syndrome caused by ST3Gal‐III deficiency. (17th December 2012) Authors: Edvardson, Simon; Baumann, Anna‐Maria; Mühlenhoff, Martina; Stephan, Oliver; Kuss, Andreas W.; Shaag, Avraham; He, Liqun; Zenvirt, Shamir; Tanzi, Raimo; Gerardy‐Schahn, Rita; Elpeleg, Orly Journal: Epilepsia Issue: Volume 54:issue 2(2013:Feb.) Page Start: e24 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗