1. A multi-centre clinico-genetic analysis of the VPS35 gene in Parkinson disease indicates reduced penetrance for disease-associated variants. Issue 11 (2nd November 2012) Authors: Sharma, Manu; Ioannidis, John P A; Aasly, Jan O; Annesi, Grazia; Brice, Alexis; Bertram, Lars; Bozi, Maria; Barcikowska, Maria; Crosiers, David; Clarke, Carl E; Facheris, Maurizio F; Farrer, Matthew; Garraux, Gaetan; Gispert, Suzana; Auburger, Georg; Vilariño-Güell, Carles; Hadjigeorgiou, Georgio... Journal: Journal of medical genetics Issue: Volume 49:Issue 11(2012) Page Start: 721 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Analysis of Plasminogen Genetic Variants in Multiple Sclerosis Patients. Issue 7 (1st July 2016) Authors: Sadovnick, A Dessa; Traboulsee, Anthony L; Bernales, Cecily Q; Ross, Jay P; Forwell, Amanda L; Yee, Irene M; Guillot-Noel, Lena; Fontaine, Bertrand; Cournu-Rebeix, Isabelle; Alcina, Antonio; Fedetz, Maria; Izquierdo, Guillermo; Matesanz, Fuencisla; Hilven, Kelly; Dubois, Bénédicte; Goris, An; Ast... Journal: G3 Issue: Volume 6:Issue 7(2016) Page Start: 2073 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Co‐incidental C9orf72 expansion mutation‐related frontotemporal lobar degeneration pathology and sporadic Creutzfeldt−Jakob disease. (1st December 2020) Authors: Klotz, Sigrid; König, Theresa; Erdler, Marcus; Ulram, Andreas; Nguyen, Anita; Ströbel, Thomas; Zimprich, Alexander; Stögmann, Elisabeth; Regelsberger, Günther; Höftberger, Romana; Budka, Herbert; Kovacs, Gabor G.; Gelpi, Ellen Journal: European journal of neurology Issue: Volume 28:Number 3(2021) Page Start: 1009 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study. Issue 4 (8th January 2022) Authors: Domenighetti, Cloé; Sugier, Pierre‐Emmanuel; Ashok Kumar Sreelatha, Ashwin; Schulte, Claudia; Grover, Sandeep; Mohamed, Océane; Portugal, Berta; May, Patrick; Bobbili, Dheeraj R.; Radivojkov‐Blagojevic, Milena; Lichtner, Peter; Singleton, Andrew B.; Hernandez, Dena G.; Edsall, Connor; Mellick, Ge... Journal: Movement disorders Issue: Volume 37:Issue 4(2022) Page Start: 857 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Development of a multiplexed targeted mass spectrometry assay for LRRK2-phosphorylated Rabs and Ser910/Ser935 biomarker sites. Issue 2 (29th January 2021) Authors: Nirujogi, Raja S.; Tonelli, Francesca; Taylor, Matthew; Lis, Pawel; Zimprich, Alexander; Sammler, Esther; Alessi, Dario R. Journal: Biochemical journal Issue: Volume 478:Issue 2(2021) Page Start: 299 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Diagnostic exome sequencing in non-acquired focal epilepsies highlights a major role of GATOR1 complex genes. Issue 9 (21st February 2020) Authors: Krenn, Martin; Wagner, Matias; Hotzy, Christoph; Graf, Elisabeth; Weber, Sandrina; Brunet, Theresa; Lorenz-Depiereux, Bettina; Kasprian, Gregor; Aull-Watschinger, Susanne; Pataraia, Ekaterina; Stogmann, Elisabeth; Zimprich, Alexander; Strom, Tim M; Meitinger, Thomas; Zimprich, Fritz Journal: Journal of medical genetics Issue: Volume 57:Issue 9(2020) Page Start: 624 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. FP247The urinary microbiome during acute kidney injury in renal transplant recipients versus non-transplant recipients. (13th June 2019) Authors: Knafl, Daniela; Winnicki, Wolfgang; Zimprich, Alexander; Hotzy, Christoph; Barousch, Wolfgang; Lang, Rita Maria; Lobmeyr, Elisabeth; Baumgartner-Parzer, Sabina; Wagner, Ludwig Journal: Nephrology dialysis transplantation Issue: Volume 34(2019)Supplement 1 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Genome-wide Association and Meta-analysis of Age at Onset in Parkinson Disease: Evidence From the COURAGE-PD Consortium. (16th August 2022) Authors: Grover, Sandeep; Kumar Sreelatha, Ashwin Ashok; Pihlstrom, Lasse; Domenighetti, Cloé; Schulte, Claudia; Sugier, Pierre-Emmanuel; Radivojkov-Blagojevic, Milena; Lichtner, Peter; Mohamed, Océane; Portugal, Berta; Landoulsi, Zied; May, Patrick; Bobbili, Dheeraj; Edsall, Connor; Bartusch, Felix; Hanu... Journal: Neurology Issue: Volume 99:Number 7(2022) Page Start: e698 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Genome-wide significant association with seven novel multiple sclerosis risk loci. Issue 12 (16th October 2015) Authors: Lill, Christina M; Luessi, Felix; Alcina, Antonio; Sokolova, Ekaterina A; Ugidos, Nerea; de la Hera, Belén; Guillot-Noël, Léna; Malhotra, Sunny; Reinthaler, Eva; Schjeide, Brit-Maren M; Mescheriakova, Julia Y; Mashychev, Andriy; Wohlers, Inken; Akkad, Denis A; Aktas, Orhan; Alloza, Iraide; Antigü... Journal: Journal of medical genetics Issue: Volume 52:Issue 12(2015) Page Start: 848 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Lack of association between ABCC2 gene variants and treatment response in epilepsy. (January 2012) Authors: Hilger, Eva; Reinthaler, Eva Maria; Stogmann, Elisabeth; Hotzy, Christoph; Pataraia, Ekaterina; Baumgartner, Christoph; Zimprich, Alexander; Zimprich, Fritz Journal: Pharmacogenomics Issue: Volume 13:Number 2(2012) Page Start: 185 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗