Human Genome Epidemiology Literature Finder
|
Records 1 - 8 (of 8 Records) |
| Query Trace: Disease and GP2[original query] |
|---|
| Genetic analysis of the glycoprotein 2 gene in patients with chronic pancreatitis. Pancreas 2010 Apr 39 (3): 353-8. Masson Emmanuelle, Paliwal Sumit, Bhaskar Seema, Prakash Soami, Scotet Virginie, Reddy D Nageshwar, Le Maréchal Cédric, Ratan Chandak Giriraj, Chen Jian-Min, Férec Clau |
| Anti-GP2 IgA autoantibodies are associated with poor survival and cholangiocarcinoma in primary sclerosing cholangitis. Gut 2017 01 66 (1): 137-144. Jendrek Sebastian Torben, Gotthardt Daniel, Nitzsche Thomas, Widmann Laila, Korf Tobias, Michaels Maike Anna, Weiss Karl-Heinz, Liaskou Evaggelia, Vesterhus Mette, Karlsen Tom Hemming, Mindorf Swantje, Schemmer Peter, Bär Florian, Teegen Bianca, Schröder Torsten, Ehlers Marc, Hammers Christoph Matthias, Komorowski Lars, Lehnert Hendrik, Fellermann Klaus, Derer Stefanie, Hov Johannes Roksund, Sina Christi |
| Serologic Anti-GP2 Antibodies Are Associated with Genetic Polymorphisms, Fibrostenosis, and Need for Surgical Resection in Crohn's Disease. Inflammatory bowel diseases 2016 Nov 22 (11): 2648-2657. Degenhardt Frauke, Dirmeier Andrea, Lopez Rocio, Lang Sylvia, Kunst Claudia, Roggenbuck Dirk, Reinhold Dirk, Szymczak Silke, Rogler Gerhard, Klebl Frank, Franke Andre, Rieder Flori |
| Author Correction: Elucidating causative gene variants in hereditary Parkinson's disease in the Global Parkinson's Genetics Program (GP2). NPJ Parkinson's disease 2023 9 9 (1): 133. Lara M Lange, Micol Avenali, Melina Ellis, Anastasia Illarionova, Ignacio J Keller Sarmiento, Ai-Huey Tan, Harutyun Madoev, Caterina Galandra, Johanna Junker, Karisha Roopnarain, Justin Solle, Claire Wegel, Zih-Hua Fang, Peter Heutink, Kishore R Kumar, Shen-Yang Lim, Enza Maria Valente, Mike Nalls, Cornelis Blauwendraat, Andrew Singleton, Niccolo Mencacci, Katja Lohmann, Christine Klein, |
| Genetic screening of Filipinos suspected with familial Parkinson's disease: A pilot study. Parkinsonism & related disorders 2023 2 108 105319. Caritativo Erin Camille A, Yu Jeryl Ritzi T, Bautista Juan Miguel P, Nishioka Kenya, Jamora Roland Dominic G, Yalung Patrick M, Ng Arlene R, Hattori Nobuta |
| Increased burden of rare risk variants across gene expression networks predisposes to sporadic Parkinson's disease. bioRxiv : the preprint server for biology 2024 9 . Elena Eubanks, Katelyn VanderSleen, Jiya Mody, Neha Patel, Benjamin Sacks, Mahsa Darestani Farahani, Jinying Wang, Jordan Elliott, Nora Jaber, Fulya Akçimen, Sara Bandres-Ciga, Fadel Helweh, Jun Liu, Sanjana Archakam, Robert Kimelman, Bineet Sharma, Philip Socha, Ananya Guntur, Tim Bartels, Ulf Dettmer, M Maral Mouradian, Amir Houshang Bahrami, Wei Dai, Jean Baum, Zheng Shi, John Hardy, Eleanna Ka |
| RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses. The Lancet. Neurology 2024 4 . Emil K Gustavsson, Jordan Follett, Joanne Trinh, Sandeep K Barodia, Raquel Real, Zhiyong Liu, Melissa Grant-Peters, Jesse D Fox, Silke Appel-Cresswell, A Jon Stoessl, Alex Rajput, Ali H Rajput, Roland Auer, Russel Tilney, Marc Sturm, Tobias B Haack, Suzanne Lesage, Christelle Tesson, Alexis Brice, Carles Vilariño-Güell, Mina Ryten, Matthew S Goldberg, Andrew B West, Michele T Hu, Huw R Morris, Manu Sharma, Ziv Gan-Or, Bedia Samanci, Pawel Lis, Maria Teresa Periñan, Rim Amouri, Samia Ben Sassi, Faycel Hentati, , Francesca Tonelli, Dario R Alessi, Matthew J Farr |
| The LRRK2 p.L1795F variant causes Parkinson's disease in the European population. Research square 2024 10 . Lara M Lange, Kristin Levine, Susan H Fox, Connie Marras, Nazish Ahmed, Nicole Kuznetsov, Dan Vitale, Hirotaka Iwaki, Katja Lohmann, Luca Marsili, Alberto J Espay, Peter Bauer, Christian Beetz, Jessica Martin, Stewart A Factor, Lenora A Higginbotham, Honglei Chen, Hampton Leonard, Mike Nalls, Niccolo E Mencacci, Huw R Morris, Christine Klein, Cornelis Blauwendraat, Zih-Hua Fang, |
- Page last reviewed:Feb 1, 2024
- Content source:

