Human Genome Epidemiology Literature Finder

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Records 1 - 15 (of 15 Records)

Query Trace: Parkinson Disease and PARK2[original query]
Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early-onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patients. Human mutation 2004 May 23 (5): 525. Djarmati A, Hedrich K, Svetel M, Schäfer N, Juric V, Vukosavic S, Hering R, Riess O, Romac S, Klein C, Kostic V Similar articles in PubMed
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease. Neurology 2004 Feb 62 (3): 389-94. Hedrich K, Djarmati A, Schäfer N, Hering R, Wellenbrock C, Weiss P H, Hilker R, Vieregge P, Ozelius L J, Heutink P, Bonifati V, Schwinger E, Lang A E, Noth J, Bressman S B, Pramstaller P P, Riess O, Klein Similar articles in PubMed
Parkin polymorphisms and environmental exposure: decrease in age at onset of Parkinson's disease. Neurotoxicology 2007 May 28 (3): 698-701. Ghione Isabella, Di Fonzo Alessio, Saladino Francesca, Del Bo Roberto, Bresolin Nereo, Comi Giacomo Pietro, Rango Mar Similar articles in PubMed
Genetic screening reveals high frequency of PARK2 mutations and reduced Parkin expression conferring risk for Parkinsonism in North West India. Journal of neurology, neurosurgery, and psychiatry 2010 Feb 81 (2): 166-70. Vinish Monika, Prabhakar Sudesh, Khullar Madhu, Verma Indu, Anand Aksh Similar articles in PubMed
Low frequency of the PARK2 gene mutations in Polish patients with the early-onset form of Parkinson disease. Parkinsonism & related disorders 2010 Feb 16 (2): 136-8. Koziorowski Dariusz, Hoffman-Zacharska Dorota, S?awek Jaros?aw, Szirkowiec Walentyna, Janik Piotr, Bal Jerzy, Friedman Andrz Similar articles in PubMed
Relative contribution of simple mutations vs. copy number variations in five Parkinson disease genes in the Belgian population. Human mutation 2009 Jul 30 (7): 1054-61. Nuytemans Karen, Meeus Bram, Crosiers David, Brouwers Nathalie, Goossens Dirk, Engelborghs Sebastiaan, Pals Philippe, Pickut Barbara, Van den Broeck Marleen, Corsmit Ellen, Cras Patrick, De Deyn Peter P, Del-Favero Jurgen, Van Broeckhoven Christine, Theuns Jess Similar articles in PubMed
A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2. Neurology 2010 Sep 75 (13): 1189-94. Kay D M, Stevens C F, Hamza T H, Montimurro J S, Zabetian C P, Factor S A, Samii A, Griffith A, Roberts J W, Molho E S, Higgins D S, Gancher S, Moses L, Zareparsi S, Poorkaj P, Bird T, Nutt J, Schellenberg G D, Payami Similar articles in PubMed
Copy number variation in familial Parkinson disease. PloS one 2011 6 (8): e20988. Pankratz Nathan, Dumitriu Alexandra, Hetrick Kurt N, Sun Mei, Latourelle Jeanne C, Wilk Jemma B, Halter Cheryl, Doheny Kimberly F, Gusella James F, Nichols William C, Myers Richard H, Foroud Tatiana, DeStefano Anita L, Similar articles in PubMed
Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. Molecular psychiatry 2014 Jan 19 (1): 115-21. Jarick I, Volckmar A-L, Pütter C, Pechlivanis S, Nguyen T T, Dauvermann M R, Beck S, Albayrak Ö, Scherag S, Gilsbach S, Cichon S, Hoffmann P, Degenhardt F, Nöthen M M, Schreiber S, Wichmann H-E, Jöckel K-H, Heinrich J, Tiesler C M T, Faraone S V, Walitza S, Sinzig J, Freitag C, Meyer J, Herpertz-Dahlmann B, Lehmkuhl G, Renner T J, Warnke A, Romanos M, Lesch K-P, Reif A, Schimmelmann B G, Hebebrand J, Scherag A, Hinney Similar articles in PubMed
Incidence of mutations in the PARK2, PINK1, PARK7 genes in Polish early-onset Parkinson disease patients. Neurologia i neurochirurgia polska 0 47 (4): 319-24. Koziorowski D, Hoffman-Zacharska D, S?awek J, Jamrozik Z, Janik P, Potulska-Chromik A, Roszmann A, Tataj R, Bal J, Friedman Similar articles in PubMed
High-resolution survey in familial Parkinson disease genes reveals multiple independent copy number variation events in PARK2. Human mutation 2013 Aug 34 (8): 1071-4. Wang Liyong, Nuytemans Karen, Bademci Guney, Jauregui Cherylyn, Martin Eden R, Scott William K, Vance Jeffery M, Zuchner Steph Similar articles in PubMed
Analysis of Leucine-rich repeat kinase 2 (LRRK2) and Parkinson protein 2 (parkin, PARK2) genes mutations in Slovak Parkinson disease patients. General physiology and biophysics 2013 Mar 32 (1): 55-66. Bognar Csaba, Baldovic Marian, Benetin Jan, Kadasi Ludovit, Zatkova Andr Similar articles in PubMed
High-resolution arrays reveal burden of copy number variations on Parkinson disease genes associated with increased disease risk in random cohorts. Neurological research 2016 Jul 1-11. Murthy Megha N, Veerappa Avinash M, Seshachalam Keshava B, Ramachandra Nallur Similar articles in PubMed
Genomic mechanisms underlying PARK2 large deletions identified in a cohort of patients with PD. Neurology. Genetics 2016 Jun 2 (3): e73. Morais Sara, Bastos-Ferreira Rita, Sequeiros Jorge, Alonso Isab Similar articles in PubMed
Expanding the canvas of PRKN mutations in familial and early-onset Parkinson disease. Parkinsonism & related disorders 2019 8 66 216-219. Pandey Sanjay, Tomar Laxmikant Ramkumarsingh, Kumar Sumeet, Dinesh Shreya, Thelma B Similar articles in PubMed