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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 4
2001 1
2002 11
2003 4
2004 11
2005 6
2006 16
2007 17
2008 15
2009 15
2010 39
2011 42
2012 34
2013 35
2014 30
2015 32
2016 22
2017 40
2018 40
2019 35
2020 46
2021 54
2022 37
2023 55
2024 23

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593 results

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Page 1
PINK1 Type of Young-Onset Parkinson Disease.
Lange LM, Klein C. Lange LM, et al. Among authors: klein c. 2010 Mar 16 [updated 2024 Apr 25]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2010 Mar 16 [updated 2024 Apr 25]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301792 Free Books & Documents. Review.
Stability of Mosaic Divergent Repeat Interruptions in X-Linked Dystonia-Parkinsonism.
Laß J, Lüth T, Schlüter K, Schaake S, Laabs BH, Much C, Jamora RD, Rosales RL, Saranza G, Diesta CCE, Pearson CE, König IR, Brüggemann N, Klein C, Westenberger A, Trinh J. Laß J, et al. Among authors: klein c. Mov Disord. 2024 Apr 14. doi: 10.1002/mds.29809. Online ahead of print. Mov Disord. 2024. PMID: 38616406
Genotype-phenotype correlation in PRKN-associated Parkinson's disease.
Menon PJ, Sambin S, Criniere-Boizet B, Courtin T, Tesson C, Casse F, Ferrien M, Mariani LL, Carvalho S, Lejeune FX, Rebbah S, Martet G, Houot M, Lanore A, Mangone G, Roze E, Vidailhet M, Aasly J, Gan Or Z, Yu E, Dauvilliers Y, Zimprich A, Tomantschger V, Pirker W, Álvarez I, Pastor P, Di Fonzo A, Bhatia KP, Magrinelli F, Houlden H, Real R, Quattrone A, Limousin P, Korlipara P, Foltynie T, Grosset D, Williams N, Narendra D, Lin HP, Jovanovic C, Svetel M, Lynch T, Gallagher A, Vandenberghe W, Gasser T, Brockmann K, Morris HR, Borsche M, Klein C, Corti O, Brice A, Lesage S, Corvol JC; French Parkinson disease Genetics Study Group (PDG). Menon PJ, et al. Among authors: klein c. NPJ Parkinsons Dis. 2024 Mar 29;10(1):72. doi: 10.1038/s41531-024-00677-3. NPJ Parkinsons Dis. 2024. PMID: 38553467 Free PMC article.
Understanding monogenic Parkinson's disease at a global scale.
Junker J, Lange LM, Vollstedt EJ, Roopnarain K, Doquenia MLM, Annuar AA, Avenali M, Bardien S, Bahr N, Ellis M, Galandra C, Gasser T, Heutink P, Illarionova A, Kanana Y, Keller Sarmiento IJ, Kumar KR, Lim SY, Madoev H, Mata IF, Mencacci NE, Nalls MA, Padmanabhan S, Shambetova C, Solle J, Tan AH, Trinh J, Valente EM, Singleton A, Blauwendraat C, Lohmann K, Fang ZH, Klein C; Global Parkinson’s Genetics Program (GP2). Junker J, et al. Among authors: klein c. medRxiv [Preprint]. 2024 Apr 9:2024.03.12.24304154. doi: 10.1101/2024.03.12.24304154. medRxiv. 2024. PMID: 38529492 Free PMC article. Preprint.
RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia.
Milovanović A, Dragaševic-Mišković N, Thomsen M, Borsche M, Hinrichs F, Westenberger A, Klein C, Brüggemann N, Branković M, Marjanović A, Svetel M, Kostić VS, Lohmann K. Milovanović A, et al. Among authors: klein c. Mov Disord Clin Pract. 2024 Mar 15. doi: 10.1002/mdc3.14020. Online ahead of print. Mov Disord Clin Pract. 2024. PMID: 38487929
How Do I Report Genes in a Paper?
Gabbert C, Klein C, Trinh J. Gabbert C, et al. Among authors: klein c. Mov Disord Clin Pract. 2024 Mar 12. doi: 10.1002/mdc3.13984. Online ahead of print. Mov Disord Clin Pract. 2024. PMID: 38469948
ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series.
Milovanović A, Westenberger A, Stanković I, Tamaš O, Branković M, Marjanović A, Laabs BH, Brand M, Rajalingam R, Marras C, Lohmann K, Branković V, Novaković I, Petrović I, Svetel M, Klein C, Kostić VS, Dragašević-Mišković N. Milovanović A, et al. Among authors: klein c. Mov Disord. 2024 Mar 12. doi: 10.1002/mds.29729. Online ahead of print. Mov Disord. 2024. PMID: 38469933
593 results