BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

879 related articles for article (PubMed ID: 25662902)

  • 1. CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study.
    Funayama M; Ohe K; Amo T; Furuya N; Yamaguchi J; Saiki S; Li Y; Ogaki K; Ando M; Yoshino H; Tomiyama H; Nishioka K; Hasegawa K; Saiki H; Satake W; Mogushi K; Sasaki R; Kokubo Y; Kuzuhara S; Toda T; Mizuno Y; Uchiyama Y; Ohno K; Hattori N
    Lancet Neurol; 2015 Mar; 14(3):274-82. PubMed ID: 25662902
    [TBL] [Abstract][Full Text] [Related]  

  • 2. CHCHD2 gene mutations in familial and sporadic Parkinson's disease.
    Shi CH; Mao CY; Zhang SY; Yang J; Song B; Wu P; Zuo CT; Liu YT; Ji Y; Yang ZH; Wu J; Zhuang ZP; Xu YM
    Neurobiol Aging; 2016 Feb; 38():217.e9-217.e13. PubMed ID: 26705026
    [TBL] [Abstract][Full Text] [Related]  

  • 3. CHCHD2 and Parkinson's disease.
    Foo JN; Liu J; Tan EK
    Lancet Neurol; 2015 Jul; 14(7):681-2. PubMed ID: 26067114
    [No Abstract]   [Full Text] [Related]  

  • 4. CHCHD2 and Parkinson's disease.
    Iqbal Z; Toft M
    Lancet Neurol; 2015 Jul; 14(7):680-1. PubMed ID: 26067113
    [No Abstract]   [Full Text] [Related]  

  • 5. CHCHD2 and Parkinson's disease.
    Liu G; Li K
    Lancet Neurol; 2015 Jul; 14(7):679-80. PubMed ID: 26067112
    [No Abstract]   [Full Text] [Related]  

  • 6. CHCHD2 and Parkinson's disease.
    Puschmann A; Dickson DW; Englund E; Wszolek ZK; Ross OA
    Lancet Neurol; 2015 Jul; 14(7):679. PubMed ID: 26067111
    [No Abstract]   [Full Text] [Related]  

  • 7. CHCHD2 and Parkinson's disease--authors' reply.
    Funayama M; Hattori N
    Lancet Neurol; 2015 Jul; 14(7):682-3. PubMed ID: 26067115
    [No Abstract]   [Full Text] [Related]  

  • 8. CHCHD2 and Parkinson's disease.
    Jansen IE; Bras JM; Lesage S; Schulte C; Gibbs JR; Nalls MA; Brice A; Wood NW; Morris H; Hardy JA; Singleton AB; Gasser T; Heutink P; Sharma M;
    Lancet Neurol; 2015 Jul; 14(7):678-9. PubMed ID: 26067110
    [No Abstract]   [Full Text] [Related]  

  • 9. Analysis of CHCHD2 gene in familial Parkinson's disease from Calabria.
    Gagliardi M; Iannello G; Colica C; Annesi G; Quattrone A
    Neurobiol Aging; 2017 Feb; 50():169.e5-169.e6. PubMed ID: 27839905
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A new gene for Parkinson's disease: should we care?
    Singleton A
    Lancet Neurol; 2015 Mar; 14(3):238-9. PubMed ID: 25728432
    [No Abstract]   [Full Text] [Related]  

  • 11. Generation of induced pluripotent stem cell line (ZZUi007-A) from a 52-year-old patient with a novel CHCHD2 gene mutation in Parkinson's disease.
    Wang Y; Wang Z; Sun H; Mao C; Yang J; Liu Y; Liu H; Zhang S; Zhang J; Xu Y; Shi C
    Stem Cell Res; 2018 Oct; 32():87-90. PubMed ID: 30237140
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutation analysis of CHCHD2 in Canadian patients with familial Parkinson's disease.
    Zhang M; Xi Z; Fang S; Ghani M; Sato C; Moreno D; Liang Y; Lang AE; Rogaeva E
    Neurobiol Aging; 2016 Feb; 38():217.e7-217.e8. PubMed ID: 26639156
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Lack of CHCHD2 mutations in Parkinson's disease in a Taiwanese population.
    Fan TS; Lin HI; Lin CH; Wu RM
    Neurobiol Aging; 2016 Feb; 38():218.e1-218.e2. PubMed ID: 26725463
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic analysis of CHCHD2 in a southern Spanish population.
    Tejera-Parrado C; Jesús S; Huertas-Fernández I; Bernal-Bernal I; Bonilla-Toribio M; Córdoba-Tevar I; Abreu-Rodríguez I; Carrillo F; Bernal-Escudero M; Vargas-González L; Carballo M; Gómez-Garre P; Mir P
    Neurobiol Aging; 2017 Feb; 50():169.e1-169.e2. PubMed ID: 27839904
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutation analysis of CHCHD2 gene in Chinese Han familial essential tremor patients and familial Parkinson's disease patients.
    Gao C; Chen YM; Sun Q; He YC; Huang P; Wang T; Li DH; Liang L; Liu J; Xiao Q; Chen SD
    Neurobiol Aging; 2017 Jan; 49():218.e9-218.e11. PubMed ID: 27814991
    [TBL] [Abstract][Full Text] [Related]  

  • 16. CHCHD2 mutational screening in Brazilian patients with familial Parkinson's disease.
    Voigt DD; Nascimento CM; de Souza RB; Cabello Acero PH; Campos Júnior M; da Silva CP; Pereira JS; Rosso AL; Araujo Leite MA; Vasconcellos LFR; Della Coletta MV; da Silva DJ; Nicaretta DH; Gonçalves AP; Dos Santos JM; Calassara V; Santos-Rebouças CB; Pimentel MMG
    Neurobiol Aging; 2019 Feb; 74():236.e7-236.e8. PubMed ID: 30342766
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mitochondrial UQCRC1 mutations cause autosomal dominant parkinsonism with polyneuropathy.
    Lin CH; Tsai PI; Lin HY; Hattori N; Funayama M; Jeon B; Sato K; Abe K; Mukai Y; Takahashi Y; Li Y; Nishioka K; Yoshino H; Daida K; Chen ML; Cheng J; Huang CY; Tzeng SR; Wu YS; Lai HJ; Tsai HH; Yen RF; Lee NC; Lo WC; Hung YC; Chan CC; Ke YC; Chao CC; Hsieh ST; Farrer M; Wu RM
    Brain; 2020 Dec; 143(11):3352-3373. PubMed ID: 33141179
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutation analysis of CHCHD2 gene in Chinese familial Parkinson's disease.
    Liu Z; Guo J; Li K; Qin L; Kang J; Shu L; Zhang Y; Wei Y; Yang N; Luo Y; Sun Q; Xu Q; Yan X; Tang B
    Neurobiol Aging; 2015 Nov; 36(11):3117.e7-3117.e8. PubMed ID: 26343503
    [TBL] [Abstract][Full Text] [Related]  

  • 19. DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study.
    Trinh J; Gustavsson EK; Vilariño-Güell C; Bortnick S; Latourelle J; McKenzie MB; Tu CS; Nosova E; Khinda J; Milnerwood A; Lesage S; Brice A; Tazir M; Aasly JO; Parkkinen L; Haytural H; Foroud T; Myers RH; Sassi SB; Hentati E; Nabli F; Farhat E; Amouri R; Hentati F; Farrer MJ
    Lancet Neurol; 2016 Nov; 15(12):1248-1256. PubMed ID: 27692902
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic analysis of CHCHD2 gene in Chinese Parkinson's disease.
    Li NN; Wang L; Tan EK; Cheng L; Sun XY; Lu ZJ; Li JY; Zhang JH; Peng R
    Am J Med Genet B Neuropsychiatr Genet; 2016 Dec; 171(8):1148-1152. PubMed ID: 27626775
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 44.