These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

206 related articles for article (PubMed ID: 30537300)

  • 21. Genetic analysis of TRIM family genes for early-onset Parkinson's disease in Chinese population.
    Li C; Ou R; Hou Y; Chen Y; Gu X; Wei Q; Cao B; Zhang L; Liu K; Chen X; Song W; Zhao B; Wu Y; Shang H
    Parkinsonism Relat Disord; 2021 Sep; 90():105-113. PubMed ID: 34419804
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing.
    Jansen IE; Ye H; Heetveld S; Lechler MC; Michels H; Seinstra RI; Lubbe SJ; Drouet V; Lesage S; Majounie E; Gibbs JR; Nalls MA; Ryten M; Botia JA; Vandrovcova J; Simon-Sanchez J; Castillo-Lizardo M; Rizzu P; Blauwendraat C; Chouhan AK; Li Y; Yogi P; Amin N; van Duijn CM; ; Morris HR; Brice A; Singleton AB; David DC; Nollen EA; Jain S; Shulman JM; Heutink P
    Genome Biol; 2017 Jan; 18(1):22. PubMed ID: 28137300
    [TBL] [Abstract][Full Text] [Related]  

  • 23. PLA2G6 mutations in PARK14-linked young-onset parkinsonism and sporadic Parkinson's disease.
    Lu CS; Lai SC; Wu RM; Weng YH; Huang CL; Chen RS; Chang HC; Wu-Chou YH; Yeh TH
    Am J Med Genet B Neuropsychiatr Genet; 2012 Mar; 159B(2):183-91. PubMed ID: 22213678
    [TBL] [Abstract][Full Text] [Related]  

  • 24. GCH1 variants contribute to the risk and earlier age-at-onset of Parkinson's disease: a two-cohort case-control study.
    Pan HX; Zhao YW; Mei JP; Fang ZH; Wang Y; Zhou X; Zhou YJ; Zhang R; Zhang KL; Jiang L; Zeng Q; He Y; Wang Z; Liu ZH; Xu Q; Sun QY; Yang Y; Hu YC; Chen YS; Du J; Lei LF; Zhang HN; Wang CY; Yan XX; Shen L; Jiang H; Tan JQ; Li JC; Tang BS; Guo JF
    Transl Neurodegener; 2020 Aug; 9(1):31. PubMed ID: 32746945
    [TBL] [Abstract][Full Text] [Related]  

  • 25. ANXA1 and the risk for early-onset Parkinson's disease.
    Li C; Ou R; Gu X; Hou Y; Chen Y; Wei Q; Zhang L; Lin J; Liu K; Huang J; Chen X; Song W; Zhao B; Wu Y; Shang H
    Neurobiol Aging; 2022 Apr; 112():212-214. PubMed ID: 35240489
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease.
    Gaare JJ; Nido GS; Sztromwasser P; Knappskog PM; Dahl O; Lund-Johansen M; Maple-Grødem J; Alves G; Tysnes OB; Johansson S; Haugarvoll K; Tzoulis C
    Mov Disord; 2018 Oct; 33(10):1591-1600. PubMed ID: 30256453
    [TBL] [Abstract][Full Text] [Related]  

  • 27. PLA2G6 variant in Parkinson's disease.
    Tomiyama H; Yoshino H; Ogaki K; Li L; Yamashita C; Li Y; Funayama M; Sasaki R; Kokubo Y; Kuzuhara S; Hattori N
    J Hum Genet; 2011 May; 56(5):401-3. PubMed ID: 21368765
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Novel deep intronic mutation in PLA2G6 causing early-onset Parkinson's disease with brain iron accumulation through pseudo-exon activation.
    Cavestro C; Panteghini C; Reale C; Nasca A; Fenu S; Salsano E; Chiapparini L; Garavaglia B; Pareyson D; Di Meo I; Tiranti V
    Neurogenetics; 2021 Oct; 22(4):347-351. PubMed ID: 34387792
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Mutation Analysis of DNAJC Family for Early-Onset Parkinson's Disease in a Chinese Cohort.
    Li C; Ou R; Chen Y; Gu X; Wei Q; Cao B; Zhang L; Hou Y; Liu K; Chen X; Song W; Zhao B; Wu Y; Shang H
    Mov Disord; 2020 Nov; 35(11):2068-2076. PubMed ID: 32662538
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The Genetic Drivers of Juvenile, Young, and Early-Onset Parkinson's Disease in India.
    Andrews SV; Kukkle PL; Menon R; Geetha TS; Goyal V; Kandadai RM; Kumar H; Borgohain R; Mukherjee A; Wadia PM; Yadav R; Desai S; Kumar N; Joshi D; Murugan S; Biswas A; Pal PK; Oliver M; Nair S; Kayalvizhi A; Samson PL; Deshmukh M; Bassi A; Sandeep C; Mandloi N; Davis OB; Roberts MA; Leto DE; Henry AG; Di Paolo G; Muthane U; Das SK; Peterson AS; Sandmann T; Gupta R; Ramprasad VL;
    Mov Disord; 2024 Feb; 39(2):339-349. PubMed ID: 38014556
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Genetic Analysis of HSP40/DNAJ Family Genes in Parkinson's Disease: a Large Case-Control Study.
    Zhang K; Pan H; Zhao Y; Wang Y; Zeng Q; Zhou X; He R; Zhou X; Xiang Y; Zhou Z; Li Y; Xu Q; Sun Q; Tan J; Yan X; Li J; Guo J; Tang B; Liu Z
    Mol Neurobiol; 2022 Sep; 59(9):5443-5451. PubMed ID: 35715682
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Targeted next-generation sequencing identifies novel variants in candidate genes for Parkinson's disease in Black South African and Nigerian patients.
    Oluwole OG; Kuivaniemi H; Abrahams S; Haylett WL; Vorster AA; van Heerden CJ; Kenyon CP; Tabb DL; Fawale MB; Sunmonu TA; Ajose A; Olaogun MO; Rossouw AC; van Hillegondsberg LS; Carr J; Ross OA; Komolafe MA; Tromp G; Bardien S
    BMC Med Genet; 2020 Feb; 21(1):23. PubMed ID: 32019516
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The genetic landscape of Parkinson's disease.
    Lunati A; Lesage S; Brice A
    Rev Neurol (Paris); 2018 Nov; 174(9):628-643. PubMed ID: 30245141
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Harmonizing Genetic Testing for Parkinson's Disease: Results of the PARKNET Multicentric Study.
    Di Fonzo A; Percetti M; Monfrini E; Palmieri I; Albanese A; Avenali M; Bartoletti-Stella A; Blandini F; Brescia G; Calandra-Buonaura G; Campopiano R; Capellari S; Colangelo I; Comi GP; Cuconato G; Ferese R; Galandra C; Gambardella S; Garavaglia B; Gaudio A; Giardina E; Invernizzi F; Mandich P; Mineri R; Panteghini C; Reale C; Trevisan L; Zampatti S; Cortelli P; Valente EM;
    Mov Disord; 2023 Dec; 38(12):2241-2248. PubMed ID: 37750340
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Whole-Exome Sequencing Study of Consanguineous Parkinson's Disease Families and Related Phenotypes: Report of Twelve Novel Variants.
    Soudyab M; Shariati M; Esfehani RJ; Shalaei N; Vafadar S; Nouri V; Zech M; Winkelmann J; Shoeibi A; Sadr-Nabavi A
    J Mol Neurosci; 2022 Dec; 72(12):2486-2496. PubMed ID: 36520381
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Genetics of Parkinson's disease--state of the art, 2013.
    Bonifati V
    Parkinsonism Relat Disord; 2014 Jan; 20 Suppl 1():S23-8. PubMed ID: 24262182
    [TBL] [Abstract][Full Text] [Related]  

  • 37. A genetic analysis of a Spanish population with early onset Parkinson's disease.
    Cristina TP; Pablo M; Teresa PM; Lydia VD; Irene AR; Araceli AC; Inmaculada BB; Marta BT; Dolores BR; José CM; Rocío GR; José GP; Ismael HF; Silvia J; Labrador MA; Lydia LM; Carlos MJ; Posada IJ; Ana RS; Cristina RH; Javier DV; Gómez-Garre P
    PLoS One; 2020; 15(9):e0238098. PubMed ID: 32870915
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The RAB39B p.G192R mutation causes X-linked dominant Parkinson's disease.
    Mata IF; Jang Y; Kim CH; Hanna DS; Dorschner MO; Samii A; Agarwal P; Roberts JW; Klepitskaya O; Shprecher DR; Chung KA; Factor SA; Espay AJ; Revilla FJ; Higgins DS; Litvan I; Leverenz JB; Yearout D; Inca-Martinez M; Martinez E; Thompson TR; Cholerton BA; Hu SC; Edwards KL; Kim KS; Zabetian CP
    Mol Neurodegener; 2015 Sep; 10():50. PubMed ID: 26399558
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease.
    Smaili I; Tesson C; Regragui W; Bertrand H; Rahmani M; Bouslam N; Benomar A; Brice A; Lesage S; Bouhouche A
    J Mol Neurosci; 2021 Jan; 71(1):142-152. PubMed ID: 32557143
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Low-frequency and rare coding variants of NUS1 contribute to susceptibility and phenotype of Parkinson's disease.
    Jiang L; Mei JP; Zhao YW; Zhang R; Pan HX; Yang Y; Sun QY; Xu Q; Yan XX; Tan JQ; Li JC; Tang BS; Guo JF
    Neurobiol Aging; 2022 Feb; 110():106-112. PubMed ID: 34635350
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.