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 *

118 related articles for article (PubMed ID: 37139776)

  • 1. Re-evaluation of Genetic Variants in Parkinson's Disease Using Targeted Panel and Next-Generation Sequencing.
    Kablan A; Silan F; Ozdemir O
    Twin Res Hum Genet; 2023 Apr; 26(2):164-170. PubMed ID: 37139776
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Interpreting Genetic Variants: Hints from a Family Cluster of Parkinson's Disease.
    Cali F; Cantone M; Cosentino FII; Lanza G; Ruggeri G; Chiavetta V; Salluzzo R; Ragalmuto A; Vinci M; Ferri R
    J Parkinsons Dis; 2019; 9(1):203-206. PubMed ID: 30400105
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic Mutation Analysis of Parkinson's Disease Patients Using Multigene Next-Generation Sequencing Panels.
    Gorostidi A; Martí-Massó JF; Bergareche A; Rodríguez-Oroz MC; López de Munain A; Ruiz-Martínez J
    Mol Diagn Ther; 2016 Oct; 20(5):481-91. PubMed ID: 27294386
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Clinical and genetic analysis of Vietnamese patients diagnosed with early-onset Parkinson's disease.
    Do MD; Tran TN; Luong AB; Le LHG; Van Le T; Le KT; Van Vo NT; Le TN; Vu HA; Mai TP
    Brain Behav; 2023 Apr; 13(4):e2950. PubMed ID: 36879366
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson's Disease in Sporadic Moroccan Patients.
    Smaili I; Tibar H; Rahmani M; Machkour N; Razine R; Darai HN; Bouslam N; Benomar A; Regragui W; Bouhouche A
    J Mol Neurosci; 2023 Jun; 73(6):391-402. PubMed ID: 37256495
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing.
    Lin CH; Chen PL; Tai CH; Lin HI; Chen CS; Chen ML; Wu RM
    Mov Disord; 2019 Apr; 34(4):506-515. PubMed ID: 30788857
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical and molecular genetic findings of hereditary Parkinson's patients from Turkey.
    Emekli I; Tepgeç F; Samancı B; Toksoy G; Hasanoğulları Kına G; Tüfekçioğlu Z; Başaran S; Bilgiç B; Gürvit IH; Emre M; Uyguner ZO; Hanagasi HA
    Parkinsonism Relat Disord; 2021 Dec; 93():35-39. PubMed ID: 34781237
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Clinical next generation sequencing in developmental and epileptic encephalopathies: Diagnostic relevance of data re-analysis and variants re-interpretation.
    Salinas V; Martínez N; Maturo JP; Rodriguez-Quiroga SA; Zavala L; Medina N; Amartino H; Sfaello I; Agosta G; Serafín EM; Morón DG; Kauffman MA; Vega P
    Eur J Med Genet; 2021 Dec; 64(12):104363. PubMed ID: 34673242
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease.
    Schormair B; Kemlink D; Mollenhauer B; Fiala O; Machetanz G; Roth J; Berutti R; Strom TM; Haslinger B; Trenkwalder C; Zahorakova D; Martasek P; Ruzicka E; Winkelmann J
    Clin Genet; 2018 Mar; 93(3):603-612. PubMed ID: 28862745
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Genetic Analysis of Prosaposin, the Lysosomal Storage Disorder Gene in Parkinson's Disease.
    Chen YP; Gu XJ; Ou RW; Zhang LY; Hou YB; Liu KC; Cao B; Wei QQ; Song W; Zhao B; Wu Y; Cheng JQ; Shang HF
    Mol Neurobiol; 2021 Apr; 58(4):1583-1592. PubMed ID: 33219486
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. The role of genetics in Parkinson's disease: a large cohort study in Chinese mainland population.
    Zhao Y; Qin L; Pan H; Liu Z; Jiang L; He Y; Zeng Q; Zhou X; Zhou X; Zhou Y; Fang Z; Wang Z; Xiang Y; Yang H; Wang Y; Zhang K; Zhang R; He R; Zhou X; Zhou Z; Yang N; Liang D; Chen J; Zhang X; Zhou Y; Liu H; Deng P; Xu K; Xu K; Zhou C; Zhong J; Xu Q; Sun Q; Li B; Zhao G; Wang T; Chen L; Shang H; Liu W; Chan P; Xue Z; Wang Q; Guo L; Wang X; Xu C; Zhang Z; Chen T; Lei L; Zhang H; Wang C; Tan J; Yan X; Shen L; Jiang H; Zhang Z; Hu Z; Xia K; Yue Z; Li J; Guo J; Tang B
    Brain; 2020 Jul; 143(7):2220-2234. PubMed ID: 32613234
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. A DNA resequencing array for genes involved in Parkinson's disease.
    Wilkins EJ; Rubio JP; Kotschet KE; Cowie TF; Boon WC; O'Hely M; Burfoot R; Wang W; Sue CM; Speed TP; Stankovitch J; Horne MK
    Parkinsonism Relat Disord; 2012 May; 18(4):386-90. PubMed ID: 22243833
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Mutation Analysis of the Genes Associated with Parkinson's Disease in a Finnish Cohort of Early-Onset Dementia.
    Luukkainen L; Huttula S; Väyrynen H; Helisalmi S; Kytövuori L; Haapasalo A; Hiltunen M; Remes AM; Krüger J
    J Alzheimers Dis; 2020; 76(3):955-965. PubMed ID: 32568194
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of Heterozygous PRKN Variants and Copy-Number Variations in Parkinson's Disease.
    Yu E; Rudakou U; Krohn L; Mufti K; Ruskey JA; Asayesh F; Estiar MA; Spiegelman D; Surface M; Fahn S; Waters CH; Greenbaum L; Espay AJ; Dauvilliers Y; Dupré N; Rouleau GA; Hassin-Baer S; Fon EA; Alcalay RN; Gan-Or Z
    Mov Disord; 2021 Jan; 36(1):178-187. PubMed ID: 32970363
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.