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 *

659 related articles for article (PubMed ID: 33150996)

  • 1. Genome-Wide Analysis of Copy Number Variation in Latin American Parkinson's Disease Patients.
    Sarihan EI; Pérez-Palma E; Niestroj LM; Loesch D; Inca-Martinez M; Horimoto ARVR; Cornejo-Olivas M; Torres L; Mazzetti P; Cosentino C; Sarapura-Castro E; Rivera-Valdivia A; Dieguez E; Raggio V; Lescano A; Tumas V; Borges V; Ferraz HB; Rieder CR; Schumacher-Schuh AF; Santos-Lobato BL; Velez-Pardo C; Jimenez-Del-Rio M; Lopera F; Moreno S; Chana-Cuevas P; Fernandez W; Arboleda G; Arboleda H; Arboleda-Bustos CE; Yearout D; Zabetian CP; Thornton TA; O'Connor TD; Lal D; Mata IF;
    Mov Disord; 2021 Feb; 36(2):434-441. PubMed ID: 33150996
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's disease.
    Zhu W; Huang X; Yoon E; Bandres-Ciga S; Blauwendraat C; Billingsley KJ; Cade JH; Wu BP; Williams VH; Schindler AB; Brooks J; Gibbs JR; Hernandez DG; Ehrlich D; Singleton AB; Narendra DP
    Brain; 2022 Jun; 145(6):2077-2091. PubMed ID: 35640906
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. X-Chromosome Association Study in Latin American Cohorts Identifies New Loci in Parkinson's Disease.
    Leal TP; Rao SC; French-Kwawu JN; Gouveia MH; Borda V; Bandres-Ciga S; Inca-Martinez M; Mason EA; Horimoto ARVR; Loesch DP; Sarihan EI; Cornejo-Olivas MR; Torres LE; Mazzetti-Soler PE; Cosentino C; Sarapura-Castro EH; Rivera-Valdivia A; Medina AC; Dieguez EM; Raggio VE; Lescano A; Tumas V; Borges V; Ferraz HB; Rieder CR; Schumacher Schuh A; Santos-Lobato BL; Velez-Pardo C; Jimenez-Del-Rio M; Lopera F; Moreno S; Chana-Cuevas P; Fernandez W; Arboleda G; Arboleda H; Arboleda Bustos CE; Yearout D; Barbosa MT; Cardoso FEC; Caramelli P; Cunningham MCQ; Maia DP; Lima-Costa MF; Tarazona-Santos E; Zabetian CP; ; Thornton TA; O'Connor TD; Mata IF;
    Mov Disord; 2023 Sep; 38(9):1625-1635. PubMed ID: 37469269
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data.
    Mok KY; Sheerin U; Simón-Sánchez J; Salaka A; Chester L; Escott-Price V; Mantripragada K; Doherty KM; Noyce AJ; Mencacci NE; Lubbe SJ; ; Williams-Gray CH; Barker RA; van Dijk KD; Berendse HW; Heutink P; Corvol JC; Cormier F; Lesage S; Brice A; Brockmann K; Schulte C; Gasser T; Foltynie T; Limousin P; Morrison KE; Clarke CE; Sawcer S; Warner TT; Lees AJ; Morris HR; Nalls MA; Singleton AB; Hardy J; Abramov AY; Plagnol V; Williams NM; Wood NW
    Lancet Neurol; 2016 May; 15(6):585-96. PubMed ID: 27017469
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Parkinson's Disease Gene Screening in Familial Cases from Central and South America.
    Lorenzo-Betancor O; Mehta S; Ramchandra J; Mumuney S; Schumacher-Schuh AF; Cornejo-Olivas M; Sarapura-Castro EH; Torres L; Inca-Martinez MA; Mazzetti P; Cosentino C; Micheli F; Tumas V; Dieguez E; Raggio V; Borges V; Ferraz HB; Chana-Cuevas P; Jimenez-Del-Rio M; Velez-Pardo C; Moreno S; Lopera F; Orozco-Velez JL; Muñoz-Ospina B; Rieder CRM; Medina-Escobar A; Yearout D; Zabetian CP; Mata IF;
    Mov Disord; 2024 Oct; 39(10):1843-1855. PubMed ID: 39051491
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study.
    Rizig M; Bandres-Ciga S; Makarious MB; Ojo OO; Crea PW; Abiodun OV; Levine KS; Abubakar SA; Achoru CO; Vitale D; Adeniji OA; Agabi OP; Koretsky MJ; Agulanna U; Hall DA; Akinyemi RO; Xie T; Ali MW; Shamim EA; Ani-Osheku I; Padmanaban M; Arigbodi OM; Standaert DG; Bello AH; Dean MN; Erameh CO; Elsayed I; Farombi TH; Okunoye O; Fawale MB; Billingsley KJ; Imarhiagbe FA; Jerez PA; Iwuozo EU; Baker B; Komolafe MA; Malik L; Nwani PO; Daida K; Nwazor EO; Miano-Burkhardt A; Nyandaiti YW; Fang ZH; Obiabo YO; Kluss JH; Odeniyi OA; Hernandez DG; Odiase FE; Tayebi N; Ojini FI; Sidranksy E; Onwuegbuzie GA; D'Souza AM; Osaigbovo GO; Berhe B; Osemwegie N; Reed X; Oshinaike OO; Leonard HL; Otubogun FM; Alvarado CX; Oyakhire SI; Ozomma SI; Samuel SC; Taiwo FT; Wahab KW; Zubair YA; Iwaki H; Kim JJ; Morris HR; Hardy J; Nalls MA; Heilbron K; Norcliffe-Kaufmann L; ; ; ; ; Blauwendraat C; Houlden H; Singleton A; Okubadejo NU;
    Lancet Neurol; 2023 Nov; 22(11):1015-1025. PubMed ID: 37633302
    [TBL] [Abstract][Full Text] [Related]  

  • 8. RIC3 variants are not associated with Parkinson's disease in large European, Latin American, or East Asian cohorts.
    Brolin K; Bandres-Ciga S; Leonard H; Makarious MB; Blauwendraat C; Mata IF; Foo JN; Pihlstrøm L; Swanberg M; Gan-Or Z; Tan MM;
    Neurobiol Aging; 2022 Jan; 109():264-268. PubMed ID: 34538707
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.
    Blauwendraat C; Reed X; Krohn L; Heilbron K; Bandres-Ciga S; Tan M; Gibbs JR; Hernandez DG; Kumaran R; Langston R; Bonet-Ponce L; Alcalay RN; Hassin-Baer S; Greenbaum L; Iwaki H; Leonard HL; Grenn FP; Ruskey JA; Sabir M; Ahmed S; Makarious MB; Pihlstrøm L; Toft M; van Hilten JJ; Marinus J; Schulte C; Brockmann K; Sharma M; Siitonen A; Majamaa K; Eerola-Rautio J; Tienari PJ; ; Pantelyat A; Hillis AE; Dawson TM; Rosenthal LS; Albert MS; Resnick SM; Ferrucci L; Morris CM; Pletnikova O; Troncoso J; Grosset D; Lesage S; Corvol JC; Brice A; Noyce AJ; Masliah E; Wood N; Hardy J; Shulman LM; Jankovic J; Shulman JM; Heutink P; Gasser T; Cannon P; Scholz SW; Morris H; Cookson MR; Nalls MA; Gan-Or Z; Singleton AB
    Brain; 2020 Jan; 143(1):234-248. PubMed ID: 31755958
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Somatic copy number gains of α-synuclein (SNCA) in Parkinson's disease and multiple system atrophy brains.
    Mokretar K; Pease D; Taanman JW; Soenmez A; Ejaz A; Lashley T; Ling H; Gentleman S; Houlden H; Holton JL; Schapira AHV; Nacheva E; Proukakis C
    Brain; 2018 Aug; 141(8):2419-2431. PubMed ID: 29917054
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Characterizing the Genetic Architecture of Parkinson's Disease in Latinos.
    Loesch DP; Horimoto ARVR; Heilbron K; Sarihan EI; Inca-Martinez M; Mason E; Cornejo-Olivas M; Torres L; Mazzetti P; Cosentino C; Sarapura-Castro E; Rivera-Valdivia A; Medina AC; Dieguez E; Raggio V; Lescano A; Tumas V; Borges V; Ferraz HB; Rieder CR; Schumacher-Schuh A; Santos-Lobato BL; Velez-Pardo C; Jimenez-Del-Rio M; Lopera F; Moreno S; Chana-Cuevas P; Fernandez W; Arboleda G; Arboleda H; Arboleda-Bustos CE; Yearout D; Zabetian CP; ; Cannon P; Thornton TA; O'Connor TD; Mata IF;
    Ann Neurol; 2021 Sep; 90(3):353-365. PubMed ID: 34227697
    [TBL] [Abstract][Full Text] [Related]  

  • 14. LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study.
    Quadri M; Mandemakers W; Grochowska MM; Masius R; Geut H; Fabrizio E; Breedveld GJ; Kuipers D; Minneboo M; Vergouw LJM; Carreras Mascaro A; Yonova-Doing E; Simons E; Zhao T; Di Fonzo AB; Chang HC; Parchi P; Melis M; Correia Guedes L; Criscuolo C; Thomas A; Brouwer RWW; Heijsman D; Ingrassia AMT; Calandra Buonaura G; Rood JP; Capellari S; Rozemuller AJ; Sarchioto M; Fen Chien H; Vanacore N; Olgiati S; Wu-Chou YH; Yeh TH; Boon AJW; Hoogers SE; Ghazvini M; IJpma AS; van IJcken WFJ; Onofrj M; Barone P; Nicholl DJ; Puschmann A; De Mari M; Kievit AJ; Barbosa E; De Michele G; Majoor-Krakauer D; van Swieten JC; de Jong FJ; Ferreira JJ; Cossu G; Lu CS; Meco G; Cortelli P; van de Berg WDJ; Bonifati V;
    Lancet Neurol; 2018 Jul; 17(7):597-608. PubMed ID: 29887161
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genome-wide contribution of common short-tandem repeats to Parkinson's disease genetic risk.
    Bustos BI; Billingsley K; Blauwendraat C; Gibbs JR; Gan-Or Z; Krainc D; Singleton AB; Lubbe SJ;
    Brain; 2023 Jan; 146(1):65-74. PubMed ID: 36347471
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Targeted sequencing of Parkinson's disease loci genes highlights SYT11, FGF20 and other associations.
    Rudakou U; Yu E; Krohn L; Ruskey JA; Asayesh F; Dauvilliers Y; Spiegelman D; Greenbaum L; Fahn S; Waters CH; Dupré N; Rouleau GA; Hassin-Baer S; Fon EA; Alcalay RN; Gan-Or Z
    Brain; 2021 Mar; 144(2):462-472. PubMed ID: 33349842
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Sulfotransferase 1A3/4 copy number variation is associated with neurodegenerative disease.
    Butcher NJ; Horne MK; Mellick GD; Fowler CJ; Masters CL; ; Minchin RF
    Pharmacogenomics J; 2018 Apr; 18(2):209-214. PubMed ID: 28374858
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Improving Diversity in Parkinson's Disease Genetics: Findings from the First-Ever Genome-Wide Association Study in Latinos.
    Elsayed I; Foote IF
    Mov Disord; 2021 Nov; 36(11):2505. PubMed ID: 34476843
    [No Abstract]   [Full Text] [Related]  

  • 20. Genome-wide Association Identifies Novel Etiological Insights Associated with Parkinson's Disease in African and African Admixed Populations.
    Rizig M; Bandres-Ciga S; Makarious MB; Ojo O; Crea PW; Abiodun O; Levine KS; Abubakar S; Achoru C; Vitale D; Adeniji O; Agabi O; Koretsky MJ; Agulanna U; Hall DA; Akinyemi R; Xie T; Ali M; Shamim EA; Ani-Osheku I; Padmanaban M; Arigbodi O; Standaert DG; Bello A; Dean M; Erameh C; Elsayed I; Farombi T; Okunoye O; Fawale M; Billingsley KJ; Imarhiagbe F; Jerez PA; Iwuozo E; Baker B; Komolafe M; Malik L; Nwani P; Daida K; Nwazor E; Miano-Burkhardt A; Nyandaiti Y; Fang ZH; Obiabo Y; Kluss JH; Odeniyi O; Hernandez D; Odiase F; Tayebi N; Ojini F; Sidranksy E; Onwuegbuzie G; D'Souza AM; Osaigbovo G; Berhe B; Osemwegie N; Reed X; Oshinaike O; Leonard H; Otubogun F; Alvarado CX; Oyakhire S; Ozomma S; Samuel S; Taiwo F; Wahab K; Zubair Y; Iwaki H; Kim JJ; Morris HR; Hardy J; Nalls M; Heilbron K; Norcliffe-Kaufmann L; ; Blauwendraat C; Houlden H; Singleton A; Okubadejo N
    medRxiv; 2023 May; ():. PubMed ID: 37398408
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 33.