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 *

163 related articles for article (PubMed ID: 32672555)

  • 41. Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.
    Aung T; Ozaki M; Lee MC; Schlötzer-Schrehardt U; Thorleifsson G; Mizoguchi T; Igo RP; Haripriya A; Williams SE; Astakhov YS; Orr AC; Burdon KP; Nakano S; Mori K; Abu-Amero K; Hauser M; Li Z; Prakadeeswari G; Bailey JNC; Cherecheanu AP; Kang JH; Nelson S; Hayashi K; Manabe SI; Kazama S; Zarnowski T; Inoue K; Irkec M; Coca-Prados M; Sugiyama K; Järvelä I; Schlottmann P; Lerner SF; Lamari H; Nilgün Y; Bikbov M; Park KH; Cha SC; Yamashiro K; Zenteno JC; Jonas JB; Kumar RS; Perera SA; Chan ASY; Kobakhidze N; George R; Vijaya L; Do T; Edward DP; de Juan Marcos L; Pakravan M; Moghimi S; Ideta R; Bach-Holm D; Kappelgaard P; Wirostko B; Thomas S; Gaston D; Bedard K; Greer WL; Yang Z; Chen X; Huang L; Sang J; Jia H; Jia L; Qiao C; Zhang H; Liu X; Zhao B; Wang YX; Xu L; Leruez S; Reynier P; Chichua G; Tabagari S; Uebe S; Zenkel M; Berner D; Mossböck G; Weisschuh N; Hoja U; Welge-Luessen UC; Mardin C; Founti P; Chatzikyriakidou A; Pappas T; Anastasopoulos E; Lambropoulos A; Ghosh A; Shetty R; Porporato N; Saravanan V; Venkatesh R; Shivkumar C; Kalpana N; Sarangapani S; Kanavi MR; Beni AN; Yazdani S; Lashay A; Naderifar H; Khatibi N; Fea A; Lavia C; Dallorto L; Rolle T; Frezzotti P; Paoli D; Salvi E; Manunta P; Mori Y; Miyata K; Higashide T; Chihara E; Ishiko S; Yoshida A; Yanagi M; Kiuchi Y; Ohashi T; Sakurai T; Sugimoto T; Chuman H; Aihara M; Inatani M; Miyake M; Gotoh N; Matsuda F; Yoshimura N; Ikeda Y; Ueno M; Sotozono C; Jeoung JW; Sagong M; Park KH; Ahn J; Cruz-Aguilar M; Ezzouhairi SM; Rafei A; Chong YF; Ng XY; Goh SR; Chen Y; Yong VHK; Khan MI; Olawoye OO; Ashaye AO; Ugbede I; Onakoya A; Kizor-Akaraiwe N; Teekhasaenee C; Suwan Y; Supakontanasan W; Okeke S; Uche NJ; Asimadu I; Ayub H; Akhtar F; Kosior-Jarecka E; Lukasik U; Lischinsky I; Castro V; Grossmann RP; Sunaric Megevand G; Roy S; Dervan E; Silke E; Rao A; Sahay P; Fornero P; Cuello O; Sivori D; Zompa T; Mills RA; Souzeau E; Mitchell P; Wang JJ; Hewitt AW; Coote M; Crowston JG; Astakhov SY; Akopov EL; Emelyanov A; Vysochinskaya V; Kazakbaeva G; Fayzrakhmanov R; Al-Obeidan SA; Owaidhah O; Aljasim LA; Chowbay B; Foo JN; Soh RQ; Sim KS; Xie Z; Cheong AWO; Mok SQ; Soo HM; Chen XY; Peh SQ; Heng KK; Husain R; Ho SL; Hillmer AM; Cheng CY; Escudero-Domínguez FA; González-Sarmiento R; Martinon-Torres F; Salas A; Pathanapitoon K; Hansapinyo L; Wanichwecharugruang B; Kitnarong N; Sakuntabhai A; Nguyn HX; Nguyn GTT; Nguyn TV; Zenz W; Binder A; Klobassa DS; Hibberd ML; Davila S; Herms S; Nöthen MM; Moebus S; Rautenbach RM; Ziskind A; Carmichael TR; Ramsay M; Álvarez L; García M; González-Iglesias H; Rodríguez-Calvo PP; Fernández-Vega Cueto L; Oguz Ç; Tamcelik N; Atalay E; Batu B; Aktas D; Kasım B; Wilson MR; Coleman AL; Liu Y; Challa P; Herndon L; Kuchtey RW; Kuchtey J; Curtin K; Chaya CJ; Crandall A; Zangwill LM; Wong TY; Nakano M; Kinoshita S; den Hollander AI; Vesti E; Fingert JH; Lee RK; Sit AJ; Shingleton BJ; Wang N; Cusi D; Qamar R; Kraft P; Pericak-Vance MA; Raychaudhuri S; Heegaard S; Kivelä T; Reis A; Kruse FE; Weinreb RN; Pasquale LR; Haines JL; Thorsteinsdottir U; Jonasson F; Allingham RR; Milea D; Ritch R; Kubota T; Tashiro K; Vithana EN; Micheal S; Topouzis F; Craig JE; Dubina M; Sundaresan P; Stefansson K; Wiggs JL; Pasutto F; Khor CC
    Nat Genet; 2017 Jul; 49(7):993-1004. PubMed ID: 28553957
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Association of clusterin (CLU) variants and exfoliation syndrome: An analysis in two Caucasian studies and a meta-analysis.
    Fan BJ; Pasquale LR; Kang JH; Levkovitch-Verbin H; Haines JL; Wiggs JL
    Exp Eye Res; 2015 Oct; 139():115-22. PubMed ID: 26272660
    [TBL] [Abstract][Full Text] [Related]  

  • 43. LOXL1 gene sequence variants and vascular disease in exfoliation syndrome and exfoliative glaucoma.
    Holló G; Gál A; Kóthy P; Molnár JM
    J Glaucoma; 2011 Mar; 20(3):143-7. PubMed ID: 20436359
    [TBL] [Abstract][Full Text] [Related]  

  • 44. The management of exfoliative glaucoma.
    Ritch R
    Prog Brain Res; 2008; 173():211-24. PubMed ID: 18929111
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Evaluation of MMP1 and MMP3 gene polymorphisms in exfoliation syndrome and exfoliation glaucoma.
    Tsironi EE; Pefkianaki M; Tsezou A; Kotoula MG; Dardiotis E; Almpanidou P; Papathanasiou AA; Rodopoulou P; Chatzoulis DZ; Hadjigeorgiou GM
    Mol Vis; 2009 Dec; 15():2890-5. PubMed ID: 20038976
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Genetics of pseudoexfoliation syndrome.
    Challa P
    Curr Opin Ophthalmol; 2009 Mar; 20(2):88-91. PubMed ID: 19240540
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Association of non-synonymous single nucleotide polymorphisms in the LOXL1 gene with pseudoexfoliation syndrome in India.
    Ramprasad VL; George R; Soumittra N; Sharmila F; Vijaya L; Kumaramanickavel G
    Mol Vis; 2008 Feb; 14():318-22. PubMed ID: 18334947
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Exfoliation syndrome in sub-Saharan Africa.
    Olawoye OO; Pasquale LR; Ritch R
    Int Ophthalmol; 2014 Oct; 34(5):1165-73. PubMed ID: 24844849
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Association of exfoliation syndrome and central retinal vein occlusion: an ultrastructural analysis.
    Ritch R; Prata TS; de Moraes CG; Vessani RM; Costa VP; Konstas AG; Liebmann JM; Schlötzer-Schrehardt U
    Acta Ophthalmol; 2010 Feb; 88(1):91-5. PubMed ID: 19725816
    [TBL] [Abstract][Full Text] [Related]  

  • 50. LOXL1 Polymorphisms: Genetic Biomarkers that Presage Environmental Determinants of Exfoliation Syndrome.
    Pasquale LR; Kang JH; Fan B; Levkovitch-Verbin H; Wiggs JL
    J Glaucoma; 2018 Jul; 27 Suppl 1(Suppl 1):S20-S23. PubMed ID: 29965898
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Systemic associations and prevalence of exfoliation syndrome in patients scheduled for cataract surgery.
    Sekeroglu MA; Bozkurt B; Irkec M; Ustunel S; Orhan M; Saracbasi O
    Eur J Ophthalmol; 2008; 18(4):551-5. PubMed ID: 18609473
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Expression and regulation of LOXL1 and elastin-related genes in eyes with exfoliation syndrome.
    Wiggs JL; Pasquale LR
    J Glaucoma; 2014; 23(8 Suppl 1):S62-3. PubMed ID: 25275910
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Prevalence of exfoliation syndrome and cardiovascular diseases in patients scheduled for cataract surgery].
    Tijani M; Albaroudi N; Boutimzine N; Cherkaoui O; Laghmari M
    J Fr Ophtalmol; 2017 Oct; 40(8):623-628. PubMed ID: 28865939
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Solar exposure and residential geographic history in relation to exfoliation syndrome in the United States and Israel.
    Pasquale LR; Jiwani AZ; Zehavi-Dorin T; Majd A; Rhee DJ; Chen T; Turalba A; Shen L; Brauner S; Grosskreutz C; Gardiner M; Chen S; Borboli-Gerogiannis S; Greenstein SH; Chang K; Ritch R; Loomis S; Kang JH; Wiggs JL; Levkovitch-Verbin H
    JAMA Ophthalmol; 2014 Dec; 132(12):1439-45. PubMed ID: 25188364
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Exfoliation syndrome: assembling the puzzle pieces.
    Pasquale LR; Borrás T; Fingert JH; Wiggs JL; Ritch R
    Acta Ophthalmol; 2016 Sep; 94(6):e505-12. PubMed ID: 26648185
    [TBL] [Abstract][Full Text] [Related]  

  • 56. LOXL1 GENE VARIANTS IN ASSOCIATION WITH EXFOLIATION SYNDROME IN GEORGIAN POPULATION.
    Kobakhidze N; Tabagari S; Chichua G
    Georgian Med News; 2019 Jan; (286):32-36. PubMed ID: 30829585
    [TBL] [Abstract][Full Text] [Related]  

  • 57. LOXL1 deficiency in the lamina cribrosa as candidate susceptibility factor for a pseudoexfoliation-specific risk of glaucoma.
    Schlötzer-Schrehardt U; Hammer CM; Krysta AW; Hofmann-Rummelt C; Pasutto F; Sasaki T; Kruse FE; Zenkel M
    Ophthalmology; 2012 Sep; 119(9):1832-43. PubMed ID: 22633114
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Hearing Loss in Exfoliation Syndrome: Systematic Review and Meta-Analysis.
    Shih MC; Gordis TM; Lambert PR; Nguyen SA; Meyer TA
    Laryngoscope; 2023 May; 133(5):1025-1035. PubMed ID: 36087028
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Common sequence variants in the LOXL1 gene confer susceptibility to exfoliation glaucoma.
    Thorleifsson G; Magnusson KP; Sulem P; Walters GB; Gudbjartsson DF; Stefansson H; Jonsson T; Jonasdottir A; Jonasdottir A; Stefansdottir G; Masson G; Hardarson GA; Petursson H; Arnarsson A; Motallebipour M; Wallerman O; Wadelius C; Gulcher JR; Thorsteinsdottir U; Kong A; Jonasson F; Stefansson K
    Science; 2007 Sep; 317(5843):1397-400. PubMed ID: 17690259
    [TBL] [Abstract][Full Text] [Related]  

  • 60. LOXL1 folding in exfoliation glaucoma.
    Bernstein AM; Ritch R; Wolosin JM
    Adv Protein Chem Struct Biol; 2019; 118():273-288. PubMed ID: 31928728
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.