학술논문

The genetic architecture of membranous nephropathy and its potential to improve non-invasive diagnosis
Document Type
article
Author
Jingyuan XieLili LiuNikol MladkovaYifu LiHong RenWeiming WangZhao CuiLi LinXiaofan HuXialian YuJing XuGang LiuYasar CaliskanCarlo SidoreOlivia BalderesRaphael J. RosenMonica BodriaFrancesca ZanoniJun Y. ZhangPriya KrithivasanKarla MehlMaddalena MarasaAtlas KhanFatih OzayPietro A. CanettaAndrew S. BombackGerald B. AppelSimone Sanna-CherchiMatthew G. SampsonLaura H. MarianiAgnieszka Perkowska-PtasinskaMagdalena DurlikKrzysztof MuchaBarbara MoszczukBartosz ForoncewiczLeszek PączekIreneusz HaburaElisabet ArsJose BallarinLaila-Yasmin ManiBruno VogtSavas OzturkAbdülmecit YildizNurhan SeyahiHakki ArikanMehmet KocTaner BasturkGonca KarahanSebahat Usta AkgulMehmet Sukru SeverDan ZhangDomenico SantoroMario BonominiFrancesco LondrinoLoreto GesualdoJana ReiterovaVladimir TesarClaudia IzziSilvana SavoldiDonatella SpottiCarmelita MarcantoniPiergiorgio MessaMarco GallianiDario RoccatelloSimona GranataGianluigi ZazaFrancesca LuganiGianMarco GhiggeriIsabella PisaniLandino AllegriBen SprangersJin-Ho ParkBeLong ChoYon Su KimDong Ki KimHitoshi SuzukiAntonio AmorosoDaniel C. CattranFernando C. FervenzaAntonello PaniPatrick HamiltonShelly HarrisSanjana GuptaChris CheshireStephanie DufekNaomi IsslerRuth J. PepperJohn ConnollyStephen PowisDetlef BockenhauerHoria C. StanescuNeil AshmanRuth J. F. LoosEimear E. KennyMatthias WuttkeKai-Uwe EckardtAnna KöttgenJulia M. HofstraMarieke J. H. CoenenLambertus A. KiemeneyShreeram AkileshMatthias KretzlerLawrence H. BeckBenedicte StengelHanna DebiecPierre RoncoJack F. M. WetzelsMagdalena ZoledziewskaFrancesco CuccaIuliana Ionita-LazaHajeong LeeElion HoxhaRolf A. K. StahlPaul BrenchleyFrancesco ScolariMing-hui ZhaoAli G. GharaviRobert KletaNan ChenKrzysztof Kiryluk
Source
Nature Communications, Vol 11, Iss 1, Pp 1-18 (2020)
Subject
Science
Language
English
ISSN
2041-1723
Abstract
Membranous nephropathy (MN) is a rare autoimmune disease of podocyte-directed antibodies, such as anti-phospholipase A2 receptor. Here, the authors report a genome-wide association study for MN and identify two previously unreported loci encompassing the NFKB1 and IRF4 genes and additional ancestry-specific effects.