BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

377 related articles for article (PubMed ID: 31328266)

  • 1. Genetic spectrum of renal disease for 1001 Chinese children based on a multicenter registration system.
    Rao J; Liu X; Mao J; Tang X; Shen Q; Li G; Sun L; Bi Y; Wang X; Qian Y; Wu B; Wang H; Zhou W; Ma D; Zheng B; Shen Y; Chen Z; Luan J; Wang X; Wang M; Dang X; Wang Y; Wu Y; Hou L; Sun S; Li Q; Liu X; Bai H; Yang Y; Shao X; Li Y; Zheng S; Han M; Liu C; Cao G; Zhao L; Qiu S; Dong Y; Zhu Y; Wang F; Zhang D; Li Y; Zhao L; Yang C; Luo X; Chen L; Jiang X; Zhang A; Xu H;
    Clin Genet; 2019 Nov; 96(5):402-410. PubMed ID: 31328266
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genetic Architecture of Childhood Kidney and Urological Diseases in China.
    Fang Y; Shi H; Xiang T; Liu J; Liu J; Tang X; Fang X; Chen J; Zhai Y; Shen Q; Li G; Sun L; Bi Y; Wang X; Qian Y; Wu B; Wang H; Zhou W; Ma D; Mao J; Jiang X; Sun S; Shen Y; Liu X; Zhang A; Wang X; Huang W; Li Q; Wang M; Gao X; Wu Y; Deng F; Zhang R; Liu C; Yu L; Zhuang J; Sun Q; Dang X; Bai H; Zhu Y; Lu S; Zhang B; Shao X; Liu X; Han M; Zhao L; Liu Y; Gao J; Bao Y; Zhang D; Ma Q; Zhao L; Xia Z; Lu B; Wang Y; Zhao M; Zhang J; Jian S; He G; Zhang H; Zhao B; Li X; Wang F; Li Y; Zhu H; Luo X; Li J; Rao J; Xu H
    Phenomics; 2021 Jun; 1(3):91-104. PubMed ID: 36939782
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Whole-Exome Sequencing Enables a Precision Medicine Approach for Kidney Transplant Recipients.
    Mann N; Braun DA; Amann K; Tan W; Shril S; Connaughton DM; Nakayama M; Schneider R; Kitzler TM; van der Ven AT; Chen J; Ityel H; Vivante A; Majmundar AJ; Daga A; Warejko JK; Lovric S; Ashraf S; Jobst-Schwan T; Widmeier E; Hugo H; Mane SM; Spaneas L; Somers MJG; Ferguson MA; Traum AZ; Stein DR; Baum MA; Daouk GH; Lifton RP; Manzi S; Vakili K; Kim HB; Rodig NM; Hildebrandt F
    J Am Soc Nephrol; 2019 Feb; 30(2):201-215. PubMed ID: 30655312
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Spectrum of congenital anomalies of the kidney and urinary tract (CAKUT) including renal parenchymal malformations during fetal life and the implementation of prenatal exome sequencing (WES).
    Koenigbauer JT; Fangmann L; Reinhardt C; Weichert A; Henrich W; Saskia B; Gabriel HP
    Arch Gynecol Obstet; 2024 Jun; 309(6):2613-2622. PubMed ID: 37535131
    [TBL] [Abstract][Full Text] [Related]  

  • 5. COL4A1 mutations as a potential novel cause of autosomal dominant CAKUT in humans.
    Kitzler TM; Schneider R; Kohl S; Kolvenbach CM; Connaughton DM; Dai R; Mann N; Nakayama M; Majmundar AJ; Wu CW; Kari JA; El Desoky SM; Senguttuvan P; Bogdanovic R; Stajic N; Valivullah Z; Lek M; Mane S; Lifton RP; Tasic V; Shril S; Hildebrandt F
    Hum Genet; 2019 Oct; 138(10):1105-1115. PubMed ID: 31230195
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Responsible genes in children with primary vesicoureteral reflux: findings from the Chinese Children Genetic Kidney Disease Database.
    Liu JL; Shen Q; Wu MY; Zhu GH; Li YF; Wang XW; Tang XS; Bi YL; Gong YN; Chen J; Fang XY; Zhai YH; Wu BB; Li GM; Sun YB; Gao XJ; Liu CH; Jiang XY; Hao S; Kang YL; Gong YL; Rong LP; Li D; Wang S; Ma D; Rao J; Xu H;
    World J Pediatr; 2021 Aug; 17(4):409-418. PubMed ID: 34059960
    [TBL] [Abstract][Full Text] [Related]  

  • 7. New insights from trio whole-exome sequencing in the children with kidney disease: A single-center retrospective cohort study.
    Chen Y; Zhang Y; Huang J; Zeng Y; Qian Y; Chen J; Chen G; Xia G; Wang C; Feng A; Li Z; Chen L; Zheng S; Li F; Weng Z; Zhang C; Yang Y; Lin J; Wu J; Zhang H; Ouyang W; Nie X
    Mol Genet Genomic Med; 2023 Jul; 11(7):e2163. PubMed ID: 37248651
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Monogenic causes of chronic kidney disease in adults.
    Connaughton DM; Kennedy C; Shril S; Mann N; Murray SL; Williams PA; Conlon E; Nakayama M; van der Ven AT; Ityel H; Kause F; Kolvenbach CM; Dai R; Vivante A; Braun DA; Schneider R; Kitzler TM; Moloney B; Moran CP; Smyth JS; Kennedy A; Benson K; Stapleton C; Denton M; Magee C; O'Seaghdha CM; Plant WD; Griffin MD; Awan A; Sweeney C; Mane SM; Lifton RP; Griffin B; Leavey S; Casserly L; de Freitas DG; Holian J; Dorman A; Doyle B; Lavin PJ; Little MA; Conlon PJ; Hildebrandt F
    Kidney Int; 2019 Apr; 95(4):914-928. PubMed ID: 30773290
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Copy Number Variation Analysis Facilitates Identification of Genetic Causation in Patients with Congenital Anomalies of the Kidney and Urinary Tract.
    Wu CW; Lim TY; Wang C; Seltzsam S; Zheng B; Schierbaum L; Schneider S; Mann N; Connaughton DM; Nakayama M; van der Ven AT; Dai R; Kolvenbach CM; Kause F; Ottlewski I; Stajic N; Soliman NA; Kari JA; El Desoky S; Fathy HM; Milosevic D; Turudic D; Al Saffar M; Awad HS; Eid LA; Ramanathan A; Senguttuvan P; Mane SM; Lee RS; Bauer SB; Lu W; Hilger AC; Tasic V; Shril S; Sanna-Cherchi S; Hildebrandt F
    Eur Urol Open Sci; 2022 Oct; 44():106-112. PubMed ID: 36185583
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A Clinical Workflow for Cost-Saving High-Rate Diagnosis of Genetic Kidney Diseases.
    Becherucci F; Landini S; Palazzo V; Cirillo L; Raglianti V; Lugli G; Tiberi L; Dirupo E; Bellelli S; Mazzierli T; Lomi J; Ravaglia F; Sansavini G; Allinovi M; Giannese D; Somma C; Spatoliatore G; Vergani D; Artuso R; Rosati A; Cirami C; Dattolo PC; Campolo G; De Chiara L; Papi L; Vaglio A; Lazzeri E; Anders HJ; Mazzinghi B; Romagnani P
    J Am Soc Nephrol; 2023 Apr; 34(4):706-720. PubMed ID: 36753701
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Whole exome sequencing identifies monogenic forms of nephritis in a previously unsolved cohort of children with steroid-resistant nephrotic syndrome and hematuria.
    Xiao H; Hildebrandt F
    Pediatr Nephrol; 2022 Jul; 37(7):1567-1574. PubMed ID: 34762194
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Fluorescence in situ hybridization for the diagnosis of NPHP1 deletion-related nephronophthisis on renal biopsy.
    Larsen CP; Bonsib SM; Beggs ML; Wilson JD
    Hum Pathol; 2018 Nov; 81():71-77. PubMed ID: 29949740
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Exome Sequencing and Identification of Phenocopies in Patients With Clinically Presumed Hereditary Nephropathies.
    Riedhammer KM; Braunisch MC; Günthner R; Wagner M; Hemmer C; Strom TM; Schmaderer C; Renders L; Tasic V; Gucev Z; Nushi-Stavileci V; Putnik J; Stajić N; Weidenbusch M; Uetz B; Montoya C; Strotmann P; Ponsel S; Lange-Sperandio B; Hoefele J
    Am J Kidney Dis; 2020 Oct; 76(4):460-470. PubMed ID: 32359821
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic diagnosis of kidney disease by whole exome sequencing and its clinical application.
    Jung J; Lee JH; Seo GH; Keum C; Kang HG; Cho H; Lee H; Park SK; Baek CH; Han R; Lee ST; Cho MH; Yim HE; Koo JW; Lee BH
    Clin Genet; 2023 Sep; 104(3):298-312. PubMed ID: 37270787
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Molecular diagnostic in fetuses with isolated congenital anomalies of the kidney and urinary tract by whole-exome sequencing.
    Zhou X; Wang Y; Shao B; Wang C; Hu P; Qiao F; Xu Z
    J Clin Lab Anal; 2020 Nov; 34(11):e23480. PubMed ID: 32779812
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Analysis of 26 fetuses with congenital anomalies of the kidney and urinary tract by whole exome sequencing].
    Lei T; Fu F; Li R; Wang D; Yang D; Wang F; Yang X; Pan M; Zhen L; Han J; Li D; Liao C
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Dec; 35(6):856-859. PubMed ID: 30512163
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study.
    Lata S; Marasa M; Li Y; Fasel DA; Groopman E; Jobanputra V; Rasouly H; Mitrotti A; Westland R; Verbitsky M; Nestor J; Slater LM; D'Agati V; Zaniew M; Materna-Kiryluk A; Lugani F; Caridi G; Rampoldi L; Mattoo A; Newton CA; Rao MK; Radhakrishnan J; Ahn W; Canetta PA; Bomback AS; Appel GB; Antignac C; Markowitz GS; Garcia CK; Kiryluk K; Sanna-Cherchi S; Gharavi AG
    Ann Intern Med; 2018 Jan; 168(2):100-109. PubMed ID: 29204651
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Whole-exome sequencing in the evaluation of fetal congenital anomalies of the kidney and urinary tract detected by ultrasonography.
    Lei TY; Fu F; Li R; Yu QX; Du K; Zhang WW; Deng Q; Li LS; Wang D; Yang X; Zhen L; Li DZ; Liao C
    Prenat Diagn; 2020 Sep; 40(10):1290-1299. PubMed ID: 32436246
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Early diagnosis of WT1 nephropathy and follow up in a Chinese multicenter cohort.
    Sun S; Xu L; Bi Y; Wang J; Zhang Z; Tang X; Cao Q; Zhai Y; Chen J; Fang X; Liu J; Fang Y; Xiang T; Qian Y; Wu B; Wang H; Zhou W; Shen J; Dong K; Liu X; Zheng B; Zhang A; Wang X; Wu Y; Ma D; Shen Q; Rao J; Xu H
    Eur J Med Genet; 2020 Nov; 63(11):104047. PubMed ID: 32891756
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Dominant PAX2 mutations may cause steroid-resistant nephrotic syndrome and FSGS in children.
    Vivante A; Chacham OS; Shril S; Schreiber R; Mane SM; Pode-Shakked B; Soliman NA; Koneth I; Schiffer M; Anikster Y; Hildebrandt F
    Pediatr Nephrol; 2019 Sep; 34(9):1607-1613. PubMed ID: 31001663
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 19.