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5. Publisher Correction: Integrated exome and RNA sequencing of dedifferentiated liposarcoma. Hirata M; Asano N; Katayama K; Yoshida A; Tsuda Y; Sekimizu M; Mitani S; Kobayashi E; Komiyama M; Fujimoto H; Goto T; Iwamoto Y; Naka N; Iwata S; Nishida Y; Hiruma T; Hiraga H; Kawano H; Motoi T; Oda Y; Matsubara D; Fujita M; Shibata T; Nakagawa H; Nakayama R; Kondo T; Imoto S; Miyano S; Kawai A; Yamaguchi R; Ichikawa H; Matsuda K Nat Commun; 2020 Feb; 11(1):1024. PubMed ID: 32075980 [TBL] [Abstract][Full Text] [Related]
6. Author Correction: Exome sequencing of Finnish isolates enhances rare-variant association power. Locke AE; Steinberg KM; Chiang CWK; Service SK; Havulinna AS; Stell L; Pirinen M; Abel HJ; Chiang CC; Fulton RS; Jackson AU; Kang CJ; Kanchi KL; Koboldt DC; Larson DE; Nelson J; Nicholas TJ; Pietilä A; Ramensky V; Ray D; Scott LJ; Stringham HM; Vangipurapu J; Welch R; Yajnik P; Yin X; Eriksson JG; Ala-Korpela M; Järvelin MR; Männikkö M; Laivuori H; ; Dutcher SK; Stitziel NO; Wilson RK; Hall IM; Sabatti C; Palotie A; Salomaa V; Laakso M; Ripatti S; Boehnke M; Freimer NB Nature; 2019 Nov; 575(7783):E4. PubMed ID: 31686056 [TBL] [Abstract][Full Text] [Related]
7. Author Correction: Development and performance of a targeted whole exome sequencing enrichment kit for the dog (Canis Familiaris Build 3.1). Broeckx BJG; Coopman F; Verhoeven GEC; Bavegems V; De Keulenaer S; De Meester E; Van Nieuwerburgh F; Deforce D Sci Rep; 2020 Apr; 10(1):6285. PubMed ID: 32269259 [TBL] [Abstract][Full Text] [Related]
8. Publisher Correction: Exome sequencing highlights the role of wild-relative introgression in shaping the adaptive landscape of the wheat genome. He F; Pasam R; Shi F; Kant S; Keeble-Gagnere G; Kay P; Forrest K; Fritz A; Hucl P; Wiebe K; Knox R; Cuthbert R; Pozniak C; Akhunova A; Morrell PL; Davies JP; Webb SR; Spangenberg G; Hayes B; Daetwyler H; Tibbits J; Hayden M; Akhunov E Nat Genet; 2019 Jul; 51(7):1194. PubMed ID: 31197271 [TBL] [Abstract][Full Text] [Related]
9. Author Correction: Genetic Characteristics of Korean Patients with Autosomal Dominant Polycystic Kidney Disease by Targeted Exome Sequencing. Kim H; Park HC; Ryu H; Kim H; Lee HS; Heo J; Lee C; Kim NKD; Park WY; Hwang YH; Lee KB; Oh KH; Oh YK; Ahn C Sci Rep; 2020 Apr; 10(1):6033. PubMed ID: 32238825 [TBL] [Abstract][Full Text] [Related]
10. Author Correction: Whole exome sequencing for the identification of CYP3A7 variants associated with tacrolimus concentrations in kidney transplant patients. Sohn M; Kim MG; Han N; Kim IW; Gim J; Min SI; Song EY; Kim YS; Jung HS; Shin YK; Ha J; Oh JM Sci Rep; 2020 Feb; 10(1):2486. PubMed ID: 32034192 [TBL] [Abstract][Full Text] [Related]
12. Publisher Correction: Personalized early detection and prevention of breast cancer: ENVISION consensus statement. Pashayan N; Antoniou AC; Ivanus U; Esserman LJ; Easton DF; French D; Sroczynski G; Hall P; Cuzick J; Evans DG; Simard J; Garcia-Closas M; Schmutzler R; Wegwarth O; Pharoah P; Moorthie S; De Montgolfier S; Baron C; Herceg Z; Turnbull C; Balleyguier C; Rossi PG; Wesseling J; Ritchie D; Tischkowitz M; Broeders M; Reisel D; Metspalu A; Callender T; de Koning H; Devilee P; Delaloge S; Schmidt MK; Widschwendter M Nat Rev Clin Oncol; 2020 Nov; 17(11):716. PubMed ID: 32601456 [TBL] [Abstract][Full Text] [Related]
13. Correction: Whole-exome sequencing identifies a novel CCDC151 mutation, c.325GT (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus. Zhang W; Li D; Wei S; Guo T; Wang J; Luo H; Yang Y; Tan Z J Hum Genet; 2019 Aug; 64(8):829. PubMed ID: 31178588 [TBL] [Abstract][Full Text] [Related]
15. Correction: The importance of a valid assessment of salt intake in individuals and populations. A scientific statement of the British and Irish Hypertension Society. Cappuccio FP; Sever PS; J Hum Hypertens; 2020 Apr; 34(4):338. PubMed ID: 32103155 [TBL] [Abstract][Full Text] [Related]
16. Author Correction: An exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer. Oh JJ; Shivakumar M; Miller J; Verma S; Lee H; Hong SK; Lee SE; Lee Y; Lee SJ; Sung J; Kim D; Byun SS Sci Rep; 2020 Feb; 10(1):2481. PubMed ID: 32034279 [TBL] [Abstract][Full Text] [Related]
17. Author Correction: The spatiotemporal organization of episodic memory and its disruption in a neurodevelopmental disorder. Mastrogiuseppe M; Bertelsen N; Bedeschi MF; Lee SA Sci Rep; 2020 Oct; 10(1):18814. PubMed ID: 33110174 [TBL] [Abstract][Full Text] [Related]
18. Correction: GATAD2B-associated neurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-related disorder. Shieh C; Jones N; Vanle B; Au M; Huang AY; Silva APG; Lee H; Douine ED; Otero MG; Choi A; Grand K; Taff IP; Delgado MR; Hajianpour MJ; Seeley A; Rohena L; Vernon H; Gripp KW; Vergano SA; Mahida S; Naidu S; Sousa AB; Wain KE; Challman TD; Beek G; Basel D; Ranells J; Smith R; Yusupov R; Freckmann ML; Ohden L; Davis-Keppen L; Chitayat D; Dowling JJ; Finkel R; Dauber A; Spillmann R; Pena LDM; ; Metcalfe K; Splitt M; Lachlan K; McKee SA; Hurst J; Fitzpatrick DR; Morton JEV; Cox H; Venkateswaran S; Young JI; Marsh ED; Nelson SF; Martinez JA; Graham JM; Kini U; Mackay JP; Pierson TM Genet Med; 2020 Apr; 22(4):822. PubMed ID: 32047287 [TBL] [Abstract][Full Text] [Related]
19. Comparison of the diagnostic yield of aCGH and genome-wide sequencing across different neurodevelopmental disorders. Martinez-Granero F; Blanco-Kelly F; Sanchez-Jimeno C; Avila-Fernandez A; Arteche A; Bustamante-Aragones A; Rodilla C; Rodríguez-Pinilla E; Riveiro-Alvarez R; Tahsin-Swafiri S; Trujillo-Tiebas MJ; Ayuso C; Rodríguez de Alba M; Lorda-Sanchez I; Almoguera B NPJ Genom Med; 2021 Mar; 6(1):25. PubMed ID: 33767182 [TBL] [Abstract][Full Text] [Related]
20. Genetic Analysis of Children With Unexplained Developmental Delay and/or Intellectual Disability by Whole-Exome Sequencing. Xiang J; Ding Y; Yang F; Gao A; Zhang W; Tang H; Mao J; He Q; Zhang Q; Wang T Front Genet; 2021; 12():738561. PubMed ID: 34858471 [No Abstract] [Full Text] [Related] [Next] [New Search]