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.
7. Exome sequencing a review of new strategies for rare genomic disease research. Brown TL; Meloche TM Genomics; 2016 Oct; 108(3-4):109-114. PubMed ID: 27387609 [TBL] [Abstract][Full Text] [Related]
8. How to proceed after "negative" exome: A review on genetic diagnostics, limitations, challenges, and emerging new multiomics techniques. Wortmann SB; Oud MM; Alders M; Coene KLM; van der Crabben SN; Feichtinger RG; Garanto A; Hoischen A; Langeveld M; Lefeber D; Mayr JA; Ockeloen CW; Prokisch H; Rodenburg R; Waterham HR; Wevers RA; van de Warrenburg BPC; Willemsen MAAP; Wolf NI; Vissers LELM; van Karnebeek CDM J Inherit Metab Dis; 2022 Jul; 45(4):663-681. PubMed ID: 35506430 [TBL] [Abstract][Full Text] [Related]
9. Prospective Evaluation of the Utility of Whole Exome Sequencing in Dilated Cardiomyopathy. Ramchand J; Wallis M; Macciocca I; Lynch E; Farouque O; Martyn M; Phelan D; Chong B; Lockwood S; Weintraub R; Thompson T; Trainer A; Zentner D; Vohra J; Chetrit M; Hare DL; James P J Am Heart Assoc; 2020 Jan; 9(2):e013346. PubMed ID: 31931689 [TBL] [Abstract][Full Text] [Related]
10. Challenges and opportunities in the application of artificial intelligence in gastroenterology and hepatology. Christou CD; Tsoulfas G World J Gastroenterol; 2021 Oct; 27(37):6191-6223. PubMed ID: 34712027 [TBL] [Abstract][Full Text] [Related]
11. Whole genome and exome sequencing reference datasets from a multi-center and cross-platform benchmark study. Zhao Y; Fang LT; Shen TW; Choudhari S; Talsania K; Chen X; Shetty J; Kriga Y; Tran B; Zhu B; Chen Z; Chen W; Wang C; Jaeger E; Meerzaman D; Lu C; Idler K; Ren L; Zheng Y; Shi L; Petitjean V; Sultan M; Hung T; Peters E; Drabek J; Vojta P; Maestro R; Gasparotto D; Kõks S; Reimann E; Scherer A; Nordlund J; Liljedahl U; Foox J; Mason CE; Xiao C; Hong H; Xiao W Sci Data; 2021 Nov; 8(1):296. PubMed ID: 34753956 [TBL] [Abstract][Full Text] [Related]
12. Frequency and management of medically actionable incidental findings from genome and exome sequencing data: a systematic review. Elfatih A; Mohammed I; Abdelrahman D; Mifsud B Physiol Genomics; 2021 Sep; 53(9):373-384. PubMed ID: 34250816 [TBL] [Abstract][Full Text] [Related]
13. From sub-microscopic variants to the resolution of a single base pair: Exome sequencing in prenatal diagnosis. He P; Xu LL; Li DZ Eur J Med Genet; 2020 Apr; 63(4):103779. PubMed ID: 31586466 [No Abstract] [Full Text] [Related]
14. A novel knowledge-derived data potentizing method revealed unique liver cancer-associated genetic variants. Sultana N; Rahman M; Myti S; Islam J; Mustafa MG; Nag K Hum Genomics; 2019 Jul; 13(1):30. PubMed ID: 31272500 [TBL] [Abstract][Full Text] [Related]
15. Whole-exome sequencing in familial keratoconus: the challenges of a genetically complex disorder. Magalhães OA; Kowalski TW; Wachholz GE; Schuler-Faccini L Arq Bras Oftalmol; 2019; 82(6):453-459. PubMed ID: 31482965 [TBL] [Abstract][Full Text] [Related]
16. Controversy and debate on clinical genomics sequencing-paper 2: clinical genome-wide sequencing: don't throw out the baby with the bathwater! Adam S; Friedman JM J Clin Epidemiol; 2017 Dec; 92():7-10. PubMed ID: 28916491 [TBL] [Abstract][Full Text] [Related]
17. Scientific publications in gastroenterology and hepatology in Taiwan: An analysis of Web of Science from 1993 to 2013. Chang HT; Lin MH; Hwang IH; Chen TJ; Lin HC; Hou MC; Hwang SJ J Chin Med Assoc; 2017 Feb; 80(2):80-85. PubMed ID: 28341083 [TBL] [Abstract][Full Text] [Related]
18. Single-cell exome sequencing reveals multiple subclones in metastatic colorectal carcinoma. Tang J; Tu K; Lu K; Zhang J; Luo K; Jin H; Wang L; Yang L; Xiao W; Zhang Q; Liu X; Ge XY; Li G; Zhou Z; Xie D Genome Med; 2021 Sep; 13(1):148. PubMed ID: 34507604 [TBL] [Abstract][Full Text] [Related]
19. Actionable secondary findings in 1116 Hong Kong Chinese based on exome sequencing data. Yu MHC; Mak CCY; Fung JLF; Lee M; Tsang MHY; Chau JFT; Chung PH; Yang W; Chan GCF; Lee SL; Lau YL; Tam PKH; Tang CSM; Yeung KS; Chung BHY J Hum Genet; 2021 Jun; 66(6):637-641. PubMed ID: 33223521 [TBL] [Abstract][Full Text] [Related]
20. Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies. Mackley MP; Fletcher B; Parker M; Watkins H; Ormondroyd E Genet Med; 2017 Mar; 19(3):283-293. PubMed ID: 27584911 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]