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Showing results for guo yi han
Search for Guoyi Han instead (2 results)
The course of clinical diagnosis and treatment of a case infected with coronavirus disease 2019.
Han W, Quan B, Guo Y, Zhang J, Lu Y, Feng G, Wu Q, Fang F, Cheng L, Jiao N, Li X, Chen Q. Han W, et al. Among authors: guo y. J Med Virol. 2020 May;92(5):461-463. doi: 10.1002/jmv.25711. Epub 2020 Mar 1. J Med Virol. 2020. PMID: 32073161 Free PMC article. No abstract available.
Clinical and Autoimmune Characteristics of Severe and Critical Cases of COVID-19.
Zhou Y, Han T, Chen J, Hou C, Hua L, He S, Guo Y, Zhang S, Wang Y, Yuan J, Zhao C, Zhang J, Jia Q, Zuo X, Li J, Wang L, Cao Q, Jia E. Zhou Y, et al. Among authors: guo y. Clin Transl Sci. 2020 Nov;13(6):1077-1086. doi: 10.1111/cts.12805. Epub 2020 May 14. Clin Transl Sci. 2020. PMID: 32315487 Free PMC article.
Conversion Discriminative Analysis on Mild Cognitive Impairment Using Multiple Cortical Features from MR Images.
Guo S, Lai C, Wu C, Cen G; Alzheimer's Disease Neuroimaging Initiative. Guo S, et al. Front Aging Neurosci. 2017 May 18;9:146. doi: 10.3389/fnagi.2017.00146. eCollection 2017. Front Aging Neurosci. 2017. PMID: 28572766 Free PMC article.
A COL4A5 Missense Variant in a Han-Chinese Family with X-linked Alport Syndrome.
Wu Y, Guo Y, Yuan J, Xu H, Chen Y, Zhang H, Yuan M, Deng H, Yuan L. Wu Y, et al. Among authors: guo y. Curr Mol Med. 2019;19(10):758-765. doi: 10.2174/1566524019666190906144214. Curr Mol Med. 2019. PMID: 31490752
OBJECTIVE: The purpose of this research is to detect the genetic defect responsible for renal disorder in a 3-generation Han-Chinese pedigree. METHODS: Detailed family history and clinical data of the family members were collected and recorded. ...
OBJECTIVE: The purpose of this research is to detect the genetic defect responsible for renal disorder in a 3-generation Han-Chinese …
Identification of novel pathogenic ABCA4 variants in a Han Chinese family with Stargardt disease.
Xiang Q, Cao Y, Xu H, Guo Y, Yang Z, Xu L, Yuan L, Deng H. Xiang Q, et al. Among authors: guo y. Biosci Rep. 2019 Jan 15;39(1):BSR20180872. doi: 10.1042/BSR20180872. Print 2019 Jan 31. Biosci Rep. 2019. PMID: 30563929 Free PMC article.
Here, we sought to identify gene mutations associated with STGD1 in a three-generation Han Chinese pedigree by whole exome sequencing and Sanger sequencing. ...
Here, we sought to identify gene mutations associated with STGD1 in a three-generation Han Chinese pedigree by whole exome sequencing …
Identifying a BRCA2 c.5722_5723del mutation in a Han-Chinese family with breast cancer.
Guo Y, Wang P, Li X, Zhu S, Xu H, Li S, Deng H, Yuan L. Guo Y, et al. Biosci Rep. 2019 Apr 30;39(4):BSR20182471. doi: 10.1042/BSR20182471. Print 2019 Apr 30. Biosci Rep. 2019. PMID: 30940775 Free PMC article.
The present study found a heterozygous c.5722_5723del mutation in the BRCA2 exon 11 of a large Han-Chinese BC family using whole exome sequencing and Sanger sequencing. ...
The present study found a heterozygous c.5722_5723del mutation in the BRCA2 exon 11 of a large Han-Chinese BC family using whole exom …
Heterozygous RHO p.R135W missense mutation in a large Han-Chinese family with retinitis pigmentosa and different refractive errors.
Wu Y, Guo Y, Yi J, Xu H, Yuan L, Yang Z, Deng H. Wu Y, et al. Among authors: guo y. Biosci Rep. 2019 Jul 12;39(7):BSR20182198. doi: 10.1042/BSR20182198. Print 2019 Jul 31. Biosci Rep. 2019. PMID: 31239368 Free PMC article.
The present study aims to identify the disease-causing mutation in a numerous, four-generation Han-Chinese family with adRP detected by whole exome sequencing and Sanger sequencing. ...
The present study aims to identify the disease-causing mutation in a numerous, four-generation Han-Chinese family with adRP detected …
Identification of a novel EVC variant in a Han-Chinese family with Ellis-van Creveld syndrome.
Huang X, Guo Y, Xu H, Yang Z, Deng X, Deng H, Yuan L. Huang X, et al. Among authors: guo y. Mol Genet Genomic Med. 2019 Sep;7(9):e885. doi: 10.1002/mgg3.885. Epub 2019 Jul 23. Mol Genet Genomic Med. 2019. PMID: 31338997 Free PMC article. Clinical Trial.
The aim of this study was to identify the genetic defect for EVC in a five-generation consanguineous Han-Chinese pedigree. METHODS: A five-generation, 12-member Han-Chinese pedigree was enrolled in this study. ...CONCLUSION: The identified novel homozygous EVC varia …
The aim of this study was to identify the genetic defect for EVC in a five-generation consanguineous Han-Chinese pedigree. METHODS: A …
COL1A2 p.Gly1066Val variant identified in a Han Chinese family with osteogenesis imperfecta type I.
Wang M, Guo Y, Rong P, Xu H, Gong L, Deng H, Yuan L. Wang M, et al. Among authors: guo y. Mol Genet Genomic Med. 2019 May;7(5):e619. doi: 10.1002/mgg3.619. Epub 2019 Mar 4. Mol Genet Genomic Med. 2019. PMID: 30829463 Free PMC article.
This study sought to identify pathogenic gene variants in a four-generation Han Chinese family with OI type I. METHODS: In order to unveil the molecular genetic factors underlying the disease phenotype, whole exome sequencing in a member, with OI type I, of a Han Ch …
This study sought to identify pathogenic gene variants in a four-generation Han Chinese family with OI type I. METHODS: In order to u …
The epidemiological characteristics of cluster transmission of coronavirus disease 2019 (COVID-19): a multi-center study in Jiangsu Province.
Han T, Hua L, He S, Zhou Y, Hou C, Chen J, Yuan J, Guo Y, Zhang S, Jia Q, Zhao C, Zhang J, Cao Q, Jia E. Han T, et al. Among authors: guo y. Am J Transl Res. 2020 Oct 15;12(10):6434-6444. eCollection 2020. Am J Transl Res. 2020. PMID: 33194041 Free PMC article.
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