| Year |
Citation |
Score |
| 2025 |
Liu P, Li W, Li J, Wang Z, Chen X, Yu S, Zheng X, Xie C, Tang Z, Wu S, Li W, Yang C, Zhang J. Interfacial Work Function Modulation of Wide Bandgap Perovskite Solar Cell for Efficient Perovskite/CIGS Tandem Solar Cell. Small Methods. e2401802. PMID 39865980 DOI: 10.1002/smtd.202401802 |
0.346 |
|
| 2023 |
Liu L, Li J, Li J, Hu H, Liu J, Tang P. Novel heterozygous mutation in the SHOX gene leading to familial idiopathic short stature: A case report and literature review. Medicine. 102: e35471. PMID 37832088 DOI: 10.1097/MD.0000000000035471 |
0.316 |
|
| 2023 |
Xu N, Cai Y, Li J, Tao T, Liu C, Shen Y, Li X, Zhang L, Zhao M, Shi X, Li J, Huang L. An SNX31 variant underlies dominant familial exudative vitreoretinopathy-like pathogenesis. Jci Insight. PMID 37053012 DOI: 10.1172/jci.insight.167032 |
0.3 |
|
| 2022 |
Tang P, Li J, Li J, Yang J, Zhu J. Prenatal diagnosis and genetic analysis of a fetus with Branchio-oto-renal syndrome: A case report. Medicine. 101: e31172. PMID 36316881 DOI: 10.1097/MD.0000000000031172 |
0.317 |
|
| 2022 |
Lai D, Wang L, Li JR, Chen C, Zhao WL, Yuan Q, Ma X, Zhang X. Corrigendum: Transcriptional progressive patterns from mild to severe renal ischemia/reperfusion-induced kidney injury in mice. Frontiers in Genetics. 13: 1011276. PMID 36176290 DOI: 10.3389/fgene.2022.1011276 |
0.368 |
|
| 2022 |
Lai D, Wang L, Li JR, Chen C, Zhao WL, Yuan Q, Ma X, Zhang X. Transcriptional progressive patterns from mild to severe renal ischemia/reperfusion-induced kidney injury in mice. Frontiers in Genetics. 13: 874189. PMID 35938014 DOI: 10.3389/fgene.2022.874189 |
0.405 |
|
| 2019 |
Zhang Q, Yang X, Wang J, Li J, Wu Q, Wen Y, Zhao Y, Zhang X, Yao H, Wu X, Yu S, Wei L, Bao X. Correction: Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30783265 DOI: 10.1038/S41436-019-0461-X |
0.624 |
|
| 2019 |
Zhou WZ, Zhang J, Li Z, Lin X, Li J, Wang S, Yang C, Wu Q, Ye AY, Wang M, Wang D, Pu TZ, Wu YY, Wei L. Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations. Human Mutation. PMID 30763456 DOI: 10.1002/Humu.23724 |
0.76 |
|
| 2018 |
Zhang Q, Yang X, Wang J, Li J, Wu Q, Wen Y, Zhao Y, Zhang X, Yao H, Wu X, Yu S, Wei L, Bao X. Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30405208 DOI: 10.1038/S41436-018-0348-2 |
0.678 |
|
| 2018 |
Yang C, Li J, Wu Q, Yang X, Huang AY, Zhang J, Ye AY, Dou Y, Yan L, Zhou WZ, Kong L, Wang M, Ai C, Yang D, Wei L. AutismKB 2.0: a knowledgebase for the genetic evidence of autism spectrum disorder. Database : the Journal of Biological Databases and Curation. 2018. PMID 30339214 DOI: 10.1093/Database/Bay106 |
0.676 |
|
| 2017 |
Wang J, Gao H, Bao X, Zhang Q, Li J, Wei L, Wu X, Chen Y, Yu S. SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures. Bmc Medical Genetics. 18: 104. PMID 28923014 DOI: 10.1186/S12881-017-0460-1 |
0.607 |
|
| 2017 |
Zhang Q, Wang J, Li J, Bao X, Zhao Y, Zhang X, Wei L, Wu X. Novel FOXG1 mutations in Chinese patients with Rett syndrome or Rett-like mental retardation. Bmc Medical Genetics. 18: 96. PMID 28851325 DOI: 10.1186/S12881-017-0455-Y |
0.51 |
|
| 2017 |
Dou Y, Yang X, Li Z, Wang S, Zhang Z, Ye AY, Yan L, Yang C, Wu Q, Li J, Zhao B, Huang AY, Wei L. Post-zygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations. Human Mutation. PMID 28503910 DOI: 10.1002/Humu.23255 |
0.666 |
|
| 2017 |
Zhang Q, Zhao Y, Bao X, Luo J, Zhang X, Li J, Wei L, Wu X. Familial cases and male cases with MECP2 mutations. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. PMID 28394482 DOI: 10.1002/Ajmg.B.32534 |
0.522 |
|
| 2015 |
Xu X, Yang X, Wu Q, Liu A, Yang X, Ye AY, Huang AY, Li J, Wang M, Yu Z, Wang S, Zhang Z, Wu X, Wei L, Zhang Y. Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of "de novo" SCN1A Mutations in Children with Dravet Syndrome. Human Mutation. PMID 26096185 DOI: 10.1002/Humu.22819 |
0.711 |
|
| 2014 |
Zhao Y, Zhang X, Bao X, Zhang Q, Zhang J, Cao G, Zhang J, Li J, Wei L, Pan H, Wu X. Clinical features and gene mutational spectrum of CDKL5-related diseases in a cohort of Chinese patients. Bmc Medical Genetics. 15: 24. PMID 24564546 DOI: 10.1186/1471-2350-15-24 |
0.539 |
|
| 2012 |
Xu LM, Li JR, Huang Y, Zhao M, Tang X, Wei L. AutismKB: an evidence-based knowledgebase of autism genetics. Nucleic Acids Research. 40: D1016-22. PMID 22139918 DOI: 10.1093/Nar/Gkr1145 |
0.593 |
|
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