Year |
Citation |
Score |
2008 |
Melara RD, Wang H, Vu KP, Proctor RW. Attentional origins of the Simon effect: behavioral and electrophysiological evidence. Brain Research. 1215: 147-59. PMID 18474363 DOI: 10.1016/J.Brainres.2008.03.026 |
0.433 |
|
2005 |
Melara RD, Chen S, Wang H. Inhibiting change: effects of memory on auditory selective attention. Brain Research. Cognitive Brain Research. 25: 431-42. PMID 16157478 DOI: 10.1016/J.Cogbrainres.2005.07.002 |
0.558 |
|
Low-probability matches (unlikely to be authored by this person) |
2021 |
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, ... ... Wang H, et al. Genetic Architecture of Childhood Kidney and Urological Diseases in China. Phenomics (Cham, Switzerland). 1: 91-104. PMID 36939782 DOI: 10.1007/s43657-021-00014-1 |
0.193 |
|
2021 |
Yang X, Li Y, Fang Y, Shi H, Xiang T, Liu J, Liu J, Tang X, Fang X, Chen J, Zhai Y, Shen Q, Bi Y, Qian Y, Wu B, ... Wang H, et al. Phenotypic spectrum and genetics of PAX2-related disorder in the Chinese cohort. Bmc Medical Genomics. 14: 250. PMID 34696790 DOI: 10.1186/s12920-021-01102-x |
0.184 |
|
2020 |
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, et al. Early diagnosis of WT1 nephropathy and follow up in a Chinese multicenter cohort. European Journal of Medical Genetics. 104047. PMID 32891756 DOI: 10.1016/J.Ejmg.2020.104047 |
0.173 |
|
2020 |
Song X, Fang X, Tang X, Cao Q, Zhai Y, Chen J, Liu J, Zhang Z, Xiang T, Qian Y, Wu B, Wang H, Zhou W, Liu C, Shen Q, et al. COQ8B nephropathy: Early detection and optimal treatment. Molecular Genetics & Genomic Medicine. e1360. PMID 32543055 DOI: 10.1002/Mgg3.1360 |
0.158 |
|
2021 |
Xu L, Wei F, Feng J, Liu J, Liu J, Tang X, Fang X, Chen J, Zhai Y, Liu H, Sun L, Qian Y, Wu B, Wang H, Shen Q, et al. Characteristics and outcomes of glomerulonephritis with membranoproliferative pattern in children. Translational Pediatrics. 10: 2985-2996. PMID 34976764 DOI: 10.21037/tp-21-286 |
0.148 |
|
2018 |
Li S, Liu S, Chen W, Yuan Y, Gu R, Song Y, Li J, Cao Y, Lin Y, Xu J, Wang H, Ma D, Ma X, Sheng W, Huang G. A novel ZIC3 gene mutation identified in patients with heterotaxy and congenital heart disease. Scientific Reports. 8: 12386. PMID 30120289 DOI: 10.1038/s41598-018-30204-3 |
0.142 |
|
2023 |
Zhu J, Li W, Yu S, Lu W, Xu Q, Wang S, Qian Y, Guo Q, Xu S, Wang Y, Zhang P, Zhao X, Ni Q, Liu R, Li X, ... ... Wang H, et al. Further delineation of EBF3-related syndromic neurodevelopmental disorder in twelve Chinese patients. Frontiers in Pediatrics. 11: 1091532. PMID 36937983 DOI: 10.3389/fped.2023.1091532 |
0.14 |
|
2023 |
Pan F, Wang Z, Wang H, Zhang J, Su C, Jia X, Du W, Jiang H, Li W, Wang L, Hao L, Zhang B, Ding G. Association between Ultra-Processed Food Consumption and Metabolic Syndrome among Adults in China-Results from the China Health and Nutrition Survey. Nutrients. 15. PMID 36771458 DOI: 10.3390/nu15030752 |
0.133 |
|
2003 |
Wang Y, Tian S, Wang H, Cui L, Zhang Y, Zhang X. Event-related potentials evoked by multi-feature conflict under different attentive conditions. Experimental Brain Research. 148: 451-7. PMID 12582828 DOI: 10.1007/s00221-002-1319-y |
0.132 |
|
2019 |
Huang L, Wang H, Wang Z, Zhang J, Zhang B, Ding G. Regional Disparities in the Association between Cereal Consumption and Metabolic Syndrome: Results from the China Health and Nutrition Survey. Nutrients. 11. PMID 30939825 DOI: 10.3390/nu11040764 |
0.13 |
|
2016 |
Hao S, Jin L, Wang H, Li C, Zheng F, Ma D, Zhang T. Mutational Analysis of TCOF1, GSC, and HOXA2 in Patients With Treacher Collins Syndrome. The Journal of Craniofacial Surgery. PMID 27526242 DOI: 10.1097/SCS.0000000000002934 |
0.127 |
|
2021 |
Zhang Y, Qin W, Wang H, Lin Z, Tang Z, Xu Z. Novel pathogenic variants in the RECQL4 gene causing Rothmund-Thomson syndrome in three Chinese patients. The Journal of Dermatology. PMID 34155702 DOI: 10.1111/1346-8138.16015 |
0.126 |
|
2020 |
Liu B, Wu B, Lu Y, Zhang P, Xiao F, Li G, Wang H, Dong X, Liu R, Li Y, Xie X, Zhou W, Wang J, Lu Y. A novel recurrent 3.6-kb deletion in the PYGL gene contributes to glycogen storage disease type VI. The Journal of Molecular Diagnostics : Jmd. PMID 32961316 DOI: 10.1016/j.jmoldx.2020.08.006 |
0.125 |
|
2021 |
Yu S, Chen WX, Zhang YF, Ni Y, Lu P, Wang B, Wang Y, Wu B, Ni Q, Wang H, Xu ZM. Apparent homozygosity for a novel splicing variant in EPS8 causes congenital profound hearing loss. European Journal of Medical Genetics. 104362. PMID 34637946 DOI: 10.1016/j.ejmg.2021.104362 |
0.125 |
|
2022 |
Jiao Y, Li W, Wang L, Jiang H, Wang S, Jia X, Wang Z, Wang H, Zhang B, Ding G. Relationship between Dietary Magnesium Intake and Metabolic Syndrome. Nutrients. 14. PMID 35631154 DOI: 10.3390/nu14102013 |
0.125 |
|
2020 |
Huang L, Wang Z, Wang H, Zhao L, Jiang H, Zhang B, Ding G. Nutrition transition and related health challenges over decades in China. European Journal of Clinical Nutrition. PMID 32620907 DOI: 10.1038/s41430-020-0674-8 |
0.124 |
|
2023 |
Zhang J, Du W, Huang F, Li L, Bai J, Wei Y, Wang Z, Zhang B, Wang H. Longitudinal study of dietary patterns and hypertension in adults: China Health and Nutrition Survey 1991-2018. Hypertension Research : Official Journal of the Japanese Society of Hypertension. PMID 37337099 DOI: 10.1038/s41440-023-01322-x |
0.122 |
|
2022 |
Peng X, Dong X, Wang Y, Wu B, Wang H, Lu W, Xiao F, Yang L, Li G, Zhou W, Liu B, Lu Y. Overcoming the pitfalls of NGS-based molecular diagnosis of Shwachman-Diamond syndrome. The Journal of Molecular Diagnostics : Jmd. PMID 36162759 DOI: 10.1016/j.jmoldx.2022.09.002 |
0.122 |
|
2002 |
Wang Y, Tian S, Wang H, Cui L, Zhang Y. Event-related potentials in a No-go task involving response-tendency conflict. Clinical Eeg (Electroencephalography). 33: 82-5. PMID 12025736 DOI: 10.1177/155005940203300207 |
0.12 |
|
2020 |
Huang Q, Wang L, Jiang H, Wang H, Zhang B, Zhang J, Jia X, Wang Z. Intra-Individual Double Burden of Malnutrition among Adults in China: Evidence from the China Health and Nutrition Survey 2015. Nutrients. 12. PMID 32937736 DOI: 10.3390/nu12092811 |
0.12 |
|
2022 |
Shen Q, Feng Y, Gong X, Jia Y, Gao Q, Jiao X, Qi S, Liu X, Wei H, Huang B, Zhao N, Song X, Ma Y, Liang S, Zhang D, ... ... Wang H, et al. A Phenogenetic Axis that Modulates Clinical Manifestation and Predicts Treatment Outcome in Primary Myeloid Neoplasms. Cancer Research Communications. 2: 258-276. PMID 36873623 DOI: 10.1158/2767-9764.CRC-21-0194 |
0.12 |
|
2015 |
Su C, Jia X, Wang Z, Wang H, Zhang B. Trends in dietary cholesterol intake among Chinese adults: a longitudinal study from the China Health and Nutrition Survey, 1991-2011. Bmj Open. 5: e007532. PMID 26038359 DOI: 10.1136/bmjopen-2014-007532 |
0.12 |
|
2022 |
Pan F, Wang Z, Wang H, Su C, Zhang J, Du W, Jia X, Wang L, Jiang H, Li W, Zhang B, Ding G. Association between Free Sugars Intake and Risk of Metabolic Syndrome in Chinese Adults: Results from the China Health and Nutrition Survey, 2000-2018. Nutrients. 14. PMID 36558544 DOI: 10.3390/nu14245385 |
0.119 |
|
2009 |
Zhai F, Wang H, Du S, He Y, Wang Z, Ge K, Popkin BM. Prospective study on nutrition transition in China. Nutrition Reviews. S56-61. PMID 19453679 DOI: 10.1111/J.1753-4887.2009.00160.X |
0.119 |
|
2022 |
Zhao X, Wu B, Chen H, Zhang P, Qian Y, Peng X, Dong X, Wang Y, Li G, Dong C, Wang H. Case report: A novel truncating variant of associated with rare feature of craniosynostosis and global developmental delay. Frontiers in Pediatrics. 10: 982361. PMID 36275064 DOI: 10.3389/fped.2022.982361 |
0.118 |
|
2012 |
Gao Y, Ma XJ, Huang GY, Zhang J, Wang HJ, Ma D, Wu Y. DNA sequencing of TGFβ2 in sporadic patients with tetralogy of Fallot. Experimental and Therapeutic Medicine. 3: 878-880. PMID 22969986 DOI: 10.3892/etm.2012.492 |
0.118 |
|
2023 |
Qian Y, Jiang Y, Wang J, Li G, Wu B, Zhou Y, Xu X, Wang H. Novel Variants of PPP2R1A in Catalytic Subunit Binding Domain and Genotype-Phenotype Analysis in Neurodevelopmentally Delayed Patients. Genes. 14. PMID 37761890 DOI: 10.3390/genes14091750 |
0.118 |
|
2017 |
Ge MM, Hu L, Li Z, Cheng G, Yan K, Kong Y, Wang H, Yang L, Zhou W. Novel compound heterozygous mutations in the PEX1 gene in two Chinese newborns with Zellweger syndrome based on whole exome sequencing. Clinica Chimica Acta; International Journal of Clinical Chemistry. PMID 28432012 DOI: 10.1016/j.cca.2017.04.016 |
0.117 |
|
2019 |
Yu S, Wu B, Qian Y, Zhang P, Lu Y, Dong X, Wang Q, Zhao X, Liu R, Zhou W, Wang H. Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein-Taybi Syndrome kids with high frequency of polydactyly. Molecular Genetics & Genomic Medicine. e1009. PMID 31637876 DOI: 10.1002/mgg3.1009 |
0.117 |
|
2020 |
Zhong W, Hu L, Cao X, Zhao J, Zhang X, Lee M, Wang H, Zhang J, Chen Q, Feng C, Duo L, Wang X, Tang L, Lin Z, Yang Y. Genotype-Phenotype Correlation of TRPV3-Related Olmsted Syndrome. The Journal of Investigative Dermatology. PMID 32795529 DOI: 10.1016/J.Jid.2020.06.035 |
0.117 |
|
2016 |
Zhou EY, Wang H, Lin Z, Xu G, Ma Z, Zhao J, Feng C, Duo L, Yin J, Yang Y. Clinical and molecular epidemiological study of xeroderma pigmentosum in China: A case series of 19 patients. The Journal of Dermatology. PMID 27607234 DOI: 10.1111/1346-8138.13576 |
0.117 |
|
2020 |
Sun WH, Zhuang DY, Wang Y, Xiao FF, Wu MY, Dong XR, Zhang P, Wang HJ, Zhou WH, Wu BB. [Clinical features and SLC6A8 gene mutations of cerebral creatine deficiency syndrome I: an analysis of two families]. Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics. 22: 482-487. PMID 32434645 DOI: 10.7499/j.issn.1008-8830.2002012 |
0.116 |
|
2017 |
Su C, Zhao J, Wu Y, Wang H, Wang Z, Wang Y, Zhang B. Temporal Trends in Dietary Macronutrient Intakes among Adults in Rural China from 1991 to 2011: Findings from the CHNS. Nutrients. 9. PMID 28273878 DOI: 10.3390/nu9030227 |
0.115 |
|
2022 |
Wang J, Yan Y, Xiong W, Song G, Wang Y, Zhao J, Jia Y, Li C, Yu Z, Yu Y, Chen J, Jiao Y, Wang T, Lyu R, Li Q, ... ... Wang H, et al. The landscape of immunoglobulin heavy chain gene repertoire and its clinical relevance in LPL/WM. Blood Advances. PMID 35537114 DOI: 10.1182/bloodadvances.2022007279 |
0.115 |
|
2021 |
Yi S, Yan Y, Jin M, Bhattacharya S, Wang Y, Wu Y, Yang L, Giné E, Clot G, Chen L, Yu Y, Zou D, Wang J, Phan AT, Cui R, ... ... Wang H, et al. Genomic and transcriptomic profiling reveals distinct molecular subsets associated with outcomes in mantle cell lymphoma. The Journal of Clinical Investigation. PMID 34882582 DOI: 10.1172/JCI153283 |
0.115 |
|
2023 |
Huang Z, Lu W, Zhang P, Lu Y, Chen L, Kang W, Yang L, Li G, Zhu J, Wu B, Zhou W, Wang H. Early onset critically ill infants with Schaaf-Yang syndrome: a retrospective study from the China neonatal genomes project and literature review. Annals of Translational Medicine. 11: 312. PMID 37404980 DOI: 10.21037/atm-22-4396 |
0.114 |
|
2015 |
Zhang J, Wang H, Wang Y, Xue H, Wang Z, Du W, Su C, Zhang J, Jiang H, Zhai F, Zhang B. Dietary patterns and their associations with childhood obesity in China. The British Journal of Nutrition. 113: 1978-84. PMID 25944159 DOI: 10.1017/S0007114515001154 |
0.114 |
|
2015 |
Li L, Dong J, Wang X, Guo H, Wang H, Zhao J, Qiu Y, Abuduxikuer K, Wang J. JAG1 Mutation Spectrum and Origin in Chinese Children with Clinical Features of Alagille Syndrome. Plos One. 10: e0130355. PMID 26076142 DOI: 10.1371/journal.pone.0130355 |
0.114 |
|
2023 |
Guo L, Huang F, Liu M, Zhang Y, Zhang J, Zhang B, Wang H. Generational Differences in Food Consumption among Chinese Adults of Different Ages. Nutrients. 15. PMID 37892526 DOI: 10.3390/nu15204451 |
0.113 |
|
2014 |
Yang L, Shen C, Mei M, Zhan G, Zhao Y, Wang H, Huang G, Qiu Z, Lu W, Zhou W. De novo GLI3 mutation in esophageal atresia: reproducing the phenotypic spectrum of Gli3 defects in murine models. Biochimica Et Biophysica Acta. 1842: 1755-61. PMID 24819706 DOI: 10.1016/j.bbadis.2014.05.001 |
0.113 |
|
2017 |
Chen X, Wang H, Wu B, Dong X, Liu B, Chen H, Lu Y, Zhou W, Yang L. One novel 2.43Kb deletion and one single nucleotide mutation of the INSR gene in a Chinese neonate with Rabson-Mendenhall syndrome. Journal of Clinical Research in Pediatric Endocrinology. PMID 29082893 DOI: 10.4274/jcrpe.5080 |
0.113 |
|
2021 |
Qian Y, Zhou Y, Wu B, Chen H, Xu S, Wang Y, Zhang P, Li G, Xu Q, Zhou W, Xu X, Wang H. Novel Variants of the SMARCA4 Gene Associated with Autistic Features Rather Than Typical Coffin-Siris Syndrome in Eight Chinese Pediatric Patients. Journal of Autism and Developmental Disorders. PMID 34813034 DOI: 10.1007/s10803-021-05365-2 |
0.112 |
|
2021 |
Zhang X, Zhang J, Du W, Su C, Ouyang Y, Huang F, Jia X, Li L, Bai J, Zhang B, Wang Z, Du S, Wang H. Multi-Trajectories of Macronutrient Intake and Their Associations with Obesity among Chinese Adults from 1991 to 2018: A Prospective Study. Nutrients. 14. PMID 35010888 DOI: 10.3390/nu14010013 |
0.112 |
|
2020 |
Yu S, Chen WX, Lu W, Chen C, Ni Y, Duan B, Wang B, Wang H, Xu ZM. Novel heterozygous GATA3 and SLC34A3 variants in a 6-year-old boy with Barakat syndrome and hypercalciuria. Molecular Genetics & Genomic Medicine. e1222. PMID 32155322 DOI: 10.1002/Mgg3.1222 |
0.112 |
|
2015 |
Fan ZC, Ni JW, Yang L, Hu LY, Ma SM, Mei M, Sun BJ, Wang HJ, Zhou WH. Uncovering the molecular pathogenesis of congenital hyperinsulinism by panel gene sequencing in 32 Chinese patients. Molecular Genetics & Genomic Medicine. 3: 526-36. PMID 26740944 DOI: 10.1002/mgg3.162 |
0.112 |
|
2015 |
Liu F, Yang F, Wen D, Xia W, Hao L, Hu J, Zong J, Shen X, Ma J, Jiang N, Sun S, Zhang J, Wang H, Wang X, Ma Z, et al. Grhl1 deficiency affects inner ear development in zebrafish. The International Journal of Developmental Biology. PMID 25896282 DOI: 10.1387/ijdb.140230FL |
0.111 |
|
2017 |
Hao S, Jin L, Li C, Wang H, Zheng F, Ma D, Zhang T. Mutational analysis of GSC, HOXA2 and PRKRA in 106 Chinese patients with microtia. International Journal of Pediatric Otorhinolaryngology. 93: 78-82. PMID 28109504 DOI: 10.1016/j.ijporl.2016.12.026 |
0.111 |
|
2021 |
Hu X, Jiang H, Wang H, Zhang B, Zhang J, Jia X, Wang L, Wang Z, Ding G. Intraindividual Double Burden of Malnutrition in Chinese Children and Adolescents Aged 6-17 Years: Evidence from the China Health and Nutrition Survey 2015. Nutrients. 13. PMID 34578974 DOI: 10.3390/nu13093097 |
0.111 |
|
2012 |
Lin Z, Chen Q, Shi L, Lee M, Giehl KA, Tang Z, Wang H, Zhang J, Yin J, Wu L, Xiao R, Liu X, Dai L, Zhu X, Li R, et al. Loss-of-function mutations in HOXC13 cause pure hair and nail ectodermal dysplasia. American Journal of Human Genetics. 91: 906-11. PMID 23063621 DOI: 10.1016/j.ajhg.2012.08.029 |
0.111 |
|
2022 |
Zhang S, Wang L, Jia X, Zhang J, Jiang H, Li W, Huang F, Wang H, Zhang B, Ding G, Wang Z. A Comparison between Dietary Consumption Status and Healthy Dietary Pattern among Adults Aged 55 and Older in China. Nutrients. 14. PMID 35807958 DOI: 10.3390/nu14132778 |
0.11 |
|
2022 |
Peng X, Lu Y, Wang H, Wu B, Gan M, Xu S, Zhuang D, Wang J, Sun J, Wang X, Zhou W. Further Delineation of the Spectrum of XMEN Disease in Six Chinese Pediatric Patients. Frontiers in Genetics. 13: 768000. PMID 35145548 DOI: 10.3389/fgene.2022.768000 |
0.109 |
|
2018 |
Wang H, Xu Z, Lee BH, Vu S, Hu L, Lee M, Bu D, Cao X, Hwang S, Yang Y, Zheng J, Lin Z. Gain-of-function mutations in TRPM4 activation gate cause progressive symmetric erythrokeratoderma. The Journal of Investigative Dermatology. PMID 30528822 DOI: 10.1016/J.Jid.2018.10.044 |
0.109 |
|
2024 |
Yin T, Qian Y, Zhang X, Liao Y, Wu B, Wang S, Wang H. Derivation of an induced pluripotent stem cell line (FDCHi014-A) from PBMCs of a seven-year-old patient with a truncating NOVA2 variant (c.625del). Stem Cell Research. 76: 103369. PMID 38430735 DOI: 10.1016/j.scr.2024.103369 |
0.109 |
|
2004 |
Wang Y, Cui L, Wang H, Tian S, Zhang X. The sequential processing of visual feature conjunction mismatches in the human brain. Psychophysiology. 41: 21-9. PMID 14692997 DOI: 10.1111/j.1469-8986.2003.00134.x |
0.108 |
|
2016 |
Liu LY, Liu F, Du SC, Jiang SY, Wang HJ, Zhang J, Wang W, Ma D. A Novel Functional Missense Mutation p.T219A in Type 1 Gaucher's Disease. Chinese Medical Journal. 129: 1072-1077. PMID 27098793 DOI: 10.4103/0366-6999.180523 |
0.108 |
|
2012 |
Lin Z, Chen Q, Lee M, Cao X, Zhang J, Ma D, Chen L, Hu X, Wang H, Wang X, Zhang P, Liu X, Guan L, Tang Y, Yang H, et al. Exome sequencing reveals mutations in TRPV3 as a cause of Olmsted syndrome. American Journal of Human Genetics. 90: 558-64. PMID 22405088 DOI: 10.1016/J.Ajhg.2012.02.006 |
0.108 |
|
2021 |
Su Y, Zhang H, Wang H, Wu B, Yang J, Zhou W, Li L. Case Report: Progressive Cholestasis: Severe Phenotype of MEGDEL Syndrome With SATB2-Associated Syndrome. Frontiers in Pediatrics. 9: 713458. PMID 34660482 DOI: 10.3389/fped.2021.713458 |
0.108 |
|
2021 |
Ma H, Tang Z, Xiao F, Li L, Li Y, Tang W, Chen L, Kang W, Lu Y, Dong X, Cheng G, Wang L, Lu W, Yang L, Ni Q, ... ... Wang H, et al. Neonatal Metabolic Acidosis in the Neonatal Intensive Care Unit: What Are the Genetic Causes? Frontiers in Pediatrics. 9: 727301. PMID 34733806 DOI: 10.3389/fped.2021.727301 |
0.107 |
|
2021 |
Yu S, Chen WX, Zhang YF, Chen C, Ni Y, Duan B, Wang H, Xu ZM. Recessive LOXHD1 variants cause a prelingual down-sloping hearing loss: genotype-phenotype correlation and three additional children with novel variants. International Journal of Pediatric Otorhinolaryngology. 145: 110715. PMID 33892339 DOI: 10.1016/j.ijporl.2021.110715 |
0.107 |
|
2015 |
Wang H, Cao X, Lin Z, Lee M, Jia X, Ren Y, Dai L, Guan L, Zhang J, Lin X, Zhang J, Chen Q, Feng C, Zhou EY, Yin J, et al. Exome sequencing reveals mutation in GJA1 as a cause of keratoderma-hypotrichosis-leukonychia totalis syndrome. Human Molecular Genetics. 24: 243-50. PMID 25168385 DOI: 10.1093/Hmg/Ddu442 |
0.107 |
|
2022 |
Wu J, Zhang W, Zhang P, Qin T, Xu Z, Sun Q, Jia Y, Qu S, Wang H, Pan L, Liu J, Zhang Y, Yan X, Gale RP, Xiao Z. Distinguishing MDS with MF-2/3 from TN-PMF based on clinical and genetic covariates. Hematological Oncology. PMID 36265165 DOI: 10.1002/hon.3091 |
0.107 |
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2020 |
Zhang P, Zhao J, Peng XM, Qian YY, Zhao XM, Zhou WH, Wang JS, Wu BB, Wang HJ. Cholestasis as a dominating symptom of patients with CYP27A1 mutations: An analysis of 17 Chinese infants. Journal of Clinical Lipidology. PMID 33414089 DOI: 10.1016/j.jacl.2020.12.004 |
0.107 |
|
2023 |
Zhang P, Zhang J, Rosewarne E, Li Y, Dong L, He FJ, Brown M, Pettigrew S, Yamamoto R, Nishida C, Liu A, Yang X, Zhang B, Ding G, Wang H. Setting sodium targets for pre-packaged foods in China - an exploratory study. Frontiers in Nutrition. 10: 1231979. PMID 38024347 DOI: 10.3389/fnut.2023.1231979 |
0.107 |
|
2021 |
Zhang X, Ouyang Y, Huang F, Zhang J, Su C, Jia X, Du W, Li L, Bai J, Zhang B, Wang Z, Du S, Wang H. Modifiable factors of twenty-year blood pressure trajectories among normotensives and their associations with hypertension: A prospective study. The British Journal of Nutrition. 1-25. PMID 34470677 DOI: 10.1017/S0007114521003378 |
0.107 |
|
2014 |
Wang ZH, Zhai FY, Wang HJ, Zhang JG, Du WW, Su C, Zhang J, Jiang HR, Zhang B. Secular trends in meat and seafood consumption patterns among Chinese adults, 1991-2011. European Journal of Clinical Nutrition. 69: 227-33. PMID 25351649 DOI: 10.1038/ejcn.2014.225 |
0.106 |
|
2021 |
Guan F, Du W, Zhang J, Su C, Zhang B, Deng K, Du S, Wang H. Amino Acids and Lipids Associated with Long-Term and Short-Term Red Meat Consumption in the Chinese Population: An Untargeted Metabolomics Study. Nutrients. 13. PMID 34960119 DOI: 10.3390/nu13124567 |
0.106 |
|
2015 |
Zhang J, Duo L, Lin Z, Wang H, Yin J, Cao X, Zhao J, Dai L, Liu X, Zhang J, Yang Y, Tang Z. Exome sequencing reveals novel BCS1L mutations in siblings with hearing loss and hypotrichosis. Gene. 566: 84-8. PMID 25895478 DOI: 10.1016/J.Gene.2015.04.039 |
0.106 |
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2013 |
Yao G, Chen D, Wang H, Li S, Zhang J, Feng Z, Guo L, Yang Z, Yang S, Sun C, Zhang X, Ma D. Novel mutations of SLC26A4 in Chinese patients with nonsyndromic hearing loss. Acta Oto-Laryngologica. 133: 833-41. PMID 23638949 DOI: 10.3109/00016489.2013.777160 |
0.106 |
|
2022 |
Yang F, Jiang X, Zhu Y, Lee M, Xu Z, Zhang J, Li Q, Lin MY, Wang H, Lin Z. Bi-allelic Variants in LSS Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2. The Journal of Investigative Dermatology. PMID 35413293 DOI: 10.1016/j.jid.2022.03.023 |
0.106 |
|
2022 |
Zhang Y, Wu J, Xu Z, Qin T, Qu S, Pan L, Wang H, Sun Q, Li C, Jia Y, Cai W, Yan X, Gong J, Gao Q, Li B, et al. Impact of the International Consensus Classification of myelodysplastic syndromes. British Journal of Haematology. PMID 36575970 DOI: 10.1111/bjh.18628 |
0.106 |
|
2020 |
Wang Z, Huang Q, Wang L, Jiang H, Wang Y, Wang H, Zhang J, Zhai F, Zhang B. Moderate Intake of Lean Red Meat was Associated with Lower Risk of Elevated Blood Pressure in Chinese Women: Results from the China Health and Nutrition Survey, 1991-2015. Nutrients. 12. PMID 32403294 DOI: 10.3390/nu12051369 |
0.106 |
|
2015 |
Wang H, Qian Y, Wu B, Zhang P, Zhou W. KRAS G12D mosaic mutation in a Chinese linear nevus sebaceous syndrome infant. Bmc Medical Genetics. 16: 101. PMID 26521233 DOI: 10.1186/s12881-015-0247-1 |
0.105 |
|
2015 |
Ouyang Y, Wang H, Su C, Wang Z, Song Y, Xiao Y, Du W, Zhang B. Use of quantile regression to investigate changes in the body mass index distribution of Chinese adults aged 18-60 years: a longitudinal study. Bmc Public Health. 15: 278. PMID 25885045 DOI: 10.1186/s12889-015-1606-8 |
0.105 |
|
2020 |
Wang Y, Wang H, Howard AG, Tsilimigras MCB, Avery CL, Meyer KA, Sha W, Sun S, Zhang J, Su C, Wang Z, Fodor AA, Zhang B, Gordon-Larsen P. Gut Microbiota and Host Plasma Metabolites in Association with Blood Pressure in Chinese Adults. Hypertension (Dallas, Tex. : 1979). HYPERTENSIONAHA12016. PMID 33342240 DOI: 10.1161/HYPERTENSIONAHA.120.16154 |
0.104 |
|
2014 |
Du S, Neiman A, Batis C, Wang H, Zhang B, Zhang J, Popkin BM. Understanding the patterns and trends of sodium intake, potassium intake, and sodium to potassium ratio and their effect on hypertension in China. The American Journal of Clinical Nutrition. 99: 334-43. PMID 24257724 DOI: 10.3945/Ajcn.113.059121 |
0.104 |
|
2021 |
Zhao J, Zuo L, Sun J, Su C, Wang H. Trends and Urban-Rural Disparities of Energy Intake and Macronutrient Composition among Chinese Children: Findings from the China Health and Nutrition Survey (1991 to 2015). Nutrients. 13. PMID 34199924 DOI: 10.3390/nu13061933 |
0.104 |
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Xiong J, Wang H, Zhu Y, Zhou Y, Pang Y, Zhang L. The Right Internal Jugular at the Cricoid Cartilage Level May Represent the Optimal Central Vein Puncture Site in Pediatric Patients. Frontiers in Pediatrics. 10: 833845. PMID 35273930 DOI: 10.3389/fped.2022.833845 |
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Du P, Wang HJ, Zhang B, Qi SF, Mi YJ, Liu DW, Tian QB. Prevalence of abdominal obesity among Chinese adults in 2011. Journal of Epidemiology. PMID 28427831 DOI: 10.1016/j.je.2017.03.001 |
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Guo P, Wang S, Liang W, Wang W, Wang H, Zhao M, Liu X. Salvianolic acid B reverses multidrug resistance in HCT‑8/VCR human colorectal cancer cells by increasing ROS levels. Molecular Medicine Reports. PMID 28000873 DOI: 10.3892/mmr.2016.6049 |
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Wang Y, Wang Z, Su C, Jia X, Ouyang Y, Zhang B, Wang H. [Longitudinal multilevel analysis of correlative factors of abdominal obesity among Chinese reproductive women]. Wei Sheng Yan Jiu = Journal of Hygiene Research. 49: 19-27. PMID 32290909 DOI: 10.19813/j.cnki.weishengyanjiu.2020.01.004 |
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Yi S, Li Z, Zou D, An G, Cui R, Zhong S, Li H, Xiong W, Li C, Chen W, Liu W, Lv R, Yu Z, Wang H, Xu Y, et al. Intratumoral genetic heterogeneity and number of cytogenetic aberrations provide additional prognostic significance in chronic lymphocytic leukemia. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 27467457 DOI: 10.1038/gim.2016.81 |
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Sun J, Wang H, Yuan W, Chen H. Spatial-temporal features of intense snowfall events in China and their possible change Journal of Geophysical Research. 115. DOI: 10.1029/2009JD013541 |
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Wang Y, Jia X, Su C, Du W, Wang Z, Zhang B, Wang H. [Dietary cholesterol intake status and the correlation analysis with serum cholesterol level of the residents aged 60 and above in 15 provinces (autonomous regions and municipality) of China in 2015]. Wei Sheng Yan Jiu = Journal of Hygiene Research. 48: 33-40. PMID 31032765 |
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Mi YJ, Zhang B, Wang HJ, Yan J, Han W, Zhao J, Liu DW, Tian QB. Prevalence and Secular Trends in Obesity Among Chinese Adults, 1991-2011. American Journal of Preventive Medicine. PMID 26275960 DOI: 10.1016/j.amepre.2015.05.005 |
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