Huijun Wang, Ph.D. - Publications

Affiliations: 
Psychological Sciences Purdue University, West Lafayette, IN, United States 

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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
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
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
2021 Yan W, Zhang B, Wang H, Mo R, Jiang X, Qin W, Ma L, Lin Z. Somatic frameshift mutation in PIK3CA causes CLOVES syndrome by provoking PI3K/AKT/mTOR pathway. Hereditas. 158: 18. PMID 34074347 DOI: 10.1186/s41065-021-00184-y  0.104
2020 Liu B, Lu Y, Wu B, Yang L, Liu R, Wang H, Dong X, Li G, Qin Q, Zhou W. SMN gene copy number analysis by exome-seq: assisting SMA diagnosis and carrier screening. The Journal of Molecular Diagnostics : Jmd. PMID 32092542 DOI: 10.1016/j.jmoldx.2020.01.015  0.104
2021 Wang H, Xiao F, Dong X, Lu Y, Cheng G, Wang L, Lu W, Yang L, Chen L, Kang W, Li L, Pan X, Wei Q, Zhuang D, Chen D, et al. Diagnostic and clinical utility of next-generation sequencing in children born with multiple congenital anomalies in the China neonatal genomes project (CNGP). Human Mutation. PMID 33502061 DOI: 10.1002/humu.24170  0.103
2021 Zhang J, Wang H, Wang Z, Huang F, Zhang X, Du W, Su C, Ouyang Y, Li L, Bai J, Zhang B, Du S, Ding G. Trajectories of Dietary Patterns and Their Associations with Overweight/Obesity among Chinese Adults: China Health and Nutrition Survey 1991-2018. Nutrients. 13. PMID 34444995 DOI: 10.3390/nu13082835  0.102
2021 Xiao F, Lu Y, Wu B, Liu B, Li G, Zhang P, Zhou Q, Sun J, Wang H, Zhou W. High-Frequency Exon Deletion of DNA Cross-Link Repair 1C Accounting for Severe Combined Immunodeficiency May Be Missed by Whole-Exome Sequencing. Frontiers in Genetics. 12: 677748. PMID 34421990 DOI: 10.3389/fgene.2021.677748  0.102
2020 Lv X, Wang H, Wu R, Shen X, Ye G. The Active Compounds of Yixin Ningshen Tablet and Their Potential Action Mechanism in Treating Coronary Heart Disease- A Network Pharmacology and Proteomics Approach. Evidence-Based Complementary and Alternative Medicine : Ecam. 2020: 4912395. PMID 32419806 DOI: 10.1155/2020/4912395  0.102
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2023 Chen YX, Xiao TT, Chen HY, Chen X, Wang YQ, Ni Q, Wu BB, Wang HJ, Lu YL, Hu LY, Cao Y, Cheng GQ, Wang LS, Xiao FF, Yang L, et al. Risk stratification of hemodynamically significant patent ductus arteriosus by clinical and genetic factors. World Journal of Pediatrics : Wjp. PMID 37318723 DOI: 10.1007/s12519-023-00733-7  0.071
2018 Yang L, Kong Y, Dong X, Hu L, Lin Y, Chen X, Ni Q, Lu Y, Wu B, Wang H, Lu QR, Zhou W. Clinical and genetic spectrum of a large cohort of children with epilepsy in China. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 29930392 DOI: 10.1038/s41436-018-0091-8  0.071
2014 Yuan Y, Gao Y, Wang H, Ma X, Ma D, Huang G. Promoter methylation and expression of the VANGL2 gene in the myocardium of pediatric patients with tetralogy of fallot. Birth Defects Research. Part a, Clinical and Molecular Teratology. 100: 973-84. PMID 25200836 DOI: 10.1002/bdra.23291  0.071
2021 Yan Q, Korty R, Zhang Z, Brierley C, Li X, Wang H. Large shift of the Pacific Walker Circulation across the Cenozoic. National Science Review. 8: nwaa101. PMID 34691627 DOI: 10.1093/nsr/nwaa101  0.071
2020 Lyu Y, Jiang H, Jia X, Su C, Huang F, Niu R, Zhang B, Wang H, Wang Z. [Perceived stress level and its related factors in Chinese adult residents aged 18-65 in 15 provinces (autonomous regions and municipalities) in 2015]. Wei Sheng Yan Jiu = Journal of Hygiene Research. 49: 201-207. PMID 32290935 DOI: 10.19813/j.cnki.weishengyanjiu.2020.02.006  0.071
2014 Qiao D, Xu J, Le C, Huang E, Liu C, Qiu P, Lin Z, Xie WB, Wang H. Insulin-like growth factor binding protein 5 (IGFBP5) mediates methamphetamine-induced dopaminergic neuron apoptosis. Toxicology Letters. 230: 444-53. PMID 25127757 DOI: 10.1016/j.toxlet.2014.08.010  0.071
2022 Chen J, Mei MS, Xu Y, Xiong S, Zhao Y, Liu R, Shi S, Wang H, Wang S. The impact of the methyl esters of homogalacturonan on cellular uptake dependent hypoglycemic activity in IR-HepG2 cells. Carbohydrate Polymers. 293: 119741. PMID 35798434 DOI: 10.1016/j.carbpol.2022.119741  0.071
2014 Cao X, Yin J, Wang H, Zhao J, Zhang J, Dai L, Zhang J, Jiang H, Lin Z, Yang Y. Mutation in AQP5, encoding aquaporin 5, causes palmoplantar keratoderma Bothnia type. The Journal of Investigative Dermatology. 134: 284-7. PMID 23867895 DOI: 10.1038/Jid.2013.302  0.071
2007 Zhai F, Wang H, Du S, He Y, Wang Z, Ge K, Popkin BM. Lifespan nutrition and changing socio-economic conditions in China. Asia Pacific Journal of Clinical Nutrition. 374-82. PMID 17392135  0.071
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2021 Mei H, Yang L, Xiao T, Wang S, Wu B, Wang H, Lu Y, Dong X, Yang H, Zhou W. Genetic Spectrum Identified by Exome Sequencing in a Chinese Pediatric Cerebral Palsy Cohort. The Journal of Pediatrics. PMID 34788679 DOI: 10.1016/j.jpeds.2021.11.019  0.07
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2022 Wang H, Wei K. Transcranial Direct-Current Stimulation Does Not Affect Implicit Sensorimotor Adaptation: A Randomized Sham-Controlled Trial. Brain Sciences. 12. PMID 36291258 DOI: 10.3390/brainsci12101325  0.068
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2021 He Y, Wang H, Fang Y, Xia J, Lian Y, Su C. [China prime diet quality score]. Wei Sheng Yan Jiu = Journal of Hygiene Research. 50: 198-204. PMID 33985626 DOI: 10.19813/j.cnki.weishengyanjiu.2021.02.006  0.068
2022 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  0.068
2021 Qu S, Jia Y, Wang H, Ai X, Xu Z, Qin T, Pan L, Li B, Huang G, Gale RP, Xiao Z. and mutations have unique distribution in T-cell large granular lymphocyte proliferations and advanced myeloid neoplasms. Leukemia & Lymphoma. 1-9. PMID 33410350 DOI: 10.1080/10428194.2020.1869964  0.068
2017 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  0.068
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2022 Xu Y, Chen J, Shi S, Gao W, Wu J, Gong H, Zhao Y, Chen W, Wang H, Wang S. Structure characterization of pectin from the pollen of Typha angustifolia L. and the inhibition activity of lipid accumulation in oleic acid induced L02 cells. Carbohydrate Polymers. 303: 120452. PMID 36657842 DOI: 10.1016/j.carbpol.2022.120452  0.068
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2019 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  0.068
2015 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  0.068
2020 Wang L, Chen R, Weng Q, Lin S, Wang H, Li L, Fuchs BB, Tan X, Mylonakis E. Regulates the Hog1-MAPK Pathway and Is Involved in Response to Hyperosmotic Stress. Frontiers in Microbiology. 11: 213. PMID 32153525 DOI: 10.3389/fmicb.2020.00213  0.067
2023 Gao W, Zhang L, Wu J, Xu Y, Qi S, Liu W, Liu P, Shi S, Wang H, Zhang Q, Wang Y, Wang S. Extraction, characterization, and anti-nonalcoholic steatohepatitis activity of a (1,3) (1,6)-β-D-glucan from the Polyporus umbellatus (Pers.) Fries. International Journal of Biological Macromolecules. 230: 123252. PMID 36639082 DOI: 10.1016/j.ijbiomac.2023.123252  0.067
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2011 Zhao SX, Zhang HM, Dong SX, Liu JH, Zhou Z, Wang HJ, Zhu XF, Mi YC, Ru YX. [Characteristics and clinical significance of CD73 expression in subtypes of leukemia] Zhongguo Shi Yan Xue Ye Xue Za Zhi / Zhongguo Bing Li Sheng Li Xue Hui = Journal of Experimental Hematology / Chinese Association of Pathophysiology. 19: 1141-1144. PMID 22040959  0.067
2020 Zou Q, Wang H, Su C, Du W, Ouyang Y, Jia X, Wang Z, Ding G, Zhang B. Longitudinal association between physical activity and blood pressure, risk of hypertension among Chinese adults: China Health and Nutrition Survey 1991-2015. European Journal of Clinical Nutrition. PMID 32404900 DOI: 10.1038/s41430-020-0653-0  0.067
2024 Song X, Wang H, Su C, Zhang M, Zhang L, Meng J, Zhang B. Distribution of daily protein intake and appendicular skeletal muscle mass in healthy free-living Chinese older adults. European Journal of Nutrition. PMID 38563983 DOI: 10.1007/s00394-024-03364-4  0.067
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2022 Xiao H, Zhang JT, Dong XR, Lu YL, Wu BB, Wang HJ, Zhao ZY, Yang L, Zhou WH. Secondary genomic findings in the 2020 China Neonatal Genomes Project participants. World Journal of Pediatrics : Wjp. PMID 35727495 DOI: 10.1007/s12519-022-00558-w  0.067
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2022 Miao Z, Du W, Xiao C, Su C, Gou W, Shen L, Zhang J, Fu Y, Jiang Z, Wang Z, Jia X, Zheng JS, Wang H. Gut microbiota signatures of long-term and short-term plant-based dietary pattern and cardiometabolic health: a prospective cohort study. Bmc Medicine. 20: 204. PMID 35701845 DOI: 10.1186/s12916-022-02402-4  0.067
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