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[wareness and knowledge of oral cancer among 1 483 residents in Beijing].
Zhou XH, Huang Y, Yuan C, Zheng SG, Zhang J, Zhang JG. Zhou XH, et al. Among authors: zhang jg, zhang j. Beijing Da Xue Xue Bao Yi Xue Ban. 2020 Apr 18;52(2):323-331. doi: 10.19723/j.issn.1671-167X.2020.02.021. Beijing Da Xue Xue Bao Yi Xue Ban. 2020. PMID: 32306018 Free PMC article. Chinese.
First observation of the M1 transition ψ(3686)→γη(c)(2S).
Ablikim M, Achasov MN, Ambrose DJ, An FF, An Q, An ZH, Bai JZ, Ban Y, Becker J, Berger N, Bertani M, Bian JM, Boger E, Bondarenko O, Boyko I, Briere RA, Bytev V, Cai X, Calcaterra A, Cao GF, Chang JF, Chelkov G, Chen G, Chen HS, Chen JC, Chen ML, Chen SJ, Chen Y, Chen YB, Cheng HP, Chu YP, Cronin-Hennessy D, Dai HL, Dai JP, Dedovich D, Deng ZY, Denig A, Denysenko I, Destefanis M, Ding WM, Ding Y, Dong LY, Dong MY, Du SX, Fang J, Fang SS, Fava L, Feldbauer F, Feng CQ, Ferroli RB, Fu CD, Fu JL, Gao Y, Geng C, Goetzen K, Gong WX, Gradl W, Greco M, Gu MH, Gu YT, Guan YH, Guo AQ, Guo LB, Guo YP, Han YL, Hao XQ, Harris FA, He KL, He M, He ZY, Held T, Heng YK, Hou ZL, Hu HM, Hu JF, Hu T, Huang B, Huang GM, Huang JS, Huang XT, Huang YP, Hussain T, Ji CS, Ji Q, Ji XB, Ji XL, Jia LK, Jiang LL, Jiang XS, Jiao JB, Jiao Z, Jin DP, Jin S, Jing FF, Kalantar-Nayestanaki N, Kavatsyuk M, Kuehn W, Lai W, Lange JS, Leung JK, Li CH, Li C, Li C, Li DM, Li F, Li G, Li HB, Li JC, Li K, Li L, Li NB, Li QJ, Li SL, Li WD, Li WG, Li XL, Li XN, Li XQ, Li XR, Li ZB, Liang H, Liang YF, Liang YT, Liao GR, Liao XT, Liu BJ, Liu BJ, Liu CL, Liu CX, Liu CY, Liu FH, Liu F, Liu F, Liu H, Liu HB, Liu HH, Liu HM, Liu HW… See abstract for full author list ➔ Ablikim M, et al. Among authors: zhang jq, zhang dh, zhang l, zhang tr, zhang zy, zhang jg, zhang j, zhang cc, zhang hh, zhang xy, zhang bx, zhang zp, zhang by, zhang sh, zhang ys, zhang jy, zhang yh, zhang jw, zhang xj, zhang jz, zhang hy, zhang y. Phys Rev Lett. 2012 Jul 27;109(4):042003. doi: 10.1103/PhysRevLett.109.042003. Epub 2012 Jul 24. Phys Rev Lett. 2012. PMID: 23006078 Free article.
Evidence for the direct two-photon transition from ψ(3686) to J/ψ.
Ablikim M, Achasov MN, Ambrose DJ, An FF, An Q, An ZH, Bai JZ, Ferroli RB, Ban Y, Becker J, Berger N, Bertani MB, Bian JM, Boger E, Bondarenko O, Boyko I, Briere RA, Bytev V, Cai X, Calcaterra AC, Cao GF, Chang JF, Chelkov G, Chen G, Chen HS, Chen JC, Chen ML, Chen SJ, Chen Y, Chen YB, Cheng HP, Chu YP, Cronin-Hennessy D, Dai HL, Dai JP, Dedovich D, Deng ZY, Denig A, Denysenko I, Destefanis M, Ding WM, Ding Y, Dong LY, Dong MY, Du SX, Fang J, Fang SS, Fava L, Feldbauer F, Feng CQ, Fu CD, Fu JL, Gao Y, Geng C, Goetzen K, Gong WX, Gradl W, Greco M, Gu MH, Gu YT, Guan YH, Guo AQ, Guo LB, Guo YP, Han YL, Hao XQ, Harris FA, He KL, He M, He ZY, Held T, Heng YK, Hou ZL, Hu HM, Hu JF, Hu T, Huang B, Huang GM, Huang JS, Huang XT, Huang YP, Hussain T, Ji CS, Ji Q, Ji XB, Ji XL, Jia LK, Jiang LL, Jiang XS, Jiao JB, Jiao Z, Jin DP, Jin S, Jing FF, Kalantar-Nayestanaki N, Kavatsyuk M, Kuehn W, Lai W, Lange JS, Leung JK, Li CH, Li C, Li C, Li DM, Li F, Li G, Li HB, Li JC, Li K, Li L, Li NB, Li QJ, Li SL, Li WD, Li WG, Li XL, Li XN, Li XQ, Li XR, Li ZB, Liang H, Liang YF, Liang YT, Liao GR, Liao XT, Liu BJ, Liu BJ, Liu CL, Liu CX, Liu CY, Liu FH, Liu F, Liu F, Liu H, Liu HB, Liu HH, Liu HM, Liu … See abstract for full author list ➔ Ablikim M, et al. Among authors: zhang jq, zhang dh, zhang l, zhang tr, zhang zy, zhang jg, zhang j, zhang cc, zhang hh, zhang xy, zhang bx, zhang zp, zhang by, zhang sh, zhang ys, zhang jy, zhang yh, zhang jw, zhang xj, zhang jz, zhang hy, zhang y. Phys Rev Lett. 2012 Oct 26;109(17):172002. doi: 10.1103/PhysRevLett.109.172002. Epub 2012 Oct 24. Phys Rev Lett. 2012. PMID: 23215179
Observation of two new N* resonances in the decay ψ(3686)→ppπ0.
Ablikim M, Achasov MN, Ambrose DJ, An FF, An Q, An ZH, Bai JZ, Ban Y, Becker J, Berger N, Bertani M, Bian JM, Boger E, Bondarenko O, Boyko I, Briere RA, Bytev V, Cai X, Calcaterra A, Cao GF, Chang JF, Chelkov G, Chen G, Chen HS, Chen JC, Chen ML, Chen SJ, Chen Y, Chen YB, Cheng HP, Chu YP, Cronin-Hennessy D, Dai HL, Dai JP, Dedovich D, Deng ZY, Denig A, Denysenko I, Destefanis M, Ding WM, Ding Y, Dong LY, Dong MY, Du SX, Fang J, Fang SS, Fava L, Feldbauer F, Feng CQ, Ferroli RB, Fu CD, Fu JL, Gao Y, Geng C, Goetzen K, Gong WX, Gradl W, Greco M, Gu MH, Gu YT, Guan YH, Guo AQ, Guo LB, Guo YP, Han YL, Hao XQ, Harris FA, He KL, He M, He ZY, Held T, Heng YK, Hou ZL, Hu HM, Hu JF, Hu T, Huang B, Huang GM, Huang JS, Huang XT, Huang YP, Hussain T, Ji CS, Ji Q, Ji XB, Ji XL, Jia LK, Jiang LL, Jiang XS, Jiao JB, Jiao Z, Jin DP, Jin S, Jing FF, Kalantar-Nayestanaki N, Kavatsyuk M, Kühn W, Lai W, Lange JS, Leung JK, Li CH, Li C, Li C, Li DM, Li F, Li G, Li HB, Li JC, Li K, Li L, Li NB, Li QJ, Li SL, Li WD, Li WG, Li XL, Li XN, Li XQ, Li XR, Li ZB, Liang H, Liang YF, Liang YT, Liao GR, Liao XT, Liu BJ, Liu BJ, Liu CL, Liu CX, Liu CY, Liu FH, Liu F, Liu F, Liu H, Liu HB, Liu HH, Liu HM, Liu HW,… See abstract for full author list ➔ Ablikim M, et al. Among authors: zhang jq, zhang dh, zhang l, zhang tr, zhang zy, zhang jg, zhang j, zhang cc, zhang hh, zhang xy, zhang bx, zhang zp, zhang by, zhang sh, zhang ys, zhang jy, zhang yh, zhang jw, zhang xj, zhang jz, zhang hy, zhang y. Phys Rev Lett. 2013 Jan 11;110(2):022001. doi: 10.1103/PhysRevLett.110.022001. Epub 2013 Jan 11. Phys Rev Lett. 2013. PMID: 23383891 Free article.
Mutational landscape and genetic signatures of cell-free DNA in tumour-induced osteomalacia.
Wu N, Zhang Z, Zhou X, Zhao H, Ming Y, Wu X, Zhang X, Yang XZ, Zhou M, Bao H, Chen W, Wu Y, Liu S, Wang H, Niu Y, Li Y, Zheng Y, Shao Y, Gao N, Yang Y, Liu Y, Li W, Liu J, Zhang N, Yang X, Xu Y, Li M, Sun Y, Su J, Zhang J, Xia W, Qiu G, Liu Y, Liu J, Wu Z. Wu N, et al. J Cell Mol Med. 2020 May;24(9):4931-4943. doi: 10.1111/jcmm.14991. Epub 2020 Apr 11. J Cell Mol Med. 2020. PMID: 32277576 Free PMC article.
Phenotypic and genetic spectrum of isolated macrodactyly: somatic mosaicism of PIK3CA and AKT1 oncogenic variants.
Tian W, Huang Y, Sun L, Guo Y, Zhao S, Lin M, Dong X, Zhong W, Yin Y, Chen Z, Zhang N, Zhang Y, Wang L, Lin J, Yan Z, Yang X, Zhao J, Qiu G, Zhang J, Wu Z, Wu N; (Deciphering Disorders Involving Scoliosis, COmorbidities) study group. Tian W, et al. Orphanet J Rare Dis. 2020 Oct 14;15(1):288. doi: 10.1186/s13023-020-01572-9. Orphanet J Rare Dis. 2020. PMID: 33054853 Free PMC article.
Identification of novel FBN1 variations implicated in congenital scoliosis.
Lin M, Zhao S, Liu G, Huang Y, Yu C, Zhao Y, Wang L, Zhang Y, Yan Z, Wang S, Liu S, Liu J, Ye Y, Chen Y, Yang X, Tong B, Wang Z, Yang X, Niu Y, Li X, Wang Y, Su J, Yuan J, Zhao H, Zhang S, Qiu G; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study; Ikegawa S, Zhang J, Wu Z, Wu N. Lin M, et al. J Hum Genet. 2020 Mar;65(3):221-230. doi: 10.1038/s10038-019-0698-x. Epub 2019 Dec 11. J Hum Genet. 2020. PMID: 31827250 Free PMC article.
Diagnostic yield and clinical impact of exome sequencing in early-onset scoliosis (EOS).
Zhao S, Zhang Y, Chen W, Li W, Wang S, Wang L, Zhao Y, Lin M, Ye Y, Lin J, Zheng Y, Liu J, Zhao H, Yan Z, Yang Y, Huang Y, Lin G, Chen Z, Zhang Z, Liu S, Jin L, Wang Z, Chen J, Niu Y, Li X, Wu Y, Wang Y, Du R, Gao N, Zhao H, Yang Y, Liu Y, Tian Y, Li W, Zhao Y, Liu J, Yu B, Zhang N, Yu K, Yang X, Li S, Xu Y, Hu J, Liu Z, Shen J, Zhang S, Su J, Khanshour AM, Kidane YH, Ramo B, Rios JJ, Liu P, Sutton VR, Posey JE, Wu Z, Qiu G, Wise CA, Zhang F, Lupski JR, Zhang J, Wu N; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study. Zhao S, et al. J Med Genet. 2021 Jan;58(1):41-47. doi: 10.1136/jmedgenet-2019-106823. Epub 2020 May 7. J Med Genet. 2021. PMID: 32381727 Free PMC article.
DrABC: deep learning accurately predicts germline pathogenic mutation status in breast cancer patients based on phenotype data.
Liu J, Zhao H, Zheng Y, Dong L, Zhao S, Huang Y, Huang S, Qian T, Zou J, Liu S, Li J, Yan Z, Li Y, Zhang S, Huang X, Wang W, Li Y, Wang J, Ming Y, Li X, Xing Z, Qin L, Zhao Z, Jia Z, Li J, Liu G, Zhang M, Feng K, Wu J, Zhang J, Yang Y, Wu Z, Liu Z, Ying J, Wang X, Su J, Wang X, Wu N. Liu J, et al. Genome Med. 2022 Feb 25;14(1):21. doi: 10.1186/s13073-022-01027-9. Genome Med. 2022. PMID: 35209950 Free PMC article.
Cost-effectiveness analysis of using the TBX6-associated congenital scoliosis risk score (TACScore) in genetic diagnosis of congenital scoliosis.
Chen Z, Yan Z, Yu C, Liu J, Zhang Y, Zhao S, Lin J, Zhang Y, Wang L, Lin M, Huang Y, Li X, Niu Y, Wang S, Wu Z; DISCO (Deciphering disorders Involving Scoliosis and COmorbidities) study group; Qiu G, Zhang TJ, Wu N. Chen Z, et al. Orphanet J Rare Dis. 2020 Sep 15;15(1):250. doi: 10.1186/s13023-020-01537-y. Orphanet J Rare Dis. 2020. PMID: 32933559 Free PMC article.
Perturbations of genes essential for Müllerian duct and Wölffian duct development in Mayer-Rokitansky-Küster-Hauser syndrome.
Chen N, Zhao S, Jolly A, Wang L, Pan H, Yuan J, Chen S, Koch A, Ma C, Tian W, Jia Z, Kang J, Zhao L, Qin C, Fan X, Rall K, Coban-Akdemir Z, Chen Z, Jhangiani S, Liang Z, Niu Y, Li X, Yan Z, Wu Y, Dong S, Song C, Qiu G, Zhang S, Liu P, Posey JE, Zhang F, Luo G, Wu Z; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study group; Su J, Zhang J, Chen EY, Rouskas K, Glentis S, Bacopoulou F, Deligeoroglou E, Chrousos G, Lyonnet S, Polak M, Rosenberg C, Dingeldein I, Bonilla X, Borel C, Gibbs RA, Dietrich JE, Dimas AS, Antonarakis SE, Brucker SY, Lupski JR, Wu N, Zhu L. Chen N, et al. Am J Hum Genet. 2021 Feb 4;108(2):337-345. doi: 10.1016/j.ajhg.2020.12.014. Am J Hum Genet. 2021. PMID: 33434492 Free PMC article.
The draft genome of watermelon (Citrullus lanatus) and resequencing of 20 diverse accessions.
Guo S, Zhang J, Sun H, Salse J, Lucas WJ, Zhang H, Zheng Y, Mao L, Ren Y, Wang Z, Min J, Guo X, Murat F, Ham BK, Zhang Z, Gao S, Huang M, Xu Y, Zhong S, Bombarely A, Mueller LA, Zhao H, He H, Zhang Y, Zhang Z, Huang S, Tan T, Pang E, Lin K, Hu Q, Kuang H, Ni P, Wang B, Liu J, Kou Q, Hou W, Zou X, Jiang J, Gong G, Klee K, Schoof H, Huang Y, Hu X, Dong S, Liang D, Wang J, Wu K, Xia Y, Zhao X, Zheng Z, Xing M, Liang X, Huang B, Lv T, Wang J, Yin Y, Yi H, Li R, Wu M, Levi A, Zhang X, Giovannoni JJ, Wang J, Li Y, Fei Z, Xu Y. Guo S, et al. Nat Genet. 2013 Jan;45(1):51-8. doi: 10.1038/ng.2470. Epub 2012 Nov 25. Nat Genet. 2013. PMID: 23179023 Free article.
A genetic variation map for chicken with 2.8 million single-nucleotide polymorphisms.
Wong GK, Liu B, Wang J, Zhang Y, Yang X, Zhang Z, Meng Q, Zhou J, Li D, Zhang J, Ni P, Li S, Ran L, Li H, Zhang J, Li R, Li S, Zheng H, Lin W, Li G, Wang X, Zhao W, Li J, Ye C, Dai M, Ruan J, Zhou Y, Li Y, He X, Zhang Y, Wang J, Huang X, Tong W, Chen J, Ye J, Chen C, Wei N, Li G, Dong L, Lan F, Sun Y, Zhang Z, Yang Z, Yu Y, Huang Y, He D, Xi Y, Wei D, Qi Q, Li W, Shi J, Wang M, Xie F, Wang J, Zhang X, Wang P, Zhao Y, Li N, Yang N, Dong W, Hu S, Zeng C, Zheng W, Hao B, Hillier LW, Yang SP, Warren WC, Wilson RK, Brandström M, Ellegren H, Crooijmans RP, van der Poel JJ, Bovenhuis H, Groenen MA, Ovcharenko I, Gordon L, Stubbs L, Lucas S, Glavina T, Aerts A, Kaiser P, Rothwell L, Young JR, Rogers S, Walker BA, van Hateren A, Kaufman J, Bumstead N, Lamont SJ, Zhou H, Hocking PM, Morrice D, de Koning DJ, Law A, Bartley N, Burt DW, Hunt H, Cheng HH, Gunnarsson U, Wahlberg P, Andersson L, Kindlund E, Tammi MT, Andersson B, Webber C, Ponting CP, Overton IM, Boardman PE, Tang H, Hubbard SJ, Wilson SA, Yu J, Wang J, Yang H; International Chicken Polymorphism Map Consortium. Wong GK, et al. Nature. 2004 Dec 9;432(7018):717-22. doi: 10.1038/nature03156. Nature. 2004. PMID: 15592405 Free PMC article.
The Genomes of Oryza sativa: a history of duplications.
Yu J, Wang J, Lin W, Li S, Li H, Zhou J, Ni P, Dong W, Hu S, Zeng C, Zhang J, Zhang Y, Li R, Xu Z, Li S, Li X, Zheng H, Cong L, Lin L, Yin J, Geng J, Li G, Shi J, Liu J, Lv H, Li J, Wang J, Deng Y, Ran L, Shi X, Wang X, Wu Q, Li C, Ren X, Wang J, Wang X, Li D, Liu D, Zhang X, Ji Z, Zhao W, Sun Y, Zhang Z, Bao J, Han Y, Dong L, Ji J, Chen P, Wu S, Liu J, Xiao Y, Bu D, Tan J, Yang L, Ye C, Zhang J, Xu J, Zhou Y, Yu Y, Zhang B, Zhuang S, Wei H, Liu B, Lei M, Yu H, Li Y, Xu H, Wei S, He X, Fang L, Zhang Z, Zhang Y, Huang X, Su Z, Tong W, Li J, Tong Z, Li S, Ye J, Wang L, Fang L, Lei T, Chen C, Chen H, Xu Z, Li H, Huang H, Zhang F, Xu H, Li N, Zhao C, Li S, Dong L, Huang Y, Li L, Xi Y, Qi Q, Li W, Zhang B, Hu W, Zhang Y, Tian X, Jiao Y, Liang X, Jin J, Gao L, Zheng W, Hao B, Liu S, Wang W, Yuan L, Cao M, McDermott J, Samudrala R, Wang J, Wong GK, Yang H. Yu J, et al. PLoS Biol. 2005 Feb;3(2):e38. doi: 10.1371/journal.pbio.0030038. Epub 2005 Feb 1. PLoS Biol. 2005. PMID: 15685292 Free PMC article.
Exome sequencing reveals genetic architecture in patients with isolated or syndromic short stature.
Fan X, Zhao S, Yu C, Wu D, Yan Z, Fan L, Song Y, Wang Y, Li C, Ming Y, Gui B, Niu Y, Li X, Yang X, Luo S, Zhang Q, Zhao X, Pan H, Li M, Xia W, Qiu G, Liu P, Zhang S, Zhang J, Wu Z; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study; Lupski JR, Posey JE, Chen S, Gong C, Wu N. Fan X, et al. J Genet Genomics. 2021 May 20;48(5):396-402. doi: 10.1016/j.jgg.2021.02.008. Epub 2021 Mar 22. J Genet Genomics. 2021. PMID: 34006472
[Dietary sodium intake of adult residents in 15 provinces of China in 2015].
Zhang JG, Wang ZH, Du WW, Su C, Jiang HR, Huang FF, Jia XF, Ouyang YF, Li L, Wang Y, Zhang B, Wang HJ. Zhang JG, et al. Among authors: zhang b. Zhonghua Yu Fang Yi Xue Za Zhi. 2019 May 6;53(5):455-458. doi: 10.3760/cma.j.issn.0253-9624.2019.05.004. Zhonghua Yu Fang Yi Xue Za Zhi. 2019. PMID: 31091600 Chinese.
A draft sequence for the genome of the domesticated silkworm (Bombyx mori).
Xia Q, Zhou Z, Lu C, Cheng D, Dai F, Li B, Zhao P, Zha X, Cheng T, Chai C, Pan G, Xu J, Liu C, Lin Y, Qian J, Hou Y, Wu Z, Li G, Pan M, Li C, Shen Y, Lan X, Yuan L, Li T, Xu H, Yang G, Wan Y, Zhu Y, Yu M, Shen W, Wu D, Xiang Z, Yu J, Wang J, Li R, Shi J, Li H, Li G, Su J, Wang X, Li G, Zhang Z, Wu Q, Li J, Zhang Q, Wei N, Xu J, Sun H, Dong L, Liu D, Zhao S, Zhao X, Meng Q, Lan F, Huang X, Li Y, Fang L, Li C, Li D, Sun Y, Zhang Z, Yang Z, Huang Y, Xi Y, Qi Q, He D, Huang H, Zhang X, Wang Z, Li W, Cao Y, Yu Y, Yu H, Li J, Ye J, Chen H, Zhou Y, Liu B, Wang J, Ye J, Ji H, Li S, Ni P, Zhang J, Zhang Y, Zheng H, Mao B, Wang W, Ye C, Li S, Wang J, Wong GK, Yang H; Biology Analysis Group. Xia Q, et al. Science. 2004 Dec 10;306(5703):1937-40. doi: 10.1126/science.1102210. Science. 2004. PMID: 15591204
[Analysis of endoscopic screening compliance and related factors among high risk population of upper gastrointestinal cancer in urban areas of Henan Province from 2013 to 2017].
Guo LW, Zhang SK, Liu SZ, Yang FN, Zheng LY, Chen Q, Cao XQ, Sun XB, Zhang JG. Guo LW, et al. Among authors: zhang sk, zhang jg. Zhonghua Yu Fang Yi Xue Za Zhi. 2020 May 6;54(5):523-528. doi: 10.3760/cma.j.cn112150-20200304-00238. Zhonghua Yu Fang Yi Xue Za Zhi. 2020. PMID: 32388953 Chinese.
Glaucoma-like optic neuropathy in patients with intracranial tumours.
Qu Y, Wang YX, Xu L, Zhang L, Zhang J, Zhang J, Wang L, Yang L, Yang A, Wang J, Jonas JB. Qu Y, et al. Acta Ophthalmol. 2011 Aug;89(5):e428-33. doi: 10.1111/j.1755-3768.2011.02118.x. Epub 2011 Feb 18. Acta Ophthalmol. 2011. PMID: 21332674 Free article.
Genetic and molecular mechanism for distinct clinical phenotypes conveyed by allelic truncating mutations implicated in FBN1.
Lin M, Liu Z, Liu G, Zhao S, Li C, Chen W, Coban Akdemir Z, Lin J, Song X, Wang S, Xu Q, Zhao Y, Wang L, Zhang Y, Yan Z, Liu S, Liu J, Chen Y, Zuo Y, Yang X, Sun T, Yang XZ, Niu Y, Li X, You W, Qiu B, Ding C, Liu P, Zhang S, Carvalho CMB, Posey JE, Qiu G; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study; Lupski JR, Wu Z, Zhang J, Wu N. Lin M, et al. Mol Genet Genomic Med. 2020 Jan;8(1):e1023. doi: 10.1002/mgg3.1023. Epub 2019 Nov 27. Mol Genet Genomic Med. 2020. PMID: 31774634 Free PMC article.
Whole-Genome Methylation Analysis of Phenotype Discordant Monozygotic Twins Reveals Novel Epigenetic Perturbation Contributing to the Pathogenesis of Adolescent Idiopathic Scoliosis.
Liu G, Wang L, Wang X, Yan Z, Yang X, Lin M, Liu S, Zuo Y, Niu Y, Zhao S, Zhao Y, Zhang J, Shen J, Wang Y, Qiu G, Wu Z, Wu N. Liu G, et al. Front Bioeng Biotechnol. 2019 Dec 10;7:364. doi: 10.3389/fbioe.2019.00364. eCollection 2019. Front Bioeng Biotechnol. 2019. PMID: 31921798 Free PMC article.
A novel COMP mutation in a Chinese family with multiple epiphyseal dysplasia.
Shao J, Zhao S, Yan Z, Wang L, Zhang Y, Lin M, Yu C, Wang S, Niu Y, Li X, Qiu G, Zhang J; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study; Wu Z, Wu N. Shao J, et al. BMC Med Genet. 2020 May 27;21(1):115. doi: 10.1186/s12881-020-01040-y. BMC Med Genet. 2020. PMID: 32460719 Free PMC article.
TBX6 missense variants expand the mutational spectrum in a non-Mendelian inheritance disease.
Chen W, Lin J, Wang L, Li X, Zhao S, Liu J, Akdemir ZC, Zhao Y, Du R, Ye Y, Song X, Zhang Y, Yan Z, Yang X, Lin M, Shen J, Wang S, Gao N, Yang Y, Liu Y, Li W, Liu J, Zhang N, Yang X, Xu Y, Zhang J, Delgado MR, Posey JE, Qiu G, Rios JJ, Liu P, Wise CA, Zhang F, Wu Z, Lupski JR, Wu N. Chen W, et al. Hum Mutat. 2020 Jan;41(1):182-195. doi: 10.1002/humu.23907. Epub 2019 Sep 26. Hum Mutat. 2020. PMID: 31471994 Free PMC article.
Human and mouse studies establish TBX6 in Mendelian CAKUT and as a potential driver of kidney defects associated with the 16p11.2 microdeletion syndrome.
Yang N, Wu N, Dong S, Zhang L, Zhao Y, Chen W, Du R, Song C, Ren X, Liu J, Pehlivan D, Liu Z, Rao J, Wang C, Zhao S, Breman AM, Xue H, Sun H, Shen J, Zhang S, Posey JE, Xu H, Jin L, Zhang J, Liu P, Sanna-Cherchi S, Qiu G, Wu Z, Lupski JR, Zhang F. Yang N, et al. Kidney Int. 2020 Oct;98(4):1020-1030. doi: 10.1016/j.kint.2020.04.045. Epub 2020 May 22. Kidney Int. 2020. PMID: 32450157 Free PMC article.
[Clinical Characteristics and Genetic Analysis of Klippel-Feil Syndrome].
Li ZQ, Geng MZ, Zhao S, Wu ZH, Zhang JG, Wu N, Wang YP. Li ZQ, et al. Among authors: zhang jg. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2021 Feb 28;43(1):25-31. doi: 10.3881/j.issn.1000-503X.12629. Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2021. PMID: 33663658 Chinese.
Chinese guideline on the application of anti-seizure medications in the perioperative period of supratentorial craniocerebral surgery.
Liang S, Fan X, Chen F, Liu Y, Qiu B, Zhang K, Qi S, Zhang G, Liu J, Zhang J, Wang J, Wang X, Song Z, Luan G, Yang X, Jiang R, Zhang H, Wang L, You Y, Shu K, Lu X, Gao G, Zhang B, Zhou J, Jin H, Han K, Li Y, Wei J, Yang K, You G, Ji H, Jiang Y, Wang Y, Lin Z, Li Y, Liu X, Hu J, Zhu J, Li W, Wang Y, Kang D, Feng H, Liu T, Chen X, Pan Y, Liu Z, Li G, Li Y, Ge M, Fu X, Wang Y, Zhou D, Li S, Jiang T, Hou L, Hong Z. Liang S, et al. Ther Adv Neurol Disord. 2022 Aug 16;15:17562864221114357. doi: 10.1177/17562864221114357. eCollection 2022. Ther Adv Neurol Disord. 2022. PMID: 35992894 Free PMC article. Review.
Mutational burden and potential oligogenic model of TBX6-mediated genes in congenital scoliosis.
Yang Y, Zhao S, Zhang Y, Wang S, Shao J, Liu B, Li Y, Yan Z, Niu Y, Li X, Wang L, Ye Y, Weng X, Wu Z; Deciphering Disorders Involving Scoliosis and COmorbidities (DISCO) study; Zhang J, Wu N. Yang Y, et al. Mol Genet Genomic Med. 2020 Oct;8(10):e1453. doi: 10.1002/mgg3.1453. Epub 2020 Aug 20. Mol Genet Genomic Med. 2020. PMID: 32815649 Free PMC article.
Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family.
Bigoni S, Neri M, Scotton C, Farina R, Sabatelli P, Jiang C, Zhang J, Falzarano MS, Rossi R, Ognibene D, Selvatici R, Gualandi F, Bosshardt D, Perri P, Campa C, Brancati F, Salvatore M, De Stefano MC, Taruscio D, Trombelli L, Fang M, Ferlini A. Bigoni S, et al. Front Genet. 2019 Jan 21;9:723. doi: 10.3389/fgene.2018.00723. eCollection 2018. Front Genet. 2019. PMID: 30740127 Free PMC article.
Contribution of basal ganglia activity to REM sleep disorder in Parkinson's disease.
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