Bing-Lan Wu - Publications


71 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Wu BL, Hu CL, Mao FF, Tang RL, Mao JG. Highly polarizable Hg induced a strong SHG signal and large birefringence in LiHgPO. Journal of the American Chemical Society. PMID 31204805 DOI: 10.1021/jacs.9b05125  0.64
2019 Mao FF, Hu CL, Chen J, Tang RL, Wu BL, Mao JG. (HO)HCsNb(IO) and SrNbO(IO): a facile synthetic method using hydrofluoric acid as a solubilizer. Chemical Communications (Cambridge, England). PMID 31134976 DOI: 10.1039/c9cc02774b  0.64
2019 Wu YG, Wang KW, Zhao ZR, Zhang P, Liu H, Zhou GJ, Cheng Y, Wu WJ, Cai YH, Wu BL, Chen FY. A novel polysaccharide from Dendrobium devonianum serves as a TLR4 agonist for activating macrophages. International Journal of Biological Macromolecules. PMID 31004640 DOI: 10.1016/j.ijbiomac.2019.04.125  0.32
2019 Mao FF, Hu CL, Chen J, Wu BL, Mao JG. HBa(IO)(IO) and HBa(IO)(IO): Explorations of Second-Order Nonlinear Optical Materials in the Alkali-Earth Polyiodate System. Inorganic Chemistry. PMID 30840444 DOI: 10.1021/acs.inorgchem.9b00075  0.64
2018 Lan X, Li N, Wan H, Luo L, Wu Y, Li S, An Y, Wu BL. Developing a one-step triplet-repeat primed PCR assay for diagnosing myotonic dystrophy. Journal of Genetics and Genomics = Yi Chuan Xue Bao. PMID 30297192 DOI: 10.1016/j.jgg.2018.06.008  0.92
2018 Zhu Y, Zhao YL, Li J, Liu H, Zhao Q, Wu BL, Yang ZL. Molecular binding mode of PF-232798, a clinical anti-HIV candidate, at chemokine receptor CCR5. Acta Pharmacologica Sinica. PMID 29941870 DOI: 10.1038/s41401-018-0054-2  0.32
2018 Bai CY, Zhang JY, Shi TW, Bai YQ, Wu BL, Du ZP, Wu ZY, Xu XE, Wang SH, Wu JY, Te RY, Zhang JY, Xu LY, Li EM. Association between 5-lipoxygenase expression, and malignant behaviors and poor prognosis in esophageal squamous cell carcinoma. Oncology Letters. 15: 9353-9360. PMID 29805660 DOI: 10.3892/ol.2018.8527  0.4
2017 Zhan XH, Jiao JW, Zhang HF, Li CQ, Zhao JM, Liao LD, Wu JY, Wu BL, Wu ZY, Wang SH, Du ZP, Shen JH, Zou HY, Neufeld G, Xu LY, et al. A three-gene signature from protein-protein interaction network of LOXL2- and actin-related proteins for esophageal squamous cell carcinoma prognosis. Cancer Medicine. PMID 28556501 DOI: 10.1002/cam4.1096  0.4
2017 Zhang W, Song X, Ni F, Cheng J, Wu BL, Jiang H. Association analysis between HFM1 variations and idiopathic azoospermia or severe oligozoospermia in Chinese Men. Science China. Life Sciences. 60: 315-318. PMID 28303456 DOI: 10.1007/s11427-016-0274-9  0.48
2017 Xu HY, Nie EM, Deng G, Lai LZ, Sun FY, Tian H, Fang FC, Zou YG, Wu BL, Ou-Yang J. Periostin is essential for periodontal ligament remodeling during orthodontic treatment. Molecular Medicine Reports. PMID 28260019 DOI: 10.3892/mmr.2017.6200  0.48
2017 Li CQ, Huang GW, Wu ZY, Xu YJ, Li XC, Xue YJ, Zhu Y, Zhao JM, Li M, Zhang J, Wu JY, Lei F, Wang QY, Li S, Zheng CP, ... ... Wu BL, et al. Integrative analyses of transcriptome sequencing identify novel functional lncRNAs in esophageal squamous cell carcinoma. Oncogenesis. 6: e297. PMID 28194033 DOI: 10.1038/oncsis.2017.1  0.44
2017 Dang T, Duan WY, Yu B, Tong DL, Cheng C, Zhang YF, Wu W, Ye K, Zhang WX, Wu M, Wu BB, An Y, Qiu ZL, Wu BL. Autism-associated Dyrk1a truncation mutants impair neuronal dendritic and spine growth and interfere with postnatal cortical development. Molecular Psychiatry. PMID 28167836 DOI: 10.1038/mp.2016.253  0.92
2016 Chen J, Wu BL, Lu QB. [Diurnal activity pattern and seasonal variations of captive Papio hamadryas.] Ying Yong Sheng Tai Xue Bao = the Journal of Applied Ecology. 27: 3719-3726. PMID 29696873 DOI: 10.13287/j.1001-9332.201611.006  0.4
2016 Chen X, An Y, Gao Y, Guo L, Rui L, Xie H, Sun M, Lam Hung S, Sheng X, Zou J, Bao Y, Guan H, Niu B, Li Z, Finnell RH, ... ... Wu BL, et al. Rare Deleterious PARD3 Variants in the aPKC-Binding Region are Implicated in the Pathogenesis of Human Cranial Neural Tube Defects via Disrupting Apical Tight Junction Formation. Human Mutation. PMID 27925688 DOI: 10.1002/humu.23153  0.92
2016 Zhang JX, Chen ZH, Xu Y, Chen JW, Weng HW, Yun M, Zheng ZS, Chen C, Wu BL, Li EM, Fu JH, Ye S, Xie D. Downregulation of MicroRNA-644a Promotes Esophageal Squamous Cell Carcinoma Aggressiveness and Stem-cell-like Phenotype via Dysregulation of PITX2. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. PMID 27407092 DOI: 10.1158/1078-0432.CCR-16-0414  0.32
2016 Zou HY, Lv GQ, Dai LH, Zhan XH, Jiao JW, Liao LD, Zhou TM, Li CQ, Wu BL, Xu LY, Li EM. A truncated splice variant of human lysyl oxidase-like 2 promotes migration and invasion in esophageal squamous cell carcinoma. The International Journal of Biochemistry & Cell Biology. PMID 27063404 DOI: 10.1016/j.biocel.2016.04.003  0.4
2016 Li CY, Gao BL, Guo FQ, Zhang XJ, Fan QY, Wu BL, Xiang C, Liu XW, Pan T. Quantitative evaluation of left ventricular volume and function in middle-aged healthy chinese people with 3 Tesla MRI. Journal of Magnetic Resonance Imaging : Jmri. PMID 27015960 DOI: 10.1002/jmri.25243  0.56
2015 Pu D, Wang C, Cao J, Shen Y, Wu BL, Liu J, Wu J. Association analysis between HFM1 variation and primary ovarian insufficiency in Chinese women. Clinical Genetics. PMID 26679638 DOI: 10.1111/cge.12718  0.92
2015 Liu MF, Hu YY, Jin T, Xu K, Wang SH, Du GZ, Wu BL, Li LY, Xu LY, Li EM, Xu HX. Matrix Metalloproteinase-9/Neutrophil Gelatinase-Associated Lipocalin Complex Activity in Human Glioma Samples Predicts Tumor Presence and Clinical Prognosis. Disease Markers. 2015: 138974. PMID 26663949 DOI: 10.1155/2015/138974  0.4
2015 Gong Y, Du Y, Li H, Zhang X, An Y, Wu B. Parenting stress and affective symptoms in parents of autistic children. Science China. Life Sciences. PMID 26335730 DOI: 10.1007/s11427-012-4293-z  0.92
2015 Du ZP, Wu BL, Xie JJ, Lin XH, Qiu XY, Zhan XF, Wang SH, Shen JH, Li EM, Xu LY. Network Analyses of Gene Expression following Fascin Knockdown in Esophageal Squamous Cell Carcinoma Cells. Asian Pacific Journal of Cancer Prevention : Apjcp. 16: 5445-51. PMID 26225692  0.4
2015 Du ZP, Wu BL, Xie YM, Zhang YL, Liao LD, Zhou F, Xie JJ, Zeng FM, Xu XE, Fang WK, Li EM, Xu LY. Lipocalin 2 promotes the migration and invasion of esophageal squamous cell carcinoma cells through a novel positive feedback loop. Biochimica Et Biophysica Acta. 1853: 2240-2250. PMID 26190820 DOI: 10.1016/j.bbamcr.2015.07.007  0.4
2015 Du ZP, Wu BL, Wu X, Lin XH, Qiu XY, Zhan XF, Wang SH, Shen JH, Zheng CP, Wu ZY, Xu LY, Wang D, Li EM. A systematic analysis of human lipocalin family and its expression in esophageal carcinoma. Scientific Reports. 5: 12010. PMID 26131602 DOI: 10.1038/srep12010  0.4
2015 Brigandi SA, Shao H, Qian SY, Shen Y, Wu BL, Kang JX. Autistic children exhibit decreased levels of essential Fatty acids in red blood cells. International Journal of Molecular Sciences. 16: 10061-76. PMID 25946342 DOI: 10.3390/ijms160510061  0.36
2015 Zhang LM, An Y, Pan G, Ding YF, Zhou YF, Yao YH, Wu BL, Zhou SZ. Reduced Penetrance of PRRT2 Mutation in a Chinese Family With Infantile Convulsion and Choreoathetosis Syndrome. Journal of Child Neurology. 30: 1263-9. PMID 25403460 DOI: 10.1177/0883073814556887  0.92
2014 Lv GQ, Zou HY, Liao LD, Cao HH, Zeng FM, Wu BL, Xie JJ, Fang WK, Xu LY, Li EM. Identification of a novel lysyl oxidase-like 2 alternative splicing isoform, LOXL2 Δe13, in esophageal squamous cell carcinoma. Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire. 92: 379-89. PMID 25275797 DOI: 10.1139/bcb-2014-0046  0.4
2014 Wu BL, Lv GQ, Zou HY, Du ZP, Wu JY, Zhang PX, Xu LY, Li EM. Exploration of potential roles of a new LOXL2 splicing variant using network knowledge in esophageal squamous cell carcinoma. Thescientificworldjournal. 2014: 431792. PMID 25254241 DOI: 10.1155/2014/431792  0.4
2014 Du ZP, Wu BL, Wang SH, Shen JH, Lin XH, Zheng CP, Wu ZY, Qiu XY, Zhan XF, Xu LY, Li EM. Shortest path analyses in the protein-protein interaction network of NGAL (neutrophil gelatinase-associated lipocalin) overexpression in esophageal squamous cell carcinoma. Asian Pacific Journal of Cancer Prevention : Apjcp. 15: 6899-904. PMID 25169543  0.4
2014 Jamuar SS, Lam AT, Kircher M, D'Gama AM, Wang J, Barry BJ, Zhang X, Hill RS, Partlow JN, Rozzo A, Servattalab S, Mehta BK, Topcu M, Amrom D, Andermann E, ... ... Wu BL, et al. Somatic mutations in cerebral cortical malformations. The New England Journal of Medicine. 371: 733-43. PMID 25140959 DOI: 10.1056/NEJMoa1314432  0.36
2014 Wu BL, Li CQ, Du ZP, Zhou F, Xie JJ, Luo LW, Wu JY, Zhang PX, Xu LY, Li EM. Functional analysis of the mRNA profile of neutrophil gelatinase‑associated lipocalin overexpression in esophageal squamous cell carcinoma using multiple bioinformatic tools. Molecular Medicine Reports. 10: 1800-12. PMID 25109818 DOI: 10.3892/mmr.2014.2465  0.4
2014 Ye Y, Lan X, Cong J, Li N, Wu Y, Zhang M, Liu J, Cui Y, Wu BL, An Y, Wu J. Analysis of CGG repeats in FMR1 in Chinese women with idiopathic premature ovarian failure. Reproductive Biomedicine Online. 29: 382-7. PMID 24912415 DOI: 10.1016/j.rbmo.2014.05.004  0.36
2014 Olson H, Shen Y, Avallone J, Sheidley BR, Pinsky R, Bergin AM, Berry GT, Duffy FH, Eksioglu Y, Harris DJ, Hisama FM, Ho E, Irons M, Jacobsen CM, James P, ... ... Wu BL, et al. Copy number variation plays an important role in clinical epilepsy. Annals of Neurology. 75: 943-58. PMID 24811917 DOI: 10.1002/ana.24178  0.36
2014 Wu BL, Zou HY, Lv GQ, Du ZP, Wu JY, Zhang PX, Xu LY, Li EM. Protein-protein interaction network analyses for elucidating the roles of LOXL2-delta72 in esophageal squamous cell carcinoma. Asian Pacific Journal of Cancer Prevention : Apjcp. 15: 2345-51. PMID 24716982  0.4
2014 Wang J, Zhang W, Jiang H, Wu BL. Mutations in HFM1 in recessive primary ovarian insufficiency. The New England Journal of Medicine. 370: 972-4. PMID 24597873 DOI: 10.1056/NEJMc1310150  0.48
2014 Lionel AC, Tammimies K, Vaags AK, Rosenfeld JA, Ahn JW, Merico D, Noor A, Runke CK, Pillalamarri VK, Carter MT, Gazzellone MJ, Thiruvahindrapuram B, Fagerberg C, Laulund LW, Pellecchia G, ... ... Wu BL, et al. Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes. Human Molecular Genetics. 23: 2752-68. PMID 24381304 DOI: 10.1093/hmg/ddt669  0.36
2014 Zhang HF, Zhang K, Liao LD, Li LY, Du ZP, Wu BL, Wu JY, Xu XE, Zeng FM, Chen B, Cao HH, Zhu MX, Dai LH, Long L, Wu ZY, et al. miR-200b suppresses invasiveness and modulates the cytoskeletal and adhesive machinery in esophageal squamous cell carcinoma cells via targeting Kindlin-2. Carcinogenesis. 35: 292-301. PMID 24064224 DOI: 10.1093/carcin/bgt320  0.4
2013 Wu BL, Luo LW, Li CQ, Xie JJ, Du ZP, Wu JY, Zhang PX, Xu LY, Li EM. Comprehensive bioinformation analysis of the mRNA profile of fascin knockdown in esophageal squamous cell carcinoma. Asian Pacific Journal of Cancer Prevention : Apjcp. 14: 7221-7. PMID 24460279  0.4
2013 Wang H, Lin ZX, Wu BL. [Concentration levels and sources analysis of additives element in engine oil]. Guang Pu Xue Yu Guang Pu Fen Xi = Guang Pu. 33: 2579-82. PMID 24369676  0.48
2013 An Y, Amr SS, Torres A, Weissman L, Raffalli P, Cox G, Sheng X, Lip V, Bi W, Patel A, Stankiewicz P, Wu BL, Shen Y. SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delay. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 162: 832-40. PMID 24019301 DOI: 10.1002/ajmg.b.32187  0.36
2013 Fang WK, Liao LD, Li LY, Xie YM, Xu XE, Zhao WJ, Wu JY, Zhu MX, Wu ZY, Du ZP, Wu BL, Xie D, Guo MZ, Xu LY, Li EM. Down-regulated desmocollin-2 promotes cell aggressiveness through redistributing adherens junctions and activating beta-catenin signalling in oesophageal squamous cell carcinoma. The Journal of Pathology. 231: 257-70. PMID 23836524 DOI: 10.1002/path.4236  0.4
2013 Wu BL, Song B. Reply to Dr. Jeffrey Brent. Neurotoxicology. 37: 220. PMID 23711744 DOI: 10.1016/j.neuro.2013.05.013  0.32
2013 Mason-Suares H, Kim W, Grimmett L, Williams ES, Horner VL, Kunig D, Goldlust IS, Wu BL, Shen Y, Miller DT, Martin CL, Rudd MK. Density matters: comparison of array platforms for detection of copy-number variation and copy-neutral abnormalities. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 15: 706-12. PMID 23558256 DOI: 10.1038/gim.2013.36  0.36
2013 Chen X, Shen Y, Zhang F, Chiang C, Pillalamarri V, Blumenthal I, Talkowski M, Wu BL, Gusella JF. Molecular analysis of a deletion hotspot in the NRXN1 region reveals the involvement of short inverted repeats in deletion CNVs. American Journal of Human Genetics. 92: 375-86. PMID 23472757 DOI: 10.1016/j.ajhg.2013.02.006  0.36
2013 Wu BL, Song B. Reply to drs. John andrew tomenson and clive campbell. Neurotoxicology. 36: 105. PMID 23454660 DOI: 10.1016/j.neuro.2013.02.011  0.32
2013 Chen X, Shen Y, Gao Y, Zhao H, Sheng X, Zou J, Lip V, Xie H, Guo J, Shao H, Bao Y, Shen J, Niu B, Gusella JF, Wu BL, et al. Detection of copy number variants reveals association of cilia genes with neural tube defects. Plos One. 8: e54492. PMID 23349908 DOI: 10.1371/journal.pone.0054492  0.36
2013 Beunders G, Voorhoeve E, Golzio C, Pardo LM, Rosenfeld JA, Talkowski ME, Simonic I, Lionel AC, Vergult S, Pyatt RE, van de Kamp J, Nieuwint A, Weiss MM, Rizzu P, Verwer LE, ... ... Wu BL, et al. Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus. American Journal of Human Genetics. 92: 210-20. PMID 23332918 DOI: 10.1016/j.ajhg.2012.12.011  0.36
2013 Mademont-Soler I, Morales C, Soler A, Martínez-Crespo JM, Shen Y, Margarit E, Clusellas N, Obón M, Wu BL, Sánchez A. Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis. Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology. 41: 375-82. PMID 23233332 DOI: 10.1002/uog.12372  0.92
2012 Yu Y, Wu BL, Wu J, Shen Y. Exome and whole-genome sequencing as clinical tests: a transformative practice in molecular diagnostics. Clinical Chemistry. 58: 1507-9. PMID 23065473 DOI: 10.1373/clinchem.2012.193128  0.92
2012 Ernst C, Marshall CR, Shen Y, Metcalfe K, Rosenfeld J, Hodge JC, Torres A, Blumenthal I, Chiang C, Pillalamarri V, Crapper L, Diallo AB, Ruderfer D, Pereira S, Sklar P, ... ... Wu BL, et al. Highly penetrant alterations of a critical region including BDNF in human psychopathology and obesity. Archives of General Psychiatry. 69: 1238-46. PMID 23044507 DOI: 10.1001/archgenpsychiatry.2012.660  0.36
2012 Song B, Wu BL, Sun SJ, Zhang R, Tan FZ, Niu YJ. [The effects of low pre-pregnant lead exposure level on maternal bone turnover during gestation and lactation in mice]. Zhonghua Lao Dong Wei Sheng Zhi Ye Bing Za Zhi = Zhonghua Laodong Weisheng Zhiyebing Zazhi = Chinese Journal of Industrial Hygiene and Occupational Diseases. 30: 493-6. PMID 22931813  0.32
2012 Miller DT, Shen Y, Wu BL. Oligonucleotide microarrays for clinical diagnosis of copy number variation and zygosity status. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. Unit8.12. PMID 22786613 DOI: 10.1002/0471142905.hg0812s74  0.36
2012 Poduri A, Chopra SS, Neilan EG, Elhosary PC, Kurian MA, Meyer E, Barry BJ, Khwaja OS, Salih MA, Stödberg T, Scheffer IE, Maher ER, Sahin M, Wu BL, Berry GT, et al. Homozygous PLCB1 deletion associated with malignant migrating partial seizures in infancy. Epilepsia. 53: e146-50. PMID 22690784 DOI: 10.1111/j.1528-1167.2012.03538.x  0.36
2012 Shi Y, Ding Y, Lei YP, Yang XY, Xie GM, Wen J, Cai CQ, Li H, Chen Y, Zhang T, Wu BL, Jin L, Chen YG, Wang HY. Identification of novel rare mutations of DACT1 in human neural tube defects. Human Mutation. 33: 1450-5. PMID 22610794 DOI: 10.1002/humu.22121  0.68
2012 Shi Y, Cui YH, Wu HG, Zhang W, Zhao C, Liu HR, Guo LQ, Wu BL, Yu AZ, Zhang YY. Effects of mild-warming moxibustion on Bcl-2 and PKC expressions of peripheral blood in elderly people. Journal of Traditional Chinese Medicine = Chung I Tsa Chih Ying Wen Pan / Sponsored by All-China Association of Traditional Chinese Medicine, Academy of Traditional Chinese Medicine. 32: 45-51. PMID 22594101  0.48
2012 Talkowski ME, Rosenfeld JA, Blumenthal I, Pillalamarri V, Chiang C, Heilbut A, Ernst C, Hanscom C, Rossin E, Lindgren AM, Pereira S, Ruderfer D, Kirby A, Ripke S, Harris DJ, ... ... Wu BL, et al. Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries. Cell. 149: 525-37. PMID 22521361 DOI: 10.1016/j.cell.2012.03.028  0.36
2012 Gong X, Jiang YW, Zhang X, An Y, Zhang J, Wu Y, Wang J, Sun Y, Liu Y, Gao X, Shen Y, Wu X, Qiu Z, Jin L, Wu BL, et al. High proportion of 22q13 deletions and SHANK3 mutations in Chinese patients with intellectual disability. Plos One. 7: e34739. PMID 22509352 DOI: 10.1371/journal.pone.0034739  0.36
2012 Zhao Q, Wu BL. Ice breaking in GPCR structural biology Acta Pharmacologica Sinica. 33: 324-334. PMID 22286917 DOI: 10.1038/aps.2011.187  0.32
2012 Lin RJ, Xiao DW, Liao LD, Chen T, Xie ZF, Huang WZ, Wang WS, Jiang TF, Wu BL, Li EM, Xu LY. MiR-142-3p as a potential prognostic biomarker for esophageal squamous cell carcinoma. Journal of Surgical Oncology. 105: 175-82. PMID 21882196 DOI: 10.1002/jso.22066  0.4
2012 Waisbren SE, Potter NL, Gordon CM, Green RC, Greenstein P, Gubbels CS, Rubio-Gozalbo E, Schomer D, Welt C, Anastasoaie V, D'Anna K, Gentile J, Guo CY, Hecht L, Jackson R, ... ... Wu BL, et al. The adult galactosemic phenotype. Journal of Inherited Metabolic Disease. 35: 279-86. PMID 21779791 DOI: 10.1007/s10545-011-9372-y  0.36
2012 Yu HE, Hawash K, Picker J, Stoler J, Urion D, Wu BL, Shen Y. A recurrent 1.71 Mb genomic imbalance at 2q13 increases the risk of developmental delay and dysmorphism Clinical Genetics. 81: 257-264. PMID 21255006 DOI: 10.1111/j.1399-0004.2011.01637.x  0.92
2011 Dauber A, Yu Y, Turchin MC, Chiang CW, Meng YA, Demerath EW, Patel SR, Rich SS, Rotter JI, Schreiner PJ, Wilson JG, Shen Y, Wu BL, Hirschhorn JN. Genome-wide association of copy-number variation reveals an association between short stature and the presence of low-frequency genomic deletions. American Journal of Human Genetics. 89: 751-9. PMID 22118881 DOI: 10.1016/j.ajhg.2011.10.014  0.36
2011 Talkowski ME, Mullegama SV, Rosenfeld JA, van Bon BW, Shen Y, Repnikova EA, Gastier-Foster J, Thrush DL, Kathiresan S, Ruderfer DM, Chiang C, Hanscom C, Ernst C, Lindgren AM, Morton CC, ... ... Wu BL, et al. Assessment of 2q23.1 microdeletion syndrome implicates MBD5 as a single causal locus of intellectual disability, epilepsy, and autism spectrum disorder. American Journal of Human Genetics. 89: 551-63. PMID 21981781 DOI: 10.1016/j.ajhg.2011.09.011  0.36
2011 Wang H, Bi ZY, Zhao WD, Tian H, Jiao PF, Wu BL, Zhao WH, Liu Y. [Six degree-of-freedom acquisition and analysis of jaw opening and closing with motion capture system]. Nan Fang Yi Ke Da Xue Xue Bao = Journal of Southern Medical University. 31: 1597-9. PMID 21945776  0.48
2011 Yu Y, Zhu H, Miller DT, Gusella JF, Platt OS, Wu BL, Shen Y. Age- and gender-dependent obesity in individuals with 16p11.2 deletion. Journal of Genetics and Genomics = Yi Chuan Xue Bao. 38: 403-9. PMID 21930099 DOI: 10.1016/j.jgg.2011.08.003  0.36
2011 Jacquemont S, Reymond A, Zufferey F, Harewood L, Walters RG, Kutalik Z, Martinet D, Shen Y, Valsesia A, Beckmann ND, Thorleifsson G, Belfiore M, Bouquillon S, Campion D, de Leeuw N, ... ... Wu BL, et al. Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. Nature. 478: 97-102. PMID 21881559 DOI: 10.1038/nature10406  0.36
2011 Shen Y, An Y, Wu BL. Standardization and diversification of copy number microarray testing for clinical diagnostics--implications of the cross-platform/algorithm study on clinical diagnostic chromosomal microarray analysis. Clinical Chemistry. 57: 1354-6. PMID 21852392 DOI: 10.1373/clinchem.2011.171769  0.92
2011 Du ZP, Yuan HM, Wu BL, Chang JX, Lv Z, Shen J, Wu JY, Chen HB, Li EM, Xu LY. Neutrophil gelatinase-associated lipocalin in gastric carcinoma cells and its induction by TPA are controlled by C/EBPβ. Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire. 89: 314-24. PMID 21612443 DOI: 10.1139/o11-002  0.4
2011 Tian H, Wu BL, Bi ZY, Jiao PF, Zhao WD, Sun FY, Xu HY, Liu Y. [Application of three-dimensional laser scanning-based maxillofacial soft tissue reconstruction in orthodontic treatment]. Nan Fang Yi Ke Da Xue Xue Bao = Journal of Southern Medical University. 31: 864-6. PMID 21602144  0.48
2011 Kluk MJ, An Y, James P, Coulter D, Harris D, Wu BL, Shen Y. Avoiding pitfalls in molecular genetic testing: case studies of high-resolution array comparative genomic hybridization testing in the definitive diagnosis of Mowat-Wilson syndrome. The Journal of Molecular Diagnostics : Jmd. 13: 363-7. PMID 21497296 DOI: 10.1016/j.jmoldx.2011.01.008  0.36
2011 Shen Y, Chen X, Wang L, Guo J, Shen J, An Y, Zhu H, Zhu Y, Xin R, Bao Y, Gusella JF, Zhang T, Wu BL. Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 225-32. PMID 21302351 DOI: 10.1002/ajmg.b.31147  0.36
2011 Wu BL, Xu LY, Du ZP, Liao LD, Zhang HF, Huang Q, Fang GQ, Li EM. MiRNA profile in esophageal squamous cell carcinoma: downregulation of miR-143 and miR-145. World Journal of Gastroenterology : Wjg. 17: 79-88. PMID 21218087 DOI: 10.3748/wjg.v17.i1.79  0.4
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