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Qing Wang

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TOP 3
Gong-Qing Shen; Eric J Topol; Qiuyun Chen; Domenico Girelli; Lin Li; Nicola Martinelli; Oliviero Olivieri; Qing K Wang
Multi-allelic haplotype association identifies novel information different from single-SNP analysis: A new protective haplotype in the LRP8 gene is against familial and early-onset CAD and MI.
Susmita Chakrabarti; Keli Hu; Qing K Wang; Ling Wu; Xiaofen Wu; Zhaogang Yang; Sandro L Yong; Cuntai Zhang; Qiuyun Chen
MOG1 Rescues Defective Trafficking of Nav1.5 Mutations in Brugada Syndrome and Sick Sinus Syndrome.
Ying Liu; Xue Qin; Deng-Ke Wang; Qing K Wang; Zhang-Dong Xie; De-Zhi Jiang; Mugen Liu; Li-Ming Chen
Cloning and functional characterization of novel variants and tissue-specific expression of alternative amino and carboxyl termini of products of slc4a10.

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All Publications

2013: Gong-Qing Shen; Eric J Topol; Qiuyun Chen; Domenico Girelli; Lin Li; Nicola Martinelli; Oliviero Olivieri; Qing K Wang
Multi-allelic haplotype association identifies novel information different from single-SNP analysis: A new protective haplotype in the LRP8 gene is against familial and early-onset CAD and MI.
Gene 2013;521(1):78-81.
2013: Susmita Chakrabarti; Keli Hu; Qing K Wang; Ling Wu; Xiaofen Wu; Zhaogang Yang; Sandro L Yong; Cuntai Zhang; Qiuyun Chen
MOG1 Rescues Defective Trafficking of Nav1.5 Mutations in Brugada Syndrome and Sick Sinus Syndrome.
Circulation. Arrhythmia and electrophysiology 2013;6(2):392-401.
2013: Ying Liu; Xue Qin; Deng-Ke Wang; Qing K Wang; Zhang-Dong Xie; De-Zhi Jiang; Mugen Liu; Li-Ming Chen
Cloning and functional characterization of novel variants and tissue-specific expression of alternative amino and carboxyl termini of products of slc4a10.
PloS one 2013;8(2):e55974.
2012: Gong-Qing Shen; Lin Li; Qing K Wang
Genetic variant R952Q in LRP8 is associated with increased plasma triglyceride levels in patients with early-onset CAD and MI.
Annals of human genetics 2012;76(3):193-9.
2012: Cheng Wang; Junhan Wang; Lianqing Wang; Qing K Wang; Tao Wang; Haibo Xu; Jing Yao; Lu Zhang; Xue Zhang; Xiang-Yang Zhang; Miguel Baquero; Xiaoniu Cui; Xiaohua Dai; João R M de Oliveira; Shenglei Feng; Ian C Forster; Yong Gao; Yulei Li; Juan Liu; Mugen Liu; Hongying Ma; Xixiang Ma; Monica Patti; Beatriz Quintáns; Jie Ren; Lei Shi; María-Jesús Sobrido; Jing-Yu Liu
Mutations in SLC20A2 link familial idiopathic basal ganglia calcification with phosphate homeostasis.
Nature genetics 2012;44(3):254-6.
2011: Xiukun Cui; Rong Du; Jingyu Liu; Ying Liu; Zhaohui Tang; Qing K Wang; Feng Zeng; Tailan Zhan; Jing Zhang; Stephen Archacki; Mugen Liu
A novel SCN1A missense mutation causes generalized epilepsy with febrile seizures plus in a Chinese family.
Neuroscience letters 2011;503(1):27-30.
2011: Qinbo Yang; Qiuyun Chen; Nancy Foldvary-Schaefer; Lin Li; William G Ondo; Qing K Wang
Association studies of variants in MEIS1, BTBD9, and MAP2K5/SKOR1 with restless legs syndrome in a US population.
Sleep medicine 2011;12(8):800-4.
2011: Hu Ding; Rutai Hui; Xin Tu; Qing K Wang; Xiaojing Wang; Chenqi Xu; Yujun Xu; Xunna Bao; Guanglin Cui; Dao Wen Wang
No evidence for association of 12p13 SNPs rs11833579 and rs12425791 within NINJ2 gene with ischemic stroke in Chinese Han population.
Atherosclerosis 2011;216(2):381-2.
2011: Cong Li; Fan Wang; Yanzong Yang; Fenfen Fu; Chengqi Xu; Lisong Shi; Sisi Li; Yunlong Xia; Gang Wu; Xiang Cheng; Hui Liu; Chuchu Wang; Pengyun Wang; Jianjun Hao; Yuhe Ke; Yuanyuan Zhao; Mugen Liu; Rongfeng Zhang; Lianjun Gao; Bo Yu; Qiutang Zeng; Yuhua Liao; Bo Yang; Xin Tu; Qing K Wang
Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population.
Human genetics 2011;129(3):239-46.
2011: Qinbo Yang; Lin Li; Rong Yang; Gong-Qing Shen; Qiuyun Chen; Nancy Foldvary-Schaefer; William G Ondo; Qing K Wang
Family-based and population-based association studies validate PTPRD as a risk factor for restless legs syndrome.
Movement disorders : official journal of the Movement Disorder Society 2011;26(3):516-9.
2011: Xiang Cheng; Lisong Shi; Shaofang Nie; Fan Wang; Xiuchun Li; Chengqi Xu; Pengyun Wang; Baofeng Yang; Qingxian Li; Zhenwei Pan; Yue Li; Hao Xia; Chenhong Zheng; Yuhe Ke; Yanxia Wu; Tingting Tang; Xinxin Yan; Yan Yang; Ni Xia; Rui Yao; Binbin Wang; Xu Ma; Qiutang Zeng; Xin Tu; Yuhua Liao; Qing K Wang
The same chromosome 9p21.3 locus is associated with type 2 diabetes and coronary artery disease in a Chinese Han population.
Diabetes 2011;60(2):680-4.
2011: Ping Ouyang; Elizabeth Saarel; Ying Bai; Chunyan Luo; Qiulun Lv; Yan Xu; Fan Wang; Chun Fan; Adel Younoszai; Qiuyun Chen; Xin Tu; Qing K Wang
A de novo mutation in NKX2.5 associated with atrial septal defects, ventricular noncompaction, syncope and sudden death.
Clinica chimica acta; international journal of clinical chemistry 2011;412(1-2):170-5.
2011: Li Zhou; Yujun Xu; Xiaomin Zhang; Longxian Cheng; Guanglin Cui; Hu Ding; Meian He; Frank B Hu; Suli Huang; Ying Shi; Daowen Wang; Qing K Wang; Tangchun Wu
Genetic variants at newly identified lipid loci are associated with coronary heart disease in a Chinese Han population.
PloS one 2011;6(11):e27481.
2011: Yong Gao; Kangjuan Yang; Shujiang Xu; Cheng Wang; Juan Liu; Zibo Zhang; Mingxiong Yuan; Xiaoping Luo; Mugen Liu; Qing K Wang; Jing Yu Liu
Identification of compound heterozygous mutations in GNPTG in three siblings of a Chinese family with mucolipidosis type III gamma.
Molecular genetics and metabolism 2011;102(1):107-9.
2010: Xiaohua Dai; Yong Gao; Zhenping Xu; Xiaoniu Cui; Juan Liu; Yulei Li; Haibo Xu; Mugen Liu; Qing K Wang; Jing Yu Liu
Identification of a novel genetic locus on chromosome 8p21.1-q11.23 for idiopathic basal ganglia calcification.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010;153B(7):1305-10.
2010: Chengqi Xu; Fan Wang; Binbin Wang; Xiuchun Li; Cong Li; Dan Wang; Xin Xiong; Pengyun Wang; Qiulun Lu; Xiaojing Wang; Qin Yang; Dan Yin; Yufeng Huang; Liying Ji; Nan Wang; Shanshan Chen; Xiang Cheng; Yuhua Liao; Xu Ma; Dingfeng Su; Guohua Chen; Hao Xia; Lisong Shi; Xin Tu; Qing K Wang
Minor allele C of chromosome 1p32 single nucleotide polymorphism rs11206510 confers risk of ischemic stroke in the Chinese Han population.
Stroke; a journal of cerebral circulation 2010;41(8):1587-92.
2010: Pengyun Wang; Qinbo Yang; Xiaofen Wu; Yanzong Yang; Lisong Shi; Chuchu Wang; Gang Wu; Yunlong Xia; Bo Yang; Rongfeng Zhang; Chengqi Xu; Xiang Cheng; Sisi Li; Yuanyuan Zhao; Fenfen Fu; Yuhua Liao; Fang Fang; Qiuyun Chen; Xin Tu; Qing K Wang
Functional dominant-negative mutation of sodium channel subunit gene SCN3B associated with atrial fibrillation in a Chinese GeneID population.
Biochemical and biophysical research communications 2010;398(1):98-104.
2010: Rong Yang; Lin Li; Sara Seidelmann; Gong-Qing Shen; Sonia Sharma; Shaoqi Rao; Kalil Abdullah; Kenneth G Mackinlay; Robert C Elston; Qiuyun Chen; Eric J Topol; Qing K Wang
A genome-wide linkage scan identifies multiple quantitative trait loci for HDL-cholesterol levels in families with premature CAD and MI.
Journal of lipid research 2010;51(6):1442-51.
2010: Xiaoyan Wu; Qing K Wang; Le Gui; Mugen Liu; Xianqin Zhang; Runming Jin; Wei Li; Lu Yan; Rong Du; Qiufen Wang; Jianfang Zhu; Junguo Yang
Identification of a new lamin A/C mutation in a Chinese family affected with atrioventricular block as the prominent phenotype.
Journal of Huazhong University of Science and Technology. Medical sciences = Hua zhong ke ji da xue xue bao. Yi xue Ying De wen ban = Huazhong keji daxue xuebao. Yixue Yingdewen ban 2010;30(1):103-7.
2010: Yukan Huang; Jing Zhang; Chang Li; Guohua Yang; Mugen Liu; Qing K Wang; Zhaohui Tang
Identification of a novel homozygous nonsense mutation in EYS in a Chinese family with autosomal recessive retinitis pigmentosa.
BMC medical genetics 2010;11():121.
2009: Qi Wang; Ying Diao; Zhenping Xu; Xiaohui Li; Xiao Ping Luo; Haibo Xu; Ping Ouyang; Mugen Liu; Zhongli Hu; Qing K Wang; Jing Yu Liu
Identification of a novel splicing mutation in the growth hormone (GH)-releasing hormone receptor gene in a Chinese family with pituitary dwarfism.
Molecular and cellular endocrinology 2009;313(1-2):50-6.
2009: Lisong Shi; Cong Li; Chuchu Wang; Yunlong Xia; Gang Wu; Fan Wang; Chengqi Xu; Pengyun Wang; Xiuchun Li; Dan Wang; Xin Xiong; Ying Bai; Mugen Liu; Jingyu Liu; Xiang Ren; Lianjun Gao; Binbin Wang; Qiutang Zeng; Bo Yang; Xu Ma; Yanzong Yang; Xin Tu; Qing K Wang
Assessment of association of rs2200733 on chromosome 4q25 with atrial fibrillation and ischemic stroke in a Chinese Han population.
Human genetics 2009;126(6):843-9.
2009: Tie Ke; Cladelis Rubio Gomez; Heidi Eliana Mateus; Juan Andres Castano; Qing K Wang
Novel CACNA1S mutation causes autosomal dominant hypokalemic periodic paralysis in a South American family.
Journal of human genetics 2009;54(11):660-4.
2009: Hui Li; Tailan Zhan; Chang Li; Mugen Liu; Qing K Wang
Repression of MHC class I transcription by HPV16E7 through interaction with a putative RXRbeta motif and NF-kappaB cytoplasmic sequestration.
Biochemical and biophysical research communications 2009;388(2):383-8.
2009: Chun Fan; Qiuyun Chen; Qing K Wang
Functional role of transcriptional factor TBX5 in pre-mRNA splicing and Holt-Oram syndrome via association with SC35.
The Journal of biological chemistry 2009;284(38):25653-63.
2009: Gong-Qing Shen; Kalil Abdullah; Qing K Wang
The TaqMan method for SNP genotyping.
Methods in molecular biology (Clifton, N.J.) 2009;578():293-306.
2008: Xiao-Hua Dai; Wen-Wu Chen; Xu Wang; Qi-Hui Zhu; Cong Li; Lin Li; Mu-Gen Liu; Qing K Wang; Jing-Yu Liu
A novel genetic locus for familial febrile seizures and epilepsy on chromosome 3q26.2-q26.33.
Human genetics 2008;124(4):423-9.
2008: Y Hu; Lin Li; Sara Seidelmann; A A Timur; P H Shen; D J Driscoll; Qing K Wang
Identification of association of common AGGF1 variants with susceptibility for Klippel-Trenaunay syndrome using the structure association program.
Annals of human genetics 2008;72(Pt 5):636-43.
2008: Kalil Abdullah; Lin Li; Gong-Qing Shen; Y Hu; Y Yang; K G MacKinlay; Eric J Topol; Qing K Wang
Four SNPS on chromosome 9p21 confer risk to premature, familial CAD and MI in an American Caucasian population (GeneQuest).
Annals of human genetics 2008;72(Pt 5):654-7.
2008: Ping Liu; Shouyan Zhang; Qi Yao; Xiangyang Liu; Xu Wang; Changzheng Huang; Xinyuan Huang; Pengyun Wang; Mingxiong Yuan; Jing Yu Liu; Qing K Wang; Mugen Liu
Identification of a genetic locus for autosomal dominant disseminated superficial actinic porokeratosis on chromosome 1p31.3-p31.1.
Human genetics 2008;123(5):507-13.
2008: Shirong Zhang; Lejin Wang; Yansheng Hao; Pengyun Wang; Ping Hao; Ke Yin; Qing K Wang; Mugen Liu
T14484C and T14502C in the mitochondrial ND6 gene are associated with Leber's hereditary optic neuropathy in a Chinese family.
Mitochondrion 2008;8(3):205-10.
2008: Ping Liu; Qingyu Yang; Xu Wang; Aiping Feng; Tao Yang; Rong Yang; Pengyun Wang; Mingxiong Yuang; Mugen Liu; Jing Yu Liu; Qing K Wang
Identification of a genetic locus for ichthyosis vulgaris on chromosome 10q22.3-q24.2.
The Journal of investigative dermatology 2008;128(6):1418-22.
2008: Hui Li; Chang Li; Qiulun Lu; Ting Su; Tie Ke; David Wan-Cheng Li; Mingxiong Yuan; Jingyu Liu; Xiang Ren; Zhihong Zhang; Shaoqiong Zeng; Qing K Wang; Mugen Liu
Cataract mutation P20S of alphaB-crystallin impairs chaperone activity of alphaA-crystallin and induces apoptosis of human lens epithelial cells.
Biochimica et biophysica acta 2008;1782(5):303-9.
2008: Sara Seidelmann; Lin Li; Gong-Qing Shen; Eric J Topol; Qing K Wang
Identification of a novel locus for triglyceride on chromosome 1p31-32 in families with premature CAD and MI.
Journal of lipid research 2008;49(5):1034-8.
2008: Ling Wu; Sandro L Yong; Chun Fan; Ying Ni; Shin Yoo; Teng Zhang; Xianqin Zhang; Carlos A Obejero-Paz; Hyun-Jin Rho; Tie Ke; Przemyslaw Szafranski; Stephen W Jones; Qiuyun Chen; Qing K Wang
Identification of a new co-factor, MOG1, required for the full function of cardiac sodium channel Nav 1.5.
The Journal of biological chemistry 2008;283(11):6968-78.
2008: Jing Yu Liu; Xiaohua Dai; Jiqun Sheng; Xin Cui; Xu Wang; Xueqing Jiang; Xin Tu; Zhaohui Tang; Yan Bai; Mugen Liu; Qing K Wang
Identification and functional characterization of a novel splicing mutation in RP gene PRPF31.
Biochemical and biophysical research communications 2008;367(2):420-6.
2008: X Ren; J Y Liu; L Y Zhai; Q Yao; X Dai; Z Cai; P Liu; K Sun; C Huang; Qing K Wang; M Liu
A splicing mutation in the COL7A1 gene causes autosomal dominant dystrophic epidermolysis bullosa pruriginosa.
The British journal of dermatology 2008;158(3):618-20.
2008: Gong-Qing Shen; Lin Li; Shaoqi Rao; Kalil Abdullah; Ji Min Ban; Bok-Soo Lee; Jeong Euy Park; Qing K Wang
Four SNPs on chromosome 9p21 in a South Korean population implicate a genetic locus that confers high cross-race risk for development of coronary artery disease.
Arteriosclerosis, thrombosis, and vascular biology 2008;28(2):360-5.
2008: Shirong Zhang; Mugen Liu; Jia Mei Dong; Ke Yin; Pengyun Wang; Juan Bu; Jing Li; Yan Sheng Hao; Ping Hao; Qing K Wang; Lejin Wang
Identification of a genetic locus for autosomal dominant infantile cataract on chromosome 20p12.1-p11.23 in a Chinese family.
Molecular vision 2008;14():1893-7.
2008: Xianqin Zhang; Shenghan Chen; Li Zhang; Mugen Liu; Sharon Redfearn; Randall M Bryant; Carlos Oberti; G Michael Vincent; Qing K Wang
Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2 mutations.
BMC medical genetics 2008;9():87.
2008: Su Zhang; Ke Yin; Xiang Ren; Pengyun Wang; Shirong Zhang; Lingling Cheng; Junguo Yang; Jing Yu Liu; Mugen Liu; Qing K Wang
Identification of a novel KCNQ1 mutation associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long QT syndrome in a Chinese family.
BMC medical genetics 2008;9():24.
2008: Gong-Qing Shen; Shaoqi Rao; Nicola Martinelli; Lin Li; Oliviero Olivieri; Roberto Corrocher; Kalil Abdullah; Stanley L Hazen; Jonathan D. Smith; John Barnard; Edward F Plow; Domenico Girelli; Qing K Wang
Association between four SNPs on chromosome 9p21 and myocardial infarction is replicated in an Italian population.
Journal of human genetics 2008;53(2):144-50.
2007: Gong-Qing Shen; Lin Li; Domenico Girelli; Sara Seidelmann; Shaoqi Rao; Chun Fan; Jeong Euy Park; Quansheng Xi; Jing Li; Ying Hu; Oliviero Olivieri; Kandice Marchant; John Barnard; Roberto Corrocher; Robert Elston; June Cassano; Susan Henderson; Stanley L Hazen; Edward F Plow; Eric J Topol; Qing K Wang
An LRP8 variant is associated with familial and premature coronary artery disease and myocardial infarction.
American journal of human genetics 2007;81(4):780-91.
2007: Ling Wu; Stephen R Archacki; Teng Zhang; Qing K Wang
Induction of high STAT1 expression in transgenic mice with LQTS and heart failure.
Biochemical and biophysical research communications 2007;358(2):449-54.
2007: Teng Zhang; Sandro L Yong; Xiao-Li Tian; Qing K Wang
Cardiac-specific overexpression of SCN5A gene leads to shorter P wave duration and PR interval in transgenic mice.
Biochemical and biophysical research communications 2007;355(2):444-50.
2007: Xiao-Li Tian; Yuanna Cheng; Teng Zhang; Mei-Ling Chang Liao; Sandro L Yong; Qing K Wang
Optical mapping of ventricular arrhythmias in LQTS mice with SCN5A mutation N1325S.
Biochemical and biophysical research communications 2007;352(4):879-83.
2007: Sandro L Yong; Ying Ni; Teng Zhang; David J Tester; Michael J Ackerman; Qing K Wang
Characterization of the cardiac sodium channel SCN5A mutation, N1325S, in single murine ventricular myocytes.
Biochemical and biophysical research communications 2007;352(2):378-83.
2007: Shao-Qi Rao; Liang-De Xu; Guang-Mei Zhang; Xia Li; Lin Li; Gong-Qing Shen; Yang Jiang; Yue-Ying Yang; Bin-Sheng Gong; Wei Jiang; Fan Zhang; Yun Xiao; Qing K Wang
Familial aggregation analysis of gene expressions.
BMC proceedings 2007;1 Suppl 1():S49.
2007: Wei Chang; Qianbin Ding; Zhaohui Tang; Ping Liu; Fagang Jiang; Tie Ke; Xiang Ren; Zhi Wang; Jingyu Liu; Qing K Wang; Mugen Liu
A novel de novo frameshift mutation of RPGR ORF15 is associated with X-linked retinitis pigmentosa in a Chinese family.
Molecular vision 2007;13():1548-54.
2007: Xianqin Zhang; Lanying Chen; Jingyu Liu; Zhen Zhao; Erjun Qu; Xiaotao Wang; Wei Chang; Chengqi Xu; Qing K Wang; Mugen Liu
A novel DSPP mutation is associated with type II dentinogenesis imperfecta in a Chinese family.
BMC medical genetics 2007;8():52.
2007: Jing Yu Liu; Xiang Ren; Xiufeng Yang; Tangying Guo; Qi Yao; Lin Li; Xiaohua Dai; Mingchang Zhang; Lejin Wang; Mugen Liu; Qing K Wang
Identification of a novel GPR143 mutation in a large Chinese family with congenital nystagmus as the most prominent and consistent manifestation.
Journal of human genetics 2007;52(6):565-70.
2006: Eric J Topol; Jonathan D. Smith; Edward F Plow; Qing K Wang
Genetic susceptibility to myocardial infarction and coronary artery disease.
Human molecular genetics 2006;15 Spec No 2():R117-23.
2006: Xu Wang; Fuying Xiao; Qinbo Yang; Bo Liang; Zhaohui Tang; Linbin Jiang; Qihui Zhu; Wei Chang; Jiuxi Jiang; Chuanming Jiang; Xiang Ren; Jing-Yu Liu; Qing K Wang; Mugen Liu
A novel mutation in GDF5 causes autosomal dominant symphalangism in two Chinese families.
American journal of medical genetics. Part A 2006;140A(17):1846-53.
2006: Mugen Liu; Tie Ke; Zhaoxiang Wang; Qinbo Yang; Wei Chang; Fagang Jiang; Zhaohui Tang; Hui Li; Xiang Ren; Xu Wang; Tao Wang; Qingchun Li; Junguo Yang; Jingyu Liu; Qing K Wang
Identification of a CRYAB mutation associated with autosomal dominant posterior polar cataract in a Chinese family.
Investigative ophthalmology & visual science 2006;47(8):3461-6.
2006: Tie Ke; Qing K Wang; Binchu Ji; Xu Wang; Ping Liu; Xianqin Zhang; Zhaohui Tang; Xiang Ren; Mugen Liu
Novel HSF4 mutation causes congenital total white cataract in a Chinese family.
American journal of ophthalmology 2006;142(2):298-303.
2006: Alex Melamud; Gong-Qing Shen; D Chung; Quansheng Xi; E Simpson; Lin Li; Neal S Peachey; H Zegarra; Stephanie A Hagstrom; Qing K Wang; Elias Traboulsi
Mapping a new genetic locus for X linked retinitis pigmentosa to Xq28.
Journal of medical genetics 2006;43(6):e27.
2006: Liping Luo; Gong-Qing Shen; Karen A Stiffler; Qing K Wang; Thomas G Pretlow; Theresa P Pretlow
Loss of heterozygosity in human aberrant crypt foci (ACF), a putative precursor of colon cancer.
Carcinogenesis 2006;27(6):1153-9.
2006: Sandro L Yong; Qing K Wang
Animal models for cardiac arrhythmias.
Methods in molecular medicine 2006;129():127-48.
2006: Xiao-Li Tian; Qing K Wang
Generation of transgenic mice for cardiovascular research.
Methods in molecular medicine 2006;129():69-81.
2006: Sun-Ah You; Qing K Wang
Proteomics with two-dimensional gel electrophoresis and mass spectrometry analysis in cardiovascular research.
Methods in molecular medicine 2006;129():15-26.
2006: Stephen R Archacki; Qing K Wang
Microarray analysis of cardiovascular diseases.
Methods in molecular medicine 2006;129():1-13.
2006: Gong-Qing Shen; Albert Luo; Qing K Wang
High-throughput single-nucleotide polymorphisms genotyping: TaqMan assay and pyrosequencing assay.
Methods in molecular medicine 2006;128():209-24.
2006: Shaoqi Rao; Qing K Wang
SAGE programs: model-free linkage analysis for complex cardiovascular phenotypes.
Methods in molecular medicine 2006;128():61-89.
2006: Lin Li; Qing K Wang; Shaoqi Rao
LINKAGE programs: linkage analysis for monogenic cardiovascular diseases.
Methods in molecular medicine 2006;128():41-60.
2006: Ayse Anil Timur; Qing K Wang
Construction of somatic cell hybrid lines: fusion of mouse thymidine kinase-deficient 3T3 fibroblasts and human lymphoblastoid cells.
Methods in molecular medicine 2006;128():33-40.
2006: Ayse Anil Timur; Qing K Wang
Fluorescence in situ hybridization in cardiovascular disease.
Methods in molecular medicine 2006;128():11-21.
2006: Changzheng Huang; Qinbo Yang; Tie Ke; Haisheng Wang; Xu Wang; Jiqun Shen; Xin Tu; Jin Tian; Jing Yu Liu; Qing K Wang; Mugen Liu
A novel de novo frame-shift mutation of the EDA gene in a Chinese Han family with hypohidrotic ectodermal dysplasia.
Journal of human genetics 2006;51(12):1133-7.
2006: Mugen Liu; Xu Wang; Zhou Cai; Zhaohui Tang; Kangsheng Cao; Bo Liang; Xiang Ren; Jing Yu Liu; Qing K Wang
A novel heterozygous mutation in the Indian hedgehog gene (IHH) is associated with brachydactyly type A1 in a Chinese family.
Journal of human genetics 2006;51(8):727-31.
2006: J Y Liu; M F Ji; X R Wang; R L Luo; X Ren; M Liu; Qing K Wang
Detection of human chromosomal abnormalities using a new technique combining 4',6-diamidino-2-phenyl-indole staining and image analysis.
Clinical genetics 2006;69(1):65-71.
2006: Xia Li; Shaoqi Rao; Wei Jiang; Chuanxing Li; Yun Xiao; Zheng Guo; Qingpu Zhang; Lihong Wang; Lei Du; Jing Li; Li Li; Tianwen Zhang; Qing K Wang
Discovery of Time-Delayed Gene Regulatory Networks based on temporal gene expression profiling.
BMC bioinformatics 2006;7():26.
2005: Wei Du; Jocelyn F Bautista; Huanghe Yang; Ana Diez Sampedro; Sun-Ah You; Lejin Wang; Prakash Kotagal; Hans O Lüders; Jingyi Shi; Jianmin Cui; George B Richerson; Qing K Wang
Calcium-sensitive potassium channelopathy in human epilepsy and paroxysmal movement disorder.
Nature genetics 2005;37(7):733-8.
2005: Qing K Wang
Update on the molecular genetics of vascular anomalies.
Lymphatic research and biology 2005;3(4):226-33.