Jiong Tao

Jiong Tao

UNVERIFIED PROFILE

Are you Jiong Tao?   Register this Author

Register author
Jiong Tao

Jiong Tao

Publications by authors named "Jiong Tao"

Are you Jiong Tao?   Register this Author

35Publications

828Reads

38Profile Views

TAMM41 is required for heart valve differentiation via regulation of PINK-PARK2 dependent mitophagy.

Cell Death Differ 2019 Nov 1;26(11):2430-2446. Epub 2019 Mar 1.

CNRS-LIA Hematology and Cancer, Sino-French Research Center for Life Sciences and Genomics, State Key Laboratory of Medical Genomics, Rui Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/s41418-019-0311-zDOI Listing
November 2019

Parallel and Scalable Heat Methods for Geodesic Distance Computation.

IEEE Trans Pattern Anal Mach Intell 2019 Aug 6. Epub 2019 Aug 6.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1109/TPAMI.2019.2933209DOI Listing
August 2019

The influence of non-breathing-related sleep fragmentation on cognitive function in patients with cerebral small vessel disease.

Neuropsychiatr Dis Treat 2019 18;15:1009-1014. Epub 2019 Apr 18.

Department of Psychiatry, The Third Affiliated Hospital, Sun Yat-sen University, Guangzhou, 510630, People's Republic of China,

View Article

Download full-text PDF

Source
http://dx.doi.org/10.2147/NDT.S193869DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6476228PMC
April 2019

The clinical use of chromosomal microarray analysis in detection of fetal chromosomal rearrangements: a study from China Mainland.

Eur J Obstet Gynecol Reprod Biol 2017 May 7;212:44-50. Epub 2017 Mar 7.

Prenatal Diagnosis Center, International Peace Maternity & Child Health Hospital, Shanghai Jiao Tong University, School of Medicine, China. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ejogrb.2017.03.007DOI Listing
May 2017

Alterations of white matter fractional anisotropy in unmedicated obsessive-compulsive disorder.

Neuropsychiatr Dis Treat 2017 28;13:69-76. Epub 2016 Dec 28.

Mental Health Institute of the Second Xiangya Hospital, Central South University, Changsha.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.2147/NDT.S123669DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5207449PMC
December 2016

A genotype-phenotype correlation study reveals that a non-coding RNA might be associated with cardiovascular anomalies in fetuses with WHS.

Prenat Diagn 2016 Oct 19;36(10):979-981. Epub 2016 Aug 19.

Prenatal Diagnosis Center, International Peace Maternal & Child Health Hospital, Medical College, Shanghai JiaoTong University, Shanghai, China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/pd.4884DOI Listing
October 2016

[Analysis of AGG interspersion of the FMR1 gene in fragile X syndrome].

Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2015 Feb;32(1):11-5

Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai Institute for Pediatric Research, Shanghai 200092, P. R. China. Email:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3760/cma.j.issn.1003-9406.2015.01.003DOI Listing
February 2015

Alterations in white matter fractional anisotropy in subsyndromal perimenopausal depression.

BMC Psychiatry 2014 Dec 24;14:367. Epub 2014 Dec 24.

Department of Psychiatry, the Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, 510630, China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1186/s12888-014-0367-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4355552PMC
December 2014

A novel mutation in MID1 in a patient with X-linked Opitz G/BBB syndrome.

Gene 2014 Mar 26;537(1):140-2. Epub 2013 Dec 26.

Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, China; Shanghai Institute for Pediatric Research, China. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.gene.2013.12.018DOI Listing
March 2014

A rare case of 46, XX SRY-negative male with approximately 74-kb duplication in a region upstream of SOX9.

Eur J Med Genet 2013 Dec 18;56(12):695-8. Epub 2013 Oct 18.

Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China; Department of Genetics, Shanghai Institute for Pediatric Research, Shanghai, China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.ejmg.2013.10.001DOI Listing
December 2013

[Unbalanced subtelomic rearrangement involving 9q and 22q in a child with mental retardation and multiple congenital anomalies].

Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2013 Dec;30(6):666-9

Xinhua Hospital, Medical School of Shanghai Jiao Tong University, Shanghai Institute for Pediatric Research, Shanghai 200092, P.R. China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3760/cma.j.issn.1003-9406.2013.06.007DOI Listing
December 2013

Molecular prenatal diagnosis of autosomal recessive spinal muscular atrophies using quantification polymerase chain reaction.

Genet Test Mol Biomarkers 2013 May 28;17(5):438-42. Epub 2013 Feb 28.

Department of Prenatal Diagnosis Center, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1089/gtmb.2012.0481DOI Listing
May 2013

[A pilot study on spinal muscular atrophy carrier screening in Shanghai region using real-time PCR].

Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2013 Feb;30(1):1-4

Shanghai Jiaotong University School of Medicine, Shanghai, People's Republic of China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3760/cma.j.issn.1003-9406.2013.01.001DOI Listing
February 2013

[Molecular and cytogenetic characterization of six 46, XX males due to translocations between the short arms of X and Y chromosomes].

Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2012 Aug;29(4):408-12

Shanghai Jiaotong University School of Medicine, Shanghai, People's Republic of China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3760/cma.j.issn.1003-9406.2012.04.007DOI Listing
August 2012

[Clinical and genetic study of a case with Smith-Magenis syndrome].

Zhonghua Er Ke Za Zhi 2012 Mar;50(3):227-30

Department of Child and Adolescent Health Care, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai 200092, China.

View Article

Download full-text PDF

Source
March 2012

Serum inducible kinase is a positive regulator of cortical dendrite development and is required for BDNF-promoted dendritic arborization.

Cell Res 2012 Feb 21;22(2):387-98. Epub 2011 Jun 21.

Institute of Neuroscience and State Key Laboratory of Neuroscience, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Yueyang Road #320, ION building, Room 426, Shanghai 200031, China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/cr.2011.100DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271584PMC
February 2012

[A case with partial trisomy 7 (q34→qter) derived from a paternal reciprocal translocation t(7;14)(q34;q32)].

Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2011 Dec;28(6):654-7

Medical School of Shanghai Jiao Tong University, Shanghai Institute for Pediatric Research, Shanghai, People's Republic of China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3760/cma.j.issn.1003-9406.2011.06.012DOI Listing
December 2011

[Clinical application of multiplex ligation-dependent probe amplification for the detection exonic copy number alterations in the Dystrophin gene].

Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2011 Dec;28(6):699-704

Shanghai Institute for Pediatric Research, Shanghai Jiaotong University School of Medicine, Shanghai, People's Republic of China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3760/cma.j.issn.1003-9406.2011.06.023DOI Listing
December 2011

[Optimization of polymerase chain reaction assay combined with capillary electrophoresis to detect the pre- and full mutation of FMR1 gene].

Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2011 Aug;28(4):401-5

Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai Institute for Pediatric Research, Shanghai 200092, P. R. China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3760/cma.j.issn.1003-9406.2011.04.009DOI Listing
August 2011

[Two cases of partial trisomy 8p derived from paternal reciprocal translocation or maternal insertion translocation: clinical features and genetic abnormalities].

Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2011 Jun;28(3):247-50

Xinhua Hospital, Shanghai Jiaotong University Medical School, Shanghai Institute for Pediatric Research, Shanghai, 200092 P. R. China.

View Article

Download full-text PDF

Source
http://doi.med.wanfangdata.com.cn/10.3760/cma.j.issn.1003-94
Publisher Site
http://dx.doi.org/10.3760/cma.j.issn.1003-9406.2011.03.002DOI Listing
June 2011

CD44-SLC1A2 gene fusions in gastric cancer.

Sci Transl Med 2011 Apr;3(77):77ra30

Department of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, 5 Lower Kent Ridge Road, Singapore 119074, Singapore.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1126/scitranslmed.3001423DOI Listing
April 2011

CDKL5, a protein associated with rett syndrome, regulates neuronal morphogenesis via Rac1 signaling.

J Neurosci 2010 Sep;30(38):12777-86

Institute of Neuroscience and State Key Laboratory of Neuroscience, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200031, People's Republic of China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1523/JNEUROSCI.1102-10.2010DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6633570PMC
September 2010

[Cytogenetic and molecular genetic study of a case with 8p inverted duplication deletion syndrome].

Zhonghua Yi Xue Yi Chuan Xue Za Zhi 2010 Aug;27(4):361-6

Cytogenetic Department of Shanghai Institute for Pediatric Research, Xinhua Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, 200092 PR China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.3760/cma.j.issn.1003-9406.2010.04.001DOI Listing
August 2010

[Genetic tests and clinical re-evaluation of 85 children with suspected spinal muscular atrophy].

Zhonghua Er Ke Za Zhi 2010 Jun;48(6):425-30

Shanghai Institute for Pediatric Research, Xinhua Hospital Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai 200092, China.

View Article

Download full-text PDF

Source
June 2010

Functional SNPs in the SCGB3A2 promoter are associated with susceptibility to Graves' disease.

Hum Mol Genet 2009 Mar 6;18(6):1156-70. Epub 2009 Jan 6.

Ruijin Hospital, State Key Laboratory of Medical Genomics, Shanghai Institute of Endocrinology, Shanghai Jiao Tong University (SJTU), School of Medicine, Shanghai 20025, China.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/hmg/ddn442DOI Listing
March 2009

Integrative genomics identifies RAB23 as an invasion mediator gene in diffuse-type gastric cancer.

Cancer Res 2008 Jun;68(12):4623-30

National Cancer Centre, Department of Biochemistry, National University of Singapore, Duke-NUS Graduate Medical School, and Genome Institute of Singapore, Singapore, Singapore.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1158/0008-5472.CAN-07-5870DOI Listing
June 2008