Zhiying Xie - Revision history

Zx2300 at 00:49, 23 February 2020

2020-02-23T00:49:44Z

Zx2300 at 00:12, 23 February 2020

2020-02-23T00:12:57Z

Zx2300 at 23:01, 22 February 2020

2020-02-22T23:01:42Z

Zx2300 at 22:39, 22 February 2020

2020-02-22T22:39:07Z

Zx2300: /* Zhiying Xie MD*/

2020-02-22T22:37:38Z

‎Zhiying Xie MD

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== Zhiying Xie ==

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← Older revision		Revision as of 00:49, 23 February 2020
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		+	Visiting PhD student
	==Education==		==Education==
	* MD, Clinical medicine, Soochow University, 2016		* MD, Clinical medicine, Soochow University, 2016

@@ Line 2: / Line 2: @@
 * MD, Clinical medicine, Soochow University, 2016
 * PhD, Neurology, Peking University, 2016 – present
-* A visiting PhD student, Bioinformatics, Columbia University, 2019 – present
+* Visiting PhD student, Bioinformatics, Columbia University, 2019 – present
 ==Research Interests==
@@ Line 9: / Line 9: @@
 * Clinical and pathological research in neuromuscular disorders
-==Professional Statement==
+==Personal statement==
 I am a PhD student, majoring in Neurology, in the Department of neurology at Peking University First Hospital. My PhD advisor, Prof. Yun Yuan, is a neurologist specialized in neuromuscular disorders. Under his guidance, my PhD research has focused on clinical, genetic, and pathological aspects of dystrophinopathies. Currently, I am a visiting PhD student in the Center for Statistical Genetics, Department of Neurology at Columbia University. I now perform research in the field of Bioinformatics, under the supervision of Prof. Suzanne M. Leal, in identifying pathogenic variants for inherited myopathies.

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 ==Education==
 * MD, Clinical medicine, Soochow University, 2016
@@ Line 17: / Line 15: @@
 ==Publications==
-* Xie Z, Hou Y, Yu M, Liu Y, Fan Y, Zhang W, Wang Z, Xiong H, Yuan Y. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=Clinical+and+genetic+spectrum+of+sarcoglycanopathies+in+a+large+cohort+of+Chinese+patients.]." ''Orphanet J Rare Dis.''. 2019 Feb 14;14(1):43. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=30764848 30764848]
+* Xie Z, Hou Y, Yu M, Liu Y, Fan Y, Zhang W, Wang Z, Xiong H, Yuan Y. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=30764848 Clinical and genetic spectrum of sarcoglycanopathies in a large cohort of Chinese patients.]." ''Orphanet J Rare Dis.''. 2019 Feb 14;14(1):43. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=30764848 30764848]
-* Xie Z, Xie Z, Yu M, Zheng Y, Sun C, Liu Y, Ling C, Zhu Y, Zhang W, Xiao J, Wang Z, Yuan Y. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=Value+of+muscle+magnetic+resonance+imaging+in+the+differential+diagnosis+of+muscular+dystrophies+related+to+the+dystrophin-glycoprotein+complex.]." ''Orphanet J Rare Dis.''. 2019 Nov 12;14(1):250. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=31747956 31747956]
+* Xie Z, Xie Z, Yu M, Zheng Y, Sun C, Liu Y, Ling C, Zhu Y, Zhang W, Xiao J, Wang Z, Yuan Y. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=31747956 Value of muscle magnetic resonance imaging in the differential diagnosis of muscular dystrophies related to the dystrophin-glycoprotein complex.]." ''Orphanet J Rare Dis.''. 2019 Nov 12;14(1):250. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=31747956 31747956]
-* Xie Z, Xiao J, Zheng Y, Wang Z, Yuan Y. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=Magnetic+Resonance+Imaging+Findings+in+the+Muscle+Tissue+of+Patients+with+Limb+Girdle+Muscular+Dystrophy+Type+2I+Harboring+the+Founder+Mutation+c.545A%3EG+in+the+FKRP+Gene.]." ''Biomed Res Int.''. 2018 May 29;2018:3710814. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=30003095 30003095]
+* Xie Z, Xiao J, Zheng Y, Wang Z, Yuan Y. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=30003095 Magnetic Resonance Imaging Findings in the Muscle Tissue of Patients with Limb Girdle Muscular Dystrophy Type 2I Harboring the Founder Mutation c.545A>G in the FKRP Gene.]." ''Biomed Res Int.''. 2018 May 29;2018:3710814. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=30003095 30003095]
-* Yin L, Xie ZY, Xu HY, Zheng SS, Wang ZX, Xiao JX, Yuan Y. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=T2+Mapping+and+Fat+Quantification+of+Thigh+Muscles+in+Children+with+Duchenne+Muscular+Dystrophy.]." ''Curr Med Sci.''. 2019 Feb;39(1):138-145. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=30868504 30868504]
+* Yin L, Xie ZY, Xu HY, Zheng SS, Wang ZX, Xiao JX, Yuan Y. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=30868504 T2 Mapping and Fat Quantification of Thigh Muscles in Children with Duchenne Muscular Dystrophy.]." ''Curr Med Sci.''. 2019 Feb;39(1):138-145. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=30868504 30868504]
-* Yu M, Zhu Y, Xie Z, Zheng Y, Xiao J, Zhang W, Nishino I, Yuan Y, Wang Z. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=Novel+TTN+mutations+and+muscle+imaging+characteristics+in+congenital+titinopathy.]." ''Ann Clin Transl Neurol.''. 2019 Jul;6(7):1311-1318. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=31353864 31353864]
+* Yu M, Zhu Y, Xie Z, Zheng Y, Xiao J, Zhang W, Nishino I, Yuan Y, Wang Z. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=31353864 Novel TTN mutations and muscle imaging characteristics in congenital titinopathy.]." ''Ann Clin Transl Neurol.''. 2019 Jul;6(7):1311-1318. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=31353864 31353864]
-* Deng J, Wu W, Xie Z, Gang Q, Yu M, Liu J, Wang Q, Lv H, Zhang W, Huang Y, Wang T, Yuan Y, Hong D, Wang Z. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=Novel+and+Recurrent+Mutations+in+a+Cohort+of+Chinese+Patients+With+Young-Onset+Amyotrophic+Lateral+Sclerosis.]." ''Front Neurosci.''. 2019 Dec 6;13:1289. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=31866807 31866807]
+* Deng J, Wu W, Xie Z, Gang Q, Yu M, Liu J, Wang Q, Lv H, Zhang W, Huang Y, Wang T, Yuan Y, Hong D, Wang Z. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=31866807 Novel and Recurrent Mutations in a Cohort of Chinese Patients With Young-Onset Amyotrophic Lateral Sclerosis.]." ''Front Neurosci.''. 2019 Dec 6;13:1289. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=31866807 31866807]
-* Yuan R, Yi J, Xie Z, Zheng Y, Han M, Hou Y, Wang Z, Yuan Y. "[https://www.ncbi.nlm.nih.gov/pubmed/29976999.]." ''J Hum Genet.''. 2018 Oct;63(10):1041-1048. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=29976999 29976999]
+* Yuan R, Yi J, Xie Z, Zheng Y, Han M, Hou Y, Wang Z, Yuan Y. "[https://www.ncbi.nlm.nih.gov/pubmed/29976999 Genotype-phenotype correlation in Becker muscular dystrophy in Chinese patients.]." ''J Hum Genet.''. 2018 Oct;63(10):1041-1048. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=29976999 29976999]
-* Liu Y, Zheng Y, Gang Q, Xie Z, Jin Y, Zhang X, Deng X, Hao H, Gao F, Zhang Z, Xiong H, Zhang W, Wang Z, Yuan Y. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=Perimysial+microarteriopathy+in+dermatomyositis+with+anti-nuclear+matrix+protein-2+antibodies.]." ''Eur J Neurol.''. 2020 Mar;27(3):514-521. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=31571350 31571350]
+* Liu Y, Zheng Y, Gang Q, Xie Z, Jin Y, Zhang X, Deng X, Hao H, Gao F, Zhang Z, Xiong H, Zhang W, Wang Z, Yuan Y. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=31571350 Perimysial microarteriopathy in dermatomyositis with anti-nuclear matrix protein-2 antibodies.]." ''Eur J Neurol.''. 2020 Mar;27(3):514-521. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=31571350 31571350]
-* Deng J, Lu Y, Xie Z, Liu J, Yuan Y, Wang Z. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=RNA-seq+profiling%2C+and+impaired+autophagic+process+in+skeletal+muscle+of+MELAS.]." ''Biochem Biophys Res Commun.''. 2020 Feb 26;523(1):91-97. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=31836143 31836143]
+* Deng J, Lu Y, Xie Z, Liu J, Yuan Y, Wang Z. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=31836143 RNA-seq profiling, and impaired autophagic process in skeletal muscle of MELAS.]." ''Biochem Biophys Res Commun.''. 2020 Feb 26;523(1):91-97. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=31836143 31836143]
-* Hou Y, Xie Z, Zhao X, Yuan Y, Dou P, Wang Z. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=Appendicular+skeletal+muscle+mass%3A+A+more+sensitive+biomarker+of+disease+severity+than+BMI+in+adults+with+mitochondrial+diseases.]." ''PLoS One.''. 2019 Jul 25;14(7):e0219628. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=31344055 31344055]
+* Hou Y, Xie Z, Zhao X, Yuan Y, Dou P, Wang Z. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=31344055 Appendicular skeletal muscle mass: A more sensitive biomarker of disease severity than BMI in adults with mitochondrial diseases.]." ''PLoS One.''. 2019 Jul 25;14(7):e0219628. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=31344055 31344055]
-* Li J, Meng L, Wu R, Xie Z, Gang Q, Zhang W, Wang Z, Yuan Y. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=Sural+nerve+pathology+in+TFG-associated+motor+neuron+disease+with+sensory+neuropathy.]." ''Neuropathology''. 2019 Jun;39(3):194-199. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=30957313 30957313]
+* Li J, Meng L, Wu R, Xie Z, Gang Q, Zhang W, Wang Z, Yuan Y. "[https://www.ncbi.nlm.nih.gov/pubmed/?term=30957313 Sural nerve pathology in TFG-associated motor neuron disease with sensory neuropathy.]." ''Neuropathology''. 2019 Jun;39(3):194-199. Pubmed PMID: [http://www.ncbi.nlm.nih.gov/pubmed/?term=30957313 30957313]
-* An J, Xie Z, Jia F, Wang Z, Yuan Y, Zhang J, Fang J. "[https://aip.scitation.org/doi/10.1063/1.5126116.]." ''Chaos''. 30, 023116 (2020)
+* An J, Xie Z, Jia F, Wang Z, Yuan Y, Zhang J, Fang J. "[https://aip.scitation.org/doi/10.1063/1.5126116 Quantitative coordination evaluation for screening children with Duchenne muscular dystrophy.]." ''Chaos''. 30, 023116 (2020)
 ==Contact Information==

← Older revision		Revision as of 22:39, 22 February 2020
Line 1:		Line 1:
−	~~__NOTITLE__~~	+	__Zhiying Xie MD__

	==Education==		==Education==

@@ Line 1: / Line 1: @@
 __NOTITLE__
-== Zhiying Xie ==
+==Education==
-You can follow from the formatting of this page:
+==Research Interests==
-http://statgen.us/Suzanne_M_Leal_PhD
+==Professional Statement==
-to edit your personal information. Please slack Gao if you need help uploading your profile picture, or have other technical issues. To learn about formatting in mediawiki syntax please check out: https://www.mediawiki.org/wiki/Help:Formatting
+My major interest is in the identification of genetic etiologies of neuromuscular disorders. I have published 12 peered reviewed articles regarding to neuromuscular disorders and most of them are related to genetic research. I am either first or co-first author on 4 of these articles.