Yi-feng Yang

发表

19p13.2 Microdeletion including NFIX associated with overgrowth and intellectual disability suggestive of Malan syndrome

Xiu-ying Wang, Haiyun Dong, Hui Zeng, 2016, Molecular Cytogenetics.

Rare copy number variations containing genes involved in RASopathies: deletion of SHOC2 and duplication of PTPN11

T. Zhao, Jian Wang, Yi-feng Yang, 2014, Molecular Cytogenetics.

Rare De Novo Copy Number Variants in Patients with Congenital Pulmonary Atresia

T. Zhao, Li Xie, Jian Wang, 2014, PloS one.

Novel mutation of EXT2 identified in a large family with multiple osteochondromas

Yi-feng Yang, Z. Tan, Xiaojun Chen, 2016, Molecular medicine reports.

A 1.1Mb deletion in distal 13q deletion syndrome region with congenital heart defect and postaxial polydactyly: additional support for a CHD locus at distal 13q34 region.

Li Xie, Jian Wang, Yi-feng Yang, 2013, Gene.

Microduplication of 3p25.2 encompassing RAF1 associated with congenital heart disease suggestive of Noonan syndrome

B. Yin, Cheng Luo, Jian Wang, 2012, American journal of medical genetics. Part A.

A Novel Nonsense MMP21 Variant Causes Dextrocardia and Congenital Heart Disease in a Han Chinese Patient

Yi-feng Yang, Z. Tan, Zhuang-zhuang Yuan, 2020, Frontiers in Cardiovascular Medicine.

Duplication of 8q12 encompassing CHD7 is associated with a distinct phenotype but without duane anomaly.

Hong Luo, Li Xie, Jian Wang, 2012, European journal of medical genetics.

Case Report: BAF-Opathies/SSRIDDs Due to a de novo ACTL6A Variant, Previously Considered to Be Heart-Hand Syndrome

Xiaohui Xie, Yi-qiao Hu, Yi-feng Yang, 2021, Frontiers in Cardiovascular Medicine.

Duplication of 10q22.3–q23.3 encompassing BMPR1A and NGR3 associated with congenital heart disease, microcephaly, and mild intellectual disability

T. Zhao, Li Xie, Jian Wang, 2015, American journal of medical genetics. Part A.

A novel nonsense PKD1L1 variant cause heterotaxy syndrome with congenital asplenia in a Han Chinese patient

Xiaohui Xie, Yi-feng Yang, Z. Tan, 2022, Journal of Human Genetics.

Clinical and molecular delineation of 16p13.3 duplication in a patient with congenital heart defect and multiple congenital anomalies

Jian Wang, Yi-feng Yang, Z. Tan, 2012, American journal of medical genetics. Part A.

Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia

Cheng Lei, T. Guo, Shuizi Ding, 2021, Human Genetics.

[Lung protection of continuous pulmonary artery perfusion with oxygenated blood during cardiopulmonary bypass].

Shaoqing Liu, Li-ming Liu, B. Yin, 2005, Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences.

Mutant CARD10 in a family with progressive immunodeficiency and autoimmunity

Cheng Lei, T. Guo, Shuizi Ding, 2020, Cellular & Molecular Immunology.

Identification of anaplastic lymphoma kinase as a potential therapeutic target in ovarian cancer.

S. Beausoleil, J. Rush, T. Gu, 2012, Cancer research.

Therapeutics , Targets , and Chemical Biology Identi fi cation of Anaplastic Lymphoma Kinase as a Potential Therapeutic Target in Ovarian Cancer

S. Beausoleil, J. Rush, T. Gu, 2012 .

Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia

Cheng Lei, T. Guo, Shuizi Ding, 2021, Human Genetics.

Rare copy number variations containing genes involved in RASopathies: deletion of SHOC2 and duplication of PTPN11

Jian Wang, Yi-feng Yang, Z. Tan, 2014, Molecular Cytogenetics.

Variations in/nearby genes coding for JAZF1, TSPAN8/LGR5 and HHEX-IDE and risk of type 2 diabetes in Han Chinese

Yun Liu, G. Feng, Zhuoyou Chen, 2010, Journal of Human Genetics.

576 kb deletion in 1p36.33-p36.32 containing SKI is associated with limb malformation, congenital heart disease and epilepsy.

Jian Wang, Yi Zhang, Xin Zhu, 2013, Gene.

Whole-exome sequencing identifies Y1495X of SCN5A to be associated with familial conduction disease and sudden death

Li Xie, Jian Wang, Yi-feng Yang, 2014, Scientific Reports.

19p13.2 Microdeletion including NFIX associated with overgrowth and intellectual disability suggestive of Malan syndrome

Xiu-ying Wang, Hui Zeng, Yi-qiao Hu, 2016, Molecular Cytogenetics.

Haploinsufficiency of syncoilin leads to hypertrophic cardiomyopathy

Hui Zeng, Yi-feng Yang, Z. Tan, 2022, Genes & diseases.

An effective combination of whole-exome sequencing and runs of homozygosity for the diagnosis of primary ciliary dyskinesia in consanguineous families

T. Guo, Hong Luo, Ping Chen, 2017, Scientific Reports.

Two novel mutations of the LDL receptor gene associated with familial hypercholesterolemia in a Chinese family.

K. Xia, Zhengmao Hu, J. Xia, 2007, Chinese medical journal.

Mutations in the gene encoding gap junction protein β-3 associated with autosomal dominant hearing impairment

K. Xia, Q. Pan, H. Dai, 1998, Nature Genetics.

Congenital heart defect and mental retardation in a patient with a 13q33.1-34 deletion.

Jian Wang, Yi-feng Yang, Z. Tan, 2012, Gene.

An Isolated Congenital Left Ventricular Diverticulum with Mitral Valve Endocarditis.

Yi-feng Yang, Can Huang, Lian Xiong, 2016, Heart, lung & circulation.

A clinical and molecular analysis of a patient with Emanuel syndrome.

Hong Luo, Ming Tu, Li Xie, 2017, Molecular medicine reports.

[Prosthetic valve replacement in pediatric patients: analysis of 105 cases].

F. Liu, Xin-min Zhou, B. Yin, 2005, Zhonghua yi xue za zhi.

A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

Jian-guang Tang, Hui Zeng, Yi-feng Yang, 2017, Cytogenetic and Genome Research.

Midterm Outcomes of Crosslinked Acellular Bovine Jugular Vein Conduit for Right Ventricular Outflow Tract Reconstruction

Tao Qian, Ting Lu, Zhong-shi Wu, 2021, Frontiers in Pediatrics.

Anomalous origin of the right pulmonary artery from the ascending aorta: results of direct implantation surgical repair in 6 infants

Zhong-shi Wu, Li Xie, Yi-feng Yang, 2015, Journal of Cardiothoracic Surgery.

A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal defect

Yi-feng Yang, Z. Tan, Jinlan Chen, 2014, Journal of Zhejiang University-SCIENCE B.

A Case of Isolated Congenital Left Ventricular Diverticulum with Acute Myocarditis

Yi-feng Yang, Can Huang, Qin Wu, 2014, Iranian journal of pediatrics.

Letter

Yi-feng Yang, Can Huang, Qin Wu, 2000 .

Identification of anaplastic lymphoma kinase as a potential therapeutic target in ovarian cancer.

S. Beausoleil, J. Rush, T. Gu, 2012, Cancer research.

A Novel Homozygous SACS Mutation Identified by Whole-Exome Sequencing in a Consanguineous Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

Jian-guang Tang, Hui Zeng, Yi-feng Yang, 2017, Cytogenetic and Genome Research.

Identification of a pathogenic SMCHD1 variant in a Chinese patient with bosma arhinia microphthalmia syndrome: a case report

Yi-feng Yang, Z. Tan, Zhuang-zhuang Yuan, 2024, BMC medical genomics.