Rui Dong

发表

Analysis of clinical and genetic characteristics in 10 Chinese individuals with Cornelia de Lange syndrome and literature review

Z. Gai, Dong Wang, Jian Ma, 2020, Molecular genetics & genomic medicine.

Evaluation of a Viral Microarray Based on Simultaneous Extraction and Amplification of Viral Nucleotide Acid for Detecting Human Herpesviruses and Enteroviruses

Chun-xiu Zhang, Z. Gai, Yi Liu, 2015, PloS one.

Chromosome r(3)(p25.3q29) in a Patient with Developmental Delay and Congenital Heart Defects: A Case Report and a Brief Literature Review

Z. Gai, Kaihui Zhang, Yi Liu, 2016, Cytogenetic and Genome Research.

Refining critical regions in 15q24 microdeletion syndrome pertaining to autism

S. Scherer, M. Zarrei, Dongmei Zhao, 2020, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Chromosomal microarray analysis of 410 Han Chinese patients with autism spectrum disorder or unexplained intellectual disability and developmental delay

S. Scherer, E. Higginbotham, M. Zarrei, 2022, NPJ genomic medicine.

Generation of an induced pluripotent stem cell line (SDQLCHi008-A) from a patient with ASD and DD carrying an 830 kb de novo deletion at chr7q11.22 including the exon 1 of AUTS2 gene.

G. Pan, Z. Gai, Yi Liu, 2019, Stem cell research.

Rare de novo deletion of metabotropic glutamate receptor 7 (GRM7) gene in a patient with autism spectrum disorder

S. Scherer, M. Uddin, K. Tammimies, 2015, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Clinical characteristics and mutation analysis of five Chinese patients with maple syrup urine disease

Z. Gai, Qing Gao, Kaihui Zhang, 2018, Metabolic Brain Disease.

Genome-Wide Analysis of Long Noncoding RNA (lncRNA) Expression in Hepatoblastoma Tissues

Xianghuo He, K. Dong, P. Xue, 2014, PloS one.

De novo exon 1 deletion of AUTS2 gene in a patient with autism spectrum disorder and developmental delay: A case report and a brief literature review

S. Scherer, M. Uddin, K. Tammimies, 2015, American journal of medical genetics. Part A.

Association of IMMP2L deletions with autism spectrum disorder: A trio family study and meta‐analysis

S. Scherer, M. Uddin, M. Zarrei, 2018, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Familial intellectual disability as a result of a derivative chromosome 22 originating from a balanced translocation (3;22) in a four generation family

Y. Huang, Z. Gai, Kaihui Zhang, 2018, Molecular Cytogenetics.

Clinical Application of an Innovative Multiplex-Fluorescent-Labeled STRs Assay for Prader-Willi Syndrome and Angelman Syndrome

Shu Liu, N. Jana, Z. Gai, 2016, PloS one.

Genotypic and phenotypic characteristics of 12 chinese children with glycogen storage diseases

Z. Gai, Dong Wang, Kaihui Zhang, 2022, Frontiers in Genetics.

An induced pluripotent stem cells line (SDQLCHi014-A) derived from urine cells of a patient with ASD and hyperactivity carrying a 303 kb de novo deletion at chr3p26.1 implicating GRM7 gene.

Z. Gai, Yi Liu, Tiancheng Zhou, 2019, Stem cell research.

Establishment of a novel human iPSC line (SDQLCHi032-A) derived from a patient with primary hypertrophic osteoarthropathy caused by HPGD homozygous mutation.

Z. Gai, Yi Liu, Haiyan Zhang, 2021, Stem Cell Research.

Diagnostic application of exome sequencing in Chinese children with suspected inherited kidney diseases

Z. Gai, Dong Wang, Kaihui Zhang, 2023, Frontiers in Genetics.