Yuan Xue

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Genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing@@@Genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing

Yuan Xue, W. Wilcox, C. Stanislaw, 2016 .

Genetic evaluation and testing for hereditary forms of cancer in the era of next-generation sequencing

Yuan Xue, W. Wilcox, C. Stanislaw, 2016, Cancer biology & medicine.

Solving the molecular diagnostic testing conundrum for Mendelian disorders in the era of next-generation sequencing: single-gene, gene panel, or exome/genome sequencing

Yuan Xue, Arunkanth Ankala, M. Hegde, 2014, Genetics in Medicine.

Paternal duplication of the 11p15 centromeric imprinting control region is associated with increased expression of CDKN1C in a child with Russell–Silver syndrome

M. K. Rudd, Z. Dai, Yuan Xue, 2015, American journal of medical genetics. Part A.

Functional indel polymorphism within lncRNA GAS 5 and colorectal carcinoma risk

Yuan Xue, Chaoyang Li, Zhansheng Zhu, 2016 .

G 801 A polymorphism within SDF-1 predicts prognosis of colorectal carcinoma in a Chinese population

Yuan Xue, Chaoyang Li, Xueren Gao, 2016 .

Comparison of immune cells and diagnostic markers between spondyloarthritis and rheumatoid arthritis by bioinformatics analysis

Yuan Xue, Jiaqian Wang, Liang Zhou, 2022, Journal of translational medicine.

Functional STR within PTPN11: a novel potential risk factor for colorectal cancer.

J. Aweya, Yuan Xue, Zhansheng Zhu, 2017, International journal of clinical and experimental pathology.

FGFR3 mutation frequency in 324 cases from the International Skeletal Dysplasia Registry

D. Rimoin, W. Wilcox, Yuan Xue, 2014, Molecular genetics & genomic medicine.

Changing paradigm of cancer therapy: precision medicine by next-generation sequencing

W. Wilcox, Yuan Xue, 2016, Cancer biology & medicine.

A Novel ZRS Mutation Leads to Preaxial Polydactyly Type 2 in a Heterozygous Form and Werner Mesomelic Syndrome in a Homozygous Form

E. Jabs, N. Ahituv, W. Wilcox, 2014, Human mutation.

A novel functional indel polymorphism within long non-coding RNAs growth arrest specific 5 conferred risk for cervical squamous cell carcinoma in Chinese Han populations

Yuan Xue, Chaoyang Li, Zhansheng Zhu, 2017 .

Prognostic value of long noncoding RNA MALAT1 in various carcinomas: evidence from nine studies

Yuan Xue, Y. Teng, Yong Rui, 2015, Tumor Biology.

Exome Sequencing Identified a Splice Site Mutation in FHL1 that Causes Uruguay Syndrome, an X-Linked Disorder With Skeletal Muscle Hypertrophy and Premature Cardiac Death

Aliz R. Rao, S. Nelson, W. Wilcox, 2016, Circulation. Cardiovascular genetics.

Long noncoding RNA CCAT 2 as an independent prognostic marker in various carcinomas : evidence based on four studies

Yuan Xue, Y. Teng, Yong Rui, 2016 .