Siyu Ma

Phenotype and genotype of FXIII deficiency in two unrelated probands: identification of a novel F13A1 large deletion mediated by complex rearrangement

Wenman Wu, Q. Ding, Yan Liu, 2019, Orphanet journal of rare diseases.

Whole exome sequencing reveals novel CEP104 mutations in a Chinese patient with Joubert syndrome

Zongfu Cao, Ruikun Cai, Yufei Yu, 2019, Molecular genetics & genomic medicine.

Genetic variability of human papillomavirus type 39 based on E6, E7 and L1 genes in Southwest China

Yanru Cui, Jiaoyu He, Junhang Deng, 2021, Virology Journal.

Identification of two novel pathogenic variants of PIBF1 by whole exome sequencing in a 2-year-old boy with Joubert syndrome

Yun Peng, Zongfu Cao, Ruikun Cai, 2020, BMC medical genetics.

Incidence and risk of herpes zoster in patients with ulcerative colitis and Crohn’s disease in the USA

J. Pawlowski, S. Poston, P. Thompson-Leduc, 2022, Gastroenterology report.

Incidence of Herpes Zoster in Patients With Rheumatoid Arthritis in the United States: A Retrospective Cohort Study

S. Poston, J. Curtis, P. Thompson-Leduc, 2023, The Journal of Rheumatology.