Zheng Wang

De novo heterozygous variants in KIF5B cause kyphomelic dysplasia

Long Guo, N. Matsumoto, H. Ohashi, 2022, Clinical genetics.

Deficiency of TMEM53 causes a previously unknown sclerosing bone disorder by dysregulation of BMP-SMAD signaling

Long Guo, T. Nakashima, N. Matsumoto, 2021, Nature Communications.

Identification of six novel variants from nine Chinese families with hypophosphatemic rickets

T. Yang, S. Ikegawa, W. Xia, 2022, BMC medical genomics.

Identification of novel FBN1 variations implicated in congenital scoliosis

Zhihong Wu, Shuyang Zhang, G. Qiu, 2019, Journal of Human Genetics.

Hypomorphic Mutations in TONSL Cause SPONASTRIME Dysplasia.

O. Mäkitie, Dongsup Kim, G. Stewart, 2019, American journal of human genetics.

SLC4A2 Deficiency Causes a New Type of Osteopetrosis

Long Guo, N. Matsumoto, N. Miyake, 2021, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Exome Sequencing in Monogenic Forms of Rickets

K. Girisha, A. Dalal, S. Ikegawa, 2023, Indian Journal of Pediatrics.

Bi-allelic loss-of-function variants in TMEM53 cause a novel type of sclerosing bone disorder in human and mouse

Long Guo, S. Ikegawa, Zheng Wang, 2021 .

Novel DNA Damage-Related Subtypes Characterization Identifies Uterine Corpus Endometrial Carcinoma (UCEC) Based on Machine Learning

Yunfeng Jin, Zheng Wang, Liping Chen, 2022, Journal of oncology.

Null and missense mutations of ERI1 cause a recessive phenotypic dichotomy in humans.

J. Rosenfeld, Long Guo, J. Clayton-Smith, 2023, American journal of human genetics.

Heterozygous mutations in the straitjacket region of the latency-associated peptide domain of TGFB2 cause Camurati-Engelmann disease type II.

Long Guo, K. Yoshiura, M. Shiina, 2024, Journal of human genetics.