Jian Han

The Recurrent Mutation in PATL2 Inhibits Its Degradation Thus Causing Female Infertility Characterized by Oocyte Maturation Defect Through Regulation of the Mos-MAPK Pathway

Ling-bo Cai, Xiang Ma, Junqiang Zhang, 2021, Frontiers in Cell and Developmental Biology.

OPA1 mutations and mitochondrial DNA haplotypes in autosomal dominant optic atrophy

N. Newman, Haomiao Jia, V. Biousse, 2006, Genetics in Medicine.

RET Germline Mutations Identified by Exome Sequencing in a Chinese Multiple Endocrine Neoplasia Type 2A/Familial Medullary Thyroid Carcinoma Family

Jian-Guo Zhang, Xian-ning Zhang, Xiao-ling Chen, 2011, PloS one.

RET proto-oncogene genetic screening of families with multiple endocrine neoplasia type 2 optimizes diagnostic and clinical management in China.

Jun Cheng, Xian-ning Zhang, Xiao-ling Chen, 2012, Thyroid : official journal of the American Thyroid Association.

NLRP7 participates in the human subcortical maternal complex and its variants cause female infertility characterized by early embryo arrest

Junqiang Zhang, R. Huo, Chun Zhao, 2023, Journal of Molecular Medicine.

Assignment of a Human Voltage-Dependent Sodium Channel α-Subunit Gene (SCN6A) to 2q21-q23

A. George, M. Tamkun, G. B. Brown, 1994 .

Mutations in CCNB3 affect its location thus causing a multiplicity of phenotypes in human oocytes maturation by aberrant CDK1 activity and APC/C activity at different stages

Yuan Zhang, Junqiang Zhang, R. Huo, 2023, Journal of Ovarian Research.

Direct amplification of a single dissected chromosomal segment by polymerase chain reaction: a human brain sodium channel gene is on chromosome 2q22-q23.

G. B. Brown, T. Rado, J. Han, 1991, Proceedings of the National Academy of Sciences of the United States of America.