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张浩波
职称:副主任医师
所在单位:妇儿与生殖健康研究院
教师拼音名称:
zhanghaobo
入职时间:
1997-09-01
所在单位:
妇儿与生殖健康研究院
性别:
男
在职信息:
在职
是否在职:
1
论文成果
[1] . Absence of murine CFAP61 causes male infertility due to multiple morphological abnormalities of the flagella. Science bulletin, 2020.
[2] 张文君. The impact of the COVID-19 pandemic on semen quality of uninfected men. BASIC AND CLINICAL ANDROLOGY, 33, 2023.
[3] . The impact of the COVID-19 pandemic on semen quality of uninfected men. Basic And Clinical Andrology, 2023.
[4] 于小宸. Does ICSI outcome in obstructive azoospermia differ according to the origin of retrieved spermatozoa or the cause of epididymal obstruction? A comparative study. International urology and nephrology, 2022.
[5] zhang xu. Mutational analysis of the GATA4 gene in Chinese men with nonobstructive azoospermia. Asian Journal of Andrology, 23, 205, 2021.
[6] 刘雯. Analysis of STAG3 variants in Chinese non-obstructive azoospermia patients with germ cell maturation arrest. Scientific Reports, 11, 2021.
[7] Liu, Chao. Paternal USP26 mutations raise Klinefelter syndrome risk in the offspring of mice and humans. EMBO Journal, 40, 2021.
[8] 于小宸. A new TEX11 mutation causes azoospermia and testicular meiotic arrest. Asian Journal of Andrology, 2021.
[9] Liu, Chao. Paternal USP26 mutations raise Klinefelter syndrome risk in the offspring of mice and humans. EMBO Journal, 2021.
[10] 张栩. Variation analysis of SOX8 gene in Chinese men with non-obstructive azoospermia or oligozoospermia. Andrologia, 2020.
[11] 张栩. Variation analysis of SOX8 gene in Chinese men with non-obstructive azoospermia or oligozoospermia. Andrologia, 2020.
[12] 张栩. Mutational analysis of the GATA4 gene in Chinese men with nonobstructive azoospermia. Asian Journal of Andrology, 2021.
[13] 黄涛. Absence of murine CFAP61 causes male infertility due to multiple morphological abnormalities of the flagella. Science Bulletin, 65, 854, 2020.
[14] 游力 , 张浩波 , 王丽 , 高选 and 秦莹莹. A Genome-wide Association Study Reveals Variants within the HLA Region Are Associated with Risk for Nonobstructive Azoospermia. Am J Hum Genet, 90, 900-6, 2012.
[15] 陈子江 , 张浩波 and 秦莹莹. Mutations in KISS1 are not responsible for idiopathic hypogonadotropic hypogonadism in Chinese patients. J Assist Reprod Genet, 2015.
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