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秦莹莹 ( 主任医师 ) 赞
个人主页 https://faculty.sdu.edu.cn/qinyingying/zh_CN/index.htm

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论文成果当前位置：中文主页 >> 科学研究 >> 论文成果

[161] 秦莹莹 and 陈子江. WNT9B in 542 Chinese women with Müllerian duct abnormalities: mutation analysis. Reprod Biomed online, 2014.
[162] 秦莹莹 and 陈子江. Impaired telomere length and telomerase activity in peripheral blood leukocytes and granulosa cells in patients with biochemical primary ovarian insufficiency. Human reproduction, 2016.
[163] 秦莹莹 and 焦雪. CSB-PGBD3 Mutations Cause Premature Ovarian Failure. PLoS Genet, 2015.
[164] 秦莹莹 and 陈子江. ESR1, HK3 and BRSK1 gene variants are associated with both age at natural menopause and premature ovarian failure.. Orphanet Journal of Rare Diseases., 2012.
[165] 颜军昊 , 赵涵 , 石玉华 , 秦莹莹 , 游力 , 高选 and 陈子江. Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3.. Nature Genetics, 43, 55, 2011.
[166] 秦莹莹 and 焦雪. Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure. fertil steril, 2014.
[167] 秦莹莹 and 焦雪. Genetics of primary ovarian insufficiency: new developments and opportunities. Hum Reprod Update, 2015.
[168] 秦莹莹 and 陈子江. Ethnic Specificity of Variants of the ESR1, HK3, BRSK1 Genes and the 8q22.3 Locus: No Association with Premature Ovarian Failure (POF) in Serbian Women. Maturitas, 2013.
[169] 赵涵 , 秦莹莹 and 陈子江. PTEN gene analysis in premature ovarian failure patients. Acta Obstet Gynecol Scand, 90, 678, 2011.
[170] 秦莹莹 , 张浩波 and 游力. 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.

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