2011 PhD: Zhejiang University, School of Life Sciences
Youth Committee Member of the Chinese Society of Eugenics
Deputy Director of the Youth Committee of the Medical Genetics Physician Branch of the Zhejiang Medical Association
Youth Committee Member of the Medical Genetics Branch of the Zhejiang Medical Association
Youth Committee Member of the Rare Disease Branch of the Zhejiang Medical Association
Published over 40 SCI papers, 11 as first author
2011 - Present - Zhejiang University School of Medicine, Reproductive Genetics Department - Researcher
Research
Prenatal screening and diagnosis Molecular diagnosis of genetic diseases Pathogenic genes and mechanisms of rare genetic diseases
Validation and depth evaluation of recurrent neural network-based ultra low-pass genome sequencing for the detection of absence of heterozygosity: A multi-centre study of 409 cases, Qian YQ, Zhu JJ, Tang ZG, Sun Y, Wang ZH, Tang F, Yang Y, Fan LL, Sun YX, Liu B, Chen M, Luo YQ, Hu JJ, Yan K, Man JF, Wang LN, Jia CC, Tang P, Zhu XY, Wang CH, Tang JX, Xia YY, Guo XQ, Zhang K, Wang XL, Li SP, Song LJ, Zhu JS, Dong MY, 2024
SLC10A5 deficiency causes hypercholanemia, Xu YY, Qian YQ, Yu Y, Zhan X, Jin PZ, Hong JW, Dong MY, 2024
Validation and depth evaluation of low-pass genome sequencing in prenatal diagnosis using 387 amniotic fluid samples, Qian YQ, Sun Y, Guo XQ, Song LJ, Sun YX, Gao XY, Liu B, Xu YQ, Chen N, Luo YQ, Qiao ZH, Fan LL, Man JF, Zhang K, Wang XL, Rong TT, Wang ZH, Liu FX, Zhao J, Wei XM, Chen MF, Peng ZY, Peng HH, Sun J, Dong MY, 2023
Noninvasive Prenatal Screening for Common Fetal Aneuploidies Using Single-Molecular Sequencing, Qian YQ, Liu YF, Yan K, Xu YF, Sun YX, Gao XY, Chen N, Jin PZ, Zeng LD, Sun L, Yan Q, Dong MY, 2023
Novel deep intronic and frameshift mutations causing a TRIP11-related disorder, Qian YQ, Hu G, Chen M, Liu B, Yan K, Zhou CY, Yu YQ, Dong MY, 2021
Paternal Low-Level Mosaicism-Caused SATB2-Associated Syndrome, Qian YQ, Liu J, Yang YM, Chen M, Jin CL, Chen PL, Lei YL, Pan HY, Dong MY, 2019
Detection of fetal subchromosomal aberration with cell-free DNA screening led to diagnosis of parental translocation: Review of 11344 consecutive cases in a university hospital, Qian YQ, Wang XQ, Luo YQ, Chen M, Yan K, Yang YM, Liu B, Wang LY, Huang YZ, Li HG, Pan HY, Jin F, Dong MY, 2018
A feasible diagnostic approach for the translocation carrier from the indication of products of conception, Qian YQ, Fu XY, Wang XQ, Luo YQ, Chen M, Yan K, Yang YM, Liu B, Wang LY, Huang YZ, Li HG, Pan HY, Jin F, Dong MY, 2018
Wntless, a conserved Wnt-transport protein, is involved in the innate immune response of Macrobrachium rosenbergii, Dai ZM, Xiong Y, He W, Fang Y, Qian YQ, Zhu XJ, 2018
MSG is involved in sperm gelatinolytic activity in the prawn, Macrobrachium rosenbergii, Yang F, Qian YQ, Ma WM, Li Y, Yang JS, Yang WJ, 2013
Two Kazal-type protease inhibitors from Macrobrachium nipponense and Eriocheir sinensis: Comparative analysis of structure and activities, Qian YQ, Li Y, Yang F, Yu YQ, Yang JS, Yang WJ, 2012
CHH family peptides from an 'eyeless' deep-sea hydrothermal vent shrimp, Rimicaris kairei: characterization and sequence analysis, Qian YQ, Dai L, Yang JS, Yang F, Chen DF, Fujiwara Y, Tsuchida S, Nagasawa H, Yang WJ, 2009
Efficiency of non-invasive prenatal screening in pregnant women at advanced maternal age, Zhu H, Jin XX, Xu YQ, Zhang WH, Liu XD, Jin JL, Qian YQ, Dong MY, 2021
Galectin-14 Promotes Trophoblast Migration and Invasion by Upregulating the Expression of MMP-9 and N-Cadherin, Wang Mm, Xu YQ, Wang P, Xu YF, Jin PZ, Wu ZG, Qian YQ, Bai L, Dong MY, 2021
Non-invasive prenatal screening for Emanuel syndrome, Luo YQ, Lin J, Sun YX, Qian YQ, Wang LY, Chen M, Dong MY, Jin F, 2020
Preimplantation Genetic Testing for a Chinese Family With X-Linked Lymphoproliferative Syndrome Type 1, Chen SC, Shi WH, Qian YQ, Wang LY, Zhang JY, Li SY, Chen YY, Chang CX, Fei HJ, Zhang LL, Huang HF, Xu CM, 2020
Basonuclin 1 deficiency causes testicular premature aging: BNC1 cooperates with TAF7L to regulate spermatogenesis, Li JY, Liu YF, Xu HY, Zhang JY, Lv PP, Liu ME, Ying YY, Qian YQ, Li K, Li C, Huang Y, Xu GF, Ding GL, Mao YC, Xu CM, Liu XM, Sheng JZ, Zhang D, Huang HF, 2020
The association between the two more common genetic causes of spermatogenic failure: a 7-year retrospective study, Li HG, Fan LH, Liu B, Qian YQ, Chen M, Sun YX, Dong MY, 2020
Generation of the human induced pluripotent stem cell line (ZJUi005-A) from a patient with Pelizaeus-Merzbacher disease (PMD) carrying a novel hemizygous mutation in PLP1 gene, Liu B, Chen L, Sun J, Zhang L, Chen M, Qian YQ, Wang YL, Yan K, Hou LX, Huang YZ, Zhang D, Xu YM, Yu JL, Zhang J, Dong MY, 2020
Is Noninvasive Prenatal Screening Appropriate for Pregnant Women Age 35 or Older In Cases if Isolated Fetal Nasal Bone Abnormalities in The Chinese Han Population?, Chen Y, Lv M, Dong T, Chen QQ, Qian YQ, Zhao BH, Luo Q, 2020
Identification of a likely pathogenic structural variation in the LAMA1 gene by Bionano optical mapping, Chen M, Zhang M, Qian YQ, Yang YM, Sun YX, Liu B, Wang LY, Dong MY, 2020
Comprehensive genetic diagnosis of patients with Duchenne/Becker muscular dystrophy (DMD/BMD) and pathogenicity analysis of splice site variants in the DMD gene, Yang YM, Yan K, Liu B, Chen M, Wang LY, Huang YZ, Qian YQ, Sun YX, Li HG, Dong MY, 2019
Preimplantation genetic diagnosis and screening (PGD/S) using a semiconductor sequencing platform, Wang LY, Rao XQ, Luo YQ, Liu B, Peng CF, Chen D, Yan K, Qian YQ, Yang YM, Huang YZ, Chen M, Sun YX, Li HG, Ye YH, Jin F, Liu HL, Dong MY, 2019
A Novel Silent Mutation in the L1CAM Gene Causing Fetal Hydrocephalus Detected by Whole-Exome Sequencing, Sun YX, Li YF, Chen M, Luo YQ, Qian YQ, Yang YM, Lu H, Lou FL, Dong MY, 2019
Whole-Exome Sequencing Revealed Mutations of MED12 and EFNB1 in Fetal Agenesis of the Corpus Callosum, Jiang Y, Qian YQ, Yang MM, Zhan QT, Chen Y, Xi FF, Sagnelli M, Dong MY, Zhao BH, Luo Q, 2019
Detection of fetal duplication 16p11.2q12.1 by next-generation sequencing of maternal plasma and invasive diagnosis, Chen M, Fu XY, Luo YQ, Qian YQ, Pan L, Wang LY, Dong MY, 2019
Basonuclin 1 deficiency is a cause of primary ovarian insufficiency, Zhang D, Liu YF, Zhang Z, Lv PP, Liu Y, Li JY, Wu YQ, Zhang RJ, Huang Y, Xu GF, Qian YQ, Qian YL, Chen SC, Xu CM, Shen J, Zhu LL, Chen K, Zhu B, Ye XQ, Mao YC, Bo XS, Zhou CY, Wang TT, Chen DF, Yang WJ, Tan YJ, Song Y, Zhou DZ, Sheng JZ, Gao HJ, Zhu YM, Li MG, Wu LP, He L, Huang HF, 2018
The application of NIPT using combinatorial probe-anchor synthesis to identify sex chromosomal aneuploidies (SCAs) in a cohort of 570 pregnancies, Li HG, Lei Y, Zhu H, Luo YQ, Qian YQ, Chen M, Sun YX, Yan K, Yang YM, Liu B, Wang LY, Huang YZ, Hu JJ, Xu JY, Dong MY, 2018
XCI-escaping gene KDM5C contributes to ovarian development via downregulating miR-320a, Sun YX, Zhang YX, Zhang D, Xu CM, Chen SC, Zhang JY, Ruan YC, Chen F, Zhang RJ, Qian YQ, Liu YF, Jin LY, Yu TT, Xu HY, Luo YQ, Liu XM, Sun F, Sheng JZ, Huang HF, 2017
A copy number variation genotyping method for aneuploidy detection in spontaneous abortion specimens, Chen SC, Liu DY, Zhang JY, Li SY, Zhang LL, Fan JX, Luo YQ, Qian YQ, Huang HF, Liu C, Zhu HH, Jiang ZW, Xu CM, 2017
Identification of novel PKD1 and PKD2 mutations in a Chinese population with autosomal dominant polycystic kidney disease, Liu B, Chen SC, Yang YM, Yan K, Qian YQ, Zhang JY, Hu YT, Dong MY, Jin F, Huang HF, Xu CM, 2016
Follicle-stimulating hormone promotes age-related endometrial atrophy through cross-talk with transforming growth factor beta signal transduction pathway, Zhang D, Li JY, Xu GF, Zhang RJ, Zhou CL, Qian YQ,
Area of Focus
Genetic Diseases | Children | Mechanisms | Protein Evolution | Recombination | Gene Function | Pathogenic Mechanisms | Research | Genetics | Pediatrics
