Professor | 沙艳伟 | 数字化转型顾问

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Name	沙艳伟
Contact Information	shayanwei928@126.com
Language ability	中文, 英语
Province	福建

Upload Avatar (500 x 500)

Name

沙艳伟

Contact Information

shayanwei928@126.com

Language ability

中文, 英语

Province

福建

University/Lab Affiliation and Title	厦门大学
Faculty	Medical
Academic Background & Achievements	2002-2005 硕士学位: 吉林大学 2000-2002 临床医学: 吉林大学白求恩医学部
Work Experience	2020-至今 - 厦门大学附属妇女儿童医院 - 副教授 2016-至今 - 厦门市妇幼保健院 - 副主任医师 2012-2016 - 厦门市妇幼保健院 - 主治医师 2006-2012 - 厦门市妇幼保健院 - 住院医师
Awards	福建省高层次人才 (2021) 全国妇幼健康科学技术三等奖 (2020) 厦门市科技进步奖三等奖 (2020) 福建省医学科技进步二等奖 (2019) 全国妇幼健康科学技术三等奖 (2019) 厦门市科技进步二等奖 (2019) 厦门市科技进步二等奖 (2017) 全国妇幼健康科学技术二等奖 (2017) 厦门市医学创新奖 (2015)

University/Lab Affiliation and Title

厦门大学

Faculty

Medical

Academic Background & Achievements

2002-2005 硕士学位: 吉林大学
2000-2002 临床医学: 吉林大学白求恩医学部

Work Experience

2020-至今 - 厦门大学附属妇女儿童医院 - 副教授
2016-至今 - 厦门市妇幼保健院 - 副主任医师
2012-2016 - 厦门市妇幼保健院 - 主治医师
2006-2012 - 厦门市妇幼保健院 - 住院医师

Awards

福建省高层次人才 (2021)
全国妇幼健康科学技术三等奖 (2020)
厦门市科技进步奖三等奖 (2020)
福建省医学科技进步二等奖 (2019)
全国妇幼健康科学技术三等奖 (2019)
厦门市科技进步二等奖 (2019)
厦门市科技进步二等奖 (2017)
全国妇幼健康科学技术二等奖 (2017)
厦门市医学创新奖 (2015)

Areas of Focus	无精子症、少精子症、弱精子症、畸形精子症的致病基因及分子机制精子膜及受体异常导致不受精的致病基因及分子机制早期胚胎发育停滞的致病基因及分子机制研究反复自然流产及胚胎植入前遗传学检测技术防治研究
Publications	Defective piRNA Processing and Azoospermia, Sha Y, Li L, Yin C, 2022 Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice, Tan C, Meng L, Lv M, He X, Sha Y, Tang D, Tan Y, Hu T, He W, Tu C, Nie H, Zhang H, Du J, Lu G, Fan LQ, Cao Y, Lin G, Tan YQ, 2022 Biallelic mutations in ARMC12 cause asthenozoospermia and multiple midpiece defects in humans and mice, Liu W, Wei X, Liu X, Chen G, Zhang X, Liang X, Isachenko V, Sha Y, Wang Y, 2022 DNAH1 gene mutations and their potential association with dysplasia of the sperm fibrous sheath and infertility in the Han Chinese population, Sha Y, Yang X, Mei L, Ji Z, Wang X, Ding L, Li P, Yang S, 2017 Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility, Liu C, Miyata H, Gao Y, Sha Y, Tang S, Xu Z, Whitfield M, Patrat C, Wu H, Dulioust E, Tian S, Shimada K, Cong J, Noda T, Li H, Morohoshi A, Cazin C, Kherraf ZE, Arnoult C, Jin L, He X, Ray PF, Cao Y, Touré A, Zhang F, Ikawa M, 2020 Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotype, Sha Y, Wei X, Ding L, Ji Z, Mei L, Huang X, Su Z, Wang W, Zhang X, Lin S, 2020 Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF), Liu W, Sha Y, Li Y, Mei L, Lin S, Huang X, Lu J, Ding L, Kong S, Lu Z, 2019 Biallelic mutations in PMFBP1 cause acephalic spermatozoa, Sha YW, Wang X, Xu X, Ding L, Liu WS, Li P, Su ZY, Chen J, Mei LB, Zheng LK, Wang HL, Kong SB, You M, Wu JF, 2019

Areas of Focus

无精子症、少精子症、弱精子症、畸形精子症的致病基因及分子机制
精子膜及受体异常导致不受精的致病基因及分子机制
早期胚胎发育停滞的致病基因及分子机制研究
反复自然流产及胚胎植入前遗传学检测技术防治研究

Publications

Defective piRNA Processing and Azoospermia, Sha Y, Li L, Yin C, 2022
Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice, Tan C, Meng L, Lv M, He X, Sha Y, Tang D, Tan Y, Hu T, He W, Tu C, Nie H, Zhang H, Du J, Lu G, Fan LQ, Cao Y, Lin G, Tan YQ, 2022
Biallelic mutations in ARMC12 cause asthenozoospermia and multiple midpiece defects in humans and mice, Liu W, Wei X, Liu X, Chen G, Zhang X, Liang X, Isachenko V, Sha Y, Wang Y, 2022
DNAH1 gene mutations and their potential association with dysplasia of the sperm fibrous sheath and infertility in the Han Chinese population, Sha Y, Yang X, Mei L, Ji Z, Wang X, Ding L, Li P, Yang S, 2017
Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility, Liu C, Miyata H, Gao Y, Sha Y, Tang S, Xu Z, Whitfield M, Patrat C, Wu H, Dulioust E, Tian S, Shimada K, Cong J, Noda T, Li H, Morohoshi A, Cazin C, Kherraf ZE, Arnoult C, Jin L, He X, Ray PF, Cao Y, Touré A, Zhang F, Ikawa M, 2020
Biallelic mutations of CFAP74 may cause human primary ciliary dyskinesia and MMAF phenotype, Sha Y, Wei X, Ding L, Ji Z, Mei L, Huang X, Su Z, Wang W, Zhang X, Lin S, 2020
Loss-of-function mutations in SPEF2 cause multiple morphological abnormalities of the sperm flagella (MMAF), Liu W, Sha Y, Li Y, Mei L, Lin S, Huang X, Lu J, Ding L, Kong S, Lu Z, 2019
Biallelic mutations in PMFBP1 cause acephalic spermatozoa, Sha YW, Wang X, Xu X, Ding L, Liu WS, Li P, Su ZY, Chen J, Mei LB, Zheng LK, Wang HL, Kong SB, You M, Wu JF, 2019

无精子症少精子症弱精子症畸形精子症致病基因分子机制精子膜受体异常不受精胚胎发育

张银丽 - 浙江大学

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