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1. Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice SCIE PubMed SCOPUS

作者:Liu, WJ; He, XJ; Yang, SM; Zouari, R; Wang, JX; Wu, H; Kherraf, ZE; Liu, CY; Coutton, C; Zhao, R; Tang, DD; Tang, SY; Lv, MR; Fang, YY; Li, WY; Li, H; Zhao, JY; Wang, X; Zhao, SM; Zhang, JJ; Arnoult, C; Jin, L; Zhang, ZG; Ray, PF; Cao, YX; Zhang, F

作者机构:[Liu, Wangjie; Liu, Chunyu; Zhao, Rui; Tang, Shuyan; Li, Weiyu; Zhao, Jianyuan; Zhao, Shimin; Jin, Li; Zhang, Feng] Fudan Univ, NHC Key Lab Reprod Reg 更多

关键词:CRISPR; exome; flagella; male infertility; MMAF; sequencing; sperm; TTC21A

来源:AMERICAN JOURNAL OF HUMAN GENETICS,2019,Vol.104,Issue.4

资源类型:外文期刊论文

2. Mutations in PMFBP1 Cause Acephalic Spermatozoa Syndrome PubMed SCIE SCOPUS

作者:Zhu, FX; Liu, C; Wang, FS; Yang, XY; Zhang, JJ; Wu, H; Zhang, ZG; He, XJ; Zhang, Z; Zhou, P; Wei, ZL; Shang, YL; Wang, L; Zhang, RD; Ouyang, YC; Sun, QY; Cao, YX; Li, W

作者机构:[Zhu, Fuxi; Zhang, Jingjing; Wu, Huan; Zhang, Zhiguo; He, Xiaojin; Zhang, Zhou; Zhou, Ping; Wei, Zhaolian; Cao, Yunxia] Anhui Med Univ, Affiliated Hos 更多

关键词:acephalic spermatozoa syndrome; head-tail coupling apparatus; ICSI; male infertility; PMFBP1

来源:AMERICAN JOURNAL OF HUMAN GENETICS,2018,Vol.103,Issue.2

Scopus被引频次:3

ESI学科:MOLECULAR BIOLOGY & GENETICS

最新一期影响因子:9.025

资源类型:外文期刊论文

3. Biallelic Mutations in CFAP43 and CFAP44 Cause Male Infertility with Multiple Morphological Abnormalities of the Sperm Flagella SCIE PubMed SCOPUS

作者:Tang, SY; Wang, X; Li, WY; Yang, XY; Li, Z; Liu, WJ; Li, CH; Zhu, ZJ; Wang, LX; Wang, JX; Zhang, L; Sun, XL; Zhi, EL; Wang, HY; Li, H; Jin, L; Luo, Y; Wang, J; Yang, SM; Zhang, F

作者机构:[Tang, Shuyan; Li, Weiyu; Liu, Wangjie; Wang, Lingxiang; Zhang, Ling; Wang, Hongyan; Jin, Li; Zhang, Feng] Fudan Univ, Obstet & Gynecol Hosp, State Ke 更多

关键词:CFAP43; CFAP44; CFAP65; CGH; cilia; flagella; male infertility; motility; sequencing; sperm

来源:AMERICAN JOURNAL OF HUMAN GENETICS,2017,Vol.100,Issue.6

Scopus被引频次:1

ESI学科:MOLECULAR BIOLOGY & GENETICS

最新一期影响因子:9.025

资源类型:外文期刊论文

4. Biallelic SUN5 Mutations Cause Autosomal-Recessive Acephalic Spermatozoa Syndrome PubMed SCIE SCOPUS

作者:Zhu, FX; Wang, FS; Yang, XY; Zhang, JJ; Wu, H; Zhang, Z; Zhang, ZG; He, XJ; Zhou, P; Wei, ZL; Gecz, J; Cao, YX

作者机构:[Zhu, Fuxi; Zhang, Jingjing; Wu, Huan; Zhang, Zhou; Zhang, Zhiguo; He, Xiaojin; Zhou, Ping; Wei, Zhaolian; Cao, Yunxia] Anhui Med Univ, Affiliated Hos 更多

来源:AMERICAN JOURNAL OF HUMAN GENETICS,2016,Vol.99,Issue.4

WOS被引频次:3

Scopus被引频次:27

ESI学科:MOLECULAR BIOLOGY & GENETICS

JCR分区:Q1

当年影响因子:9.025

最新一期影响因子:9.025

资源类型:外文期刊论文

5. Characterization of Large Structural Genetic Mosaicism in Human Autosomes SCIE SCOPUS PubMed

作者:Machiela, MJ; Zhou, WY; Sampson, JN; Dean, MC; Jacobs, KB; Black, A; Brinton, LA; Chang, IS; Chen, C; Chen, C; Chen, KX; Cook, LS; Bou, MC; De Vivo, I; Doherty, J; Friedenreich, CM; Gaudet, MM; Haiman, CA; Hankinson, SE; Hartge, P; Henderson, BE; Hong, YC; Hosgood, HD; Hsiung, CA; Hu, W; Hunter, DJ; Jessop, L; Kim, HN; Kim, YH; Kim, YT; Klein, R; Kraft, P; Lan, Q; Lin, DX; Liu, JJ; Le Marchand, L; Liang, XL; Lissowska, J; Lu, LG; Magliocco, AM; Matsuo, K; Olson, SH; Orlow, I; Park, JY; Pooler, L; Prescott, J; Rastogi, R; Risch, HA; Schumacher, F; Seow, A; Setiawan, VW; Shen, HB; Sheng, X; Shin, MH; Shu, XO; VanDen Berg, D; Wang, JC; Wentzensen, N; Wong, MP; Wu, C; Wu, TC; Wu, YL; Xia, L; Yang, HP; Yang, PC; Zheng, W; Zhou, BS; Abnet, CC; Albanes, D; Aldrich, MC; Amos, C; Amundadottir, LT; Berndt, SI; Blot, WJ; Bock, CH; Bracci, PM; Burdett, L; Buring, JE; Butler, MA; Carreon, T; Chatterjee, N; Chung, CC; Cook, MB; Cullen, M; Davis, FG; Ding, T; Duell, EJ; Epstein, CG; Fan, JH; Figueroa, JD; Fraumeni, JF; Freedman, ND; Fuchs, CS; Gao, YT; Gapstur, SM; Patino-Garcia, A; Garcia-Closas, M; Gaziano, JM; Giles, GG; Gillanders, EM; Giovannucci, EL; Goldin, L; Goldstein, AM; Greene, MH; Hallmans, G; Harris, CC; Henriksson, R; Holly, EA; Hoover, RN; Hu, N; Hutchinson, A; Jenab, M; Johansen, C; Khaw, KT; Koh, WP; Kolonel, LN; Kooperberg, C; Krogh, V; Kurtz, RC; LaCroix, A; Landgren, A; Landi, MT; Li, DH; Liao, LM; Malats, N; McGlynn, KA; McNeill, LH; McWilliams, RR; Melin, BS; Mirabello, L; Peplonska, B; Peters, U; Petersen, GM; Prokunina-Olsson, L; Purdue, M; Qiao, YL; Rabe, KG; Rajaraman, P; Real, FX; Riboli, E; Rodriguez-Santiago, B; Rothman, N; Ruder, AM; Savage, SA; Schwartz, AG; Schwartz, KL; Sesso, HD; Severi, G; Silverman, DT; Spitz, MR; Stevens, VL; Stolzenberg-Solomon, R; Stram, D; Tang, ZZ; Taylor, PR; Teras, LR; Tobias, GS; Viswanathan, K; Wacholder, S; Wang, ZM; Weinstein, SJ; Wheeler, W; White, E; Wiencke, JK; Wolpin, BM; Wu, XF; Wunder, JS; Yu, K; Zanetti, KA; Zeleniuch-Jacquotte, A; Ziegler, RG; De Andrade, M; Barnes, KC; Beaty, TH; Bierut, LJ; Desch, KC; Doheny, KF; Feenstra, B; Ginsburg, D; Heit, JA; Kang, JH; Laurie, CA; Li, JZ; Lowe, WL; Marazita, ML; Melbye, M; Mirel, DB; Murray, JC; Nelson, SC; Pasquale, LR; Rice, K; Wiggs, JL; Wise, A; Tucker, M; Perez-Jurado, LA; Laurie, CC; Caporaso, NE; Yeager, M; Chanock, SJ

作者机构:[Machiela, Mitchell J.; Zhou, Weiyin; Sampson, Joshua N.; Black, Amanda; Brinton, Louise A.; Hartge, Patricia; Hosgood, H. Dean, III; Hu, Wei; Jessop, 更多

来源:AMERICAN JOURNAL OF HUMAN GENETICS,2015,Vol.96,Issue.3

WOS被引频次:11

Scopus被引频次:33

ESI学科:MOLECULAR BIOLOGY & GENETICS

JCR分区:Q1

当年影响因子:10.794

最新一期影响因子:9.025

资源类型:外文期刊论文

6. Low-Frequency Coding Variants at 6p21.33 and 20q11.21 Are Associated with Lung Cancer Risk in Chinese Populations SCIE SCOPUS PubMed

作者:Jin, GF; Zhu, M; Yin, R; Shen, W; Liu, J; Sun, J; Wang, C; Dai, JC; Ma, HX; Wu, C; Yin, ZH; Huang, JQ; Higgs, BW; Xu, L; Yao, YH; Christiani, DC; Amos, CI; Hu, ZB; Zhou, BS; Shi, YY; Lin, DX; Shen, HB

作者机构:[Jin, Guangfu; Zhu, Meng; Shen, Wei; Liu, Jia; Sun, Jie; Wang, Cheng; Dai, Juncheng; Ma, Hongxia; Hu, Zhibin; Shen, Hongbing] Nanjing Med Univ, Sch Pu 更多

来源:AMERICAN JOURNAL OF HUMAN GENETICS,2015,Vol.96,Issue.5

WOS被引频次:2

Scopus被引频次:14

ESI学科:MOLECULAR BIOLOGY & GENETICS

JCR分区:Q1

当年影响因子:10.794

最新一期影响因子:9.025

资源类型:外文期刊论文

7. A Genome-wide Association Study Reveals that Variants within the HLA Region Are Associated with Risk for Nonobstructive Azoospermia SCIE SCOPUS

作者:Zhao, H; Xu, JF; Zhang, HB; Sun, JL; Sun, YP; Wang, Z; Liu, JY; Ding, Q; Lu, SM; Shi, R; You, L; Qin, YY; Zhao, XM; Lin, XL; Li, X; Feng, JJ; Wang, L; Trent, JM; Xu, CY; Gao, Y; Zhang, B; Gao, X; Hu, JM; Chen, H; Li, GY; Zhao, JZ; Zou, SH; Jiang, H; Hao, CF; Zhao, YR; Ma, JL; Zheng, SL; Chen, ZJ

作者机构:[Zhao, Han; Zhang, Haobo; Lu, Shaoming; You, Li; Qin, Yingying; Li, Xiao; Wang, Li; Xu, Chengyan; Gao, Xuan; Hu, Jingmei; Chen, Hong; Li, Guangyu; Zha 更多

来源:AMERICAN JOURNAL OF HUMAN GENETICS,2012,Vol.90,Issue.5

WOS被引频次:22

Scopus被引频次:41

ESI学科:MOLECULAR BIOLOGY & GENETICS

JCR分区:Q1

当年影响因子:11.202

最新一期影响因子:9.025

资源类型:外文期刊论文

8. Genetic Variants at 6p21.1 and 7p15.3 Are Associated with Risk of Multiple Cancers in Han Chinese SCIE SCOPUS PubMed

作者:Jin, GF; Ma, HX; Wu, C; Dai, JC; Zhang, RY; Shi, YY; Lu, JC; Miao, XP; Wang, ML; Zhou, YF; Chen, JP; Li, HZ; Pan, SD; Chu, MJ; Lu, F; Yu, DK; Jiang, Y; Dong, J; Hu, LM; Chen, YJ; Xu, L; Shu, YQ; Pan, SY; Tan, W; Zhou, BS; Lu, DR; Wu, TC; Zhang, ZD; Chen, F; Wang, XR; Hu, ZB; Lin, DX; Shen, HB

作者机构:[Jin, Guangfu; Ma, Hongxia; Dai, Juncheng; Zhang, Ruyang; Chen, Jiaping; Li, Huizhang; Pan, Shandong; Chu, Minjie; Lu, Feng; Jiang, Yue; Dong, Jing; H 更多

来源:AMERICAN JOURNAL OF HUMAN GENETICS,2012,Vol.91,Issue.5

WOS被引频次:21

Scopus被引频次:45

ESI学科:MOLECULAR BIOLOGY & GENETICS

JCR分区:Q1

当年影响因子:11.202

最新一期影响因子:9.025

资源类型:外文期刊论文

9. Molecular and clinical characterization of a large Chinese pedigree with maternally inherited hearing loss. CPCI-S SCIE

作者:Li, R; Bu, X; Yan, M; Guan, M

作者机构:[Li, R; Bu, X; Yan, M; Guan, M]Cincinnati Childrens Hosp, Dept Human Genet, Cincinnati, OH USA., Nanjing Med Univ, Peoples Hosp Jiangsu Provin 更多

会议名称:52nd Annual Meeting of the American-Society-of-Human-Genetics

会议日期:OCT 15-19, 2002

来源:AMERICAN JOURNAL OF HUMAN GENETICS,2002,Vol.71,Issue.4

ESI学科:MOLECULAR BIOLOGY & GENETICS

JCR分区:Q1

当年影响因子:10.649

最新一期影响因子:9.025

资源类型:外文会议论文

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