譚躍球

個人簡介

譚躍球，中南大學研究員，醫學遺傳學博士，博士研究生導師，《中華醫學遺傳學雜誌》編委，中國優生優育協會理事，中華醫學會醫學細胞生物學分會委員，中國遺傳學會遺傳諮詢分會委員會委員，中國遺傳學會國際交流委員會委員，湖南省醫學會生殖醫學分會和湖南省醫學遺傳學分會委員。

研究方向

[1] 遺傳學
[2] 發育生物學

個人經歷

教育經歷

[1]1997.9-2002.6

中南大學| 遺傳學| 博士學位| 博士研究生畢業

[2]1991.9-1994.6

湖南醫科大學| 醫學遺傳學| 碩士學位| 碩士研究生畢業

[3]1987.9-1991.6

湖南師範大學| 生物學| 學士學位| 本科

工作經歷

[1]2002.9-至今

生殖與幹細胞工程研究所| 中南大學 2002年9月晉升為副研究員，2007年9月晉升為研究員

[2]1993.3-2002.8

人類生殖工程研究室| 湖南醫科大學 1997年9月晉升為助理研究員

[3]1991.7-1993.2

醫學遺傳學國家重點實驗室| 湖南醫科大學實習研究員

社會兼職

[1]海峽兩岸醫藥衛生交流協會遺傳與生殖專業委員會委員
[2]中國遺傳學會遺傳諮詢分會委員兼職時間：2017/01/01 --至今
[3]中華醫學遺傳學雜誌編輯委員會第六屆、第七屆編委會兼職時間：2013/01/01 --至今
[4]中國遺傳學會國際交流委員會委員兼職時間：2013/01/01 --至今
[5]中國優生優育協會理事兼職時間：2013/04/01 --至今
[6]湖南省婦幼保健與優生優育協會第一屆優生遺傳專業委員會委員兼職時間：2012/05/01 --至今
[7]湖南省醫學會第一屆、第二屆生殖醫學專業委員會委員兼職時間：2009/11/01 --至今
[8]中華醫學會醫學細胞生物學分會第四屆、第五屆委員會委員兼職時間：2012/04/01 --2018/04/01

學術成果

發表論文

[1] Tu C, Nie H, Meng L, Wang W, Li H, Yuan S, Cheng D, He W, Liu G, Du J, Gong F, Lu G, Lin G, Tan YQ. Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD [J]. Hum Genet, 2020,
[2] Tan YQ*,Tu CF, Meng LL, Yuan SM, Sjaarda C, Luo AX, Du J, Li W, Gong F, Zhong CG, Lu GX, Lin G. Loss-of-function mutations TDRD7 lead to a rare novel syndrome combining congenital cataract and non-obstructive azoospermia in humans [J]. Genetics in Medicine, 2019, 21(5): 1209-1217
[3] Tan YQ, Yin XY, Zhang SP, Jiang H, Tan K, Li J, Xiong B, Gong F, Zhang CL, Pan XY, Chen F, Chen SP. Clinical outcome of preimplantation genetic diagnosis and screening using next generation sequencing [J]. Gigascience, 2014, 3(30): 1-9
[4] He WB, Tu CF, Liu Q, Meng LL, Yuan SM, , He FS, Shen J, Li W, Du J, Zhong CG, Lu GX, Lin G, Tan YQ*. DMC1 mutation that causes human non-obstructive azoospermia and premature ovarian insufficiency identified by whole-exome sequencing [J]. J Med Genet, 2018, 55: 198-204
[5] Tu C, Nie H, Meng L, Yuan S, He W, Luo A, Li H, Li W, Du J, Lu G, Lin G, Tan YQ*. Identification of DNAH6 mutations in infertile men with multiple morphological abnormalities of the sperm flagella [J]. Sci Rep, 2019, 9(1): 15864
[6] Wang W, Tu C, Nie H, Meng L, Li Y, Zhang Q, Du J, Wang J, Gong F, Fan L, Lu GX, Lin G, Tan Y*. Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations [J]. J Med Genet, 2019, 56(11): 750-757
[7] Liu Q, Tan YQ*. Advances in Identifications of Susceptibility Gene Defects of Hereditary Colorectal Cancer [J]. J Cancer, 2019, 10(3): 643-653
[8] Cheng DH,Tan YQ*,Di YF,Li LY,Lu GX. Crypt Y chromosome fragment resulting from an X;Y translocation in a patient with premature ovarian failure [J]. Fertil Steril, 2009, 92(2): 828.e3-6
[9] Tan YQ*, Tan K, Zhang SP, Gong F, Cheng DH, Xiong B, Lu CF, Tang XC, Lu GX etc. Single-nucleotide polymorphism microarray-based preimplantation genetic diagnosis is likely to improve the clinical outcome for translocation carriers [J]. Hum Reprod, 2013, 28(9): 2581-2592
[10] He WB, Du J, Xie PY, Zhou S, Zhang YX, Lu GX, Lin G, Li W, Tan YQ*. X-chromosome inactivation pattern of amniocytes predicts the risk of dystrophinopathy in fetal carriers of DMD mutations [J]. Prenat Diagn, 2019, 39(8): 603-608
[11] Zhang YX, Li HY, He WB, Tu C, Du J, Li W, Lu GX, Lin G, Yang Y, Tan YQ*. XRCC2 mutation causes premature ovarian insufficiency as well as non-obstructive azoospermia in humans [J]. Clin Genet, 2019, 95(3): 442-443
[12] He WB, Banerjee S, Meng LL, Du J, Gong F, Huang H, Zhang XX, Wang YY, Lu GX, Lin G, Tan YQ*. Whole-exome sequencing identifies a homozygous donor splice-site mutation in STAG3 that causes primary ovarian insufficiency [J]. Clin Genet, 2018, 93(2): 340-344
[13] He WB, Du J, Yang XW, Li W, Tang WL, Dai C, Chen YZ, Zhang YX, Lu GX, Lin G, Gong F, Tan YQ*. Novel inactivating mutations in the FSH receptor cause premature ovarian insufficiency with resistant ovary syndrome [J]. Reprod Biomed Online, 2018, 38(3): 397-406
[14] Tan Y*, Gao Y, Lin G, Fu M, Li X, Yin X, Du J, Li J, Li W, Peng H, Yuan Y, Chen F, Jiang F, Zhang H,. Noninvasive prenatal testing (NIPT) in twin pregnancies with treatment of assistedreproductivetechniques (ART) in a single center [J]. Prenat Diagn, 2016, 36(7): 672-679
[15] Tan YQ*, Hu L, Lin G, Jonathan S.T.Sham, Gong F, Guan XY, Lu GX. Genetic changes in human fetuses from spontaneous abortion after in vitro fertilization detected by comparative genomic hybridization [J]. Biol Reprod, 2004, 70(2): 495-499
[16] Cheng DH, Gong F, Tan K, Lu CF, Lin G, Lu GX, Tan YQ*. Karyotype determination and reproductive guidance for short stature women with a hidden Y chromosome fragment [J]. Reproductive Biomedicine Online, 2013, 27(1): 89-95
[17] Meng L, Tu C, Lu G, Lin G,Tan Y*. Novel biallelic PCNT deletion causing microcephalic osteodysplastic primordial dwarfism type II with congenital heart defect [J]. Sci China Life Sci, 2019, 62(1): 144-147
[18] Cheng D, Yuan S, Yi D, Luo K, Xu F, Gong F, Lu C, Lu G, Lin G, Tan YQ*. Analysis of molecular cytogenetic features and PGT-SR for two infertile patients with small supernumerary marker chromosomes [J]. J Assist Reprod Genet, 2019, 11(12):
[19] Meng LL, Yuan SM, Tu CF, Lin G, Lu GX, Tan YQ*. Next-generation sequencing identified a novel SPTB frameshift insertion causing hereditary spherocytosis in China [J]. Ann Hematol, 2019, 98(1): 223-226
[20] Luo A, Cheng D, Yuan S, Li H, Du J, Zhang Y, Yang C,Lin G, Zhang W, Tan YQ*. Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblings [J]. Mol Cytogenet, 2018, 11: 24
[21] Yuan SM, Zhang YN, Du J, Li W, Tu CF, Meng LL,Lin G, Lu GX, Tan YQ*. Phenotypic and molecular characteristics of androgen insensitivity syndrome patients [J]. Asian J Androl, 2018, 20(5): 473-478
[22] Li H, Du J, Li W, Cheng D, He W, Yi D, Xiong B, Yuan S, Tu C, Meng L, Luo A, Lin G, Lu G, Tan YQ*. Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature [J]. Mol Cytogenet, 2018, 11: 15
[23] Yuan SM, Huang H, Tu CF, Du J, Xu DB, Lin G, Lu GX, Tan YQ*. A rare polypyrimidine tract mutation in the androgen receptor gene results in complete androgen insensitivity syndrome [J]. Asian J Androl, 2018, 20(3): 308-310
[24] He WB, Tan YQ*, Hu X, Li W, Xiong B, Luo KL, Gong F, Lu GX, Lin G, Du J. Expanded carrier screening and preimplantation genetic diagnosis in a couple who delivered a baby affected with congenital factor VII deficiency [J]. BMC Med Genet, 2018, 19(1): 15-21
[25] Yang XW, He WB, Gong F, Li W, Li XR, Zhong CG, Lu GX, Lin G, Du J, Tan YQ*. Novel FOXL2 mutations cause blepharophimosis-ptosis-epicanthus inversus syndrome with premature ovarian insufficiency [J]. Mol Genet Genomic Med, 2018, 6(2): 261-267
[26] Yuan SM, Meng LL, Zhang Y, Tu CF, Du J, Li W, Liang P, Lu GX, Tan YQ*. Genotype-phenotype correlation and identification of two novel SRD5A2 mutations in 33 Chinese patients with hypospadias [J]. Steroids, 2017, 125: 61-66
[27] Xu F, Zhang YN, Cheng DH, Tan K, Zhong CG, Lu GX, Lin G, Tan YQ*. The first patient with a pure 1p36 microtriplication associated with severe clinical phenotypes [J]. Mol Cytogenet, 2014, 7(1): 64-69
[28] Cheng DH,Gong F,Lu CF,Li LY,Lu GX,Tan YQ. Risk evaluation and preimplantation genetic diagnosis in an infertile man with an unbalanced translocation t(10;15) resulting in a healthy baby [J]. J Assist Reprod Genet, 2012, 29(11): 1299-1304
[29] Tan YQ*, Chen XM, Hu L, Guan XY, Lu GX. Prenatal diagnosis of nonmosaic tetrasomy 9p by microdissection and FISH:case report [J]. Chin Med J (Engl), 2007, 120(14): 1281-1283
[30] Tan YQ*, Lu GX. Chromosomal cryptic insertion of the terminal region and its formative mechanism determined by fluorescence in situ hybridization [J]. Chin Med J, 2002, 115(7): 1039-1042

譚躍球

基本介紹

個人簡介

研究方向

個人經歷

教育經歷

工作經歷

社會兼職

學術成果

發表論文

著作成果

科研項目

榮譽獎項

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