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[1].Hu TY, Zhang H, Meng LL, Yuan SM, Tu CF, Du J, Lu GX, Lin G, Nie HC, Tan YQ*. Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility.[J]:Hum Mutat.,2020:doi: 10.1002/humu.24138. Online ahead of print.
[2].Tu C, Wang W, Hu T, Lu G, Lin G, Tan YQ*. Genetic underpinnings of asthenozoospermia.[J]:Best Pract Res Clin Endocrinol Metab.,2020:101472
[3].Cheng D, Yuan S, Hu L, Yi D, Luo K, Gong F, Lu C, Lu G, Lin G, Tan YQ*. The genetic cause of intellectual deficiency and/or congenital malformations in two parental reciprocal translocation carriers and implications for assisted reproduction.[J]:J Assist Reprod Genet.,2020:doi: 10.1007/s10815-020-01986-1. Online ahead of print. PMID: 3309447.
[4].Li Y, Wang WL, Tu CF, Meng LL, Hu TY, Du J, Lin G, Nie HC, Tan YQ*. A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans.[J]:Asian J Androl.,2020:19.doi: 10.4103/aja.aja_56_20.Online ahead of print. PMID: 33037173.
[5].Xiao WJ, He WB, Zhang YX, Meng LL, Lu GX, Lin G, Tan YQ*, Du J*. In-Frame variants in STAG3 gene cause premature ovarian insufficiency.[J]:Front Genet.,2019,10:1016
[6].He WB, Tan C, Zhang YX, Meng LL, Gong F, Lu GX, Lin G, Du J, Tan YQ*. Homozygous variants in SYCP2L cause premature ovarian insufficiency:J Med Genet,2020:doi: 10.1136/jmedgenet-2019-106789
[7].Wang Y, Tu C, Nie H, Meng L, Li D, Wang W, Zhang H, Lu G, Lin G, Tan YQ*, Du J*. Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia.[J]:J Assist reprod Genet,2020,37(4):811-820
[8].Zhang YX, He WB, Xiao WJ, Meng LL, Tan C, Du J, Lu GX, Lin G, Tan YQ*. Novel loss-of-function mutation in MCM8 causes premature ovarian insufficiency:Mol Genet Genomic Med,2020,8(4):e1165
[9].Wang WL, Tu CF, Tan YQ*. Insight on multiple morphological abnormalities of sperm falgella in male infertility: what is new?:Asian J Androl,2020,22(3):236-245
[10].Tu C, Wang Y, Nie H, Meng L, Wang W, Li Y, Li D, Zhang H, Lu G, Lin G, Tan YQ*, Du J*. An M1AP homozygous splice-site mutation associated with severe oligozoospermia in a consanguineous family.[J]:Clin Genet,2020,97(5):741-746
[11].Tu C, Meng L, Nie H, Yuan S, Wang W, Du J, Lu G, Lin G, Tan YQ*. A homozygous RPL10L missense mutation associated with male factor infertility and severe oligozoospermia.[J]:Fertil Steril,2020,113(3):561-568
[12]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.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, Zhang Q, Tan YQ*. Novel mutations in SPEF2 causing different defects between flagella and cilia bridge: the phenotypic link between MMAF and PCD.[J]:Hum Genet,2020,139(2):257-271
[13]Tan YQ*,Tu CF, Meng LL, Yuan SM, Sjaarda C, Luo AX, Du J, Li W, Gong F, Zhong CG, Lu GX, Lin G.Tan YQ, Tu CF, Meng LL, Yuan SM, Sjaarda C, Luo AX, Du J, Li W, Gong F, Zhong CG, Deng HX, Lu GX, Liang P, 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
[14]Tan YQ, Yin XY, Zhang SP, Jiang H, Tan K, Li J, Xiong B, Gong F, Zhang CL, Pan XY, Chen F, Chen SP.Tan YQ, Yin XY, Zhang SP, Jiang H, Tan K, Li J, Xiong B, Gong F, Zhang CL, Pan XY, Chen F, Chen SP, Gong C, Lu CF, Luo KL, Gu YF, Zhang XQ, Wang W, Xu X, Vajta G, Bolund L, Yang HM, Lu GX, Du YT, Lin G. Clinical outcome of preimplantation genetic diagnosis and screening using next generation sequencing.[J]:Gigascience,2014,3(30):1-9
[15]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*.He WB, Tu CF, Liu Q, Meng LL, Yuan SM, Luo AX, He FS, Shen J, Li W, Du J, Zhong CG, Lu GX, Lin G, Fan LQ, 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(3):198-204
[16]Tu C, Nie H, Meng L, Yuan S, He W, Luo A, Li H, Li W, Du J, Lu G, Lin G, Tan YQ*.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
[17]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*.Wang W, Tu C, Nie H, Meng L, Li Y, Yuan S, Zhang Q, Du J, Wang J, Gong F, Fan L, Lu GX, Lin G, Tan YQ*. Biallelic mutations in CFAP65 lead to severe asthenoteratospermia due to acrosome hypoplasia and flagellum malformations.[J]:J Med Genet,2019,56(11):750-757
[18]Liu Q, Tan YQ*.Liu Q, Tan YQ*. Advances in Identifications of Susceptibility Gene Defects of Hereditary Colorectal Cancer.[J]:J Cancer,2019,10(3):643-653
[19]Cheng DH,Tan YQ*,Di YF,Li LY,Lu GX.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
[20]Tan YQ*, Tan K, Zhang SP, Gong F, Cheng DH, Xiong B, Lu CF, Tang XC, Lu GX etc.Tan YQ, Tan K, Zhang SP, Gong F, Cheng DH, Xiong B, Lu CF, Tang XC, Luo KL, Lin G, Lu GX. 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
[21]He WB, Du J, Xie PY, Zhou S, Zhang YX, Lu GX, Lin G, Li W, Tan YQ*.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
[22]Zhang YX, Li HY, He WB, Tu C, Du J, Li W, Lu GX, Lin G, Yang Y, Tan YQ*.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
[23]He WB, Banerjee S, Meng LL, Du J, Gong F, Huang H, Zhang XX, Wang YY, Lu GX, Lin G, Tan YQ*.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
[24]He WB, Du J, Yang XW, Li W, Tang WL, Dai C, Chen YZ, Zhang YX, Lu GX, Lin G, Gong F, Tan YQ*.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
[25]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.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, Lu G, Gong F, Wang W. Noninvasive prenatal testing (NIPT) in twin pregnancies with treatment of assisted reproductive techniques (ART) in a single center.[J]:Prenat Diagn,2016,36(7):672-679
[26]Tan YQ*, Hu L, Lin G, Jonathan S.T.Sham, Gong F, Guan XY, Lu GX.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
[27]Cheng DH, Gong F, Tan K, Lu CF, Lin G, Lu GX, Tan YQ*.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
[28]Meng L, Tu C, Lu G, Lin G,？Tan Y*.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
[29]Cheng D, Yuan S, Yi D, Luo K, Xu F, Gong F, Lu C, Lu G, Lin G, Tan YQ*.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):2533-2539
[30]Meng LL, Yuan SM, Tu CF, Lin G, Lu GX, Tan YQ*.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
[31]Luo A, Cheng D, Yuan S, Li H, Du J, Zhang Y, Yang C,？Lin G, Zhang W, Tan YQ*.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
[32]Yuan SM, Zhang YN, Du J, Li W, Tu CF, Meng LL,？Lin G, Lu GX, Tan YQ*.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
[33]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*.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
[34]Yuan SM, Huang H, Tu CF, Du J, Xu DB, Lin G, Lu GX, Tan YQ*.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
[35]He WB, Tan YQ*, Hu X, Li W, Xiong B, Luo KL, Gong F, Lu GX, Lin G, Du J.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
[36]Yang XW, He WB, Gong F, Li W, Li XR, Zhong CG, Lu GX, Lin G, Du J, Tan YQ*.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
[37]Yuan SM, Meng LL, Zhang Y, Tu CF, Du J, Li W, Liang P, Lu GX, Tan YQ*.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
[38]Xu F, Zhang YN, Cheng DH, Tan K, Zhong CG, Lu GX, Lin G, Tan YQ*.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
[39]Cheng DH,Gong F,Lu CF,Li LY,Lu GX,Tan YQ.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
[40]Tan YQ*, Chen XM, Hu L, Guan XY, Lu GX.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
[41]Tan YQ*, Lu GX.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
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