Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 65 Records) |
Query Trace: Preimplantation genetic testing[original query] |
---|
What is the threshold of mature oocytes to obtain at least one healthy transferable cleavage-stage embryo after preimplantation genetic testing for fragile X syndrome? Human reproduction (Oxford, England) 2021 9 36 (11): 3003-3013. Sonigo C, Mayeur A, Sadoun M, Pinto M, Benguigui J, Frydman N, Monnot S, Benachi A, Steffann J, Grynberg |
Case Report: Identification of Germline Chimerism in Monochorionic Dizygotic Twins. Frontiers in genetics 2021 12 12 744890. Chen Juan, Xu Jian, Chen Zhi-Heng, Yin Min-Na, Guo Xin-Yu, Sun Li |
Genetic testing, ultrasonography and preimplantation genetic testing of men with autosomal dominant polycystic kidney disease in Hunan, China. Andrologia 2021 Nov e14273. Li Weina, Liu Gang, Zhao Xingguo, Lu Yichang, Li Huanzhu, Zhang Huan, Lin |
Impact of parental chromosomal polymorphisms on the incidence of congenital anomalies and perinatal complications in a cohort of newborns conceived after ICSI?+?PGT-A. Reproductive biology and endocrinology : RB&E 2022 9 20 (1): 145. Rodriguez Freddy, Cruz Maria, Requena Anton |
Gonadotropin receptor polymorphisms (FSHR N680S and LHCGR N312S) are not predictive of clinical outcome and live birth in assisted reproductive technology. Fertility and sterility 2022 Jul . Pirtea Paul, de Ziegler Dominique, Marin Diego, Sun Li, Tao Xin, Ayoubi Jean Marc, Franasiak Jason, Scott Richard |
Relationship between paternal factors and embryonic aneuploidy of paternal origin. Fertility and sterility 2022 5 118 (2): 281-288. Bonus Marissa L, McQueen Dana B, Ruderman Rachel, Hughes Lydia, Merrion Katrina, Maisenbacher Melissa K, Feinberg Eve, Boots Christi |
Identifying Balanced Chromosomal Translocations in Human Embryos by Oxford Nanopore Sequencing and Breakpoints Region Analysis. Frontiers in genetics 2022 2 12 810900. Pei Zhenle, Deng Ke, Lei Caixai, Du Danfeng, Yu Guoliang, Sun Xiaoxi, Xu Congjian, Zhang Sh |
Association between maternal MTHFR C677T/A1298C combination polymorphisms and IVF/ICSI outcomes: a retrospective cohort study. Human reproduction open 2022 12 2023 (1): hoac055. Lu Yong-Jie, Li Qin, Chen Li-Xue, Tian Tian, Kang Jia, Hao Yong-Xiu, Zhou Jian-Suo, Wang Yuan-Yuan, Yan Li-Ying, Li Rong, Chang Liang, Qiao J |
PGT-A is associated with reduced cumulative live birth rate in first reported IVF stimulation cycles age ? 40: an analysis of 133,494 autologous cycles reported to SART CORS. Journal of assisted reproduction and genetics 2022 12 40 (1): 137-149. Kucherov Alexander, Fazzari Melissa, Lieman Harry, Ball G David, Doody Kevin, Jindal Sangi |
Investigation of the role of X chromosome inactivation and androgen receptor CAG repeat polymorphisms in patients with recurrent pregnancy loss: a prospective case-control study. BMC pregnancy and childbirth 2022 11 22 (1): 805. Sui Yilun, Fu Jing, Zhang Shuo, Li Lu, Sun Xiao |
Preimplantation genetic testing in two Danish couples affected by Peutz-Jeghers syndrome. Scandinavian journal of gastroenterology 2022 10 58 (3): 314-318. Byrjalsen Anna, Roos Laura, Diemer Tue, Karstensen John Gásdal, Løssl Kristine, Jelsig Anne Mar |
De novo variants and recombination at 4q35: Hints for preimplantation genetic testing in facioscapulohumeral muscular dystrophy. Clinical genetics 2022 10 103 (2): 242-246. Pini Sara, Napoli Floriana Maria, Tagliafico Enrico, La Marca Antonio, Bertucci Emma, Salsi Valentina, Tupler Rossel |
Impact of male age on paternal aneuploidy: single-nucleotide polymorphism microarray outcomes following blastocyst biopsy. Reproductive biomedicine online 2023 8 47 (4): 103245. Tanya Samarasekera, Elissa Willats, Mark P Green, Tristan Hardy, Luk Rombauts, Deirdre Zander-F |
Blinded rebiopsy and analysis of non-euploid embryos with two distinct preimplantation genetic testing platforms for aneuploidy. Fertility and sterility 2023 8 . Sarah Druckenmiller Cascante, Andria Besser, Hsiao-Ling Lee, Fang Wang, Caroline McCaffrey, James A Gri |
Clinical application of next generation sequencing-based haplotype linkage analysis in the preimplantation genetic testing for germline mosaicisms. Orphanet journal of rare diseases 2023 6 18 (1): 137. Dongjia Chen, Yan Xu, Yu Fu, Yali Wang, Yuliang Liu, Chenhui Ding, Bing Cai, Jiafu Pan, Jing Wang, Rong Li, Jing Guo, Han Zhang, Yanhong Zeng, Xiaoting Shen, Canquan Zh |
Preimplantation genetic testing for hereditary hearing loss in Chinese population. Journal of assisted reproduction and genetics 2023 4 . Bi Qingling, Huang Shasha, Wang Hui, Gao Xue, Ma Minyue, Han Mingyu, Lu Sijia, Kang Dongyang, Nourbakhsh Aida, Yan Denise, Blanton Susan, Liu Xuezhong, Yuan Yongyi, Yao Yuanqing, Dai |
Impact of Breast Cancer and Germline BRCA Pathogenic Variants on Fertility Preservation in Young Women. Life (Basel, Switzerland) 2023 4 13 (4): . Elze Prokurotaite, Margherita Condorelli, Julie Dechene, Jason Bouziotis, Matteo Lambertini, Isabelle Demeeste |
Retrospective Analysis of Meiotic Segregation Pattern and Reproductive Outcomes in Blastocysts from Robertsonian Preimplantation Genetic Testing Cycles. Reproductive sciences (Thousand Oaks, Calif.) 2023 4 . Miaomiao Jia, Juanzi Shi, Xia X |
Case report: A reciprocal translocation-free and pathogenic DUOX2 mutation-free embryo selected by complicated preimplantation genetic testing resulted in a healthy live birth. Frontiers in genetics 2023 3 14 1066199. Shi Biwei, Ye Yingh |
Ultra-low-coverage genome-wide association study-insights into gestational age using 17,844 embryo samples with preimplantation genetic testing.
Genome medicine 2023 2 15 (1): 10. Li Shumin, Yan Bin, Li Thomas K T, Lu Jianliang, Gu Yifan, Tan Yueqiu, Gong Fei, Lam Tak-Wah, Xie Pingyuan, Wang Yuexuan, Lin Ge, Luo Ruiba |
Correlation study of male semen parameters and embryo aneuploidy in preimplantation genetic testing for aneuploidy. Frontiers in endocrinology 2023 2 13 1072176. Yang Hongyi, Liu Yan, Niu Wenbin, Yang Zilan, Wang Yang, Jin Haixia, Li Ga |
The association between a carrier state of FMR1 premutation and numeric sex chromosome variations. Journal of assisted reproduction and genetics 2023 2 . Malcov Mira, Blickstein Ophir, Brabbing-Goldstein Dana, Reches Adi, Kalma Yael, Fouks Yuval, Azem Foad, Cohen Yo |
Clinical outcomes of preimplantation genetic testing for aneuploidy in high-risk patients: a retrospective cohort study. Clinical and experimental reproductive medicine 2023 12 . Jun Woo Kim, So Young Lee, Chang Young Hur, Jin Ho Lim, Choon Keun Pa |
A comprehensive preimplantation genetic testing approach for SEA-type ?-thalassemia by fluorescent gap-polymerase chain reaction combined with haplotype analysis. Frontiers in genetics 2023 12 14 1248358. Jing Wang, Yuanlin Ma, Jing Guo, Rong Li, Canquan Zhou, Yanwen |
Preimplantation genetic testing using comprehensive genomic copy number analysis is beneficial for balanced translocation carriers. Journal of human genetics 2023 10 . Aya Yamazaki, Tomoko Kuroda, Nami Kawasaki, Keiichi Kato, Keiko Shimojima Yamamoto, Takeshi Iwasa, Akira Kuwahara, Yuka Taniguchi, Toshiyuki Takeshita, Yosuke Kita, Mikio Mikami, Minoru Irahara, Toshiyuki Yamamo |
Robust preimplantation genetic testing of the common F8 Inv22 pathogenic variant of severe hemophilia A using a highly polymorphic multi-marker panel encompassing the paracentric inversion. Thrombosis journal 2023 10 21 (1): 108. Minh Tam Nguyen, Thanh Tung Nguyen, Duy Bac Nguyen, Thi Mai Nguyen, Kim Ngan Nguyen, Van Nhat Minh Ngo, Van Dieu Nguyen, Ngoc Anh Tran, Mulias Lian, Arnold S C Tan, Samuel S Chong, Tien Truong Da |
Association of State Insurance Mandates for Fertility Treatment With Multiple Embryo Transfer After Preimplantation Genetic Testing for Aneuploidy. JAMA network open 2023 1 6 (1): e2251739. Bedrick Bronwyn S, Nickel Katelin B, Riley Joan K, Jain Tarun, Jungheim Emily |
Fertility Preferences and Practices Among Young Women With Breast Cancer: Germline Genetic Carriers Versus Noncarriers. Clinical breast cancer 2023 1 . Lewinsohn Rebecca, Zheng Yue, Rosenberg Shoshana M, Ruddy Kathryn J, Tamimi Rulla M, Schapira Lidia, Peppercorn Jeffrey, Borges Virginia F, Come Steven, Snow Craig, Ginsburg Elizabeth S, Partridge Ann |
Hereditary deafness carrier screening in 9,993 Chinese individuals. Frontiers in genetics 2024 1 14 1327258. Yanqiu Liu, Lei Wang, Lanlai Yuan, Yaqing Li, Zhengshi Chen, Bicheng Yang, Daqing Wang, Yu S |
Extended application of PGT-M strategies for small pathogenic CNVs. Journal of assisted reproduction and genetics 2024 1 . Xiao Hu, Weili Wang, Keli Luo, Jing Dai, Yi Zhang, Zhenxing Wan, Wenbin He, Shuoping Zhang, Lanlin Yang, Qin Tan, Wen Li, Qianjun Zhang, Fei Gong, Guangxiu Lu, Yue-Qiu Tan, Ge Lin, Juan |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: