Human Genome Epidemiology Literature Finder
Reproductive and Child Health
Records 1 - 30 (of 2400 Records) |
Query Trace: Fertility Or Infertility[original query] |
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Genomic prediction of male fertility in Brown Swiss cattle. JDS communications 2024 12 5 (6): 568-571. Hendyel A Pacheco, Attilio Rossoni, Alessio Cecchinato, Francisco Peñagarica |
Koala MHCII association with chlamydia infertility remains equivocal: a need for new research approaches. Scientific reports 2024 12 14 (1): 31074. Alana Kidd, Andrea Casteriano, Mark B Krockenberger, Damien P Higgins, Belinda R Wrig |
CYP19 and ESR2 polymorphisms as potential culprits in cryptorchidism. Journal of pediatric urology 2024 12 . Tubanur Kaya Kurt, Alev Suzen, Cilem Ozdemir, Tuba Edgunlu, Muhammed Kurt, Ramazan Gungorm |
Preimplantation genetic testing for structural rearrangements by genome-wide SNP genotyping and haplotype analysis: a prospective multicenter clinical study. EBioMedicine 2024 12 111 105514. Shuo Zhang, Yuan Gao, Xiaohong Wang, Qing Li, Jichun Tan, Bo Liang, Ming Gao, Junping Wu, Xiufeng Ling, Jiayin Liu, Xiaoming Teng, Hong Li, Yun Sun, Weidong Huang, Xianhong Tong, Caixia Lei, Hongchang Li, Jun Wang, Shaoying Li, Xiaoyan Xu, Junqiang Zhang, Wei Wu, Shanshan Liang, Jian Ou, Qiongzhen Zhao, Rentao Jin, Yueping Zhang, Chenming Xu, Daru Lu, Junhao Yan, Xiaoxi Sun, Kwong Wai Choy, Congjian Xu, Zi-Jiang Ch |
Telomere length in relation to fecundability and use of assisted reproductive technologies: the Norwegian Mother, Father, and Child Cohort Study. BMC medicine 2024 12 22 (1): 580. Karoline H Skåra, Yunsung Lee, Astanand Jugessur, Håkon K Gjessing, Abraham Aviv, Ben Brumpton, Øyvind Næss, Álvaro Hernáez, Hans Ivar Hanevik, Per Magnus, Maria C Magn |
A comprehensive study of common and rare genetic variants in spermatogenesis-related loci identifies new risk factors for idiopathic severe spermatogenic failure. Human reproduction open 2024 12 2024 (4): hoae069. Andrea Guzmán-Jiménez, Sara González-Muñoz, Miriam Cerván-Martín, Nicolás Garrido, José A Castilla, M Carmen Gonzalvo, Ana Clavero, Marta Molina, Saturnino Luján, Samuel Santos-Ribeiro, Miguel Ángel Vilches, Andrea Espuch, Vicente Maldonado, Noelia Galiano-Gutiérrez, Esther Santamaría-López, Cristina González-Ravina, Fernando Quintana-Ferraz, Susana Gómez, David Amorós, Luis Martínez-Granados, Yanira Ortega-González, Miguel Burgos, Iris Pereira-Caetano, Ozgur Bulbul, Stefano Castellano, Massimo Romano, Elena Albani, Lluís Bassas, Susana Seixas, João Gonçalves, Alexandra M Lopes, Sara Larriba, Rogelio J Palomino-Morales, F David Carmona, Lara Bossini-Castil |
Effect analysis of S5-interacting genes on rice hybrid sterility using nontransgenic gamete killer. Plant science : an international journal of experimental plant biology 2024 12 352 112357. Jie Li, Fu Huang, Yingxia Jiang, Jianglei Rao, Yourong Fan, Jiangyi Ya |
Evaluating the impact of LHCGR gene polymorphism on polycystic ovary syndrome: a comprehensive meta-analysis and power assessment. Journal of the Turkish German Gynecological Association 2024 12 25 (4): 207-218. Sheena Mariam Thomas, Ramakrishnan Veerabathir |
Metabolome-Wide Mendelian Randomization Assessing the Causal Relationship Between Blood Metabolites and Primary Ovarian Insufficiency. Clinical nutrition ESPEN 2024 11 . Yijie Chen, Jun Chen, Ji Wu, Xianguo Qu, Zhifen Zha |
Gonadal changes in children and adolescents with congenital adrenal hyperplasia. Journal of pediatric endocrinology & metabolism : JPEM 2024 11 . Rana Mahmoud, Marwa Elsayed Abdelrahman, Hasnaa Hassan Mohamed, Heba Elsed |
Multi-locus high-risk alleles association from interleukin's genes with female infertility and certain comorbidities. BMC research notes 2024 11 17 (1): 344. Khalil Khashei Varnamkhasti, Samire Khashei Varnamkhasti, Najmeh Bahraini, Mohaddeseh Davoodi, Mahsa Sadeghian, Massomeh Khavanin, Raana Naeimi, Sirous Naei |
Inherited infertility: Mapping loci associated with impaired female reproduction. American journal of human genetics 2024 11 . Sanni Ruotsalainen, Juha Karjalainen, Mitja Kurki, Elisa Lahtela, Matti Pirinen, Juha Riikonen, Jarmo Ritari, Silja Tammi, Jukka Partanen, Hannele Laivuori, , Aarno Palotie, Henrike Heyne, Mark Daly, Elisabeth Wid |
Associations between maternal MTHFR polymorphisms and embryological outcomes in Korean patients with infertility undergoing IVF/ICSI cycles. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2024 11 40 (1): 2431224. Yoo Ra Ko, Tae Hyung Kim, Eum Jin Hee, Woo Sik Lee, Se Jeong K |
Epidemiology and Risk Factors for Testicular Cancer: A Systematic Review. European urology 2024 11 . Valentina Tateo, Zachary J Thompson, Scott M Gilbert, Victoria K Cortessis, Siamak Daneshmand, Timothy A Masterson, Darren R Feldman, Phillip M Pierorazio, Gagan Prakash, Axel Heidenreich, Peter Albers, Andrea Necchi, Philippe E Spie |
Blood-Based Inflammatory Markers in Female Infertility: Evidence from Mendelian Randomisation Analysis. F&S science 2024 11 . Simon Alesi, Helena Teede, Joanne Enticott, Kushan De Silva, Aya Mou |
Novel variants in DNAH9 are present in two infertile patients with severe asthenospermia. Journal of human genetics 2024 11 . Fei Yan, Weiwei Zhi, Yazhen Wei, Li Dai, Wenming Xu, Rui Zhe |
Novel Loss-of-function Variants of ZP3 Associated with Premature Ovarian Insufficiency. Reproductive sciences (Thousand Oaks, Calif.) 2024 11 . Lang Zhou, Xi Yang, Shuting Ren, Yuncheng Pan, Zixue Zhou, Yiqing Liu, Jitong Mo, Feng Zhang, Xiaojin Zhang, Yanhua |
Rare variation in LMNA underlies polycystic ovary syndrome (PCOS) pathogenesis in two independent cohorts. The Journal of clinical endocrinology and metabolism 2024 11 . Rosemary Bauer, Chloe Parker, Lidija K Gorsic, M Geoffrey Hayes, Allen R Kunselman, Richard S Legro, Corrine K Welt, Margrit Urban |
Population-Based Study of Rare Coding Variants in NR5A1/SF-1. Journal of the Endocrine Society 2024 10 8 (12): bvae178. Chrysanthi Kouri, Raina Y Jia, Katherine A Kentistou, Eugene J Gardner, John R B Perry, Christa E Flück, Ken K O |
MTHFR C677T?MTHFR A1298C?MTRR A66G and MTR A2756G polymorphisms and male infertility risk: a systematic review and meta-analysis. Reproductive biology and endocrinology : RB&E 2024 10 22 (1): 133. Feng Li, Ju-Ju Qi, Li-Xin Li, Teng-Fei Y |
Serum iron status and the risk of female infertility in European populations: A two-sample Mendelian randomization study. Medicine 2024 10 103 (43): e40220. Ziping Liu, Zelin Zhang, Ping X |
The Human 8-oxoG DNA Glycosylase 1 (OGG1) Ser326Cys Polymorphism in Infertile Men. Biomedicines 2024 10 12 (10): . César Antonio González-Díaz, María Antonieta Suárez-Souto, Elvia Pérez-Soto, Modesto Gómez-López, Jacobo Esteban Munguía-Cervantes, Nadia Mabel Pérez-Vielma, Virginia Sánchez-Monr |
Genetic Polymorphisms of Prokineticins and Prokineticin Receptors Associated with Human Disease. Life (Basel, Switzerland) 2024 10 14 (10): . Roberta Lattanzi, Rossella Mie |
The Causal Effect of Urate Level on Female Infertility: A Mendelian Randomization Study. Metabolites 2024 10 14 (10): . Jiawei Sun, Ting Shen, Yining Guan, Yixin Jiang, Xiaoling |
Human papillomavirus carriage in the semen of men consulting for infertility: prevalence and correlations with sperm characteristics. Asian journal of andrology 2024 10 . Armin Priam, Antoine Le Bozec, Vasco Dias Meireles, Fabien Saint, Rosalie Cabry, Moncef Benkhalifa, Baptiste Demey, Dorian Bosqu |
Causal association between thyroid function and the risk of infertility: a Mendelian randomization study. Frontiers in endocrinology 2024 10 15 1425639. Qinyu Liu, Yingkun Qiu, Jialin Jiang, Shushu Long, Chengyu Zhu, Gang Chen, Junping W |
Diminished DNA binding affinity of DMRT1 caused by heterozygous DM domain mutations is a cause of male infertility. Human molecular genetics 2025 1 . Tihana Mari?, Helen Castillo-Madeen, Monika Logara Klari?, Antun Bariši?, Lovro Trgovec-Greif, Mark W Murphy, Anna-Grete Juchnewitsch, Kristiina Lillepea, Avirup Dutta, Lucija Žuni?, Alexandra M Stendahl, Margus Punab, Kristjan Pomm, Daniel M Mendoza, Alexandra M Lopes, Ana Merkler Šorgi?, Oliver Vugrek, Joao Gonçalves, Kristian Almstrup, Kenneth I Aston, Robert Beluži?, Davor Ježek, Branimir Bertoša, Maris Laan, Ana Katuši? Bojanac, Donald F Conrad, Maja Barbal |
A Case-Control Study of the Association Between GSTP1 Gene Polymorphisms (rs1695 and rs1138272) and the Susceptibility to Male Infertility in the Moroccan Population. Genetic testing and molecular biomarkers 2025 1 . Houda Harmak, Salaheddine Redouane, Hicham Charoute, Ouafaa Aniq Filali, Abdelhamid Barakat, Hassan Rou |
Maternal X chromosome pericentric inversion resulting in the genetic analysis of offspring pedigrees with deletions at Xp22.33 and Xp22.33p11.3, and duplications at Xq27.3q28: Case report. Medicine 2025 1 104 (2): e41255. Guo-Sheng Deng, Yu-Qing Lai, Bo-Wen Luo, Yu-Di Luo, Ling-Ling Zhu, Zeng-Yu Yang, Keng Feng, De-Rong Li, Xiang |
Utilization of natural alleles and haplotypes of Ctb1 for rice cold adaptability. Gene 2025 1 941 149225. Lingling Li, Gongye Cheng, Wenyu Li, Di Zhang, Jianghui Yu, Huang Zhou, Xiaoping Ding, Zhijun Wang, Wanjing Zhu, Jiajia Li, Jiwai He, Meijuan Duan, Citao L |
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