Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 1648 Records) |
Query Trace: Infertility[original query] |
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Gene Polymorphism, Microdeletion, and Gene Expression of PRM1, PRM2, AZFc in Infertile Males. Reports of biochemistry & molecular biology 2023 9 12 (1): 173-184. Nashwah Jabbar Kadhim, Narges Dastmalchi, Parisa Banamolaei, Reza Safaralizad |
Detection of GSTM1-null Genotype in Women Undergoing IVF Treatment. Journal of clinical medicine 2023 12 12 (23): . Ioannis Chrysanthopoulos, Angelos Petsavas, Despoina Mavrogianni, Anastasios Potiris, Nikolaos Machairiotis, Eirini Drakaki, Dionysios Vrachnis, Pavlos Machairoudias, Theodoros Karampitsakos, Paraskevas Perros, Christos Koratzanis, Peter Drakakis, Sofoklis Stavr |
Type 2 diabetes mellitus and the risk of male infertility: a Mendelian randomization study. Frontiers in endocrinology 2023 12 14 1279058. Xiao-Bin Zhu, Zhi-Hong Niu, Wei-Min Fan, Chang-Sheng Sheng, Qian Ch |
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 |
Association Between Endometritis and Endometrial Polyp: A Mendelian Randomization Study. International journal of women's health 2023 12 15 1963-1970. Longlong Wei, Yan Zhao, Siyue Xu, Cuilian Zha |
To Test or Not to Test: Routine Thrombophilia Diagnostic Screening of Women with Reproductive Failures. Journal of clinical medicine 2023 12 12 (24): . Urszula Wysocka, Kinga Sa?aci?ska, Iwona Pinkier, ?ukasz K?pczy?ski, Wojciech A?aszewski, Lech Dudarewicz, Agnieszka Ga |
Causal association between aspirin use and risk of endometrioid carcinoma: a Mendelian randomization study. European review for medical and pharmacological sciences 2023 12 27 (23): 11597-11605. X Chang, S-J Liu, L H |
Single nucleotide polymorphism rs527236194 of the cytochrome B gene (MT-CYB) is associated with alterations in sperm parameters. Molecular biology reports 2023 11 . Yulia Yu Gromenko, Kamil S Galimov, Irina R Gilyazova, Elmira F Galimova, Kirill V Bulygin, Sergey N Ryagin, Shamil N Galimov, Peter F Litvitskiy, Gennadii A Piavchenko, Valentin N Pavl |
Causal association between lipid-lowering drugs and female reproductive endocrine diseases: a drug-targeted Mendelian randomization study. Frontiers in endocrinology 2023 11 14 1295412. Jing Zhao, Runfang Wang, Liyun Song, Hua Han, Pei Wang, Yuan Zhao, Yunxia Zhang, Hongzhen Zha |
Whole exome sequencing reveals novel candidate variants for endometriosis utilizing multiple affected members in a single family. Molecular genetics & genomic medicine 2023 11 e2312. Busra Gizem Kina, Nura Fitnat Topbas Selcuki, Pinar Yalcin Bahat, Taner Usta, Sevcan Aydin, Nilufer Rahmioglu, Feyza Nur Tuncer, Engin Or |
Polymorphisms and expression levels of TNP2, SYCP3, and AZFa genes in patients with azoospermia. Clinical and experimental reproductive medicine 2023 11 50 (4): 253-261. Mohammad Ismael Ibrahim Jebur, Narges Dastmalchi, Parisa Banamolaei, Reza Safaralizad |
Association of GSTM1 Polymorphism and Redox Potential with Idiopathic Male Infertility. Journal of clinical medicine 2023 11 12 (21): . Anastasios Potiris, Anastasia Voitse, Despoina Mavrogianni, Nikolaos Machairiotis, Eirini Drakaki, Myrto Papamentzelopoulou, Theodoros Karampitsakos, Athanasios Zikopoulos, Evangelini Evgeni, Peter Drakakis, Sofoklis Stavr |
Novel Mutations Reduce Expression of Meiotic Regulators SYCE1 and BOLL in Testis of Azoospermic Men from West Bengal, India. Reproductive sciences (Thousand Oaks, Calif.) 2023 11 . Samudra Pal, Pranab Paladhi, Saurav Dutta, Rupam Basu Mullick, Gunja Bose, Papiya Ghosh, Ratna Chattopadhyay, Sujay Gho |
Compound heterozygous mutations in TBPL2 were identified in an infertile woman with impaired ovarian folliculogenesis. Journal of assisted reproduction and genetics 2023 10 . Tian Du, Meiling Li, Li Chen, Yong Shao, Yichun Wang, Hui Wang, Jinzhao Ma, Bing Y |
Changing the standardised obstetric care by expanded carrier screening and counselling: a multicentre prospective cohort study. Journal of medical genetics 2023 10 . Han-Ying Chen, Shin-Yu Lin, Jin-Chung Shih, Jessica Kang, Yi-Yun Tai, Steven W Shaw, Kuang-Cheng Chen, Kevin Mai, Chien-Nan L |
A Comprehensive Genetic Study of Microtubule-Associated Gene Clusters for Male Infertility in a Taiwanese Cohort. International journal of molecular sciences 2023 10 24 (20): . Chying-Chyuan Chan, Te-Hsin Yen, Hao-Chen Tseng, Brang Mai, Pin-Kuan Ho, Jian-Liang Chou, Gwo-Jang Wu, Yu-Chuan Hua |
Correction to: A novel nonsense mutation of PNLDC1 associated with male infertility due to oligo-astheno-teratozoospermia in a consanguineous Chinese family. QJM : monthly journal of the Association of Physicians 2023 10 116 (10): 890. Authors are not available |
Unraveling the Genetic Associations of DENND1A (rs9696009) and ERBB4 (rs2178575) with Infertile Polycystic Ovary Syndrome Females in Pakistan. Biochemical genetics 2023 10 . Zainab Hanif Samma, Haq Nawaz Khan, Sumaira Riffat, Mussarat Ashraf, Rehana Rehm |
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 |
ESX1 gene as a potential candidate responsible for male infertility in nonobstructive azoospermia. Scientific reports 2023 10 13 (1): 16563. Agnieszka Malcher, Zuzanna Graczyk, Hermann Bauer, Tomasz Stokowy, Andrea Berman, Miko?aj Smolibowski, Dominika Blaszczyk, Piotr Jedrzejczak, Alexander N Yatsenko, Maciej Kurpi |
Correlation between LHCGR and NR5A1 genes polymorphism and male infertility risk. Actas urologicas espanolas 2023 10 . M Behvarz, S A Rahmani, E Siasi Torbati, S Danaei Mehrabad, M Bikhof Torba |
Identification of a Single Nucleotide Polymorphism of Vitamin D Receptor (VDR) and Vitamin D Binding Protein (VDBP) Gene and Its Dysregulated Pathway Through VDR-VDBP Interaction Network Analysis in Vitamin D-Deficient Infertile Females. Cureus 2024 4 16 (3): e55602. Zil E Rubab, Sumaira Naz, Mussarat Ashraf, Saba Shahid, Rehana Rehm |
A report of two homozygous TERB1 protein-truncating variants in two unrelated women with primary infertility. Journal of assisted reproduction and genetics 2024 1 . Zeynep Yalcin, Manqi Liang, Ibrahim M Abdelrazek, Corinna Friedrich, Eric Bareke, Amira Nabil, Frank Tüttelmann, Jacek Majewski, Ebtesam Abdalla, Seang-Lin Tan, Rima Sl |
Y chromosome polymorphisms contribute to an increased risk of non-obstructive azoospermia: a retrospective study of 32,055 Chinese men. Journal of assisted reproduction and genetics 2024 1 . Jing-Ping Li, Feng-Bin Zhang, Le-Jun Li, Wei-Kang Chen, Jing-Gen Wu, Yong-Hong Tian, Zhong-Yan Liang, Chong Chen, Fan J |
Russian Regional Differences in Allele Frequencies of CFTR Gene Variants: Genetic Monitoring of Infertile Couples. Genes 2024 1 15 (1): . Andrey S Glotov, Vyacheslav B Chernykh, Olga A Solovova, Aleksander V Polyakov, Maksim Yu Donnikov, Ludmila V Kovalenko, Yury A Barbitoff, Yulia A Nasykhova, Tatyana E Lazareva, Oleg S Glot |
Investigating the association of previously identified genome-wide significant loci (rs10739076 and rs1784692) with PCOS susceptibility and its related traits in Indian women. European journal of obstetrics, gynecology, and reproductive biology 2024 1 294 156-162. Roshan Dadachanji, Sushma Khavale, Anushree Patil, Srabani Mukherj |
The Effect of FSHR (G2039A) Polymorphism on Müllerian Duct Development and Hormonal Profile of Women with Primary Amenorrhea. Journal of reproduction & infertility 2024 1 24 (4): 240-247. Priyanka Sanghavi, Divya Chand |
The causal relationship of female infertility and psychiatric disorders in the European population: a bidirectional two-sample Mendelian randomization study. BMC women's health 2024 1 24 (1): 54. Pengfei Zeng, Hanxiao Zhang, Liyue Lu, Yanting Li, Tong Yu, Jun Zhang, Hang Zh |
A cryptozoospermic infertile male with Y chromosome AZFc microdeletion and low FSH levels due to a simultaneous polymorphism in the FSHB gene: a case report. Human reproduction (Oxford, England) 2024 1 . Andrea Graziani, Maurizio Merico, Giuseppe Grande, Antonella Di Mambro, Cinzia Vinanzi, Maria Santa Rocca, Riccardo Selice, Alberto Ferl |
Genetic Architecture of Pregnancy Loss: Co-inheritance of Risk Factors in Bosnian Women. Folia biologica 2024 1 69 (3): 75-80. Gra?yna Adler, Mateusz A Adler, Emir Mahmutbegov |
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- Page last updated:Apr 16, 2024
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