Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 45 Records) |
Query Trace: FOXL2[original query] |
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DICER1 and FOXL2 mutations in ovarian sex cord-stromal tumours: a GINECO Group study. Histopathology 2015 Jun . Goulvent Thibault, Ray-Coquard Isabelle, Borel Stéphane, Haddad Véronique, Devouassoux-Shisheboran Mojgan, Vacher-Lavenu Marie-Cecile, Pujade-Laurraine Eric, Savina Ariel, Maillet Denis, Gillet Germain, Treilleux Isabelle, Rimokh Ru |
Polymorphism of the CTNNB1 and FOXL2 Genes is not Associated with Canine XX Testicular/Ovotesticular Disorder of Sex Development. Folia biologica 2015 63 (1): 57-62. Salamon Sylwia, Nowacka-Woszuk Joanna, Switonski Mar |
A novel FOXL2 gene mutation and BMP15 variants in a woman with primary ovarian insufficiency and blepharophimosis-ptosis-epicanthus inversus syndrome. Menopause (New York, N.Y.) 2015 May . Settas Nikolaos, Anapliotou Margarita, Kanavakis Emmanuel, Fryssira Helen, Sofocleous Christalena, Dacou-Voutetakis Catherine, Chrousos George P, Voutetakis Anton |
SNP rs1511412 in FOXL2 gene as a risk factor for keloid by meta analysis. International journal of clinical and experimental medicine 2015 8 (2): 2766-71. Lu Wensheng, Zheng Xiaodong, Liu Shengli, Ding Maoqian, Xie Jian, Yao Xiuhua, Zhang Lanfang, Hu B |
Refining prognosis and identifying targetable pathways for high-risk endometrial cancer; a TransPORTEC initiative. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2015 Jun 28 (6): 836-44. Stelloo Ellen, Bosse Tjalling, Nout Remi A, MacKay Helen J, Church David N, Nijman Hans W, Leary Alexandra, Edmondson Richard J, Powell Melanie E, Crosbie Emma J, Kitchener Henry C, Mileshkin Linda, Pollock Pamela M, Smit Vincent T, Creutzberg Carien |
A survey of DICER1 hotspot mutations in ovarian and testicular sex cord-stromal tumors. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2015 Oct . Conlon Niamh, Schultheis Anne M, Piscuoglio Salvatore, Silva Annacarolina, Guerra Esther, Tornos Carmen, Reuter Victor E, Soslow Robert A, Young Robert H, Oliva Esther, Weigelt Brit |
Identification of Multiple Gene Mutations Accounts for a new Genetic Architecture of Primary Ovarian Insufficiency. The Journal of clinical endocrinology and metabolism 2016 Sep jc20162152. Bouilly Justine, Beau Isabelle, Barraud Sara, Bernard Valérie, Azibi Kemal, Fagart Jérôme, Fèvre Anne, Todeschini Anne Laure, Veitia Reiner A, Beldjord Chérif, Delemer Brigitte, Dodé Catherine, Young Jacques, Binart Nadi |
Prognostic factors in the myoepithelial-like spindle cell type of metaplastic breast cancer. Virchows Archiv : an international journal of pathology 2016 May . Leo Fabian, Bartels Stephan, Mägel Lavinia, Framke Theodor, Büsche Guntram, Jonigk Danny, Christgen Matthias, Lehmann Ulrich, Kreipe Ha |
Mutational heterogeneity in non-serous ovarian cancers. Scientific reports 2017 Aug 7 (1): 9728. Teer Jamie K, Yoder Sean, Gjyshi Anxhela, Nicosia Santo V, Zhang Chaomei, Monteiro Alvaro N |
FOXL2 Mutation Analysis of Ovarian Sex Cord-Stromal Tumors: Genotype-Phenotype Correlation With Diagnostic Considerations. International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists 2017 Jul . Buza Natalia, Wong Serena, Hui P |
Seven Novel and Three Known Mutations in FOXL2 in 10 Chinese Families with Blepharophimosis Syndrome. Current molecular medicine 2018 9 18 (3): 152-159. Lin B, Zeng B, Zhao J, Xu T, Wang Y, Hu B, Li F, Zhao Q, Liu R, Liu J, Chen J M, Huang D, Wang |
Mutational Landscape of Ovarian Adult Granulosa Cell Tumors from Whole Exome and Targeted TERT Promoter Sequencing. Molecular cancer research : MCR 2018 9 17 (1): 177-185. Alexiadis Maria, Rowley Simone M, Chu Simon, Leung Dilys T H, Stewart Colin J R, Amarasinghe Kaushalya C, Campbell Ian G, Fuller Peter |
KMT2D/MLL2 inactivation is associated with recurrence in adult-type granulosa cell tumors of the ovary. Nature communications 2018 Jun 9 (1): 2496. Hillman R Tyler, Celestino Joseph, Terranova Christopher, Beird Hannah C, Gumbs Curtis, Little Latasha, Nguyen Tri, Thornton Rebecca, Tippen Samantha, Zhang Jianhua, Lu Karen H, Gershenson David M, Rai Kunal, Broaddus Russell R, Futreal P Andr |
"Evaluation of four genes associated with primary ovarian insufficiency in a cohort of Mexican women". Journal of assisted reproduction and genetics 2018 Jun . Juárez-Rendón K J, García-Ortiz J |
Novel Genetic Variants of Sporadic Atrial Septal Defect (ASD) in a Chinese Population Identified by Whole-Exome Sequencing (WES). Medical science monitor : international medical journal of experimental and clinical research 2018 Mar 24 1340-1358. Liu Yong, Cao Yu, Li Yaxiong, Lei Dongyun, Li Lin, Hou Zong Liu, Han Shen, Meng Mingyao, Shi Jianlin, Zhang Yayong, Wang Yi, Niu Zhaoyi, Xie Yanhua, Xiao Benshan, Wang Yuanfei, Li Xiao, Yang Lirong, Wang Wenju, Jiang Liho |
Loss of Function of the Nuclear Receptor NR2F2, Encoding COUP-TF2, Causes Testis Development and Cardiac Defects in 46,XX Children. American journal of human genetics 2018 2 102 (3): 487-493. Bashamboo Anu, Eozenou Caroline, Jorgensen Anne, Bignon-Topalovic Joelle, Siffroi Jean-Pierre, Hyon Capucine, Tar Attila, Nagy Péter, Sólyom Janos, Halász Zita, Paye-Jaouen Annnabel, Lambert Sophie, Rodriguez-Buritica David, Bertalan Rita, Martinerie Laetitia, Rajpert-De Meyts Ewa, Achermann John C, McElreavey K |
A Novel FOXL2 Mutation Implying Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Type I. Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2018 1 45 (1): 203-211. Li Fang, Chai Peiwei, Fan Jiayan, Wang Xi, Lu Wenjuan, Li Jin, Ge Shengfang, Jia Renbing, Zhang He, Fan Xianq |
Clinical characterization and identification of five novel FOXL2 pathogenic variants in a cohort of 12 Mexican subjects with the syndrome of blepharophimosis-ptosis-epicanthus inversus. Gene 2019 5 706 62-68. Chacón-Camacho Oscar F, Salgado-Medina Acatzin, Alcaraz-Lares Nayeli, López-Moreno Daniel, Barragán-Arévalo Tania, Nava-Castañeda Angel, Rodríguez-Uribe Genaro, Lieberman Esther, Rodríguez-Cabrera Lourdes, González-Del Angel Ariadna, Borbolla Ana María, Fernández-Hernández Liliana, Graue-Hernández Enrique O, Zenteno Juan Carl |
Whole-exome sequencing in patients with premature ovarian insufficiency: early detection and early intervention. Journal of ovarian research 2020 9 13 (1): 114. Liu Hongli, Wei Xiaoli, Sha Yanwei, Liu Wensheng, Gao Haijie, Lin Jin, Li Youzhu, Tang Yaling, Wang Yifeng, Wang Yanlong, Su Zhiyi |
Whole Genome Analysis of Ovarian Granulosa Cell Tumors Reveals Tumor Heterogeneity and a High-Grade TP53-Specific Subgroup. Cancers 2020 5 12 (5): . Roze Joline, Monroe Glen, Kutzera Joachim, Groeneweg Jolijn, Stelloo Ellen, Paijens Sterre, Nijman Hans, Meurs Hannah van, Lonkhuijzen Luc van, Piek Jurgen, Lok Christianne, Jonges Geertruida, Witteveen Petronella, Verheijen René, Haaften Gijs van, Zweemer Rona |
Genomic profiling of primary and recurrent adult granulosa cell tumors of the ovary. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2020 Mar . Da Cruz Paula Arnaud, da Silva Edaise M, Segura Sheila E, Pareja Fresia, Bi Rui, Selenica Pier, Kim Sarah H, Ferrando Lorenzo, Vahdatinia Mahsa, Soslow Robert A, Vidal August, Gatius Sonia, Przybycin Christopher G, Abu-Rustum Nadeem R, Matias-Guiu Xavier, Rubin Brian P, Reis-Filho Jorge S, DeLair Deborah F, Weigelt Brit |
FOXL2 homozygous genotype and chromosome instability are associated with recurrence in adult granulosa cell tumors of the ovary. Oncotarget 2020 2 11 (4): 419-428. Kraus Francois, Dremaux Julie, Altakfi Wajd, Goux Magalie, Pontois Léa, Sevestre Henri, Trudel Stéphan |
Next Generation Sequencing Should Be Proposed to Every Woman With "Idiopathic" Primary Ovarian Insufficiency. Journal of the Endocrine Society 2021 6 5 (7): bvab032. Eskenazi Sarah, Bachelot Anne, Hugon-Rodin Justine, Plu-Bureau Genevieve, Gompel Anne, Catteau-Jonard Sophie, Molina-Gomes Denise, Dewailly Didier, Dodé Catherine, Christin-Maitre Sophie, Touraine Philip |
Genetic etiologic analysis in 74 Chinese Han women with idiopathic premature ovarian insufficiency by combined molecular genetic testing. Journal of assisted reproduction and genetics 2021 Feb . Shen Jiandong, Qu Dianyun, Gao Yan, Sun Fangxi, Xie Jiazi, Sun Xueping, Wang Daowu, Ma Xiang, Cui Yugui, Liu Jiayin, Diao Feiya |
Upfront Next Generation Sequencing in Non-Small Cell Lung Cancer. Current oncology (Toronto, Ont.) 2022 Jun 29 (7): 4428-4437. Kuang Shelley, Fung Andrea S, Perdrizet Kirstin A, Chen Kaitlin, Li Janice J N, Le Lisa W, Cabanero Michael, Karsaneh Ola Abu Al, Tsao Ming S, Morganstein Josh, Ranich Laura, Smith Adam C, Wei Cuihong, Cheung Carol, Shepherd Frances A, Liu Geoffrey, Bradbury Penelope, Pal Prodipto, Schwock Joerg, Sacher Adrian G, Law Jennifer H, Stockley Tracy L, Leighl Natasha |
Genetic variations in triple-negative breast cancers undergoing neo-adjuvant chemotherapy. Cancer drug resistance (Alhambra, Calif.) 2022 5 2 (3): 877-884. Mori Miki, Watanabe Tomoko, Akashi-Tanaka Sadako, Ueda Kumiko, Makino Reiko, Hirota Yuko, Nakamura Sei |
Ovarian Reserve and ART Outcomes in Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome Patients With FOXL2 Mutations. Frontiers in endocrinology 2022 5 13 829153. Meng Tingting, Zhang Wenzhe, Zhang Rongrong, Li Jie, Gao Yuan, Qin Yingying, Jiao X |
CHEK2 Mutation Is Associated with Increased Risk of Adult-Type Ovarian Granulosa Cell Tumors. Cancers 2022 3 14 (5): . Švajdler Peter, Vasov?ák Peter, Švajdler Marián, Šedivcová Monika, Urbán Veronika, Michal Michal, Mezencev Rom |
Identification and functional analyses of a novel FOXL2 pathogenic variant causing blepharophimosis, ptosis, and epicanthus inversus syndrome. International journal of ophthalmology 2023 5 16 (5): 680-686. Yu-Cheng Yan, Lu Zhou, Jin-Cai F |
Next-generation sequencing of 500 POI patients identified novel responsible monogenic and oligogenic variants. Journal of ovarian research 2023 2 16 (1): 39. Luo Wei, Ke Hanni, Tang Shuyan, Jiao Xue, Li Zhuqing, Zhao Shidou, Zhang Feng, Guo Ting, Qin Yingyi |
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- Page last updated:Apr 29, 2024
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