Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Hyperparathyroidism and GCM2[original query] |
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| Increased prevalence of the GCM2 polymorphism, Y282D, in primary hyperparathyroidism: analysis of three Italian cohorts. The Journal of clinical endocrinology and metabolism 2014 Dec 99 (12): E2794-8. D'Agruma Leonardo, Coco Michela, Guarnieri Vito, Battista Claudia, Canaff Lucie, Salcuni Antonio S, Corbetta Sabrina, Cetani Filomena, Minisola Salvatore, Chiodini Iacopo, Eller-Vainicher Cristina, Spada Anna, Marcocci Claudio, Guglielmi Giuseppe, Zini Michele, Clemente Rosanna, Wong Betty Y L, de Martino Danilo, Scillitani Alfredo, Hendy Geoffrey N, Cole David E |
| Ethnicity of Patients With Germline GCM2-Activating Variants and Primary Hyperparathyroidism. Journal of the Endocrine Society 2017 12 1 (5): 488-499. Guan Bin, Welch James M, Vemulapalli Meghana, Li Yulong, Ling Hua, Kebebew Electron, Simonds William F, Marx Stephen J, Agarwal Sunita |
| Familial isolated primary hyperparathyroidism associated with germline GCM2 mutations is more aggressive and has a lesser rate of biochemical cure. Surgery 2017 11 163 (1): 31-34. El Lakis Mustapha, Nockel Pavel, Guan Bin, Agarwal Sunita, Welch James, Simonds William F, Marx Stephen, Li Yulong, Nilubol Naris, Patel Dhaval, Yang Lily, Merkel Roxanne, Kebebew Electr |
| Should the GCM2 gene be tested when screening for familial primary hyperparathyroidism? European journal of endocrinology 2019 11 182 (1): 57-65. Coppin Lucie, Dufosse Margaux, Romanet Pauline, Giraud Sophie, North Marie-Odile, Cardot Bauters Catherine, Borson-Chazot Françoise, Duchesne Laurence, Métallo Mélanie, Lovecchio Tonio, Barlier Anne, Odou Marie-Françoi |
| Analysis of Activating GCM2 Sequence Variants in Sporadic Parathyroid Adenomas. The Journal of clinical endocrinology and metabolism 2019 1 104 (6): 1948-1952. Riccardi Aaliyah, Aspir Tori, Shen Lilia, Kuo Chia-Ling, Brown Taylor C, Korah Reju, Murtha Timothy D, Bellizzi Justin, Parham Kourosh, Carling Tobias, Costa-Guda Jessica, Arnold Andr |
| GERMLINE GCM2 MUTATION SCREENING IN CHINESE PRIMARY HYPERPARATHYROIDISM PATIENTS. Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2020 6 . Song An, Yang Yi, Wang Yabing, Liu Shuzhong, Nie Min, Jiang Yan, Li Mei, Xia Weibo, Wang Ou, Xing Xiaopi |
| Integrated Whole-Exome and Transcriptome Sequencing of Sporadic Parathyroid Adenoma. Frontiers in endocrinology 2021 5 12 631680. Hu Ya, Zhang Xiang, Wang Ou, Cui Ming, Li Xiaobin, Wang Mengyi, Hua Surong, Liao Qu |
| Five patients with disorders of calcium metabolism presented with GCM2 gene variants. Scientific reports 2021 2 11 (1): 2968. García-Castaño Alejandro, Madariaga Leire, Gómez-Conde Sara, Cordo Carmen Lourdes Rey, López-Iglesias María, Garcia-Fernández Yolanda, Martín Alicia, González Pedro, Goicolea Ignacio, de Nanclares Gustavo Pérez, De la Hoz Ana Belén, Aguayo Aníbal, de LaPiscina Idoia Martínez, Martínez Rosa, Saso Laura, Urrutia Inés, Velasco Olaia, Castaño Luis, Gaztambide Son |
| GCM2 Variants in Familial and Multiglandular Primary Hyperparathyroidism. The Journal of clinical endocrinology and metabolism 2021 12 107 (5): e2021-e2026. Vincze Sarah, Peters Nicholas V, Kuo Chia-Ling, Brown Taylor C, Korah Reju, Murtha Timothy D, Bellizzi Justin, Riccardi Aaliyah, Parham Kourosh, Carling Tobias, Costa-Guda Jessica, Arnold Andr |
| Germline GCM2 Mutation Screening in Chinese Primary Hyperparathyroidism Patients. Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists 2020 Oct 26 (10): 1093-1104. Song An, Yang Yi, Wang Yabing, Liu Shuzhong, Nie Min, Jiang Yan, Li Mei, Xia Weibo, Wang Ou, Xing Xiaopi |
| Germline Mutations Related to Primary Hyperparathyroidism Identified by Next-Generation Sequencing. Frontiers in endocrinology 2022 5 13 853171. Park Hye-Sun, Lee Yeon Hee, Hong Namki, Won Dongju, Rhee Yum |
| Novel Glial Cells Missing-2 (GCM2) variants in parathyroid disorders. European journal of endocrinology 2022 1 186 (3): 351-366. Canaff Lucie, Guarnieri Vito, Kim Yoojung, Wong Betty Y L, Nolin-Lapalme Alexis, Cole David E C, Minisola Salvatore, Eller-Vainicher Cristina, Cetani Filomena, Repaci Andrea, Turchetti Daniela, Corbetta Sabrina, Scillitani Alfredo, Goltzman Dav |
| Genetic and clinical screening for hereditary primary hyperparathyroidism in a large Chinese cohort: a single-center study. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2023 7 . An Song, Yi Yang, Yue Jiang, Min Nie, Yan Jiang, Mei Li, Weibo Xia, Xiaoping Xing, Ou Wa |
| Variant Tyr 394Ser in the GCM2 Gene Is Rare in a Cohort of Ashkenazi Jews With Primary Hyperparathyroidism. Journal of the Endocrine Society 2023 6 7 (7): bvad086. Lior Tolkin, Vanessa Klein, Meir Frankel, Gheona Altarescu, Rachel Beeri, Gabriel Munt |
| Genetic testing for familial hyperparathyroidism: clinical-genetic profile in a Mediterranean cohort. Frontiers in endocrinology 2023 10 14 1244361. Isabel Mazarico-Altisent, Ismael Capel, Neus Baena, Maria Rosa Bella-Cueto, Santi Barcons, Xavier Guirao, Rocío Pareja, Andreea Muntean, Valeria Arsentales, Assumpta Caixàs, Mercedes Rig |
- Page last reviewed:Oct 1, 2023
- Page last updated:Dec 04, 2023
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