Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Syndrome and HMGA2[original query] |
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| Smallness for gestational age interacts with high mobility group A2 gene genetic variation to modulate height. European journal of endocrinology / European Federation of Endocrine Societies 2009 Apr 160 (4): 557-60. Bouatia-Naji Nabila, Marchand Marion, Cavalcanti-Proença Christine, Daghmoun Samia, Durand Emmanuelle, Tichet Jean, Marre Michel, Balkau Beverley, Froguel Philippe, Lévy-Marchal Clai |
| Cross-ethnic meta-analysis of genetic variants for polycystic ovary syndrome. The Journal of clinical endocrinology and metabolism 2013 Dec 98 (12): E2006-12. Louwers Yvonne V, Stolk Lisette, Uitterlinden André G, Laven Joop S |
| A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype. Journal of human genetics 2015 Jun 60 (6): 287-93. De Crescenzo Agostina, Citro Valentina, Freschi Andrea, Sparago Angela, Palumbo Orazio, Cubellis Maria Vittoria, Carella Massimo, Castelluccio Pia, Cavaliere Maria Luigia, Cerrato Flavia, Riccio Andr |
| Variant Alleles of the ESR1, PPARG, HMGA2, and MTHFR Genes Are Associated With Polycystic Ovary Syndrome Risk in a Chinese Population: A Case-Control Study. Frontiers in endocrinology 2018 9 504. Jiao Xianting, Chen Weiwei, Zhang Jun, Wang Weiye, Song Junjiao, Chen Dan, Zhu Wenting, Shi Yuhua, Yu Xiaod |
| MED12 mutations and fumarate hydratase inactivation in uterine adenomyomas. Human reproduction open 2018 2018 (4): hoy020. Heikkinen Tuomas, Äyräväinen Anna, Hänninen Janne, Ahvenainen Terhi, Bützow Ralf, Pasanen Annukka, Vahteristo P |
| Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients. Clinical epigenetics 2020 6 12 (1): 86. Inoue Takanobu, Nakamura Akie, Iwahashi-Odano Megumi, Tanase-Nakao Kanako, Matsubara Keiko, Nishioka Junko, Maruo Yoshihiro, Hasegawa Yukihiro, Suzumura Hiroshi, Sato Seiji, Kobayashi Yoshiyuki, Murakami Nobuyuki, Nakabayashi Kazuhiko, Yamazawa Kazuki, Fuke Tomoko, Narumi Satoshi, Oka Akira, Ogata Tsutomu, Fukami Maki, Kagami Masa |
| A Comprehensive Overview of Common Polymorphic Variants in Genes Related to Polycystic Ovary Syndrome. Reproductive sciences (Thousand Oaks, Calif.) 2020 Nov . Castillo-Higuera Tatiana, Alarcón-Granados María Camila, Marin-Suarez Johana, Moreno-Ortiz Harold, Esteban-Pérez Clara Inés, Ferrebuz-Cardozo Atilio Junior, Forero-Castro Maribel, Camargo-Vill Alba Glor |
| Genotype based Risk Predictors for Polycystic Ovary Syndrome in Western Saudi Arabia. Bioinformation 2019 15 (11): 812-819. Bakhashab Sherin, Ahmed Na |
| One test for all: whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver-Russell syndrome. Orphanet journal of rare diseases 2021 1 16 (1): 42. Meyer Robert, Begemann Matthias, Hübner Christian Thomas, Dey Daniela, Kuechler Alma, Elgizouli Magdeldin, Schara Ulrike, Ambrozaityte Laima, Burnyte Birute, Schröder Carmen, Kenawy Asmaa, Kroisel Peter, Demuth Stephanie, Fekete Gyorgy, Opladen Thomas, Elbracht Miriam, Eggermann Thom |
| Genetic Variants of Steroidogenesis and Gonadotropin Pathways and Polycystic Ovary Syndrome Susceptibility: A Systematic Review and Meta-analysis. Metabolic syndrome and related disorders 2023 10 . Priya Sharma, Abhilash Kumar Singh, Sabyasachi Senapati, Harmanpreet Singh Kapoor, Lajya Devi Goyal, Balpreet Kaur, Pooja Kamra, Preeti Khetarp |
| Clinical and molecular risk factors for repeat interventions due to symptomatic uterine leiomyomas. American journal of obstetrics and gynecology 2024 8 . Sara Khamaiseh, Anna Äyräväinen, Maare Arffman, Siiri Reinikka, Miika Mehine, Päivi Härkki, Ralf Bützow, Annukka Pasanen, Pia Vahteris |
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