HuGE Literature Finder
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Association of Genetic Variants in IGF2-Related Genes With Risk of Metabolic Syndrome in the Chinese Han Population. Frontiers in endocrinology 2021 12 654747. Gui Weiwei, Liang Julong, Lin Xihua, Shi Nanjing, Zhu Yiyi, Tan Bowen, Li Ho |
Validating genetic markers of response to recombinant human growth hormone in children with growth hormone deficiency and Turner syndrome: the PREDICT validation study. European journal of endocrinology 2016 Dec 175 (6): 633-643. Stevens Adam, Murray Philip, Wojcik Jerome, Raelson John, Koledova Ekaterina, Chatelain Pierre, Clayton Peter, |
Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups. American journal of medical genetics. Part A 2016 Jul . Maas Saskia M, Vansenne Fleur, Kadouch Daniel J M, Ibrahim Abdulla, Bliek Jet, Hopman Saskia, Mannens Marcel M, Merks Johannes H M, Maher Eamonn R, Hennekam Raoul |
No association between genetic or epigenetic variation in insulin growth factors and antipsychotic-induced metabolic disturbances in a cross-sectional sample. Pharmacogenomics 2014 May 15 (7): 951-62. Moons Tim, De Hert Marc, Kenis Gunther, Viechtbauer Wolfgang, van Os Jim, Gohlke Henning, Claes Stephan, van Winkel Ru |
No evidence for copy number and methylation variation in H19 and KCNQ10T1 imprinting control regions in children born small for gestational age. BMC medical genetics 2014 15 67. Murphy Rinki, Thompson John Md, Tost Jörg, Mitchell Edwin A, |
Genetic polymorphisms associated with steroids metabolism and insulin action in polycystic ovary syndrome. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2012 Mar 28 (3): 190-4. Ramos Cirilo Priscila Daniele, Rosa Fabíola Encinas, Moreira Ferraz Maria Fernanda, Rainho Cláudia Aparecida, Pontes Anaglória, Rogatto Silvia Regi |
No evidence for mutations of CTCFL/BORIS in Silver-Russell syndrome patients with IGF2/H19 imprinting control region 1 hypomethylation. PloS one 2009 4 (8): e6631. Bernier-Latmani Jeremiah, Baumer Alessandra, Shaw Phill |
Association of the polycystic ovary syndrome with genomic variants related to insulin resistance, type 2 diabetes mellitus, and obesity. The Journal of clinical endocrinology and metabolism 2004 Jun 89 (6): 2640-6. San Millán José L, Cortón Marta, Villuendas Gemma, Sancho José, Peral Belén, Escobar-Morreale Héctor |
Haplotypic analyses of the IGF2-INS-TH gene cluster in relation to cardiovascular risk traits. Human molecular genetics 2004 Apr 13 (7): 715-25. Rodríguez Santiago, Gaunt Tom R, O'Dell Sandra D, Chen Xiao-He, Gu Dongfeng, Hawe Emma, Miller George J, Humphries Stephen E, Day Ian N |
An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: interaction between genotype and epigenotype. Human molecular genetics 2004 Jan 13 (2): 247-55. Murrell Adele, Heeson Sarah, Cooper Wendy N, Douglas Eleanor, Apostolidou Sophia, Moore Gudrun E, Maher Eamonn R, Reik Wo |
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