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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 15 (of 15 Records)

Query Trace: Syndrome and IGF2[original query]
Evidence that insulin is imprinted in the human yolk sac.
Diabetes 2001 1 50 (1): 199-203.
Moore G E, Abu-Amero S N, Bell G, Wakeling E L, Kingsnorth A, Stanier P, Jauniaux E, Bennett S
Insulin-like growth factor 2 (IGF2 ) and IGF-binding protein 1 (IGFBP1) gene variants are associated with overfeeding-induced metabolic changes.
Diabetologia 2002 1 44 (12): 2231-6.
Ukkola O, Sun G, Bouchard
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
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
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
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 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,
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
Search for cis-acting factors and maternal effect variants in Silver-Russell patients with ICR1 hypomethylation and their mothers.
European journal of human genetics : EJHG 2018 9 27 (1): 42-48.
Soellner Lukas, Kraft Florian, Sauer Sabrina, Begemann Matthias, Kurth Ingo, Elbracht Miriam, Eggermann Thom
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
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
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
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