HuGE Literature Finder
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| A homozygous mutation in the insulin gene (INS) causing autosomal recessive neonatal diabetes in Saudi families. Annals of pediatric endocrinology & metabolism 2020 4 25 (1): 42-45. Shaikh Adnan Al, Shirah Bader, Alzelaye Soma |
| Maturity onset diabetes of the young (MODY) in Chinese children: genes and clinical phenotypes. Journal of pediatric endocrinology & metabolism : JPEM 2019 6 32 (7): 759-765. Ming-Qiang Zhu, Yang-Li Dai, Ke Huang, Wei Wu, Jun-Fen Fu, Chao-Chun Zou, Guan-Ping Do |
| Associative role of TYMS6bpdel polymorphism and resulting hyperhomocysteinemia in the pathogenesis of preterm delivery and associated complications: A study from Northeast India. Gene 2017 Jun . Tiwari Diptika, Das Chandana Ray, Bose Purabi Deka, Bose Suj |
| Fetal growth interacts with multilocus genetic score reflecting dopamine signaling capacity to predict spontaneous sugar intake in children. Appetite 2017 10 120 596-601. Silveira Patrícia P, Pokhvisneva Irina, Gaudreau Hélène, Atkinson Leslie, Fleming Alison S, Sokolowski Marla B, Steiner Meir, Kennedy James L, Dubé Laurette, Levitan Robert D, Meaney Michael J, |
| The influence of INS VNTR class III allele on auxological parameters, glucose, insulin, lipids, and adipocytokines secretion in prepubertal children born small for gestational age. Endokrynologia Polska 2016 67 (6): 585-591. Stawerska Renata, Sza?apska Ma?gorzata, Borowiec Maciej, Antosik Karolina, M?ynarski Wojciech, Lewi?ski Andrz |
| Association analysis of ten candidate genes in a large multinational cohort of small for gestational age children and children with idiopathic short stature (NESTEGG study). Hormone research in pædiatrics 2013 80 (6): 466-76. de Graaff L C G, Clark A J L, Tauber M, Ranke M B, Johnston L B, Caliebe J, Molinas C, Amin N, van Duijn C, Wollmann H, Wallaschofski H, Savage M O, Hokken-Koelega A C |
| Maternal homozygocity for a 14 base pair insertion in exon 8 of the HLA-G gene and carriage of HLA class II alleles restricting HY immunity predispose to unexplained secondary recurrent miscarriage and low birth weight in children born to these patients. Human immunology 2012 Jul 73 (7): 699-705. Christiansen Ole B, Kolte Astrid M, Dahl Mette, Larsen Elisabeth C, Steffensen Rudi, Nielsen Henriette S, Hviid Thomas |
| Influence of polymorphisms in genes encoding for insulin-like growth factor (IGF)-I, insulin, and IGF-binding protein (IGFBP)-3 on IGF-I, IGF-II, and IGFBP-3 levels in umbilical cord plasma. Hormone research in pædiatrics 2012 77 (6): 341-50. Landmann Eva, Kollerits Barbara, Kreuder Joachim Gerhard, Blum Werner Friedrich, Kronenberg Florian, Rudloff Silv |
| Does the relative risk for type 1 diabetes conferred by HLA-DQ, INS, and PTPN22 polymorphisms vary with maternal age, birth weight, or cesarean section? Pediatric diabetes 2011 Mar 12 (2): 91-4. Stene Lars C, Rønningen Kjersti S, Undlien Dag E, Joner Ge |
| Insulin VNTR and IGF-1 promoter region polymorphisms are not associated with body composition in early childhood: the generation R study. Hormone research in pædiatrics 2010 73 (2): 120-7. Maas Janneke A J B M, Mook-Kanamori Dennis O, Ay Lamise, Steegers Eric A P, van Duijn Cornelia M, Hofman Albert, Hokken-Koelega Anita C S, Jaddoe Vincent W |
| Common polymorphic variation in the genetically diverse African insulin gene and its association with size at birth. Human genetics 2009 Sep 126 (3): 375-84. Petry Clive J, Rayco-Solon Pura, Fulford Anthony J C, Stead John D H, Wingate Dianne L, Ong Ken K, Sirugo Giorgio, Prentice Andrew M, Dunger David |
| INS VNTR is not associated with childhood obesity in 1,023 families: a family-based study. Obesity (Silver Spring, Md.) 2008 Jun 16 (6): 1471-5. Bouatia-Naji Nabila, De Graeve Franck, Brönner Günter, Lecoeur Cécile, Vatin Vincent, Durand Emmanuelle, Lichtner Peter, Nguyen Thuy T, Heude Barbara, Weill Jacques, Lévy-Marchal Claire, Hebebrand Johannes, Froguel Philippe, Meyre Dav |
| Insulin gene variable number of tandem repeats is not associated with weight from fetal life until infancy: the Generation R Study. European journal of endocrinology / European Federation of Endocrine Societies 2007 Dec 157 (6): 741-8. Mook-Kanamori Dennis O, Miranda Geelhoed J J, Steegers Eric A P, Witteman Jacqueline C M, Hofman Albert, Moll Henriëtte A, van Duijn Cornelia M, Hokken-Koelega Anita C S, Jaddoe Vincent W |
| Absence of the wild-type allele (192 base pairs) of a polymorphism in the promoter region of the IGF-I gene but not a polymorphism in the insulin gene variable number of tandem repeat locus is associated with accelerated weight gain in infancy. Pediatrics 2006 Dec 118 (6): 2374-9. Landmann Eva, Geller Frank, Schilling Jutta, Rudloff Silvia, Foeller-Gaudier Eleonore, Gortner Ludw |
| Genetic polymorphisms of hemostasis genes and primary outcome of very low birth weight infants. Pediatrics 2006 Aug 118 (2): 683-9. Härtel Christoph, König Inke, Köster Stefan, Kattner Evelyn, Kuhls Eckhardt, Küster Helmut, Möller Jens, Müller Dirk, Kribs Angela, Segerer Hugo, Wieg Christian, Herting Egbert, Göpel Wolfga |
| The INS VNTR locus does not associate with smallness for gestational age (SGA) but interacts with SGA to increase insulin resistance in young adults. The Journal of clinical endocrinology and metabolism 2006 Jun 91 (6): 2437-40. Vu-Hong Thuy-Ai, Durand Emmanuelle, Deghmoun Samia, Boutin Philippe, Meyre David, Chevenne Didier, Czernichow Paul, Froguel Philippe, Levy-Marchal Clai |
| Polymorphisms of haemostasis genes as risk factors for preterm delivery. Thrombosis and haemostasis 2005 Jul 94 (1): 88-92. Härtel Christoph, von Otte Sören, Koch Julia, Ahrens Peter, Kattner Evelyn, Segerer Hugo, Möller Jens, Diedrich Klaus, Göpel Wolfga |
| Variation at the insulin gene VNTR (variable number tandem repeat) polymorphism and early growth: studies in a large Finnish birth cohort. Diabetes 2004 Aug 53 (8): 2126-31. Bennett Amanda J, Sovio Ulla, Ruokonen Aimo, Martikainen Hannu, Pouta Anneli, Taponen Saara, Hartikainen Anna-Liisa, King Vanessa J, Elliott Paul, Järvelin Marjo-Riitta, McCarthy Mark |
| Lack of support for a role of the insulin gene variable number of tandem repeats minisatellite (INS-VNTR) locus in fetal growth or type 2 diabetes-related intermediate traits in United Kingdom populations. The Journal of clinical endocrinology and metabolism 2004 Jan 89 (1): 310-7. Mitchell Simon M S, Hattersley Andrew T, Knight Beatrice, Turner Tina, Metcalf Bradley S, Voss Linda D, Davies David, McCarthy Anne, Wilkin Terence J, Smith George Davey, Ben-Shlomo Yoav, Frayling Timothy |
| Association of insulin gene VNTR polymorphism with polycystic ovary syndrome. Annals of the New York Academy of Sciences 2002 Jun 967 (): 558-65. Vanková Markéta, Vrbíková Jana, Hill Martin, Cinek Ondrej, Bendlová Be |
| The insulin gene variable number tandem repeat class I/III polymorphism is in linkage disequilibrium with birth weight but not Type 2 diabetes in the Pima population. Diabetes 2002 12 52 (1): 187-93. Lindsay Robert S, Hanson Robert L, Wiedrich Chris, Knowler William C, Bennett Peter H, Baier Leslie |
| Insulin gene variable number of tandem repeat genotype and the low birth weight, precocious pubarche, and hyperinsulinism sequence. The Journal of clinical endocrinology and metabolism 2001 Dec 86 (12): 5788-93. Ibáñez L, Ong K, Potau N, Marcos M V, de Zegher F, Dunger |
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