Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 31 Records) |
Query Trace: FOXC2[original query] |
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Genetic variation in the human winged helix/forkhead transcription factor gene FOXC2 in Pima Indians. Diabetes 2003 May 52 (5): 1292-5. Kovacs Peter, Lehn-Stefan Angela, Stumvoll Michael, Bogardus Clifton, Baier Leslie |
The FOXC2 -512C>T variant is associated with hypertriglyceridaemia and increased serum C-peptide in Danish Caucasian glucose-tolerant subjects. Diabetologia 2003 Nov 46 (11): 1576-80. Yanagisawa K, Hingstrup Larsen L, Andersen G, Drivsholm T, Cederberg A, Westergren R, Borch-Johnsen K, Pedersen O, Enerbäck S, Hansen |
The FOXC2 C-512T polymorphism is associated with obesity and dyslipidemia. Obesity research 2004 Nov 12 (11): 1738-43. Carlsson Emma, Almgren Peter, Hoffstedt Johan, Groop Leif, Ridderstråle Mart |
Role of the FOXC2 -512C>T polymorphism in type 2 diabetes: possible association with the dysmetabolic syndrome. International journal of obesity (2005) 2005 Mar 29 (3): 268-74. Carlsson E, Groop L, Ridderstråle |
Genetic determinants of insulin action in polycystic ovary syndrome. Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2005 May 113 (5): 275-81. Haap M, Machicao F, Stefan N, Thamer C, Tschritter O, Schnuck F, Wallwiener D, Stumvoll M, Häring H-U, Fritsche |
Association of polymorphisms in forkhead box C2 and perilipin genes with bone mineral density in community-dwelling Japanese individuals. International journal of molecular medicine 2006 Jul 18 (1): 119-27. Yamada Yoshiji, Ando Fujiko, Shimokata Hiros |
A variant in the transcription factor 7-like 2 (TCF7L2) gene is associated with an increased risk of gestational diabetes mellitus. Diabetologia 2007 May 50 (5): 972-9. Shaat N, Lernmark A, Karlsson E, Ivarsson S, Parikh H, Berntorp K, Groop |
HGF and MET mutations in primary and secondary lymphedema. Lymphatic research and biology 2008 6 (2): 65-8. Finegold David N, Schacht Vivien, Kimak Mark A, Lawrence Elizabeth C, Foeldi Etelka, Karlsson Jenny M, Baty Catherine J, Ferrell Robert |
Candidate gene analysis in primary lymphedema. Lymphatic research and biology 2008 6 (2): 69-76. Ferrell Robert E, Kimak Mark A, Lawrence Elizabeth C, Finegold David |
A recurrent ITGA9 missense mutation in human fetuses with severe chylothorax: possible correlation with poor response to fetal therapy. Prenatal diagnosis 2008 Nov 28 (11): 1057-63. Ma Gwo-Chin, Liu Chin-San, Chang Shun-Ping, Yeh Kun-Tu, Ke Yu-Yuan, Chen Tze-Ho, Wang Boris Bao-Tyan, Kuo Shou-Jen, Shih Jin-Chung, Chen Mi |
High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2009 Dec 24 (12): 2039-49. Yerges Laura M, Klei Lambertus, Cauley Jane A, Roeder Kathryn, Kammerer Candace M, Moffett Susan P, Ensrud Kristine E, Nestlerode Cara S, Marshall Lynn M, Hoffman Andrew R, Lewis Cora, Lang Thomas F, Barrett-Connor Elizabeth, Ferrell Robert E, Orwoll Eric S, Zmuda Joseph M, |
Gestational diabetes mellitus shares polymorphisms of genes associated with insulin resistance and type 2 diabetes in the Greek population. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2011 Apr 27 (4): 267-72. Pappa Kalliopi I, Gazouli Maria, Economou Konstantinos, Daskalakis George, Anastasiou Eleni, Anagnou Nicholas P, Antsaklis Aristid |
Expanding the spectrum of FOXC1 and PITX2 mutations and copy number changes in patients with anterior segment malformations. Investigative ophthalmology & visual science 2011 Jan 52 (1): 324-33. D'haene Barbara, Meire Françoise, Claerhout Ilse, Kroes Hester Y, Plomp Astrid, Arens Yvonne H, de Ravel Thomy, Casteels Ingele, De Jaegere Sarah, Hooghe Sally, Wuyts Wim, van den Ende Jenneke, Roulez Françoise, Veenstra-Knol Hermine E, Oldenburg Rogier A, Giltay Jacques, Verheij Johanna B G M, de Faber Jan-Tjeerd, Menten Björn, De Paepe Anne, Kestelyn Philippe, Leroy Bart P, De Baere Elfri |
Studies of the association of Arg72Pro of tumor suppressor protein p53 with type 2 diabetes in a combined analysis of 55,521 Europeans. PloS one 2011 6 (1): e15813. Burgdorf Kristoffer Sølvsten, Grarup Niels, Justesen Johanne Marie, Harder Marie Neergaard, Witte Daniel Rinse, Jørgensen Torben, Sandbæk Annelli, Lauritzen Torsten, Madsbad Sten, Hansen Torben, , Pedersen Ol |
Possible genetic predisposition to lymphedema after breast cancer. Lymphatic research and biology 2012 Mar 10 (1): 2-13. Newman Beth, Lose Felicity, Kedda Mary-Anne, Francois Mathias, Ferguson Kaltin, Janda Monika, Yates Patsy, Spurdle Amanda B, Hayes Sandra |
Connexin 47 mutations increase risk for secondary lymphedema following breast cancer treatment. Clinical cancer research : an official journal of the American Association for Cancer Research 2012 Apr 18 (8): 2382-90. Finegold David N, Baty Catherine J, Knickelbein Kelly Z, Perschke Shelley, Noon Sarah E, Campbell Diana, Karlsson Jenny M, Huang Diana, Kimak Mark A, Lawrence Elizabeth C, Feingold Eleanor, Meriney Stephen D, Brufsky Adam M, Ferrell Robert |
Mutations in the VEGFR3 signaling pathway explain 36% of familial lymphedema. Molecular syndromology 2013 Sep 4 (6): 257-66. Mendola A, Schlögel M J, Ghalamkarpour A, Irrthum A, Nguyen H L, Fastré E, Bygum A, van der Vleuten C, Fagerberg C, Baselga E, Quere I, Mulliken J B, Boon L M, Brouillard P, Vikkula M, |
Forkhead box C2 promoter variant c.-512C>T is associated with increased susceptibility to chronic venous diseases. PloS one 2014 9 (3): e90682. Surendran Sumi, Girijamma Athira, Nair Radhakrishnan, Ramegowda Kalpana S, Nair Divya H, Thulaseedharan Jissa V, Lakkappa Ravikumar B, Kamalapurkar Giridhar, Kartha Chandrasekharan |
FOXC2 and FLT4 Gene Variants in Lymphatic Filariasis. Lymphatic research and biology 2015 Jun 13 (2): 112-9. Sheik Yasmeen, Qureshi Sameera Fatima, Mohhammed Basheeruddin, Nallari Pratib |
Genome-wide association study of sepsis in extremely premature infants.
Archives of disease in childhood. Fetal and neonatal edition 2017 Mar . Srinivasan Lakshmi, Page Grier, Kirpalani Haresh, Murray Jeffrey C, Das Abhik, Higgins Rosemary D, Carlo Waldemar A, Bell Edward F, Goldberg Ronald N, Schibler Kurt, Sood Beena G, Stevenson David K, Stoll Barbara J, Van Meurs Krisa P, Johnson Karen J, Levy Joshua, McDonald Scott A, Zaterka-Baxter Kristin M, Kennedy Kathleen A, Sánchez Pablo J, Duara Shahnaz, Walsh Michele C, Shankaran Seetha, Wynn James L, Cotten C Michael, |
Minor alleles of genetic variants in second heart field increase the risk of hypoplastic right heart syndrome. Journal of genetics 2019 6 98 (2): . Wang Enshi, Nie Yu, Fan Xuesong, Zheng Zhe, Gu Haiyong, Zhang Hao, Hu Shengsh |
Role of FOXC2 and PITX2 rare variants associated with mild functional alterations as modifier factors in congenital glaucoma. PloS one 2019 1 14 (1): e0211029. Medina-Trillo Cristina, Aroca-Aguilar José-Daniel, Ferre-Fernández Jesús-José, Alexandre-Moreno Susana, Morales Laura, Méndez-Hernández Carmen-Dora, García-Feijoo Julián, Escribano Jul |
Delving into Early-onset Pancreatic Ductal Adenocarcinoma: How Does Age Fit In? Clinical cancer research : an official journal of the American Association for Cancer Research 2020 9 27 (1): 246-254. Tsang Erica S, Topham James T, Karasinska Joanna M, Lee Michael K C, Williamson Laura M, Mendis Shehara, Denroche Robert E, Jang Gun Ho, Kalloger Steve E, Moore Richard A, Mungall Andrew J, Bathe Oliver F, Tang Patricia A, Notta Faiyaz, Wilson Julie M, Laskin Janessa, O'Kane Grainne M, Knox Jennifer J, Goodwin Rachel A, Loree Jonathan M, Jones Steven J M, Marra Marco A, Gallinger Steven, Schaeffer David F, Renouf Daniel |
Functional polymorphisms in FOXC2 gene and Epithelial ovarian Cancer susceptibility in Chinese population. Journal of ovarian research 2020 Mar 13 (1): 34. Zhou Zhijiao, Ou Xiang, Zou Qiong, Chu Ling, Quan Xiyun, Chen Yong, Liu Ya |
[Genetic characteristics of varicocele: An almost unexplored area]. Zhonghua nan ke xue = National journal of andrology 2020 3 24 (10): 867-870. Dong Qiang, Yang Bo, Ren Zheng- |
[Genetic analysis and clinical phenotype of a family with lymphedema-distichiasis syndrome]. Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences 2020 11 49 (5): 581-585. Hu Gang, Liu Bei, Chen Min, Qian Yeqing, Dong Miny |
Improvement of quality of life by intake of hydroxytyrosol in patients with lymphedema and association of lymphedema genes with obesity. European review for medical and pharmacological sciences 2021 12 25 (1 Suppl): 33-42. Dhuli K, Ceccarini M R, Precone V, Maltese P E, Bonetti G, Paolacci S, Dautaj A, Guerri G, Marceddu G, Beccari T, Michelini S, Bertelli |
First genome-wide association study of esophageal atresia identifies three genetic risk loci at CTNNA3, FOXF1/FOXC2/FOXL1, and HNF1B.
HGG advances 2022 2 3 (2): 100093. Gehlen Jan, Giel Ann-Sophie, Köllges Ricarda, Haas Stephan L, Zhang Rong, Trcka Jiri, Sungur Ayse Ö, Renziehausen Florian, Bornholdt Dorothea, Jung Daphne, Hoyer Paul D, Nordenskjöld Agneta, Tibboel Dick, Vlot John, Spaander Manon C W, Smigiel Robert, Patkowski Dariusz, Roeleveld Nel, van Rooij Iris Alm, de Blaauw Ivo, Hölscher Alice, Pauly Marcus, Leutner Andreas, Fuchs Joerg, Niethammer Joel, Melissari Maria-Theodora, Jenetzky Ekkehart, Zwink Nadine, Thiele Holger, Hilger Alina Christine, Hess Timo, Trautmann Jessica, Marks Matthias, Baumgarten Martin, Bläss Gaby, Landén Mikael, Fundin Bengt, Bulik Cynthia M, Pennimpede Tracie, Ludwig Michael, Ludwig Kerstin U, Mangold Elisabeth, Heilmann-Heimbach Stefanie, Moebus Susanne, Herrmann Bernhard G, Alsabeah Kristina, Burgos Carmen M, Lilja Helene E, Azodi Sahar, Stenström Pernilla, Arnbjörnsson Einar, Frybova Barbora, Lebensztejn Dariusz M, Debek Wojciech, Kolodziejczyk Elwira, Kozera Katarzyna, Kierkus Jaroslaw, Kalici?ski Piotr, Stefanowicz Marek, Socha-Banasiak Anna, Kolejwa Michal, Piaseczna-Piotrowska Anna, Czkwianianc Elzbieta, Nöthen Markus M, Grote Phillip, Rygl Michal, Reinshagen Konrad, Spychalski Nicole, Ludwikowski Barbara, Hubertus Jochen, Heydweiller Andreas, Ure Benno, Muensterer Oliver J, Aubert Ophelia, Gosemann Jan-Hendrik, Lacher Martin, Degenhardt Petra, Boemers Thomas M, Mokrowiecka Anna, Ma?ecka-Panas Ewa, Wöhr Markus, Knapp Michael, Seitz Guido, de Klein Annelies, Oracz Grzegorz, Brosens Erwin, Reutter Heiko, Schumacher Johann |
Analysis of pathogenic variants in 605 Chinese children with non-syndromic cardiac conotruncal defects based on targeted sequencing. Genomics 2023 7 115 (5): 110676. JiaJun Ye, Yiwei Niu, Yongxuan Peng, Jihong Huang, Huiying Wang, Qihua Fu, Fen Li, Rang Xu, Sun Chen, Yuejuan Xu, Kun S |
Whole-exome sequencing revealed novel genetic alterations in patients with tetralogy of Fallot. Translational pediatrics 2023 11 12 (10): 1835-1841. Yu Pan, Manli Liu, Songsong Zhang, Huaxian Mei, Jing |
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- Page last updated:Apr 22, 2024
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