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Records 1-10

Query Trace: Genetic Diseases, Inborn and VEGFA[orginal query]

Single-nucleotide polymorphisms of VEGF-A and VEGFR-2 genes and risk of infantile hemangioma. International journal of dermatology 2018 Jul . Oszajca Katarzyna, Szemraj Janusz, Wyrzykowski Dariusz, Chrzanowska Barbara, Salamon Aneta, Przewratil Przemysl Similar articles in PubMed
Efficiency of exome sequencing for the molecular diagnosis of pseudoxanthoma elasticum. The Journal of investigative dermatology 2015 Apr 135 (4): 992-8. Hosen Mohammad J, Van Nieuwerburgh Filip, Steyaert Wouter, Deforce Dieter, Martin Ludovic, Leftheriotis Georges, De Paepe Anne, Coucke Paul J, Vanakker Olivier Similar articles in PubMed
Impact of VEGFA -583C?>?T polymorphism on serum VEGF levels and the susceptibility to acute chest syndrome in pediatric patients with sickle cell disease. Pediatric blood & cancer 2014 Dec 61 (12): 2310-2. Redha Noor A, Mahdi Najat, Al-Habboubi Hebah H, Almawi Wassim Similar articles in PubMed
Correlation of VEGF genetic polymorphisms and lipid profile to aortic calcification. Gene 2014 Oct 550 (1): 33-9. Yadav Binod Kumar, Hong Yoochan, Shin Byoung-S Similar articles in PubMed
Single nucleotide polymorphism in the FLT4 gene is associated with atopic dermatitis in Koreans. Cytokine 2013 Apr 62 (1): 110-4. Namkung Jung-Hyun, Lee Jong-Eun, Kim Eugene, Huh Ik-Soo, Park Taesung, Shin Eun-Soon, Cho Eun-Young, Yang Jun- Similar articles in PubMed
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nature genetics 2012 Dec . Köttgen A, Albrecht E, Teumer A, Vitart V, Krumsiek J, Hundertmark C, Pistis G, Ruggiero D, O'Seaghdha CM, Haller T, Yang Q, Tanaka T, Johnson AD, Kutalik Z, Smith AV, Shi J, Struchalin M, Middelberg RP, Brown MJ, Gaffo AL, Pirastu N, Li G, Hayward C, Zemunik T, Huffman J, Yengo L, Zhao JH, Demirkan A, Feitosa MF, Liu X, Malerba G, Lopez LM, van der Harst P, Li X, Kleber ME, Hicks AA, Nolte IM, Johansson A, Murgia F, Wild SH, Bakker SJ, Peden JF, Dehghan A, Steri M, Tenesa A, Lagou V, Salo P, Mangino M, Rose LM, Lehtimäki T, Woodward OM, Okada Y, Tin A, Müller C, Oldmeadow C, Putku M, Czamara D, Kraft P, Frogheri L, Thun GA, Grotevendt A, Gislason GK, Harris TB, Launer LJ, McArdle P, Shuldiner AR, Boerwinkle E, Coresh J, Schmidt H, Schallert M, Martin NG, Montgomery GW, Kubo M, Nakamura Y, Tanaka T, Munroe PB, Samani NJ, Jacobs DR, Liu K, D'Adamo P, Ulivi S, Rotter JI, Psaty BM, Vollenweider P, Waeber G, Campbell S, Devuyst O, Navarro P, Kolcic I, Hastie N, Balkau B, Froguel P, Esko T, Salumets A, Khaw KT, Langenberg C, Wareham NJ, Isaacs A, Kraja A, Zhang Q, Wild PS, Scott RJ, Holliday EG, Org E, Viigimaa M, Bandinelli S, Metter JE, Lupo A, Trabetti E, Sorice R, Döring A, Lattka E, Strauch K, Theis F, Waldenberger M, Wichmann HE, Davies G, Gow AJ, Bruinenberg M, Stolk RP, Kooner JS, Zhang W, Winkelmann BR, Boehm BO, Lucae S, Penninx BW, Smit JH, Curhan G, Mudgal P, Plenge RM, Portas L, Persico I, Kirin M, Wilson JF, Leach IM, van Gilst WH, Goel A, Ongen H, Hofman A, Rivadeneira F, Uitterlinden AG, Imboden M, von Eckardstein A, Cucca F, Nagaraja R, Piras MG, Nauck M, Schurmann C, Budde K, Ernst F, Farrington SM, Theodoratou E, Prokopenko I, Stumvoll M, Jula A, Perola M, Salomaa V, Shin SY, Spector TD, Sala C, Ridker PM, Kähönen M, Viikari J, Hengstenberg C, Nelson CP, Meschia JF, Nalls MA, Sharma P, Singleton AB, Kamatani N, Zeller T, Burnier M, Attia J, Laan M, Klopp N, Hillege HL, Kloiber S, Choi H, Pirastu M, Tore S, Probst-Hensch NM, Völzke H, Gudnason V, Parsa A, Schmidt R, Whitfield JB, Fornage M, Gasparini P, Siscovick DS, Polašek O, Campbell H, Rudan I, Bouatia-Naji N, Metspalu A, Loos RJ, van Duijn CM, Borecki IB, Ferrucci L, Gambaro G, Deary IJ, Wolffenbuttel BH, Chambers JC, März W, Pramstaller PP, Snieder H, Gyllensten U, Wright AF, Navis G, Watkins H, Witteman JC, Sanna S, Schipf S, Dunlop MG, Tönjes A, Ripatti S, Soranzo N, Toniolo D, Chasman DI, Raitakari O, Kao WH, Ciullo M, Fox CS, Caulfield M, Bochud M, Gieger C Similar articles in PubMed
The relation of vascular endothelial growth factor (VEGF) gene polymorphisms on VEGF levels and the risk of vasoocclusive crisis in sickle cell disease. European journal of haematology 2012 Nov 89 (5): 403-9. Al-Habboubi Hebah H, Mahdi Najat, Abu-Hijleh Tala M, Abu-Hijleh Farah M, Sater Mai S, Almawi Wassim Similar articles in PubMed
Pazopanib-induced hyperbilirubinemia is associated with Gilbert's syndrome UGT1A1 polymorphism. British journal of cancer 2010 Apr 102 (9): 1371-7. Xu C-F, Reck B H, Xue Z, Huang L, Baker K L, Chen M, Chen E P, Ellens H E, Mooser V E, Cardon L R, Spraggs C F, Pandite Similar articles in PubMed
Vascular endothelial growth factor gene polymorphisms as prognostic markers for ocular manifestations in pseudoxanthoma elasticum. Human molecular genetics 2009 Sep 18 (17): 3344-51. Zarbock Ralf, Hendig Doris, Szliska Christiane, Kleesiek Knut, Götting Christi Similar articles in PubMed
Analysis of vascular endothelial growth factor gene 936 C/T polymorphism in patients with familial Mediterranean fever. International journal of immunogenetics 2008 Feb 35 (1): 33-6. Gunesacar R, Erken E, Ozer H T E, Bozkurt B, Dinkci S, Deveci Similar articles in PubMed

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