List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Coronary heart disease. The EFO term coronary heart disease was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
F Takeuchi, M Yokota, K Yamamoto, E Nakashima, T Katsuya, H Asano, M Isono, T Nabika, T Sugiyama, A Fujioka, N Awata, K Ohnaka, M Nakatochi, H Kitajima, H Rakugi, J Nakamura, T Ohkubo, Y Imai, K Shimamoto, Y Yamori, S Yamaguchi, S Kobayashi, R Takayanagi, T Ogihara, N Kato
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Myocardial infarction. The EFO term myocardial infarction was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
A Helgadottir, G Thorleifsson, A Manolescu, S Gretarsdottir, T Blondal, A Jonasdottir, A Jonasdottir, A Sigurdsson, A Baker, A Palsson, G Masson, DF Gudbjartsson, KP Magnusson, K Andersen, AI Levey, VM Backman, S Matthiasdottir, T Jonsdottir, S Palsson, H Einarsdottir, S Gunnarsdottir, A Gylfason, V Vaccarino, WC Hooper, MP Reilly, CB Granger, H Austin, DJ Rader, SH Shah, AA Quyyumi, JR Gulcher, G Thorgeirsson, U Thorsteinsdottir, A Kong, K Stefansson
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Intracranial aneurysm. The EFO term brain aneurysm was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
K Bilguvar, K Yasuno, M Niemelä, YM Ruigrok, M von Und Zu Fraunberg, CM van Duijn, LH van den Berg, S Mane, CE Mason, M Choi, E Gaál, Y Bayri, L Kolb, Z Arlier, S Ravuri, A Ronkainen, A Tajima, A Laakso, A Hata, H Kasuya, T Koivisto, J Rinne, J Ohman, MM Breteler, C Wijmenga, MW State, GJ Rinkel, J Hernesniemi, JE Jääskeläinen, A Palotie, I Inoue, RP Lifton, M Günel
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Type 2 diabetes. The EFO term type II diabetes mellitus was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
R Saxena, BF Voight, V Lyssenko, NP Burtt, PI de Bakker, H Chen, JJ Roix, S Kathiresan, JN Hirschhorn, MJ Daly, TE Hughes, L Groop, D Altshuler, P Almgren, JC Florez, J Meyer, K Ardlie, K Bengtsson Boström, B Isomaa, G Lettre, U Lindblad, HN Lyon, O Melander, C Newton-Cheh, P Nilsson, M Orho-Melander, L Råstam, EK Speliotes, MR Taskinen, T Tuomi, C Guiducci, A Berglund, J Carlson, L Gianniny, R Hackett, L Hall, J Holmkvist, E Laurila, M Sjögren, M Sterner, A Surti, M Svensson, M Svensson, R Tewhey, B Blumenstiel, M Parkin, M Defelice, R Barry, W Brodeur, J Camarata, N Chia, M Fava, J Gibbons, B Handsaker, C Healy, K Nguyen, C Gates, C Sougnez, D Gage, M Nizzari, SB Gabriel, GW Chirn, Q Ma, H Parikh, D Richardson, D Ricke, S Purcell
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Type 2 diabetes. The EFO term type II diabetes mellitus was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
LJ Scott, KL Mohlke, LL Bonnycastle, CJ Willer, Y Li, WL Duren, MR Erdos, HM Stringham, PS Chines, AU Jackson, L Prokunina-Olsson, CJ Ding, AJ Swift, N Narisu, T Hu, R Pruim, R Xiao, XY Li, KN Conneely, NL Riebow, AG Sprau, M Tong, PP White, KN Hetrick, MW Barnhart, CW Bark, JL Goldstein, L Watkins, F Xiang, J Saramies, TA Buchanan, RM Watanabe, TT Valle, L Kinnunen, GR Abecasis, EW Pugh, KF Doheny, RN Bergman, J Tuomilehto, FS Collins, M Boehnke
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Type 2 diabetes. The EFO term type II diabetes mellitus was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
E Zeggini, MN Weedon, CM Lindgren, TM Frayling, KS Elliott, H Lango, NJ Timpson, JR Perry, NW Rayner, RM Freathy, JC Barrett, B Shields, AP Morris, S Ellard, CJ Groves, LW Harries, JL Marchini, KR Owen, B Knight, LR Cardon, M Walker, GA Hitman, AD Morris, AS Doney, MI McCarthy, AT Hattersley
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Glioma. The EFO term central nervous system cancer was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
S Shete, FJ Hosking, LB Robertson, SE Dobbins, M Sanson, B Malmer, M Simon, Y Marie, B Boisselier, JY Delattre, K Hoang-Xuan, S El Hallani, A Idbaih, D Zelenika, U Andersson, R Henriksson, AT Bergenheim, M Feychting, S Lönn, A Ahlbom, J Schramm, M Linnebank, K Hemminki, R Kumar, SJ Hepworth, A Price, G Armstrong, Y Liu, X Gu, R Yu, C Lau, M Schoemaker, K Muir, A Swerdlow, M Lathrop, M Bondy, RS Houlston
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Melanoma. The EFO term melanoma was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
DT Bishop, F Demenais, MM Iles, M Harland, JC Taylor, E Corda, J Randerson-Moor, JF Aitken, MF Avril, E Azizi, B Bakker, G Bianchi-Scarrà , B Bressac-de Paillerets, D Calista, LA Cannon-Albright, T Chin-A-Woeng, T Debniak, G Galore-Haskel, P Ghiorzo, I Gut, J Hansson, M Hocevar, V Höiom, JL Hopper, C Ingvar, PA Kanetsky, RF Kefford, MT Landi, J Lang, J Lubiński, R Mackie, J Malvehy, GJ Mann, NG Martin, GW Montgomery, FA van Nieuwpoort, S Novakovic, H Olsson, S Puig, M Weiss, W van Workum, D Zelenika, KM Brown, AM Goldstein, EM Gillanders, A Boland, P Galan, DE Elder, NA Gruis, NK Hayward, GM Lathrop, JH Barrett, JA Bishop
List of positional candidate genes after correcting for multiple testing and controlling the false discovery rate from genome wide association studies (GWAS) retrieved from the NHGRI-EBI Catalog of published genome-wide association studies (http://www.ebi.ac.uk/gwas/). The disease/trait examined in this study, as reported by the authors, was Intracranial aneurysm. The EFO term brain aneurysm was annotated to this set after curation by NHGRI-EBI. Intergenic SNPS were mapped to both the upstream and downstream gene. P-value uploaded. This gene set was generated using gwas2gs v. 0.1.8 and the GWAS Catalog v. 1.0.1.
Authors:
K Yasuno, K Bilguvar, P Bijlenga, SK Low, B Krischek, G Auburger, M Simon, D Krex, Z Arlier, N Nayak, YM Ruigrok, M Niemelä, A Tajima, M von und zu Fraunberg, T Dóczi, F Wirjatijasa, A Hata, J Blasco, A Oszvald, H Kasuya, G Zilani, B Schoch, P Singh, C Stüer, R Risselada, J Beck, T Sola, F Ricciardi, A Aromaa, T Illig, S Schreiber, CM van Duijn, LH van den Berg, C Perret, C Proust, C Roder, AK Ozturk, E Gaál, D Berg, C Geisen, CM Friedrich, P Summers, AF Frangi, MW State, HE Wichmann, MM Breteler, C Wijmenga, S Mane, L Peltonen, V Elio, MC Sturkenboom, P Lawford, J Byrne, J Macho, EI Sandalcioglu, B Meyer, A Raabe, H Steinmetz, D Rüfenacht, JE Jääskeläinen, J Hernesniemi, GJ Rinkel, H Zembutsu, I Inoue, A Palotie, F Cambien, Y Nakamura, RP Lifton, M Günel
Genes associated with Homo sapiens that interact with the MeSH term 'Copper Sulfate' (D019327). Incorporates data from 72 publications curated by the Comparative Toxicogenomics Database (CTD). ODE Gene scores represent number of supporting publications per gene.
chr9p21
Genes in cytogenetic band chr9p21
c1 - Positional genesets for each human chromosome and cytogenetic band.
Molecular Signatures Database (MSigDB) Geneset. This geneset was imported from one of the MSigDB collections.
gene2msig v. 0.1.0
Last updated 2015.08.31
Pathological conditions involving the CARDIOVASCULAR SYSTEM including the HEART; the BLOOD VESSELS; or the PERICARDIUM.
Generated by gene2mesh v. 1.1.1
Pathological processes involving any of the BLOOD VESSELS in the cardiac or peripheral circulation. They include diseases of ARTERIES; VEINS; and rest of the vasculature system in the body.
Generated by gene2mesh v. 1.1.1
The medium-sized, submetacentric human chromosomes, called group C in the human chromosome classification. This group consists of chromosome pairs 6, 7, 8, 9, 10, 11, and 12 and the X chromosome.
Generated by gene2mesh v. 1.1.1
The processes, properties and biological objects that are involved in maintaining, expressing, and transmitting from one organism to another, genetically encoded traits.
Generated by gene2mesh v. 1.1.1
Abnormal anatomical or physiological conditions and objective or subjective manifestations of disease, not classified as disease or syndrome.
Generated by gene2mesh v. 1.1.1
The fundamental, structural, and functional units or subunits of living organisms. They are composed of CYTOPLASM containing various ORGANELLES and a CELL MEMBRANE boundary.
Generated by gene2mesh v. 1.1.1
GeneWeaver