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 Pancreatic cancer. The EFO term pancreatic carcinoma 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:
M Zhang, Z Wang, O Obazee, J Jia, EJ Childs, J Hoskins, G Figlioli, E Mocci, I Collins, CC Chung, C Hautman, AA Arslan, L Beane-Freeman, PM Bracci, J Buring, EJ Duell, S Gallinger, GG Giles, GE Goodman, PJ Goodman, A Kamineni, LN Kolonel, MH Kulke, N Malats, SH Olson, HD Sesso, K Visvanathan, E White, W Zheng, CC Abnet, D Albanes, G Andreotti, L Brais, HB Bueno-de-Mesquita, D Basso, SI Berndt, MC Boutron-Ruault, MF Bijlsma, H Brenner, L Burdette, D Campa, NE Caporaso, G Capurso, GM Cavestro, M Cotterchio, E Costello, J Elena, U Boggi, JM Gaziano, M Gazouli, EL Giovannucci, M Goggins, M Gross, CA Haiman, M Hassan, KJ Helzlsouer, N Hu, DJ Hunter, E Iskierka-Jazdzewska, M Jenab, R Kaaks, TJ Key, KT Khaw, EA Klein, M Kogevinas, V Krogh, J Kupcinskas, RC Kurtz, MT Landi, S Landi, L Le Marchand, A Mambrini, S Mannisto, RL Milne, RE Neale, AL Oberg, S Panico, AV Patel, PH Peeters, U Peters, R Pezzilli, M Porta, M Purdue, JR Quiros, E Riboli, N Rothman, A Scarpa, G Scelo, XO Shu, DT Silverman, P Soucek, O Strobel, M Sund, E Małecka-Panas, PR Taylor, F Tavano, RC Travis, M Thornquist, A Tjønneland, GS Tobias, D Trichopoulos, Y Vashist, P Vodicka, J Wactawski-Wende, N Wentzensen, H Yu, K Yu, A Zeleniuch-Jacquotte, C Kooperberg, HA Risch, EJ Jacobs, D Li, C Fuchs, R Hoover, P Hartge, SJ Chanock, GM Petersen, RS Stolzenberg-Solomon, BM Wolpin, P Kraft, AP Klein, F Canzian, LT Amundadottir
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 Pancreatic cancer. The EFO term pancreatic carcinoma 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:
GM Petersen, L Amundadottir, CS Fuchs, P Kraft, RZ Stolzenberg-Solomon, KB Jacobs, AA Arslan, HB Bueno-de-Mesquita, S Gallinger, M Gross, K Helzlsouer, EA Holly, EJ Jacobs, AP Klein, A LaCroix, D Li, MT Mandelson, SH Olson, HA Risch, W Zheng, D Albanes, WR Bamlet, CD Berg, MC Boutron-Ruault, JE Buring, PM Bracci, F Canzian, S Clipp, M Cotterchio, M de Andrade, EJ Duell, JM Gaziano, EL Giovannucci, M Goggins, G Hallmans, SE Hankinson, M Hassan, B Howard, DJ Hunter, A Hutchinson, M Jenab, R Kaaks, C Kooperberg, V Krogh, RC Kurtz, SM Lynch, RR McWilliams, JB Mendelsohn, DS Michaud, H Parikh, AV Patel, PH Peeters, A Rajkovic, E Riboli, L Rodriguez, D Seminara, XO Shu, G Thomas, A Tjønneland, GS Tobias, D Trichopoulos, SK Van Den Eeden, J Virtamo, J Wactawski-Wende, Z Wang, BM Wolpin, H Yu, K Yu, A Zeleniuch-Jacquotte, JF Fraumeni, RN Hoover, P Hartge, SJ Chanock
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 Pancreatic cancer. The EFO term pancreatic carcinoma 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:
EJ Childs, E Mocci, D Campa, PM Bracci, S Gallinger, M Goggins, D Li, RE Neale, SH Olson, G Scelo, LT Amundadottir, WR Bamlet, MF Bijlsma, A Blackford, M Borges, P Brennan, H Brenner, HB Bueno-de-Mesquita, F Canzian, G Capurso, GM Cavestro, KG Chaffee, SJ Chanock, SP Cleary, M Cotterchio, L Foretova, C Fuchs, N Funel, M Gazouli, M Hassan, JM Herman, I Holcatova, EA Holly, RN Hoover, RJ Hung, V Janout, TJ Key, J Kupcinskas, RC Kurtz, S Landi, L Lu, E Malecka-Panas, A Mambrini, B Mohelnikova-Duchonova, JP Neoptolemos, AL Oberg, I Orlow, C Pasquali, R Pezzilli, C Rizzato, A Saldia, A Scarpa, RZ Stolzenberg-Solomon, O Strobel, F Tavano, YK Vashist, P Vodicka, BM Wolpin, H Yu, GM Petersen, HA Risch, AP Klein
Whole Brain Gene Expression Correlates for NEPCOUNT30 measured in BXD RI Females obtained using INIA Brain mRNA M430 (Jun06) RMA. The NEPCOUNT30 measures Novel environment locomotion (activity beam breaks) 15-30 min in the periphery under the domain Morphine. The correlates were thresholded at a p-value of less than 0.001.
Whole Brain Gene Expression Correlates for NEPDIST30 measured in BXD RI Females obtained using INIA Brain mRNA M430 (Jun06) RMA. The NEPDIST30 measures Novel environment distance (cm) travelled min 15-30 under the domain Morphine. The correlates were thresholded at a p-value of less than 0.001.
Cerebellum Gene Expression Correlates for TAILCLIP_LAT_SEC measured in BXD RI Males obtained using SJUT Cerebellum mRNA M430 (Mar05) RMA. The TAILCLIP_LAT_SEC measures Mechanical Nociception - Tail Clip Test under the domain Pain. The correlates were thresholded at a p-value of less than 0.001.
Authors:
Philip VM, Duvvuru S, Gomero B, Ansah TA, Blaha CD, Cook MN, Hamre KM, Lariviere WR, Matthews DB, Mittleman G, Goldowitz D, Chesler EJ
Whole Brain Gene Expression Correlates for AMCNT105 measured in BXD RI Females obtained using INIA Brain mRNA M430 (Jun06) RMA. The AMCNT105 measures Morphine photocell counts minutes 90-105 under the domain Morphine. The correlates were thresholded at a p-value of less than 0.001.
Authors:
Philip VM, Duvvuru S, Gomero B, Ansah TA, Blaha CD, Cook MN, Hamre KM, Lariviere WR, Matthews DB, Mittleman G, Goldowitz D, Chesler EJ
Whole Brain Gene Expression Correlates for AMCNT90 measured in BXD RI Females obtained using INIA Brain mRNA M430 (Jun06) RMA. The AMCNT90 measures Morphine photocell counts minutes 75-90 under the domain Morphine. The correlates were thresholded at a p-value of less than 0.001.
Authors:
Philip VM, Duvvuru S, Gomero B, Ansah TA, Blaha CD, Cook MN, Hamre KM, Lariviere WR, Matthews DB, Mittleman G, Goldowitz D, Chesler EJ
By comparing transcript profiles of normal mucosa and CRC samples in two independent sample sets, covering a total of 20 normal mucosa and 424 adenocarcinoma samples, we identified 51 TFs that showed a significant (P<10−4, Benjamini and Hochberg corrected) fold change (of at least 2) from normal to cancer in both data sets.
QTL for high-dose ethanol actions on Chr1 at D1Mit45 (135.76 Mbp , Build 37)
Description:
high-dose ethanol actions spans 110.76 - 160.76 Mbp (NCBI Build 37) on Chr1. This interval was obtained by using an interval width of 25 Mbp around the peak marker (Build 37, MGI, http://informatics.jax.org).
Authors:
Erwin VG, Markel PD, Johnson TE, Gehle VM, Jones BC
QTL for alcohol preference on Chr1 at NA (138.98 Mbp , Build 37)
Description:
alcohol preference spans 113.98 - 163.98 Mbp (NCBI Build 37) on Chr1. This interval was obtained by using an interval width of 25 Mbp around the peak marker (Build 37, MGI, http://informatics.jax.org).
Chronic cocaine - Cocaine-paired (conditioned place preference) vs. Control (saline or cocaine-non-paired) DNA microarray All genes on microarray presented After the pre-conditioning phase where animals were allowed access to either compartment for 15 minutes for 4 consecutive days, the conditioning phase for the cocaine-paired groups and cocaine non-paired groups began, consisting of eight subsequent daily sessions. For both groups, cocaine (10 mg / kg) or saline injections were administered on alternate days. For the cocaine-paired groups, rats were immediately placed in one of the two compartments for 30 min with the door in place restricting a z transformation followed by z test and anova followed by Student-Newman-Keuls' post hoc test. Gene expression profile was assessed 24 h after the last conditioning session that corresponded to 48 h after last cocaine exposure, when drug has been eliminated from the body and transient transcriptional changes are likely to be minimal. Therefore, changes in gene expression at this time-point are likely to reflect longer lasting adaptations that may account for maintenance of cocaine-induced memories. The complete lists of normalized gene expression values for the hippocampus of saline-treated, cocaine non-paired and cocaine-paired groups are presented. Analyses revealed that 214 transcripts were differentially regulated in the hippocampus of cocaine-paired rats vs. non-paired and saline-treated controls. Cocaine-induced conditioned place preference caused significant increases in the expression of 151 genes and caused decreases in the expression of 63 genes. (NIF Table ID 130.1 [83])
Authors:
Krasnova IN, Li SM, Wood WH, McCoy MT, Prabhu VV, Becker KG, Katz JL, Cadet JL
Chronic cocaine - Cocaine-paired (conditioned place preference) vs. Control (saline or cocaine-non-paired) DNA microarray All genes on microarray presented After the pre-conditioning phase where animals were allowed access to either compartment for 15 minutes for 4 consecutive days, the conditioning phase for the cocaine-paired groups and cocaine non-paired groups began, consisting of eight subsequent daily sessions. For both groups, cocaine (10 mg / kg) or saline injections were administered on alternate days. For the cocaine-paired groups, rats were immediately placed in one of the two compartments for 30 min with the door in place restricting a z transformation followed by z test and anova followed by Student-Newman-Keuls' post hoc test. Gene expression profile was assessed 24 h after the last conditioning session that corresponded to 48 h after last cocaine exposure, when drug has been eliminated from the body and transient transcriptional changes are likely to be minimal. Therefore, changes in gene expression at this time-point are likely to reflect longer lasting adaptations that may account for maintenance of cocaine-induced memories. The complete lists of normalized gene expression values for the frontal cortex of saline-treated, cocaine non-paired and cocaine-paired groups are presented. Differences in the expression of 39 transcripts in the frontal cortex were related to the conditioned place preference paradigm. These include increases in the level of 22 genes and decreases in 17 genes. (NIF Table ID 130.3 [83.5])
Authors:
Krasnova IN, Li SM, Wood WH, McCoy MT, Prabhu VV, Becker KG, Katz JL, Cadet JL
Genes associated with Homo sapiens that interact with the MeSH term 'Arsenic' (D001151). Incorporates data from 87 publications curated by the Comparative Toxicogenomics Database (CTD). ODE Gene scores represent number of supporting publications per gene.
Genes associated with Homo sapiens that interact with the MeSH term 'LG 100268' (C095104). Incorporates data from 102 publications curated by the Comparative Toxicogenomics Database (CTD). ODE Gene scores represent number of supporting publications per gene.
Genes associated with Homo sapiens that interact with the MeSH term 'Demecolcine' (D003703). Incorporates data from 3 publications curated by the Comparative Toxicogenomics Database (CTD). ODE Gene scores represent number of supporting publications per gene.
Genes associated with Homo sapiens that interact with the MeSH term 'arsenite' (C015001). Incorporates data from 3 publications curated by the Comparative Toxicogenomics Database (CTD). ODE Gene scores represent number of supporting publications per gene.
Genes associated with Homo sapiens that interact with the MeSH term 'alitretinoin' (C103303). Incorporates data from 8 publications curated by the Comparative Toxicogenomics Database (CTD). ODE Gene scores represent number of supporting publications per gene.
Genes associated with Homo sapiens that interact with the MeSH term 'Vinca Alkaloids' (D014748). Incorporates data from 1138 publications curated by the Comparative Toxicogenomics Database (CTD). ODE Gene scores represent number of supporting publications per gene.
Genes associated with Homo sapiens that interact with the MeSH term 'Tretinoin' (D014212). Incorporates data from 1 publications curated by the Comparative Toxicogenomics Database (CTD). ODE Gene scores represent number of supporting publications per gene.
Genes associated with Bos taurus that interact with the MeSH term 'Colforsin' (D005576). Incorporates data from 1 publications curated by the Comparative Toxicogenomics Database (CTD). ODE Gene scores represent number of supporting publications per gene.
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