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 Height. The EFO term body height 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 Johansson, F Marroni, C Hayward, CS Franklin, AV Kirichenko, I Jonasson, AA Hicks, V Vitart, A Isaacs, T Axenovich, S Campbell, MG Dunlop, J Floyd, N Hastie, A Hofman, S Knott, I Kolcic, I Pichler, O Polasek, F Rivadeneira, A Tenesa, AG Uitterlinden, SH Wild, IV Zorkoltseva, T Meitinger, JF Wilson, I Rudan, H Campbell, C Pattaro, P Pramstaller, BA Oostra, AF Wright, CM van Duijn, YS Aulchenko, U Gyllensten
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 Systemic lupus erythematosus and Systemic sclerosis. The EFO term systemic lupus erythematosus 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:
JE Martin, S Assassi, LM Diaz-Gallo, JC Broen, CP Simeon, I Castellvi, E Vicente-Rabaneda, V Fonollosa, N Ortego-Centeno, MA González-Gay, G Espinosa, P Carreira, M Camps, JM Sabio, S D'alfonso, MC Vonk, AE Voskuyl, AJ Schuerwegh, A Kreuter, T Witte, G Riemekasten, N Hunzelmann, P Airo, L Beretta, R Scorza, C Lunardi, J Van Laar, MM Chee, J Worthington, A Herrick, C Denton, C Fonseca, FK Tan, F Arnett, X Zhou, JD Reveille, O Gorlova, BP Koeleman, TR Radstake, T Vyse, MD Mayes, ME Alarcón-Riquelme, J Martin
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, LJ Scott, R Saxena, BF Voight, JL Marchini, T Hu, PI de Bakker, GR Abecasis, P Almgren, G Andersen, K Ardlie, KB Boström, RN Bergman, LL Bonnycastle, K Borch-Johnsen, NP Burtt, H Chen, PS Chines, MJ Daly, P Deodhar, CJ Ding, AS Doney, WL Duren, KS Elliott, MR Erdos, TM Frayling, RM Freathy, L Gianniny, H Grallert, N Grarup, CJ Groves, C Guiducci, T Hansen, C Herder, GA Hitman, TE Hughes, B Isomaa, AU Jackson, T Jørgensen, A Kong, K Kubalanza, FG Kuruvilla, J Kuusisto, C Langenberg, H Lango, T Lauritzen, Y Li, CM Lindgren, V Lyssenko, AF Marvelle, C Meisinger, K Midthjell, KL Mohlke, MA Morken, AD Morris, N Narisu, P Nilsson, KR Owen, CN Palmer, F Payne, JR Perry, E Pettersen, C Platou, I Prokopenko, L Qi, L Qin, NW Rayner, M Rees, JJ Roix, A Sandbaek, B Shields, M Sjögren, V Steinthorsdottir, HM Stringham, AJ Swift, G Thorleifsson, U Thorsteinsdottir, NJ Timpson, T Tuomi, J Tuomilehto, M Walker, RM Watanabe, MN Weedon, CJ Willer, T Illig, K Hveem, FB Hu, M Laakso, K Stefansson, O Pedersen, NJ Wareham, I Barroso, AT Hattersley, FS Collins, L Groop, MI McCarthy, M Boehnke, D Altshuler
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 Height. The EFO term body height 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:
N Soranzo, F Rivadeneira, U Chinappen-Horsley, I Malkina, JB Richards, N Hammond, L Stolk, A Nica, M Inouye, A Hofman, J Stephens, E Wheeler, P Arp, R Gwilliam, PM Jhamai, S Potter, A Chaney, MJ Ghori, R Ravindrarajah, S Ermakov, K Estrada, HA Pols, FM Williams, WL McArdle, JB van Meurs, RJ Loos, ET Dermitzakis, KR Ahmadi, DJ Hart, WH Ouwehand, NJ Wareham, I Barroso, MS Sandhu, DP Strachan, G Livshits, TD Spector, AG Uitterlinden, P Deloukas
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 Prostate cancer. The EFO term prostate 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:
G Thomas, KB Jacobs, M Yeager, P Kraft, S Wacholder, N Orr, K Yu, N Chatterjee, R Welch, A Hutchinson, A Crenshaw, G Cancel-Tassin, BJ Staats, Z Wang, J Gonzalez-Bosquet, J Fang, X Deng, SI Berndt, EE Calle, HS Feigelson, MJ Thun, C Rodriguez, D Albanes, J Virtamo, S Weinstein, FR Schumacher, E Giovannucci, WC Willett, O Cussenot, A Valeri, GL Andriole, ED Crawford, M Tucker, DS Gerhard, JF Fraumeni, R Hoover, RB Hayes, DJ Hunter, SJ Chanock
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
The regular and simultaneous occurrence in a single interbreeding population of two or more discontinuous genotypes. The concept includes differences in genotypes ranging in size from a single nucleotide site (POLYMORPHISM, SINGLE NUCLEOTIDE) to large nucleotide sequences visible at a chromosomal level.
Generated by gene2mesh v. 1.1.1
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 Systemic lupus erythematosus and Systemic sclerosis. The EFO term systemic scleroderma, systemic lupus erythematosus 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:
JE Martin, S Assassi, LM Diaz-Gallo, JC Broen, CP Simeon, I Castellvi, E Vicente-Rabaneda, V Fonollosa, N Ortego-Centeno, MA González-Gay, G Espinosa, P Carreira, M Camps, JM Sabio, S D'alfonso, MC Vonk, AE Voskuyl, AJ Schuerwegh, A Kreuter, T Witte, G Riemekasten, N Hunzelmann, P Airo, L Beretta, R Scorza, C Lunardi, J Van Laar, MM Chee, J Worthington, A Herrick, C Denton, C Fonseca, FK Tan, F Arnett, X Zhou, JD Reveille, O Gorlova, BP Koeleman, TR Radstake, T Vyse, MD Mayes, ME Alarcón-Riquelme, J Martin
The total transcriptome including genes that are differentially expressed in cocaine addicts compared to control subjects. Post-mortem brain samples were collected from the dorsolateral prefrontal cortex (dlPFC) of the cocaine addict group and the control group. To assess gene expression, RNA-seq was performed. Data taken from Supplementary Table 2. Values presented are k.diff values. Data available from GEO with accession number GSE99349."
Authors:
Efrain A Ribeiro, Joseph R Scarpa, Susanna P Garamszegi, Andrew Kasarskis, Deborah C Mash, Eric J Nestler
Data from GEO GSE194368 and analyzed using GEO2R, only top gene shown. Authors identified transcriptional adaptations of GR signaling in the amygdala of humans with OUD. Thus, GRs, their coregulators and downstream systems may represent viable therapeutic targets to treat the “stress side” of OUD.
Authors:
Stephanie A Carmack, Janaina C M Vendruscolo, M Adrienne McGinn, Jorge Miranda-Barrientos, Vez Repunte-Canonigo, Gabriel D Bosse, Daniele Mercatelli, Federico M Giorgi, Yu Fu, Anthony J Hinrich, Francine M Jodelka, Karen Ling, Robert O Messing, Randall T Peterson, Frank Rigo, Scott Edwards, Pietro P Sanna, Marisela Morales, Michelle L Hastings, George F Koob, Leandro F Vendruscolo
Opioid use disorder_human_dorsolateral prefrontal cortex_coefficient
Description:
RNA sequencing on the dorsolateral prefrontal cortex (DLPFC) and nucleus accumbens (NAc) from unaffected comparison subjects (n = 20) and subjects diagnosed with opioid use disorder OUD (n = 20). Transcriptomic analyses identified differentially expressed transcripts and investigated the transcriptional coherence between brain regions using rank-rank hypergeometric orderlap.transcriptional differences by brain region in unaffected comparison subjects, finding unique transcriptional profiles in the DLPFC and NAc
Authors:
Marianne L Seney, Sam-Moon Kim, Jill R Glausier, Mariah A Hildebrand, Xiangning Xue, Wei Zong, Jiebiao Wang, Micah A Shelton, BaDoi N Phan, Chaitanya Srinivasan, Andreas R Pfenning, George C Tseng, David A Lewis, Zachary Freyberg, Ryan W Logan
Opioid use disorder_human_nucleus accumbens_coefficient
Description:
RNA sequencing on the dorsolateral prefrontal cortex (DLPFC) and nucleus accumbens (NAc) from unaffected comparison subjects (n = 20) and subjects diagnosed with opioid use disorder OUD (n = 20). Transcriptomic analyses identified differentially expressed transcripts and investigated the transcriptional coherence between brain regions using rank-rank hypergeometric orderlap.transcriptional differences by brain region in unaffected comparison subjects, finding unique transcriptional profiles in the DLPFC and NAc
Authors:
Marianne L Seney, Sam-Moon Kim, Jill R Glausier, Mariah A Hildebrand, Xiangning Xue, Wei Zong, Jiebiao Wang, Micah A Shelton, BaDoi N Phan, Chaitanya Srinivasan, Andreas R Pfenning, George C Tseng, David A Lewis, Zachary Freyberg, Ryan W Logan
Cerebellum Gene Expression Correlates for LM_PAIR1 measured in BXD RI Females & Males obtained using SJUT Cerebellum mRNA M430 (Mar05) RMA. The LM_PAIR1 measures Activity during 1st tone shock pairing under the domain Basal Behavior. 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 MDMA_ACT_MDA_1 measured in BXD RI Males obtained using INIA Brain mRNA M430 (Jun06) RMA. The MDMA_ACT_MDA_1 measures Locomotor response of 10 mg/kg MDMA injected on Day 2 under the domain MDMA. 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
cocaine related behavior 7 (Cocrb7) spans 28.968906 - 78.968906 Mbp (NCBI Build 37) on Chr 6. Obtained from MGI (http://www.informatics.jax.org) by searching for QTLs containing the keyword .
QTL for cocaine related behavior on Chr6 at D6Mit183 (53.97 Mbp , Build 37)
Description:
cocaine related behavior spans 28.97 - 78.97 Mbp (NCBI Build 37) on Chr6. This interval was obtained by using an interval width of 25 Mbp around the peak marker (Build 37, MGI, http://informatics.jax.org).
QTL for METH responses for body temperature on Chr6 at D6Ncvs34 (54.50 Mbp , Build 37)
Description:
METH responses for body temperature spans 29.50 - 79.50 Mbp (NCBI Build 37) on Chr6. This interval was obtained by using an interval width of 25 Mbp around the peak marker (Build 37, MGI, http://informatics.jax.org).
QTL for ethanol induced locomotion on Chr6 at NA (64.65 Mbp , Build 37)
Description:
ethanol induced locomotion spans 39.65 - 89.65 Mbp (NCBI Build 37) on Chr6. This interval was obtained by using an interval width of 25 Mbp around the peak marker (Build 37, MGI, http://informatics.jax.org).
Authors:
Hitzemann R, Demarest K, Koyner J, Cipp L, Patel N, Rasmussen E, McCaughran J Jr
QTL for METH responses for home cage activity on Chr6 at D6Nds3 (67.84 Mbp , Build 37)
Description:
METH responses for home cage activity spans 42.84 - 92.84 Mbp (NCBI Build 37) on Chr6. This interval was obtained by using an interval width of 25 Mbp around the peak marker (Build 37, MGI, http://informatics.jax.org).
QTL for METH responses for body temperature on Chr6 at D6MIt16 (67.84 Mbp , Build 37)
Description:
METH responses for body temperature spans 42.84 - 92.84 Mbp (NCBI Build 37) on Chr6. This interval was obtained by using an interval width of 25 Mbp around the peak marker (Build 37, MGI, http://informatics.jax.org).
Genome-wide association study identifies a locus at 7p15.2 associated with endometriosis.
Authors:
Painter JN, Anderson CA, Nyholt DR, Macgregor S, Lin J, Lee SH, Lambert A, Zhao ZZ, Roseman F, Guo Q, Gordon SD, Wallace L, Henders AK, Visscher PM, Kraft P, Martin NG, Morris AP, Treloar SA, Kennedy SH, Missmer SA, Montgomery GW, Zondervan KT
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