NR3C1 c.2298T>C ;(p.N766=)

Variant ID: 5-142661490-A-G

NM_000176.2(NR3C1):c.2298T>C;(p.N766=)

This variant was identified in 51 publications

View GRCh38 version.




Publications:


Comprehensive proteogenomic characterization of early duodenal cancer reveals the carcinogenesis tracks of different subtypes.

Nature Communications
Li, Lingling L; Jiang, Dongxian D; Liu, Hui H; Guo, Chunmei C; Zhao, Rui R; Zhang, Qiao Q; Xu, Chen C; Qin, Zhaoyu Z; Feng, Jinwen J; Liu, Yang Y; Wang, Haixing H; Chen, Weijie W; Zhang, Xue X; Li, Bin B; Bai, Lin L; Tian, Sha S; Tan, Subei S; Yu, Zixiang Z; Chen, Lingli L; Huang, Jie J; Zhao, Jian-Yuan JY; Hou, Yingyong Y; Ding, Chen C
Publication Date: 2023-03-29

Variant appearance in text: NR3C1: N766N; rs6196
PubMed Link: 36991000
Variant Present in the following documents:
  • 41467_2023_37221_MOESM5_ESM.xlsx, sheet 3
View BVdb publication page



The role of the glucocorticoid receptor and its impact on steroid response in moderate-severe COVID-19 patients.

European Journal Of Pharmacology
Aliska, Gestina G; Nafrialdi, Nafrialdi N; Lie, Khie Chen KC; Setiabudy, Rianto R; Putra, Andani Eka AE; Widyahening, Indah Suci IS; Harahap, Alida Roswita AR
Publication Date: 2023-01-28

Variant appearance in text: rs6196
PubMed Link: 36720399
Variant Present in the following documents:
  • Main text
  • main.pdf
View BVdb publication page



Establishment and characterization of a new mantle cell lymphoma cell line with a NOTCH2 mutation, Arbo.

Ejhaem
Safa, Firas F; Rasmussen, Terri T; Lobelle-Rich, Patricia P; Collier, Stephanie S; Milligan, Nicholas N; Schmeig, John J; Schmid, Janet J; Wiewiorowski, Carol C; Totaro, Denise D; Brown, Theresa C TC; Satyavarapu, Ishwarya I; Badoo, Melody M; Ungerleider, Nathan N; Flemington, Erik K EK; Safah, Hana H; Saba, Nakhle S NS
Publication Date: 2022-11

Variant appearance in text: NR3C1: N766N; rs6196
PubMed Link: 36467812
Variant Present in the following documents:
  • JHA2-3-1326-s001.xlsx, sheet 1
View BVdb publication page



Familial Linkage and Association of the NR3C1 Gene with Type 2 Diabetes and Depression Comorbidity.

International Journal Of Molecular Sciences
Amin, Mutaz M; Syed, Shumail S; Wu, Rongling R; Postolache, Teodor Tudorel TT; Gragnoli, Claudia C
Publication Date: 2022-10-08

Variant appearance in text: rs6196
PubMed Link: 36233250
Variant Present in the following documents:
  • Main text
  • ijms-23-11951.pdf
View BVdb publication page



Association of singlenucleotide NR3C1 gene polymorphisms with glucocorticosteroid responsiveness in patients with pemphigus vulgaris.

Dermatology Reports
Le, Thai Van Thanh TVT; Nguyen, Duy Quan DQ; Tran, Ngoc Dang ND; Tu Trinh, Hoang Kim HK
Publication Date: 2022-06-16

Variant appearance in text: rs6196
PubMed Link: 35795836
Variant Present in the following documents:
  • Main text
  • dr-14-2-9190.pdf
View BVdb publication page



Investigation of single-nucleotide polymorphisms in the NR3C1a glucocorticoid receptor gene in Cocker Spaniels with primary immune thrombocytopenia.

Journal Of Veterinary Internal Medicine
Tayler, Sarah S; Hazuchova, Katarina K; Riddle, Anna A; Swann, James W JW; Glanemann, Barbara B
Publication Date: 2022-07

Variant appearance in text: rs6196
PubMed Link: 35689373
Variant Present in the following documents:
  • Main text
  • JVIM-36-1281.pdf
View BVdb publication page



Effect of Glucocorticosteroids in Diamond-Blackfan Anaemia: Maybe Not as Elusive as It Seems.

International Journal Of Molecular Sciences
Macečková, Zuzana Z; Kubíčková, Agáta A; Sanctis, Juan Bautista De JB; Hajdúch, Marian M
Publication Date: 2022-02-08

Variant appearance in text: rs6196
PubMed Link: 35163808
Variant Present in the following documents:
  • Main text
  • ijms-23-01886.pdf
View BVdb publication page



Effect of Glucocorticosteroids in Diamond-Blackfan Anaemia: Maybe Not as Elusive as It Seems.

International Journal Of Molecular Sciences
Macečková, Zuzana Z; Kubíčková, Agáta A; De Sanctis, Juan Bautista JB; Hajdúch, Marian M
Publication Date: 2022-02-08

Variant appearance in text: rs6196
PubMed Link: 35163808
Variant Present in the following documents:
  • Main text
  • ijms-23-01886.pdf
View BVdb publication page



Editorial: Genetics and Genomics of Red Blood Cells.

Frontiers In Physiology
Iolascon, Achille A; Russo, Roberta R; Andolfo, Immacolata I
Publication Date: 2021

Variant appearance in text: rs6196
PubMed Link: 35069269
Variant Present in the following documents:
  • Main text
  • fphys-12-822156.pdf
View BVdb publication page



NR3C1 Glucocorticoid Receptor Gene Polymorphisms Are Associated with Membranous and IgA Nephropathies.

Cells
Pac, Michał M; Krata, Natalia N; Moszczuk, Barbara B; Wyczałkowska-Tomasik, Aleksandra A; Kaleta, Beata B; Foroncewicz, Bartosz B; Rudnicki, Witold W; Pączek, Leszek L; Mucha, Krzysztof K
Publication Date: 2021-11-16

Variant appearance in text: rs6196
PubMed Link: 34831409
Variant Present in the following documents:
  • Main text
  • cells-10-03186.pdf
View BVdb publication page



The Glucocorticoid Receptor Polymorphism Landscape in Patients With Diamond Blackfan Anemia Reveals an Association Between Two Clinically Relevant Single Nucleotide Polymorphisms and Time to Diagnosis.

Frontiers In Physiology
Lonetti, Annalisa A; Indio, Valentina V; Dianzani, Irma I; Ramenghi, Ugo U; Da Costa, Lydie L; Pospíšilová, Dagmar D; Migliaccio, Anna Rita AR
Publication Date: 2021

Variant appearance in text: rs6196
PubMed Link: 34721069
Variant Present in the following documents:
  • Main text
  • fphys-12-745032.pdf
View BVdb publication page



Association and Genetic Expression between Genes Involved in HPA Axis and Suicide Behavior: A Systematic Review.

Genes
Hernández-Díaz, Yazmín Y; Genis-Mendoza, Alma Delia AD; González-Castro, Thelma Beatriz TB; Tovilla-Zárate, Carlos Alfonso CA; Juárez-Rojop, Isela Esther IE; López-Narváez, María Lilia ML; Nicolini, Humberto H
Publication Date: 2021-10-13

Variant appearance in text: rs6196
PubMed Link: 34681002
Variant Present in the following documents:
  • Main text
  • genes-12-01608.pdf
View BVdb publication page



Comprehensive analysis of important pharmacogenes in Koreans using the DMET™ platform.

Translational And Clinical Pharmacology
Kim, Byungwook B; Yoon, Deok Yong DY; Lee, SeungHwan S; Jang, In-Jin IJ; Yu, Kyung-Sang KS; Cho, Joo-Youn JY; Oh, Jaeseong J
Publication Date: 2021-09

Variant appearance in text: NR3C1: 2298T>C; N766N; rs6196
PubMed Link: 34621706
Variant Present in the following documents:
  • tcp-29-135-s001.xls, sheet 1
View BVdb publication page



Association between NR3C1 gene polymorphisms and age-related hearing impairment in Qingdao Chinese elderly.

Bmc Medical Genomics
Song, Wanxue W; Cao, Hainan H; Zhang, Dongfeng D; Xu, Haiyan H; Zhang, Qianqian Q; Wang, Zhaoguo Z; Li, Suyun S; Wang, Weijing W; Hu, Wenchao W; Wang, Bingling B; Duan, Haiping H
Publication Date: 2021-07-28

Variant appearance in text: rs6196
PubMed Link: 34320993
Variant Present in the following documents:
  • Main text
  • 12920_2021_Article_1044.pdf
View BVdb publication page



Fragmentation patterns and personalized sequencing of cell-free DNA in urine and plasma of glioma patients.

Embo Molecular Medicine
Mouliere, Florent F; Smith, Christopher G CG; Heider, Katrin K; Su, Jing J; van der Pol, Ymke Y; Thompson, Mareike M; Morris, James J; Wan, Jonathan C M JCM; Chandrananda, Dineika D; Hadfield, James J; Grzelak, Marta M; Hudecova, Irena I; Couturier, Dominique-Laurent DL; Cooper, Wendy W; Zhao, Hui H; Gale, Davina D; Eldridge, Matthew M; Watts, Colin C; Brindle, Kevin K; Rosenfeld, Nitzan N; Mair, Richard R
Publication Date: 2021-08-09

Variant appearance in text: rs6196
PubMed Link: 34291583
Variant Present in the following documents:
  • EMMM-13-e12881-s010.xlsx, sheet 1
View BVdb publication page



Disseminated Talaromyces marneffei Infection in a Non-HIV Infant With a Homozygous Private Variant of RELB.

Frontiers In Cellular And Infection Microbiology
Ding, Xiaofang X; Huang, Han H; Zhong, Lili L; Chen, Min M; Peng, Fang F; Zhang, Bing B; Cui, Xinyu X; Yang, Xiu-An XA
Publication Date: 2021

Variant appearance in text: NR3C1: N766N; rs6196
PubMed Link: 33791233
Variant Present in the following documents:
  • Table_2.xlsx, sheet 1
View BVdb publication page



Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss.

Bmc Medical Genomics
Yang, Guangxian G; Yin, Yi Y; Tan, Zhiping Z; Liu, Jian J; Deng, Xicheng X; Yang, Yifeng Y
Publication Date: 2021-01-21

Variant appearance in text: NR3C1: 2298T>C; N766N; rs6196
PubMed Link: 33478437
Variant Present in the following documents:
  • 12920_2021_871_MOESM2_ESM.xls, sheet 1
View BVdb publication page



Computational Functional Genomics-Based AmpliSeq™ Panel for Next-Generation Sequencing of Key Genes of Pain.

International Journal Of Molecular Sciences
Kringel, Dario D; Malkusch, Sebastian S; Kalso, Eija E; Lötsch, Jörn J
Publication Date: 2021-01-16

Variant appearance in text: rs6196
PubMed Link: 33467215
Variant Present in the following documents:
  • Main text
  • ijms-22-00878.pdf
View BVdb publication page



The Pathways between Cortisol-Related Regulation Genes and PTSD Psychotherapy.

Healthcare (Basel, Switzerland)
Castro-Vale, Ivone I; Carvalho, Davide D
Publication Date: 2020-10-01

Variant appearance in text: rs6196
PubMed Link: 33019527
Variant Present in the following documents:
  • Main text
  • healthcare-08-00376.pdf
View BVdb publication page



PGG.SNV: understanding the evolutionary and medical implications of human single nucleotide variations in diverse populations.

Genome Biology
Zhang, Chao C; Gao, Yang Y; Ning, Zhilin Z; Lu, Yan Y; Zhang, Xiaoxi X; Liu, Jiaojiao J; Xie, Bo B; Xue, Zhe Z; Wang, Xiaoji X; Yuan, Kai K; Ge, Xueling X; Pan, Yuwen Y; Liu, Chang C; Tian, Lei L; Wang, Yuchen Y; Lu, Dongsheng D; Hoh, Boon-Peng BP; Xu, Shuhua S
Publication Date: 2019-10-22

Variant appearance in text: NR3C1: 2298T>C; rs6196
PubMed Link: 31640808
Variant Present in the following documents:
  • 13059_2019_1838_MOESM3_ESM.xlsx, sheet 1
View BVdb publication page



Distinctive mutational spectrum and karyotype disruption in long-term cisplatin-treated urothelial carcinoma cell lines.

Scientific Reports
Skowron, Margaretha A MA; Petzsch, Patrick P; Hardt, Karin K; Wagner, Nicholas N; Beier, Manfred M; Stepanow, Stefanie S; Drechsler, Matthias M; Rieder, Harald H; Köhrer, Karl K; Niegisch, Günter G; Hoffmann, Michèle J MJ; Schulz, Wolfgang A WA
Publication Date: 2019-10-09

Variant appearance in text: NR3C1: N766N; rs6196
PubMed Link: 31597922
Variant Present in the following documents:
  • 41598_2019_50891_MOESM6_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM9_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM7_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM4_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM8_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM5_ESM.xlsx, sheet 1
View BVdb publication page



Reproducibility of pharmacogenetics findings for paclitaxel in a heterogeneous population of patients with lung cancer.

Plos One
Sissung, Tristan M TM; Rajan, Arun A; Blumenthal, Gideon M GM; Liewehr, David J DJ; Steinberg, Seth M SM; Berman, Arlene A; Giaccone, Giuseppe G; Figg, William D WD
Publication Date: 2019

Variant appearance in text: NR3C1: N766N; rs6196
PubMed Link: 30817750
Variant Present in the following documents:
  • Main text
  • pone.0212097.pdf
View BVdb publication page



Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology
Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P
Publication Date: 2018

Variant appearance in text: NR3C1: 2298T>C; rs6196
PubMed Link: 30319441
Variant Present in the following documents:
  • Table_7.xlsx, sheet 1
View BVdb publication page



A likely pathogenic variant putatively affecting splicing of PIGA identified in a multiple congenital anomalies hypotonia-seizures syndrome 2 (MCAHS2) family pedigree via whole-exome sequencing.

Molecular Genetics & Genomic Medicine
Yang, Junli J; Wang, Qiong Q; Zhuo, Qingcui Q; Tian, Huiling H; Li, Wen W; Luo, Fang F; Zhang, Jinghui J; Bi, Dan D; Peng, Jing J; Zhou, Dong D; Xin, Huawei H
Publication Date: 2018-09

Variant appearance in text: NR3C1: 2298T>C; rs6196
PubMed Link: 29974678
Variant Present in the following documents:
  • MGG3-6-739-s002.xlsx, sheet 6
View BVdb publication page



Sequencing the exons of human glucocorticoid receptor (NR3C1) gene in Han Chinese with high-altitude pulmonary edema.

Journal Of Physiological Anthropology
Du, Hui H; Zhao, Jing J; Su, Zhanhai Z; Liu, Yongnian Y; Yang, Yingzhong Y
Publication Date: 2018-03-27

Variant appearance in text: rs6196
PubMed Link: 29587872
Variant Present in the following documents:
  • Main text
View BVdb publication page



Pharmacology and pharmacogenetics of prednisone and prednisolone in patients with nephrotic syndrome.

Pediatric Nephrology (Berlin, Germany)
Schijvens, Anne M AM; Ter Heine, Rob R; de Wildt, Saskia N SN; Schreuder, Michiel F MF
Publication Date: 2019-03

Variant appearance in text: rs6196
PubMed Link: 29549463
Variant Present in the following documents:
  • Main text
  • 467_2018_Article_3929.pdf
View BVdb publication page



Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget
Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH
Publication Date: 2017-11-10

Variant appearance in text: NR3C1: N766N; rs6196
PubMed Link: 29221171
Variant Present in the following documents:
  • oncotarget-08-95841-s002.xlsx, sheet 4
  • oncotarget-08-95841-s002.xlsx, sheet 1
View BVdb publication page



Pharmacogenomics in the treatment of mood disorders: Strategies and Opportunities for personalized psychiatry.

The Epma Journal
Amare, Azmeraw T AT; Schubert, Klaus Oliver KO; Baune, Bernhard T BT
Publication Date: 2017-09

Variant appearance in text: rs6196
PubMed Link: 29021832
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetics of generalized anxiety disorder and related traits.

Dialogues In Clinical Neuroscience
Gottschalk, Michael G MG; Domschke, Katharina K
Publication Date: 2017-06

Variant appearance in text: rs6196
PubMed Link: 28867940
Variant Present in the following documents:
  • Main text
  • DialoguesClinNeurosci-19-159.pdf
View BVdb publication page



Pharmacogenetics of steroid-responsive acute graft-versus-host disease.

Clinical Transplantation
Arora, Mukta M; Weisdorf, Daniel J DJ; Shanley, Ryan M RM; Thyagarajan, Bharat B
Publication Date: 2017-05

Variant appearance in text: rs6196
PubMed Link: 28266732
Variant Present in the following documents:
  • Main text
View BVdb publication page



A systematic review of the association between fatigue and genetic polymorphisms.

Brain, Behavior, And Immunity
Wang, Tengteng T; Yin, Jie J; Miller, Andrew H AH; Xiao, Canhua C
Publication Date: 2017-05

Variant appearance in text: rs6196
PubMed Link: 28089639
Variant Present in the following documents:
  • Main text
View BVdb publication page



GLUCOCORTICOID RECEPTOR-RELATED GENES: GENOTYPE AND BRAIN GENE EXPRESSION RELATIONSHIPS TO SUICIDE AND MAJOR DEPRESSIVE DISORDER.

Depression And Anxiety
Yin, Honglei H; Galfalvy, Hanga H; Pantazatos, Spiro P SP; Huang, Yung-Yu YY; Rosoklija, Gorazd B GB; Dwork, Andrew J AJ; Burke, Ainsley A; Arango, Victoria V; Oquendo, Maria A MA; Mann, J John JJ
Publication Date: 2016-06

Variant appearance in text: rs6196
PubMed Link: 27030168
Variant Present in the following documents:
  • Main text
View BVdb publication page



Glucocorticoid Receptors, Brain-Derived Neurotrophic Factor, Serotonin and Dopamine Neurotransmission are Associated with Interferon-Induced Depression.

The International Journal Of Neuropsychopharmacology
Udina, M M; Navinés, R R; Egmond, E E; Oriolo, G G; Langohr, K K; Gimenez, D D; Valdés, M M; Gómez-Gil, E E; Grande, I I; Gratacós, M M; Kapczinski, F F; Artigas, F F; Vieta, E E; Solà, R R; Martín-Santos, R R
Publication Date: 2016-04

Variant appearance in text: rs6196
PubMed Link: 26721949
Variant Present in the following documents:
  • Main text
  • pyv135.pdf
View BVdb publication page



Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget
Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S
Publication Date: 2015-06-20

Variant appearance in text: NR3C1: N766N; rs6196
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
View BVdb publication page



The Affymetrix DMET Plus platform reveals unique distribution of ADME-related variants in ethnic Arabs.

Disease Markers
Wakil, Salma M SM; Nguyen, Cao C; Muiya, Nzioka P NP; Andres, Editha E; Lykowska-Tarnowska, Agnieszka A; Baz, Batoul B; Tahir, Asma I AI; Meyer, Brian F BF; Morahan, Grant G; Dzimiri, Nduna N
Publication Date: 2015

Variant appearance in text: rs6196
PubMed Link: 25802476
Variant Present in the following documents:
  • 542543.f1.xlsx, sheet 1
View BVdb publication page



A study of genes encoding cytokines (IL6, IL10, TNF), cytokine receptors (IL6R, IL6ST), and glucocorticoid receptor (NR3C1) and susceptibility to bronchopulmonary dysplasia.

Bmc Medical Genetics
Huusko, Johanna M JM; Karjalainen, Minna K MK; Mahlman, Mari M; Haataja, Ritva R; Kari, M Anneli MA; Andersson, Sture S; Toldi, Gergely G; Tammela, Outi O; Rämet, Mika M; Lavoie, Pascal M PM; Hallman, Mikko M; ,
Publication Date: 2014-11-01

Variant appearance in text: rs6196
PubMed Link: 25409741
Variant Present in the following documents:
  • Main text
  • 12881_2014_Article_120.pdf
View BVdb publication page



Whole-genome sequencing of the world's oldest people.

Plos One
Gierman, Hinco J HJ; Fortney, Kristen K; Roach, Jared C JC; Coles, Natalie S NS; Li, Hong H; Glusman, Gustavo G; Markov, Glenn J GJ; Smith, Justin D JD; Hood, Leroy L; Coles, L Stephen LS; Kim, Stuart K SK
Publication Date: 2014

Variant appearance in text: NR3C1: N766N; rs6196
PubMed Link: 25390934
Variant Present in the following documents:
  • pone.0112430.s004.xlsx, sheet 1
View BVdb publication page



The RPTEC/TERT1 cell line models key renal cell responses to the environmental toxicants, benzo[a]pyrene and cadmium.

Toxicology Reports
Simon, B R BR; Wilson, M J MJ; Wickliffe, J K JK
Publication Date: 2014

Variant appearance in text: rs6196
PubMed Link: 25126521
Variant Present in the following documents:
  • mmc1.xls, sheet 1
View BVdb publication page



Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.

Febs Open Bio
Szeto, Carol Ying-Ying CY; Lin, Chi Ho CH; Choi, Siu Chung SC; Yip, Timothy T C TT; Ngan, Roger Kai-Cheong RK; Tsao, George Sai-Wah GS; Li Lung, Maria M
Publication Date: 2014

Variant appearance in text: NR3C1: N766N; rs6196
PubMed Link: 24490137
Variant Present in the following documents:
  • mmc5.xlsx, sheet 2
View BVdb publication page



Influence of genetic polymorphisms involved in the hypothalamic-pituitary-adrenal axis and their interactions with environmental factors on antidepressant response.

Cns Neuroscience & Therapeutics
Geng, Lei-Yu LY; Ye, Dong-Qing DQ; Shi, Yan-Yan YY; Xu, Zhi Z; Pu, Meng-Jia MJ; Li, Zan-Yuan ZY; Li, Xiao-Li XL; Li, Yang Y; Zhang, Zhi-Jun ZJ
Publication Date: 2014-03

Variant appearance in text: rs6196
PubMed Link: 24422887
Variant Present in the following documents:
  • Main text
View BVdb publication page



Association, haplotype, and gene-gene interactions of the HPA axis genes with suicidal behaviour in affective disorders.

Thescientificworldjournal
Leszczyńska-Rodziewicz, Anna A; Szczepankiewicz, Aleksandra A; Pawlak, Joanna J; Dmitrzak-Weglarz, Monika M; Hauser, Joanna J
Publication Date: 2013

Variant appearance in text: rs6196
PubMed Link: 24379738
Variant Present in the following documents:
  • Main text
  • TSWJ2013-207361.pdf
View BVdb publication page



Effect of a poly(ADP-ribose) polymerase-1 inhibitor against esophageal squamous cell carcinoma cell lines.

Cancer Science
Nasuno, Tomomitsu T; Mimaki, Sachiyo S; Okamoto, Makito M; Esumi, Hiroyasu H; Tsuchihara, Katsuya K
Publication Date: 2014-02

Variant appearance in text: rs6196
PubMed Link: 24219164
Variant Present in the following documents:
  • cas0105-0202-SD3.xlsx, sheet 1
View BVdb publication page



Glucocorticoid receptor mRNA and protein isoform alterations in the orbitofrontal cortex in schizophrenia and bipolar disorder.

Bmc Psychiatry
Sinclair, Duncan D; Webster, Maree J MJ; Fullerton, Janice M JM; Weickert, Cynthia Shannon CS
Publication Date: 2012-07-20

Variant appearance in text: NR3C1: N766N; rs6196
PubMed Link: 22812453
Variant Present in the following documents:
  • Main text
View BVdb publication page



Glucocorticoid receptor 1B and 1C mRNA transcript alterations in schizophrenia and bipolar disorder, and their possible regulation by GR gene variants.

Plos One
Sinclair, Duncan D; Fullerton, Janice M JM; Webster, Maree J MJ; Shannon Weickert, Cynthia C
Publication Date: 2012

Variant appearance in text: NR3C1: N766N; rs6196
PubMed Link: 22427805
Variant Present in the following documents:
  • Main text
View BVdb publication page



Identification of significant genes in genomics using Bayesian variable selection methods.

Advances And Applications In Bioinformatics And Chemistry : Aabc
Lin, Eugene E; Huang, Lung-Cheng LC
Publication Date: 2008

Variant appearance in text: rs6196
PubMed Link: 21918603
Variant Present in the following documents:
  • Main text
  • aabc-1-13.pdf
View BVdb publication page



Identification of rare DNA variants in mitochondrial disorders with improved array-based sequencing.

Nucleic Acids Research
Wang, Wenyi W; Shen, Peidong P; Thiyagarajan, Sreedevi S; Lin, Shengrong S; Palm, Curtis C; Horvath, Rita R; Klopstock, Thomas T; Cutler, David D; Pique, Lynn L; Schrijver, Iris I; Davis, Ronald W RW; Mindrinos, Michael M; Speed, Terence P TP; Scharfe, Curt C
Publication Date: 2011-01

Variant appearance in text: rs6196
PubMed Link: 20843780
Variant Present in the following documents:
  • supp_gkq750_NAR-WangWetal-SuppTable-6.xls, sheet 1
View BVdb publication page



Glucocorticoid receptor gene haplotype structure and steroid therapy outcome in IBD patients.

World Journal Of Gastroenterology
Mwinyi, Jessica J; Wenger, Christa C; Eloranta, Jyrki J JJ; Kullak-Ublick, Gerd A GA
Publication Date: 2010-08-21

Variant appearance in text: NR3C1: N766N; rs6196
PubMed Link: 20712049
Variant Present in the following documents:
  • Main text
View BVdb publication page



A comparison of classification methods for predicting Chronic Fatigue Syndrome based on genetic data.

Journal Of Translational Medicine
Huang, Lung-Cheng LC; Hsu, Sen-Yen SY; Lin, Eugene E
Publication Date: 2009-09-22

Variant appearance in text: rs6196
PubMed Link: 19772600
Variant Present in the following documents:
  • Main text
  • 1479-5876-7-81.pdf
View BVdb publication page



Human glucocorticoid receptor alpha gene (NR3C1) pharmacogenomics: gene resequencing and functional genomics.

The Journal Of Clinical Endocrinology And Metabolism
Niu, Nifang N; Manickam, Venkatraman V; Kalari, Krishna R KR; Moon, Irene I; Pelleymounter, Linda L LL; Eckloff, Bruce W BW; Wieben, Eric D ED; Schaid, Daniel J DJ; Wang, Liewei L
Publication Date: 2009-08

Variant appearance in text: rs6196
PubMed Link: 19435830
Variant Present in the following documents:
  • Main text
View BVdb publication page



Cohort profile: risk patterns and processes for psychopathology emerging during adolescence: the ROOTS project.

International Journal Of Epidemiology
Goodyer, Ian M IM; Croudace, Tim T; Dunn, Valerie V; Herbert, Joe J; Jones, Peter B PB
Publication Date: 2010-04

Variant appearance in text: rs6196
PubMed Link: 19359258
Variant Present in the following documents:
  • Main text
View BVdb publication page



Glucocorticoid receptor gene variant in the 3' untranslated region is associated with multiple measures of blood pressure.

The Journal Of Clinical Endocrinology And Metabolism
Chung, Charles C CC; Shimmin, Lawrence L; Natarajan, Sivamani S; Hanis, Craig L CL; Boerwinkle, Eric E; Hixson, James E JE
Publication Date: 2009-01

Variant appearance in text: rs6196
PubMed Link: 18854398
Variant Present in the following documents:
  • Main text
View BVdb publication page



Polymorphisms affecting gene transcription and mRNA processing in pharmacogenetic candidate genes: detection through allelic expression imbalance in human target tissues.

Pharmacogenetics And Genomics
Johnson, Andrew D AD; Zhang, Ying Y; Papp, Audrey C AC; Pinsonneault, Julia K JK; Lim, Jeong-Eun JE; Saffen, David D; Dai, Zunyan Z; Wang, Danxin D; Sadée, Wolfgang W
Publication Date: 2008-09

Variant appearance in text: rs6196
PubMed Link: 18698231
Variant Present in the following documents:
  • Main text
View BVdb publication page