NRG1 c.866T>C ;(p.M289T)

Variant ID: 8-32613983-T-C

NM_013964.3(NRG1):c.866T>C;(p.M289T)

This variant was identified in 35 publications

View GRCh38 version.




Publications:


A Phase II Trial of Guadecitabine plus Atezolizumab in Metastatic Urothelial Carcinoma Progressing after Initial Immune Checkpoint Inhibitor Therapy.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Jang, H Josh HJ; Hostetter, Galen G; MacFarlane, Alexander W AW; Madaj, Zachary Z; Ross, Eric A EA; Hinoue, Toshinori T; Kulchycki, Justin R JR; Burgos, Ryan S RS; Tafseer, Mahvish M; Alpaugh, R Katherine RK; Schwebel, Candice L CL; Kokate, Rutika R; Geynisman, Daniel M DM; Zibelman, Matthew R MR; Ghatalia, Pooja P; Nichols, Peter W PW; Chung, Woonbok W; Madzo, Jozef J; Hahn, Noah M NM; Quinn, David I DI; Issa, Jean-Pierre J JJ; Topper, Michael J MJ; Baylin, Stephen B SB; Shen, Hui H; Campbell, Kerry S KS; Jones, Peter A PA; Plimack, Elizabeth R ER
Publication Date: 2023-03-16

Variant appearance in text: NRG1: M289T
PubMed Link: 36928921
Variant Present in the following documents:
  • ccr-22-3642_supplementary_tables_1_suppts1.xlsx, sheet 3
View BVdb publication page



Response prediction in patients with gastric and esophagogastric adenocarcinoma under neoadjuvant chemotherapy using targeted gene expression analysis and next-generation sequencing in pre-therapeutic biopsies.

Journal Of Cancer Research And Clinical Oncology
Kleo, Karsten K; Jovanovic, Vladimir M VM; Arndold, Alexander A; Lehmann, Annika A; Lammert, Hedwig H; Berg, Erika E; Harloff, Hannah H; Treese, Christoph C; Hummel, Michael M; Daum, Severin S
Publication Date: 2022-03-05

Variant appearance in text: rs10503929
PubMed Link: 35246724
Variant Present in the following documents:
  • 432_2022_3944_MOESM1_ESM.xlsx, sheet 1
View BVdb publication page



The mutational load and a T-cell inflamed tumour phenotype identify ovarian cancer patients rendering tumour-reactive T cells from PD-1+ tumour-infiltrating lymphocytes.

British Journal Of Cancer
Salas-Benito, Diego D; Conde, Enrique E; Tamayo-Uria, Ibon I; Mancheño, Uxua U; Elizalde, Edurne E; Garcia-Ros, David D; Aramendia, Jose M JM; Muruzabal, Juan C JC; Alcaide, Julia J; Guillen-Grima, Francisco F; Minguez, Jose A JA; Amores-Tirado, Jose J; Gonzalez-Martin, Antonio A; Sarobe, Pablo P; Lasarte, Juan J JJ; Ponz-Sarvise, Mariano M; De Andrea, Carlos E CE; Hervas-Stubbs, Sandra S
Publication Date: 2021-03

Variant appearance in text: NRG1: 866T>C; Met289Thr; rs10503929
PubMed Link: 33402737
Variant Present in the following documents:
  • 41416_2020_1218_MOESM2_ESM.xlsx, sheet 1
View BVdb publication page



NRG1, PIP4K2A, and HTR2C as Potential Candidate Biomarker Genes for Several Clinical Subphenotypes of Depression and Bipolar Disorder.

Frontiers In Genetics
Levchenko, Anastasia A; Vyalova, Natalia M NM; Nurgaliev, Timur T; Pozhidaev, Ivan V IV; Simutkin, German G GG; Bokhan, Nikolay A NA; Ivanova, Svetlana A SA
Publication Date: 2020

Variant appearance in text: rs10503929
PubMed Link: 33193575
Variant Present in the following documents:
  • Main text
  • fgene-11-00936.pdf
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: NRG1: M289T; rs10503929
PubMed Link: 31597922
Variant Present in the following documents:
  • 41598_2019_50891_MOESM10_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM9_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM3_ESM.xlsx, sheet 1
  • 41598_2019_50891_MOESM8_ESM.xlsx, sheet 1
View BVdb publication page



Nrg1 Intracellular Signaling Is Neuroprotective upon Stroke.

Oxidative Medicine And Cellular Longevity
Navarro-González, Carmen C; Huerga-Gómez, Alba A; Fazzari, Pietro P
Publication Date: 2019

Variant appearance in text: rs10503929
PubMed Link: 31583038
Variant Present in the following documents:
  • Main text
  • OMCL2019-3930186.pdf
View BVdb publication page



Clinical-Pharmacogenetic Predictive Models for Time to Occurrence of Levodopa Related Motor Complications in Parkinson's Disease.

Frontiers In Genetics
Redenšek, Sara S; Jenko Bizjan, Barbara B; Trošt, Maja M; Dolžan, Vita V
Publication Date: 2019

Variant appearance in text: rs10503929
PubMed Link: 31156712
Variant Present in the following documents:
  • Main text
  • fgene-10-00461.pdf
View BVdb publication page



Usefulness of Single Nucleotide Polymorphisms as Predictors of Sudden Cardiac Death.

The American Journal Of Cardiology
Tamariz, Leonardo L; Balda, Javier J; Pareja, Dennise D; Palacio, Ana A; Myerburg, Robert J RJ; Conway, Douglas D; Davis, Lea L; Goldberger, Jeffrey J JJ
Publication Date: 2019-06-15

Variant appearance in text: rs10503929
PubMed Link: 31053292
Variant Present in the following documents:
  • Main text
View BVdb publication page



A reference collection of patient-derived cell line and xenograft models of proneural, classical and mesenchymal glioblastoma.

Scientific Reports
Stringer, Brett W BW; Day, Bryan W BW; D'Souza, Rochelle C J RCJ; Jamieson, Paul R PR; Ensbey, Kathleen S KS; Bruce, Zara C ZC; Lim, Yi Chieh YC; Goasdoué, Kate K; Offenhäuser, Carolin C; Akgül, Seçkin S; Allan, Suzanne S; Robertson, Thomas T; Lucas, Peter P; Tollesson, Gert G; Campbell, Scott S; Winter, Craig C; Do, Hongdo H; Dobrovic, Alexander A; Inglis, Po-Ling PL; Jeffree, Rosalind L RL; Johns, Terrance G TG; Boyd, Andrew W AW
Publication Date: 2019-03-20

Variant appearance in text: rs10503929
PubMed Link: 30894629
Variant Present in the following documents:
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 9
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 2
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 3
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 13
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 6
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 5
  • 41598_2019_41277_MOESM4_ESM.xlsx, sheet 10
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Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases.

Cell Death & Disease
Grassi, Ludovica L; Alfonsi, Romina R; Francescangeli, Federica F; Signore, Michele M; De Angelis, Maria Laura ML; Addario, Antonio A; Costantini, Manuela M; Flex, Elisabetta E; Ciolfi, Andrea A; Pizzi, Simone S; Bruselles, Alessandro A; Pallocca, Matteo M; Simone, Giuseppe G; Haoui, Mustapha M; Falchi, Mario M; Milella, Michele M; Sentinelli, Steno S; Di Matteo, Paola P; Stellacci, Emilia E; Gallucci, Michele M; Muto, Giovanni G; Tartaglia, Marco M; De Maria, Ruggero R; Bonci, Désirée D
Publication Date: 2019-02-27

Variant appearance in text: rs10503929
PubMed Link: 30814510
Variant Present in the following documents:
  • 41419_2019_1453_MOESM27_ESM.xlsx, sheet 1
  • 41419_2019_1453_MOESM27_ESM.xlsx, sheet 2
View BVdb publication page



Prediction Analysis for Transition to Schizophrenia in Individuals at Clinical High Risk for Psychosis: The Relationship of DAO, DAOA, and NRG1 Variants with Negative Symptoms and Cognitive Deficits.

Frontiers In Psychiatry
Jagannath, Vinita V; Theodoridou, Anastasia A; Gerstenberg, Miriam M; Franscini, Maurizia M; Heekeren, Karsten K; Correll, Christoph U CU; Rössler, Wulf W; Grünblatt, Edna E; Walitza, Susanne S
Publication Date: 2017

Variant appearance in text: rs10503929
PubMed Link: 29326614
Variant Present in the following documents:
  • Main text
  • fpsyt-08-00292.pdf
View BVdb publication page



BACE1-Dependent Neuregulin-1 Signaling: An Implication for Schizophrenia.

Frontiers In Molecular Neuroscience
Zhang, Zhengrong Z; Huang, Jing J; Shen, Yong Y; Li, Rena R
Publication Date: 2017

Variant appearance in text: rs10503929
PubMed Link: 28993723
Variant Present in the following documents:
  • Main text
  • fnmol-10-00302.pdf
View BVdb publication page



Meta-analysis reveals associations between genetic variation in the 5' and 3' regions of Neuregulin-1 and schizophrenia.

Translational Psychiatry
Mostaid, M S MS; Mancuso, S G SG; Liu, C C; Sundram, S S; Pantelis, C C; Everall, I P IP; Bousman, C A CA
Publication Date: 2017-01-17

Variant appearance in text: rs10503929
PubMed Link: 28094814
Variant Present in the following documents:
  • Main text
View BVdb publication page



A Common Variant in SCN5A and the Risk of Ventricular Fibrillation Caused by First ST-Segment Elevation Myocardial Infarction.

Plos One
Jabbari, Reza R; Glinge, Charlotte C; Jabbari, Javad J; Risgaard, Bjarke B; Winkel, Bo Gregers BG; Terkelsen, Christian Juhl CJ; Tilsted, Hans-Henrik HH; Jensen, Lisette Okkels LO; Hougaard, Mikkel M; Haunsø, Stig S; Engstrøm, Thomas T; Albert, Christine M CM; Tfelt-Hansen, Jacob J
Publication Date: 2017

Variant appearance in text: rs10503929
PubMed Link: 28085969
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic Consideration of Schizotypal Traits: A Review.

Frontiers In Psychology
Walter, Emma E EE; Fernandez, Francesca F; Snelling, Mollie M; Barkus, Emma E
Publication Date: 2016

Variant appearance in text: rs10503929
PubMed Link: 27895608
Variant Present in the following documents:
  • Main text
  • fpsyg-07-01769.pdf
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Three-dimensional modelling identifies novel genetic dependencies associated with breast cancer progression in the isogenic MCF10 model.

The Journal Of Pathology
Maguire, Sarah L SL; Peck, Barrie B; Wai, Patty T PT; Campbell, James J; Barker, Holly H; Gulati, Aditi A; Daley, Frances F; Vyse, Simon S; Huang, Paul P; Lord, Christopher J CJ; Farnie, Gillian G; Brennan, Keith K; Natrajan, Rachael R
Publication Date: 2016-11

Variant appearance in text: NRG1: M289T; rs10503929
PubMed Link: 27512948
Variant Present in the following documents:
  • PATH-240-315-s015.xlsx, sheet 1
View BVdb publication page



Reproducible Analysis of Post-Translational Modifications in Proteomes--Application to Human Mutations.

Plos One
Holehouse, Alex S AS; Naegle, Kristen M KM
Publication Date: 2015

Variant appearance in text: rs10503929
PubMed Link: 26659599
Variant Present in the following documents:
  • pone.0144692.s002.xlsx, sheet 1
View BVdb publication page



Etiology of cardiovascular disease in patients with schizophrenia: current perspectives.

Neuropsychiatric Disease And Treatment
Emul, Murat M; Kalelioglu, Tevfik T
Publication Date: 2015

Variant appearance in text: rs10503929
PubMed Link: 26491327
Variant Present in the following documents:
  • Main text
View BVdb publication page



Hierarchical Classes Analysis (HICLAS): A novel data reduction method to examine associations between biallelic SNPs and perceptual organization phenotypes in schizophrenia.

Schizophrenia Research. Cognition
Joseph, Jamie J; Gara, Michael A MA; Silverstein, Steven M SM
Publication Date: 2015-06-01

Variant appearance in text: rs10503929
PubMed Link: 26346124
Variant Present in the following documents:
  • Main text
View BVdb publication page



Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALS.

Scientific Reports
Steinberg, Karyn Meltz KM; Yu, Bing B; Koboldt, Daniel C DC; Mardis, Elaine R ER; Pamphlett, Roger R
Publication Date: 2015-03-16

Variant appearance in text: rs10503929
PubMed Link: 25773295
Variant Present in the following documents:
  • srep09124-s3.xls, sheet 1
View BVdb publication page



Investigation of gene effects and epistatic interactions between Akt1 and neuregulin 1 in the regulation of behavioral phenotypes and social functions in genetic mouse models of schizophrenia.

Frontiers In Behavioral Neuroscience
Huang, Ching-Hsun CH; Pei, Ju-Chun JC; Luo, Da-Zhong DZ; Chen, Ching C; Chen, Yi-Wen YW; Lai, Wen-Sung WS
Publication Date: 2014

Variant appearance in text: rs10503929
PubMed Link: 25688191
Variant Present in the following documents:
  • Main text
  • fnbeh-08-00455.pdf
View BVdb publication page



Study of five novel non-synonymous polymorphisms in human brain-expressed genes in a Colombian sample.

Annals Of Neurosciences
Ojeda, Diego A DA; Forero, Diego A DA
Publication Date: 2014-10

Variant appearance in text: NRG1: Met289Thr; rs10503929
PubMed Link: 25452674
Variant Present in the following documents:
  • Main text
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: NRG1: M289T; rs10503929
PubMed Link: 25390934
Variant Present in the following documents:
  • pone.0112430.s004.xlsx, sheet 1
View BVdb publication page



Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium.

Human Genetics
Li, Qing Q; Wojciechowski, Robert R; Simpson, Claire L CL; Hysi, Pirro G PG; Verhoeven, Virginie J M VJ; Ikram, Mohammad Kamran MK; Höhn, René R; Vitart, Veronique V; Hewitt, Alex W AW; Oexle, Konrad K; Mäkelä, Kari-Matti KM; MacGregor, Stuart S; Pirastu, Mario M; Fan, Qiao Q; Cheng, Ching-Yu CY; St Pourcain, Beaté B; McMahon, George G; Kemp, John P JP; Northstone, Kate K; Rahi, Jugnoo S JS; Cumberland, Phillippa M PM; Martin, Nicholas G NG; Sanfilippo, Paul G PG; Lu, Yi Y; Wang, Ya Xing YX; Hayward, Caroline C; Polašek, Ozren O; Campbell, Harry H; Bencic, Goran G; Wright, Alan F AF; Wedenoja, Juho J; Zeller, Tanja T; Schillert, Arne A; Mirshahi, Alireza A; Lackner, Karl K; Yip, Shea Ping SP; Yap, Maurice K H MK; Ried, Janina S JS; Gieger, Christian C; Murgia, Federico F; Wilson, James F JF; Fleck, Brian B; Yazar, Seyhan S; Vingerling, Johannes R JR; Hofman, Albert A; Uitterlinden, André A; Rivadeneira, Fernando F; Amin, Najaf N; Karssen, Lennart L; Oostra, Ben A BA; Zhou, Xin X; Teo, Yik-Ying YY; Tai, E Shyong ES; Vithana, Eranga E; Barathi, Veluchamy V; Zheng, Yingfeng Y; Siantar, Rosalynn Grace RG; Neelam, Kumari K; Shin, Youchan Y; Lam, Janice J; Yonova-Doing, Ekaterina E; Venturini, Cristina C; Hosseini, S Mohsen SM; Wong, Hoi-Suen HS; Lehtimäki, Terho T; Kähönen, Mika M; Raitakari, Olli O; Timpson, Nicholas J NJ; Evans, David M DM; Khor, Chiea-Chuen CC; Aung, Tin T; Young, Terri L TL; Mitchell, Paul P; Klein, Barbara B; van Duijn, Cornelia M CM; Meitinger, Thomas T; Jonas, Jost B JB; Baird, Paul N PN; Mackey, David A DA; Wong, Tien Yin TY; Saw, Seang-Mei SM; Pärssinen, Olavi O; Stambolian, Dwight D; Hammond, Christopher J CJ; Klaver, Caroline C W CC; Williams, Cathy C; Paterson, Andrew D AD; Bailey-Wilson, Joan E JE; Guggenheim, Jeremy A JA; ,
Publication Date: 2015-02

Variant appearance in text: rs10503929
PubMed Link: 25367360
Variant Present in the following documents:
  • Main text
  • 439_2014_Article_1500.pdf
View BVdb publication page



Neuregulin-ERBB signaling in the nervous system and neuropsychiatric diseases.

Neuron
Mei, Lin L; Nave, Klaus-Armin KA
Publication Date: 2014-07-02

Variant appearance in text: rs10503929
PubMed Link: 24991953
Variant Present in the following documents:
  • Main text
View BVdb publication page



Cognitive outcome and gamma noise power unrelated to neuregulin 1 and 3 variation in schizophrenia.

Annals Of General Psychiatry
Díez, Alvaro A; Cieza-Borrella, Clara C; Suazo, Vanessa V; González-Sarmiento, Rogelio R; Papiol, Sergi S; Molina, Vicente V
Publication Date: 2014

Variant appearance in text: rs10503929
PubMed Link: 24976857
Variant Present in the following documents:
  • Main text
  • 1744-859X-13-18.pdf
View BVdb publication page



Analysis of schizophrenia-related genes and electrophysiological measures reveals ZNF804A association with amplitude of P300b elicited by novel sounds.

Translational Psychiatry
Del Re, E C EC; Bergen, S E SE; Mesholam-Gately, R I RI; Niznikiewicz, M A MA; Goldstein, J M JM; Woo, T U TU; Shenton, M E ME; Seidman, L J LJ; McCarley, R W RW; Petryshen, T L TL
Publication Date: 2014-01-14

Variant appearance in text: rs10503929
PubMed Link: 24424392
Variant Present in the following documents:
View BVdb publication page



A common missense variant in the neuregulin 1 gene is associated with both schizophrenia and sudden cardiac death.

Heart Rhythm
Huertas-Vazquez, Adriana A; Teodorescu, Carmen C; Reinier, Kyndaron K; Uy-Evanado, Audrey A; Chugh, Harpriya H; Jerger, Katherine K; Ayala, Jo J; Gunson, Karen K; Jui, Jonathan J; Newton-Cheh, Christopher C; Albert, Christine M CM; Chugh, Sumeet S SS
Publication Date: 2013-07

Variant appearance in text: rs10503929
PubMed Link: 23524320
Variant Present in the following documents:
  • Main text
View BVdb publication page



Prepulse inhibition of startle response: recent advances in human studies of psychiatric disease.

Clinical Psychopharmacology And Neuroscience : The Official Scientific Journal Of The Korean College Of Neuropsychopharmacology
Takahashi, Hidetoshi H; Hashimoto, Ryota R; Iwase, Masao M; Ishii, Ryouhei R; Kamio, Yoko Y; Takeda, Masatoshi M
Publication Date: 2011-12

Variant appearance in text: rs10503929
PubMed Link: 23429840
Variant Present in the following documents:
  • Main text
  • cpn-9-102.pdf
View BVdb publication page



Paradox of schizophrenia genetics: is a paradigm shift occurring?

Behavioral And Brain Functions : Bbf
Doi, Nagafumi N; Hoshi, Yoko Y; Itokawa, Masanari M; Yoshikawa, Takeo T; Ichikawa, Tomoe T; Arai, Makoto M; Usui, Chie C; Tachikawa, Hirokazu H
Publication Date: 2012-05-31

Variant appearance in text: rs10503929
PubMed Link: 22650965
Variant Present in the following documents:
  • Main text
  • 1744-9081-8-28.pdf
View BVdb publication page



Comprehensive analysis of NRG1 common and rare variants in Hirschsprung patients.

Plos One
Luzón-Toro, Berta B; Torroglosa, Ana A; Núñez-Torres, Rocío R; Enguix-Riego, María Valle MV; Fernández, Raquel María RM; de Agustín, Juan Carlos JC; Antiñolo, Guillermo G; Borrego, Salud S
Publication Date: 2012

Variant appearance in text: rs10503929
PubMed Link: 22574178
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic associations between neuregulin-1 SNPs and neurocognitive function in multigenerational, multiplex schizophrenia families.

Psychiatric Genetics
Yokley, Jessica L JL; Prasad, Konasale M KM; Chowdari, Kodavali V KV; Talkowski, Michael E ME; Wood, Joel J; Gur, Ruben C RC; Gur, Raquel E RE; Almasy, Laura L; Nimgaonkar, Vishwajit L VL; Pogue-Geile, Michael F MF
Publication Date: 2012-04

Variant appearance in text: rs10503929
PubMed Link: 22183611
Variant Present in the following documents:
  • Main text
View BVdb publication page



Biological validation of increased schizophrenia risk with NRG1, ERBB4, and AKT1 epistasis via functional neuroimaging in healthy controls.

Archives Of General Psychiatry
Nicodemus, Kristin K KK; Law, Amanda J AJ; Radulescu, Eugenia E; Luna, Augustin A; Kolachana, Bhaskar B; Vakkalanka, Radhakrishna R; Rujescu, Dan D; Giegling, Ina I; Straub, Richard E RE; McGee, Kate K; Gold, Bert B; Dean, Michael M; Muglia, Pierandrea P; Callicott, Joseph H JH; Tan, Hao-Yang HY; Weinberger, Daniel R DR
Publication Date: 2010-10

Variant appearance in text: rs10503929
PubMed Link: 20921115
Variant Present in the following documents:
  • Main text
View BVdb publication page



Neuregulin 1 in neural development, synaptic plasticity and schizophrenia.

Nature Reviews. Neuroscience
Mei, Lin L; Xiong, Wen-Cheng WC
Publication Date: 2008-06

Variant appearance in text: rs10503929
PubMed Link: 18478032
Variant Present in the following documents:
  • Main text
View BVdb publication page