COMT c.616-367C>A

Variant ID: 22-19955692-C-A

NM_000754.3(COMT):c.616-367C>A

This variant was identified in 57 publications

View GRCh38 version.




Publications:


Pharmacogenetic Analysis Enables Optimization of Pain Therapy: A Case Report of Ineffective Oxycodone Therapy.

Journal Of Personalized Medicine
Wiss, Florine M FM; Stäuble, Céline K CK; Meyer Zu Schwabedissen, Henriette E HE; Allemann, Samuel S SS; Lampert, Markus L ML
Publication Date: 2023-05-13

Variant appearance in text: rs9332377
PubMed Link: 37240999
Variant Present in the following documents:
  • jpm-13-00829.pdf
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A Missense Variant in COMT Associated with Hearing Loss among Young Adults: The National Longitudinal Study of Adolescent to Adult Health (Add Health).

Biomedicines
Li, Chuan-Ming CM; Chen, Le L; Chen, Guanjie G; Zhang, Jianhua J; Hoffman, Howard J HJ
Publication Date: 2022-10-31

Variant appearance in text: rs9332377
PubMed Link: 36359276
Variant Present in the following documents:
  • Main text
  • biomedicines-10-02756.pdf
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Sex hormone-related polymorphisms in endometriosis and migraine: A narrative review.

Women'S Health (London, England)
van der Vaart, Joy-Fleur JF; Merki-Feld, Gabriele Susanne GS
Publication Date: 2022

Variant appearance in text: rs9332377
PubMed Link: 35848345
Variant Present in the following documents:
  • Main text
  • 10.1177_17455057221111315.pdf
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Brain Radiotoxicity-Related 15CAcBRT Gene Expression Signature Predicts Survival Prognosis of Glioblastoma Patients.

Neuro-Oncology
Reyes-González, Jesús J; Barajas-Olmos, Francisco F; García-Ortiz, Humberto H; Magraner-Pardo, Lorena L; Pons, Tirso T; Moreno, Sergio S; Aguirre-Cruz, Lucinda L; Reyes-Abrahantes, Andy A; Martínez-Hernández, Angélica A; Contreras-Cubas, Cecilia C; Barrios-Payan, Jorge J; Ruiz-Garcia, Henry J HJ; Hernandez-Pando, Rogelio R; Quiñones-Hinojosa, Alfredo A; Orozco, Lorena L; Abrahantes-Pérez, María Del Carmen MDC
Publication Date: 2022-07-08

Variant appearance in text: rs9332377
PubMed Link: 35802478
Variant Present in the following documents:
  • Main text
  • noac171.pdf
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A Computational Data Mining Strategy to Identify the Common Genetic Markers of Temporomandibular Joint Disorders and Osteoarthritis.

Global Medical Genetics
Jayaseelan, Vijayashree Priyadharsini VP; Arumugam, Paramasivam P
Publication Date: 2022-06

Variant appearance in text: rs9332377
PubMed Link: 35707787
Variant Present in the following documents:
  • Main text
  • 10-1055-s-0042-1743571.pdf
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Genetic overlap between temporomandibular disorders and primary headaches: A systematic review.

The Japanese Dental Science Review
Cruz, Diogo D; Monteiro, Francisca F; Paço, Maria M; Vaz-Silva, Manuel M; Lemos, Carolina C; Alves-Ferreira, Miguel M; Pinho, Teresa T
Publication Date: 2022-11

Variant appearance in text: rs9332377
PubMed Link: 35242249
Variant Present in the following documents:
  • Main text
  • main.pdf
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Genetic diversity of 'Very Important Pharmacogenes' in two South-Asian populations.

Peerj
Bharti, Neeraj N; Banerjee, Ruma R; Achalere, Archana A; Kasibhatla, Sunitha Manjari SM; Joshi, Rajendra R
Publication Date: 2021

Variant appearance in text: rs9332377
PubMed Link: 34824904
Variant Present in the following documents:
  • Main text
  • peerj-09-12294.pdf
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Abstracts from the 53rd European Society of Human Genetics (ESHG) Conference: e-Posters.

European Journal Of Human Genetics : Ejhg
Publication Date: 2020-12

Variant appearance in text: rs9332377
PubMed Link: 33262486
Variant Present in the following documents:
  • Main text
  • 41431_2020_Article_741.pdf
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The Impact of Genetic Polymorphisms in Organic Cation Transporters on Renal Drug Disposition.

International Journal Of Molecular Sciences
Zazuli, Zulfan Z; Duin, Naut J C B NJCB; Jansen, Katja K; Vijverberg, Susanne J H SJH; Maitland-van der Zee, Anke H AH; Masereeuw, Rosalinde R
Publication Date: 2020-09-10

Variant appearance in text: rs9332377
PubMed Link: 32927790
Variant Present in the following documents:
  • Main text
  • ijms-21-06627.pdf
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Pharmacogenomics as a Tool to Limit Acute and Long-Term Adverse Effects of Chemotherapeutics: An Update in Pediatric Oncology.

Frontiers In Pharmacology
Bernsen, Emma C EC; Hagleitner, Melanie M MM; Kouwenberg, Theodorus W TW; Hanff, Lidwien M LM
Publication Date: 2020

Variant appearance in text: rs9332377
PubMed Link: 32848787
Variant Present in the following documents:
  • Main text
  • Table_1.pdf
  • fphar-11-01184.pdf
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Pharmacogenomics and Pharmacogenetics in Osteosarcoma: Translational Studies and Clinical Impact.

International Journal Of Molecular Sciences
Hattinger, Claudia Maria CM; Patrizio, Maria Pia MP; Luppi, Silvia S; Serra, Massimo M
Publication Date: 2020-06-30

Variant appearance in text: rs9332377
PubMed Link: 32629971
Variant Present in the following documents:
  • Main text
  • ijms-21-04659.pdf
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MTHFR and VDR Polymorphisms Improve the Prognostic Value of MYCN Status on Overall Survival in Neuroblastoma Patients.

International Journal Of Molecular Sciences
Olivera, Gladys G GG; Yáñez, Yania Y; Gargallo, Pablo P; Sendra, Luis L; Aliño, Salvador F SF; Segura, Vanessa V; Sanz, Miguel Ángel MÁ; Cañete, Adela A; Castel, Victoria V; Font De Mora, Jaime J; Hervás, David D; Berlanga, Pablo P; Herrero, María José MJ
Publication Date: 2020-04-14

Variant appearance in text: rs9332377
PubMed Link: 32295184
Variant Present in the following documents:
  • Main text
View BVdb publication page



Influence of Genetic Variation in COMT on Cisplatin-Induced Nephrotoxicity in Cancer Patients.

Genes
Agema, Bram C BC; Koolen, Stijn L W SLW; With, Mirjam de M; Doorn, Nadia van NV; Heersche, Niels N; Hoop, Esther Oomen-de EO; Visser, Sabine S; Aerts, Joachim G J V JGJV; Bins, Sander S; Schaik, Ron H N van RHNV; Mathijssen, Ron H J RHJ
Publication Date: 2020-03-27

Variant appearance in text: rs9332377
PubMed Link: 32230800
Variant Present in the following documents:
  • Main text
  • genes-11-00358.pdf
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Genetic Influence on Efficacy of Pharmacotherapy for Pediatric Attention-Deficit/Hyperactivity Disorder: Overview and Current Status of Research.

Cns Drugs
Elsayed, Nada A NA; Yamamoto, Kaila M KM; Froehlich, Tanya E TE
Publication Date: 2020-04

Variant appearance in text: rs9332377
PubMed Link: 32133580
Variant Present in the following documents:
  • Main text
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Genetic variants and cognitive functions in patients with brain tumors.

Neuro-Oncology
Correa, Denise D DD; Satagopan, Jaya J; Martin, Axel A; Braun, Erica E; Kryza-Lacombe, Maria M; Cheung, Kenneth K; Sharma, Ajay A; Dimitriadoy, Sofia S; O'Connell, Kelli K; Leong, Siok S; Karimi, Sasan S; Lyo, John J; DeAngelis, Lisa M LM; Orlow, Irene I
Publication Date: 2019-10-09

Variant appearance in text: rs9332377
PubMed Link: 31123752
Variant Present in the following documents:
  • Main text
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Mechanisms of Cisplatin-Induced Ototoxicity and Prevention.

Seminars In Hearing
Rybak, Leonard P LP; Mukherjea, Debashree D; Ramkumar, Vickram V
Publication Date: 2019-05

Variant appearance in text: rs9332377
PubMed Link: 31036996
Variant Present in the following documents:
  • Main text
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Genetic Variants as Predictive Markers for Ototoxicity and Nephrotoxicity in Patients with Locally Advanced Head and Neck Cancer Treated with Cisplatin-Containing Chemoradiotherapy (The PRONE Study).

Cancers
Driessen, Chantal M CM; Ham, Janneke C JC; Te Loo, Maroeska M; van Meerten, Esther E; van Lamoen, Maurits M; Hakobjan, Marina H MH; Takes, Robert P RP; van der Graaf, Winette T WT; Kaanders, Johannes H JH; Coenen, Marieke J H MJH; van Herpen, Carla M CM
Publication Date: 2019-04-17

Variant appearance in text: rs9332377
PubMed Link: 30999660
Variant Present in the following documents:
  • Main text
  • cancers-11-00551.pdf
View BVdb publication page



The genetic vulnerability to cisplatin ototoxicity: a systematic review.

Scientific Reports
Tserga, Evangelia E; Nandwani, Tara T; Edvall, Niklas K NK; Bulla, Jan J; Patel, Poulam P; Canlon, Barbara B; Cederroth, Christopher R CR; Baguley, David M DM
Publication Date: 2019-03-05

Variant appearance in text: rs9332377
PubMed Link: 30837596
Variant Present in the following documents:
  • Main text
  • 41598_2019_Article_40138.pdf
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Analytical Validation of Variants to Aid in Genotype-Guided Therapy for Oncology.

The Journal Of Molecular Diagnostics : Jmd
Swart, Marelize M; Stansberry, Wesley M WM; Pratt, Victoria M VM; Medeiros, Elizabeth B EB; Kiel, Patrick J PJ; Shen, Fei F; Schneider, Bryan P BP; Skaar, Todd C TC
Publication Date: 2019-05

Variant appearance in text: COMT: 616-367C>A; rs9332377
PubMed Link: 30794985
Variant Present in the following documents:
  • Main text
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Genetic and Modifiable Risk Factors Contributing to Cisplatin-induced Toxicities.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Trendowski, Matthew R MR; El Charif, Omar O; Dinh, Paul C PC; Travis, Lois B LB; Dolan, M Eileen ME
Publication Date: 2019-02-15

Variant appearance in text: rs9332377
PubMed Link: 30305294
Variant Present in the following documents:
  • Main text
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Whole genome sequencing identifies high-impact variants in well-known pharmacogenomic genes.

The Pharmacogenomics Journal
Choi, Jihoon J; Tantisira, Kelan G KG; Duan, Qing Ling QL
Publication Date: 2019-04

Variant appearance in text: rs9332377
PubMed Link: 30214008
Variant Present in the following documents:
  • NIHMS1503453-supplement-3.xlsx, sheet 1
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The Impact of COMT and Childhood Maltreatment on Suicidal Behaviour in Affective Disorders.

Scientific Reports
Bernegger, Alexandra A; Kienesberger, Klemens K; Carlberg, Laura L; Swoboda, Patrick P; Ludwig, Birgit B; Koller, Romina R; Inaner, Michelle M; Zotter, Melanie M; Kapusta, Nestor N; Aigner, Martin M; Haslacher, Helmuth H; Kasper, Siegfried S; Schosser, Alexandra A
Publication Date: 2018-01-12

Variant appearance in text: rs9332377
PubMed Link: 29330410
Variant Present in the following documents:
  • Main text
  • 41598_2017_Article_19040.pdf
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Attempts to replicate genetic associations with schizophrenia in a cohort from north India.

Npj Schizophrenia
Prasad, Suman S; Bhatia, Triptish T; Kukshal, Prachi P; Nimgaonkar, Vishwajit L VL; Deshpande, Smita N SN; Thelma, B K BK
Publication Date: 2017-08-30

Variant appearance in text: rs9332377
PubMed Link: 28855605
Variant Present in the following documents:
  • Main text
  • 41537_2017_Article_30.pdf
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Pharmacogenetic analysis of irreversible severe cisplatin-induced nephropathy: a case report of a 27-year-old woman.

British Journal Of Clinical Pharmacology
de Jong, Corine C; Sanders, Stefan S; Creemers, Geert-Jan GJ; Burylo, Artur M AM; Taks, Margot M; Schellens, Jan H M JHM; Deenen, Maarten J MJ
Publication Date: 2017-09

Variant appearance in text: rs9332377
PubMed Link: 28560854
Variant Present in the following documents:
  • Main text
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TPMT, COMT and ACYP2 genetic variants in paediatric cancer patients with cisplatin-induced ototoxicity.

Pharmacogenetics And Genomics
Thiesen, Signe S; Yin, Peng P; Jorgensen, Andrea L AL; Zhang, Jieying Eunice JE; Manzo, Valentina V; McEvoy, Laurence L; Barton, Christopher C; Picton, Susan S; Bailey, Simon S; Brock, Penelope P; Vyas, Harish H; Walker, David D; Makin, Guy G; Bandi, Srinivas S; Pizer, Barry B; Hawcutt, Daniel B DB; Pirmohamed, Munir M
Publication Date: 2017-06

Variant appearance in text: rs9332377
PubMed Link: 28445188
Variant Present in the following documents:
  • Main text
View BVdb publication page



Associations Between Neurotransmitter Genes and Fatigue and Energy Levels in Women After Breast Cancer Surgery.

Journal Of Pain And Symptom Management
Eshragh, Jasmine J; Dhruva, Anand A; Paul, Steven M SM; Cooper, Bruce A BA; Mastick, Judy J; Hamolsky, Deborah D; Levine, Jon D JD; Miaskowski, Christine C; Kober, Kord M KM
Publication Date: 2017-01

Variant appearance in text: rs9332377
PubMed Link: 27720787
Variant Present in the following documents:
  • Main text
View BVdb publication page



Attention-deficit hyperactivity disorder in adults: A systematic review and meta-analysis of genetic, pharmacogenetic and biochemical studies.

Molecular Psychiatry
Bonvicini, C C; Faraone, S V SV; Scassellati, C C
Publication Date: 2016-07

Variant appearance in text: rs9332377
PubMed Link: 27217152
Variant Present in the following documents:
  • Main text
  • mp201674a.pdf
View BVdb publication page



COMT, BDNF, and DTNBP1 polymorphisms and cognitive functions in patients with brain tumors.

Neuro-Oncology
Correa, Denise D DD; Satagopan, Jaya J; Cheung, Kenneth K; Arora, Arshi K AK; Kryza-Lacombe, Maria M; Xu, Youming Y; Karimi, Sasan S; Lyo, John J; DeAngelis, Lisa M LM; Orlow, Irene I
Publication Date: 2016-10

Variant appearance in text: rs9332377
PubMed Link: 27091610
Variant Present in the following documents:
  • Main text
View BVdb publication page



Variations in opioid receptor genes in neonatal abstinence syndrome.

Drug And Alcohol Dependence
Wachman, Elisha M EM; Hayes, Marie J MJ; Sherva, Richard R; Brown, Mark S MS; Davis, Jonathan M JM; Farrer, Lindsay A LA; Nielsen, David A DA
Publication Date: 2015-10-01

Variant appearance in text: rs9332377
PubMed Link: 26233486
Variant Present in the following documents:
  • Main text
View BVdb publication page



Look beyond Catechol-O-Methyltransferase genotype for cathecolamines derangement in migraine: the BioBIM rs4818 and rs4680 polymorphisms study.

The Journal Of Headache And Pain
De Marchis, Maria Laura ML; Barbanti, Piero P; Palmirotta, Raffaele R; Egeo, Gabriella G; Aurilia, Cinzia C; Fofi, Luisa L; Piroso, Serena S; Ialongo, Cristiano C; Della-Morte, David D; D'Andrea, Giovanni G; Ferroni, Patrizia P; Guadagni, Fiorella F
Publication Date: 2015

Variant appearance in text: rs9332377
PubMed Link: 25929431
Variant Present in the following documents:
  • Main text
View BVdb publication page



Pharmacogenomics--how close/far are we to practising individualized medicine for children?

British Journal Of Clinical Pharmacology
Sing, Chor-Wing CW; Cheung, Ching-Lung CL; Wong, Ian C K IC
Publication Date: 2015-03

Variant appearance in text: rs9332377
PubMed Link: 25855823
Variant Present in the following documents:
  • Main text
View BVdb publication page



Human OCT2 variant c.808G>T confers protection effect against cisplatin-induced ototoxicity.

Pharmacogenomics
Lanvers-Kaminsky, Claudia C; Sprowl, Jason A JA; Malath, Ingrid I; Deuster, Dirk D; Eveslage, Maria M; Schlatter, Eberhard E; Mathijssen, Ron Hj RH; Boos, Joachim J; Jürgens, Heribert H; Am Zehnhoff-Dinnesen, Antionette G AG; Sparreboom, Alex A; Ciarimboli, Giuliano G
Publication Date: 2015

Variant appearance in text: rs9332377
PubMed Link: 25823781
Variant Present in the following documents:
  • Main text
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COMT and MAO-A polymorphisms and obsessive-compulsive disorder: a family-based association study.

Plos One
Sampaio, Aline Santos AS; Hounie, Ana Gabriela AG; Petribú, Kátia K; Cappi, Carolina C; Morais, Ivanil I; Vallada, Homero H; do Rosário, Maria Conceição MC; Stewart, S Evelyn SE; Fargeness, Jesen J; Mathews, Carol C; Arnold, Paul P; Hanna, Gregory L GL; Richter, Margaret M; Kennedy, James J; Fontenelle, Leonardo L; de Bragança Pereira, Carlos Alberto CA; Pauls, David L DL; Miguel, Eurípedes Constantino EC
Publication Date: 2015

Variant appearance in text: rs9332377
PubMed Link: 25793616
Variant Present in the following documents:
  • Main text
View BVdb publication page



Influence of genetic variants in TPMT and COMT associated with cisplatin induced hearing loss in patients with cancer: two new cohorts and a meta-analysis reveal significant heterogeneity between cohorts.

Plos One
Hagleitner, Melanie M MM; Coenen, Marieke J H MJ; Patino-Garcia, Ana A; de Bont, Eveline S J M ES; Gonzalez-Neira, Anna A; Vos, Hanneke I HI; van Leeuwen, Frank N FN; Gelderblom, Hans H; Hoogerbrugge, Peter M PM; Guchelaar, Henk-Jan HJ; Te Loo, Maroeska W M MW
Publication Date: 2014

Variant appearance in text: rs9332377
PubMed Link: 25551397
Variant Present in the following documents:
  • Main text
  • pone.0115869.pdf
View BVdb publication page



Can pharmacogenetics explain efficacy and safety of cisplatin pharmacotherapy?

Frontiers In Genetics
Roco, Angela A; Cayún, Juan J; Contreras, Stephania S; Stojanova, Jana J; Quiñones, Luis L
Publication Date: 2014

Variant appearance in text: rs9332377
PubMed Link: 25452763
Variant Present in the following documents:
  • Main text
  • fgene-05-00391.pdf
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Screening for 392 polymorphisms in 141 pharmacogenes.

Biomedical Reports
Kim, Jason Yongha JY; Cheong, Hyun Sub HS; Park, Tae-Joon TJ; Shin, Hee Jung HJ; Seo, Doo Won DW; Na, Han Sung HS; Chung, Myeon Woo MW; Shin, Hyoung Doo HD
Publication Date: 2014-07

Variant appearance in text: rs9332377
PubMed Link: 24944790
Variant Present in the following documents:
  • Main text
View BVdb publication page



Pharmacogenomics and adverse drug reactions in children.

Frontiers In Genetics
Rieder, Michael J MJ; Carleton, Bruce B
Publication Date: 2014

Variant appearance in text: rs9332377
PubMed Link: 24795743
Variant Present in the following documents:
  • Main text
  • fgene-05-00078.pdf
View BVdb publication page



Effect of catechol-o-methyltransferase-gene (COMT) variants on experimental and acute postoperative pain in 1,000 women undergoing surgery for breast cancer.

Anesthesiology
Kambur, Oleg O; Kaunisto, Mari A MA; Tikkanen, Emmi E; Leal, Suzanne M SM; Ripatti, Samuli S; Kalso, Eija A EA
Publication Date: 2013-12

Variant appearance in text: rs9332377
PubMed Link: 24343288
Variant Present in the following documents:
  • Main text
View BVdb publication page



Dopaminergic gene polymorphisms and cognitive function in a north Indian schizophrenia cohort.

Journal Of Psychiatric Research
Kukshal, Prachi P; Kodavali, Venkat Chowdari VC; Srivastava, Vibhuti V; Wood, Joel J; McClain, Lora L; Bhatia, Triptish T; Bhagwat, A M AM; Deshpande, Smita Neelkanth SN; Nimgaonkar, Vishwajit Laxmikant VL; Thelma, B K BK
Publication Date: 2013-11

Variant appearance in text: rs9332377
PubMed Link: 23932573
Variant Present in the following documents:
  • Main text
View BVdb publication page



No association between germline variation in catechol-O-methyltransferase and colorectal cancer survival in postmenopausal women.

Menopause (New York, N.Y.)
Passarelli, Michael N MN; Newcomb, Polly A PA; Makar, Karen W KW; Burnett-Hartman, Andrea N AN; Phipps, Amanda I AI; David, Sean P SP; Hsu, Li L; Harrison, Tabitha A TA; Hutter, Carolyn M CM; Duggan, David J DJ; White, Emily E; Chan, Andrew T AT; Peters, Ulrike U
Publication Date: 2014-04

Variant appearance in text: rs9332377
PubMed Link: 23880798
Variant Present in the following documents:
  • Main text
View BVdb publication page



The role of inherited TPMT and COMT genetic variation in cisplatin-induced ototoxicity in children with cancer.

Clinical Pharmacology And Therapeutics
Yang, J J JJ; Lim, J Y S JY; Huang, J J; Bass, J J; Wu, J J; Wang, C C; Fang, J J; Stewart, E E; Harstead, E H EH; E, S S; Robinson, G W GW; Evans, W E WE; Pappo, A A; Zuo, J J; Relling, M V MV; Onar-Thomas, A A; Gajjar, A A; Stewart, C F CF
Publication Date: 2013-08

Variant appearance in text: rs9332377
PubMed Link: 23820299
Variant Present in the following documents:
  • Main text
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A genome-wide integrative study of microRNAs in human liver.

Bmc Genomics
Gamazon, Eric R ER; Innocenti, Federico F; Wei, Rongrong R; Wang, Libo L; Zhang, Min M; Mirkov, Snezana S; Ramírez, Jacqueline J; Huang, R Stephanie RS; Cox, Nancy J NJ; Ratain, Mark J MJ; Liu, Wanqing W
Publication Date: 2013-06-13

Variant appearance in text: rs9332377
PubMed Link: 23758991
Variant Present in the following documents:
  • Main text
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Perspective: Identification of genetic variants associated with dopaminergic compensatory mechanisms in early Parkinson's disease.

Frontiers In Neuroscience
Greenbaum, Lior L; Lorberboym, Mordechai M; Melamed, Eldad E; Rigbi, Amihai A; Barhum, Yael Y; Kohn, Yoav Y; Khlebtovsky, Alexander A; Lerer, Bernard B; Djaldetti, Ruth R
Publication Date: 2013

Variant appearance in text: rs9332377
PubMed Link: 23596382
Variant Present in the following documents:
  • Main text
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Replication of TPMT and ABCC3 genetic variants highly associated with cisplatin-induced hearing loss in children.

Clinical Pharmacology And Therapeutics
Pussegoda, K K; Ross, C J CJ; Visscher, H H; Yazdanpanah, M M; Brooks, B B; Rassekh, S R SR; Zada, Y F YF; Dubé, M-P MP; Carleton, B C BC; Hayden, M R MR; ,
Publication Date: 2013-08

Variant appearance in text: rs9332377
PubMed Link: 23588304
Variant Present in the following documents:
  • Main text
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Higher frequency of genetic variants conferring increased risk for ADRs for commonly used drugs treating cancer, AIDS and tuberculosis in persons of African descent.

The Pharmacogenomics Journal
Aminkeng, F F; Ross, C J D CJ; Rassekh, S R SR; Brunham, L R LR; Sistonen, J J; Dube, M-P MP; Ibrahim, M M; Nyambo, T B TB; Omar, S A SA; Froment, A A; Bodo, J-M JM; Tishkoff, S S; Carleton, B C BC; Hayden, M R MR; ,
Publication Date: 2014-04

Variant appearance in text: rs9332377
PubMed Link: 23588107
Variant Present in the following documents:
  • Main text
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Chemotherapy refractory testicular germ cell tumor is associated with a variant in Armadillo Repeat gene deleted in Velco-Cardio-Facial syndrome (ARVCF).

Frontiers In Endocrinology
Fung, Chunkit C; Vaughn, David J DJ; Mitra, Nandita N; Ciosek, Stephanie L SL; Vardhanabhuti, Saran S; Nathanson, Katherine L KL; Kanetsky, Peter A PA
Publication Date: 2012

Variant appearance in text: rs9332377
PubMed Link: 23248619
Variant Present in the following documents:
  • Main text
  • fendo-03-00163.pdf
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Using germline genomics to individualize pediatric cancer treatments.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Pinto, Navin N; Cohn, Susan L SL; Dolan, M Eileen ME
Publication Date: 2012-05-15

Variant appearance in text: rs9332377
PubMed Link: 22589487
Variant Present in the following documents:
  • Main text
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Platinum-induced ototoxicity in children: a consensus review on mechanisms, predisposition, and protection, including a new International Society of Pediatric Oncology Boston ototoxicity scale.

Journal Of Clinical Oncology : Official Journal Of The American Society Of Clinical Oncology
Brock, Penelope R PR; Knight, Kristin R KR; Freyer, David R DR; Campbell, Kathleen C M KC; Steyger, Peter S PS; Blakley, Brian W BW; Rassekh, Shahrad R SR; Chang, Kay W KW; Fligor, Brian J BJ; Rajput, Kaukab K; Sullivan, Michael M; Neuwelt, Edward A EA
Publication Date: 2012-07-01

Variant appearance in text: rs9332377
PubMed Link: 22547603
Variant Present in the following documents:
  • Main text
View BVdb publication page