Publications:

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Polymorphisms in COMT and OPRM1 Collectively Contribute to Chronic Shoulder Pain and Disability in South African Breast Cancer Survivors'.

Genes

Firfirey, Firzana F; Shamley, Delva D; September, Alison V AV

Publication Date: 2022-12-21

Variant appearance in text: rs740602

PubMed Link: 36672750

Variant Present in the following documents:

• Main text
• genes-14-00009.pdf

View BVdb publication page

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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: rs740602

PubMed Link: 35802478

Variant Present in the following documents:

• noac171_suppl_suplementary_table_s1.xlsx, sheet 1
• noac171_suppl_suplementary_table_s7.xlsx, sheet 1

View BVdb publication page

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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: rs740602

PubMed Link: 35242249

Variant Present in the following documents:

• Main text
• main.pdf

View BVdb publication page

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Decoding variants in drug-metabolizing enzymes and transporters in solid tumor patients by whole-exome sequencing.

Saudi Journal Of Biological Sciences

Aboul-Soud, Mourad A M MAM; Alzahrani, Alhussain J AJ; Mahmoud, Amer A

Publication Date: 2021-01

Variant appearance in text: rs740602

PubMed Link: 33424349

Variant Present in the following documents:

• mmc1.xlsx, sheet 1

View BVdb publication page

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A pan-cancer analysis of synonymous mutations.

Nature Communications

Sharma, Yogita Y; Miladi, Milad M; Dukare, Sandeep S; Boulay, Karine K; Caudron-Herger, Maiwen M; Groß, Matthias M; Backofen, Rolf R; Diederichs, Sven S

Publication Date: 2019-06-12

Variant appearance in text: COMT: 219G>A

PubMed Link: 31189880

Variant Present in the following documents:

• 41467_2019_10489_MOESM7_ESM.xlsx, sheet 1

View BVdb publication page

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Targeted next generation sequencing as a tool for precision medicine.

Bmc Medical Genomics

Gulilat, Markus M; Lamb, Tyler T; Teft, Wendy A WA; Wang, Jian J; Dron, Jacqueline S JS; Robinson, John F JF; Tirona, Rommel G RG; Hegele, Robert A RA; Kim, Richard B RB; Schwarz, Ute I UI

Publication Date: 2019-06-03

Variant appearance in text: rs740602

PubMed Link: 31159795

Variant Present in the following documents:

• 12920_2019_527_MOESM1_ESM.xlsx, sheet 6

View BVdb publication page

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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: rs740602

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

View BVdb publication page

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The Role of Genetic Polymorphisms in Chronic Pain Patients.

International Journal Of Molecular Sciences

Knezevic, Nebojsa Nick NN; Tverdohleb, Tatiana T; Knezevic, Ivana I; Candido, Kenneth D KD

Publication Date: 2018-06-08

Variant appearance in text: rs740602

PubMed Link: 29890676

Variant Present in the following documents:

• Main text
• ijms-19-01707.pdf

View BVdb publication page

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Deleterious coding variants in multi-case families with non-syndromic cleft lip and/or palate phenotypes.

Scientific Reports

Pengelly, Reuben J RJ; Arias, Liliana L; Martínez, Julio J; Upstill-Goddard, Rosanna R; Seaby, Eleanor G EG; Gibson, Jane J; Ennis, Sarah S; Collins, Andrew A; Briceño, Ignacio I

Publication Date: 2016-07-26

Variant appearance in text: COMT: Q73Q; rs740602

PubMed Link: 27456059

Variant Present in the following documents:

• srep30457-s2.xls, sheet 2
• srep30457-s2.xls, sheet 1

View BVdb publication page

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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: COMT: Q73Q; rs740602

PubMed Link: 25390934

Variant Present in the following documents:

• pone.0112430.s004.xlsx, sheet 1

View BVdb publication page

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A clinical tool for reducing central nervous system depression among neonates exposed to codeine through breast milk.

Plos One

Kelly, Lauren E LE; Chaudhry, Shahnaz A SA; Rieder, Michael J MJ; 't Jong, Geert G; Moretti, Myla E ME; Lausman, Andrea A; Ross, Colin C; Berger, Howard H; Carleton, Bruce B; Hayden, Michael R MR; Madadi, Parvaz P; Koren, Gideon G

Publication Date: 2013

Variant appearance in text: rs740602

PubMed Link: 23922910

Variant Present in the following documents:

• Main text
• pone.0070073.pdf

View BVdb publication page

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Low enzymatic activity haplotypes of the human catechol-O-methyltransferase gene: enrichment for marker SNPs.

Plos One

Nackley, Andrea G AG; Shabalina, Svetlana A SA; Lambert, Jason E JE; Conrad, Mathew S MS; Gibson, Dustin G DG; Spiridonov, Alexey N AN; Satterfield, Sarah K SK; Diatchenko, Luda L

Publication Date: 2009

Variant appearance in text: rs740602

PubMed Link: 19365560

Variant Present in the following documents:

• Main text
• pone.0005237.pdf

View BVdb publication page

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Panic disorder is associated with the serotonin transporter gene (SLC6A4) but not the promoter region (5-HTTLPR).

Molecular Psychiatry

Strug, L J LJ; Suresh, R R; Fyer, A J AJ; Talati, A A; Adams, P B PB; Li, W W; Hodge, S E SE; Gilliam, T C TC; Weissman, M M MM

Publication Date: 2010-02

Variant appearance in text: rs740602

PubMed Link: 18663369

Variant Present in the following documents:

• Main text

View BVdb publication page

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The complex global pattern of genetic variation and linkage disequilibrium at catechol-O-methyltransferase.

Molecular Psychiatry

Mukherjee, N N; Kidd, K K KK; Pakstis, A J AJ; Speed, W C WC; Li, H H; Tarnok, Z Z; Barta, C C; Kajuna, S L B SL; Kidd, J R JR

Publication Date: 2010-02

Variant appearance in text: rs740602

PubMed Link: 18574484

Variant Present in the following documents:

• Main text

View BVdb publication page

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