Publications:

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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: rs5993882

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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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: rs5993882

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

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Prediction of opioid dose in cancer pain patients using genetic profiling: not yet an option with support vector machine learning.

Bmc Research Notes

Olesen, Anne Estrup AE; Grønlund, Debbie D; Gram, Mikkel M; Skorpen, Frank F; Drewes, Asbjørn Mohr AM; Klepstad, Pål P

Publication Date: 2018-01-27

Variant appearance in text: rs5993882

PubMed Link: 29374492

Variant Present in the following documents:

• Main text
• 13104_2018_Article_3194.pdf

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Neurocognitive Functioning of Children Treated for High-Risk B-Acute Lymphoblastic Leukemia Randomly Assigned to Different Methotrexate and Corticosteroid Treatment Strategies: A Report From the Children's Oncology Group.

Journal Of Clinical Oncology : Official Journal Of The American Society Of Clinical Oncology

Hardy, Kristina K KK; Embry, Leanne L; Kairalla, John A JA; Helian, Shanjun S; Devidas, Meenakshi M; Armstrong, Daniel D; Hunger, Stephen S; Carroll, William L WL; Larsen, Eric E; Raetz, Elizabeth A EA; Loh, Mignon L ML; Yang, Wenjian W; Relling, Mary V MV; Noll, Robert B RB; Winick, Naomi N

Publication Date: 2017-08-10

Variant appearance in text: rs5993882

PubMed Link: 28671857

Variant Present in the following documents:

• Main text

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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: rs5993882

PubMed Link: 28089639

Variant Present in the following documents:

• Main text

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Genetic variation and cognitive dysfunction in opioid-treated patients with cancer.

Brain And Behavior

Kurita, Geana Paula GP; Ekholm, Ola O; Kaasa, Stein S; Klepstad, Pål P; Skorpen, Frank F; Sjøgren, Per P

Publication Date: 2016-07

Variant appearance in text: rs5993882

PubMed Link: 27247849

Variant Present in the following documents:

• Main text
• BRB3-6-e00471.pdf

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Interaction between COMT rs5993883 and second generation antipsychotics is linked to decreases in verbal cognition and cognitive control in bipolar disorder.

Bmc Psychology

Flowers, Stephanie A SA; Ryan, Kelly A KA; Lai, Zongshan Z; McInnis, Melvin G MG; Ellingrod, Vicki L VL

Publication Date: 2016-04-02

Variant appearance in text: rs5993882

PubMed Link: 27039372

Variant Present in the following documents:

• Main text
• 40359_2016_Article_118.pdf

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Clinical and genetic factors related to cancer-induced bone pain and bone pain relief.

The Oncologist

Scarpi, Emanuela E; Calistri, Daniele D; Klepstad, Pål P; Kaasa, Stein S; Skorpen, Frank F; Habberstad, Ragnhild R; Nanni, Oriana O; Amadori, Dino D; Maltoni, Marco M

Publication Date: 2014-12

Variant appearance in text: rs5993882

PubMed Link: 25342315

Variant Present in the following documents:

• Main text

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Association of COMT and COMT-DRD2 interaction with creative potential.

Frontiers In Human Neuroscience

Zhang, Shun S; Zhang, Muzi M; Zhang, Jinghuan J

Publication Date: 2014

Variant appearance in text: rs5993882

PubMed Link: 24782743

Variant Present in the following documents:

• Main text
• fnhum-08-00216.pdf

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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: rs5993882

PubMed Link: 24343288

Variant Present in the following documents:

• Main text

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Polymorphisms of genes in neurotransmitter systems were associated with alcohol use disorders in a Tibetan population.

Plos One

Xu, Yan Y; Guo, Wan-Jun WJ; Wang, Qiang Q; Lanzi, Gongga G; Luobu, Ouzhu O; Ma, Xiao-Hong XH; Wang, Ying-Cheng YC; Zhen, Puo P; Deng, Wei W; Liu, Xiang X; Zhuoma, Basang B; Liu, Xie-He XH; Li, Tao T; Hu, Xun X

Publication Date: 2013

Variant appearance in text: rs5993882

PubMed Link: 24312204

Variant Present in the following documents:

• Main text
• pone.0080206.pdf

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Genome-wide association study meta-analysis of chronic widespread pain: evidence for involvement of the 5p15.2 region.

Annals Of The Rheumatic Diseases

Peters, Marjolein J MJ; Broer, Linda L; Willemen, Hanneke L D M HL; Eiriksdottir, Gudny G; Hocking, Lynne J LJ; Holliday, Kate L KL; Horan, Michael A MA; Meulenbelt, Ingrid I; Neogi, Tuhina T; Popham, Maria M; Schmidt, Carsten O CO; Soni, Anushka A; Valdes, Ana M AM; Amin, Najaf N; Dennison, Elaine M EM; Eijkelkamp, Niels N; Harris, Tamara B TB; Hart, Deborah J DJ; Hofman, Albert A; Huygen, Frank J P M FJ; Jameson, Karen A KA; Jones, Gareth T GT; Launer, Lenore J LJ; Kerkhof, Hanneke J M HJ; de Kruijf, Marjolein M; McBeth, John J; Kloppenburg, Margreet M; Ollier, William E WE; Oostra, Ben B; Payton, Antony A; Rivadeneira, Fernando F; Smith, Blair H BH; Smith, Albert V AV; Stolk, Lisette L; Teumer, Alexander A; Thomson, Wendy W; Uitterlinden, André G AG; Wang, Ke K; van Wingerden, Sophie H SH; Arden, Nigel K NK; Cooper, Cyrus C; Felson, David D; Gudnason, Vilmundur V; Macfarlane, Gary J GJ; Pendleton, Neil N; Slagboom, P Eline PE; Spector, Tim D TD; Völzke, Henry H; Kavelaars, Annemieke A; van Duijn, Cornelia M CM; Williams, Frances M K FM; van Meurs, Joyce B J JB

Publication Date: 2013-03

Variant appearance in text: rs5993882

PubMed Link: 22956598

Variant Present in the following documents:

• annrheumdis-2012-201742-s1.pdf

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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: rs5993882

PubMed Link: 21918603

Variant Present in the following documents:

• Main text
• aabc-1-13.pdf

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Localizing putative markers in genetic association studies by incorporating linkage disequilibrium into bayesian hierarchical models.

Human Heredity

Fridley, Brooke L BL; Jenkins, Gregory D GD

Publication Date: 2010

Variant appearance in text: rs5993882

PubMed Link: 20551675

Variant Present in the following documents:

• Main text

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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: rs5993882

PubMed Link: 19772600

Variant Present in the following documents:

• Main text

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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: rs5993882

PubMed Link: 18574484

Variant Present in the following documents:

• Main text

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Genetic predictors for acute experimental cold and heat pain sensitivity in humans.

Journal Of Medical Genetics

Kim, H H; Mittal, D P DP; Iadarola, M J MJ; Dionne, R A RA

Publication Date: 2006-08

Variant appearance in text: rs5993882

PubMed Link: 16882734

Variant Present in the following documents:

• Main text

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Genetic polymorphisms in monoamine neurotransmitter systems show only weak association with acute post-surgical pain in humans.

Molecular Pain

Kim, Hyungsuk H; Lee, Hyewon H; Rowan, Janet J; Brahim, Jaime J; Dionne, Raymond A RA

Publication Date: 2006-07-18

Variant appearance in text: rs5993882

PubMed Link: 16848906

Variant Present in the following documents:

• Main text
• 1744-8069-2-24.pdf

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