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: rs976881

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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Pharmacogenetics of Biological Agents Used in Inflammatory Bowel Disease: A Systematic Review.

Biomedicines

Lauro, Rita R; Mannino, Federica F; Irrera, Natasha N; Squadrito, Francesco F; Altavilla, Domenica D; Squadrito, Giovanni G; Pallio, Giovanni G; Bitto, Alessandra A

Publication Date: 2021-11-23

Variant appearance in text: rs976881

PubMed Link: 34944563

Variant Present in the following documents:

• Main text
• biomedicines-09-01748.pdf

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Pharmacogenetics of Biological Agents Used in Inflammatory Bowel Disease: A Systematic Review.

Biomedicines

Lauro, Rita R; Mannino, Federica F; Irrera, Natasha N; Squadrito, Francesco F; Altavilla, Domenica D; Squadrito, Giovanni G; Pallio, Giovanni G; Bitto, Alessandra A

Publication Date: 2021-11-23

Variant appearance in text: rs976881

PubMed Link: 34944563

Variant Present in the following documents:

• Main text
• biomedicines-09-01748.pdf

View BVdb publication page

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The Genetic Contribution to Drug Response in Spondyloarthritis: A Systematic Literature Review.

Frontiers In Genetics

Ortolan, Augusta A; Cozzi, Giacomo G; Lorenzin, Mariagrazia M; Galozzi, Paola P; Doria, Andrea A; Ramonda, Roberta R

Publication Date: 2021

Variant appearance in text: rs976881

PubMed Link: 34354741

Variant Present in the following documents:

• Main text
• fgene-12-703911.pdf

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TNFRSF1B Gene Variants and Related Soluble TNFR2 Levels Impact Resilience in Alzheimer's Disease.

Frontiers In Aging Neuroscience

Pillai, Jagan A JA; Bebek, Gurkan G; Khrestian, Maria M; Bena, James J; Bergmann, Cornelia C CC; Bush, William S WS; Leverenz, James B JB; Bekris, Lynn M LM

Publication Date: 2021

Variant appearance in text: rs976881

PubMed Link: 33716716

Variant Present in the following documents:

• Main text
• fnagi-13-638922.pdf

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Pre-Treatment Biomarkers of Anti-Tumour Necrosis Factor Therapy Response in Crohn's Disease-A Systematic Review and Gene Ontology Analysis.

Cells

Gole, Boris B; Potočnik, Uroš U

Publication Date: 2019-05-28

Variant appearance in text: rs976881

PubMed Link: 31141991

Variant Present in the following documents:

• Main text
• cells-08-00515.pdf

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Factors predicting the therapeutic response to infliximab during maintenance therapy in Japanese patients with Crohn's disease.

Plos One

Matsuoka, Katsuyoshi K; Hamada, Shunsuke S; Shimizu, Mikiko M; Nanki, Kosaku K; Mizuno, Shinta S; Kiyohara, Hiroki H; Arai, Mari M; Sugimoto, Shinya S; Iwao, Yasushi Y; Ogata, Haruhiko H; Hisamatsu, Tadakazu T; Naganuma, Makoto M; Kanai, Takanori T; Mochizuki, Mayumi M; Hashiguchi, Masayuki M

Publication Date: 2018

Variant appearance in text: rs976881

PubMed Link: 30286108

Variant Present in the following documents:

• Main text
• pone.0204632.pdf

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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: rs976881

PubMed Link: 27247849

Variant Present in the following documents:

• Main text
• BRB3-6-e00471.pdf

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A population-based case-control study of genetic variation in cytokine genes associated with risk of cervical and vulvar cancers.

Gynecologic Oncology

Hardikar, Sheetal S; Johnson, Lisa G LG; Malkki, Mari M; Petersdorf, Effie W EW; Galloway, Denise A DA; Schwartz, Stephen M SM; Madeleine, Margaret M MM

Publication Date: 2015-10

Variant appearance in text: rs976881

PubMed Link: 26241630

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic variation in TLR or NFkappaB pathways and the risk of breast cancer: a case-control study.

Bmc Cancer

Resler, Alexa J AJ; Malone, Kathleen E KE; Johnson, Lisa G LG; Malkki, Mari M; Petersdorf, Effie W EW; McKnight, Barbara B; Madeleine, Margaret M MM

Publication Date: 2013-05-01

Variant appearance in text: rs976881

PubMed Link: 23634849

Variant Present in the following documents:

View BVdb publication page

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P-selectin genotype is associated with the development of cancer cachexia.

Embo Molecular Medicine

Tan, Benjamin H L BH; Fladvad, Torill T; Braun, Theodore P TP; Vigano, Antonio A; Strasser, Florian F; Deans, D A Christopher DA; Skipworth, Richard J E RJ; Solheim, Tora S TS; Damaraju, Sambasivarao S; Ross, James A JA; Kaasa, Stein S; Marks, Daniel L DL; Baracos, Vickie E VE; Skorpen, Frank F; Fearon, Kenneth C H KC; ,

Publication Date: 2012-06

Variant appearance in text: rs976881

PubMed Link: 22473907

Variant Present in the following documents:

• Main text
• emmm0004-0462.pdf

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Molecular genetic studies of gene identification for osteoporosis: the 2009 update.

Endocrine Reviews

Xu, Xiang-Hong XH; Dong, Shan-Shan SS; Guo, Yan Y; Yang, Tie-Lin TL; Lei, Shu-Feng SF; Papasian, Christopher J CJ; Zhao, Ming M; Deng, Hong-Wen HW

Publication Date: 2010-08

Variant appearance in text: rs976881

PubMed Link: 20357209

Variant Present in the following documents:

• Main text

View BVdb publication page

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Multiple common variants for celiac disease influencing immune gene expression.

Nature Genetics

Dubois, Patrick C A PC; Trynka, Gosia G; Franke, Lude L; Hunt, Karen A KA; Romanos, Jihane J; Curtotti, Alessandra A; Zhernakova, Alexandra A; Heap, Graham A R GA; Adány, Róza R; Aromaa, Arpo A; Bardella, Maria Teresa MT; van den Berg, Leonard H LH; Bockett, Nicholas A NA; de la Concha, Emilio G EG; Dema, Bárbara B; Fehrmann, Rudolf S N RS; Fernández-Arquero, Miguel M; Fiatal, Szilvia S; Grandone, Elvira E; Green, Peter M PM; Groen, Harry J M HJ; Gwilliam, Rhian R; Houwen, Roderick H J RH; Hunt, Sarah E SE; Kaukinen, Katri K; Kelleher, Dermot D; Korponay-Szabo, Ilma I; Kurppa, Kalle K; MacMathuna, Padraic P; Mäki, Markku M; Mazzilli, Maria Cristina MC; McCann, Owen T OT; Mearin, M Luisa ML; Mein, Charles A CA; Mirza, Muddassar M MM; Mistry, Vanisha V; Mora, Barbara B; Morley, Katherine I KI; Mulder, Chris J CJ; Murray, Joseph A JA; Núñez, Concepción C; Oosterom, Elvira E; Ophoff, Roel A RA; Polanco, Isabel I; Peltonen, Leena L; Platteel, Mathieu M; Rybak, Anna A; Salomaa, Veikko V; Schweizer, Joachim J JJ; Sperandeo, Maria Pia MP; Tack, Greetje J GJ; Turner, Graham G; Veldink, Jan H JH; Verbeek, Wieke H M WH; Weersma, Rinse K RK; Wolters, Victorien M VM; Urcelay, Elena E; Cukrowska, Bozena B; Greco, Luigi L; Neuhausen, Susan L SL; McManus, Ross R; Barisani, Donatella D; Deloukas, Panos P; Barrett, Jeffrey C JC; Saavalainen, Paivi P; Wijmenga, Cisca C; van Heel, David A DA

Publication Date: 2010-04

Variant appearance in text: rs976881

PubMed Link: 20190752

Variant Present in the following documents:

• Main text
• ukmss-28740.pdf

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