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: rs759162

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

View BVdb publication page

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Stemness underpinning all steps of human colorectal cancer defines the core of effective therapeutic strategies.

Ebiomedicine

Visioli, Alberto A; Giani, Fabrizio F; Trivieri, Nadia N; Pracella, Riccardo R; Miccinilli, Elide E; Cariglia, Maria Grazia MG; Palumbo, Orazio O; Arleo, Andrea A; Dezi, Fabio F; Copetti, Massimiliano M; Cajola, Laura L; Restelli, Silvia S; Papa, Valerio V; Sciuto, Antonio A; Latiano, Tiziana Pia TP; Carella, Massimo M; Amadori, Dino D; Gallerani, Giulia G; Ricci, Riccardo R; Alfieri, Sergio S; Pesole, Graziano G; Vescovi, Angelo L AL; Binda, Elena E

Publication Date: 2019-06

Variant appearance in text: EGFR: 1498+142C>T

PubMed Link: 31056474

Variant Present in the following documents:

• mmc1.xls, sheet 1

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Genetic Evidence Supporting the Role of the Calcium Channel, CACNA1S, in Tooth Cusp and Root Patterning.

Frontiers In Physiology

Laugel-Haushalter, Virginie V; Morkmued, Supawich S; Stoetzel, Corinne C; Geoffroy, Véronique V; Muller, Jean J; Boland, Anne A; Deleuze, Jean-François JF; Chennen, Kirsley K; Pitiphat, Waranuch W; Dollfus, Hélène H; Niederreither, Karen K; Bloch-Zupan, Agnès A; Pungchanchaikul, Patimaporn P

Publication Date: 2018

Variant appearance in text: EGFR: 1498+142C>T; rs759162

PubMed Link: 30319441

Variant Present in the following documents:

• Table_7.xlsx, sheet 1
• Table_5.xlsx, sheet 1
• Table_6.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: rs759162

PubMed Link: 30214008

Variant Present in the following documents:

• NIHMS1503453-supplement-3.xlsx, sheet 1

View BVdb publication page

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Shared genetic risk between corticobasal degeneration, progressive supranuclear palsy, and frontotemporal dementia.

Acta Neuropathologica

Yokoyama, Jennifer S JS; Karch, Celeste M CM; Fan, Chun C CC; Bonham, Luke W LW; Kouri, Naomi N; Ross, Owen A OA; Rademakers, Rosa R; Kim, Jungsu J; Wang, Yunpeng Y; Höglinger, Günter U GU; Müller, Ulrich U; Ferrari, Raffaele R; Hardy, John J; , ; Momeni, Parastoo P; Sugrue, Leo P LP; Hess, Christopher P CP; James Barkovich, A A; Boxer, Adam L AL; Seeley, William W WW; Rabinovici, Gil D GD; Rosen, Howard J HJ; Miller, Bruce L BL; Schmansky, Nicholas J NJ; Fischl, Bruce B; Hyman, Bradley T BT; Dickson, Dennis W DW; Schellenberg, Gerard D GD; Andreassen, Ole A OA; Dale, Anders M AM; Desikan, Rahul S RS

Publication Date: 2017-05

Variant appearance in text: rs759162

PubMed Link: 28271184

Variant Present in the following documents:

• Main text

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Genetic variability in EGFR, Src and HER2 and risk of colorectal adenoma and cancer.

International Journal Of Molecular Epidemiology And Genetics

Poole, Elizabeth M EM; Curtin, Karen K; Hsu, Li L; Kulmacz, Richard J RJ; Duggan, David J DJ; Makar, Karen W KW; Xiao, Liren L; Carlson, Christopher S CS; Slattery, Martha L ML; Caan, Bette J BJ; Potter, John D JD; Ulrich, Cornelia M CM

Publication Date: 2011

Variant appearance in text: rs759162

PubMed Link: 22199994

Variant Present in the following documents:

• Main text

View BVdb publication page

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