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: rs6604026

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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Genetic Variants of RPL5 and RPL9 Genes among Saudi Patients Diagnosed with Thrombosis.

Medical Archives (Sarajevo, Bosnia And Herzegovina)

Hassan, Fathelrahman Mahdi FM; Alsultan, Afnan A; Alzehrani, Faisal F; Albuali, Waleed W; Bubshait, Dalal D; Abass, Elfadil E; Elbasheer, Mudathir M; Alkhanbashi, Abdulmohsen A

Publication Date: 2021-06

Variant appearance in text: rs6604026

PubMed Link: 34483448

Variant Present in the following documents:

• Main text
• medarch-75-188.pdf

View BVdb publication page

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Replication analysis of variants associated with multiple sclerosis risk.

Scientific Reports

Dashti, Mohammad M; Ateyah, Khadijah K; Alroughani, Raed R; Al-Temaimi, Rabeah R

Publication Date: 2020-04-30

Variant appearance in text: rs6604026

PubMed Link: 32355262

Variant Present in the following documents:

• 41598_2020_64432_MOESM1_ESM.pdf

View BVdb publication page

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Breakdown of multiple sclerosis genetics to identify an integrated disease network and potential variant mechanisms.

Physiological Genomics

Shepard, C Joy CJ; Cline, Sara G SG; Hinds, David D; Jahanbakhsh, Seyedehameneh S; Prokop, Jeremy W JW

Publication Date: 2019-11-01

Variant appearance in text: rs6604026

PubMed Link: 31482761

Variant Present in the following documents:

• Main text

View BVdb publication page

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A non-synonymous single-nucleotide polymorphism associated with multiple sclerosis risk affects the EVI5 interactome.

Human Molecular Genetics

Didonna, Alessandro A; Isobe, Noriko N; Caillier, Stacy J SJ; Li, Kathy H KH; Burlingame, Alma L AL; Hauser, Stephen L SL; Baranzini, Sergio E SE; Patsopoulos, Nikolaos A NA; Oksenberg, Jorge R JR

Publication Date: 2015-12-15

Variant appearance in text: rs6604026

PubMed Link: 26433934

Variant Present in the following documents:

• Main text

View BVdb publication page

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A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1).

Plos Genetics

Rubicz, Rohina R; Yolken, Robert R; Drigalenko, Eugene E; Carless, Melanie A MA; Dyer, Thomas D TD; Bauman, Lara L; Melton, Phillip E PE; Kent, Jack W JW; Harley, John B JB; Curran, Joanne E JE; Johnson, Matthew P MP; Cole, Shelley A SA; Almasy, Laura L; Moses, Eric K EK; Dhurandhar, Nikhil V NV; Kraig, Ellen E; Blangero, John J; Leach, Charles T CT; Göring, Harald H H HH

Publication Date: 2013

Variant appearance in text: rs6604026

PubMed Link: 23326239

Variant Present in the following documents:

• Main text
• pgen.1003147.pdf

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Revealing the genetic basis of multiple sclerosis: are we there yet?

Current Opinion In Genetics & Development

Baranzini, Sergio E SE

Publication Date: 2011-06

Variant appearance in text: rs6604026

PubMed Link: 21247752

Variant Present in the following documents:

• Main text

View BVdb publication page

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The effect of single nucleotide polymorphisms from genome wide association studies in multiple sclerosis on gene expression.

Plos One

Handel, Adam E AE; Handunnetthi, Lahiru L; Berlanga, Antonio J AJ; Watson, Corey T CT; Morahan, Julia M JM; Ramagopalan, Sreeram V SV

Publication Date: 2010-04-13

Variant appearance in text: rs6604026

PubMed Link: 20405052

Variant Present in the following documents:

• Main text
• pone.0010142.pdf

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Multiple sclerosis susceptibility-associated SNPs do not influence disease severity measures in a cohort of Australian MS patients.

Plos One

Jensen, Cathy J CJ; Stankovich, Jim J; Van der Walt, Anneke A; Bahlo, Melanie M; Taylor, Bruce V BV; van der Mei, Ingrid A F IA; Foote, Simon J SJ; Kilpatrick, Trevor J TJ; Johnson, Laura J LJ; Wilkins, Ella E; Field, Judith J; Danoy, Patrick P; Brown, Matthew A MA; , ; Rubio, Justin P JP; Butzkueven, Helmut H

Publication Date: 2010-04-02

Variant appearance in text: rs6604026

PubMed Link: 20368992

Variant Present in the following documents:

• Main text

View BVdb publication page

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Tag-SNP analysis of the GFI1-EVI5-RPL5-FAM69 risk locus for multiple sclerosis.

European Journal Of Human Genetics : Ejhg

Alcina, Antonio A; Fernández, Oscar O; Gonzalez, Juan Ramón JR; Catalá-Rabasa, Antonio A; Fedetz, María M; Ndagire, Dorothy D; Leyva, Laura L; Guerrero, Miguel M; Arnal, Carmen C; Delgado, Concepción C; Lucas, Miguel M; Izquierdo, Guillermo G; Matesanz, Fuencisla F

Publication Date: 2010-07

Variant appearance in text: rs6604026

PubMed Link: 20087403

Variant Present in the following documents:

• Main text

View BVdb publication page

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