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: rs260461

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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Comprehensive analysis of long noncoding RNA expression in dorsal root ganglion reveals cell-type specificity and dysregulation after nerve injury.

Pain

Baskozos, Georgios G; Dawes, John M JM; Austin, Jean S JS; Antunes-Martins, Ana A; McDermott, Lucy L; Clark, Alex J AJ; Trendafilova, Teodora T; Lees, Jon G JG; McMahon, Stephen B SB; Mogil, Jeffrey S JS; Orengo, Christine C; Bennett, David L DL

Publication Date: 2019-02

Variant appearance in text: rs260461

PubMed Link: 30335683

Variant Present in the following documents:

• jop-160-463.pdf

View BVdb publication page

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Association study of schizophrenia with variants in miR-137 binding sites.

Schizophrenia Research

Curtis, David D; Emmett, Warren W

Publication Date: 2018-07

Variant appearance in text: rs260461

PubMed Link: 29158013

Variant Present in the following documents:

• Main text

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Identification of EML4-ALK as an alternative fusion gene in epithelioid inflammatory myofibroblastic sarcoma.

Orphanet Journal Of Rare Diseases

Jiang, Quan Q; Tong, Han-Xing HX; Hou, Ying-Yong YY; Zhang, Yong Y; Li, Jing-Lei JL; Zhou, Yu-Hong YH; Xu, Jing J; Wang, Jiong-Yuan JY; Lu, Wei-Qi WQ

Publication Date: 2017-05-23

Variant appearance in text: rs260461

PubMed Link: 28535796

Variant Present in the following documents:

• 13023_2017_647_MOESM1_ESM.xlsx, sheet 4

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Preliminary evidence for association of genetic variants in pri-miR-34b/c and abnormal miR-34c expression with attention deficit and hyperactivity disorder.

Translational Psychiatry

Garcia-Martínez, I I; Sánchez-Mora, C C; Pagerols, M M; Richarte, V V; Corrales, M M; Fadeuilhe, C C; Cormand, B B; Casas, M M; Ramos-Quiroga, J A JA; Ribasés, M M

Publication Date: 2016-08-30

Variant appearance in text: rs260461

PubMed Link: 27576168

Variant Present in the following documents:

View BVdb publication page

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Brain expression genome-wide association study (eGWAS) identifies human disease-associated variants.

Plos Genetics

Zou, Fanggeng F; Chai, High Seng HS; Younkin, Curtis S CS; Allen, Mariet M; Crook, Julia J; Pankratz, V Shane VS; Carrasquillo, Minerva M MM; Rowley, Christopher N CN; Nair, Asha A AA; Middha, Sumit S; Maharjan, Sooraj S; Nguyen, Thuy T; Ma, Li L; Malphrus, Kimberly G KG; Palusak, Ryan R; Lincoln, Sarah S; Bisceglio, Gina G; Georgescu, Constantin C; Kouri, Naomi N; Kolbert, Christopher P CP; Jen, Jin J; Haines, Jonathan L JL; Mayeux, Richard R; Pericak-Vance, Margaret A MA; Farrer, Lindsay A LA; Schellenberg, Gerard D GD; , ; Petersen, Ronald C RC; Graff-Radford, Neill R NR; Dickson, Dennis W DW; Younkin, Steven G SG; Ertekin-Taner, Nilüfer N

Publication Date: 2012

Variant appearance in text: rs260461

PubMed Link: 22685416

Variant Present in the following documents:

• Main text
• pgen.1002707.pdf

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Genome-wide association studies in ADHD.

Human Genetics

Franke, Barbara B; Neale, Benjamin M BM; Faraone, Stephen V SV

Publication Date: 2009-07

Variant appearance in text: rs260461

PubMed Link: 19384554

Variant Present in the following documents:

• Main text
• 439_2009_Article_663.pdf

View BVdb publication page

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