Publications:

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: rs1187280

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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Case Report: Primary Leptomeningeal Medulloblastoma in a Child: Clinical Case Report and Literature Review.

Frontiers In Pediatrics

Morgacheva, Daria D; Daks, Alexandra A; Smirnova, Anna A; Kim, Aleksandr A; Ryzhkova, Daria D; Mitrofanova, Lubov L; Staliarova, Alena A; Omelina, Evgeniya E; Pindyurin, Alexey A; Fedorova, Olga O; Shuvalov, Oleg O; Petukhov, Alexey A; Dinikina, Yulia Y

Publication Date: 2022

Variant appearance in text: NTRK2: 1396+49825A>G; rs1187280

PubMed Link: 35899134

Variant Present in the following documents:

• Table_1.xlsx, sheet 1

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A major role for common genetic variation in anxiety disorders.

Molecular Psychiatry

Purves, Kirstin L KL; Coleman, Jonathan R I JRI; Meier, Sandra M SM; Rayner, Christopher C; Davis, Katrina A S KAS; Cheesman, Rosa R; Bækvad-Hansen, Marie M; Børglum, Anders D AD; Wan Cho, Shing S; Jürgen Deckert, J J; Gaspar, Héléna A HA; Bybjerg-Grauholm, Jonas J; Hettema, John M JM; Hotopf, Matthew M; Hougaard, David D; Hübel, Christopher C; Kan, Carol C; McIntosh, Andrew M AM; Mors, Ole O; Bo Mortensen, Preben P; Nordentoft, Merete M; Werge, Thomas T; Nicodemus, Kristin K KK; Mattheisen, Manuel M; Breen, Gerome G; Eley, Thalia C TC

Publication Date: 2020-12

Variant appearance in text: rs1187280

PubMed Link: 31748690

Variant Present in the following documents:

• Main text

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Intraventricular meningiomas frequently harbor NF2 mutations but lack common genetic alterations in TRAF7, AKT1, SMO, KLF4, PIK3CA, and TERT.

Acta Neuropathologica Communications

Jungwirth, Gerhard G; Warta, Rolf R; Beynon, Christopher C; Sahm, Felix F; von Deimling, Andreas A; Unterberg, Andreas A; Herold-Mende, Christel C; Jungk, Christine C

Publication Date: 2019-08-30

Variant appearance in text: rs1187280

PubMed Link: 31470906

Variant Present in the following documents:

• 40478_2019_793_MOESM1_ESM.xlsx, sheet 2

View BVdb publication page