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: rs1124480

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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Variants of WNT7A and GPR124 are associated with hemorrhagic transformation following intravenous thrombolysis in ischemic stroke.

Cns Neuroscience & Therapeutics

Ta, Song S; Rong, Xianfang X; Guo, Zhen-Ni ZN; Jin, Hang H; Zhang, Peng P; Li, Fenge F; Li, Zhihuan Z; Lin, Lilong L; Zheng, Chenqing C; Gu, Qingquan Q; Zhang, Yuan Y; Liu, Wenlan W; Yang, Yi Y; Chang, Junlei J

Publication Date: 2021-01

Variant appearance in text: rs1124480

PubMed Link: 32991049

Variant Present in the following documents:

• Main text
• CNS-27-71-s001.pdf
• CNS-27-71.pdf

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EGLN2 and RNF150 genetic variants are associated with chronic obstructive pulmonary disease risk in the Chinese population.

International Journal Of Chronic Obstructive Pulmonary Disease

Ding, Yipeng Y; Niu, Huan H; Yang, Hua H; Sun, Pei P; Chen, Yu Y; Duan, Mengling M; Xu, Dongchuan D; Xu, Junxue J; Jin, Tianbo T

Publication Date: 2015

Variant appearance in text: rs1124480

PubMed Link: 25609945

Variant Present in the following documents:

• Main text
• copd-10-145.pdf

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Wnt signaling pathway pharmacogenetics in non-small cell lung cancer.

The Pharmacogenomics Journal

Stewart, D J DJ; Chang, D W DW; Ye, Y Y; Spitz, M M; Lu, C C; Shu, X X; Wampfler, J A JA; Marks, R S RS; Garces, Y I YI; Yang, P P; Wu, X X

Publication Date: 2014-12

Variant appearance in text: rs1124480

PubMed Link: 24980784

Variant Present in the following documents:

• Main text

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Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate.

Human Molecular Genetics

Chiquet, Brett T BT; Blanton, Susan H SH; Burt, Amber A; Ma, Deqiong D; Stal, Samuel S; Mulliken, John B JB; Hecht, Jacqueline T JT

Publication Date: 2008-07-15

Variant appearance in text: rs1124480

PubMed Link: 18413325

Variant Present in the following documents:

• Main text

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