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: rs11724758

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

View BVdb publication page

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SNPs in miRNAs and Target Sequences: Role in Cancer and Diabetes.

Frontiers In Genetics

Chhichholiya, Yogita Y; Suryan, Aman Kumar AK; Suman, Prabhat P; Munshi, Anjana A; Singh, Sandeep S

Publication Date: 2021

Variant appearance in text: rs11724758

PubMed Link: 34925466

Variant Present in the following documents:

• Main text
• fgene-12-793523.pdf

View BVdb publication page

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Genetic analysis of sinonasal undifferentiated carcinoma discovers recurrent SWI/SNF alterations and a novel PGAP3-SRPK1 fusion gene.

Bmc Cancer

Heft Neal, Molly E ME; Birkeland, Andrew C AC; Bhangale, Apurva D AD; Zhai, Jingyi J; Kulkarni, Aditi A; Foltin, Susan K SK; Jewell, Brittany M BM; Ludwig, Megan L ML; Pinatti, Lisa L; Jiang, Hui H; McHugh, Jonathan B JB; Marentette, Lawence L; McKean, Erin L EL; Brenner, J Chad JC

Publication Date: 2021-05-29

Variant appearance in text: rs11724758

PubMed Link: 34051734

Variant Present in the following documents:

• 12885_2021_8370_MOESM15_ESM.xlsx, sheet 1

View BVdb publication page

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Integrated genetic and metabolic landscapes predict vulnerabilities of temozolomide resistant glioblastoma cells.

Npj Systems Biology And Applications

Immanuel, Selva Rupa Christinal SRC; Ghanate, Avinash D AD; Parmar, Dharmeshkumar S DS; Yadav, Ritu R; Uthup, Riya R; Panchagnula, Venkateswarlu V; Raghunathan, Anu A

Publication Date: 2021-01-08

Variant appearance in text: rs11724758

PubMed Link: 33420045

Variant Present in the following documents:

• 41540_2020_161_MOESM3_ESM.xlsx, sheet 3
• 41540_2020_161_MOESM3_ESM.xlsx, sheet 2

View BVdb publication page

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Next-generation sequencing identified novel Desmoplakin frame-shift variant in patients with Arrhythmogenic cardiomyopathy.

Bmc Cardiovascular Disorders

Lin, Xiaoping X; Ma, Yuankun Y; Cai, Zhejun Z; Wang, Qiyuan Q; Wang, Lihua L; Huo, Zhaoxia Z; Hu, Dan D; Wang, Jian'an J; Xiang, Meixiang M

Publication Date: 2020-02-11

Variant appearance in text: rs11724758

PubMed Link: 32046637

Variant Present in the following documents:

• 12872_2020_1369_MOESM1_ESM.xlsx, sheet 1

View BVdb publication page

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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: rs11724758

PubMed Link: 30319441

Variant Present in the following documents:

• Table_5.xlsx, sheet 1
• Table_6.xlsx, sheet 1

View BVdb publication page

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Proteogenomic analysis prioritises functional single nucleotide variants in cancer samples.

Oncotarget

Ma, Shiyong S; Menon, Ranjeeta R; Poulos, Rebecca C RC; Wong, Jason W H JWH

Publication Date: 2017-11-10

Variant appearance in text: rs11724758

PubMed Link: 29221171

Variant Present in the following documents:

• oncotarget-08-95841-s002.xlsx, sheet 4

View BVdb publication page

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Beyond the Protein-Coding Sequence: Noncoding RNAs in the Pathogenesis of Type 2 Diabetes.

The Review Of Diabetic Studies : Rds

DiStefano, Johanna K JK

Publication Date: 2015

Variant appearance in text: rs11724758

PubMed Link: 26859655

Variant Present in the following documents:

• Main text

View BVdb publication page

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Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes.

Oncotarget

Keerthikumar, Shivakumar S; Gangoda, Lahiru L; Liem, Michael M; Fonseka, Pamali P; Atukorala, Ishara I; Ozcitti, Cemil C; Mechler, Adam A; Adda, Christopher G CG; Ang, Ching-Seng CS; Mathivanan, Suresh S

Publication Date: 2015-06-20

Variant appearance in text: rs11724758

PubMed Link: 25944692

Variant Present in the following documents:

• oncotarget-06-15375-s005.xlsx, sheet 2

View BVdb publication page

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Influence of microRNA-related polymorphisms on clinical outcomes in coronary artery disease.

American Journal Of Translational Research

Li, Qianzhen Q; Chen, Liangwan L; Chen, Daozhong D; Wu, Xijie X; Chen, Meifang M

Publication Date: 2015

Variant appearance in text: rs11724758

PubMed Link: 25901206

Variant Present in the following documents:

• Main text

View BVdb publication page

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Four genetic loci influencing electrocardiographic indices of left ventricular hypertrophy.

Circulation. Cardiovascular Genetics

Shah, Sonia S; Nelson, Christopher P CP; Gaunt, Tom R TR; van der Harst, Pim P; Barnes, Timothy T; Braund, Peter S PS; Lawlor, Debbie A DA; Casas, Juan-Pablo JP; Padmanabhan, Sandosh S; Drenos, Fotios F; Kivimaki, Mika M; Talmud, Philippa J PJ; Humphries, Steve E SE; Whittaker, John J; Morris, Richard W RW; Whincup, Peter H PH; Dominiczak, Anna A; Munroe, Patricia B PB; Johnson, Toby T; Goodall, Alison H AH; Cambien, Francois F; Diemert, Patrick P; Hengstenberg, Christian C; Ouwehand, Willem H WH; Felix, Janine F JF; Glazer, Nicole L NL; Tomaszewski, Maciej M; Burton, Paul R PR; Tobin, Martin D MD; van Veldhuisen, Dirk J DJ; de Boer, Rudolf A RA; Navis, Gerjan G; van Gilst, Wiek H WH; Mayosi, Bongani M BM; Thompson, John R JR; Kumari, Meena M; MacFarlane, Peter W PW; Day, Ian N M IN; Hingorani, Aroon D AD; Samani, Nilesh J NJ

Publication Date: 2011-12

Variant appearance in text: rs11724758

PubMed Link: 21965548

Variant Present in the following documents:

• Main text

View BVdb publication page

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