Publications:

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Role of the Gut-Brain Axis in the Shared Genetic Etiology Between Gastrointestinal Tract Diseases and Psychiatric Disorders: A Genome-Wide Pleiotropic Analysis.

Jama Psychiatry

Gong, Weiming W; Guo, Ping P; Li, Yuanming Y; Liu, Lu L; Yan, Ran R; Liu, Shuai S; Wang, Shukang S; Xue, Fuzhong F; Zhou, Xiang X; Yuan, Zhongshang Z

Publication Date: 2023-02-08

Variant appearance in text: rs5177

PubMed Link: 36753304

Variant Present in the following documents:

• jamapsychiatry-e224974-s001.pdf

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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: rs5177

PubMed Link: 34051734

Variant Present in the following documents:

• 12885_2021_8370_MOESM15_ESM.xlsx, sheet 1

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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: rs5177

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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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: rs5177

PubMed Link: 29221171

Variant Present in the following documents:

• oncotarget-08-95841-s002.xlsx, sheet 1

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Multiple genetic imaging study of the association between cholesterol metabolism and brain functional alterations in individuals with risk factors for Alzheimer's disease.

Oncotarget

Bai, Feng F; Yuan, Yonggui Y; Shi, Yongmei Y; Zhang, Zhijun Z

Publication Date: 2016-03-29

Variant appearance in text: rs5177

PubMed Link: 26985771

Variant Present in the following documents:

• Main text
• oncotarget-07-15315.pdf

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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: rs5177

PubMed Link: 25944692

Variant Present in the following documents:

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

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Genome-wide association study combined with biological context can reveal more disease-related SNPs altering microRNA target seed sites.

Bmc Genomics

Wu, Di D; Yang, Gang G; Zhang, Lifang L; Xue, Jiwei J; Wen, Zhining Z; Li, Menglong M

Publication Date: 2014-08-08

Variant appearance in text: rs5177

PubMed Link: 25106527

Variant Present in the following documents:

• Main text
• 12864_2014_Article_6678.pdf

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A novel molecular diagnostic marker for familial and early-onset coronary artery disease and myocardial infarction in the LRP8 gene.

Circulation. Cardiovascular Genetics

Shen, Gong-Qing GQ; Girelli, Domenico D; Li, Lin L; Rao, Shaoqi S; Archacki, Stephen S; Olivieri, Oliviero O; Martinelli, Nicola N; Park, Jeong Euy JE; Chen, Qiuyun Q; Topol, Eric J EJ; Wang, Qing K QK

Publication Date: 2014-08

Variant appearance in text: rs5177

PubMed Link: 24867879

Variant Present in the following documents:

• Main text

View BVdb publication page

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Integrated mRNA and microRNA transcriptome sequencing characterizes sequence variants and mRNA-microRNA regulatory network in nasopharyngeal carcinoma model systems.

Febs Open Bio

Szeto, Carol Ying-Ying CY; Lin, Chi Ho CH; Choi, Siu Chung SC; Yip, Timothy T C TT; Ngan, Roger Kai-Cheong RK; Tsao, George Sai-Wah GS; Li Lung, Maria M

Publication Date: 2014

Variant appearance in text: rs5177

PubMed Link: 24490137

Variant Present in the following documents:

• mmc5.xlsx, sheet 2

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Multi-allelic haplotype association identifies novel information different from single-SNP analysis: a new protective haplotype in the LRP8 gene is against familial and early-onset CAD and MI.

Gene

Shen, Gong-Qing GQ; Girelli, Domenico D; Li, Lin L; Olivieri, Oliviero O; Martinelli, Nicola N; Chen, Qiuyun Q; Topol, Eric J EJ; Wang, Qing K QK

Publication Date: 2013-05-25

Variant appearance in text: rs5177

PubMed Link: 23524007

Variant Present in the following documents:

• Main text

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Association study of candidate gene polymorphisms with amnestic mild cognitive impairment in a Chinese population.

Plos One

Liu, Xiaoyan X; Yue, Chunxian C; Xu, Zhi Z; Shu, Hao H; Pu, Mengjia M; Yu, Hui H; Shi, Yongmei Y; Zhuang, Liying L; Xu, Xiaohui X; Zhang, Zhijun Z

Publication Date: 2012

Variant appearance in text: rs5177

PubMed Link: 22911757

Variant Present in the following documents:

• Main text
• pone.0041198.pdf

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GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia.

Molecular Psychiatry

Chen, X X; Lee, G G; Maher, B S BS; Fanous, A H AH; Chen, J J; Zhao, Z Z; Guo, A A; van den Oord, E E; Sullivan, P F PF; Shi, J J; Levinson, D F DF; Gejman, P V PV; Sanders, A A; Duan, J J; Owen, M J MJ; Craddock, N J NJ; O'Donovan, M C MC; Blackman, J J; Lewis, D D; Kirov, G K GK; Qin, W W; Schwab, S S; Wildenauer, D D; Chowdari, K K; Nimgaonkar, V V; Straub, R E RE; Weinberger, D R DR; O'Neill, F A FA; Walsh, D D; Bronstein, M M; Darvasi, A A; Lencz, T T; Malhotra, A K AK; Rujescu, D D; Giegling, I I; Werge, T T; Hansen, T T; Ingason, A A; Nöethen, M M MM; Rietschel, M M; Cichon, S S; Djurovic, S S; Andreassen, O A OA; Cantor, R M RM; Ophoff, R R; Corvin, A A; Morris, D W DW; Gill, M M; Pato, C N CN; Pato, M T MT; Macedo, A A; Gurling, H M D HM; McQuillin, A A; Pimm, J J; Hultman, C C; Lichtenstein, P P; Sklar, P P; Purcell, S M SM; Scolnick, E E; St Clair, D D; Blackwood, D H R DH; Kendler, K S KS; , ; ,

Publication Date: 2011-11

Variant appearance in text: rs5177

PubMed Link: 20838396

Variant Present in the following documents:

• Main text

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