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: rs603446

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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Integrated proteogenomic characterization across major histological types of pituitary neuroendocrine tumors.

Cell Research

Zhang, Fan F; Zhang, Qilin Q; Zhu, Jiajun J; Yao, Boyuan B; Ma, Chi C; Qiao, Nidan N; He, Shiman S; Ye, Zhao Z; Wang, Yunzhi Y; Han, Rui R; Feng, Jinwen J; Wang, Yongfei Y; Qin, Zhaoyu Z; Ma, Zengyi Z; Li, Kai K; Zhang, Yichao Y; Tian, Sha S; Chen, Zhengyuan Z; Tan, Subei S; Wu, Yue Y; Ran, Peng P; Wang, Ye Y; Ding, Chen C; Zhao, Yao Y

Publication Date: 2022-12

Variant appearance in text: rs603446

PubMed Link: 36307579

Variant Present in the following documents:

• 41422_2022_736_MOESM10_ESM.xlsx, sheet 3

View BVdb publication page

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"Big Data" Approaches for Prevention of the Metabolic Syndrome.

Frontiers In Genetics

Jiang, Xinping X; Yang, Zhang Z; Wang, Shuai S; Deng, Shuanglin S

Publication Date: 2022

Variant appearance in text: rs603446

PubMed Link: 35571045

Variant Present in the following documents:

• Main text
• fgene-13-810152.pdf

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Analysis of Tryptophan and Its Main Metabolite Kynurenine and the Risk of Multiple Cancers Based on the Bidirectional Mendelian Randomization Analysis.

Frontiers In Oncology

Li, Ran R; Wang, Xuanyang X; Zhang, Yuntao Y; Xu, Xiaoqing X; Wang, Lulu L; Wei, Chunbo C; Liu, Lin L; Wang, Ziqi Z; Li, Ying Y

Publication Date: 2022

Variant appearance in text: rs603446

PubMed Link: 35494045

Variant Present in the following documents:

• Main text
• fonc-12-852718.pdf

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Polymorphism rs10105606 of LPL as a Novel Risk Factor for Microalbuminuria.

Journal Of Inflammation Research

Lim, Zhu Wei ZW; Chen, Wei Liang WL

Publication Date: 2021

Variant appearance in text: rs603446

PubMed Link: 34934334

Variant Present in the following documents:

• Main text
• jir-14-6833.pdf

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Genetic factors increase the identification efficiency of predictive models for dyslipidaemia: a prospective cohort study.

Lipids In Health And Disease

Niu, Miaomiao M; Zhang, Liying L; Wang, Yikang Y; Tu, Runqi R; Liu, Xiaotian X; Hou, Jian J; Huo, Wenqian W; Mao, Zhenxing Z; Wang, Zhenfei Z; Wang, Chongjian C

Publication Date: 2021-02-12

Variant appearance in text: rs603446

PubMed Link: 33579296

Variant Present in the following documents:

• Main text
• 12944_2021_Article_1439.pdf

View BVdb publication page

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Plasma lipid levels and risk of primary open angle glaucoma: a genetic study using Mendelian randomization.

Bmc Ophthalmology

Xu, Mengqiao M; Li, Shengguo S; Zhu, Jundong J; Luo, Dawei D; Song, Weitao W; Zhou, Minwen M

Publication Date: 2020-10-02

Variant appearance in text: rs603446

PubMed Link: 33008364

Variant Present in the following documents:

• Main text
• 12886_2020_Article_1661.pdf

View BVdb publication page

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Genome-wide association study of metabolic syndrome in Korean populations.

Plos One

Oh, Seung-Won SW; Lee, Jong-Eun JE; Shin, Eunsoon E; Kwon, Hyuktae H; Choe, Eun Kyung EK; Choi, Su-Yeon SY; Rhee, Hwanseok H; Choi, Seung Ho SH

Publication Date: 2020

Variant appearance in text: rs603446

PubMed Link: 31910446

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetic Determinants of Lipids and Cardiovascular Disease Outcomes: A Wide-Angled Mendelian Randomization Investigation.

Circulation. Genomic And Precision Medicine

Allara, Elias E; Morani, Gabriele G; Carter, Paul P; Gkatzionis, Apostolos A; Zuber, Verena V; Foley, Christopher N CN; Rees, Jessica M B JMB; Mason, Amy M AM; Bell, Steven S; Gill, Dipender D; Lindström, Sara S; Butterworth, Adam S AS; Di Angelantonio, Emanuele E; Peters, James J; Burgess, Stephen S; ,

Publication Date: 2019-12

Variant appearance in text: rs603446

PubMed Link: 31756303

Variant Present in the following documents:

• hcg-12-e002711-s001.pdf

View BVdb publication page

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Effect of Interaction between Early Menarche and Genetic Polymorphisms on Triglyceride.

Oxidative Medicine And Cellular Longevity

Lee, Ho-Sun HS; Leem, Sangseob S; Oh, Bermseok B; Park, Taesung T

Publication Date: 2019

Variant appearance in text: rs603446

PubMed Link: 30931082

Variant Present in the following documents:

• Main text

View BVdb publication page

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The Korea Biobank Array: Design and Identification of Coding Variants Associated with Blood Biochemical Traits.

Scientific Reports

Moon, Sanghoon S; Kim, Young Jin YJ; Han, Sohee S; Hwang, Mi Yeong MY; Shin, Dong Mun DM; Park, Min Young MY; Lu, Yontao Y; Yoon, Kyungheon K; Jang, Hye-Mi HM; Kim, Yun Kyoung YK; Park, Tae-Joon TJ; Song, Dae Sub DS; Park, Jae Kyung JK; Lee, Jong-Eun JE; Kim, Bong-Jo BJ

Publication Date: 2019-02-04

Variant appearance in text: rs603446

PubMed Link: 30718733

Variant Present in the following documents:

• 41598_2018_37832_MOESM1_ESM.pdf

View BVdb publication page

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Multiple genotype-phenotype association study reveals intronic variant pair on SIDT2 associated with metabolic syndrome in a Korean population.

Human Genomics

Moon, Sanghoon S; Lee, Young Y; Won, Sungho S; Lee, Juyoung J

Publication Date: 2018-11-01

Variant appearance in text: rs603446

PubMed Link: 30382898

Variant Present in the following documents:

• Main text

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: ZPR1: 892-100G>A; rs603446

PubMed Link: 30319441

Variant Present in the following documents:

• Table_7.xlsx, sheet 1
• Table_5.xlsx, sheet 1

View BVdb publication page

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A Mendelian randomization study of the effects of blood lipids on breast cancer risk.

Nature Communications

Nowak, Christoph C; Ärnlöv, Johan J

Publication Date: 2018-09-27

Variant appearance in text: rs603446

PubMed Link: 30262900

Variant Present in the following documents:

• 41467_2018_6467_MOESM1_ESM.pdf

View BVdb publication page

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Role of Blood Lipids in the Development of Ischemic Stroke and its Subtypes: A Mendelian Randomization Study.

Stroke

Hindy, George G; Engström, Gunnar G; Larsson, Susanna C SC; Traylor, Matthew M; Markus, Hugh S HS; Melander, Olle O; Orho-Melander, Marju M; ,

Publication Date: 2018-04

Variant appearance in text: rs603446

PubMed Link: 29535274

Variant Present in the following documents:

• str-49-820-s001.pdf

View BVdb publication page

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Whole-exome sequencing analysis of Waardenburg syndrome in a Chinese family.

Human Genome Variation

Chen, Dezhong D; Zhao, Na N; Wang, Jing J; Li, Zhuoyu Z; Wu, Changxin C; Fu, Jie J; Xiao, Han H

Publication Date: 2017

Variant appearance in text: rs603446

PubMed Link: 28690861

Variant Present in the following documents:

• hgv201727-s1.xls, sheet 1

View BVdb publication page

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Mendelian Randomization Implicates High-Density Lipoprotein Cholesterol-Associated Mechanisms in Etiology of Age-Related Macular Degeneration.

Ophthalmology

Burgess, Stephen S; Davey Smith, George G

Publication Date: 2017-08

Variant appearance in text: rs603446

PubMed Link: 28456421

Variant Present in the following documents:

• Main text
• main.pdf

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Two-stage association study to identify the genetic susceptibility of a novel common variant of rs2075290 in ZPR1 to type 2 diabetes.

Scientific Reports

Guan, Fanglin F; Niu, Yu Y; Zhang, Tianxiao T; Liu, Songfang S; Ma, Lei L; Qi, Ting T; Feng, Jia J; Zuo, Hong H; Li, Guohong G; Liu, Xufeng X; Wang, Shujin S

Publication Date: 2016-07-14

Variant appearance in text: rs603446

PubMed Link: 27411854

Variant Present in the following documents:

• Main text

View BVdb publication page

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Distinct Patterns of Association of Variants at 11q23.3 Chromosomal Region with Coronary Artery Disease and Dyslipidemia in the Population of Andhra Pradesh, India.

Plos One

Pranav Chand, Rayabarapu R; Kumar, Arramraju Sreenivas AS; Anuj, Kapadia K; Vishnupriya, Satti S; Mohan Reddy, Battini B

Publication Date: 2016

Variant appearance in text: rs603446

PubMed Link: 27257688

Variant Present in the following documents:

• Main text
• pone.0153720.pdf

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Multiple susceptibility loci at chromosome 11q23.3 are associated with plasma triglyceride in East Asians.

Journal Of Lipid Research

Gombojav, Bayasgalan B; Lee, Soo Ji SJ; Kho, Minjung M; Song, Yun-Mi YM; Lee, Kayoung K; Sung, Joohon J

Publication Date: 2016-02

Variant appearance in text: rs603446

PubMed Link: 26634697

Variant Present in the following documents:

• Main text

View BVdb publication page

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Family-based association analysis: a fast and efficient method of multivariate association analysis with multiple variants.

Bmc Bioinformatics

Won, Sungho S; Kim, Wonji W; Lee, Sungyoung S; Lee, Young Y; Sung, Joohon J; Park, Taesung T

Publication Date: 2015-02-15

Variant appearance in text: rs603446

PubMed Link: 25887481

Variant Present in the following documents:

• Main text
• 12859_2015_Article_484.pdf

View BVdb publication page

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A comparative encyclopedia of DNA elements in the mouse genome.

Nature

Yue, Feng F; Cheng, Yong Y; Breschi, Alessandra A; Vierstra, Jeff J; Wu, Weisheng W; Ryba, Tyrone T; Sandstrom, Richard R; Ma, Zhihai Z; Davis, Carrie C; Pope, Benjamin D BD; Shen, Yin Y; Pervouchine, Dmitri D DD; Djebali, Sarah S; Thurman, Robert E RE; Kaul, Rajinder R; Rynes, Eric E; Kirilusha, Anthony A; Marinov, Georgi K GK; Williams, Brian A BA; Trout, Diane D; Amrhein, Henry H; Fisher-Aylor, Katherine K; Antoshechkin, Igor I; DeSalvo, Gilberto G; See, Lei-Hoon LH; Fastuca, Meagan M; Drenkow, Jorg J; Zaleski, Chris C; Dobin, Alex A; Prieto, Pablo P; Lagarde, Julien J; Bussotti, Giovanni G; Tanzer, Andrea A; Denas, Olgert O; Li, Kanwei K; Bender, M A MA; Zhang, Miaohua M; Byron, Rachel R; Groudine, Mark T MT; McCleary, David D; Pham, Long L; Ye, Zhen Z; Kuan, Samantha S; Edsall, Lee L; Wu, Yi-Chieh YC; Rasmussen, Matthew D MD; Bansal, Mukul S MS; Kellis, Manolis M; Keller, Cheryl A CA; Morrissey, Christapher S CS; Mishra, Tejaswini T; Jain, Deepti D; Dogan, Nergiz N; Harris, Robert S RS; Cayting, Philip P; Kawli, Trupti T; Boyle, Alan P AP; Euskirchen, Ghia G; Kundaje, Anshul A; Lin, Shin S; Lin, Yiing Y; Jansen, Camden C; Malladi, Venkat S VS; Cline, Melissa S MS; Erickson, Drew T DT; Kirkup, Vanessa M VM; Learned, Katrina K; Sloan, Cricket A CA; Rosenbloom, Kate R KR; Lacerda de Sousa, Beatriz B; Beal, Kathryn K; Pignatelli, Miguel M; Flicek, Paul P; Lian, Jin J; Kahveci, Tamer T; Lee, Dongwon D; Kent, W James WJ; Ramalho Santos, Miguel M; Herrero, Javier J; Notredame, Cedric C; Johnson, Audra A; Vong, Shinny S; Lee, Kristen K; Bates, Daniel D; Neri, Fidencio F; Diegel, Morgan M; Canfield, Theresa T; Sabo, Peter J PJ; Wilken, Matthew S MS; Reh, Thomas A TA; Giste, Erika E; Shafer, Anthony A; Kutyavin, Tanya T; Haugen, Eric E; Dunn, Douglas D; Reynolds, Alex P AP; Neph, Shane S; Humbert, Richard R; Hansen, R Scott RS; De Bruijn, Marella M; Selleri, Licia L; Rudensky, Alexander A; Josefowicz, Steven S; Samstein, Robert R; Eichler, Evan E EE; Orkin, Stuart H SH; Levasseur, Dana D; Papayannopoulou, Thalia T; Chang, Kai-Hsin KH; Skoultchi, Arthur A; Gosh, Srikanta S; Disteche, Christine C; Treuting, Piper P; Wang, Yanli Y; Weiss, Mitchell J MJ; Blobel, Gerd A GA; Cao, Xiaoyi X; Zhong, Sheng S; Wang, Ting T; Good, Peter J PJ; Lowdon, Rebecca F RF; Adams, Leslie B LB; Zhou, Xiao-Qiao XQ; Pazin, Michael J MJ; Feingold, Elise A EA; Wold, Barbara B; Taylor, James J; Mortazavi, Ali A; Weissman, Sherman M SM; Stamatoyannopoulos, John A JA; Snyder, Michael P MP; Guigo, Roderic R; Gingeras, Thomas R TR; Gilbert, David M DM; Hardison, Ross C RC; Beer, Michael A MA; Ren, Bing B; ,

Publication Date: 2014-11-20

Variant appearance in text: rs603446

PubMed Link: 25409824

Variant Present in the following documents:

• Main text

View BVdb publication page

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Effects of apolipoprotein A5 haplotypes on the ratio of triglyceride to high-density lipoprotein cholesterol and the risk for metabolic syndrome in Koreans.

Lipids In Health And Disease

Cha, Seongwon S; Yu, Hyunjoo H; Park, Ah Yeon AY; Song, Kwang Hoon KH

Publication Date: 2014-03-12

Variant appearance in text: rs603446

PubMed Link: 24618354

Variant Present in the following documents:

• Main text
• 1476-511X-13-45.pdf

View BVdb publication page

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Effect of genetic predisposition on blood lipid traits using cumulative risk assessment in the korean population.

Genomics & Informatics

Go, Min Jin MJ; Hwang, Joo-Yeon JY; Kim, Dong-Joon DJ; Lee, Hye-Ja HJ; Jang, Han Byul HB; Park, Kyung-Hee KH; Song, Jihyun J; Lee, Jong-Young JY

Publication Date: 2012-06

Variant appearance in text: rs603446

PubMed Link: 23105936

Variant Present in the following documents:

• Main text
• gni-10-99.pdf

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The Genetic Analysis Workshop 16 Problem 3: simulation of heritable longitudinal cardiovascular phenotypes based on actual genome-wide single-nucleotide polymorphisms in the Framingham Heart Study.

Bmc Proceedings

Kraja, Aldi T AT; Culverhouse, Robert R; Daw, E Warwick EW; Wu, Jun J; Van Brunt, Andrew A; Province, Michael A MA; Borecki, Ingrid B IB

Publication Date: 2009-12-15

Variant appearance in text: rs603446

PubMed Link: 20018031

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genome-wide association and linkage analysis of quantitative traits: comparison of likelihood-ratio test and conditional score statistic.

Bmc Proceedings

Hendricks, Audrey E AE; Zhu, Yanyan Y; Dupuis, Josée J

Publication Date: 2009-12-15

Variant appearance in text: rs603446

PubMed Link: 20017964

Variant Present in the following documents:

• Main text

View BVdb publication page

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Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk.

Human Molecular Genetics

Drenos, Fotios F; Talmud, Philippa J PJ; Casas, Juan P JP; Smeeth, Liam L; Palmen, Jutta J; Humphries, Steve E SE; Hingorani, Aroon D AD

Publication Date: 2009-06-15

Variant appearance in text: rs603446

PubMed Link: 19336475

Variant Present in the following documents:

• ddp159_1.pdf

View BVdb publication page

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GRM7 variants confer susceptibility to age-related hearing impairment.

Human Molecular Genetics

Friedman, Rick A RA; Van Laer, Lut L; Huentelman, Matthew J MJ; Sheth, Sonal S SS; Van Eyken, Els E; Corneveaux, Jason J JJ; Tembe, Waibhav D WD; Halperin, Rebecca F RF; Thorburn, Ashley Q AQ; Thys, Sofie S; Bonneux, Sarah S; Fransen, Erik E; Huyghe, Jeroen J; Pyykkö, Ilmari I; Cremers, Cor W R J CW; Kremer, Hannie H; Dhooge, Ingeborg I; Stephens, Dafydd D; Orzan, Eva E; Pfister, Markus M; Bille, Michael M; Parving, Agnete A; Sorri, Martti M; Van de Heyning, Paul H PH; Makmura, Linna L; Ohmen, Jeffrey D JD; Linthicum, Frederick H FH; Fayad, Jose N JN; Pearson, John V JV; Craig, David W DW; Stephan, Dietrich A DA; Van Camp, Guy G

Publication Date: 2009-02-15

Variant appearance in text: rs603446

PubMed Link: 19047183

Variant Present in the following documents:

• Main text

View BVdb publication page

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Haplotype analysis of the apolipoprotein gene cluster on human chromosome 11.

Genomics

Olivier, Michael M; Wang, Xujing X; Cole, Regina R; Gau, Brian B; Kim, Jessica J; Rubin, Edward M EM; Pennacchio, Len A LA

Publication Date: 2004-05

Variant appearance in text: rs603446

PubMed Link: 15081120

Variant Present in the following documents:

• Main text

View BVdb publication page

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