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: rs10790162

PubMed Link: 36467812

Variant Present in the following documents:

• JHA2-3-1326-s001.xlsx, sheet 1

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HGFAC is a ChREBP regulated hepatokine that enhances glucose and lipid homeostasis.

Jci Insight

Sargsyan, Ashot A; Doridot, Ludivine L; Hannou, Sarah Anissa SA; Tong, Wenxin W; Srinivasan, Harini H; Ivison, Rachael R; Monn, Ruby R; Kou, Henry H HH; Haldeman, Jonathan M JM; Arlotto, Michelle M; White, Phillip J PJ; Grimsrud, Paul A PA; Astapova, Inna I; Tsai, Linus T-Y LT; Herman, Mark A MA

Publication Date: 2022-11-22

Variant appearance in text: rs10790162

PubMed Link: 36413406

Variant Present in the following documents:

• jciinsight-8-153740.pdf

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Assessing 48 SNPs in Hypertensive Paediatric Patients and Young Adults with Review of Genetic Background of Essential Hypertension.

Children (Basel, Switzerland)

Močnik, Mirjam M; Zagradišnik, Boris B; Marčun Varda, Nataša N

Publication Date: 2022-08-21

Variant appearance in text: rs10790162

PubMed Link: 36010152

Variant Present in the following documents:

• Main text
• children-09-01262.pdf

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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: rs10790162

PubMed Link: 35571045

Variant Present in the following documents:

• Main text
• fgene-13-810152.pdf

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Inferred expression regulator activities suggest genes mediating cardiometabolic genetic signals.

Plos Computational Biology

Hoskins, Jason W JW; Chung, Charles C CC; O'Brien, Aidan A; Zhong, Jun J; Connelly, Katelyn K; Collins, Irene I; Shi, Jianxin J; Amundadottir, Laufey T LT

Publication Date: 2021-11

Variant appearance in text: rs10790162

PubMed Link: 34793442

Variant Present in the following documents:

• Main text
• pcbi.1009563.pdf

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Genome-wide landscape establishes novel association signals for metabolic traits in the Arab population.

Human Genetics

Hebbar, Prashantha P; Abubaker, Jehad Ahmed JA; Abu-Farha, Mohamed M; Alsmadi, Osama O; Elkum, Naser N; Alkayal, Fadi F; John, Sumi Elsa SE; Channanath, Arshad A; Iqbal, Rasheeba R; Pitkaniemi, Janne J; Tuomilehto, Jaakko J; Sladek, Robert R; Al-Mulla, Fahd F; Thanaraj, Thangavel Alphonse TA

Publication Date: 2021-03

Variant appearance in text: rs10790162

PubMed Link: 32902719

Variant Present in the following documents:

• Main text

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A robust and efficient method for Mendelian randomization with hundreds of genetic variants.

Nature Communications

Burgess, Stephen S; Foley, Christopher N CN; Allara, Elias E; Staley, James R JR; Howson, Joanna M M JMM

Publication Date: 2020-01-17

Variant appearance in text: rs10790162

PubMed Link: 31953392

Variant Present in the following documents:

• 41467_2019_Article_14156.pdf

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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: rs10790162

PubMed Link: 31756303

Variant Present in the following documents:

• hcg-12-e002711-s001.pdf

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Scaffold-Free Endometrial Organoids Respond to Excess Androgens Associated With Polycystic Ovarian Syndrome.

The Journal Of Clinical Endocrinology And Metabolism

Wiwatpanit, Teerawat T; Murphy, Alina R AR; Lu, Zhenxiao Z; Urbanek, Margrit M; Burdette, Joanna E JE; Woodruff, Teresa K TK; Kim, J Julie JJ

Publication Date: 2020-03-01

Variant appearance in text: rs10790162

PubMed Link: 31614364

Variant Present in the following documents:

• Main text

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Identification of 12 novel loci that confer susceptibility to early-onset dyslipidemia.

International Journal Of Molecular Medicine

Yamada, Yoshiji Y; Kato, Kimihiko K; Oguri, Mitsutoshi M; Horibe, Hideki H; Fujimaki, Tetsuo T; Yasukochi, Yoshiki Y; Takeuchi, Ichiro I; Sakuma, Jun J

Publication Date: 2019-01

Variant appearance in text: rs10790162

PubMed Link: 30365130

Variant Present in the following documents:

• Main text

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Genetic and secondary causes of severe HDL deficiency and cardiovascular disease.

Journal Of Lipid Research

Geller, Andrew S AS; Polisecki, Eliana Y EY; Diffenderfer, Margaret R MR; Asztalos, Bela F BF; Karathanasis, Sotirios K SK; Hegele, Robert A RA; Schaefer, Ernst J EJ

Publication Date: 2018-12

Variant appearance in text: rs10790162

PubMed Link: 30333156

Variant Present in the following documents:

• Main text

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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: rs10790162

PubMed Link: 30262900

Variant Present in the following documents:

• 41467_2018_6467_MOESM1_ESM.pdf

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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: rs10790162

PubMed Link: 29535274

Variant Present in the following documents:

• str-49-820-s001.pdf

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Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes.

Scientific Reports

Jäger, Susanne S; Wahl, Simone S; Kröger, Janine J; Sharma, Sapna S; Hoffmann, Per P; Floegel, Anna A; Pischon, Tobias T; Prehn, Cornelia C; Adamski, Jerzy J; Müller-Nurasyid, Martina M; Waldenberger, Melanie M; Strauch, Konstantin K; Peters, Annette A; Gieger, Christian C; Suhre, Karsten K; Grallert, Harald H; Boeing, Heiner H; Schulze, Matthias B MB; Meidtner, Karina K

Publication Date: 2017-07-20

Variant appearance in text: rs10790162

PubMed Link: 28729637

Variant Present in the following documents:

• Main text

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Association of BUD13 polymorphisms with metabolic syndrome in Chinese population: a case-control study.

Lipids In Health And Disease

Zhang, Lili L; You, Yueyue Y; Wu, Yanhua Y; Zhang, Yangyu Y; Wang, Mohan M; Song, Yan Y; Liu, Xinyu X; Kou, Changgui C

Publication Date: 2017-06-28

Variant appearance in text: rs10790162

PubMed Link: 28659142

Variant Present in the following documents:

• Main text

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Identification of eight genetic variants as novel determinants of dyslipidemia in Japanese by exome-wide association studies.

Oncotarget

Yamada, Yoshiji Y; Sakuma, Jun J; Takeuchi, Ichiro I; Yasukochi, Yoshiki Y; Kato, Kimihiko K; Oguri, Mitsutoshi M; Fujimaki, Tetsuo T; Horibe, Hideki H; Muramatsu, Masaaki M; Sawabe, Motoji M; Fujiwara, Yoshinori Y; Taniguchi, Yu Y; Obuchi, Shuichi S; Kawai, Hisashi H; Shinkai, Shoji S; Mori, Seijiro S; Arai, Tomio T; Tanaka, Masashi M

Publication Date: 2017-06-13

Variant appearance in text: rs10790162

PubMed Link: 28473662

Variant Present in the following documents:

• Main text
• oncotarget-08-38950.pdf

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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: rs10790162

PubMed Link: 28456421

Variant Present in the following documents:

• Main text

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Multiphenotype association study of patients randomized to initiate antiretroviral regimens in AIDS Clinical Trials Group protocol A5202.

Pharmacogenetics And Genomics

Verma, Anurag A; Bradford, Yuki Y; Verma, Shefali S SS; Pendergrass, Sarah A SA; Daar, Eric S ES; Venuto, Charles C; Morse, Gene D GD; Ritchie, Marylyn D MD; Haas, David W DW

Publication Date: 2017-03

Variant appearance in text: rs10790162

PubMed Link: 28099408

Variant Present in the following documents:

• Main text
• fpc-27-101.pdf

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Association and interaction of APOA5, BUD13, CETP, LIPA and health-related behavior with metabolic syndrome in a Taiwanese population.

Scientific Reports

Lin, Eugene E; Kuo, Po-Hsiu PH; Liu, Yu-Li YL; Yang, Albert C AC; Kao, Chung-Feng CF; Tsai, Shih-Jen SJ

Publication Date: 2016-11-09

Variant appearance in text: rs10790162

PubMed Link: 27827461

Variant Present in the following documents:

• Main text
• srep36830.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: rs10790162

PubMed Link: 27411854

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genetics of Insulin Resistance and the Metabolic Syndrome.

Current Cardiology Reports

Brown, Audrey E AE; Walker, Mark M

Publication Date: 2016-08

Variant appearance in text: rs10790162

PubMed Link: 27312935

Variant Present in the following documents:

• Main text

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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: rs10790162

PubMed Link: 27257688

Variant Present in the following documents:

• Main text
• pone.0153720.pdf

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Meta-analysis of lipid-traits in Hispanics identifies novel loci, population-specific effects, and tissue-specific enrichment of eQTLs.

Scientific Reports

Below, Jennifer E JE; Parra, Esteban J EJ; Gamazon, Eric R ER; Torres, Jason J; Krithika, S S; Candille, Sophie S; Lu, Yingchang Y; Manichakul, Ani A; Peralta-Romero, Jesus J; Duan, Qing Q; Li, Yun Y; Morris, Andrew P AP; Gottesman, Omri O; Bottinger, Erwin E; Wang, Xin-Qun XQ; Taylor, Kent D KD; Ida Chen, Y-D YD; Rotter, Jerome I JI; Rich, Stephen S SS; Loos, Ruth J F RJ; Tang, Hua H; Cox, Nancy J NJ; Cruz, Miguel M; Hanis, Craig L CL; Valladares-Salgado, Adan A

Publication Date: 2016-01-19

Variant appearance in text: rs10790162

PubMed Link: 26780889

Variant Present in the following documents:

• Main text
• srep19429-s1.pdf

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Genome-wide association study identifies African-ancestry specific variants for metabolic syndrome.

Molecular Genetics And Metabolism

Tekola-Ayele, Fasil F; Doumatey, Ayo P AP; Shriner, Daniel D; Bentley, Amy R AR; Chen, Guanjie G; Zhou, Jie J; Fasanmade, Olufemi O; Johnson, Thomas T; Oli, Johnnie J; Okafor, Godfrey G; Eghan, Benjami A BA; Agyenim-Boateng, Kofi K; Adebamowo, Clement C; Amoah, Albert A; Acheampong, Joseph J; Adeyemo, Adebowale A; Rotimi, Charles N CN

Publication Date: 2015-12

Variant appearance in text: rs10790162

PubMed Link: 26507551

Variant Present in the following documents:

• Main text

View BVdb publication page

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Genome-wide association study of metabolic syndrome in koreans.

Genomics & Informatics

Jeong, Seok Won SW; Chung, Myungguen M; Park, Soo-Jung SJ; Cho, Seong Beom SB; Hong, Kyung-Won KW

Publication Date: 2014-12

Variant appearance in text: rs10790162

PubMed Link: 25705157

Variant Present in the following documents:

• gni-12-187.pdf

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Association between the MLX interacting protein-like, BUD13 homolog and zinc finger protein 259 gene polymorphisms and serum lipid levels.

Scientific Reports

Aung, Lynn-Htet-Htet LH; Yin, Rui-Xing RX; Wu, Jin-Zhen JZ; Wu, Dong-Feng DF; Wang, Wei W; Li, Hui H

Publication Date: 2014-07-03

Variant appearance in text: BUD13: 237+1741T>C; rs10790162

PubMed Link: 24989072

Variant Present in the following documents:

• Main text

View BVdb publication page

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Association of the variants in the BUD13-ZNF259 genes and the risk of hyperlipidaemia.

Journal Of Cellular And Molecular Medicine

Aung, Lynn Htet Htet LH; Yin, Rui-Xing RX; Wu, Dong-Feng DF; Wang, Wei W; Liu, Cheng-Wu CW; Pan, Shang-Ling SL

Publication Date: 2014-07

Variant appearance in text: rs10790162

PubMed Link: 24780069

Variant Present in the following documents:

• Main text
• jcmm0018-1417.pdf

View BVdb publication page

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Common variants associated with plasma triglycerides and risk for coronary artery disease.

Nature Genetics

Do, Ron R; Willer, Cristen J CJ; Schmidt, Ellen M EM; Sengupta, Sebanti S; Gao, Chi C; Peloso, Gina M GM; Gustafsson, Stefan S; Kanoni, Stavroula S; Ganna, Andrea A; Chen, Jin J; Buchkovich, Martin L ML; Mora, Samia S; Beckmann, Jacques S JS; Bragg-Gresham, Jennifer L JL; Chang, Hsing-Yi HY; Demirkan, Ayşe A; Den Hertog, Heleen M HM; Donnelly, Louise A LA; Ehret, Georg B GB; Esko, Tõnu T; Feitosa, Mary F MF; Ferreira, Teresa T; Fischer, Krista K; Fontanillas, Pierre P; Fraser, Ross M RM; Freitag, Daniel F DF; Gurdasani, Deepti D; Heikkilä, Kauko K; Hyppönen, Elina E; Isaacs, Aaron A; Jackson, Anne U AU; Johansson, Asa A; Johnson, Toby T; Kaakinen, Marika M; Kettunen, Johannes J; Kleber, Marcus E ME; Li, Xiaohui X; Luan, Jian'an J; Lyytikäinen, Leo-Pekka LP; Magnusson, Patrik K E PK; Mangino, Massimo M; Mihailov, Evelin E; Montasser, May E ME; Müller-Nurasyid, Martina M; Nolte, Ilja M IM; O'Connell, Jeffrey R JR; Palmer, Cameron D CD; Perola, Markus M; Petersen, Ann-Kristin AK; Sanna, Serena S; Saxena, Richa R; Service, Susan K SK; Shah, Sonia S; Shungin, Dmitry D; Sidore, Carlo C; Song, Ci C; Strawbridge, Rona J RJ; Surakka, Ida I; Tanaka, Toshiko T; Teslovich, Tanya M TM; Thorleifsson, Gudmar G; Van den Herik, Evita G EG; Voight, Benjamin F BF; Volcik, Kelly A KA; Waite, Lindsay L LL; Wong, Andrew A; Wu, Ying Y; Zhang, Weihua W; Absher, Devin D; Asiki, Gershim G; Barroso, Inês I; Been, Latonya F LF; Bolton, Jennifer L JL; Bonnycastle, Lori L LL; Brambilla, Paolo P; Burnett, Mary S MS; Cesana, Giancarlo G; Dimitriou, Maria M; Doney, Alex S F AS; Döring, Angela A; Elliott, Paul P; Epstein, Stephen E SE; Eyjolfsson, Gudmundur Ingi GI; Gigante, Bruna B; Goodarzi, Mark O MO; Grallert, Harald H; Gravito, Martha L ML; Groves, Christopher J CJ; Hallmans, Göran G; Hartikainen, Anna-Liisa AL; Hayward, Caroline C; Hernandez, Dena D; Hicks, Andrew A AA; Holm, Hilma H; Hung, Yi-Jen YJ; Illig, Thomas T; Jones, Michelle R MR; Kaleebu, Pontiano P; Kastelein, John J P JJ; Khaw, Kay-Tee KT; Kim, Eric E; Klopp, Norman N; Komulainen, Pirjo P; Kumari, Meena M; Langenberg, Claudia C; Lehtimäki, Terho T; Lin, Shih-Yi SY; Lindström, Jaana J; Loos, Ruth J F RJ; Mach, François F; McArdle, Wendy L WL; Meisinger, Christa C; Mitchell, Braxton D BD; Müller, Gabrielle G; Nagaraja, Ramaiah R; Narisu, Narisu N; Nieminen, Tuomo V M TV; Nsubuga, Rebecca N RN; Olafsson, Isleifur I; Ong, Ken K KK; Palotie, Aarno A; Papamarkou, Theodore T; Pomilla, Cristina C; Pouta, Anneli A; Rader, Daniel J DJ; Reilly, Muredach P MP; Ridker, Paul M PM; Rivadeneira, Fernando F; Rudan, Igor I; Ruokonen, Aimo A; Samani, Nilesh N; Scharnagl, Hubert H; Seeley, Janet J; Silander, Kaisa K; Stančáková, Alena A; Stirrups, Kathleen K; Swift, Amy J AJ; Tiret, Laurence L; Uitterlinden, Andre G AG; van Pelt, L Joost LJ; Vedantam, Sailaja S; Wainwright, Nicholas N; Wijmenga, Cisca C; Wild, Sarah H SH; Willemsen, Gonneke G; Wilsgaard, Tom T; Wilson, James F JF; Young, Elizabeth H EH; Zhao, Jing Hua JH; Adair, Linda S LS; Arveiler, Dominique D; Assimes, Themistocles L TL; Bandinelli, Stefania S; Bennett, Franklyn F; Bochud, Murielle M; Boehm, Bernhard O BO; Boomsma, Dorret I DI; Borecki, Ingrid B IB; Bornstein, Stefan R SR; Bovet, Pascal P; Burnier, Michel M; Campbell, Harry H; Chakravarti, Aravinda A; Chambers, John C JC; Chen, Yii-Der Ida YD; Collins, Francis S FS; Cooper, Richard S RS; Danesh, John J; Dedoussis, George G; de Faire, Ulf U; Feranil, Alan B AB; Ferrières, Jean J; Ferrucci, Luigi L; Freimer, Nelson B NB; Gieger, Christian C; Groop, Leif C LC; Gudnason, Vilmundur V; Gyllensten, Ulf U; Hamsten, Anders A; Harris, Tamara B TB; Hingorani, Aroon A; Hirschhorn, Joel N JN; Hofman, Albert A; Hovingh, G Kees GK; Hsiung, Chao Agnes CA; Humphries, Steve E SE; Hunt, Steven C SC; Hveem, Kristian K; Iribarren, Carlos C; Järvelin, Marjo-Riitta MR; Jula, Antti A; Kähönen, Mika M; Kaprio, Jaakko J; Kesäniemi, Antero A; Kivimaki, Mika M; Kooner, Jaspal S JS; Koudstaal, Peter J PJ; Krauss, Ronald M RM; Kuh, Diana D; Kuusisto, Johanna J; Kyvik, Kirsten O KO; Laakso, Markku M; Lakka, Timo A TA; Lind, Lars L; Lindgren, Cecilia M CM; Martin, Nicholas G NG; März, Winfried W; McCarthy, Mark I MI; McKenzie, Colin A CA; Meneton, Pierre P; Metspalu, Andres A; Moilanen, Leena L; Morris, Andrew D AD; Munroe, Patricia B PB; Njølstad, Inger I; Pedersen, Nancy L NL; Power, Chris C; Pramstaller, Peter P PP; Price, Jackie F JF; Psaty, Bruce M BM; Quertermous, Thomas T; Rauramaa, Rainer R; Saleheen, Danish D; Salomaa, Veikko V; Sanghera, Dharambir K DK; Saramies, Jouko J; Schwarz, Peter E H PE; Sheu, Wayne H-H WH; Shuldiner, Alan R AR; Siegbahn, Agneta A; Spector, Tim D TD; Stefansson, Kari K; Strachan, David P DP; Tayo, Bamidele O BO; Tremoli, Elena E; Tuomilehto, Jaakko J; Uusitupa, Matti M; van Duijn, Cornelia M CM; Vollenweider, Peter P; Wallentin, Lars L; Wareham, Nicholas J NJ; Whitfield, John B JB; Wolffenbuttel, Bruce H R BH; Altshuler, David D; Ordovas, Jose M JM; Boerwinkle, Eric E; Palmer, Colin N A CN; Thorsteinsdottir, Unnur U; Chasman, Daniel I DI; Rotter, Jerome I JI; Franks, Paul W PW; Ripatti, Samuli S; Cupples, L Adrienne LA; Sandhu, Manjinder S MS; Rich, Stephen S SS; Boehnke, Michael M; Deloukas, Panos P; Mohlke, Karen L KL; Ingelsson, Erik E; Abecasis, Goncalo R GR; Daly, Mark J MJ; Neale, Benjamin M BM; Kathiresan, Sekar S

Publication Date: 2013-11

Variant appearance in text: rs10790162

PubMed Link: 24097064

Variant Present in the following documents:

• Main text

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A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium.

Diabetes

Kraja, Aldi T AT; Vaidya, Dhananjay D; Pankow, James S JS; Goodarzi, Mark O MO; Assimes, Themistocles L TL; Kullo, Iftikhar J IJ; Sovio, Ulla U; Mathias, Rasika A RA; Sun, Yan V YV; Franceschini, Nora N; Absher, Devin D; Li, Guo G; Zhang, Qunyuan Q; Feitosa, Mary F MF; Glazer, Nicole L NL; Haritunians, Talin T; Hartikainen, Anna-Liisa AL; Knowles, Joshua W JW; North, Kari E KE; Iribarren, Carlos C; Kral, Brian B; Yanek, Lisa L; O'Reilly, Paul F PF; McCarthy, Mark I MI; Jaquish, Cashell C; Couper, David J DJ; Chakravarti, Aravinda A; Psaty, Bruce M BM; Becker, Lewis C LC; Province, Michael A MA; Boerwinkle, Eric E; Quertermous, Thomas T; Palotie, Leena L; Jarvelin, Marjo-Riitta MR; Becker, Diane M DM; Kardia, Sharon L R SL; Rotter, Jerome I JI; Chen, Yii-Der Ida YD; Borecki, Ingrid B IB

Publication Date: 2011-04

Variant appearance in text: rs10790162

PubMed Link: 21386085

Variant Present in the following documents:

• Main text
• 1329.pdf

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