CELSR2 c.*521A>G

Variant ID: 1-109817192-A-G

NM_001408.2(CELSR2):c.*521A>G

This variant was identified in 50 publications

View GRCh38 version.




Publications:


Sortilin enhances fibrosis and calcification in aortic valve disease by inducing interstitial cell heterogeneity.

European Heart Journal
Iqbal, Farwah F; Schlotter, Florian F; Becker-Greene, Dakota D; Lupieri, Adrien A; Goettsch, Claudia C; Hutcheson, Joshua D JD; Rogers, Maximillian A MA; Itoh, Shinsuke S; Halu, Arda A; Lee, Lang Ho LH; Blaser, Mark C MC; Mlynarchik, Andrew K AK; Hagita, Sumihiko S; Kuraoka, Shiori S; Chen, Hao Yu HY; Engert, James C JC; Passos, Livia S A LSA; Jha, Prabhash K PK; Osborn, Eric A EA; Jaffer, Farouc A FA; Body, Simon C SC; Robson, Simon C SC; Thanassoulis, George G; Aikawa, Masanori M; Singh, Sasha A SA; Sonawane, Abhijeet R AR; Aikawa, Elena E
Publication Date: 2023-01-20

Variant appearance in text: rs7528419
PubMed Link: 36660854
Variant Present in the following documents:
  • Main text
  • ehac818.pdf
View BVdb publication page



The Role of Calcium, 25-Hydroxyvitamin D, and Parathyroid Hormone in Irritable Bowel Syndrome: A Bidirectional Two-Sample Mendelian Randomization Study.

Nutrients
Xie, Ning N; Xie, Jiale J; Wang, Ziwei Z; Shu, Qiuai Q; Shi, Haitao H; Wang, Jinhai J; Liu, Na N; Xu, Feng F; Wu, Jian J
Publication Date: 2022-12-01

Variant appearance in text: rs7528419
PubMed Link: 36501135
Variant Present in the following documents:
  • Main text
  • nutrients-14-05109.pdf
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Genetic Determinants of 25-Hydroxyvitamin D Concentrations and Their Relevance to Public Health.

Nutrients
Hyppönen, Elina E; Vimaleswaran, Karani S KS; Zhou, Ang A
Publication Date: 2022-10-20

Variant appearance in text: rs7528419
PubMed Link: 36297091
Variant Present in the following documents:
  • nutrients-14-04408.pdf
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Beneficial effects of mifepristone treatment in breast cancer patients selected by the progesterone receptor isoform ratio: Results from the MIPRA trial.

Clinical Cancer Research : An Official Journal Of The American Association For Cancer Research
Elía, Andrés A; Saldain, Leo L; Vanzulli, Silvia I SI; Helguero, Luisa A LA; Lamb, Caroline A CA; Fabris, Victoria V; Pataccini, Gabriela G; Martínez-Vazquez, Paula P; Burruchaga, Javier J; Caillet-Bois, Ines I; Spengler, Eunice E; Acosta Haab, Gabriela G; Liguori, Marcos M; Castets, Alejandra A; Lovisi, Silvia S; Abascal, María F MF; Novaro, Virginia V; Sánchez, Jana J; Muñoz, Javier J; Belizán, Jose M JM; Abba, Martín C MC; Gass, Hugo H; Rojas, Paola P; Lanari, Claudia C
Publication Date: 2022-10-21

Variant appearance in text: rs7528419
PubMed Link: 36269797
Variant Present in the following documents:
  • ccr-22-2060_supplementary_table_s5_suppts5.xlsx, sheet 1
View BVdb publication page



Validation of Polygenic Risk Scores for Coronary Heart Disease in a Middle Eastern Cohort Using Whole Genome Sequencing.

Circulation. Genomic And Precision Medicine
Saad, Mohamad M; El-Menyar, Ayman A; Kunji, Khalid K; Ullah, Ehsan E; Al Suwaidi, Jassim J; Kullo, Iftikhar J IJ
Publication Date: 2022-10-12

Variant appearance in text: rs7528419
PubMed Link: 36252120
Variant Present in the following documents:
  • Main text
View BVdb publication page



Inflammatory and Prothrombotic Biomarkers, DNA Polymorphisms, MicroRNAs and Personalized Medicine for Patients with Peripheral Arterial Disease.

International Journal Of Molecular Sciences
Poredoš, Pavel P; Šabovič, Mišo M; Božič Mijovski, Mojca M; Nikolajević, Jovana J; Antignani, Pier Luigi PL; Paraskevas, Kosmas I KI; Mikhailidis, Dimitri P DP; Blinc, Aleš A
Publication Date: 2022-10-10

Variant appearance in text: rs7528419
PubMed Link: 36233355
Variant Present in the following documents:
  • Main text
  • ijms-23-12054.pdf
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Etiologic Puzzle of Coronary Artery Disease: How Important Is Genetic Component?

Life (Basel, Switzerland)
Butnariu, Lăcrămioara Ionela LI; Florea, Laura L; Badescu, Minerva Codruta MC; Țarcă, Elena E; Costache, Irina-Iuliana II; Gorduza, Eusebiu Vlad EV
Publication Date: 2022-06-09

Variant appearance in text: rs7528419
PubMed Link: 35743896
Variant Present in the following documents:
  • life-12-00865.pdf
View BVdb publication page



Machine Learning Revealed Ferroptosis Features and a Novel Ferroptosis-Based Classification for Diagnosis in Acute Myocardial Infarction.

Frontiers In Genetics
Huang, Dan D; Zheng, Shiya S; Liu, Zhuyuan Z; Zhu, Kongbo K; Zhi, Hong H; Ma, Genshan G
Publication Date: 2022

Variant appearance in text: rs7528419
PubMed Link: 35145551
Variant Present in the following documents:
  • Main text
  • fgene-13-813438.pdf
View BVdb publication page



Mendelian randomization study updates the effect of 25-hydroxyvitamin D levels on the risk of multiple sclerosis.

Journal Of Translational Medicine
Wang, Renxi R
Publication Date: 2022-01-03

Variant appearance in text: rs7528419
PubMed Link: 34980161
Variant Present in the following documents:
  • Main text
View BVdb publication page



Mendelian randomization study updates the effect of 25-hydroxyvitamin D levels on the risk of multiple sclerosis.

Journal Of Translational Medicine
Wang, Renxi R
Publication Date: 2022-01-03

Variant appearance in text: rs7528419
PubMed Link: 34980161
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetic evidence for vitamin D and cardiovascular disease: choice of variants is critical.

European Heart Journal
Burgess, Stephen S; Gill, Dipender D
Publication Date: 2022-05-07

Variant appearance in text: rs7528419
PubMed Link: 34972215
Variant Present in the following documents:
  • EMS171110.pdf
View BVdb publication page



Stroke and Myocardial Infarction: A Bidirectional Mendelian Randomization Study.

International Journal Of General Medicine
Sun, Wenxian W; Zhang, Luyang L; Liu, Weishi W; Tian, Mengke M; Wang, Xin X; Liang, Jing J; Wang, Yuying Y; Ding, Lan L; Pei, Lulu L; Lu, Jie J; Xu, Yuming Y; Song, Bo B
Publication Date: 2021

Variant appearance in text: rs7528419
PubMed Link: 34916835
Variant Present in the following documents:
  • Main text
  • ijgm-14-9537.pdf
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Generalizability of GWA-Identified Genetic Risk Variants for Metabolic Traits to Populations from the Arabian Peninsula.

Genes
Hebbar, Prashantha P; Abu-Farha, Mohamed M; Abubaker, Jehad J; Channanath, Arshad Mohamed AM; Al-Mulla, Fahd F; Thanaraj, Thangavel Alphonse TA
Publication Date: 2021-10-18

Variant appearance in text: rs7528419
PubMed Link: 34681031
Variant Present in the following documents:
  • Main text
  • genes-12-01637.pdf
View BVdb publication page



Identification of novel genetic susceptibility loci for thoracic and abdominal aortic aneurysms via genome-wide association study using the UK Biobank Cohort.

Plos One
Ashvetiya, Tamara T; Fan, Sherry X SX; Chen, Yi-Ju YJ; Williams, Charles H CH; O'Connell, Jeffery R JR; Perry, James A JA; Hong, Charles C CC
Publication Date: 2021

Variant appearance in text: rs7528419
PubMed Link: 34469433
Variant Present in the following documents:
  • Main text
  • pone.0247287.pdf
View BVdb publication page



Is vitamin D a modifiable risk factor for dental caries?

Wellcome Open Research
Dodhia, Serena A SA; West, Nicola X NX; Thomas, Steven J SJ; Timpson, Nicholas J NJ; Johansson, Ingegerd I; Lif Holgerson, Pernilla P; Dudding, Tom T; Haworth, Simon S
Publication Date: 2020

Variant appearance in text: rs7528419
PubMed Link: 34386609
Variant Present in the following documents:
  • Main text
  • wellcomeopenres-5-18849.pdf
View BVdb publication page



Sortilin as a Biomarker for Cardiovascular Disease Revisited.

Frontiers In Cardiovascular Medicine
Møller, Peter Loof PL; Rohde, Palle D PD; Winther, Simon S; Breining, Peter P; Nissen, Louise L; Nykjaer, Anders A; Bøttcher, Morten M; Nyegaard, Mette M; Kjolby, Mads M
Publication Date: 2021

Variant appearance in text: rs7528419
PubMed Link: 33937362
Variant Present in the following documents:
  • Main text
View BVdb publication page



The rs599839 A>G Variant Disentangles Cardiovascular Risk and Hepatocellular Carcinoma in NAFLD Patients.

Cancers
Meroni, Marica M; Longo, Miriam M; Paolini, Erika E; Alisi, Anna A; Miele, Luca L; De Caro, Emilia Rita ER; Pisano, Giuseppina G; Maggioni, Marco M; Soardo, Giorgio G; Valenti, Luca Vittorio LV; Fracanzani, Anna Ludovica AL; Dongiovanni, Paola P
Publication Date: 2021-04-08

Variant appearance in text: rs7528419
PubMed Link: 33917919
Variant Present in the following documents:
  • Main text
View BVdb publication page



Incorporation of DNA methylation into eQTL mapping in African Americans.

Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing
Singh, Anmol A; Zhong, Yizhen Y; Nahlawi, Layan L; Park, C Sehwan CS; De, Tanima T; Alarcon, Cristina C; Perera, Minoli A MA
Publication Date: 2021

Variant appearance in text: rs7528419
PubMed Link: 33691021
Variant Present in the following documents:
  • Main text
  • nihms-1650926.pdf
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Integrative Analysis of Transcriptome-Wide Association Study and mRNA Expression Profiles Identified Candidate Genes and Pathways Associated With Acute Myocardial Infarction.

Frontiers In Genetics
Chen, Guanzhong G; Liu, Liwei L; Li, Huanqiang H; Lun, Zhubin Z; Mai, Ziling Z; Lai, Wenguang W; Chen, Enzhao E; Zhou, Chunyun C; Yu, Sijia S; Yang, Junqing J; Chen, Shiqun S; Chen, Jiyan J; Liu, Yong Y
Publication Date: 2021

Variant appearance in text: rs7528419
PubMed Link: 33603775
Variant Present in the following documents:
  • Main text
  • fgene-12-616492.pdf
View BVdb publication page



Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease.

Nature Communications
Nielsen, Jonas B JB; Rom, Oren O; Surakka, Ida I; Graham, Sarah E SE; Zhou, Wei W; Roychowdhury, Tanmoy T; Fritsche, Lars G LG; Gagliano Taliun, Sarah A SA; Sidore, Carlo C; Liu, Yuhao Y; Gabrielsen, Maiken E ME; Skogholt, Anne Heidi AH; Wolford, Brooke B; Overton, William W; Zhao, Ying Y; Chen, Jin J; Zhang, He H; Hornsby, Whitney E WE; Acheampong, Akua A; Grooms, Austen A; Schaefer, Amanda A; Zajac, Gregory J M GJM; Villacorta, Luis L; Zhang, Jifeng J; Brumpton, Ben B; Løset, Mari M; Rai, Vivek V; Lundegaard, Pia R PR; Olesen, Morten S MS; Taylor, Kent D KD; Palmer, Nicholette D ND; Chen, Yii-Der YD; Choi, Seung H SH; Lubitz, Steven A SA; Ellinor, Patrick T PT; Barnes, Kathleen C KC; Daya, Michelle M; Rafaels, Nicholas N; Weiss, Scott T ST; Lasky-Su, Jessica J; Tracy, Russell P RP; Vasan, Ramachandran S RS; Cupples, L Adrienne LA; Mathias, Rasika A RA; Yanek, Lisa R LR; Becker, Lewis C LC; Peyser, Patricia A PA; Bielak, Lawrence F LF; Smith, Jennifer A JA; Aslibekyan, Stella S; Hidalgo, Bertha A BA; Arnett, Donna K DK; Irvin, Marguerite R MR; Wilson, James G JG; Musani, Solomon K SK; Correa, Adolfo A; Rich, Stephen S SS; Guo, Xiuqing X; Rotter, Jerome I JI; Konkle, Barbara A BA; Johnsen, Jill M JM; Ashley-Koch, Allison E AE; Telen, Marilyn J MJ; Sheehan, Vivien A VA; Blangero, John J; Curran, Joanne E JE; Peralta, Juan M JM; Montgomery, Courtney C; Sheu, Wayne H-H WH; Chung, Ren-Hua RH; Schwander, Karen K; Nouraie, Seyed M SM; Gordeuk, Victor R VR; Zhang, Yingze Y; Kooperberg, Charles C; Reiner, Alexander P AP; Jackson, Rebecca D RD; Bleecker, Eugene R ER; Meyers, Deborah A DA; Li, Xingnan X; Das, Sayantan S; Yu, Ketian K; LeFaive, Jonathon J; Smith, Albert A; Blackwell, Tom T; Taliun, Daniel D; Zollner, Sebastian S; Forer, Lukas L; Schoenherr, Sebastian S; Fuchsberger, Christian C; Pandit, Anita A; Zawistowski, Matthew M; Kheterpal, Sachin S; Brummett, Chad M CM; Natarajan, Pradeep P; Schlessinger, David D; Lee, Seunggeun S; Kang, Hyun Min HM; Cucca, Francesco F; Holmen, Oddgeir L OL; Åsvold, Bjørn O BO; Boehnke, Michael M; Kathiresan, Sekar S; Abecasis, Goncalo R GR; Chen, Y Eugene YE; Willer, Cristen J CJ; Hveem, Kristian K
Publication Date: 2020-12-18

Variant appearance in text: rs7528419
PubMed Link: 33339817
Variant Present in the following documents:
  • 41467_2020_20086_MOESM4_ESM.xlsx, sheet 4
  • 41467_2020_20086_MOESM4_ESM.xlsx, sheet 2
View BVdb publication page



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: rs7528419
PubMed Link: 32902719
Variant Present in the following documents:
  • Main text
View BVdb publication page



Genetically programmed changes in transcription of the novel progranulin regulator.

Journal Of Molecular Medicine (Berlin, Germany)
Keller, Maria M; Gebhardt, Claudia C; Huth, Sandra S; Schleinitz, Dorit D; Heyne, Henrike H; Scholz, Markus M; Stumvoll, Michael M; Böttcher, Yvonne Y; Tönjes, Anke A; Kovacs, Peter P
Publication Date: 2020-08

Variant appearance in text: rs7528419
PubMed Link: 32620998
Variant Present in the following documents:
  • Main text
  • 109_2020_Article_1942.pdf
View BVdb publication page



Discovery of novel hepatocyte eQTLs in African Americans.

Plos Genetics
Zhong, Yizhen Y; De, Tanima T; Alarcon, Cristina C; Park, C Sehwan CS; Lec, Bianca B; Perera, Minoli A MA
Publication Date: 2020-04

Variant appearance in text: rs7528419
PubMed Link: 32310939
Variant Present in the following documents:
  • Main text
  • pgen.1008662.pdf
View BVdb publication page



Sarcopenia-related traits and coronary artery disease: a bi-directional Mendelian randomization study.

Aging
Liu, Hui-Min HM; Zhang, Qiang Q; Shen, Wen-Di WD; Li, Bo-Yang BY; Lv, Wan-Qiang WQ; Xiao, Hong-Mei HM; Deng, Hong-Wen HW
Publication Date: 2020-02-16

Variant appearance in text: rs7528419
PubMed Link: 32062614
Variant Present in the following documents:
  • Main text
View BVdb publication page



The impact of adjusting for baseline in pharmacogenomic genome-wide association studies of quantitative change.

Npj Genomic Medicine
Oni-Orisan, Akinyemi A; Haldar, Tanushree T; Ranatunga, Dilrini K DK; Medina, Marisa W MW; Schaefer, Catherine C; Krauss, Ronald M RM; Iribarren, Carlos C; Risch, Neil N; Hoffmann, Thomas J TJ
Publication Date: 2020

Variant appearance in text: rs7528419
PubMed Link: 31969989
Variant Present in the following documents:
  • Main text
  • 41525_2019_Article_109.pdf
View BVdb publication page



A phenome-wide association study (PheWAS) in the Population Architecture using Genomics and Epidemiology (PAGE) study reveals potential pleiotropy in African Americans.

Plos One
Pendergrass, Sarah A SA; Buyske, Steven S; Jeff, Janina M JM; Frase, Alex A; Dudek, Scott S; Bradford, Yuki Y; Ambite, Jose-Luis JL; Avery, Christy L CL; Buzkova, Petra P; Deelman, Ewa E; Fesinmeyer, Megan D MD; Haiman, Christopher C; Heiss, Gerardo G; Hindorff, Lucia A LA; Hsu, Chun-Nan CN; Jackson, Rebecca D RD; Lin, Yi Y; Le Marchand, Loic L; Matise, Tara C TC; Monroe, Kristine R KR; Moreland, Larry L; North, Kari E KE; Park, Sungshim L SL; Reiner, Alex A; Wallace, Robert R; Wilkens, Lynne R LR; Kooperberg, Charles C; Ritchie, Marylyn D MD; Crawford, Dana C DC
Publication Date: 2019

Variant appearance in text: rs7528419
PubMed Link: 31891604
Variant Present in the following documents:
  • Main text
  • pone.0226771.pdf
View BVdb publication page



Genome-wide association study of peripheral artery disease in the Million Veteran Program.

Nature Medicine
Klarin, Derek D; Lynch, Julie J; Aragam, Krishna K; Chaffin, Mark M; Assimes, Themistocles L TL; Huang, Jie J; Lee, Kyung Min KM; Shao, Qing Q; Huffman, Jennifer E JE; Natarajan, Pradeep P; Arya, Shipra S; Small, Aeron A; Sun, Yan V YV; Vujkovic, Marijana M; Freiberg, Matthew S MS; Wang, Lu L; Chen, Jinbo J; Saleheen, Danish D; Lee, Jennifer S JS; Miller, Donald R DR; Reaven, Peter P; Alba, Patrick R PR; Patterson, Olga V OV; DuVall, Scott L SL; Boden, William E WE; Beckman, Joshua A JA; Gaziano, J Michael JM; Concato, John J; Rader, Daniel J DJ; Cho, Kelly K; Chang, Kyong-Mi KM; Wilson, Peter W F PWF; O'Donnell, Christopher J CJ; Kathiresan, Sekar S; , ; Tsao, Philip S PS; Damrauer, Scott M SM
Publication Date: 2019-08

Variant appearance in text: rs7528419
PubMed Link: 31285632
Variant Present in the following documents:
  • Main text
  • nihms-1529756.pdf
View BVdb publication page



Reverse GWAS: Using genetics to identify and model phenotypic subtypes.

Plos Genetics
Dahl, Andy A; Cai, Na N; Ko, Arthur A; Laakso, Markku M; Pajukanta, Päivi P; Flint, Jonathan J; Zaitlen, Noah N
Publication Date: 2019-04

Variant appearance in text: rs7528419
PubMed Link: 30951530
Variant Present in the following documents:
  • Main text
  • pgen.1008009.s001.pdf
  • pgen.1008009.pdf
View BVdb publication page



Tissue-specific Network Analysis of Genetic Variants Associated with Coronary Artery Disease.

Scientific Reports
Miao, Xiao X; Chen, Xinlin X; Xie, Zhijun Z; Lin, Honghuang H
Publication Date: 2018-07-31

Variant appearance in text: rs7528419
PubMed Link: 30065343
Variant Present in the following documents:
  • Main text
  • 41598_2018_Article_29904.pdf
View BVdb publication page



Oxidized phospholipids regulate amino acid metabolism through MTHFD2 to facilitate nucleotide release in endothelial cells.

Nature Communications
Hitzel, Juliane J; Lee, Eunjee E; Zhang, Yi Y; Bibli, Sofia Iris SI; Li, Xiaogang X; Zukunft, Sven S; Pflüger, Beatrice B; Hu, Jiong J; Schürmann, Christoph C; Vasconez, Andrea Estefania AE; Oo, James A JA; Kratzer, Adelheid A; Kumar, Sandeep S; Rezende, Flávia F; Josipovic, Ivana I; Thomas, Dominique D; Giral, Hector H; Schreiber, Yannick Y; Geisslinger, Gerd G; Fork, Christian C; Yang, Xia X; Sigala, Fragiska F; Romanoski, Casey E CE; Kroll, Jens J; Jo, Hanjoong H; Landmesser, Ulf U; Lusis, Aldons J AJ; Namgaladze, Dmitry D; Fleming, Ingrid I; Leisegang, Matthias S MS; Zhu, Jun J; Brandes, Ralf P RP
Publication Date: 2018-06-12

Variant appearance in text: rs7528419
PubMed Link: 29895827
Variant Present in the following documents:
  • Main text
  • 41467_2018_Article_4602.pdf
View BVdb publication page



Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes.

Cardiovascular Diabetology
Charmet, Romain R; Duffy, Seamus S; Keshavarzi, Sareh S; Gyorgy, Beata B; Marre, Michel M; Rossing, Peter P; McKnight, Amy Jayne AJ; Maxwell, Alexander P AP; Ahluwalia, Tarun Veer Singh TVS; Paterson, Andrew D AD; Trégouët, David-Alexandre DA; Hadjadj, Samy S
Publication Date: 2018-04-25

Variant appearance in text: rs7528419
PubMed Link: 29695241
Variant Present in the following documents:
  • Main text
  • 12933_2018_Article_705.pdf
View BVdb publication page



Genetic variants in mRNA untranslated regions.

Wiley Interdisciplinary Reviews. Rna
Steri, Maristella M; Idda, M Laura ML; Whalen, Michael B MB; Orrù, Valeria V
Publication Date: 2018-07

Variant appearance in text: rs7528419
PubMed Link: 29582564
Variant Present in the following documents:
  • Main text
View BVdb publication page



Mendelian Randomization Analysis Identifies CpG Sites as Putative Mediators for Genetic Influences on Cardiovascular Disease Risk.

American Journal Of Human Genetics
Richardson, Tom G TG; Zheng, Jie J; Davey Smith, George G; Timpson, Nicholas J NJ; Gaunt, Tom R TR; Relton, Caroline L CL; Hemani, Gibran G
Publication Date: 2017-10-05

Variant appearance in text: rs7528419
PubMed Link: 28985495
Variant Present in the following documents:
  • Main text
  • mmc3.pdf
  • main.pdf
View BVdb publication page



Bayesian association scan reveals loci associated with human lifespan and linked biomarkers.

Nature Communications
McDaid, Aaron F AF; Joshi, Peter K PK; Porcu, Eleonora E; Komljenovic, Andrea A; Li, Hao H; Sorrentino, Vincenzo V; Litovchenko, Maria M; Bevers, Roel P J RPJ; Rüeger, Sina S; Reymond, Alexandre A; Bochud, Murielle M; Deplancke, Bart B; Williams, Robert W RW; Robinson-Rechavi, Marc M; Paccaud, Fred F; Rousson, Valentin V; Auwerx, Johan J; Wilson, James F JF; Kutalik, Zoltán Z
Publication Date: 2017-07-27

Variant appearance in text: rs7528419
PubMed Link: 28748955
Variant Present in the following documents:
  • Main text
View BVdb publication page



Common and rare genetic markers of lipid variation in subjects with type 2 diabetes from the ACCORD clinical trial.

Peerj
Marvel, Skylar W SW; Rotroff, Daniel M DM; Wagner, Michael J MJ; Buse, John B JB; Havener, Tammy M TM; McLeod, Howard L HL; Motsinger-Reif, Alison A AA; ,
Publication Date: 2017

Variant appearance in text: rs7528419
PubMed Link: 28480134
Variant Present in the following documents:
  • Main text
  • peerj-05-3187.pdf
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Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease.

Journal Of The American College Of Cardiology
Webb, Thomas R TR; Erdmann, Jeanette J; Stirrups, Kathleen E KE; Stitziel, Nathan O NO; Masca, Nicholas G D NG; Jansen, Henning H; Kanoni, Stavroula S; Nelson, Christopher P CP; Ferrario, Paola G PG; König, Inke R IR; Eicher, John D JD; Johnson, Andrew D AD; Hamby, Stephen E SE; Betsholtz, Christer C; Ruusalepp, Arno A; Franzén, Oscar O; Schadt, Eric E EE; Björkegren, Johan L M JL; Weeke, Peter E PE; Auer, Paul L PL; Schick, Ursula M UM; Lu, Yingchang Y; Zhang, He H; Dube, Marie-Pierre MP; Goel, Anuj A; Farrall, Martin M; Peloso, Gina M GM; Won, Hong-Hee HH; Do, Ron R; van Iperen, Erik E; Kruppa, Jochen J; Mahajan, Anubha A; Scott, Robert A RA; Willenborg, Christina C; Braund, Peter S PS; van Capelleveen, Julian C JC; Doney, Alex S F AS; Donnelly, Louise A LA; Asselta, Rosanna R; Merlini, Pier A PA; Duga, Stefano S; Marziliano, Nicola N; Denny, Josh C JC; Shaffer, Christian C; El-Mokhtari, Nour Eddine NE; Franke, Andre A; Heilmann, Stefanie S; Hengstenberg, Christian C; Hoffmann, Per P; Holmen, Oddgeir L OL; Hveem, Kristian K; Jansson, Jan-Håkan JH; Jöckel, Karl-Heinz KH; Kessler, Thorsten T; Kriebel, Jennifer J; Laugwitz, Karl L KL; Marouli, Eirini E; Martinelli, Nicola N; McCarthy, Mark I MI; Van Zuydam, Natalie R NR; Meisinger, Christa C; Esko, Tõnu T; Mihailov, Evelin E; Escher, Stefan A SA; Alver, Maris M; Moebus, Susanne S; Morris, Andrew D AD; Virtamo, Jarma J; Nikpay, Majid M; Olivieri, Oliviero O; Provost, Sylvie S; AlQarawi, Alaa A; Robertson, Neil R NR; Akinsansya, Karen O KO; Reilly, Dermot F DF; Vogt, Thomas F TF; Yin, Wu W; Asselbergs, Folkert W FW; Kooperberg, Charles C; Jackson, Rebecca D RD; Stahl, Eli E; Müller-Nurasyid, Martina M; Strauch, Konstantin K; Varga, Tibor V TV; Waldenberger, Melanie M; , ; Zeng, Lingyao L; Chowdhury, Rajiv R; Salomaa, Veikko V; Ford, Ian I; Jukema, J Wouter JW; Amouyel, Philippe P; Kontto, Jukka J; , ; Nordestgaard, Børge G BG; Ferrières, Jean J; Saleheen, Danish D; Sattar, Naveed N; Surendran, Praveen P; Wagner, Aline A; Young, Robin R; Howson, Joanna M M JM; Butterworth, Adam S AS; Danesh, John J; Ardissino, Diego D; Bottinger, Erwin P EP; Erbel, Raimund R; Franks, Paul W PW; Girelli, Domenico D; Hall, Alistair S AS; Hovingh, G Kees GK; Kastrati, Adnan A; Lieb, Wolfgang W; Meitinger, Thomas T; Kraus, William E WE; Shah, Svati H SH; McPherson, Ruth R; Orho-Melander, Marju M; Melander, Olle O; Metspalu, Andres A; Palmer, Colin N A CN; Peters, Annette A; Rader, Daniel J DJ; Reilly, Muredach P MP; Loos, Ruth J F RJ; Reiner, Alex P AP; Roden, Dan M DM; Tardif, Jean-Claude JC; Thompson, John R JR; Wareham, Nicholas J NJ; Watkins, Hugh H; Willer, Cristen J CJ; Samani, Nilesh J NJ; Schunkert, Heribert H; Deloukas, Panos P; Kathiresan, Sekar S; ,
Publication Date: 2017-02-21

Variant appearance in text: rs7528419
PubMed Link: 28209224
Variant Present in the following documents:
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The Genetic Architecture of Coronary Artery Disease: Current Knowledge and Future Opportunities.

Current Atherosclerosis Reports
Hartiala, Jaana J; Schwartzman, William S WS; Gabbay, Julian J; Ghazalpour, Anatole A; Bennett, Brian J BJ; Allayee, Hooman H
Publication Date: 2017-02

Variant appearance in text: rs7528419
PubMed Link: 28130654
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  • Main text
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Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies.

Genome Biology
Joehanes, Roby R; Zhang, Xiaoling X; Huan, Tianxiao T; Yao, Chen C; Ying, Sai-Xia SX; Nguyen, Quang Tri QT; Demirkale, Cumhur Yusuf CY; Feolo, Michael L ML; Sharopova, Nataliya R NR; Sturcke, Anne A; Schäffer, Alejandro A AA; Heard-Costa, Nancy N; Chen, Han H; Liu, Po-Ching PC; Wang, Richard R; Woodhouse, Kimberly A KA; Tanriverdi, Kahraman K; Freedman, Jane E JE; Raghavachari, Nalini N; Dupuis, Josée J; Johnson, Andrew D AD; O'Donnell, Christopher J CJ; Levy, Daniel D; Munson, Peter J PJ
Publication Date: 2017-01-25

Variant appearance in text: rs7528419
PubMed Link: 28122634
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  • Main text
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Meta-Analysis of Genome-Wide Association Studies for Abdominal Aortic Aneurysm Identifies Four New Disease-Specific Risk Loci.

Circulation Research
Jones, Gregory T GT; Tromp, Gerard G; Kuivaniemi, Helena H; Gretarsdottir, Solveig S; Baas, Annette F AF; Giusti, Betti B; Strauss, Ewa E; Van't Hof, Femke N G FN; Webb, Thomas R TR; Erdman, Robert R; Ritchie, Marylyn D MD; Elmore, James R JR; Verma, Anurag A; Pendergrass, Sarah S; Kullo, Iftikhar J IJ; Ye, Zi Z; Peissig, Peggy L PL; Gottesman, Omri O; Verma, Shefali S SS; Malinowski, Jennifer J; Rasmussen-Torvik, Laura J LJ; Borthwick, Kenneth M KM; Smelser, Diane T DT; Crosslin, David R DR; de Andrade, Mariza M; Ryer, Evan J EJ; McCarty, Catherine A CA; Böttinger, Erwin P EP; Pacheco, Jennifer A JA; Crawford, Dana C DC; Carrell, David S DS; Gerhard, Glenn S GS; Franklin, David P DP; Carey, David J DJ; Phillips, Victoria L VL; Williams, Michael J A MJ; Wei, Wenhua W; Blair, Ross R; Hill, Andrew A AA; Vasudevan, Thodor M TM; Lewis, David R DR; Thomson, Ian A IA; Krysa, Jo J; Hill, Geraldine B GB; Roake, Justin J; Merriman, Tony R TR; Oszkinis, Grzegorz G; Galora, Silvia S; Saracini, Claudia C; Abbate, Rosanna R; Pulli, Raffaele R; Pratesi, Carlo C; Saratzis, Athanasios A; Verissimo, Ana R AR; Bumpstead, Suzannah S; Badger, Stephen A SA; Clough, Rachel E RE; Cockerill, Gillian G; Hafez, Hany H; Scott, D Julian A DJ; Futers, T Simon TS; Romaine, Simon P R SP; Bridge, Katherine K; Griffin, Kathryn J KJ; Bailey, Marc A MA; Smith, Alberto A; Thompson, Matthew M MM; van Bockxmeer, Frank M FM; Matthiasson, Stefan E SE; Thorleifsson, Gudmar G; Thorsteinsdottir, Unnur U; Blankensteijn, Jan D JD; Teijink, Joep A W JA; Wijmenga, Cisca C; de Graaf, Jacqueline J; Kiemeney, Lambertus A LA; Lindholt, Jes S JS; Hughes, Anne A; Bradley, Declan T DT; Stirrups, Kathleen K; Golledge, Jonathan J; Norman, Paul E PE; Powell, Janet T JT; Humphries, Steve E SE; Hamby, Stephen E SE; Goodall, Alison H AH; Nelson, Christopher P CP; Sakalihasan, Natzi N; Courtois, Audrey A; Ferrell, Robert E RE; Eriksson, Per P; Folkersen, Lasse L; Franco-Cereceda, Anders A; Eicher, John D JD; Johnson, Andrew D AD; Betsholtz, Christer C; Ruusalepp, Arno A; Franzén, Oscar O; Schadt, Eric E EE; Björkegren, Johan L M JL; Lipovich, Leonard L; Drolet, Anne M AM; Verhoeven, Eric L EL; Zeebregts, Clark J CJ; Geelkerken, Robert H RH; van Sambeek, Marc R MR; van Sterkenburg, Steven M SM; de Vries, Jean-Paul JP; Stefansson, Kari K; Thompson, John R JR; de Bakker, Paul I W PI; Deloukas, Panos P; Sayers, Robert D RD; Harrison, Seamus C SC; van Rij, Andre M AM; Samani, Nilesh J NJ; Bown, Matthew J MJ
Publication Date: 2017-01-20

Variant appearance in text: rs7528419
PubMed Link: 27899403
Variant Present in the following documents:
  • res-120-341-s002.pdf
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Common Genetic Polymorphisms Influence Blood Biomarker Measurements in COPD.

Plos Genetics
Sun, Wei W; Kechris, Katerina K; Jacobson, Sean S; Drummond, M Bradley MB; Hawkins, Gregory A GA; Yang, Jenny J; Chen, Ting-Huei TH; Quibrera, Pedro Miguel PM; Anderson, Wayne W; Barr, R Graham RG; Basta, Patricia V PV; Bleecker, Eugene R ER; Beaty, Terri T; Casaburi, Richard R; Castaldi, Peter P; Cho, Michael H MH; Comellas, Alejandro A; Crapo, James D JD; Criner, Gerard G; Demeo, Dawn D; Christenson, Stephanie A SA; Couper, David J DJ; Curtis, Jeffrey L JL; Doerschuk, Claire M CM; Freeman, Christine M CM; Gouskova, Natalia A NA; Han, MeiLan K MK; Hanania, Nicola A NA; Hansel, Nadia N NN; Hersh, Craig P CP; Hoffman, Eric A EA; Kaner, Robert J RJ; Kanner, Richard E RE; Kleerup, Eric C EC; Lutz, Sharon S; Martinez, Fernando J FJ; Meyers, Deborah A DA; Peters, Stephen P SP; Regan, Elizabeth A EA; Rennard, Stephen I SI; Scholand, Mary Beth MB; Silverman, Edwin K EK; Woodruff, Prescott G PG; O'Neal, Wanda K WK; Bowler, Russell P RP; , ; ,
Publication Date: 2016-08

Variant appearance in text: rs7528419
PubMed Link: 27532455
Variant Present in the following documents:
  • Main text
  • pgen.1006011.pdf
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Efficient Integrative Multi-SNP Association Analysis via Deterministic Approximation of Posteriors.

American Journal Of Human Genetics
Wen, Xiaoquan X; Lee, Yeji Y; Luca, Francesca F; Pique-Regi, Roger R
Publication Date: 2016-06-02

Variant appearance in text: rs7528419
PubMed Link: 27236919
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  • Main text
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From Loci to Biology: Functional Genomics of Genome-Wide Association for Coronary Disease.

Circulation Research
Nurnberg, Sylvia T ST; Zhang, Hanrui H; Hand, Nicholas J NJ; Bauer, Robert C RC; Saleheen, Danish D; Reilly, Muredach P MP; Rader, Daniel J DJ
Publication Date: 2016-02-19

Variant appearance in text: rs7528419
PubMed Link: 26892960
Variant Present in the following documents:
  • Main text
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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: rs7528419
PubMed Link: 26780889
Variant Present in the following documents:
  • Main text
  • srep19429-s1.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: rs7528419
PubMed Link: 25944692
Variant Present in the following documents:
  • oncotarget-06-15375-s005.xlsx, sheet 2
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A multivariate genome-wide association analysis of 10 LDL subfractions, and their response to statin treatment, in 1868 Caucasians.

Plos One
Shim, Heejung H; Chasman, Daniel I DI; Smith, Joshua D JD; Mora, Samia S; Ridker, Paul M PM; Nickerson, Deborah A DA; Krauss, Ronald M RM; Stephens, Matthew M
Publication Date: 2015

Variant appearance in text: rs7528419
PubMed Link: 25898129
Variant Present in the following documents:
  • Main text
  • pone.0120758.pdf
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Strategies to fine-map genetic associations with lipid levels by combining epigenomic annotations and liver-specific transcription profiles.

Genomics
Lo, Ken Sin KS; Vadlamudi, Swarooparani S; Fogarty, Marie P MP; Mohlke, Karen L KL; Lettre, Guillaume G
Publication Date: 2014-08

Variant appearance in text: rs7528419
PubMed Link: 24997396
Variant Present in the following documents:
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An association study between genetic polymorphisms related to lipoprotein-associated phospholipase A(2) and coronary heart disease.

Experimental And Therapeutic Medicine
Xu, Limin L; Zhou, Jianqing J; Huang, Stephanie S; Huang, Yi Y; LE, Yanping Y; Jiang, Danjie D; Wang, Feiming F; Yang, Xi X; Xu, Weifeng W; Huang, Xiaoyan X; Dong, Changzheng C; Zhang, Lina L; Ye, Meng M; Lian, Jiangfang J; Duan, Shiwei S
Publication Date: 2013-03

Variant appearance in text: rs7528419
PubMed Link: 23404648
Variant Present in the following documents:
  • Main text
  • etm-05-03-0742.pdf
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Multi-ethnic analysis of lipid-associated loci: the NHLBI CARe project.

Plos One
Musunuru, Kiran K; Romaine, Simon P R SP; Lettre, Guillaume G; Wilson, James G JG; Volcik, Kelly A KA; Tsai, Michael Y MY; Taylor, Herman A HA; Schreiner, Pamela J PJ; Rotter, Jerome I JI; Rich, Stephen S SS; Redline, Susan S; Psaty, Bruce M BM; Papanicolaou, George J GJ; Ordovas, Jose M JM; Liu, Kiang K; Krauss, Ronald M RM; Glazer, Nicole L NL; Gabriel, Stacey B SB; Fornage, Myriam M; Cupples, L Adrienne LA; Buxbaum, Sarah G SG; Boerwinkle, Eric E; Ballantyne, Christie M CM; Kathiresan, Sekar S; Rader, Daniel J DJ
Publication Date: 2012

Variant appearance in text: rs7528419
PubMed Link: 22629316
Variant Present in the following documents:
  • Main text
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