A citation-based method for searching scientific literature

Eduardo Mundstock, Edgar E Sarria, Helen Zatti, Fernanda Mattos Louzada, Lucas Kich Grun, Marcus Herbert Jones, Fátima T C R Guma, João Mazzola In Memoriam, Matias Epifanio, Renato T Stein, Florencia M Barbé-Tuana, Rita Mattiello. Obesity (Silver Spring) 2015
Times Cited: 98







List of co-cited articles
822 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


FBN1: The disease-causing gene for Marfan syndrome and other genetic disorders.
Lynn Y Sakai, Douglas R Keene, Marjolijn Renard, Julie De Backer. Gene 2016
92
1

The genetics of alcohol dependence.
Danielle M Dick, Laura J Bierut. Curr Psychiatry Rep 2006
91
1

The impact of epigenetics on cardiovascular disease.
Dimple Prasher, Steven C Greenway, Raja B Singh. Biochem Cell Biol 2020
18
5


Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters.
K E Berge, H Tian, G A Graf, L Yu, N V Grishin, J Schultz, P Kwiterovich, B Shan, R Barnes, H H Hobbs. Science 2000
1

miRNAs at the heart of the matter.
Zhiguo Wang, Xioabin Luo, Yanjie Lu, Baofeng Yang. J Mol Med (Berl) 2008
63
1

Genetics of Familial Hypercholesterolemia: New Insights.
Michal Vrablik, Lukas Tichý, Tomas Freiberger, Vladimir Blaha, Martin Satny, Jaroslav A Hubacek. Front Genet 2020
2
50

Profiling of circulating microRNAs: from single biomarkers to re-wired networks.
Anna Zampetaki, Peter Willeit, Ignat Drozdov, Stefan Kiechl, Manuel Mayr. Cardiovasc Res 2012
184
1

Multiple distinct risk loci for nicotine dependence identified by dense coverage of the complete family of nicotinic receptor subunit (CHRN) genes.
Nancy L Saccone, Scott F Saccone, Anthony L Hinrichs, Jerry A Stitzel, Weimin Duan, Michele L Pergadia, Arpana Agrawal, Naomi Breslau, Richard A Grucza, Dorothy Hatsukami,[...]. Am J Med Genet B Neuropsychiatr Genet 2009
168
1

Histone methylation and transcriptional regulation in cardiovascular disease.
Yong Xu, Fei Fang. Cardiovasc Hematol Disord Drug Targets 2014
3
33

Sixty-five common genetic variants and prediction of type 2 diabetes.
Philippa J Talmud, Jackie A Cooper, Richard W Morris, Frank Dudbridge, Tina Shah, Jorgen Engmann, Caroline Dale, Jon White, Stela McLachlan, Delilah Zabaneh,[...]. Diabetes 2015
61
1

Sortilin: A novel regulator in lipid metabolism and atherogenesis.
Li-Yuan Zhong, Francisco S Cayabyab, Chao-Ke Tang, Xi-Long Zheng, Tian-Hong Peng, Yun-Cheng Lv. Clin Chim Acta 2016
19
5

Analysis of circulating miRNAs in patients with familial hypercholesterolaemia treated by LDL/Lp(a) apheresis.
Dana Dlouha, Milan Blaha, Vladimir Blaha, Ilona Fatorova, Jaroslav A Hubacek, Petr Stavek, Vera Lanska, Alena Parikova, Jan Pitha. Atheroscler Suppl 2017
8
12

The Role of MicroRNAs in Myocardial Infarction: From Molecular Mechanism to Clinical Application.
Teng Sun, Yan-Han Dong, Wei Du, Chun-Ying Shi, Kun Wang, Muhammad-Akram Tariq, Jian-Xun Wang, Pei-Feng Li. Int J Mol Sci 2017
83
1



The FTO gene polymorphism is associated with end-stage renal disease: two large independent case-control studies in a general population.
Jaroslav A Hubacek, Ondrej Viklicky, Dana Dlouha, Silvie Bloudickova, Ruzena Kubinova, Anne Peasey, Hynek Pikhart, Vera Adamkova, Irena Brabcova, Eva Pokorna,[...]. Nephrol Dial Transplant 2012
32
3

Genetic Risk Scores.
Robert P Igo, Tyler G Kinzy, Jessica N Cooke Bailey. Curr Protoc Hum Genet 2019
5
20

The era of clinical application of gene diagnosis in cardiovascular diseases is coming.
Yu-Bao Zou, Ru-Tai Hui, Lei Song. Chronic Dis Transl Med 2020
1
100

Distribution of the alcohol dehydrogenase ADH1B*47His allele in Eurasia.
Svetlana Borinskaya, Nina Kal'ina, Andrey Marusin, Gulnaz Faskhutdinova, Irina Morozova, Ildus Kutuev, Vladimir Koshechkin, Elza Khusnutdinova, Vadim Stepanov, Valery Puzyrev,[...]. Am J Hum Genet 2009
14
7

MicroRNA-146a Induces Lineage-Negative Bone Marrow Cell Apoptosis and Senescence by Targeting Polo-Like Kinase 2 Expression.
Shanming Deng, Huilan Wang, Chunling Jia, Shoukang Zhu, Xianming Chu, Qi Ma, Jianqin Wei, Emily Chen, Wei Zhu, Conrad J Macon,[...]. Arterioscler Thromb Vasc Biol 2017
23
4

Personalized risk prediction for type 2 diabetes: the potential of genetic risk scores.
Kristi Läll, Reedik Mägi, Andrew Morris, Andres Metspalu, Krista Fischer. Genet Med 2017
49
2

Genomics in Personalized Nutrition: Can You "Eat for Your Genes"?
Veronica A Mullins, William Bresette, Laurel Johnstone, Brian Hallmark, Floyd H Chilton. Nutrients 2020
7
14

Sortilin as a regulator of lipoprotein metabolism.
Alanna Strong, Daniel J Rader. Curr Atheroscler Rep 2012
28
3


Statin-associated myopathy: from genetic predisposition to clinical management.
M Vrablik, L Zlatohlavek, T Stulc, V Adamkova, M Prusikova, L Schwarzova, J A Hubacek, R Ceska. Physiol Res 2014
37
2

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants.
Laura J Scott, Karen L Mohlke, Lori L Bonnycastle, Cristen J Willer, Yun Li, William L Duren, Michael R Erdos, Heather M Stringham, Peter S Chines, Anne U Jackson,[...]. Science 2007
1

Discordance of DNA methylation variance between two accessible human tissues.
Ruiwei Jiang, Meaghan J Jones, Edith Chen, Sarah M Neumann, Hunter B Fraser, Gregory E Miller, Michael S Kobor. Sci Rep 2015
40
2


Role of Personalized Nutrition in Chronic-Degenerative Diseases.
Laura Di Renzo, Paola Gualtieri, Lorenzo Romano, Giulia Marrone, Annalisa Noce, Alberto Pujia, Marco Alfonso Perrone, Vincenzo Aiello, Carmela Colica, Antonino De Lorenzo. Nutrients 2019
26
3

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels.
Richa Saxena, Benjamin F Voight, Valeriya Lyssenko, Noël P Burtt, Paul I W de Bakker, Hong Chen, Jeffrey J Roix, Sekar Kathiresan, Joel N Hirschhorn, Mark J Daly,[...]. Science 2007
1

The Gene Score for Predicting Hypertriglyceridemia: New Insights from a Czech Case-Control Study.
Jaroslav A Hubacek, Dana Dlouha, Vera Adamkova, Lucie Schwarzova, Vera Lanska, Richard Ceska, Martin Satny, Michal Vrablik. Mol Diagn Ther 2019
5
20

Marginal role for 53 common genetic variants in cardiovascular disease prediction.
Richard W Morris, Jackie A Cooper, Tina Shah, Andrew Wong, Fotios Drenos, Jorgen Engmann, Stela McLachlan, Barbara Jefferis, Caroline Dale, Rebecca Hardy,[...]. Heart 2016
19
5

Familial Hypercholesterolemia: New Horizons for Diagnosis and Effective Management.
Maria Mytilinaiou, Ioannis Kyrou, Mike Khan, Dimitris K Grammatopoulos, Harpal S Randeva. Front Pharmacol 2018
14
7

Non-coding RNAs as regulators of gene expression and epigenetics.
Minna U Kaikkonen, Michael T Y Lam, Christopher K Glass. Cardiovasc Res 2011
276
1

The association between the FTO gene variant and alcohol consumption and binge and problem drinking in different gene-environment background: The HAPIEE study.
Jaroslav A Hubacek, Hynek Pikhart, Anne Peasey, Sofia Malyutina, Andrzej Pajak, Abdonas Tamosiunas, Mikhail Voevoda, Michael V Holmes, Martin Bobak. Gene 2019
2
50


The obesity-associated Fto gene is a transcriptional coactivator.
Qiong Wu, Rudel A Saunders, Maria Szkudlarek-Mikho, Ivana de la Serna, Khew-Voon Chin. Biochem Biophys Res Commun 2010
65
1


Genomewide association analysis of coronary artery disease.
Nilesh J Samani, Jeanette Erdmann, Alistair S Hall, Christian Hengstenberg, Massimo Mangino, Bjoern Mayer, Richard J Dixon, Thomas Meitinger, Peter Braund, H-Erich Wichmann,[...]. N Engl J Med 2007
1

Whole-Genome Sequencing to Characterize Monogenic and Polygenic Contributions in Patients Hospitalized With Early-Onset Myocardial Infarction.
Amit V Khera, Mark Chaffin, Seyedeh M Zekavat, Ryan L Collins, Carolina Roselli, Pradeep Natarajan, Judith H Lichtman, Gail D'Onofrio, Jennifer Mattera, Rachel Dreyer,[...]. Circulation 2019
78
1

Dietary Intervention Modifies DNA Methylation Age Assessed by the Epigenetic Clock.
Chanachai Sae-Lee, Sarah Corsi, Timothy M Barrow, Gunter G C Kuhnle, Valentina Bollati, John C Mathers, Hyang-Min Byun. Mol Nutr Food Res 2018
25
4

Sugar-sweetened beverage intake, chromosome 9p21 variants, and risk of myocardial infarction in Hispanics.
Yan Zheng, Yanping Li, Tao Huang, Han-Ling Cheng, Hannia Campos, Lu Qi. Am J Clin Nutr 2016
17
5

Risk of Premature Atherosclerotic Disease in Patients With Monogenic Versus Polygenic Familial Hypercholesterolemia.
Mark Trinder, Xuan Li, Maria Liza DeCastro, Luba Cermakova, Singh Sadananda, Linda M Jackson, Hawmid Azizi, G B John Mancini, Gordon A Francis, Jiri Frohlich,[...]. J Am Coll Cardiol 2019
41
2

Towards clinical utility of polygenic risk scores.
Samuel A Lambert, Gad Abraham, Michael Inouye. Hum Mol Genet 2019
82
1

Polymorphisms in CYP-7A1, not APOE, influence the change in plasma lipids in response to population dietary change in an 8 year follow-up; results from the Czech MONICA study.
Jaroslav A Hubacek, Jan Pitha, Zdena Skodová, Rudolf Poledne, Vera Lánská, Dawn M Waterworth, Steve E Humphries, Philippa J Talmud. Clin Biochem 2003
33
3

A survey of 246 suggested coronary risk factors.
P N Hopkins, R R Williams. Atherosclerosis 1981
239
1

Different prevalence of T2DM risk alleles in Roma population in comparison with the majority Czech population.
Jaroslav A Hubáček, Lenka Šedová, Věra Olišarová, Věra Adámková, Valérie Tóthová. Mol Genet Genomic Med 2020
3
33


Differential effect of the rs4149056 variant in SLCO1B1 on myopathy associated with simvastatin and atorvastatin.
L R Brunham, P J Lansberg, L Zhang, F Miao, C Carter, G K Hovingh, H Visscher, J W Jukema, A F Stalenhoef, C J D Ross,[...]. Pharmacogenomics J 2012
126
1


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.