A citation-based method for searching scientific literature

Hayato Tada, Soichiro Usui, Kenji Sakata, Masayuki Takamura, Masa-Aki Kawashiri. J Atheroscler Thromb 2021
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.
Ron Do, Nathan O Stitziel, Hong-Hee Won, Anders Berg Jørgensen, Stefano Duga, Pier Angelica Merlini, Adam Kiezun, Martin Farrall, Anuj Goel, Or Zuk,[...]. Nature 2015
406
100

Genetics of Coronary Artery Disease.
Ruth McPherson, Anne Tybjaerg-Hansen. Circ Res 2016
161
100

ANGPTL3 Deficiency and Protection Against Coronary Artery Disease.
Nathan O Stitziel, Amit V Khera, Xiao Wang, Andrew J Bierhals, A Christina Vourakis, Alexandra E Sperry, Pradeep Natarajan, Derek Klarin, Connor A Emdin, Seyedeh M Zekavat,[...]. J Am Coll Cardiol 2017
200
100

Worldwide Prevalence of Familial Hypercholesterolemia: Meta-Analyses of 11 Million Subjects.
Sabina O Beheshti, Christian M Madsen, Anette Varbo, Børge G Nordestgaard. J Am Coll Cardiol 2020
77
100

PCSK9 R46L, low-density lipoprotein cholesterol levels, and risk of ischemic heart disease: 3 independent studies and meta-analyses.
Marianne Benn, Børge G Nordestgaard, Peer Grande, Peter Schnohr, Anne Tybjaerg-Hansen. J Am Coll Cardiol 2010
221
100

A catalog of the pathogenic mutations of LDL receptor gene in Japanese familial hypercholesterolemia.
Hayato Tada, Mika Hori, Akihiro Nomura, Kazuyoshi Hosomichi, Atsushi Nohara, Masa-Aki Kawashiri, Mariko Harada-Shiba. J Clin Lipidol 2020
6
100

70-year legacy of the Framingham Heart Study.
Charlotte Andersson, Andrew D Johnson, Emelia J Benjamin, Daniel Levy, Ramachandran S Vasan. Nat Rev Cardiol 2019
45
100

The Framingham Heart Study and the epidemiology of cardiovascular disease: a historical perspective.
Syed S Mahmood, Daniel Levy, Ramachandran S Vasan, Thomas J Wang. Lancet 2014
477
100

Clinical Diagnostic Criteria of Familial Hypercholesterolemia - A Comparison of the Japan Atherosclerosis Society and Dutch Lipid Clinic Network Criteria.
Hayato Tada, Hirofumi Okada, Akihiro Nomura, Soichiro Usui, Kenji Sakata, Atsushi Nohara, Masakazu Yamagishi, Masayuki Takamura, Masa-Aki Kawashiri. Circ J 2021
3
100

Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease.
Akihiro Nomura, Hong-Hee Won, Amit V Khera, Fumihiko Takeuchi, Kaoru Ito, Shane McCarthy, Connor A Emdin, Derek Klarin, Pradeep Natarajan, Seyedeh M Zekavat,[...]. Circ Res 2017
46
100

Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.
Valérie Turcot, Yingchang Lu, Heather M Highland, Claudia Schurmann, Anne E Justice, Rebecca S Fine, Jonathan P Bradfield, Tõnu Esko, Ayush Giri, Mariaelisa Graff,[...]. Nat Genet 2018
145
100

Rare Protein-Truncating Variants in APOB, Lower Low-Density Lipoprotein Cholesterol, and Protection Against Coronary Heart Disease.
Gina M Peloso, Akihiro Nomura, Amit V Khera, Mark Chaffin, Hong-Hee Won, Diego Ardissino, John Danesh, Heribert Schunkert, James G Wilson, Nilesh Samani,[...]. Circ Genom Precis Med 2019
27
100

Left ventricular noncompaction cardiomyopathy: Recent update on genetics, usefulness of biomarker, and speckle imaging.
Tauseef Akhtar, Dhrubajyoti Bandyopadhyay, Raktim K Ghosh, Samhati Mondal. J Cardiol 2019
1
100

Genetics of human cardiovascular disease.
Sekar Kathiresan, Deepak Srivastava. Cell 2012
244
100

Rare and Deleterious Mutations in ABCG5/ABCG8 Genes Contribute to Mimicking and Worsening of Familial Hypercholesterolemia Phenotype.
Hayato Tada, Hirofumi Okada, Akihiro Nomura, Satoshi Yashiro, Atsushi Nohara, Yasushi Ishigaki, Masayuki Takamura, Masa-Aki Kawashiri. Circ J 2019
32
100

Usefulness of cardiovascular family history data for population-based preventive medicine and medical research (the Health Family Tree Study and the NHLBI Family Heart Study).
R R Williams, S C Hunt, G Heiss, M A Province, J T Bensen, M Higgins, R M Chamberlain, J Ware, P N Hopkins. Am J Cardiol 2001
181
100

Polygenic Risk Score Identifies Subgroup With Higher Burden of Atherosclerosis and Greater Relative Benefit From Statin Therapy in the Primary Prevention Setting.
Pradeep Natarajan, Robin Young, Nathan O Stitziel, Sandosh Padmanabhan, Usman Baber, Roxana Mehran, Samantha Sartori, Valentin Fuster, Dermot F Reilly, Adam Butterworth,[...]. Circulation 2017
201
100


Association of Rare and Common Variation in the Lipoprotein Lipase Gene With Coronary Artery Disease.
Amit V Khera, Hong-Hee Won, Gina M Peloso, Colm O'Dushlaine, Dajiang Liu, Nathan O Stitziel, Pradeep Natarajan, Akihiro Nomura, Connor A Emdin, Namrata Gupta,[...]. JAMA 2017
98
100

Loss-of-function mutations in APOC3, triglycerides, and coronary disease.
Jacy Crosby, Gina M Peloso, Paul L Auer, David R Crosslin, Nathan O Stitziel, Leslie A Lange, Yingchang Lu, Zheng-zheng Tang, He Zhang, George Hindy,[...]. N Engl J Med 2014
650
100

A trafficking-deficient KCNQ1 mutation, T587M, causes a severe phenotype of long QT syndrome by interfering with intracellular hERG transport.
Jie Wu, Tomoko Sakaguchi, Kotoe Takenaka, Futoshi Toyoda, Keiko Tsuji, Hiroshi Matsuura, Minoru Horie. J Cardiol 2019
6
100

Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease.
Satoshi Koyama, Kaoru Ito, Chikashi Terao, Masato Akiyama, Momoko Horikoshi, Yukihide Momozawa, Hiroshi Matsunaga, Hirotaka Ieki, Kouichi Ozaki, Yoshihiro Onouchi,[...]. Nat Genet 2020
27
100

Familial Hypercholesterolemia: A Narrative Review on Diagnosis and Management Strategies for Children and Adolescents.
Hayato Tada, Masayuki Takamura, Masa-Aki Kawashiri. Vasc Health Risk Manag 2021
2
100

Genetic variants associated with Lp(a) lipoprotein level and coronary disease.
Robert Clarke, John F Peden, Jemma C Hopewell, Theodosios Kyriakou, Anuj Goel, Simon C Heath, Sarah Parish, Simona Barlera, Maria Grazia Franzosi, Stephan Rust,[...]. N Engl J Med 2009
822
100

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
Amit V Khera, Mark Chaffin, Krishna G Aragam, Mary E Haas, Carolina Roselli, Seung Hoan Choi, Pradeep Natarajan, Eric S Lander, Steven A Lubitz, Patrick T Ellinor,[...]. Nat Genet 2018
838
100

Risk prediction by genetic risk scores for coronary heart disease is independent of self-reported family history.
Hayato Tada, Olle Melander, Judy Z Louie, Joseph J Catanese, Charles M Rowland, James J Devlin, Sekar Kathiresan, Dov Shiffman. Eur Heart J 2016
134
100

Acute myocardial infarction in a 25-year-old woman with sitosterolemia.
Ryuki Kawamura, Hitoshi Saiki, Hayato Tada, Akihiro Hata. J Clin Lipidol 2018
14
100

Twelve-single nucleotide polymorphism genetic risk score identifies individuals at increased risk for future atrial fibrillation and stroke.
Hayato Tada, Dov Shiffman, J Gustav Smith, Marketa Sjögren, Steven A Lubitz, Patrick T Ellinor, Judy Z Louie, Joseph J Catanese, Gunnar Engström, James J Devlin,[...]. Stroke 2014
72
100

Fifteen new risk loci for coronary artery disease highlight arterial-wall-specific mechanisms.
Joanna M M Howson, Wei Zhao, Daniel R Barnes, Weang-Kee Ho, Robin Young, Dirk S Paul, Lindsay L Waite, Daniel F Freitag, Eric B Fauman, Elias L Salfati,[...]. Nat Genet 2017
152
100

Japan Atherosclerosis Society (JAS) Guidelines for Prevention of Atherosclerotic Cardiovascular Diseases 2017.
Makoto Kinoshita, Koutaro Yokote, Hidenori Arai, Mami Iida, Yasushi Ishigaki, Shun Ishibashi, Seiji Umemoto, Genshi Egusa, Hirotoshi Ohmura, Tomonori Okamura,[...]. J Atheroscler Thromb 2018
265
100

Personalized medicine for cardiovascular diseases.
Hayato Tada, Noboru Fujino, Akihiro Nomura, Chiaki Nakanishi, Kenshi Hayashi, Masayuki Takamura, Masa-Aki Kawashiri. J Hum Genet 2021
3
100

Characterization of noncoding regulatory DNA in the human genome.
Ran Elkon, Reuven Agami. Nat Biotechnol 2017
45
100

Comparison of novel risk markers for improvement in cardiovascular risk assessment in intermediate-risk individuals.
Joseph Yeboah, Robyn L McClelland, Tamar S Polonsky, Gregory L Burke, Christopher T Sibley, Daniel O'Leary, Jeffery J Carr, David C Goff, Philip Greenland, David M Herrington. JAMA 2012
678
100


Genetic analysis in UK Biobank links insulin resistance and transendothelial migration pathways to coronary artery disease.
Derek Klarin, Qiuyu Martin Zhu, Connor A Emdin, Mark Chaffin, Steven Horner, Brian J McMillan, Alison Leed, Michael E Weale, Chris C A Spencer, François Aguet,[...]. Nat Genet 2017
107
100

Genetic Variations, Triglycerides, and Atherosclerotic Disease.
Hayato Tada, Masa-Aki Kawashiri. J Atheroscler Thromb 2019
9
100

Inactivating mutations in NPC1L1 and protection from coronary heart disease.
Nathan O Stitziel, Hong-Hee Won, Alanna C Morrison, Gina M Peloso, Ron Do, Leslie A Lange, Pierre Fontanillas, Namrata Gupta, Stefano Duga, Anuj Goel,[...]. N Engl J Med 2014
284
100

Parental cardiovascular disease as a risk factor for cardiovascular disease in middle-aged adults: a prospective study of parents and offspring.
Donald M Lloyd-Jones, Byung-Ho Nam, Ralph B D'Agostino, Daniel Levy, Joanne M Murabito, Thomas J Wang, Peter W F Wilson, Christopher J O'Donnell. JAMA 2004
450
100

Heritability of death from coronary heart disease: a 36-year follow-up of 20 966 Swedish twins.
S Zdravkovic, A Wienke, N L Pedersen, M E Marenberg, A I Yashin, U De Faire. J Intern Med 2002
262
100

Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity.
Danish Saleheen, Pradeep Natarajan, Irina M Armean, Wei Zhao, Asif Rasheed, Sumeet A Khetarpal, Hong-Hee Won, Konrad J Karczewski, Anne H O'Donnell-Luria, Kaitlin E Samocha,[...]. Nature 2017
166
100

A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses.
Samuli Ripatti, Emmi Tikkanen, Marju Orho-Melander, Aki S Havulinna, Kaisa Silander, Amitabh Sharma, Candace Guiducci, Markus Perola, Antti Jula, Juha Sinisalo,[...]. Lancet 2010
372
100

Genetics of Common, Complex Coronary Artery Disease.
Kiran Musunuru, Sekar Kathiresan. Cell 2019
67
100

Extreme Contrast of Postprandial Remnant-Like Particles Formed in Abetalipoproteinemia and Homozygous Familial Hypobetalipoproteinemia.
Masa-Aki Kawashiri, Hayato Tada, Marowa Hashimoto, Matsuo Taniyama, Takamitsu Nakano, Katsuyuki Nakajima, Takeshi Inoue, Mika Mori, Chiaki Nakanishi, Tetsuo Konno,[...]. JIMD Rep 2015
7
100



Post-prandial Remnant Lipoprotein Metabolism in Sitosterolemia.
Hayato Tada, Akihiro Nomura, Atsushi Nohara, Akihiro Inazu, Hiroshi Mabuchi, Masakazu Yamagishi, Masa-Aki Kawashiri. J Atheroscler Thromb 2018
6
100

Genetic risk, coronary heart disease events, and the clinical benefit of statin therapy: an analysis of primary and secondary prevention trials.
J L Mega, N O Stitziel, J G Smith, D I Chasman, M Caulfield, J J Devlin, F Nordio, C Hyde, C P Cannon, F Sacks,[...]. Lancet 2015
322
100

Validation of a Genome-Wide Polygenic Score for Coronary Artery Disease in South Asians.
Minxian Wang, Ramesh Menon, Sanghamitra Mishra, Aniruddh P Patel, Mark Chaffin, Deepak Tanneeru, Manjari Deshmukh, Oshin Mathew, Sanika Apte, Christina S Devanboo,[...]. J Am Coll Cardiol 2020
13
100

Prognostic impact of cascade screening for familial hypercholesterolemia on cardiovascular events.
Hayato Tada, Hirofumi Okada, Akihiro Nomura, Atsushi Nohara, Masakazu Yamagishi, Masayuki Takamura, Masa-Aki Kawashiri. J Clin Lipidol 2021
5
100

Low-Density Lipoprotein Cholesterol Level cannot be too Low: Considerations from Clinical Trials, Human Genetics, and Biology.
Hayato Tada, Soichiro Usui, Kenji Sakata, Masayuki Takamura, Masa-Aki Kawashiri. J Atheroscler Thromb 2020
6
100


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.