A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Defining and setting national goals for cardiovascular health promotion and disease reduction: the American Heart Association's strategic Impact Goal through 2020 and beyond.
Donald M Lloyd-Jones, Yuling Hong, Darwin Labarthe, Dariush Mozaffarian, Lawrence J Appel, Linda Van Horn, Kurt Greenlund, Stephen Daniels, Graham Nichol, Gordon F Tomaselli,[...]. Circulation 2010
33

Points to consider in the reevaluation and reanalysis of genomic test results: a statement of the American College of Medical Genetics and Genomics (ACMG).
Joshua L Deignan, Wendy K Chung, Hutton M Kearney, Kristin G Monaghan, Catherine W Rehder, Elizabeth C Chao. Genet Med 2019
56
33

Advances in the treatment of hereditary transthyretin amyloidosis: A review.
Morie A Gertz, Michelle L Mauermann, Martha Grogan, Teresa Coelho. Brain Behav 2019
40
33

Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy.
Nadine Norton, Duanxiang Li, Mark J Rieder, Jill D Siegfried, Evadnie Rampersaud, Stephan Züchner, Steve Mangos, Jorge Gonzalez-Quintana, Libin Wang, Sean McGee,[...]. Am J Hum Genet 2011
246
33

Neptune: an environment for the delivery of genomic medicine.
Venner Eric, Victoria Yi, David Murdock, Sara E Kalla, Tsung-Jung Wu, Aniko Sabo, Shoudong Li, Qingchang Meng, Xia Tian, Mullai Murugan,[...]. Genet Med 2021
1
100

Determination of lipoprotein(a) kringle repeat number from genomic DNA: copy number variation genotyping using qPCR.
Matthew B Lanktree, Chandheeb Rajakumar, J Howard Brunt, Marlys L Koschinsky, Philip W Connelly, Robert A Hegele. J Lipid Res 2009
36
33

Coronary heart disease mortality in treated familial hypercholesterolaemia: Update of the UK Simon Broome FH register.
S E Humphries, J A Cooper, M Seed, N Capps, P N Durrington, B Jones, I F W McDowell, H Soran, H A W Neil. Atherosclerosis 2018
50
33

The clinical pharmacogenetics implementation consortium guideline for SLCO1B1 and simvastatin-induced myopathy: 2014 update.
L B Ramsey, S G Johnson, K E Caudle, C E Haidar, D Voora, R A Wilke, W D Maxwell, H L McLeod, R M Krauss, D M Roden,[...]. Clin Pharmacol Ther 2014
244
33

Current priorities for public health practice in addressing the role of human genomics in improving population health.
Muin J Khoury, Michael S Bowen, Wylie Burke, Ralph J Coates, Nicole F Dowling, James P Evans, Michele Reyes, Jeannette St Pierre. Am J Prev Med 2011
53
33

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
223
33

Prior Authorization Requirements for Proprotein Convertase Subtilisin/Kexin Type 9 Inhibitors Across US Private and Public Payers.
Jalpa A Doshi, Justin T Puckett, Michael S Parmacek, Daniel J Rader. Circ Cardiovasc Qual Outcomes 2018
21
33

Genetic Testing for Inherited Cardiovascular Diseases: A Scientific Statement From the American Heart Association.
Kiran Musunuru, Ray E Hershberger, Sharlene M Day, N Jennifer Klinedinst, Andrew P Landstrom, Victoria N Parikh, Siddharth Prakash, Christopher Semsarian, Amy C Sturm. Circ Genom Precis Med 2020
78
33

Clinical Pharmacogenetics Implementation Consortium (CPIC) Guideline for Pharmacogenetics-Guided Warfarin Dosing: 2017 Update.
J A Johnson, K E Caudle, L Gong, M Whirl-Carrillo, C M Stein, S A Scott, M T Lee, B F Gage, S E Kimmel, M A Perera,[...]. Clin Pharmacol Ther 2017
283
33

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
884
33

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
33

Evolocumab and Clinical Outcomes in Patients with Cardiovascular Disease.
Marc S Sabatine, Robert P Giugliano, Anthony C Keech, Narimon Honarpour, Stephen D Wiviott, Sabina A Murphy, Julia F Kuder, Huei Wang, Thomas Liu, Scott M Wasserman,[...]. N Engl J Med 2017
33

Deaths: Leading Causes for 2018.
Melonie Heron. Natl Vital Stat Rep 2021
13
33

HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA).
Michael J Ackerman, Silvia G Priori, Stephan Willems, Charles Berul, Ramon Brugada, Hugh Calkins, A John Camm, Patrick T Ellinor, Michael Gollob, Robert Hamilton,[...]. Europace 2011
487
33

Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations.
Fernando Domínguez, Sofía Cuenca, Zofia Bilińska, Rocío Toro, Eric Villard, Roberto Barriales-Villa, Juan Pablo Ochoa, Folkert Asselbergs, Arjan Sammani, Maria Franaszczyk,[...]. J Am Coll Cardiol 2018
54
33

Genomic considerations for FHIR®; eMERGE implementation lessons.
Mullai Murugan, Lawrence J Babb, Casey Overby Taylor, Luke V Rasmussen, Robert R Freimuth, Eric Venner, Fei Yan, Victoria Yi, Stephen J Granite, Hana Zouk,[...]. J Biomed Inform 2021
5
33

Expert consensus recommendations on the cardiogenetic care for patients with thoracic aortic disease and their first-degree relatives.
Judith M A Verhagen, Marlies Kempers, Luc Cozijnsen, Berto J Bouma, Anthonie L Duijnhouwer, Jan G Post, Yvonne Hilhorst-Hofstee, Sebastiaan C A M Bekkers, Wilhelmina S Kerstjens-Frederikse, Thomas J van Brakel,[...]. Int J Cardiol 2018
31
33

Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel.
Theodore Chiang, Xiuping Liu, Tsung-Jung Wu, Jianhong Hu, Fritz J Sedlazeck, Simon White, Daniel Schaid, Mariza de Andrade, Gail P Jarvik, David Crosslin,[...]. Genet Med 2019
13
33

ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG).
David T Miller, Kristy Lee, Wendy K Chung, Adam S Gordon, Gail E Herman, Teri E Klein, Douglas R Stewart, Laura M Amendola, Kathy Adelman, Sherri J Bale,[...]. Genet Med 2021
91
33

Overcoming the reimbursement barriers for clinical sequencing.
Patricia A Deverka, David Kaufman, Amy L McGuire. JAMA 2014
27
33

Genetic variants in the apolipoprotein(a) gene and coronary heart disease.
Yonghong Li, May M Luke, Dov Shiffman, James J Devlin. Circ Cardiovasc Genet 2011
49
33

Underdiagnosis of Hereditary Breast Cancer: Are Genetic Testing Guidelines a Tool or an Obstacle?
Peter D Beitsch, Pat W Whitworth, Kevin Hughes, Rakesh Patel, Barry Rosen, Gia Compagnoni, Paul Baron, Rache Simmons, Linda Ann Smith, Ian Grady,[...]. J Clin Oncol 2019
151
33

Loeys-Dietz syndrome: a primer for diagnosis and management.
Gretchen MacCarrick, James H Black, Sarah Bowdin, Ismail El-Hamamsy, Pamela A Frischmeyer-Guerrerio, Anthony L Guerrerio, Paul D Sponseller, Bart Loeys, Harry C Dietz. Genet Med 2014
254
33

National Trends in Statin Use and Expenditures in the US Adult Population From 2002 to 2013: Insights From the Medical Expenditure Panel Survey.
Joseph A Salami, Haider Warraich, Javier Valero-Elizondo, Erica S Spatz, Nihar R Desai, Jamal S Rana, Salim S Virani, Ron Blankstein, Amit Khera, Michael J Blaha,[...]. JAMA Cardiol 2017
212
33

Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, Daniel P Judge, Paul F Kantor, Kim L McBride, Ana Morales, Matthew R G Taylor, Matteo Vatta, Stephanie M Ware. Genet Med 2018
92
33

Identification of Transthyretin Cardiac Amyloidosis Using Serum Retinol-Binding Protein 4 and a Clinical Prediction Model.
Marios Arvanitis, Clarissa M Koch, Gloria G Chan, Celia Torres-Arancivia, Michael P LaValley, Daniel R Jacobson, John L Berk, Lawreen H Connors, Frederick L Ruberg. JAMA Cardiol 2017
35
33

Diagnostic Utility of Exome Sequencing for Kidney Disease.
Emily E Groopman, Maddalena Marasa, Sophia Cameron-Christie, Slavé Petrovski, Vimla S Aggarwal, Hila Milo-Rasouly, Yifu Li, Junying Zhang, Jordan Nestor, Priya Krithivasan,[...]. N Engl J Med 2019
218
33

Diagnostic yield of genetic testing in a heterogeneous cohort of 1376 HCM patients.
Julie Hathaway, Krista Heliö, Inka Saarinen, Jonna Tallila, Eija H Seppälä, Sari Tuupanen, Hannu Turpeinen, Tiia Kangas-Kontio, Jennifer Schleit, Johanna Tommiska,[...]. BMC Cardiovasc Disord 2021
3
33

Germline Cancer Susceptibility Gene Testing in Unselected Patients With Colorectal Adenocarcinoma: A Multicenter Prospective Study.
Pedro L S Uson, Douglas Riegert-Johnson, Lisa Boardman, John Kisiel, Luke Mountjoy, Neej Patel, Blanca Lizaola-Mayo, Mitesh J Borad, Daniel Ahn, Mohamad B Sonbol,[...]. Clin Gastroenterol Hepatol 2022
11
33


OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders.
Joanna S Amberger, Carol A Bocchini, François Schiettecatte, Alan F Scott, Ada Hamosh. Nucleic Acids Res 2015
893
33

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
33

Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline.
Jeffrey G Reid, Andrew Carroll, Narayanan Veeraraghavan, Mahmoud Dahdouli, Andreas Sundquist, Adam English, Matthew Bainbridge, Simon White, William Salerno, Christian Buhay,[...]. BMC Bioinformatics 2014
136
33

Genetic Risk, Adherence to a Healthy Lifestyle, and Coronary Disease.
Amit V Khera, Connor A Emdin, Isabel Drake, Pradeep Natarajan, Alexander G Bick, Nancy R Cook, Daniel I Chasman, Usman Baber, Roxana Mehran, Daniel J Rader,[...]. N Engl J Med 2016
565
33

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
Sue Richards, Nazneen Aziz, Sherri Bale, David Bick, Soma Das, Julie Gastier-Foster, Wayne W Grody, Madhuri Hegde, Elaine Lyon, Elaine Spector,[...]. Genet Med 2015
33

Lipoprotein(a)-antisense therapy.
Anja Vogt. Clin Res Cardiol Suppl 2019
8
33

Towards clinical utility of polygenic risk scores.
Samuel A Lambert, Gad Abraham, Michael Inouye. Hum Mol Genet 2019
155
33

Phenotypic signatures in clinical data enable systematic identification of patients for genetic testing.
Theodore J Morley, Lide Han, Victor M Castro, Jonathan Morra, Roy H Perlis, Nancy J Cox, Lisa Bastarache, Douglas M Ruderfer. Nat Med 2021
4
33

Familial hypercholesterolemia: screening, diagnosis and management of pediatric and adult patients: clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia.
Anne C Goldberg, Paul N Hopkins, Peter P Toth, Christie M Ballantyne, Daniel J Rader, Jennifer G Robinson, Stephen R Daniels, Samuel S Gidding, Sarah D de Ferranti, Matthew K Ito,[...]. J Clin Lipidol 2011
186
33

Advances in oligonucleotide drug delivery.
Thomas C Roberts, Robert Langer, Matthew J A Wood. Nat Rev Drug Discov 2020
394
33

Multifunctional polymeric nanoparticles for oral delivery of TNF-α siRNA to macrophages.
Chunbai He, Lichen Yin, Cui Tang, Chunhua Yin. Biomaterials 2013
82
33

Statin therapy for primary prevention of cardiovascular disease.
Fiona C Taylor, Mark Huffman, Shah Ebrahim. JAMA 2013
91
33

Metabolic Induction of Trained Immunity through the Mevalonate Pathway.
Siroon Bekkering, Rob J W Arts, Boris Novakovic, Ioannis Kourtzelis, Charlotte D C C van der Heijden, Yang Li, Calin D Popa, Rob Ter Horst, Julia van Tuijl, Romana T Netea-Maier,[...]. Cell 2018
305
33

Atherosclerosis.
Peter Libby, Julie E Buring, Lina Badimon, Göran K Hansson, John Deanfield, Márcio Sommer Bittencourt, Lale Tokgözoğlu, Eldrin F Lewis. Nat Rev Dis Primers 2019
657
33

Increasing HDL Cholesterol Levels.
H Bryan Brewer. N Engl J Med 2004
100
33

Inflammation and its resolution in atherosclerosis: mediators and therapeutic opportunities.
Magnus Bäck, Arif Yurdagul, Ira Tabas, Katariina Öörni, Petri T Kovanen. Nat Rev Cardiol 2019
410
33


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.