A citation-based method for searching scientific literature

Venner Eric, Victoria Yi, David Murdock, Sara E Kalla, Tsung-Jung Wu, Aniko Sabo, Shoudong Li, Qingchang Meng, Xia Tian, Mullai Murugan, Michelle Cohen, Christie Kovar, Wei-Qi Wei, Wendy K Chung, Chunhua Weng, Georgia L Wiesner, Gail P Jarvik, Donna Muzny, Richard A Gibbs. Genet Med 2021
Times Cited: 1







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
100

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
58
100

Advances in the treatment of hereditary transthyretin amyloidosis: A review.
Morie A Gertz, Michelle L Mauermann, Martha Grogan, Teresa Coelho. Brain Behav 2019
42
100

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
247
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
100

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
51
100

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
247
100

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
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
229
100

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
100

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
84
100

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
286
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
892
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
100

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
100

Deaths: Leading Causes for 2018.
Melonie Heron. Natl Vital Stat Rep 2021
14
100

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
100

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
55
100

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
6
100

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
32
100

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
100

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
100
100

Overcoming the reimbursement barriers for clinical sequencing.
Patricia A Deverka, David Kaufman, Amy L McGuire. JAMA 2014
27
100

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
100

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
155
100

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
259
100

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
100

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
100

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
36
100

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
223
100

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
100

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
13
100


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
907
100

A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
100

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
100

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
574
100

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
100

Lipoprotein(a)-antisense therapy.
Anja Vogt. Clin Res Cardiol Suppl 2019
8
100

Towards clinical utility of polygenic risk scores.
Samuel A Lambert, Gad Abraham, Michael Inouye. Hum Mol Genet 2019
160
100


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
100

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
187
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.