A citation-based method for searching scientific literature

Julio D Duarte, Larisa H Cavallari. Nat Rev Cardiol 2021
Times Cited: 2







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



Times Cited
  Times     Co-cited
Similarity


A deliberative study of public attitudes towards sharing genomic data within NHS genomic medicine services in England.
Lamiece Hassan, Ann Dalton, Carrie Hammond, Mary Patricia Tully. Public Underst Sci 2020
3
50

Challenges in the clinical application of whole-genome sequencing.
Kelly E Ormond, Matthew T Wheeler, Louanne Hudgins, Teri E Klein, Atul J Butte, Russ B Altman, Euan A Ashley, Henry T Greely. Lancet 2010
153
50


Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics.
Carla G van El, Martina C Cornel, Pascal Borry, Ros J Hastings, Florence Fellmann, Shirley V Hodgson, Heidi C Howard, Anne Cambon-Thomsen, Bartha M Knoppers, Hanne Meijers-Heijboer,[...]. Eur J Hum Genet 2013
206
50

Admixture in Latin America: geographic structure, phenotypic diversity and self-perception of ancestry based on 7,342 individuals.
Andrés Ruiz-Linares, Kaustubh Adhikari, Victor Acuña-Alonzo, Mirsha Quinto-Sanchez, Claudia Jaramillo, William Arias, Macarena Fuentes, María Pizarro, Paola Everardo, Francisco de Avila,[...]. PLoS Genet 2014
224
50

Probing small non-coding RNAs structures.
Jean-Vincent Philippe, Lilia Ayadi, Christiane Branlant, Isabelle Behm-Ansmant. Methods Mol Biol 2015
3
50

Maternal genetic history of southern East Asians over the past 12,000 years.
Yalin Liu, Tianyi Wang, Xichao Wu, Xuechun Fan, Wei Wang, Guangmao Xie, Zhen Li, Qingping Yang, Peng Cao, Ruowei Yang,[...]. J Genet Genomics 2021
1
100

Construct validity of the SF-12 in three different samples.
Ulf Jakobsson, Albert Westergren, Susanne Lindskov, Peter Hagell. J Eval Clin Pract 2012
46
50

Open access data sharing in genomic research.
Stacey Pereira, Richard A Gibbs, Amy L McGuire. Genes (Basel) 2014
16
50


Exome sequencing as a tool for Mendelian disease gene discovery.
Michael J Bamshad, Sarah B Ng, Abigail W Bigham, Holly K Tabor, Mary J Emond, Deborah A Nickerson, Jay Shendure. Nat Rev Genet 2011
50


Modeling 3D facial shape from DNA.
Peter Claes, Denise K Liberton, Katleen Daniels, Kerri Matthes Rosana, Ellen E Quillen, Laurel N Pearson, Brian McEvoy, Marc Bauchet, Arslan A Zaidi, Wei Yao,[...]. PLoS Genet 2014
100
50

Data sharing in genomics--re-shaping scientific practice.
Jane Kaye, Catherine Heeney, Naomi Hawkins, Jantina de Vries, Paula Boddington. Nat Rev Genet 2009
145
50

Public access to genome-wide data: five views on balancing research with privacy and protection.
George Church, Catherine Heeney, Naomi Hawkins, Jantina de Vries, Paula Boddington, Jane Kaye, Martin Bobrow, Bruce Weir. PLoS Genet 2009
58
50

Large-scale pharmacogenomic studies and drug response prediction for personalized cancer medicine.
Fangyoumin Feng, Bihan Shen, Xiaoqin Mou, Yixue Li, Hong Li. J Genet Genomics 2021
3
50



The Patient as Genomic Data Manager - Evaluation of the PROMISE App.
Lena Griebel, Marc Hinderer, Ali Amr, Benjamin Meder, Marc Schweig, Dominic Deuber, Christoph Egger, Claudia Kawohl, Annika Krämer, Isabell Flade,[...]. Stud Health Technol Inform 2020
1
100

Genetics in genomic era.
Eugenia Poliakov, David N Cooper, Elena I Stepchenkova, Igor B Rogozin. Genet Res Int 2015
2
50

The growth and gaps of genetic data sharing policies in the United States.
Jalayne J Arias, Genevieve Pham-Kanter, Eric G Campbell. J Law Biosci 2014
9
50

Assessing the privacy risks of data sharing in genomics.
C Heeney, N Hawkins, J de Vries, P Boddington, J Kaye. Public Health Genomics 2011
61
50

The mental component of the short-form 12 health survey (SF-12) as a measure of depressive disorders in the general population: results with three alternative scoring methods.
Gemma Vilagut, Carlos G Forero, Alejandra Pinto-Meza, Josep M Haro, Ron de Graaf, Ronny Bruffaerts, Viviane Kovess, Giovanni de Girolamo, Herbert Matschinger, Montserrat Ferrer,[...]. Value Health 2013
125
50

Whole genome sequencing in pharmacogenomics.
Theodora Katsila, George P Patrinos. Front Pharmacol 2015
25
50

Facial asymmetry and genetic ancestry in Latin American admixed populations.
Mirsha Quinto-Sánchez, Kaustubh Adhikari, Victor Acuña-Alonzo, Celia Cintas, Caio Cesar Silva de Cerqueira, Virginia Ramallo, Lucia Castillo, Arodi Farrera, Claudia Jaramillo, Williams Arias,[...]. Am J Phys Anthropol 2015
14
50

Open sharing of genomic data: Who does it and why?
Tobias Haeusermann, Bastian Greshake, Alessandro Blasimme, Darja Irdam, Martin Richards, Effy Vayena. PLoS One 2017
28
50

The need to redefine genomic data sharing: A focus on data accessibility.
Tempest A van Schaik, Nadezda V Kovalevskaya, Elena Protopapas, Hamza Wahid, Fiona G G Nielsen. Appl Transl Genom 2014
13
50

From genetic privacy to open consent.
Jeantine E Lunshof, Ruth Chadwick, Daniel B Vorhaus, George M Church. Nat Rev Genet 2008
217
50

De-identified genomic data sharing: the research participant perspective.
Deborah Goodman, Catherine O Johnson, Deborah Bowen, Megan Smith, Lari Wenzel, Karen Edwards. J Community Genet 2017
24
50

Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric Medicine.
Dimitri J Stavropoulos, Daniele Merico, Rebekah Jobling, Sarah Bowdin, Nasim Monfared, Bhooma Thiruvahindrapuram, Thomas Nalpathamkalam, Giovanna Pellecchia, Ryan K C Yuen, Michael J Szego,[...]. NPJ Genom Med 2016
174
50

Finding the missing heritability of complex diseases.
Teri A Manolio, Francis S Collins, Nancy J Cox, David B Goldstein, Lucia A Hindorff, David J Hunter, Mark I McCarthy, Erin M Ramos, Lon R Cardon, Aravinda Chakravarti,[...]. Nature 2009
50

The NCI Genomic Data Commons as an engine for precision medicine.
Mark A Jensen, Vincent Ferretti, Robert L Grossman, Louis M Staudt. Blood 2017
100
50

Implications of the admixture process in skin color molecular assessment.
Caio Cesar Silva de Cerqueira, Tábita Hünemeier, Jorge Gomez-Valdés, Virgínia Ramallo, Carla Daiana Volasko-Krause, Ana Angélica Leal Barbosa, Pedro Vargas-Pinilla, Rodrigo Ciconet Dornelles, Danaê Longo, Francisco Rothhammer,[...]. PLoS One 2014
12
50

The validity of the Hospital Anxiety and Depression Scale. An updated literature review.
Ingvar Bjelland, Alv A Dahl, Tone Tangen Haug, Dag Neckelmann. J Psychosom Res 2002
50

De novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEP.
Krishna R Veeramah, Janelle E O'Brien, Miriam H Meisler, Xiaoyang Cheng, Sulayman D Dib-Hajj, Stephen G Waxman, Dinesh Talwar, Santhosh Girirajan, Evan E Eichler, Linda L Restifo,[...]. Am J Hum Genet 2012
259
50

Precision Medicine in the Management of Dilated Cardiomyopathy: JACC State-of-the-Art Review.
Diane Fatkin, Inken G Huttner, Jason C Kovacic, J G Seidman, Christine E Seidman. J Am Coll Cardiol 2019
26
50

Are Next-Generation Sequencing Tools Ready for the Cloud?
Antonio Celesti, Fabrizio Celesti, Maria Fazio, Placido Bramanti, Massimo Villari. Trends Biotechnol 2017
7
50

Toward better governance of human genomic data.
Kieran C O'Doherty, Mahsa Shabani, Edward S Dove, Heidi Beate Bentzen, Pascal Borry, Michael M Burgess, Don Chalmers, Jantina De Vries, Lisa Eckstein, Stephanie M Fullerton,[...]. Nat Genet 2021
4
50

Genomic medicine and data sharing.
Sobia Raza, Alison Hall. Br Med Bull 2017
10
50

Research participants' attitudes towards the confidentiality of genomic sequence information.
Leila Jamal, Julie C Sapp, Katie Lewis, Tatiane Yanes, Flavia M Facio, Leslie G Biesecker, Barbara B Biesecker. Eur J Hum Genet 2014
29
50

On the future of genomic data.
Scott D Kahn. Science 2011
104
50

Potential of whole-genome sequencing for determining risk and personalizing therapy: focus on AML.
Uma Borate, Devin Absher, Harry P Erba, Boris Pasche. Expert Rev Anticancer Ther 2012
2
50

Making sense of big data in health research: Towards an EU action plan.
Charles Auffray, Rudi Balling, Inês Barroso, László Bencze, Mikael Benson, Jay Bergeron, Enrique Bernal-Delgado, Niklas Blomberg, Christoph Bock, Ana Conesa,[...]. Genome Med 2016
98
50

Cytochrome P450 2C9 polymorphisms: a comprehensive review of the in-vitro and human data.
Craig R Lee, Joyce A Goldstein, John A Pieper. Pharmacogenetics 2002
493
50

Effects of ACE and ADD1 gene polymorphisms on blood pressure response to hydrochlorothiazide: a meta-analysis.
Hye Duck Choi, Jee Hyun Suh, Jeong Yoon Lee, Soo Kyung Bae, Hee Eun Kang, Myung Gull Lee, Wan Gyoon Shin. Int J Clin Pharmacol Ther 2013
15
50

Genetic and clinical predictors of warfarin dose requirements in African Americans.
L H Cavallari, T Y Langaee, K M Momary, N L Shapiro, E A Nutescu, W A Coty, M A G Viana, S R Patel, J A Johnson. Clin Pharmacol Ther 2010
145
50

Human P450 metabolism of warfarin.
L S Kaminsky, Z Y Zhang. Pharmacol Ther 1997
590
50

Use of pharmacogenetic and clinical factors to predict the therapeutic dose of warfarin.
B F Gage, C Eby, J A Johnson, E Deych, M J Rieder, P M Ridker, P E Milligan, G Grice, P Lenzini, A E Rettie,[...]. Clin Pharmacol Ther 2008
547
50

Genetic determinants of lipid-lowering response to atorvastatin therapy in an Indian population.
P Kadam, T F Ashavaid, C K Ponde, R M Rajani. J Clin Pharm Ther 2016
16
50

Global Burden of Cardiovascular Diseases and Risk Factors, 1990-2019: Update From the GBD 2019 Study.
Gregory A Roth, George A Mensah, Catherine O Johnson, Giovanni Addolorato, Enrico Ammirati, Larry M Baddour, Noël C Barengo, Andrea Z Beaton, Emelia J Benjamin, Catherine P Benziger,[...]. J Am Coll Cardiol 2020
362
50


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.