A citation-based method for searching scientific literature

Christian Domilongo Bope, Emile R Chimusa, Victoria Nembaware, Gaston K Mazandu, Jantina de Vries, Ambroise Wonkam. Front Genet 2019
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity



Genomics is failing on diversity.
Alice B Popejoy, Stephanie M Fullerton. Nature 2016
573
50

Genetic Misdiagnoses and the Potential for Health Disparities.
Arjun K Manrai, Birgit H Funke, Heidi L Rehm, Morten S Olesen, Bradley A Maron, Peter Szolovits, David M Margulies, Joseph Loscalzo, Isaac S Kohane. N Engl J Med 2016
320
50

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
37

Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
Laura M Amendola, Michael O Dorschner, Peggy D Robertson, Joseph S Salama, Ragan Hart, Brian H Shirts, Mitzi L Murray, Mari J Tokita, Carlos J Gallego, Daniel Seung Kim,[...]. Genome Res 2015
225
25

ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
25

Assembly of a pan-genome from deep sequencing of 910 humans of African descent.
Rachel M Sherman, Juliet Forman, Valentin Antonescu, Daniela Puiu, Michelle Daya, Nicholas Rafaels, Meher Preethi Boorgula, Sameer Chavan, Candelaria Vergara, Victor E Ortega,[...]. Nat Genet 2019
115
25

Association of trypanolytic ApoL1 variants with kidney disease in African Americans.
Giulio Genovese, David J Friedman, Michael D Ross, Laurence Lecordier, Pierrick Uzureau, Barry I Freedman, Donald W Bowden, Carl D Langefeld, Taras K Oleksyk, Andrea L Uscinski Knob,[...]. Science 2010
25

Clinical use of current polygenic risk scores may exacerbate health disparities.
Alicia R Martin, Masahiro Kanai, Yoichiro Kamatani, Yukinori Okada, Benjamin M Neale, Mark J Daly. Nat Genet 2019
481
25

The Sequence Alignment/Map format and SAMtools.
Heng Li, Bob Handsaker, Alec Wysoker, Tim Fennell, Jue Ruan, Nils Homer, Gabor Marth, Goncalo Abecasis, Richard Durbin. Bioinformatics 2009
25


The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data.
Aaron McKenna, Matthew Hanna, Eric Banks, Andrey Sivachenko, Kristian Cibulskis, Andrew Kernytsky, Kiran Garimella, David Altshuler, Stacey Gabriel, Mark Daly,[...]. Genome Res 2010
25

Field guide to next-generation DNA sequencers.
Travis C Glenn. Mol Ecol Resour 2011
565
25

Who is telling the story? A systematic review of authorship for infectious disease research conducted in Africa, 1980-2016.
Rose Mbaye, Redeat Gebeyehu, Stefanie Hossmann, Nicole Mbarga, Estella Bih-Neh, Lucrece Eteki, Ohene-Agyei Thelma, Abiodun Oyerinde, Gift Kiti, Yvonne Mburu,[...]. BMJ Glob Health 2019
33
25

Uganda Genome Resource Enables Insights into Population History and Genomic Discovery in Africa.
Deepti Gurdasani, Tommy Carstensen, Segun Fatumo, Guanjie Chen, Chris S Franklin, Javier Prado-Martinez, Heleen Bouman, Federico Abascal, Marc Haber, Ioanna Tachmazidou,[...]. Cell 2019
50
25

Designing a course model for distance-based online bioinformatics training in Africa: The H3ABioNet experience.
Kim T Gurwitz, Shaun Aron, Sumir Panji, Suresh Maslamoney, Pedro L Fernandes, David P Judge, Amel Ghouila, Jean-Baka Domelevo Entfellner, Fatma Z Guerfali, Colleen Saunders,[...]. PLoS Comput Biol 2017
19
25

H3ABioNet, a sustainable pan-African bioinformatics network for human heredity and health in Africa.
Nicola J Mulder, Ezekiel Adebiyi, Raouf Alami, Alia Benkahla, James Brandful, Seydou Doumbia, Dean Everett, Faisal M Fadlelmola, Fatima Gaboun, Simani Gaseitsiwe,[...]. Genome Res 2016
56
25

Practical experience with databases for congenital heart disease: a registry versus an academic database.
William G Williams, Brian W McCrindle. Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu 2002
24
12



Cardiovascular Event Prediction by Machine Learning: The Multi-Ethnic Study of Atherosclerosis.
Bharath Ambale-Venkatesh, Xiaoying Yang, Colin O Wu, Kiang Liu, W Gregory Hundley, Robyn McClelland, Antoinette S Gomes, Aaron R Folsom, Steven Shea, Eliseo Guallar,[...]. Circ Res 2017
153
12

Regional assessment of cardiac left ventricular myocardial function via MRI statistical features.
Mariam Afshin, Ismail Ben Ayed, Kumaradevan Punithakumar, Max Law, Ali Islam, Aashish Goela, Terry Peters, Shuo Li. IEEE Trans Med Imaging 2014
21
12

Mortality resulting from congenital heart disease among children and adults in the United States, 1999 to 2006.
Suzanne M Gilboa, Jason L Salemi, Wendy N Nembhard, David E Fixler, Adolfo Correa. Circulation 2010
304
12

Health Informatics via Machine Learning for the Clinical Management of Patients.
D A Clifton, K E Niehaus, P Charlton, G W Colopy. Yearb Med Inform 2015
12
12

Cardiovascular proteomics in the era of big data: experimental and computational advances.
Maggie P Y Lam, Edward Lau, Dominic C M Ng, Ding Wang, Peipei Ping. Clin Proteomics 2016
6
16

Artificial intelligence and echocardiography.
M Alsharqi, W J Woodward, J A Mumith, D C Markham, R Upton, P Leeson. Echo Res Pract 2018
38
12

Multiplex proteomics for prediction of major cardiovascular events in type 2 diabetes.
Christoph Nowak, Axel C Carlsson, Carl Johan Östgren, Fredrik H Nyström, Moudud Alam, Tobias Feldreich, Johan Sundström, Juan-Jesus Carrero, Jerzy Leppert, Pär Hedberg,[...]. Diabetologia 2018
28
12


Integrated Proteomic and Metabolomic prediction of Term Preeclampsia.
Ray Bahado-Singh, Liona C Poon, Ali Yilmaz, Argyro Syngelaki, Onur Turkoglu, Praveen Kumar, Joseph Kirma, Matthew Allos, Veronica Accurti, Jiansheng Li,[...]. Sci Rep 2017
23
12

Machine-Learning Algorithms to Automate Morphological and Functional Assessments in 2D Echocardiography.
Sukrit Narula, Khader Shameer, Alaa Mabrouk Salem Omar, Joel T Dudley, Partho P Sengupta. J Am Coll Cardiol 2016
129
12

Profile and risk factors for congenital heart defects: A study in a tertiary care hospital.
Shaad Abqari, Akash Gupta, Tabassum Shahab, M U Rabbani, S Manazir Ali, Uzma Firdaus. Ann Pediatr Cardiol 2016
16
12


Fully Automated Echocardiogram Interpretation in Clinical Practice.
Jeffrey Zhang, Sravani Gajjala, Pulkit Agrawal, Geoffrey H Tison, Laura A Hallock, Lauren Beussink-Nelson, Mats H Lassen, Eugene Fan, Mandar A Aras, ChaRandle Jordan,[...]. Circulation 2018
198
12

Building interpretable models for polypharmacy prediction in older chronic patients based on drug prescription records.
Simon Kocbek, Primoz Kocbek, Andraz Stozer, Tina Zupanic, Tudor Groza, Gregor Stiglic. PeerJ 2018
3
33


Predictive markers of depression in hypertension.
Xiuli Song, Zhong Zhang, Rui Zhang, Miye Wang, Dongtao Lin, Tao Li, Junming Shao, Xiaohong Ma. Medicine (Baltimore) 2018
9
12

Molecular and cellular basis of congenital heart disease.
Tara L Sander, Denise B Klinkner, Aoy Tomita-Mitchell, Michael E Mitchell. Pediatr Clin North Am 2006
10
12

Analysis of gene-gene interactions among common variants in candidate cardiovascular genes in coronary artery disease.
Muntaser D Musameh, William Y S Wang, Christopher P Nelson, Carla Lluís-Ganella, Radoslaw Debiec, Isaac Subirana, Roberto Elosua, Anthony J Balmforth, Stephen G Ball, Alistair S Hall,[...]. PLoS One 2015
6
16

Peptidomic Analysis of Amniotic Fluid for Identification of Putative Bioactive Peptides in Ventricular Septal Defect.
Xing Li, Li-Jie Wu, Meng Gu, Yu-Mei Chen, Qi-Jun Zhang, Hua Li, Zi-Jie Cheng, Ping Hu, Shu-Ping Han, Zhang-Bin Yu,[...]. Cell Physiol Biochem 2016
10
12

A classifier based on the artificial neural network approach for cardiologic auscultation in pediatrics.
Sanjay R Bhatikar, Curt DeGroff, Roop L Mahajan. Artif Intell Med 2005
25
12

Predictive value of targeted proteomics for coronary plaque morphology in patients with suspected coronary artery disease.
Michiel J Bom, Evgeni Levin, Roel S Driessen, Ibrahim Danad, Cornelis C Van Kuijk, Albert C van Rossum, Jagat Narula, James K Min, Jonathon A Leipsic, João P Belo Pereira,[...]. EBioMedicine 2019
21
12

The diagnostic value of next generation sequencing in familial nonsyndromic congenital heart defects.
Yaojuan Jia, Jacoba J Louw, Jeroen Breckpot, Bert Callewaert, Catherine Barrea, Yves Sznajer, Marc Gewillig, Erika Souche, Luc Dehaspe, Joris Robert Vermeesch,[...]. Am J Med Genet A 2015
32
12

Second-trimester prediction of delivery of a small-for-gestational-age neonate: integrating sequential Doppler information, fetal biometry, and maternal characteristics.
Viola Seravalli, Dana M Block-Abraham, Ozhan M Turan, Lauren E Doyle, Miriam G Blitzer, Ahmet A Baschat. Prenat Diagn 2014
13
12

MRI misinterpretation of spontaneous echo-contrast as a large left atrial thrombus.
P Raggi, M Daniels, H Shanoudy, N F Jarmukli. Int J Card Imaging 1996
7
14

Ethnic and socioeconomic variation in incidence of congenital heart defects.
Rachel L Knowles, Deborah Ridout, Sonya Crowe, Catherine Bull, Jo Wray, Jenifer Tregay, Rodney C Franklin, David J Barron, David Cunningham, Roger C Parslow,[...]. Arch Dis Child 2017
31
12

Identification of functional mutations in GATA4 in patients with congenital heart disease.
Erli Wang, Shuna Sun, Bin Qiao, Wenyuan Duan, Guoying Huang, Yu An, Shuhua Xu, Yufang Zheng, Zhixi Su, Xun Gu,[...]. PLoS One 2013
37
12


Electronic health record system in the public health care sector of South Africa: A systematic literature review.
Munyaradzi C Katurura, Liezel Cilliers. Afr J Prim Health Care Fam Med 2018
8
12

Automated identification and predictive tools to help identify high-risk heart failure patients: pilot evaluation.
R Scott Evans, Jose Benuzillo, Benjamin D Horne, James F Lloyd, Alejandra Bradshaw, Deborah Budge, Kismet D Rasmusson, Colleen Roberts, Jason Buckway, Norma Geer,[...]. J Am Med Inform Assoc 2016
37
12

The utility of long-term blood pressure variability for cardiovascular risk prediction in primary care.
Sarah L Stevens, Richard J McManus, Richard J Stevens. J Hypertens 2019
4
25


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.