A citation-based method for searching scientific literature

Rhonda G Kost, Stephen M Poppel, Barry S Coller. J Clin Transl Sci 2017
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity



Genetics. No longer de-identified.
Amy L McGuire, Richard A Gibbs. Science 2006
106
25


A machine learning model to determine the accuracy of variant calls in capture-based next generation sequencing.
Jeroen van den Akker, Gilad Mishne, Anjali D Zimmer, Alicia Y Zhou. BMC Genomics 2018
7
25

Genomics really gets personal: how exome and whole genome sequencing challenge the ethical framework of human genetics research.
Holly K Tabor, Benjamin E Berkman, Sara Chandros Hull, Michael J Bamshad. Am J Med Genet A 2011
91
25

Implementing Machine Learning in Health Care - Addressing Ethical Challenges.
Danton S Char, Nigam H Shah, David Magnus. N Engl J Med 2018
198
25

Why Deep Learning Is Changing the Way to Approach NGS Data Processing: A Review.
Fabrizio Celesti, Antonio Celesti, Jiafu Wan, Massimo Villari. IEEE Rev Biomed Eng 2018
4
25

Public expectations for return of results from large-cohort genetic research.
Juli Murphy, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson. Am J Bioeth 2008
191
25

Clinical Versus Research Sequencing.
Yuriy Shevchenko, Sherri Bale. Cold Spring Harb Perspect Med 2016
8
25

Big Data, Large-Scale Text Analysis, and Public Health Research.
Merlin Chowkwanyun. Am J Public Health 2019
2
50

Electronic medical records for genetic research: results of the eMERGE consortium.
Abel N Kho, Jennifer A Pacheco, Peggy L Peissig, Luke Rasmussen, Katherine M Newton, Noah Weston, Paul K Crane, Jyotishman Pathak, Christopher G Chute, Suzette J Bielinski,[...]. Sci Transl Med 2011
222
25

Clinical applications of next generation sequencing in cancer: from panels, to exomes, to genomes.
Tony Shen, Stefan Hans Pajaro-Van de Stadt, Nai Chien Yeat, Jimmy C-H Lin. Front Genet 2015
51
25

Genomics in the clinic: ethical and policy challenges in clinical next-generation sequencing programs at early adopter USA institutions.
Lauren C Milner, Nanibaa' A Garrison, Mildred K Cho, Russ B Altman, Louanne Hudgins, Stephen J Galli, Henry J Lowe, Iris Schrijver, David C Magnus. Per Med 2015
1
100

Next generation sequencing in clinical medicine: Challenges and lessons for pathology and biomedical informatics.
Rama R Gullapalli, Ketaki V Desai, Lucas Santana-Santos, Jeffrey A Kant, Michael J Becich. J Pathol Inform 2012
79
25

Re-identification of familial database records.
Bradley Malin. AMIA Annu Symp Proc 2006
24
25

How is genetic testing evaluated? A systematic review of the literature.
Erica Pitini, Corrado De Vito, Carolina Marzuillo, Elvira D'Andrea, Annalisa Rosso, Antonio Federici, Emilio Di Maria, Paolo Villari. Eur J Hum Genet 2018
27
25

The need to build trust: a perspective on disparities in genetic testing.
Kalyn Saulsberry, Sharon F Terry. Genet Test Mol Biomarkers 2013
14
25

Attitudes of African Americans toward return of results from exome and whole genome sequencing.
Joon-Ho Yu, Julia Crouch, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am J Med Genet A 2013
54
25

The risk of re-identification versus the need to identify individuals in rare disease research.
Mats G Hansson, Hanns Lochmüller, Olaf Riess, Franz Schaefer, Michael Orth, Yaffa Rubinstein, Caron Molster, Hugh Dawkins, Domenica Taruscio, Manuel Posada,[...]. Eur J Hum Genet 2016
19
25

All eyes are on AI.
. Nat Biomed Eng 2018
3
33


The unintended implications of blurring the line between research and clinical care in a genomic age.
Benjamin E Berkman, Sara Chandros Hull, Lisa Eckstein. Per Med 2014
23
25






Ethical considerations associated with clinical use of next-generation sequencing in children.
John D Lantos, Michael Artman, Stephen F Kingsmore. J Pediatr 2011
12
25

Machine Learning Methods as a Tool for Predicting Risk of Illness Applying Next-Generation Sequencing Data.
Patrick Murigu Kamau Njage, Clementine Henri, Pimlapas Leekitcharoenphon, Michel-Yves Mistou, Rene S Hendriksen, Tine Hald. Risk Anal 2019
6
25

Integration of next-generation sequencing in clinical diagnostic molecular pathology laboratories for analysis of solid tumours; an expert opinion on behalf of IQN Path ASBL.
Zandra C Deans, Jose Luis Costa, Ian Cree, Els Dequeker, Anders Edsjö, Shirley Henderson, Michael Hummel, Marjolijn Jl Ligtenberg, Marco Loddo, Jose Carlos Machado,[...]. Virchows Arch 2017
48
25



Next generation sequencing: an application in forensic sciences?
Maria Jesus Alvarez-Cubero, Maria Saiz, Belén Martínez-García, Sara M Sayalero, Carmen Entrala, Jose Antonio Lorente, Luis Javier Martinez-Gonzalez. Ann Hum Biol 2017
9
25


Next-generation sequencing approach for the diagnosis of human diseases: open challenges and new opportunities.
Chiara Di Resta, Silvia Galbiati, Paola Carrera, Maurizio Ferrari. EJIFCC 2018
36
25


Disruption of AP3B1 by a chromosome 5 inversion: a new disease mechanism in Hermansky-Pudlak syndrome type 2.
Matthew L Jones, Sherina L Murden, Claire Brooks, Viv Maloney, Richard A Manning, Kimberly C Gilmour, Vandana Bharadwaj, Josu de la Fuente, Subarna Chakravorty, Andrew D Mumford. BMC Med Genet 2013
12
25


Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders.
Kate Downes, Karyn Megy, Daniel Duarte, Minka Vries, Johanna Gebhart, Stefanie Hofer, Olga Shamardina, Sri V V Deevi, Jonathan Stephens, Rutendo Mapeta,[...]. Blood 2019
46
25

A gain-of-function variant in DIAPH1 causes dominant macrothrombocytopenia and hearing loss.
Simon Stritt, Paquita Nurden, Ernest Turro, Daniel Greene, Sjoert B Jansen, Sarah K Westbury, Romina Petersen, William J Astle, Sandrine Marlin, Tadbir K Bariana,[...]. Blood 2016
69
25

A multiinstitutional survey of the Wiskott-Aldrich syndrome.
K E Sullivan, C A Mullen, R M Blaese, J A Winkelstein. J Pediatr 1994
370
25


Sphingolipid dysregulation due to lack of functional KDSR impairs proplatelet formation causing thrombocytopenia.
Tadbir K Bariana, Veerle Labarque, Jessica Heremans, Chantal Thys, Mara De Reys, Daniel Greene, Benjamin Jenkins, Luigi Grassi, Denis Seyres, Frances Burden,[...]. Haematologica 2019
6
25

A patient with Fechtner syndrome successfully treated with romiplostim.
Stefanie Gröpper, Karin Althaus, Juliane Najm, Sabine Haase, Carlo Aul, Andreas Greinacher, Aristoteles Giagounidis. Thromb Haemost 2012
11
25



Congenital hypoplastic bone marrow failure associated with a de novo partial deletion of the MECOM gene at 3q26.2.
Eigil Kjeldsen, Christopher Veigaard, Anni Aggerholm, Henrik Hasle. Gene 2018
2
50

Genetic defects and clinical characteristics of patients with a form of oculocutaneous albinism (Hermansky-Pudlak syndrome).
W A Gahl, M Brantly, M I Kaiser-Kupfer, F Iwata, S Hazelwood, V Shotelersuk, L F Duffy, E M Kuehl, J Troendle, I Bernardini. N Engl J Med 1998
169
25


One hundred percent survival after transplantation of 34 patients with Wiskott-Aldrich syndrome over 20 years.
Reem Ahmed Elfeky, Juliana M Furtado-Silva, Robert Chiesa, Kanchan Rao, Persis Amrolia, Giovanna Lucchini, Kimberly Gilmour, Stuart Adams, Shahnaz Bibi, Austen Worth,[...]. J Allergy Clin Immunol 2018
17
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.