A citation-based method for searching scientific literature

Leslie G Biesecker. Am J Hum Genet 2013
Times Cited: 33







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



Times Cited
  Times     Co-cited
Similarity


Reporting incidental findings in genomic scale clinical sequencing--a clinical laboratory perspective: a report of the Association for Molecular Pathology.
Madhuri Hegde, Sherri Bale, Pinar Bayrak-Toydemir, Jane Gibson, Linda Jo Bone Jeng, Loren Joseph, Jordan Laser, Ira M Lubin, Christine E Miller, Lainie F Ross,[...]. J Mol Diagn 2015
35
6

BRCA Share: A Collection of Clinical BRCA Gene Variants.
Christophe Béroud, Stanley I Letovsky, Corey D Braastad, Sandrine M Caputo, Olivia Beaudoux, Yves Jean Bignon, Brigitte Bressac-De Paillerets, Myriam Bronner, Crystal M Buell, Gwenaëlle Collod-Béroud,[...]. Hum Mutat 2016
37
6

dbSNP: the NCBI database of genetic variation.
S T Sherry, M H Ward, M Kholodov, J Baker, L Phan, E M Smigielski, K Sirotkin. Nucleic Acids Res 2001
6

UMD (Universal Mutation Database): 2005 update.
Christophe Béroud, Dalil Hamroun, Gwenaëlle Collod-Béroud, Catherine Boileau, Thierry Soussi, Mireille Claustres. Hum Mutat 2005
85
6

UMD-Predictor: A High-Throughput Sequencing Compliant System for Pathogenicity Prediction of any Human cDNA Substitution.
David Salgado, Jean-Pierre Desvignes, Ghadi Rai, Arnaud Blanchard, Morgane Miltgen, Amélie Pinard, Nicolas Lévy, Gwenaëlle Collod-Béroud, Christophe Béroud. Hum Mutat 2016
77
6


Secondary findings and carrier test frequencies in a large multiethnic sample.
Tomasz Gambin, Shalini N Jhangiani, Jennifer E Below, Ian M Campbell, Wojciech Wiszniewski, Donna M Muzny, Jeffrey Staples, Alanna C Morrison, Matthew N Bainbridge, Samantha Penney,[...]. Genome Med 2015
38
6


Predicting the functional effect of amino acid substitutions and indels.
Yongwook Choi, Gregory E Sims, Sean Murphy, Jason R Miller, Agnes P Chan. PLoS One 2012
6

Economic evidence on identifying clinically actionable findings with whole-genome sequencing: a scoping review.
Michael P Douglas, Uri Ladabaum, Mark J Pletcher, Deborah A Marshall, Kathryn A Phillips. Genet Med 2016
16
12

Human Splicing Finder: an online bioinformatics tool to predict splicing signals.
François-Olivier Desmet, Dalil Hamroun, Marine Lalande, Gwenaëlle Collod-Béroud, Mireille Claustres, Christophe Béroud. Nucleic Acids Res 2009
6

SIFT web server: predicting effects of amino acid substitutions on proteins.
Ngak-Leng Sim, Prateek Kumar, Jing Hu, Steven Henikoff, Georg Schneider, Pauline C Ng. Nucleic Acids Res 2012
988
6

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders.
Jenny C Taylor, Hilary C Martin, Stefano Lise, John Broxholme, Jean-Baptiste Cazier, Andy Rimmer, Alexander Kanapin, Gerton Lunter, Simon Fiddy, Chris Allan,[...]. Nat Genet 2015
193
6

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records.
Sara L Van Driest, Quinn S Wells, Sarah Stallings, William S Bush, Adam Gordon, Deborah A Nickerson, Jerry H Kim, David R Crosslin, Gail P Jarvik, David S Carrell,[...]. JAMA 2016
114
6



Genetic diagnosis of developmental disorders in the DDD study: a scalable analysis of genome-wide research data.
Caroline F Wright, Tomas W Fitzgerald, Wendy D Jones, Stephen Clayton, Jeremy F McRae, Margriet van Kogelenberg, Daniel A King, Kirsty Ambridge, Daniel M Barrett, Tanya Bayzetinova,[...]. Lancet 2015
374
6

Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders.
Ada Hamosh, Alan F Scott, Joanna S Amberger, Carol A Bocchini, Victor A McKusick. Nucleic Acids Res 2005
6


An ethics framework for a learning health care system: a departure from traditional research ethics and clinical ethics.
Ruth R Faden, Nancy E Kass, Steven N Goodman, Peter Pronovost, Sean Tunis, Tom L Beauchamp. Hastings Cent Rep 2013
278
6


Can research and care be ethically integrated?
Emily A Largent, Steven Joffe, Franklin G Miller. Hastings Cent Rep 2011
64
6

Adrift in the Gray Zone: IRB Perspectives on Research in the Learning Health System.
Sandra Soo-Jin Lee, Maureen Kelley, Mildred K Cho, Stephanie Alessi Kraft, Cyan James, Melissa Constantine, Adrienne N Meyer, Douglas Diekema, Alexander M Capron, Benjamin S Wilfond,[...]. AJOB Empir Bioeth 2016
19
10

Molecular findings among patients referred for clinical whole-exome sequencing.
Yaping Yang, Donna M Muzny, Fan Xia, Zhiyv Niu, Richard Person, Yan Ding, Patricia Ward, Alicia Braxton, Min Wang, Christian Buhay,[...]. JAMA 2014
809
6

Clinical interpretation and implications of whole-genome sequencing.
Frederick E Dewey, Megan E Grove, Cuiping Pan, Benjamin A Goldstein, Jonathan A Bernstein, Hassan Chaib, Jason D Merker, Rachel L Goldfeder, Gregory M Enns, Sean P David,[...]. JAMA 2014
292
6

Clinical exome sequencing for genetic identification of rare Mendelian disorders.
Hane Lee, Joshua L Deignan, Naghmeh Dorrani, Samuel P Strom, Sibel Kantarci, Fabiola Quintero-Rivera, Kingshuk Das, Traci Toy, Bret Harry, Michael Yourshaw,[...]. JAMA 2014
570
6

Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions.
Kelly D Farwell, Layla Shahmirzadi, Dima El-Khechen, Zöe Powis, Elizabeth C Chao, Brigette Tippin Davis, Ruth M Baxter, Wenqi Zeng, Cameron Mroske, Melissa C Parra,[...]. Genet Med 2015
290
6

Practical considerations in the clinical application of whole-exome sequencing.
V Shashi, A McConkie-Rosell, K Schoch, V Kasturi, C Rehder, Y H Jiang, D B Goldstein, M T McDonald. Clin Genet 2016
36
6

Moral Duties of Genomics Researchers: Why Personalized Medicine Requires a Collective Approach.
Shoko Vos, Johannes J M van Delden, Paul J van Diest, Annelien L Bredenoord. Trends Genet 2017
12
16

The cost-effectiveness of returning incidental findings from next-generation genomic sequencing.
Caroline S Bennette, Carlos J Gallego, Wylie Burke, Gail P Jarvik, David L Veenstra. Genet Med 2015
65
6

A proposed approach to accelerate evidence generation for genomic-based technologies in the context of a learning health system.
Christine Y Lu, Marc S Williams, Geoffrey S Ginsburg, Sengwee Toh, Jeff S Brown, Muin J Khoury. Genet Med 2018
12
16

Neonatal neuroblastoma.
Jonathan P H Fisher, Deborah A Tweddle. Semin Fetal Neonatal Med 2012
39
3

Screening for neuroblastoma: a resurrected idea?
John M Maris, William G Woods. Lancet 2008
13
7


Initial sequencing and comparative analysis of the mouse genome.
Robert H Waterston, Kerstin Lindblad-Toh, Ewan Birney, Jane Rogers, Josep F Abril, Pankaj Agarwal, Richa Agarwala, Rachel Ainscough, Marina Alexandersson, Peter An,[...]. Nature 2002
3

Exome sequencing identifies ACSF3 as a cause of combined malonic and methylmalonic aciduria.
Jennifer L Sloan, Jennifer J Johnston, Irini Manoli, Randy J Chandler, Caitlin Krause, Nuria Carrillo-Carrasco, Suma D Chandrasekaran, Justin R Sysol, Kevin O'Brien, Natalie S Hauser,[...]. Nat Genet 2011
57
3


Next-generation sequencing demands next-generation phenotyping.
Raoul C M Hennekam, Leslie G Biesecker. Hum Mutat 2012
109
3

Expanded newborn screening: implications for genomic medicine.
Linda L McCabe, Edward R B McCabe. Annu Rev Med 2008
32
3

Noninvasive prenatal diagnosis empowered by high-throughput sequencing.
Rossa W K Chiu, Y M Dennis Lo. Prenat Diagn 2012
20
5

Cancer risks for BRCA1 and BRCA2 mutation carriers: results from prospective analysis of EMBRACE.
Nasim Mavaddat, Susan Peock, Debra Frost, Steve Ellis, Radka Platte, Elena Fineberg, D Gareth Evans, Louise Izatt, Rosalind A Eeles, Julian Adlard,[...]. J Natl Cancer Inst 2013
487
3


Clinical aspects of PCSK9.
Bertrand Cariou, Cédric Le May, Philippe Costet. Atherosclerosis 2011
112
3


Determination of tumor aggressiveness in colorectal cancer by K-ras-2 analysis.
S D Finkelstein, R Sayegh, A Bakker, P Swalsky. Arch Surg 1993
102
3

Phentermine and topiramate for the management of obesity: a review.
Gina Cosentino, Ariane O Conrad, Gabriel I Uwaifo. Drug Des Devel Ther 2011
23
4

Mismatch repair genes in Lynch syndrome: a review.
Felipe Cavalcanti Carneiro da Silva, Mev Dominguez Valentin, Fábio de Oliveira Ferreira, Dirce Maria Carraro, Benedito Mauro Rossi. Sao Paulo Med J 2009
45
3

Genetic counselors' current use of personal health records-based family histories in genetic clinics and considerations for their future adoption.
Chaney Widmer, Jonathan P Deshazo, Joann Bodurtha, John Quillin, Heather Creswick. J Genet Couns 2013
5
20




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.