A citation-based method for searching scientific literature

Emmanuelle Souzeau, Kathryn P Burdon, David A Mackey, Alex W Hewitt, Ravi Savarirayan, Margaret Otlowski, Jamie E Craig.  2016
Times Cited: 6







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



Times Cited
  Times     Co-cited
Similarity


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
66

Managing incidental findings in human subjects research: analysis and recommendations.
Susan M Wolf, Frances P Lawrenz, Charles A Nelson, Jeffrey P Kahn, Mildred K Cho, Ellen Wright Clayton, Joel G Fletcher, Michael K Georgieff, Dale Hammerschmidt, Kathy Hudson,[...]. J Law Med Ethics 2008
425
50

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
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
194
33

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
201
33

Actionable, pathogenic incidental findings in 1,000 participants' exomes.
Michael O Dorschner, Laura M Amendola, Emily H Turner, Peggy D Robertson, Brian H Shirts, Carlos J Gallego, Robin L Bennett, Kelly L Jones, Mari J Tokita, James T Bennett,[...]. Am J Hum Genet 2013
262
33

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
720
33

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
79
33


Is there a duty to recontact in light of new genetic technologies? A systematic review of the literature.
Ellen Otten, Mirjam Plantinga, Erwin Birnie, Marian A Verkerk, Anneke M Lucassen, Adelita V Ranchor, Irene M Van Langen. Genet Med 2015
43
33

Recontacting in clinical practice: an investigation of the views of healthcare professionals and clinical scientists in the United Kingdom.
Daniele Carrieri, Sandi Dheensa, Shane Doheny, Angus J Clarke, Peter D Turnpenny, Anneke M Lucassen, Susan E Kelly. Eur J Hum Genet 2017
20
33

Defining and managing incidental findings in genetic and genomic practice.
Shiri Shkedi-Rafid, Sandi Dheensa, Gillian Crawford, Angela Fenwick, Anneke Lucassen. J Med Genet 2014
36
33

Recontact in clinical practice: a survey of clinical genetics services in the United Kingdom.
Daniele Carrieri, Anneke M Lucassen, Angus J Clarke, Sandi Dheensa, Shane Doheny, Peter D Turnpenny, Susan E Kelly. Genet Med 2016
24
33

Genomic research and incidental findings.
Brian Van Ness. J Law Med Ethics 2008
33
33

Guidelines for diagnostic next-generation sequencing.
Gert Matthijs, Erika Souche, Mariëlle Alders, Anniek Corveleyn, Sebastian Eck, Ilse Feenstra, Valérie Race, Erik Sistermans, Marc Sturm, Marjan Weiss,[...]. Eur J Hum Genet 2016
205
33

Interdisciplinary education to integrate pathology and epidemiology: towards molecular and population-level health science.
Shuji Ogino, Emily E King, Andrew H Beck, Mark E Sherman, Danny A Milner, Edward Giovannucci. Am J Epidemiol 2012
44
16

Different tracks for pathology informatics fellowship training: Experiences of and input from trainees in a large multisite fellowship program.
Bruce P Levy, David S McClintock, Roy E Lee, William J Lane, Veronica E Klepeis, Jason M Baron, Maristela L Onozato, Jiyeon Kim, Victor Brodsky, Bruce Beckwith,[...]. J Pathol Inform 2012
13
16

Personalized oncology through integrative high-throughput sequencing: a pilot study.
Sameek Roychowdhury, Matthew K Iyer, Dan R Robinson, Robert J Lonigro, Yi-Mi Wu, Xuhong Cao, Shanker Kalyana-Sundaram, Lee Sam, O Alejandro Balbin, Michael J Quist,[...]. Sci Transl Med 2011
409
16

From prospective biobanking to precision medicine: BIO-RAIDs - an EU study protocol in cervical cancer.
Charlotte Ngo, Sanne Samuels, Ksenia Bagrintseva, Andrea Slocker, Philippe Hupé, Gemma Kenter, Marina Popovic, Nina Samet, Patricia Tresca, Heiko von der Leyen,[...]. BMC Cancer 2015
10
16

ERIC: a new governance tool for biobanking.
Jane Reichel, Anna-Sara Lind, Mats G Hansson, Jan-Eric Litton. Eur J Hum Genet 2014
13
16

Biobanks: transnational, European and global networks.
Martin Asslaber, Kurt Zatloukal. Brief Funct Genomic Proteomic 2007
67
16

Digital pathology and image analysis in tissue biomarker research.
Peter W Hamilton, Peter Bankhead, Yinhai Wang, Ryan Hutchinson, Declan Kieran, Darragh G McArt, Jacqueline James, Manuel Salto-Tellez. Methods 2014
80
16

Paraffin treasures: do they last forever?
Vera Ademà, Erica Torres, Francesc Solé, Sergi Serrano, Beatriz Bellosillo. Biopreserv Biobank 2014
8
16


Comparison of clinical targeted next-generation sequence data from formalin-fixed and fresh-frozen tissue specimens.
David H Spencer, Jennifer K Sehn, Haley J Abel, Mark A Watson, John D Pfeifer, Eric J Duncavage. J Mol Diagn 2013
108
16


Molecular pathology - the value of an integrative approach.
Manuel Salto-Tellez, Jacqueline A James, Peter W Hamilton. Mol Oncol 2014
23
16

A data standard for sourcing fit-for-purpose biological samples in an integrated virtual network of biobanks.
Philip R Quinlan, Gita Mistry, Helen Bullbeck, Anne Carter. Biopreserv Biobank 2014
13
16

Cancer biomarker discovery: Opportunities and pitfalls in analytical methods.
Haleem J Issaq, Timothy J Waybright, Timothy D Veenstra. Electrophoresis 2011
72
16

Biobanking for better healthcare.
Peter H J Riegman, Manuel M Morente, Fay Betsou, Pasquale de Blasio, Peter Geary. Mol Oncol 2008
139
16

Extracellular Vesicles as Biomarkers and Therapeutic Targets in Breast Cancer.
Lilite Sadovska, Jānis Eglītis, Aija Linē. Anticancer Res 2015
26
16

Ethical tissue: a not-for-profit model for human tissue supply.
Kevin Adams, Sandie Martin. Cell Tissue Bank 2011
1
100

Digital imaging in pathology: whole-slide imaging and beyond.
Farzad Ghaznavi, Andrew Evans, Anant Madabhushi, Michael Feldman. Annu Rev Pathol 2013
147
16

Mining the plasma proteome for cancer biomarkers.
Samir M Hanash, Sharon J Pitteri, Vitor M Faca. Nature 2008
523
16

PICan: An integromics framework for dynamic cancer biomarker discovery.
Darragh G McArt, Jaine K Blayney, David P Boyle, Gareth W Irwin, Michael Moran, Ryan A Hutchinson, Peter Bankhead, Declan Kieran, Yinhai Wang, Philip D Dunne,[...]. Mol Oncol 2015
12
16

Biobanking: the foundation of personalized medicine.
Robert E Hewitt. Curr Opin Oncol 2011
146
16

Targeted Next Generation Sequencing as a Reliable Diagnostic Assay for the Detection of Somatic Mutations in Tumours Using Minimal DNA Amounts from Formalin Fixed Paraffin Embedded Material.
Wendy W J de Leng, Christa G Gadellaa-van Hooijdonk, Françoise A S Barendregt-Smouter, Marco J Koudijs, Ies Nijman, John W J Hinrichs, Edwin Cuppen, Stef van Lieshout, Robert D Loberg, Maja de Jonge,[...]. PLoS One 2016
57
16

What are the biggest challenges and opportunities for biorepositories in the next three to five years?
Fay Betsou, David L Rimm, Peter H Watson, Christopher Womack, Allison Hubel, Robert A Coleman, Liz Horn, Sharon F Terry, Nikolajs Zeps, Brian J Clark,[...]. Biopreserv Biobank 2010
14
16

An NCI perspective on creating sustainable biospecimen resources.
Jimmie Vaught, Joyce Rogers, Kimberly Myers, Mark David Lim, Nicole Lockhart, Helen Moore, Sherilyn Sawyer, Jeffrey L Furman, Carolyn Compton. J Natl Cancer Inst Monogr 2011
75
16

Tissue banking, bioinformatics, and electronic medical records: the front-end requirements for personalized medicine.
K Stephen Suh, Sreeja Sarojini, Maher Youssif, Kip Nalley, Natasha Milinovikj, Fathi Elloumi, Steven Russell, Andrew Pecora, Elyssa Schecter, Andre Goy. J Oncol 2013
20
16

Validation of next generation sequencing technologies in comparison to current diagnostic gold standards for BRAF, EGFR and KRAS mutational analysis.
Clare M McCourt, Darragh G McArt, Ken Mills, Mark A Catherwood, Perry Maxwell, David J Waugh, Peter Hamilton, Joe M O'Sullivan, Manuel Salto-Tellez. PLoS One 2013
72
16

A new paradigm for biospecimen banking in the personalized medicine era.
Sandra A McDonald, Mark A Watson, Joan Rossi, Colleen M Becker, David P Jaques, John D Pfeifer. Am J Clin Pathol 2011
11
16

The value of banked samples for oncology drug discovery and development.
Peter M Shaw, Scott D Patterson. J Natl Cancer Inst Monogr 2011
16
16

The role of the pathologist in tissue banking: European Consensus Expert Group Report.
Generoso Bevilacqua, Fred Bosman, Thibaut Dassesse, Heinz Höfler, Anne Janin, Rupert Langer, Denis Larsimont, Manuel M Morente, Peter Riegman, Peter Schirmacher,[...]. Virchows Arch 2010
49
16

Embracing an integromic approach to tissue biomarker research in cancer: Perspectives and lessons learned.
Gerald Li, Peter Bankhead, Philip D Dunne, Paul G O'Reilly, Jacqueline A James, Manuel Salto-Tellez, Peter W Hamilton, Darragh G McArt. Brief Bioinform 2017
5
20

The Informatics Challenges Facing Biobanks: A Perspective from a United Kingdom Biobanking Network.
Philip R Quinlan, Martin Groves, Lee B Jordan, Hilary Stobart, Colin A Purdie, Alastair M Thompson. Biopreserv Biobank 2015
7
16

Archived formalin-fixed paraffin-embedded (FFPE) blocks: A valuable underexploited resource for extraction of DNA, RNA, and protein.
Theresa J Kokkat, Miral S Patel, Diane McGarvey, Virginia A LiVolsi, Zubair W Baloch. Biopreserv Biobank 2013
71
16

The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists.
Kym Boycott, Taila Hartley, Shelin Adam, Francois Bernier, Karen Chong, Bridget A Fernandez, Jan M Friedman, Michael T Geraghty, Stacey Hume, Bartha M Knoppers,[...]. J Med Genet 2015
107
16

Ethical implications of the use of whole genome methods in medical research.
Jane Kaye, Paula Boddington, Jantina de Vries, Naomi Hawkins, Karen Melham. Eur J Hum Genet 2010
48
16

Are physicians prepared for whole genome sequencing? a qualitative analysis.
K D Christensen, J L Vassy, L Jamal, L S Lehmann, M J Slashinski, D L Perry, J O Robinson, J Blumenthal-Barby, L Z Feuerman, M F Murray,[...]. Clin Genet 2016
63
16


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.