A citation-based method for searching scientific literature

Anneke Lucassen, Richard S Houlston. Genes (Basel) 2014
Times Cited: 13







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



Times Cited
  Times     Co-cited
Similarity


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
37
23

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
23

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
203
15

Evaluating the utility of personal genomic information.
Morris W Foster, John J Mulvihill, Richard R Sharp. Genet Med 2009
123
15

Genetic testing of children: the need for a family perspective.
Anneke Lucassen, Guy Widdershoven, Suzanne Metselaar, Angela Fenwick, Michael Parker. Am J Bioeth 2014
6
33

Distinguishing research from clinical care in cancer genetics: theoretical justifications and practical strategies.
Nina Hallowell, Sarah Cooke, Gill Crawford, Anneke Lucassen, Michael Parker. Soc Sci Med 2009
30
15

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
15


The duty to rescue in genomic research.
Michael Ulrich. Am J Bioeth 2013
14
15


Exploring resources for intrafamilial communication of cancer genetic risk: we still need to talk.
Kelly A McClellan, Erika Kleiderman, Lee Black, Karine Bouchard, Michel Dorval, Jacques Simard, Bartha M Knoppers, Denise Avard. Eur J Hum Genet 2013
10
20

Personal utility in genomic testing: is there such a thing?
Eline M Bunnik, A Cecile J W Janssens, Maartje H N Schermer. J Med Ethics 2015
57
15

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
81
15


Genetic medicine and incidental findings: it is more complicated than deciding whether to disclose or not.
Gillian Crawford, Nicola Foulds, Angela Fenwick, Nina Hallowell, Anneke Lucassen. Genet Med 2013
22
15

Genetic information: a joint account?
Michael Parker, Anneke M Lucassen. BMJ 2004
71
15

Indigenous Arabs are descendants of the earliest split from ancient Eurasian populations.
Juan L Rodriguez-Flores, Khalid Fakhro, Francisco Agosto-Perez, Monica D Ramstetter, Leonardo Arbiza, Thomas L Vincent, Amal Robay, Joel A Malek, Karsten Suhre, Lotfi Chouchane,[...]. Genome Res 2016
41
15


A new initiative on precision medicine.
Francis S Collins, Harold Varmus. N Engl J Med 2015
15

Population genetic structure of the people of Qatar.
Haley Hunter-Zinck, Shaila Musharoff, Jacqueline Salit, Khalid A Al-Ali, Lotfi Chouchane, Abeer Gohar, Rebecca Matthews, Marcus W Butler, Jennifer Fuller, Neil R Hackett,[...]. Am J Hum Genet 2010
74
15

Phased whole-genome genetic risk in a family quartet using a major allele reference sequence.
Frederick E Dewey, Rong Chen, Sergio P Cordero, Kelly E Ormond, Colleen Caleshu, Konrad J Karczewski, Michelle Whirl-Carrillo, Matthew T Wheeler, Joel T Dudley, Jake K Byrnes,[...]. PLoS Genet 2011
99
15

A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
15

Exome sequencing identifies potential risk variants for Mendelian disorders at high prevalence in Qatar.
Juan L Rodriguez-Flores, Khalid Fakhro, Neil R Hackett, Jacqueline Salit, Jennifer Fuller, Francisco Agosto-Perez, Maey Gharbiah, Joel A Malek, Mahmoud Zirie, Amin Jayyousi,[...]. Hum Mutat 2014
31
15


Management of incidental findings in clinical genomic sequencing.
Joel B Krier, Robert C Green. Curr Protoc Hum Genet 2013
17
7

Genetics specialists' perspectives on disclosure of genomic incidental findings in the clinical setting.
Nancy R Downing, Janet K Williams, Sandra Daack-Hirsch, Martha Driessnack, Christian M Simon. Patient Educ Couns 2013
40
7

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
458
7

Parental attitudes, values, and beliefs toward the return of results from exome sequencing in children.
J C Sapp, D Dong, C Stark, L E Ivey, G Hooker, L G Biesecker, B B Biesecker. Clin Genet 2014
85
7

Can I be sued for that? Liability risk and the disclosure of clinically significant genetic research findings.
Amy L McGuire, Bartha Maria Knoppers, Ma'n H Zawati, Ellen Wright Clayton. Genome Res 2014
19
7

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
268
7

Lynch syndrome patients' views of and preferences for return of results following whole exome sequencing.
Kelly Hitch, Galen Joseph, Jenna Guiltinan, Jessica Kianmahd, Janey Youngblom, Amie Blanco. J Genet Couns 2014
45
7

Offering individual genetic research results: context matters.
Laura M Beskow, Wylie Burke. Sci Transl Med 2010
129
7

Managing incidental genomic findings: legal obligations of clinicians.
Ellen Wright Clayton, Susanne Haga, Patricia Kuszler, Emily Bane, Krysta Shutske, Wylie Burke. Genet Med 2013
44
7

"I want to know what's in Pandora's Box": comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing.
Anne Townsend, Shelin Adam, Patricia H Birch, Zoe Lohn, Francois Rousseau, Jan M Friedman. Am J Med Genet A 2012
120
7

Incidental findings in the era of whole genome sequencing?
Erik Parens, Paul Appelbaum, Wendy Chung. Hastings Cent Rep 2013
17
7

Empirical research on the ethics of genomic research.
Anna Middleton, Michael Parker, Caroline F Wright, Eugene Bragin, Matthew E Hurles. Am J Med Genet A 2013
11
9

Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
7

Potential clinical and economic consequences of noncardiac incidental findings on cardiac computed tomography.
Jimmy Machaalany, Yeung Yam, Terrence D Ruddy, Arun Abraham, Li Chen, Rob S Beanlands, Benjamin J W Chow. J Am Coll Cardiol 2009
110
7

Estimates of penetrance for recurrent pathogenic copy-number variations.
Jill A Rosenfeld, Bradley P Coe, Evan E Eichler, Howard Cuckle, Lisa G Shaffer. Genet Med 2013
184
7

Next-generation sequencing demands next-generation phenotyping.
Raoul C M Hennekam, Leslie G Biesecker. Hum Mutat 2012
109
7



Policy challenges of clinical genome sequencing.
Caroline F Wright, Anna Middleton, Hilary Burton, Fiona Cunningham, Steve E Humphries, Jane Hurst, Ewan Birney, Helen V Firth. BMJ 2013
38
7

A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findings.
Joo Wook Ahn, Susan Bint, Melita D Irving, Phillipa M Kyle, Ranjit Akolekar, Shehla N Mohammed, Caroline Mackie Ogilvie. PeerJ 2014
10
10

Return of results: not that complicated?
James P Evans, Barbra B Rothschild. Genet Med 2012
48
7

Point-counterpoint. Patient autonomy and incidental findings in clinical genomics.
Susan M Wolf, George J Annas, Sherman Elias. Science 2013
158
7

Self-guided management of exome and whole-genome sequencing results: changing the results return model.
Joon-Ho Yu, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Genet Med 2013
57
7

Incidental findings of therapeutic misconception in biobank-based research.
Colin M E Halverson, Lainie Friedman Ross. Genet Med 2012
30
7

Ethical issues raised by whole genome sequencing.
Wim Pinxten, Heidi Carmen Howard. Best Pract Res Clin Gastroenterol 2014
31
7

'Information is information': a public perspective on incidental findings in clinical and research genome-based testing.
S Daack-Hirsch, M Driessnack, A Hanish, V A Johnson, L L Shah, C M Simon, J K Williams. Clin Genet 2013
50
7


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.