A citation-based method for searching scientific literature

Pascal Borry, Gerry Evers-Kiebooms, Martina C Cornel, Angus Clarke, Kris Dierickx. Eur J Hum Genet 2009
Times Cited: 118







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



Times Cited
  Times     Co-cited
Similarity


Technical report: Ethical and policy issues in genetic testing and screening of children.
Lainie Friedman Ross, Howard M Saal, Karen L David, Rebecca R Anderson. Genet Med 2013
263
27

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

Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents.
Jeffrey R Botkin, John W Belmont, Jonathan S Berg, Benjamin E Berkman, Yvonne Bombard, Ingrid A Holm, Howard P Levy, Kelly E Ormond, Howard M Saal, Nancy B Spinner,[...]. Am J Hum Genet 2015
231
23





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
902
13

"You're one of us now": young people describe their experiences of predictive genetic testing for Huntington disease (HD) and familial adenomatous polyposis (FAP).
Rony E Duncan, Lynn Gillam, Julian Savulescu, Robert Williamson, John G Rogers, Martin B Delatycki. Am J Med Genet C Semin Med Genet 2008
65
16





"Holding your breath": interviews with young people who have undergone predictive genetic testing for Huntington disease.
Rony E Duncan, Lynn Gillam, Julian Savulescu, Robert Williamson, John G Rogers, Martin B Delatycki. Am J Med Genet A 2007
42
16


The return of individual research findings in paediatric genetic research.
Kristien Hens, Herman Nys, Jean-Jacques Cassiman, Kris Dierickx. J Med Ethics 2011
48
14

Genetic testing for hereditary colorectal cancer in children: long-term psychological effects.
Ann-Marie Codori, Kristin L Zawacki, Gloria M Petersen, Diana L Miglioretti, Judith A Bacon, Jill D Trimbath, Susan V Booker, Kimberly Picarello, Francis M Giardiello. Am J Med Genet A 2003
71
9

Feedback of individual genetic results to research participants: in favor of a qualified disclosure policy.
Annelien L Bredenoord, N Charlotte Onland-Moret, Johannes J M Van Delden. Hum Mutat 2011
88
7


Recommendations for the predictive genetic test in Huntington's disease.
R MacLeod, A Tibben, M Frontali, G Evers-Kiebooms, A Jones, A Martinez-Descales, R A Roos. Clin Genet 2013
117
7


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
214
7

Whole-genome sequencing for identification of Mendelian disorders in critically ill infants: a retrospective analysis of diagnostic and clinical findings.
Laurel K Willig, Josh E Petrikin, Laurie D Smith, Carol J Saunders, Isabelle Thiffault, Neil A Miller, Sarah E Soden, Julie A Cakici, Suzanne M Herd, Greyson Twist,[...]. Lancet Respir Med 2015
201
7

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
7

Disclosing individual genetic results to research participants.
Vardit Ravitsky, Benjamin S Wilfond. Am J Bioeth 2006
223
6

The challenge of developmentally appropriate care: predictive genetic testing in young people for familial adenomatous polyposis.
Rony E Duncan, Lynn Gillam, Julian Savulescu, Robert Williamson, John G Rogers, Martin B Delatycki. Fam Cancer 2010
23
26


Professional ambivalence: accounts of ethical practice in childhood genetic testing.
Michael Arribas-Ayllon, Srikant Sarangi, Angus Clarke. J Genet Couns 2009
14
42

From genetics to genomics: ethics, policy, and parental decision-making.
Benjamin Wilfond, Lainie Friedman Ross. J Pediatr Psychol 2009
57
10

An international survey of predictive genetic testing in children for adult onset conditions.
Rony E Duncan, Julian Savulescu, Lynn Gillam, Robert Williamson, Martin B Delatycki. Genet Med 2005
56
10

Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consent.
Wybo Dondorp, Birgit Sikkema-Raddatz, Christine de Die-Smulders, Guido de Wert. Hum Mutat 2012
47
12

Addressing the ethical challenges in genetic testing and sequencing of children.
Ellen Wright Clayton, Laurence B McCullough, Leslie G Biesecker, Steven Joffe, Lainie Friedman Ross, Susan M Wolf. Am J Bioeth 2014
72
8

"It was the missing piece": adolescent experiences of predictive genetic testing for adult-onset conditions.
Cara Mand, Lynn Gillam, Rony E Duncan, Martin B Delatycki. Genet Med 2013
30
20

How often do BRCA mutation carriers tell their young children of the family's risk for cancer? A study of parental disclosure of BRCA mutations to minors and young adults.
Angela R Bradbury, James J Dignam, Comfort N Ibe, Sogyong L Auh, Fay J Hlubocky, Shelly A Cummings, Melody White, Olufunmilayo I Olopade, Christopher K Daugherty. J Clin Oncol 2007
64
9


Family communication between children and their parents about inherited genetic conditions: a meta-synthesis of the research.
Alison Metcalfe, Jane Coad, Gill M Plumridge, Paramjit Gill, Peter Farndon. Eur J Hum Genet 2008
94
5

Reporting genetic results in research studies: summary and recommendations of an NHLBI working group.
Ebony B Bookman, Aleisha A Langehorne, John H Eckfeldt, Kathleen C Glass, Gail P Jarvik, Michael Klag, Greg Koski, Arno Motulsky, Benjamin Wilfond, Teri A Manolio,[...]. Am J Med Genet A 2006
162
5

"Family matters": a conceptual framework for genetic testing in children.
Allyn McConkie-Rosell, Gail A Spiridigliozzi. J Genet Couns 2004
43
11

Predictive DNA-testing for Huntington's disease and reproductive decision making: a European collaborative study.
Gerry Evers-Kiebooms, Kurt Nys, Peter Harper, Moniek Zoeteweij, Alexandra Dürr, Gioia Jacopini, Christos Yapijakis, Sheila Simpson. Eur J Hum Genet 2002
58
8

Attitudes regarding carrier testing in incompetent children: a survey of European clinical geneticists.
Pascal Borry, Tom Goffin, Herman Nys, Kris Dierickx. Eur J Hum Genet 2007
19
26

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
474
5

Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study.
Anita Villani, Uri Tabori, Joshua Schiffman, Adam Shlien, Joseph Beyene, Harriet Druker, Ana Novokmet, Jonathan Finlay, David Malkin. Lancet Oncol 2011
258
5

Carrier testing in minors: a systematic review of guidelines and position papers.
Pascal Borry, Jean-Pierre Fryns, Paul Schotsmans, Kris Dierickx. Eur J Hum Genet 2006
62
8

Health-related quality of life of children with a positive carrier status for inherited cardiovascular diseases.
Ellen M A Smets, Marinka M H Stam, Tineke M Meulenkamp, Irene M van Langen, Arthur A M Wilde, Albert Wiegman, Guido M de Wert, Aad Tibben. Am J Med Genet A 2008
38
13

Constructing "best interests": genetic testing of children in families with hypertrophic cardiomyopathy.
Els Geelen, Ine Van Hoyweghen, Pieter A Doevendans, Carlo L M Marcelis, Klasien Horstman. Am J Med Genet A 2011
19
26


Secondary variants in individuals undergoing exome sequencing: screening of 572 individuals identifies high-penetrance mutations in cancer-susceptibility genes.
Jennifer J Johnston, Wendy S Rubinstein, Flavia M Facio, David Ng, Larry N Singh, Jamie K Teer, James C Mullikin, Leslie G Biesecker. Am J Hum Genet 2012
164
5

Disclosure of incidental findings from next-generation sequencing in pediatric genomic research.
Ruqayyah Abdul-Karim, Benjamin E Berkman, David Wendler, Annette Rid, Javed Khan, Tom Badgett, Sara Chandros Hull. Pediatrics 2013
55
9

Point-counterpoint. Patient autonomy and incidental findings in clinical genomics.
Susan M Wolf, George J Annas, Sherman Elias. Science 2013
159
5

Next-generation sequencing: does the next generation still have a right to an open future?
Annelien L Bredenoord, Martine C de Vries, Johannes J M van Delden. Nat Rev Genet 2013
32
15


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.