A citation-based method for searching scientific literature

Aad Tibben, Wybo Dondorp, Candice Cornelis, Nine Knoers, Eva Brilstra, Marieke van Summeren, Ineke Bolt. Eur J Hum Genet 2021
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Genetic testing in asymptomatic minors: background considerations towards ESHG Recommendations.
Pascal Borry, Gerry Evers-Kiebooms, Martina C Cornel, Angus Clarke, Kris Dierickx. Eur J Hum Genet 2009
114
25

Secondary findings: How did we get here, and where are we going?
Kelly E Ormond, Julianne M O'Daniel, Sarah S Kalia. J Genet Couns 2019
17
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
220
25

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
206
25

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
71
25

Medical decision-making in paediatrics: Infancy to adolescence.
Kevin W Coughlin. Paediatr Child Health 2018
18
25

Whole-exome sequencing in pediatrics: parents' considerations toward return of unsolicited findings for their child.
Candice Cornelis, Aad Tibben, Wybo Dondorp, Mieke van Haelst, Annelien L Bredenoord, Nine Knoers, Marcus Düwell, Ineke Bolt, Marieke van Summeren. Eur J Hum Genet 2016
13
25

Re-examining the Ethics of Genetic Counselling in the Genomic Era.
Will Schupmann, Leila Jamal, Benjamin E Berkman. J Bioeth Inq 2020
5
25

From genetics to genomics: ethics, policy, and parental decision-making.
Benjamin Wilfond, Lainie Friedman Ross. J Pediatr Psychol 2009
55
25

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
842
25

Shared decision making, paternalism and patient choice.
Lars Sandman, Christian Munthe. Health Care Anal 2010
108
25


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
25

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

Ethical Issues in Newborn Sequencing Research: The Case Study of BabySeq.
Lainie Friedman Ross, Ellen Wright Clayton. Pediatrics 2019
12
25


"Is it going to hurt?": the impact of the diagnostic odyssey on children and their families.
Nikkola Carmichael, Judith Tsipis, Gail Windmueller, Leslie Mandel, Elicia Estrella. J Genet Couns 2015
47
25


Rethinking the "open future" argument against predictive genetic testing of children.
Jeremy R Garrett, John D Lantos, Leslie G Biesecker, Janet E Childerhose, Wendy K Chung, Ingrid A Holm, Barbara A Koenig, Jean E McEwen, Benjamin S Wilfond, Kyle Brothers. Genet Med 2019
16
25


Guidelines for return of research results from pediatric genomic studies: deliberations of the Boston Children's Hospital Gene Partnership Informed Cohort Oversight Board.
Ingrid A Holm, Sarah K Savage, Robert C Green, Eric Juengst, Amy McGuire, Susan Kornetsky, Stephanie J Brewster, Steven Joffe, Patrick Taylor. Genet Med 2014
40
25

Bioethics in practice: Addressing ethically sensitive requests in a Dutch fertility clinic.
Trudie Gerrits, Ria Reis, Didi D M Braat, Jan A M Kremer, Anita P Hardon. Soc Sci Med 2013
5
25

The psychological impact of genetic information on children: a systematic review.
Claire E Wakefield, Lucy V Hanlon, Katherine M Tucker, Andrea F Patenaude, Christina Signorelli, Jordana K McLoone, Richard J Cohn. Genet Med 2016
52
25


Ethical issues in pediatric genetic testing and screening.
Jeffrey R Botkin. Curr Opin Pediatr 2016
18
25

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
25

Statement of principles on the return of research results and incidental findings in paediatric research: a multi-site consultative process.
Karine Sénécal, Vasiliki Rahimzadeh, Bartha M Knoppers, Conrad V Fernandez, Denise Avard, Daniel Sinnett. Genome 2015
15
25

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
25


Four models of the physician-patient relationship.
E J Emanuel, L L Emanuel. JAMA 1992
25




Shared decision making: a model for clinical practice.
Glyn Elwyn, Dominick Frosch, Richard Thomson, Natalie Joseph-Williams, Amy Lloyd, Paul Kinnersley, Emma Cording, Dave Tomson, Carole Dodd, Stephen Rollnick,[...]. J Gen Intern Med 2012
25

Unsolved challenges in pediatric whole-exome sequencing: A literature analysis.
Gabrielle Bertier, Karine Sénécal, Pascal Borry, Danya F Vears. Crit Rev Clin Lab Sci 2017
14
25




Homozygous variant in MADD, encoding a Rab guanine nucleotide exchange factor, results in pleiotropic effects and a multisystemic disorder.
Bassam Abu-Libdeh, Hagar Mor-Shaked, Amir A Atawna, David Gillis, Orli Halstuk, Nava Shaul-Lotan, Mordechai Slae, Mutaz Sultan, Vardiella Meiner, Orly Elpeleg,[...]. Eur J Hum Genet 2021
2
50

Allelic and phenotypic heterogeneity in Junctophillin-3 related neurodevelopmental and movement disorders.
Thomas Bourinaris, Alkyoni Athanasiou, Stephanie Efthymiou, Sarah Wiethoff, Vincenzo Salpietro, Henry Houlden. Eur J Hum Genet 2021
1
100

Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis.
Elin Tønne, Bernt Johan Due-Tønnessen, Inger-Lise Mero, Ulrikke Straume Wiig, Mari Ann Kulseth, Magnus Dehli Vigeland, Ying Sheng, Charlotte von der Lippe, Kristian Tveten, Torstein Ragnar Meling,[...]. Eur J Hum Genet 2021
5
25

Biallelic hypomorphic mutations in HEATR5B, encoding HEAT repeat-containing protein 5B, in a neurological syndrome with pontocerebellar hypoplasia.
Shereen G Ghosh, Martin W Breuss, Zinayida Schlachetzki, Guoliang Chai, Danica Ross, Valentina Stanley, F Mujgan Sonmez, Haluk Topaloglu, Maha S Zaki, Heba Hosny,[...]. Eur J Hum Genet 2021
1
100

Novel variants in the stem cell niche factor WNT2B define the disease phenotype as a congenital enteropathy with ocular dysgenesis.
Yanjia Jason Zhang, Lissette Jimenez, Svetlana Azova, Jessica Kremen, Yee-Ming Chan, Abdelrahman M Elhusseiny, Hajirah Saeed, Jeffrey Goldsmith, Alyaa Al-Ibraheemi, Amy E O'Connell,[...]. Eur J Hum Genet 2021
2
50

ESHG warns against misuses of genetic tests and biobanks for discrimination purposes.
Francesca Forzano, Maurizio Genuardi, Yves Moreau. Eur J Hum Genet 2021
5
25


Integrating next-generation sequencing into pediatric oncology practice: An assessment of physician confidence and understanding of clinical genomics.
Liza-Marie Johnson, Jessica M Valdez, Emily A Quinn, April D Sykes, Rose B McGee, Regina Nuccio, Stacy J Hines-Dowell, Justin N Baker, Chimene Kesserwan, Kim E Nichols,[...]. Cancer 2017
32
25

Informed consent in the genomics era.
Deborah Mascalzoni, Andrew Hicks, Peter Pramstaller, Matthias Wjst. PLoS Med 2008
56
25

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
59
25

Paediatric genomics: diagnosing rare disease in children.
Caroline F Wright, David R FitzPatrick, Helen V Firth. Nat Rev Genet 2018
157
25

Genomic risk profiling: attitudes and use in personal and clinical care of primary care physicians who offer risk profiling.
Susanne B Haga, Madeline M Carrig, Julianne M O'Daniel, Lori A Orlando, Ley A Killeya-Jones, Geoffrey S Ginsburg, Alex Cho. J Gen Intern Med 2011
56
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.