A citation-based method for searching scientific literature

Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Hum Genet 2013
Times Cited: 99







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



Times Cited
  Times     Co-cited
Similarity


p.Val804Met, the Most Frequent Pathogenic Mutation in RET, Confers a Very Low Lifetime Risk of Medullary Thyroid Cancer.
Chey Loveday, Katherine Josephs, Daniel Chubb, Adam Gunning, Louise Izatt, Marc Tischkowitz, Sian Ellard, Clare Turnbull. J Clin Endocrinol Metab 2018
17
5

Opportunistic genomic screening. Recommendations of the European Society of Human Genetics.
Guido de Wert, Wybo Dondorp, Angus Clarke, Elisabeth M C Dequeker, Christophe Cordier, Zandra Deans, Carla G van El, Florence Fellmann, Ros Hastings, Sabine Hentze,[...]. Eur J Hum Genet 2021
6
16

Delivering genome sequencing for rapid genetic diagnosis in critically ill children: parent and professional views, experiences and challenges.
Melissa Hill, Jennifer Hammond, Celine Lewis, Rhiannon Mellis, Emma Clement, Lyn S Chitty. Eur J Hum Genet 2020
3
33

Patients' responses to incidentally discovered silent brain infarcts - a qualitative study.
Lester Y Leung, Paul K J Han, Christine Lundquist, Gene Weinstein, David E Thaler, David M Kent. J Patient Rep Outcomes 2019
1
100

Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG).
Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, Daniel P Judge, Paul F Kantor, Kim L McBride, Ana Morales, Matthew R G Taylor, Matteo Vatta, Stephanie M Ware. Genet Med 2018
57
1

Electronic health record phenotype in subjects with genetic variants associated with arrhythmogenic right ventricular cardiomyopathy: a study of 30,716 subjects with exome sequencing.
Christopher M Haggerty, Cynthia A James, Hugh Calkins, Crystal Tichnell, Joseph B Leader, Dustin N Hartzel, Christopher D Nevius, Sarah A Pendergrass, Thomas N Person, Marci Schwartz,[...]. Genet Med 2017
27
3


Psychological consequences of predictive genetic testing: a systematic review.
M Broadstock, S Michie, T Marteau. Eur J Hum Genet 2000
214
1

Current issues in medically assisted reproduction and genetics in Europe: research, clinical practice, ethics, legal issues and policy. European Society of Human Genetics and European Society of Human Reproduction and Embryology.
Joyce C Harper, Joep Geraedts, Pascal Borry, Martina C Cornel, Wybo Dondorp, Luca Gianaroli, Gary Harton, Tanya Milachich, Helena Kääriäinen, Inge Liebaers,[...]. Eur J Hum Genet 2013
35
2

The 'thousand-dollar genome': an ethical exploration.
Wybo J Dondorp, Guido M W R de Wert. Eur J Hum Genet 2013
33
3

Patients' Knowledge, Beliefs, and Distress Associated with Detection and Evaluation of Incidental Pulmonary Nodules for Cancer: Results from a Multicenter Survey.
Marc R Freiman, Jack A Clark, Christopher G Slatore, Michael K Gould, Steven Woloshin, Lisa M Schwartz, Renda Soylemez Wiener. J Thorac Oncol 2016
26
3

Genetic counseling and testing in families with hereditary nonpolyposis colorectal cancer.
Donald W Hadley, Jean Jenkins, Eileen Dimond, Kenneth Nakahara, Liam Grogan, David J Liewehr, Seth M Steinberg, Ilan Kirsch. Arch Intern Med 2003
113
1

Management of Secondary Genomic Findings.
Alexander E Katz, Robert L Nussbaum, Benjamin D Solomon, Heidi L Rehm, Marc S Williams, Leslie G Biesecker. Am J Hum Genet 2020
3
33

Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders.
Siddharth Srivastava, Jamie A Love-Nichols, Kira A Dies, David H Ledbetter, Christa L Martin, Wendy K Chung, Helen V Firth, Thomas Frazier, Robin L Hansen, Lisa Prock,[...]. Genet Med 2019
77
1

Impact of Receiving Secondary Results from Genomic Research: A 12-Month Longitudinal Study.
Julia Wynn, Josue Martinez, Jessica Bulafka, Jimmy Duong, Yuan Zhang, Codruta Chiuzan, Jain Preti, Maria L Cremona, Vaidehi Jobanputra, Abby J Fyer,[...]. J Genet Couns 2018
14
7

The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.
Jason L Vassy, Kurt D Christensen, Erica F Schonman, Carrie L Blout, Jill O Robinson, Joel B Krier, Pamela M Diamond, Matthew Lebo, Kalotina Machini, Danielle R Azzariti,[...]. Ann Intern Med 2017
94
1

1 in 38 individuals at risk of a dominant medically actionable disease.
Lonneke Haer-Wigman, Vyne van der Schoot, Ilse Feenstra, Anneke T Vulto-van Silfhout, Christian Gilissen, Han G Brunner, Lisenka E L M Vissers, Helger G Yntema. Eur J Hum Genet 2019
20
5

Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study.
M Ragan Hart, Barbara B Biesecker, Carrie L Blout, Kurt D Christensen, Laura M Amendola, Katie L Bergstrom, Sawona Biswas, Kevin M Bowling, Kyle B Brothers, Laura K Conlin,[...]. Genet Med 2019
40
2

Breaking bad news: the patient's viewpoint.
Maria Teresa Munoz Sastre, Paul Clay Sorum, Etienne Mullet. Health Commun 2011
34
2

Parents' motivations, concerns and understanding of genome sequencing: a qualitative interview study.
Celine Lewis, Saskia Sanderson, Melissa Hill, Chris Patch, Beverly Searle, Amy Hunter, Lyn S Chitty. Eur J Hum Genet 2020
8
12

"Not pathogenic until proven otherwise": perspectives of UK clinical genomics professionals toward secondary findings in context of a Genomic Medicine Multidisciplinary Team and the 100,000 Genomes Project.
Elizabeth Ormondroyd, Michael P Mackley, Edward Blair, Judith Craft, Julian C Knight, Jenny C Taylor, John Taylor, Hugh Watkins. Genet Med 2018
28
3

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
40
2

Clinical providers' experiences with returning results from genomic sequencing: an interview study.
Julia Wynn, Katie Lewis, Laura M Amendola, Barbara A Bernhardt, Sawona Biswas, Manasi Joshi, Carmit McMullen, Sarah Scollon. BMC Med Genomics 2018
28
3



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.