A citation-based method for searching scientific literature

Melissa Martyn, Anaita Kanga-Parabia, Elly Lynch, Paul A James, Ivan Macciocca, Alison H Trainer, Jane Halliday, Louise Keogh, Janney Wale, Ingrid Winship, Michael Bogwitz, Giulia Valente, Maie Walsh, Lilian Downie, David Amor, Mathew Wallis, Fiona Cunningham, Matthew Burgess, Natasha J Brown, Anna Jarmolowicz, Sebastian Lunke, Ilias Goranitis, Clara L Gaff. J Genet Couns 2019
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


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
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

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
58
50

Evaluation of Recipients of Positive and Negative Secondary Findings Evaluations in a Hybrid CLIA-Research Sequencing Pilot.
Julie C Sapp, Jennifer J Johnston, Kate Driscoll, Alexis R Heidlebaugh, Ane Miren Sagardia, D Nadine Dogbe, Kendall L Umstead, Erin Turbitt, Ilias Alevizos, Jeffrey Baron,[...]. Am J Hum Genet 2018
18
50

Genomics, Health Disparities, and Missed Opportunities for the Nation's Research Agenda.
Kathleen McGlone West, Erika Blacksher, Wylie Burke. JAMA 2017
39
25


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
119
25

p53 and Me.
Shekinah N C Elmore. N Engl J Med 2018
4
25

Patients-in-waiting: Living between sickness and health in the genomics era.
Stefan Timmermans, Mara Buchbinder. J Health Soc Behav 2010
143
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

Analysis of laboratory reporting practices using a quality assessment of a virtual patient.
Danya F Vears, Martin Elferink, Marjolein Kriek, Pascal Borry, Koen L van Gassen. Genet Med 2021
2
50

Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendations.
Pascal Pujol, Pierre Vande Perre, Laurence Faivre, Damien Sanlaville, Carole Corsini, Bernard Baertschi, Michèle Anahory, Dominique Vaur, Sylviane Olschwang, Nadem Soufir,[...]. Eur J Hum Genet 2018
13
25

Tumour risks and genotype-phenotype correlations associated with germline variants in succinate dehydrogenase subunit genes SDHB, SDHC and SDHD.
Katrina A Andrews, David B Ascher, Douglas Eduardo Valente Pires, Daniel R Barnes, Lindsey Vialard, Ruth T Casey, Nicola Bradshaw, Julian Adlard, Simon Aylwin, Paul Brennan,[...]. J Med Genet 2018
81
25

Revisiting Wilson and Jungner in the genomic age: a review of screening criteria over the past 40 years.
Anne Andermann, Ingeborg Blancquaert, Sylvie Beauchamp, Véronique Déry. Bull World Health Organ 2008
431
25

Ethical values supporting the disclosure of incidental and secondary findings in clinical genomic testing: a qualitative study.
Marlies Saelaert, Heidi Mertes, Tania Moerenhout, Elfride De Baere, Ignaas Devisch. BMC Med Ethics 2020
7
25


Searching for secondary findings: considering actionability and preserving the right not to know.
Bertrand Isidor, Sophie Julia, Pascale Saugier-Veber, Paul-Loup Weil-Dubuc, Stéphane Bézieau, Eric Bieth, Jean-Paul Bonnefont, Arnold Munnich, Franck Bourdeaut, Catherine Bourgain,[...]. Eur J Hum Genet 2019
8
25

Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics.
Daniele Carrieri, Heidi C Howard, Caroline Benjamin, Angus J Clarke, Sandi Dheensa, Shane Doheny, Naomi Hawkins, Tanya F Halbersma-Konings, Leigh Jackson, Hülya Kayserili,[...]. Eur J Hum Genet 2019
35
25

Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations.
Hartmut P H Neumann, Christian Pawlu, Mariola Peczkowska, Birke Bausch, Sarah R McWhinney, Mihaela Muresan, Mary Buchta, Gerlind Franke, Joachim Klisch, Thorsten A Bley,[...]. JAMA 2004
653
25

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
28
25

Quantifying prion disease penetrance using large population control cohorts.
Eric Vallabh Minikel, Sonia M Vallabh, Monkol Lek, Karol Estrada, Kaitlin E Samocha, J Fah Sathirapongsasuti, Cory Y McLean, Joyce Y Tung, Linda P C Yu, Pierluigi Gambetti,[...]. Sci Transl Med 2016
181
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

Incidental findings on imaging.
Thomas C Booth. BMJ 2018
7
25

Genome-wide polygenic scores for common diseases identify individuals with risk equivalent to monogenic mutations.
Amit V Khera, Mark Chaffin, Krishna G Aragam, Mary E Haas, Carolina Roselli, Seung Hoan Choi, Pradeep Natarajan, Eric S Lander, Steven A Lubitz, Patrick T Ellinor,[...]. Nat Genet 2018
838
25

Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness.
Franziska Severin, Pascal Borry, Martina C Cornel, Norman Daniels, Florence Fellmann, Shirley Victoria Hodgson, Heidi C Howard, Jürgen John, Helena Kääriäinen, Hülya Kayserili,[...]. Eur J Hum Genet 2015
16
25


Opportunistic screening for osteoporosis using abdominal computed tomography scans obtained for other indications.
Perry J Pickhardt, B Dustin Pooler, Travis Lauder, Alejandro Muñoz del Rio, Richard J Bruce, Neil Binkley. Ann Intern Med 2013
300
25


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

Rare Genetic Variants Associated With Sudden Cardiac Death in Adults.
Amit V Khera, Heather Mason-Suares, Deanna Brockman, Minxian Wang, Martin J VanDenburgh, Ozlem Senol-Cosar, Candace Patterson, Christopher Newton-Cheh, Seyedeh M Zekavat, Julie Pester,[...]. J Am Coll Cardiol 2019
15
25

Point-counterpoint. Patient autonomy and incidental findings in clinical genomics.
Susan M Wolf, George J Annas, Sherman Elias. Science 2013
157
25

An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome.
Arnon Adler, Valeria Novelli, Ahmad S Amin, Emanuela Abiusi, Melanie Care, Eline A Nannenberg, Harriet Feilotter, Simona Amenta, Daniela Mazza, Hennie Bikker,[...]. Circulation 2020
69
25

Referral to cancer genetic counseling: do migrant status and patients' educational background matter?
J A M van der Giessen, E van Riel, M E Velthuizen, A M van Dulmen, M G E M Ausems. J Community Genet 2017
13
25

The Medical Genome Reference Bank: a whole-genome data resource of 4000 healthy elderly individuals. Rationale and cohort design.
Paul Lacaze, Mark Pinese, Warren Kaplan, Andrew Stone, Marie-Jo Brion, Robyn L Woods, Martin McNamara, John J McNeil, Marcel E Dinger, David M Thomas. Eur J Hum Genet 2019
15
25


Analysis of polygenic risk score usage and performance in diverse human populations.
L Duncan, H Shen, B Gelaye, J Meijsen, K Ressler, M Feldman, R Peterson, B Domingue. Nat Commun 2019
201
25

Recommendations for returning genomic incidental findings? We need to talk!
Wylie Burke, Armand H Matheny Antommaria, Robin Bennett, Jeffrey Botkin, Ellen Wright Clayton, Gail E Henderson, Ingrid A Holm, Gail P Jarvik, Muin J Khoury, Bartha Maria Knoppers,[...]. Genet Med 2013
212
25

Genetic Insurance Discrimination in Sudden Arrhythmia Death Syndromes: Empirical Evidence From a Cross-Sectional Survey in North America.
Saira Mohammed, Zaneta Lim, Paige H Dean, James E Potts, Jessica N C Tang, Susan P Etheridge, Alice Lara, Pam Husband, Elizabeth D Sherwin, Michael J Ackerman,[...]. Circ Cardiovasc Genet 2017
12
25

Whole-genome sequencing in newborn screening? A statement on the continued importance of targeted approaches in newborn screening programmes.
Heidi Carmen Howard, Bartha Maria Knoppers, Martina C Cornel, Ellen Wright Clayton, Karine Sénécal, Pascal Borry. Eur J Hum Genet 2015
47
25

Diversity and inclusion in genomic research: why the uneven progress?
Amy R Bentley, Shawneequa Callier, Charles N Rotimi. J Community Genet 2017
90
25


Genetic Misdiagnoses and the Potential for Health Disparities.
Arjun K Manrai, Birgit H Funke, Heidi L Rehm, Morten S Olesen, Bradley A Maron, Peter Szolovits, David M Margulies, Joseph Loscalzo, Isaac S Kohane. N Engl J Med 2016
320
25

When genetic burden reaches threshold.
Roddy Walsh, Rafik Tadros, Connie R Bezzina. Eur Heart J 2020
8
25

Point-counterpoint. Ethics and genomic incidental findings.
Amy L McGuire, Steven Joffe, Barbara A Koenig, Barbara B Biesecker, Laurence B McCullough, Jennifer S Blumenthal-Barby, Timothy Caulfield, Sharon F Terry, Robert C Green. Science 2013
130
25

Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic tests.
P Pujol, D Stoppa Lyonnet, T Frebourg, J Blin, M C Picot, C Lasset, C Dugast, P Berthet, B Bressac de Paillerets, H Sobol,[...]. Breast Cancer Res Treat 2013
30
25



The Promise and Peril of Precision Medicine: Phenotyping Still Matters Most.
Jaeger P Ackerman, Daniel C Bartos, Jamie D Kapplinger, David J Tester, Brian P Delisle, Michael J Ackerman. Mayo Clin Proc 2016
53
25

Web-based return of BRCA2 research results: one-year genetic counselling experience in Iceland.
Vigdis Stefansdottir, Eirny Thorolfsdottir, Hakon B Hognason, Christine Patch, Carla van El, Sabine Hentze, Christophe Cordier, Álvaro Mendes, Jon J Jonsson. Eur J Hum Genet 2020
3
33

Validation of screening procedures.
A L Cochrane, W W Holland. Br Med Bull 1971
295
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.