A citation-based method for searching scientific literature

Daniele Carrieri, Sandi Dheensa, Shane Doheny, Angus J Clarke, Peter D Turnpenny, Anneke M Lucassen, Susan E Kelly. Eur J Hum Genet 2017
Times Cited: 25







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



Times Cited
  Times     Co-cited
Similarity


Is there a duty to recontact in light of new genetic technologies? A systematic review of the literature.
Ellen Otten, Mirjam Plantinga, Erwin Birnie, Marian A Verkerk, Anneke M Lucassen, Adelita V Ranchor, Irene M Van Langen. Genet Med 2015
55
72

Recontact in clinical practice: a survey of clinical genetics services in the United Kingdom.
Daniele Carrieri, Anneke M Lucassen, Angus J Clarke, Sandi Dheensa, Shane Doheny, Peter D Turnpenny, Susan E Kelly. Genet Med 2016
30
64

A 'joint venture' model of recontacting in clinical genomics: challenges for responsible implementation.
Sandi Dheensa, Daniele Carrieri, Susan Kelly, Angus Clarke, Shane Doheny, Peter Turnpenny, Anneke Lucassen. Eur J Med Genet 2017
23
56

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
36

Recontacting in clinical practice: the views and expectations of patients in the United Kingdom.
Daniele Carrieri, Sandi Dheensa, Shane Doheny, Angus J Clarke, Peter D Turnpenny, Anneke M Lucassen, Susan E Kelly. Eur J Hum Genet 2017
17
47

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
39
32

Recontacting or not recontacting? A survey of current practices in clinical genetics centres in Europe.
Fabio Sirchia, Daniele Carrieri, Sandi Dheensa, Caroline Benjamin, Hülya Kayserili, Christophe Cordier, Carla G van El, Peter D Turnpenny, Bela Melegh, Álvaro Mendes,[...]. Eur J Hum Genet 2018
21
38

Duty to re-contact.
K Hirschhorn, L D Fleisher, L Godmilow, R R Howell, R R Lebel, E R McCabe, M J McGinniss, A Milunsky, M Z Pelias, R E Pyeritz,[...]. Genet Med 1999
36
28

The duty to recontact: attitudes of genetics service providers.
J L Fitzpatrick, C Hahn, T Costa, M J Huggins. Am J Hum Genet 1999
45
24

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
85
24

Recontacting in clinical genetics and genomic medicine? We need to talk about it.
Daniele Carrieri, Sandi Dheensa, Shane Doheny, Angus J Clarke, Peter D Turnpenny, Anneke M Lucassen, Susan E Kelly. Eur J Hum Genet 2017
11
54

Recontacting in light of new genetic diagnostic techniques for patients with intellectual disability: Feasibility and parental perspectives.
Gea Beunders, Melodi Dekker, Oscar Haver, Hanne J Meijers-Heijboer, Lidewij Henneman. Eur J Med Genet 2018
10
60

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
128
20

Expanding the physician's duty of care: a duty to recontact?
Martin Letendre, Béatrice Godard. Med Law 2004
13
38



The inverse care law.
J T Hart. Lancet 1971
20

Prevalence of Variant Reclassification Following Hereditary Cancer Genetic Testing.
Jacqueline Mersch, Nichole Brown, Sara Pirzadeh-Miller, Erin Mundt, Hannah C Cox, Krystal Brown, Melissa Aston, Lisa Esterling, Susan Manley, Theodora Ross. JAMA 2018
103
20

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
16

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
936
16


Patient preferences regarding recontact by cancer genetics clinicians.
Constance A Griffin, Jennifer E Axilbund, Ann Marie Codori, Ginny Deise, Betty May, Cheryl Pendergrass, Miriam Tillery, Jill D Trimbath, Francis M Giardiello. Fam Cancer 2007
16
25


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
258
16

Making new genetic diagnoses with old data: iterative reanalysis and reporting from genome-wide data in 1,133 families with developmental disorders.
Caroline F Wright, Jeremy F McRae, Stephen Clayton, Giuseppe Gallone, Stuart Aitken, Tomas W FitzGerald, Philip Jones, Elena Prigmore, Diana Rajan, Jenny Lord,[...]. Genet Med 2018
149
16

Analysis of VUS reporting, variant reinterpretation and recontact policies in clinical genomic sequencing consent forms.
Danya F Vears, Emilia Niemiec, Heidi Carmen Howard, Pascal Borry. Eur J Hum Genet 2018
36
16

Patient re-contact after revision of genomic test results: points to consider-a statement of the American College of Medical Genetics and Genomics (ACMG).
Karen L David, Robert G Best, Leslie Manace Brenman, Lynn Bush, Joshua L Deignan, David Flannery, Jodi D Hoffman, Ingrid Holm, David T Miller, James O'Leary,[...]. Genet Med 2019
54
16

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
12

Stakeholder views on secondary findings in whole-genome and whole-exome sequencing: a systematic review of quantitative and qualitative studies.
Michael P Mackley, Benjamin Fletcher, Michael Parker, Hugh Watkins, Elizabeth Ormondroyd. Genet Med 2017
74
12


Managing incidental genomic findings: legal obligations of clinicians.
Ellen Wright Clayton, Susanne Haga, Patricia Kuszler, Emily Bane, Krysta Shutske, Wylie Burke. Genet Med 2013
45
12


The duty to recontact: benefit and harm.
N F Sharpe. Am J Hum Genet 1999
16
18

Regulations and practices of genetic counselling in 38 European countries: the perspective of national representatives.
Elina Rantanen, Marja Hietala, Ulf Kristoffersson, Irmgard Nippert, Jörg Schmidtke, Jorge Sequeiros, Helena Kääriäinen. Eur J Hum Genet 2008
18
16

What process attributes of clinical genetics services could maximise patient benefits?
Marion McAllister, Katherine Payne, Rhona Macleod, Stuart Nicholls, Dian Donnai, Linda Davies. Eur J Hum Genet 2008
31
12


Content analysis: method, applications, and issues.
B Downe-Wamboldt. Health Care Women Int 1992
682
12

Duty to re-contact: a study of families at risk for Fragile X.
Lynn E Bernard, Barbara McGillivray, Margot I Van Allen, J M Friedman, Sylvie Langlois. J Genet Couns 1999
7
42

Systematic reanalysis of clinical exome data yields additional diagnoses: implications for providers.
Aaron M Wenger, Harendra Guturu, Jonathan A Bernstein, Gill Bejerano. Genet Med 2017
158
12


Recontacting Patients with Updated Genetic Testing Recommendations for Medullary Thyroid Carcinoma and Pheochromocytoma or Paraganglioma.
Minerva A Romero Arenas, Thereasa A Rich, Samuel M Hyde, Naifa L Busaidy, Gilbert J Cote, Mimi I Hu, Robert F Gagel, Paul W Gidley, Camilo Jimenez, Michael E Kupferman,[...]. Ann Surg Oncol 2018
10
30

The impact of variant classification on the clinical management of hereditary cancer syndromes.
Scott A Turner, Smita K Rao, R Hayes Morgan, Cindy L Vnencak-Jones, Georgia L Wiesner. Genet Med 2019
21
14

Am I My Family's Keeper? Disclosure Dilemmas in Next-Generation Sequencing.
Roel H P Wouters, Rhodé M Bijlsma, Margreet G E M Ausems, Johannes J M van Delden, Emile E Voest, Annelien L Bredenoord. Hum Mutat 2016
20
10

Risk reversals in predictive testing for Huntington disease.
E Almqvist, S Adam, M Bloch, A Fuller, P Welch, D Eisenberg, D Whelan, D Macgregor, W Meschino, M R Hayden. Am J Hum Genet 1997
18
11

Provision of genetic services in Europe: current practices and issues.
Béatrice Godard, Helena Kääriäinen, Ulf Kristoffersson, Lisbeth Tranebjaerg, Domenico Coviello, Ségolène Aymé. Eur J Hum Genet 2003
62
8

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
477
8

Actionable exomic incidental findings in 6503 participants: challenges of variant classification.
Laura M Amendola, Michael O Dorschner, Peggy D Robertson, Joseph S Salama, Ragan Hart, Brian H Shirts, Mitzi L Murray, Mari J Tokita, Carlos J Gallego, Daniel Seung Kim,[...]. Genome Res 2015
238
8

Factors influencing success of clinical genome sequencing across a broad spectrum of disorders.
Jenny C Taylor, Hilary C Martin, Stefano Lise, John Broxholme, Jean-Baptiste Cazier, Andy Rimmer, Alexander Kanapin, Gerton Lunter, Simon Fiddy, Chris Allan,[...]. Nat Genet 2015
207
8

Managing incidental findings and research results in genomic research involving biobanks and archived data sets.
Susan M Wolf, Brittney N Crock, Brian Van Ness, Frances Lawrenz, Jeffrey P Kahn, Laura M Beskow, Mildred K Cho, Michael F Christman, Robert C Green, Ralph Hall,[...]. Genet Med 2012
306
8

Ethical Considerations for the Return of Incidental Findings in Ophthalmic Genomic Research.
Emmanuelle Souzeau, Kathryn P Burdon, David A Mackey, Alex W Hewitt, Ravi Savarirayan, Margaret Otlowski, Jamie E Craig. Transl Vis Sci Technol 2016
8
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.