A citation-based method for searching scientific literature

Marlies Saelaert, Heidi Mertes, Elfride De Baere, Ignaas Devisch. Eur J Hum Genet 2018
Times Cited: 10







List of co-cited articles
28 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
799
90

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
60

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
30

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
30

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
215
20


The implications of familial incidental findings from exome sequencing: the NIH Undiagnosed Diseases Program experience.
Lauren Lawrence, Murat Sincan, Thomas Markello, David R Adams, Fred Gill, Rena Godfrey, Gretchen Golas, Catherine Groden, Dennis Landis, Michele Nehrebecky,[...]. Genet Med 2014
40
20


Towards a European consensus for reporting incidental findings during clinical NGS testing.
Jayne Y Hehir-Kwa, Mireille Claustres, Ros J Hastings, Conny van Ravenswaaij-Arts, Gabrielle Christenhusz, Maurizio Genuardi, Béla Melegh, Anne Cambon-Thomsen, Philippos Patsalis, Joris Vermeesch,[...]. Eur J Hum Genet 2015
57
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
203
20


Attitudes of nearly 7000 health professionals, genomic researchers and publics toward the return of incidental results from sequencing research.
Anna Middleton, Katherine I Morley, Eugene Bragin, Helen V Firth, Matthew E Hurles, Caroline F Wright, Michael Parker. Eur J Hum Genet 2016
110
20

Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature.
J Delanne, S Nambot, A Chassagne, O Putois, A Pelissier, C Peyron, E Gautier, J Thevenon, E Cretin, A L Bruel,[...]. Eur J Med Genet 2019
17
20



International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases.
Kym M Boycott, Ana Rath, Jessica X Chong, Taila Hartley, Fowzan S Alkuraya, Gareth Baynam, Anthony J Brookes, Michael Brudno, Angel Carracedo, Johan T den Dunnen,[...]. Am J Hum Genet 2017
143
20

Guidelines for investigating causality of sequence variants in human disease.
D G MacArthur, T A Manolio, D P Dimmock, H L Rehm, J Shendure, G R Abecasis, D R Adams, R B Altman, S E Antonarakis, E A Ashley,[...]. Nature 2014
767
20

Meta-analysis of the diagnostic and clinical utility of genome and exome sequencing and chromosomal microarray in children with suspected genetic diseases.
Michelle M Clark, Zornitza Stark, Lauge Farnaes, Tiong Y Tan, Susan M White, David Dimmock, Stephen F Kingsmore. NPJ Genom Med 2018
150
20

The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities.
Jessica X Chong, Kati J Buckingham, Shalini N Jhangiani, Corinne Boehm, Nara Sobreira, Joshua D Smith, Tanya M Harrell, Margaret J McMillin, Wojciech Wiszniewski, Tomasz Gambin,[...]. Am J Hum Genet 2015
344
20

Genetics specialists' perspectives on disclosure of genomic incidental findings in the clinical setting.
Nancy R Downing, Janet K Williams, Sandra Daack-Hirsch, Martha Driessnack, Christian M Simon. Patient Educ Couns 2013
40
20

"I want to know what's in Pandora's Box": comparing stakeholder perspectives on incidental findings in clinical whole genomic sequencing.
Anne Townsend, Shelin Adam, Patricia H Birch, Zoe Lohn, Francois Rousseau, Jan M Friedman. Am J Med Genet A 2012
120
20

The incidentalome: a threat to genomic medicine.
Isaac S Kohane, Daniel R Masys, Russ B Altman. JAMA 2006
213
20

What are people willing to pay for whole-genome sequencing information, and who decides what they receive?
Deborah A Marshall, Juan Marcos Gonzalez, F Reed Johnson, Karen V MacDonald, Amy Pugh, Michael P Douglas, Kathryn A Phillips. Genet Med 2016
20
20

The communication of secondary variants: interviews with parents whose children have undergone array-CGH testing.
G M Christenhusz, K Devriendt, H Peeters, H Van Esch, K Dierickx. Clin Genet 2014
17
20

Patients' views on incidental findings from clinical exome sequencing.
Kristin E Clift, Colin M E Halverson, Alexander S Fiksdal, Ashok Kumbamu, Richard R Sharp, Jennifer B McCormick. Appl Transl Genom 2015
57
20

Attitudes of genetics professionals toward the return of incidental results from exome and whole-genome sequencing.
Joon-Ho Yu, Tanya M Harrell, Seema M Jamal, Holly K Tabor, Michael J Bamshad. Am J Hum Genet 2014
86
20

To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts.
Gabrielle M Christenhusz, Koenraad Devriendt, Kris Dierickx. Eur J Hum Genet 2013
105
20

Return of individual genomic research results: are laws and policies keeping step?
Adrian Thorogood, Gratien Dalpé, Bartha Maria Knoppers. Eur J Hum Genet 2019
32
20

Cytogenetic and epidemiological findings in Down syndrome: England and Wales 1989-2009.
Joan K Morris, Eva Alberman, David Mutton, Patricia Jacobs. Am J Med Genet A 2012
27
10

Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formation.
S L Page, J C Shin, J Y Han, K H Choo, L G Shaffer. Hum Mol Genet 1996
72
10


Rapid whole genome sequencing and precision neonatology.
Joshua E Petrikin, Laurel K Willig, Laurie D Smith, Stephen F Kingsmore. Semin Perinatol 2015
99
10

X chromosome loss and ageing.
L M Russell, P Strike, C E Browne, P A Jacobs. Cytogenet Genome Res 2007
91
10

Actionable, pathogenic incidental findings in 1,000 participants' exomes.
Michael O Dorschner, Laura M Amendola, Emily H Turner, Peggy D Robertson, Brian H Shirts, Carlos J Gallego, Robin L Bennett, Kelly L Jones, Mari J Tokita, James T Bennett,[...]. Am J Hum Genet 2013
268
10

Parental origin of the extra chromosomes in polysomy X.
C A Leal, J W Belmont, R Nachtman, J M Cantu, C Medina. Hum Genet 1994
18
10

Clinical exome sequencing: results from 2819 samples reflecting 1000 families.
Daniel Trujillano, Aida M Bertoli-Avella, Krishna Kumar Kandaswamy, Maximilian Er Weiss, Julia Köster, Anett Marais, Omid Paknia, Rolf Schröder, Jose Maria Garcia-Aznar, Martin Werber,[...]. Eur J Hum Genet 2017
172
10

Recurrent de novo mutations in neurodevelopmental disorders: properties and clinical implications.
Amy B Wilfert, Arvis Sulovari, Tychele N Turner, Bradley P Coe, Evan E Eichler. Genome Med 2017
52
10

Next generation sequencing in women affected by nonsyndromic premature ovarian failure displays new potential causative genes and mutations.
Dora Janeth Fonseca, Liliana Catherine Patiño, Yohjana Carolina Suárez, Asid de Jesús Rodríguez, Heidi Eliana Mateus, Karen Marcela Jiménez, Oscar Ortega-Recalde, Ivonne Díaz-Yamal, Paul Laissue. Fertil Steril 2015
35
10

A genomic view of mosaicism and human disease.
Leslie G Biesecker, Nancy B Spinner. Nat Rev Genet 2013
321
10


Cost analysis of whole genome sequencing in German clinical practice.
Marika Plöthner, Martin Frank, J-Matthias Graf von der Schulenburg. Eur J Health Econ 2017
17
10

Clinical application of whole-genome low-coverage next-generation sequencing to detect and characterize balanced chromosomal translocations.
D Liang, Y Wang, X Ji, H Hu, J Zhang, L Meng, Y Lin, D Ma, T Jiang, H Jiang,[...]. Clin Genet 2017
15
10

Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients.
Laura K Conlin, Whitney Kramer, Anne L Hutchinson, Xia Li, Harold Riethman, Hakon Hakonarson, John C Mulley, Ingrid E Scheffer, Samuel F Berkovic, Syed A Hosain,[...]. J Med Genet 2011
41
10


Fading competency of cytogenetic diagnostic laboratories: the alarm bell has started to ring.
Ron Hochstenbach, Anna Slunga-Tallberg, Caroline Devlin, Giovanna Floridia, Marta Rodríguez de Alba, Shama Bhola, Katrina Rack, Ros Hastings. Eur J Hum Genet 2017
4
25

Whole exome sequencing in recurrent early pregnancy loss.
Ying Qiao, Jiadi Wen, Flamingo Tang, Sally Martell, Naomi Shomer, Peter C K Leung, Mary D Stephenson, Evica Rajcan-Separovic. Mol Hum Reprod 2016
27
10

Mosaic structural variation in children with developmental disorders.
Daniel A King, Wendy D Jones, Yanick J Crow, Anna F Dominiczak, Nicola A Foster, Tom R Gaunt, Jade Harris, Stephen W Hellens, Tessa Homfray, Josie Innes,[...]. Hum Mol Genet 2015
32
10

Estimates of live birth prevalence of children with Down syndrome in the period 1991-2015 in the Netherlands.
G de Graaf, J J M Engelen, A C J Gijsbers, R Hochstenbach, M J V Hoffer, A J A Kooper, B Sikkema-Raddatz, M I Srebniak, A M F van der Kevie-Kersemaekers, L J C M van Zutven,[...]. J Intellect Disabil Res 2017
17
10

45,X/46,XX mosaicism in patients with idiopathic premature ovarian failure.
A S Devi, D A Metzger, A A Luciano, P A Benn. Fertil Steril 1998
31
10



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.