A citation-based method for searching scientific literature

Marlies Saelaert, Heidi Mertes, Elfride De Baere, Ignaas Devisch. Eur J Hum Genet 2018
Times Cited: 6







List of co-cited articles
16 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
669
100

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
66


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
39
33


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
54
33

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
189
33


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
97
33


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
33

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
38
33

"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
114
33

The incidentalome: a threat to genomic medicine.
Isaac S Kohane, Daniel R Masys, Russ B Altman. JAMA 2006
198
33

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
16
33

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
83
33

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
25
16

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
63
16


Rapid whole genome sequencing and precision neonatology.
Joshua E Petrikin, Laurel K Willig, Laurie D Smith, Stephen F Kingsmore. Semin Perinatol 2015
82
16

X chromosome loss and ageing.
L M Russell, P Strike, C E Browne, P A Jacobs. Cytogenet Genome Res 2007
83
16

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
257
16

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
17
16

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
149
16

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
192
16

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
39
16

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
30
16

A genomic view of mosaicism and human disease.
Leslie G Biesecker, Nancy B Spinner. Nat Rev Genet 2013
293
16


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
13
16

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
16

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
33
16


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
3
33

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
22
16

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
29
16

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
14
16

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
23
16


Intragenic Enhancers Attenuate Host Gene Expression.
Senthilkumar Cinghu, Pengyi Yang, Justin P Kosak, Amanda E Conway, Dhirendra Kumar, Andrew J Oldfield, Karen Adelman, Raja Jothi. Mol Cell 2017
40
16

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports.
B Menten, N Maas, B Thienpont, K Buysse, J Vandesompele, C Melotte, T de Ravel, S Van Vooren, I Balikova, L Backx,[...]. J Med Genet 2006
292
16

Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics.
Sau W Cheung, Chad A Shaw, Daryl A Scott, Ankita Patel, Trilochan Sahoo, Carlos A Bacino, Amber Pursley, Jiangzhen Li, Robert Erickson, Andrea L Gropman,[...]. Am J Med Genet A 2007
117
16


Actionable secondary findings from whole-genome sequencing of 954 East Asians.
Clara Sze-Man Tang, Saloni Dattani, Man-Ting So, Stacey S Cherny, Paul K H Tam, Pak C Sham, Maria-Mercè Garcia-Barcelo. Hum Genet 2018
16
16

The ring 14 syndrome.
Marcella Zollino, Emanuela Ponzi, Giuseppe Gobbi, Giovanni Neri. Eur J Med Genet 2012
23
16


Parental insertional balanced translocations are an important cause of apparently de novo CNVs in patients with developmental anomalies.
Beata A Nowakowska, Nicole de Leeuw, Claudia Al Ruivenkamp, Birgit Sikkema-Raddatz, John A Crolla, Reinhilde Thoelen, Marije Koopmans, Nicolette den Hollander, Arie van Haeringen, Anne-Marie van der Kevie-Kersemaekers,[...]. Eur J Hum Genet 2012
50
16

Hidden mosaicism in patients with Klinefelter's syndrome: implications for genetic reproductive counselling.
L Garcia-Quevedo, J Blanco, Z Sarrate, V Català, L Bassas, F Vidal. Hum Reprod 2011
20
16

Pathogenic aberrations revealed exclusively by single nucleotide polymorphism (SNP) genotyping data in 5000 samples tested by molecular karyotyping.
D L Bruno, S M White, D Ganesamoorthy, T Burgess, K Butler, S Corrie, D Francis, L Hills, K Prabhakara, C Ngo,[...]. J Med Genet 2011
46
16

Whole Genome Sequencing Expands Diagnostic Utility and Improves Clinical Management in Pediatric Medicine.
Dimitri J Stavropoulos, Daniele Merico, Rebekah Jobling, Sarah Bowdin, Nasim Monfared, Bhooma Thiruvahindrapuram, Thomas Nalpathamkalam, Giovanna Pellecchia, Ryan K C Yuen, Michael J Szego,[...]. NPJ Genom Med 2016
147
16


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.