A citation-based method for searching scientific literature

Stefano D'Arrigo, Francesco Gavazzi, Enrico Alfei, Orsetta Zuffardi, Cristina Montomoli, Barbara Corso, Erika Buzzi, Francesca L Sciacca, Sara Bulgheroni, Daria Riva, Chiara Pantaleoni. J Child Neurol 2016
Times Cited: 22







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



Times Cited
  Times     Co-cited
Similarity


Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.
David T Miller, Margaret P Adam, Swaroop Aradhya, Leslie G Biesecker, Arthur R Brothman, Nigel P Carter, Deanna M Church, John A Crolla, Evan E Eichler, Charles J Epstein,[...]. Am J Hum Genet 2010
72


Array CGH in patients with developmental delay or intellectual disability: are there phenotypic clues to pathogenic copy number variants?
M Shoukier, N Klein, B Auber, J Wickert, J Schröder, B Zoll, P Burfeind, I Bartels, E A Alsat, M Lingen,[...]. Clin Genet 2013
43
31

American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants.
Hutton M Kearney, Erik C Thorland, Kerry K Brown, Fabiola Quintero-Rivera, Sarah T South. Genet Med 2011
513
31


Confirmation of chromosomal microarray as a first-tier clinical diagnostic test for individuals with developmental delay, intellectual disability, autism spectrum disorders and dysmorphic features.
Agatino Battaglia, Viola Doccini, Laura Bernardini, Antonio Novelli, Sara Loddo, Anna Capalbo, Tiziana Filippi, John C Carey. Eur J Paediatr Neurol 2013
118
27

Changing interpretation of chromosomal microarray over time in a community cohort with intellectual disability.
Emma Palmer, Helen Speirs, Peter J Taylor, Glenda Mullan, Gill Turner, Stewart Einfeld, Bruce Tonge, David Mowat. Am J Med Genet A 2014
30
22




Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years' clinical application for over 8,700 patients.
Joo Wook Ahn, Susan Bint, Anne Bergbaum, Kathy Mann, Richard P Hall, Caroline Mackie Ogilvie. Mol Cytogenet 2013
36
18

Diagnostic genome profiling in mental retardation.
Bert B A de Vries, Rolph Pfundt, Martijn Leisink, David A Koolen, Lisenka E L M Vissers, Irene M Janssen, Simon van Reijmersdal, Willy M Nillesen, Erik H L P G Huys, Nicole de Leeuw,[...]. Am J Hum Genet 2005
416
18

Chromosomal microarray testing influences medical management.
Michael E Coulter, David T Miller, David J Harris, Pamela Hawley, Jonathan Picker, Amy E Roberts, Magdi M Sobeih, Mira Irons. Genet Med 2011
76
18

A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
803
18

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.
Santhosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, Francesca Antonacci, Priscillia Siswara, Andy Itsara, Laura Vives, Tom Walsh, Shane E McCarthy, Carl Baker,[...]. Nat Genet 2010
411
18

The genetics of microdeletion and microduplication syndromes: an update.
Corey T Watson, Tomas Marques-Bonet, Andrew J Sharp, Heather C Mefford. Annu Rev Genomics Hum Genet 2014
78
18

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
18

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
313
13

Large cryptic genomic rearrangements with apparently normal karyotypes detected by array-CGH.
Eleonora Di Gregorio, Elisa Savin, Elisa Biamino, Elga Fabia Belligni, Valeria Giorgia Naretto, Gaetana D'Alessandro, Giorgia Gai, Franco Fiocchi, Alessandro Calcia, Cecilia Mancini,[...]. Mol Cytogenet 2014
20
15

Interpretation of array comparative genome hybridization data: a major challenge.
A C J Gijsbers, J Schoumans, C A L Ruivenkamp. Cytogenet Genome Res 2011
25
13

The identification of microdeletion syndromes and other chromosome abnormalities: cytogenetic methods of the past, new technologies for the future.
Lisa G Shaffer, Bassem A Bejjani, Beth Torchia, Susan Kirkpatrick, Justine Coppinger, Blake C Ballif. Am J Med Genet C Semin Med Genet 2007
119
13


Insertional translocation detected using FISH confirmation of array-comparative genomic hybridization (aCGH) results.
Sung-Hae L Kang, Chad Shaw, Zhishuo Ou, Patricia A Eng, M Lance Cooper, Amber N Pursley, Trilochan Sahoo, Carlos A Bacino, A Craig Chinault, Pawel Stankiewicz,[...]. Am J Med Genet A 2010
66
13

Germline rates of de novo meiotic deletions and duplications causing several genomic disorders.
Daniel J Turner, Marcos Miretti, Diana Rajan, Heike Fiegler, Nigel P Carter, Martyn L Blayney, Stephan Beck, Matthew E Hurles. Nat Genet 2008
212
13

Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects.
Gurdeep S Sagoo, Adam S Butterworth, Simon Sanderson, Charles Shaw-Smith, Julian P T Higgins, Hilary Burton. Genet Med 2009
146
13

Clinical significance of de novo and inherited copy-number variation.
Anneke T Vulto-van Silfhout, Jayne Y Hehir-Kwa, Bregje W M van Bon, Janneke H M Schuurs-Hoeijmakers, Stephen Meader, Claudia J M Hellebrekers, Ilse J M Thoonen, Arjan P M de Brouwer, Han G Brunner, Caleb Webber,[...]. Hum Mutat 2013
73
13

Detection of pathogenic gene copy number variations in patients with mental retardation by genomewide oligonucleotide array comparative genomic hybridization.
Yao-Shan Fan, Parul Jayakar, Hongbo Zhu, Deborah Barbouth, Stephanie Sacharow, Ana Morales, Virginia Carver, Paul Benke, Peter Mundy, Louis J Elsas. Hum Mutat 2007
94
13

Application of chromosomal microarrays in the evaluation of intellectual disability/global developmental delay patients - A study from a tertiary care genetic centre in India.
Pankaj Sharma, Neerja Gupta, Madhumita Roy Chowdhury, Savita Sapra, Manju Ghosh, Sheffali Gulati, Madhulika Kabra. Gene 2016
7
42

Array-based comparative genomic hybridization analysis of 1176 consecutive clinical genetics investigations.
Diane L Pickering, James D Eudy, Ann Haskins Olney, Bhavana J Dave, Denae Golden, Jadd Stevens, Warren G Sanger. Genet Med 2008
37
13

Performance of chromosomal microarray for patients with intellectual disabilities/developmental delay, autism, and multiple congenital anomalies in a Chinese cohort.
Wilson Wai Sing Chong, Ivan Fai Man Lo, Stephen Tak Sum Lam, Chi Chiu Wang, Ho Ming Luk, Tak Yeung Leung, Kwong Wai Choy. Mol Cytogenet 2014
26
13

Chromosomal microarray impacts clinical management.
E R Riggs, K E Wain, D Riethmaier, B Smith-Packard, W A Faucett, N Hoppman, E C Thorland, V C Patel, D T Miller. Clin Genet 2014
51
13

An evidence-based approach to establish the functional and clinical significance of copy number variants in intellectual and developmental disabilities.
Erin B Kaminsky, Vineith Kaul, Justin Paschall, Deanna M Church, Brian Bunke, Dawn Kunig, Daniel Moreno-De-Luca, Andres Moreno-De-Luca, Jennifer G Mulle, Stephen T Warren,[...]. Genet Med 2011
286
13

The clinical impact of chromosomal microarray on paediatric care in Hong Kong.
Victoria Q Tao, Kelvin Y K Chan, Yoyo W Y Chu, Gary T K Mok, Tiong Y Tan, Wanling Yang, So Lun Lee, Wing Fai Tang, Winnie W Y Tso, Elizabeth T Lau,[...]. PLoS One 2014
15
20

Considering specific clinical features as evidence of pathogenic copy number variants.
Egle Preiksaitiene, Alma Molytė, Jurate Kasnauskiene, Zivile Ciuladaite, Algirdas Utkus, Philippos C Patsalis, Vaidutis Kučinskas. J Appl Genet 2014
12
25


The human genome browser at UCSC.
W James Kent, Charles W Sugnet, Terrence S Furey, Krishna M Roskin, Tom H Pringle, Alan M Zahler, David Haussler. Genome Res 2002
13


New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.
Gerarda Cappuccio, Francesco Vitiello, Alberto Casertano, Paolo Fontana, Rita Genesio, Dario Bruzzese, Virginia Maria Ginocchio, Angela Mormile, Lucio Nitsch, Generoso Andria,[...]. Ital J Pediatr 2016
10
30

Phenotype profiling of patients with intellectual disability and copy number variations.
Mónica Roselló, Francisco Martínez, Sandra Monfort, Sonia Mayo, Silvestre Oltra, Carmen Orellana. Eur J Paediatr Neurol 2014
10
30

Chromosomal microarray in clinical diagnosis: a study of 337 patients with congenital anomalies and developmental delays or intellectual disability.
Ivona Sansović, Ana-Maria Ivankov, Adriana Bobinec, Mijana Kero, Ingeborg Barišić. Croat Med J 2017
10
30

Copy number variation analysis of patients with intellectual disability from North-West Spain.
Inés Quintela, Jesús Eirís, Carmen Gómez-Lado, Laura Pérez-Gay, David Dacruz, Raquel Cruz, Manuel Castro-Gago, Luz Míguez, Ángel Carracedo, Francisco Barros. Gene 2017
11
27

Array-based comparative genomic hybridization in 190 Korean patients with developmental delay and/or intellectual disability: a single tertiary care university center study.
Cha Gon Lee, Sang-Jin Park, Jun-No Yun, Jung Min Ko, Hyon-Ju Kim, Shin-Young Yim, Young Bae Sohn. Yonsei Med J 2013
9
33


The impact of chromosomal microarray on clinical management: a retrospective analysis.
Lindsay B Henderson, Carolyn D Applegate, Elizabeth Wohler, Molly B Sheridan, Julie Hoover-Fong, Denise A S Batista. Genet Med 2014
47
13



Array analysis and karyotyping: workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands.
Ron Hochstenbach, Ellen van Binsbergen, John Engelen, Aggie Nieuwint, Abeltje Polstra, Pino Poddighe, Claudia Ruivenkamp, Birgit Sikkema-Raddatz, Dominique Smeets, Martin Poot. Eur J Med Genet 2009
124
13

European guidelines for constitutional cytogenomic analysis.
Marisa Silva, Nicole de Leeuw, Kathy Mann, Heleen Schuring-Blom, Sian Morgan, Daniela Giardino, Katrina Rack, Ros Hastings. Eur J Hum Genet 2019
31
13

Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases.
Xinyan Lu, Chad A Shaw, Ankita Patel, Jiangzhen Li, M Lance Cooper, William R Wells, Cathy M Sullivan, Trilochan Sahoo, Svetlana A Yatsenko, Carlos A Bacino,[...]. PLoS One 2007
159
9

A parallel study of different array-CGH platforms in a set of Spanish patients with developmental delay and intellectual disability.
Laia Rodríguez-Revenga, Elena Vallespín, Irene Madrigal, María Palomares, Antonio Mur, Sixto García-Miñaur, Fernando Santos, M Ángeles Mori, Pablo Lapunzina, Montserrat Mila,[...]. Gene 2013
13
15


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.