A citation-based method for searching scientific literature

Jay W Ellison, J Britt Ravnan, Jill A Rosenfeld, S Annie Morton, Nicholas J Neill, Marc S Williams, Jodi Lewis, Beth S Torchia, Cathryn Walker, Ryan N Traylor, Kimberly Moles, Elizabeth Miller, Jennifer Lantz, Caitlin Valentin, Sara L Minier, Kimberly Leiser, Berkley R Powell, Timothy M Wilks, Lisa G Shaffer. Pediatrics 2012
Times Cited: 33







List of co-cited articles
186 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
75

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
60


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
54

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
45


Clinical genetic testing for patients with autism spectrum disorders.
Yiping Shen, Kira A Dies, Ingrid A Holm, Carolyn Bridgemohan, Magdi M Sobeih, Elizabeth B Caronna, Karen J Miller, Jean A Frazier, Iris Silverstein, Jonathan Picker,[...]. Pediatrics 2010
241
30

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
30


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
27


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
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

Diagnostic yield of chromosomal microarray analysis in an autism primary care practice: which guidelines to implement?
Susan G McGrew, Brittany R Peters, Julie A Crittendon, Jeremy Veenstra-Vanderweele. J Autism Dev Disord 2012
36
18

"What does it mean?": uncertainties in understanding results of chromosomal microarray testing.
Marian Reiff, Barbara A Bernhardt, Surabhi Mulchandani, Danielle Soucier, Diana Cornell, Reed E Pyeritz, Nancy B Spinner. Genet Med 2012
75
18

Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino,[...]. N Engl J Med 2012
353
18

Trends in the prevalence of developmental disabilities in US children, 1997-2008.
Coleen A Boyle, Sheree Boulet, Laura A Schieve, Robin A Cohen, Stephen J Blumberg, Marshalyn Yeargin-Allsopp, Susanna Visser, Michael D Kogan. Pediatrics 2011
792
18




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
40

Physicians' perspectives on the uncertainties and implications of chromosomal microarray testing of children and families.
M Reiff, K Ross, S Mulchandani, K J Propert, R E Pyeritz, N B Spinner, B A Bernhardt. Clin Genet 2013
44
15


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
15

Practice parameter for the assessment and treatment of children and adolescents with autism spectrum disorder.
Fred Volkmar, Matthew Siegel, Marc Woodbury-Smith, Bryan King, James McCracken, Matthew State. J Am Acad Child Adolesc Psychiatry 2014
235
15

"It wasn't a disaster or anything": Parents' experiences of their child's uncertain chromosomal microarray result.
Ella J Wilkins, Alison D Archibald, Margaret A Sahhar, Susan M White. Am J Med Genet A 2016
17
29


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
15

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
12


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

Strong association of de novo copy number mutations with autism.
Jonathan Sebat, B Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese-Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, Alex Krasnitz, Jude Kendall,[...]. Science 2007
12

Structural variation of chromosomes in autism spectrum disorder.
Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren,[...]. Am J Hum Genet 2008
12


The genetics of Autism Spectrum Disorders--a guide for clinicians.
Karsten M Heil, Christian P Schaaf. Curr Psychiatry Rep 2013
36
12

Clinical whole exome sequencing in child neurology practice.
Siddharth Srivastava, Julie S Cohen, Hilary Vernon, Kristin Barañano, Rebecca McClellan, Leila Jamal, SakkuBai Naidu, Ali Fatemi. Ann Neurol 2014
151
12

Clinical performance of the CytoScan Dx Assay in diagnosing developmental delay/intellectual disability.
Rolph Pfundt, Kat Kwiatkowski, Alan Roter, Anju Shukla, Eric Thorland, Richard Hockett, Barbara DuPont, Eric T Fung, Alka Chaubey. Genet Med 2016
7
57

Variants of unknown significance on chromosomal microarray analysis: parental perspectives.
Stephanie Jez, Megan Martin, Sarah South, Rena Vanzo, Erin Rothwell. J Community Genet 2015
22
18

Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD population.
Nori Matsunami, Dexter Hadley, Charles H Hensel, G Bryce Christensen, Cecilia Kim, Edward Frackelton, Kelly Thomas, Renata Pellegrino da Silva, Jeff Stevens, Lisa Baird,[...]. PLoS One 2013
43
12

Clinical utility of chromosomal microarray analysis of DNA from buccal cells: detection of mosaicism in three patients.
Mallory R Sdano, Rena J Vanzo, Megan M Martin, Erin E Baldwin, Sarah T South, Alan F Rope, William P Allen, Hutton Kearney. J Genet Couns 2014
11
36

The Database of Genomic Variants: a curated collection of structural variation in the human genome.
Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
632
12

Parents' perceptions of the usefulness of chromosomal microarray analysis for children with autism spectrum disorders.
Marian Reiff, Ellen Giarelli, Barbara A Bernhardt, Ebony Easley, Nancy B Spinner, Pamela L Sankar, Surabhi Mulchandani. J Autism Dev Disord 2015
40
12

Copy number variation characteristics in subpopulations of patients with autism spectrum disorders.
Anna Bremer, MaiBritt Giacobini, Mats Eriksson, Peter Gustavsson, Viviann Nordin, Elisabeth Fernell, Christopher Gillberg, Ann Nordgren, Asa Uppströmer, Britt-Marie Anderlid,[...]. Am J Med Genet B Neuropsychiatr Genet 2011
48
12

Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder.
Kristiina Tammimies, Christian R Marshall, Susan Walker, Gaganjot Kaur, Bhooma Thiruvahindrapuram, Anath C Lionel, Ryan K C Yuen, Mohammed Uddin, Wendy Roberts, Rosanna Weksberg,[...]. JAMA 2015
197
12

Incidental copy-number variants identified by routine genome testing in a clinical population.
Philip M Boone, Zachry T Soens, Ian M Campbell, Pawel Stankiewicz, Sau Wai Cheung, Ankita Patel, Arthur L Beaudet, Sharon E Plon, Chad A Shaw, Amy L McGuire,[...]. Genet Med 2013
31
9

Whole genome scanning: resolving clinical diagnosis and management amidst complex data.
Sarah E Ali-Khan, Abdallah S Daar, Cheryl Shuman, Peter N Ray, Stephen W Scherer. Pediatr Res 2009
48
9


Impact of genotype-first diagnosis: the detection of microdeletion and microduplication syndromes with cancer predisposition by aCGH.
Sara Anne Adams, Justine Coppinger, Sulagna C Saitta, Tracy Stroud, Manikum Kandamurugu, Zheng Fan, Blake C Ballif, Lisa G Shaffer, Bassem A Bejjani. Genet Med 2009
30
10

Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation.
Anita Rauch, Juliane Hoyer, Sabine Guth, Christiane Zweier, Cornelia Kraus, Christian Becker, Martin Zenker, Ulrike Hüffmeier, Christian Thiel, Franz Rüschendorf,[...]. Am J Med Genet A 2006
224
9

Global variation in copy number in the human genome.
Richard Redon, Shumpei Ishikawa, Karen R Fitch, Lars Feuk, George H Perry, T Daniel Andrews, Heike Fiegler, Michael H Shapero, Andrew R Carson, Wenwei Chen,[...]. Nature 2006
9


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.