A citation-based method for searching scientific literature

Clara D M van Karnebeek, Maaike C E Jansweijer, Arnold G E Leenders, Martin Offringa, Raoul C M Hennekam. Eur J Hum Genet 2005
Times Cited: 151







List of co-cited articles
600 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
32

Evaluation of mental retardation: recommendations of a Consensus Conference: American College of Medical Genetics.
C J Curry, R E Stevenson, D Aughton, J Byrne, J C Carey, S Cassidy, C Cunniff, J M Graham, M C Jones, M M Kaback,[...]. Am J Med Genet 1997
251
26



Etiology of mental retardation in children referred to a tertiary care center: a prospective study.
Clara D M van Karnebeek, Frederike Y Scheper, Nico G Abeling, Marielle Alders, Peter G Barth, Jan M N Hoovers, Cindy Koevoets, Ronald J A Wanders, Raoul C M Hennekam. Am J Ment Retard 2005
63
31

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
225
18


The epidemiology of mental retardation: challenges and opportunities in the new millennium.
Helen Leonard, Xingyan Wen. Ment Retard Dev Disabil Res Rev 2002
349
16

Genetic evaluation of intellectual disabilities.
John B Moeschler. Semin Pediatr Neurol 2008
47
29

Diagnostic exome sequencing in persons with severe intellectual disability.
Joep de Ligt, Marjolein H Willemsen, Bregje W M van Bon, Tjitske Kleefstra, Helger G Yntema, Thessa Kroes, Anneke T Vulto-van Silfhout, David A Koolen, Petra de Vries, Christian Gilissen,[...]. N Engl J Med 2012
965
14


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
417
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
125
13





Diagnostic evaluation of developmental delay/mental retardation: An overview.
Agatino Battaglia, John C Carey. Am J Med Genet C Semin Med Genet 2003
74
14

Deep sequencing reveals 50 novel genes for recessive cognitive disorders.
Hossein Najmabadi, Hao Hu, Masoud Garshasbi, Tomasz Zemojtel, Seyedeh Sedigheh Abedini, Wei Chen, Masoumeh Hosseini, Farkhondeh Behjati, Stefan Haas, Payman Jamali,[...]. Nature 2011
572
11

Etiologic yield of subspecialists' evaluation of young children with global developmental delay.
M I Shevell, A Majnemer, P Rosenbaum, M Abrahamowicz. J Pediatr 2000
82
12



Yield of additional metabolic studies in neurodevelopmental disorders.
Hannelie M Engbers, Ruud Berger, Peter van Hasselt, Tom de Koning, Monique G M de Sain-van der Velden, Hester Y Kroes, Gepke Visser. Ann Neurol 2008
23
43

Evaluation of the child with idiopathic mental retardation.
G B Schaefer, J B Bodensteiner. Pediatr Clin North Am 1992
88
11

Genomic microarrays in mental retardation: from copy number variation to gene, from research to diagnosis.
Lisenka E L M Vissers, Bert B A de Vries, Joris A Veltman. J Med Genet 2010
106
10

Clinical studies on submicroscopic subtelomeric rearrangements: a checklist.
B B de Vries, S M White, S J Knight, R Regan, T Homfray, I D Young, M Super, C McKeown, M Splitt, O W Quarrell,[...]. J Med Genet 2001
200
10

Prevalence of intellectual disability: a meta-analysis of population-based studies.
Pallab K Maulik, Maya N Mascarenhas, Colin D Mathers, Tarun Dua, Shekhar Saxena. Res Dev Disabil 2011
569
10

Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Anita Rauch, Dagmar Wieczorek, Elisabeth Graf, Thomas Wieland, Sabine Endele, Thomas Schwarzmayr, Beate Albrecht, Deborah Bartholdi, Jasmin Beygo, Nataliya Di Donato,[...]. Lancet 2012
664
10


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
148
9


Genetics of early onset cognitive impairment.
Hans Hilger Ropers. Annu Rev Genomics Hum Genet 2010
221
9

A de novo paradigm for mental retardation.
Lisenka E L M Vissers, Joep de Ligt, Christian Gilissen, Irene Janssen, Marloes Steehouwer, Petra de Vries, Bart van Lier, Peer Arts, Nienke Wieskamp, Marisol del Rosario,[...]. Nat Genet 2010
545
9

Genome sequencing identifies major causes of severe intellectual disability.
Christian Gilissen, Jayne Y Hehir-Kwa, Djie Tjwan Thung, Maartje van de Vorst, Bregje W M van Bon, Marjolein H Willemsen, Michael Kwint, Irene M Janssen, Alexander Hoischen, Annette Schenck,[...]. Nature 2014
624
9

Investigation of global developmental delay.
L McDonald, A Rennie, J Tolmie, P Galloway, R McWilliam. Arch Dis Child 2006
45
17

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities.
Lisenka E L M Vissers, Bert B A de Vries, Kazutoyo Osoegawa, Irene M Janssen, Ton Feuth, Chik On Choy, Huub Straatman, Walter van der Vliet, Erik H L P G Huys, Anke van Rijk,[...]. Am J Hum Genet 2003
344
8

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
8

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.
Patrick S Tarpey, Raffaella Smith, Erin Pleasance, Annabel Whibley, Sarah Edkins, Claire Hardy, Sarah O'Meara, Calli Latimer, Ed Dicks, Andrew Menzies,[...]. Nat Genet 2009
402
8

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
805
8

Genomics, intellectual disability, and autism.
Heather C Mefford, Mark L Batshaw, Eric P Hoffman. N Engl J Med 2012
180
8

The prevalence of mental retardation: a critical review of recent literature.
N Roeleveld, G A Zielhuis, F Gabreëls. Dev Med Child Neurol 1997
247
7

The renaming of mental retardation: understanding the change to the term intellectual disability.
Robert L Schalock, Ruth A Luckasson, Karrie A Shogren, Sharon Borthwick-Duffy, Val Bradley, Wil H E Buntinx, David L Coulter, Ellis M Craig, Sharon C Gomez, Yves Lachapelle,[...]. Intellect Dev Disabil 2007
141
7

Oligonucleotide microarray analysis of genomic imbalance in children with mental retardation.
J M Friedman, Agnes Baross, Allen D Delaney, Adrian Ally, Laura Arbour, Linlea Armstrong, Jennifer Asano, Dione K Bailey, Sarah Barber, Patricia Birch,[...]. Am J Hum Genet 2006
213
7

Prospective screening for subtelomeric rearrangements in children with mental retardation of unknown aetiology: the Amsterdam experience.
C D M van Karnebeek, C Koevoets, S Sluijter, E K Bijlsma, D F M C Smeets, E J Redeker, R C M Hennekam, J M N Hoovers. J Med Genet 2002
63
11

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
7

Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH).
J Schoumans, C Ruivenkamp, E Holmberg, M Kyllerman, B-M Anderlid, M Nordenskjöld. J Med Genet 2005
144
7

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation.
J Flint, A O Wilkie, V J Buckle, R M Winter, A J Holland, H E McDermid. Nat Genet 1995
387
7


The metabolic evaluation of the child with an intellectual developmental disorder: diagnostic algorithm for identification of treatable causes and new digital resource.
Clara D M van Karnebeek, Michael Shevell, Johannes Zschocke, John B Moeschler, Sylvia Stockler. Mol Genet Metab 2014
73
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.