A citation-based method for searching scientific literature

A Verloes, D Héron, T Billette de Villemeur, A Afenjar, C Baumann, N Bahi-Buisson, P Charles, A Faudet, A Jacquette, C Mignot, M-L Moutard, S Passemard, M Rio, L Robel, C Rougeot, D Ville, L Burglen, V des Portes. Arch Pediatr 2012
Times Cited: 6







List of co-cited articles
3 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
50

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
987
33

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
677
33

The development of the corpus callosum in the healthy human brain.
Eileen Luders, Paul M Thompson, Arthur W Toga. J Neurosci 2010
136
16

Neurodevelopmental outcomes in children with cerebellar malformations: a systematic review.
Marie-Eve Bolduc, Catherine Limperopoulos. Dev Med Child Neurol 2009
91
16

Concepts of myelin and myelination in neuroradiology.
A J Barkovich. AJNR Am J Neuroradiol 2000
304
16

White matter fractional anisotropy correlates with speed of processing and motor speed in young childhood cancer survivors.
Eline J Aukema, Matthan W A Caan, Nienke Oudhuis, Charles B L M Majoie, Frans M Vos, Liesbeth Reneman, Bob F Last, Martha A Grootenhuis, Antoinette Y N Schouten-van Meeteren. Int J Radiat Oncol Biol Phys 2009
107
16

Radiological findings in autistic and developmentally delayed children.
Mijke Zeegers, Jeroen Van Der Grond, Sarah Durston, Rutger Jan Nievelstein, Theo Witkamp, Emma Van Daalen, Jan Buitelaar, Herman Van Engeland. Brain Dev 2006
17
16

Identification and evaluation of children with autism spectrum disorders.
Chris Plauché Johnson, Scott M Myers. Pediatrics 2007
900
16

Normal rates of neuroradiological findings in children with high functioning autism.
Roma A Vasa, Marin Ranta, Thierry A G M Huisman, Pedro S Pinto, Rachael M Tillman, Stewart H Mostofsky. J Autism Dev Disord 2012
10
16

MRI findings in 77 children with non-syndromic autistic disorder.
Nathalie Boddaert, Mônica Zilbovicius, Anne Philipe, Laurence Robel, Marie Bourgeois, Catherine Barthélemy, David Seidenwurm, Isabelle Meresse, Laurence Laurier, Isabelle Desguerre,[...]. PLoS One 2009
65
16

Positive correlations between corpus callosum thickness and intelligence.
Eileen Luders, Katherine L Narr, Robert M Bilder, Paul M Thompson, Philip R Szeszko, Liberty Hamilton, Arthur W Toga. Neuroimage 2007
101
16



Clinical and morphometric analysis of the hypoplastic corpus callosum.
G B Schaefer, J B Bodensteiner, J N Thompson, D A Wilson. Arch Neurol 1991
36
16


Neuroimaging findings in 41 low-functioning children with autism spectrum disorder: a single-center experience.
Alessandra Erbetta, Sara Bulgheroni, Valeria Contarino, Luisa Chiapparini, Silvia Esposito, Chiara Vago, Daria Riva. J Child Neurol 2014
10
16

Diagnostic investigations in individuals with mental retardation: a systematic literature review of their usefulness.
Clara D M van Karnebeek, Maaike C E Jansweijer, Arnold G E Leenders, Martin Offringa, Raoul C M Hennekam. Eur J Hum Genet 2005
153
16

Incomplete hippocampal inversion-is there a relation to epilepsy?
Dragan Bajic, Eva Kumlien, Peter Mattsson, Staffan Lundberg, Chen Wang, Raili Raininko. Eur Radiol 2009
35
16

The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism.
C Lord, S Risi, L Lambrecht, E H Cook, B L Leventhal, P C DiLavore, A Pickles, M Rutter. J Autism Dev Disord 2000
16

Qualitative assessment of brain anomalies in adolescents with mental retardation.
Michael D Spencer, Rod J Gibson, T William J Moorhead, Peter M Keston, Peter Hoare, Jonathan J K Best, Stephen M Lawrie, Eve C Johnstone. AJNR Am J Neuroradiol 2005
28
16


Macro cisterna magna: a marker for maldevelopment of the brain?
J B Bodensteiner, C T Gay, W A Marks, M Hamza, G B Schaefer. Pediatr Neurol 1988
26
16


Diagnostic evaluation of autism spectrum disorders.
Marisela Huerta, Catherine Lord. Pediatr Clin North Am 2012
71
16



Midsagittal corpus callosum area, intelligence, and language dominance in epilepsy.
D S Atkinson, B Abou-Khalil, P D Charles, L Welch. J Neuroimaging 1996
20
16

Chromosome 10q deletion del (10)(q26.1q26.3) is associated with cataract.
Yu-Tzu Chang, I-Ching Chou, Chung-Hsing Wang, Zheng-Nan Chin, Huang-Tsung Kuo, Chyi-Chyang Lin, Chang-Hai Tsai, Fuu-Jen Tsai. Pediatr Neonatol 2013
12
16

Genome-wide scans of three independent sets of 90 Irish multiplex schizophrenia families and follow-up of selected regions in all families provides evidence for multiple susceptibility genes.
R E Straub, C J MacLean, Y Ma, B T Webb, M V Myakishev, C Harris-Kerr, B Wormley, H Sadek, B Kadambi, F A O'Neill,[...]. Mol Psychiatry 2002
106
16

Subtelomeric deletions of 1q43q44 and severe brain impairment associated with delayed myelination.
Keiko Shimojima, Nobuhiko Okamoto, Yume Suzuki, Mari Saito, Masato Mori, Tatanori Yamagata, Mariko Y Momoi, Hideji Hattori, Yoshiyuki Okano, Ken Hisata,[...]. J Hum Genet 2012
15
16

Genome-wide inbreeding estimation within Lebanese communities using SNP arrays.
Nadine Jalkh, Mourad Sahbatou, Eliane Chouery, André Megarbane, Anne-Louise Leutenegger, Jean-Louis Serre. Eur J Hum Genet 2015
8
16

Challenges for CNV interpretation in clinical molecular karyotyping: lessons learned from a 1001 sample experience.
Karen Buysse, Barbara Delle Chiaie, Rudy Van Coster, Bart Loeys, Anne De Paepe, Geert Mortier, Frank Speleman, Björn Menten. Eur J Med Genet 2009
73
16

De novo 325 kb microdeletion in chromosome band 10q25.3 including ATRNL1 in a boy with cognitive impairment, autism and dysmorphic features.
Zornitza Stark, Damien L Bruno, Hayley Mountford, Paul J Lockhart, David J Amor. Eur J Med Genet 2010
8
16


Clinical and molecular characteristics of 1qter microdeletion syndrome: delineating a critical region for corpus callosum agenesis/hypogenesis.
B W M van Bon, D A Koolen, R Borgatti, A Magee, S Garcia-Minaur, L Rooms, W Reardon, M Zollino, M C Bonaglia, M De Gregori,[...]. J Med Genet 2008
74
16

Molecular karyotyping of patients with unexplained mental retardation by SNP arrays: a multicenter study.
Dominic J McMullan, Michael Bonin, Jayne Y Hehir-Kwa, Bert B A de Vries, Andreas Dufke, Eleanor Rattenberry, Marloes Steehouwer, Luminita Moruz, Rolph Pfundt, Nicole de Leeuw,[...]. Hum Mutat 2009
48
16

Clinical application of 2.7M Cytogenetics array for CNV detection in subjects with idiopathic autism and/or intellectual disability.
Y Qiao, C Tyson, M Hrynchak, E Lopez-Rangel, J Hildebrand, S Martell, C Fawcett, L Kasmara, K Calli, C Harvard,[...]. Clin Genet 2013
31
16

Delineation of the cryptic 1qter deletion phenotype.
J Lawrence Merritt, Ying Zou, Syed M Jalal, Virginia V Michels. Am J Med Genet A 2007
20
16

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
16

Haploinsufficiency of two histone modifier genes on 6p22.3, ATXN1 and JARID2, is associated with intellectual disability.
Tuva Barøy, Doriana Misceo, Petter Strømme, Asbjørg Stray-Pedersen, Asbjørn Holmgren, Olaug Kristin Rødningen, Anne Blomhoff, Johan Robert Helle, Alice Stormyr, Bjørn Tvedt,[...]. Orphanet J Rare Dis 2013
14
16

Identification of critical regions for clinical features of distal 10q deletion syndrome.
S A Yatsenko, M C Kruer, P I Bader, D Corzo, J Schuette, C E Keegan, B Nowakowska, S Peacock, W W Cai, D A Peiffer,[...]. Clin Genet 2009
42
16

Molecular and comparative genetics of mental retardation.
Jennifer K Inlow, Linda L Restifo. Genetics 2004
166
16


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
149
16

Characterization of a novel binding partner of the melanocortin-4 receptor: attractin-like protein.
Andrea M Haqq, Patricia René, Toshiro Kishi, Kathy Khong, Charlotte E Lee, Hongyan Liu, Jeffrey M Friedman, Joel K Elmquist, Roger D Cone. Biochem J 2003
26
16

American College of Medical Genetics and Genomics: standards and guidelines for documenting suspected consanguinity as an incidental finding of genomic testing.
Catherine W Rehder, Karen L David, Betsy Hirsch, Helga V Toriello, Carolyn M Wilson, Hutton M Kearney. Genet Med 2013
59
16

Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene.
Almuth Caliebe, Hester Y Kroes, Jasper J van der Smagt, José I Martin-Subero, Holger Tönnies, Ruben van 't Slot, Rutger A J Nievelstein, Hiltrud Muhle, Ulrich Stephani, Karsten Alfke,[...]. Eur J Med Genet 2010
63
16


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
45
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.