A citation-based method for searching scientific literature

Rolph Pfundt, Joris A Veltman. Methods Mol Biol 2012
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


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
44

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
230
33

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
33

Trinucleotide repeat disorders.
Harry T Orr, Huda Y Zoghbi. Annu Rev Neurosci 2007
972
22

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
590
22

Relative burden of large CNVs on a range of neurodevelopmental phenotypes.
Santhosh Girirajan, Zoran Brkanac, Bradley P Coe, Carl Baker, Laura Vives, Tiffany H Vu, Neil Shafer, Raphael Bernier, Giovanni B Ferrero, Margherita Silengo,[...]. PLoS Genet 2011
212
22

The epidemiology of mental retardation: challenges and opportunities in the new millennium.
Helen Leonard, Xingyan Wen. Ment Retard Dev Disabil Res Rev 2002
354
22


Fine-scale structural variation of the human genome.
Eray Tuzun, Andrew J Sharp, Jeffrey A Bailey, Rajinder Kaul, V Anne Morrison, Lisa M Pertz, Eric Haugen, Hillary Hayden, Donna Albertson, Daniel Pinkel,[...]. Nat Genet 2005
716
22

Population analysis of large copy number variants and hotspots of human genetic disease.
Andy Itsara, Gregory M Cooper, Carl Baker, Santhosh Girirajan, Jun Li, Devin Absher, Ronald M Krauss, Richard M Myers, Paul M Ridker, Daniel I Chasman,[...]. Am J Hum Genet 2009
420
22

Segmental copy number variation shapes tissue transcriptomes.
Charlotte N Henrichsen, Nicolas Vinckenbosch, Sebastian Zöllner, Evelyne Chaignat, Sylvain Pradervand, Frédéric Schütz, Manuel Ruedi, Henrik Kaessmann, Alexandre Reymond. Nat Genet 2009
226
22

Microdeletion and microduplication syndromes.
Lisenka E L M Vissers, Paweł Stankiewicz. Methods Mol Biol 2012
41
22

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
107
22

Genomic microarrays in mental retardation: a practical workflow for diagnostic applications.
David A Koolen, Rolph Pfundt, Nicole de Leeuw, Jayne Y Hehir-Kwa, Willy M Nillesen, Ineke Neefs, Ine Scheltinga, Erik Sistermans, Dominique Smeets, Han G Brunner,[...]. Hum Mutat 2009
113
22

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
820
22

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
124
22

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
358
22

Screening for subtelomeric rearrangements in 210 patients with unexplained mental retardation using multiplex ligation dependent probe amplification (MLPA).
D A Koolen, W M Nillesen, M H A Versteeg, G F M Merkx, N V A M Knoers, M Kets, S Vermeer, C M A van Ravenswaaij, C G de Kovel, H G Brunner,[...]. J Med Genet 2004
119
22

Telomeres: a diagnosis at the end of the chromosomes.
B B A De Vries, R Winter, A Schinzel, C van Ravenswaaij-Arts. J Med Genet 2003
168
22

A new diagnostic workflow for patients with mental retardation and/or multiple congenital abnormalities: test arrays first.
Antoinet C J Gijsbers, Janet Y K Lew, Cathy A J Bosch, Janneke H M Schuurs-Hoeijmakers, Arie van Haeringen, Nicolette S den Hollander, Sarina G Kant, Emilia K Bijlsma, Martijn H Breuning, Egbert Bakker,[...]. Eur J Hum Genet 2009
55
22

Prenatal and postnatal risk factors for mental retardation among children in Bangladesh.
M S Durkin, N Z Khan, L L Davidson, S Huq, S Munir, E Rasul, S S Zaman. Am J Epidemiol 2000
52
11

Tuberous sclerosis complex: advances in diagnosis, genetics, and management.
Robert A Schwartz, Geover Fernández, Katarzyna Kotulska, Sergiusz Jóźwiak. J Am Acad Dermatol 2007
194
11

Subtelomeric rearrangements: results from FISH studies in 84 families with idiopathic mental retardation.
Ewa Bocian, Zofia Hélias-Rodzewicz, Kamila Suchenek, Ewa Obersztyn, Anna Kutkowska-Kaźmierczak, Paweł Stankiewicz, Ewa Kostyk, Tadeusz Mazurczak. Med Sci Monit 2004
20
11

Autism spectrum conditions in myotonic dystrophy type 1: a study on 57 individuals with congenital and childhood forms.
Anne-Berit Ekström, Louise Hakenäs-Plate, Lena Samuelsson, Már Tulinius, Elisabet Wentz. Am J Med Genet B Neuropsychiatr Genet 2008
76
11

Behavioral functioning in individuals with mental retardation.
E Zigler, R M Hodapp. Annu Rev Psychol 1991
10
11

Malformations of cortical development: clinical spectrum in a series of 101 patients and review of the literature (Part I).
Serdal Güngör, Dilek Yalnizoğlu, Güzide Turanli, Işil Saatçi, Emel Erdoğan-Bakar, Meral Topçu. Turk J Pediatr 2007
8
12

Inborn errors of metabolism as a cause of neurological disease in adults: an approach to investigation.
R G Gray, M A Preece, S H Green, W Whitehouse, J Winer, A Green. J Neurol Neurosurg Psychiatry 2000
29
11

Frequency and stability of the myotonic dystrophy type 1 premutation.
L Martorell, D G Monckton, A Sanchez, A Lopez De Munain, M Baiget. Neurology 2001
51
11

Courting a cure for fragile X.
Gül Dölen, Mark F Bear. Neuron 2005
26
11

Germ line mosaicism.
J Zlotogora. Hum Genet 1998
164
11


DNA methylation represses FMR-1 transcription in fragile X syndrome.
J S Sutcliffe, D L Nelson, F Zhang, M Pieretti, C T Caskey, D Saxe, S T Warren. Hum Mol Genet 1992
478
11

X-linked mental retardation: many genes for a complex disorder.
Hans-Hilger Ropers. Curr Opin Genet Dev 2006
114
11

Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders.
Robert M Plenge, Roger A Stevenson, Herbert A Lubs, Charles E Schwartz, Huntington F Willard. Am J Hum Genet 2002
141
11

Cognitive impairment in myotonic dystrophy type 1 (DM1): a longitudinal follow-up study.
A Modoni, G Silvestri, M Gabriella Vita, D Quaranta, P A Tonali, C Marra. J Neurol 2008
48
11

Genetic polymorphisms: impact on the risk of fetal alcohol spectrum disorders.
Kenneth R Warren, Ting-Kai Li. Birth Defects Res A Clin Mol Teratol 2005
95
11

Genetics of early onset cognitive impairment.
Hans Hilger Ropers. Annu Rev Genomics Hum Genet 2010
228
11

Subtelomeric study of 132 patients with mental retardation reveals 9 chromosomal anomalies and contributes to the delineation of submicroscopic deletions of 1pter, 2qter, 4pter, 5qter and 9qter.
Marie Sogaard, Zeynep Tümer, Helle Hjalgrim, Johanne Hahnemann, Birgitte Friis, Paal Ledaal, Vibeke Faurholt Pedersen, Peter Baekgaard, Niels Tommerup, Sultan Cingöz,[...]. BMC Med Genet 2005
20
11

XLMR genes: update 2007.
Pietro Chiurazzi, Charles E Schwartz, Jozef Gecz, Giovanni Neri. Eur J Hum Genet 2008
123
11



The pathophysiology of fragile x syndrome.
Olga Penagarikano, Jennifer G Mulle, Stephen T Warren. Annu Rev Genomics Hum Genet 2007
258
11


[Autosomal dominant mental retardation].
A Sánchez-Díaz, C Morales-Peydró, I Madrigal-Bajo. Rev Neurol 2006
1
100

Candidate genes for recessive non-syndromic mental retardation on chromosome 3p (MRT2A).
J J Higgins, J Pucilowska, R Q Lombardi, J P Rooney. Clin Genet 2004
20
11

Molecular and comparative genetics of mental retardation.
Jennifer K Inlow, Linda L Restifo. Genetics 2004
166
11

Fragile X "gray zone" alleles: AGG patterns, expansion risks, and associated haplotypes.
N Zhong, W Ju, J Pietrofesa, D Wang, C Dobkin, W T Brown. Am J Med Genet 1996
54
11



Neurofibromatosis type 1: new insights into neurocognitive issues.
Maria T Acosta, Gerard A Gioia, Alcino J Silva. Curr Neurol Neurosci Rep 2006
55
11


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.