A citation-based method for searching scientific literature

Shin Hayashi, Issei Imoto, Yoshinori Aizu, Nobuhiko Okamoto, Seiji Mizuno, Kenji Kurosawa, Nana Okamoto, Shozo Honda, Satoshi Araki, Shuki Mizutani, Hironao Numabe, Shinji Saitoh, Tomoki Kosho, Yoshimitsu Fukushima, Hiroshi Mitsubuchi, Fumio Endo, Yasutsugu Chinen, Rika Kosaki, Torayuki Okuyama, Hirotaka Ohki, Hiroshi Yoshihashi, Masae Ono, Fumio Takada, Hiroaki Ono, Mariko Yagi, Hiroshi Matsumoto, Yoshio Makita, Akira Hata, Johji Inazawa. J Hum Genet 2011
Times Cited: 17







List of co-cited articles
95 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
58

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
29

Detection of pathogenic copy number variants in children with idiopathic intellectual disability using 500 K SNP array genomic hybridization.
Jm Friedman, Shelin Adam, Laura Arbour, Linlea Armstrong, Agnes Baross, Patricia Birch, Cornelius Boerkoel, Susanna Chan, David Chai, Allen D Delaney,[...]. BMC Genomics 2009
27
29


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
417
29

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
126
23

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
815
23

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
533
23


Array CGH in molecular diagnosis of mental retardation - A study of 150 Finnish patients.
Linda Siggberg, Sirpa Ala-Mello, Elisa Jaakkola, Esa Kuusinen, Robert Schuit, Jürgen Kohlhase, Detlef Böhm, Jaakko Ignatius, Sakari Knuutila. Am J Med Genet A 2010
29
23

Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical cases.
Bixia Xiang, Hongbo Zhu, Yiping Shen, David T Miller, Kangmo Lu, Xiaofeng Hu, Hans C Andersson, Tarachandra M Narumanchi, Yueying Wang, Jose E Martinez,[...]. J Mol Diagn 2010
56
23

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
23

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
23


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
17

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
314
17

Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arrays.
Juliane Hoyer, Alexander Dreweke, Christian Becker, Ina Göhring, Christian T Thiel, Maarit M Peippo, Ralf Rauch, Michael Hofbeck, Udo Trautmann, Christiane Zweier,[...]. J Med Genet 2007
60
17

Outcome of array CGH analysis for 255 subjects with intellectual disability and search for candidate genes using bioinformatics.
Y Qiao, C Harvard, C Tyson, X Liu, C Fawcett, P Pavlidis, J J A Holden, M E S Lewis, E Rajcan-Separovic. Hum Genet 2010
19
17

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
419
17

Detection of large-scale variation in the human genome.
A John Iafrate, Lars Feuk, Miguel N Rivera, Marc L Listewnik, Patricia K Donahoe, Ying Qi, Stephen W Scherer, Charles Lee. Nat Genet 2004
17

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
96
17

Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams,[...]. Nature 2010
17

Comparison of genome-wide array genomic hybridization platforms for the detection of copy number variants in idiopathic mental retardation.
Tracy Tucker, Alexandre Montpetit, David Chai, Susanna Chan, Sébastien Chénier, Bradley P Coe, Allen Delaney, Patrice Eydoux, Wan L Lam, Sylvie Langlois,[...]. BMC Med Genomics 2011
22
17

Array-CGH detection of micro rearrangements in mentally retarded individuals: clinical significance of imbalances present both in affected children and normal parents.
C Rosenberg, J Knijnenburg, E Bakker, A M Vianna-Morgante, W Sloos, P A Otto, M Kriek, K Hansson, A C V Krepischi-Santos, H Fiegler,[...]. J Med Genet 2006
165
17

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
17

Molecular karyotyping by array CGH in a Russian cohort of children with intellectual disability, autism, epilepsy and congenital anomalies.
Ivan Y Iourov, Svetlana G Vorsanova, Oxana S Kurinnaia, Maria A Zelenova, Alexandra P Silvanovich, Yuri B Yurov. Mol Cytogenet 2012
39
17

Copy number variations and clinical cytogenetic diagnosis of constitutional disorders.
Charles Lee, A John Iafrate, Arthur R Brothman. Nat Genet 2007
269
17

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
17

Application of array comparative genomic hybridization in 102 patients with epilepsy and additional neurodevelopmental disorders.
Magdalena Bartnik, Elżbieta Szczepanik, Katarzyna Derwińska, Barbara Wiśniowiecka-Kowalnik, Tomasz Gambin, Maciej Sykulski, Kamila Ziemkiewicz, Marta Kędzior, Monika Gos, Dorota Hoffman-Zacharska,[...]. Am J Med Genet B Neuropsychiatr Genet 2012
37
17

Dominant-negative mutations in alpha-II spectrin cause West syndrome with severe cerebral hypomyelination, spastic quadriplegia, and developmental delay.
Hirotomo Saitsu, Jun Tohyama, Tatsuro Kumada, Kiyoshi Egawa, Keisuke Hamada, Ippei Okada, Takeshi Mizuguchi, Hitoshi Osaka, Rie Miyata, Tomonori Furukawa,[...]. Am J Hum Genet 2010
112
11

De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy.
Hirotomo Saitsu, Mitsuhiro Kato, Takeshi Mizuguchi, Keisuke Hamada, Hitoshi Osaka, Jun Tohyama, Katsuhisa Uruno, Satoko Kumada, Kiyomi Nishiyama, Akira Nishimura,[...]. Nat Genet 2008
353
11

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
11

Rare de novo and transmitted copy-number variation in autistic spectrum disorders.
Dan Levy, Michael Ronemus, Boris Yamrom, Yoon-ha Lee, Anthony Leotta, Jude Kendall, Steven Marks, B Lakshmi, Deepa Pai, Kenny Ye,[...]. Neuron 2011
447
11


BAC array CGH reveals genomic aberrations in idiopathic mental retardation.
Noriko Miyake, Osamu Shimokawa, Naoki Harada, Nadia Sosonkina, Aiko Okubo, Hiroki Kawara, Nobuhiko Okamoto, Kenji Kurosawa, Hiroshi Kawame, Mie Iwakoshi,[...]. Am J Med Genet A 2006
54
11

Array comparative genomic hybridization in global developmental delay.
M I Shevell, B A Bejjani, M Srour, E A Rorem, N Hall, L G Shaffer. Am J Med Genet B Neuropsychiatr Genet 2008
39
11

Rare de novo variants associated with autism implicate a large functional network of genes involved in formation and function of synapses.
Sarah R Gilman, Ivan Iossifov, Dan Levy, Michael Ronemus, Michael Wigler, Dennis Vitkup. Neuron 2011
437
11


Fine-scale survey of X chromosome copy number variants and indels underlying intellectual disability.
Annabel C Whibley, Vincent Plagnol, Patrick S Tarpey, Fatima Abidi, Tod Fullston, Maja K Choma, Catherine A Boucher, Lorraine Shepherd, Lionel Willatt, Georgina Parkin,[...]. Am J Hum Genet 2010
85
11

Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations.
A C V Krepischi-Santos, A M Vianna-Morgante, F S Jehee, M R Passos-Bueno, J Knijnenburg, K Szuhai, W Sloos, J F Mazzeu, F Kok, C Cheroki,[...]. Cytogenet Genome Res 2006
86
11

Identification of gene copy number variations in patients with mental retardation using array-CGH: Novel syndromes in a large French series.
Sylvie Jaillard, Séverine Drunat, Claude Bendavid, Azzedine Aboura, Amandine Etcheverry, Hubert Journel, Andrée Delahaye, Laurent Pasquier, Dominique Bonneau, Annick Toutain,[...]. Eur J Med Genet 2010
26
11

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
11

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
11

DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation.
H Engels, A Brockschmidt, A Hoischen, C Landwehr, K Bosse, C Walldorf, G Toedt, B Radlwimmer, P Propping, P Lichter,[...]. Neurology 2007
73
11

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
Erin L Heinzen, Rodney A Radtke, Thomas J Urban, Gianpiero L Cavalleri, Chantal Depondt, Anna C Need, Nicole M Walley, Paola Nicoletti, Dongliang Ge, Claudia B Catarino,[...]. Am J Hum Genet 2010
176
11

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
11

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources.
Helen V Firth, Shola M Richards, A Paul Bevan, Stephen Clayton, Manuel Corpas, Diana Rajan, Steven Van Vooren, Yves Moreau, Roger M Pettett, Nigel P Carter. Am J Hum Genet 2009
972
11

A double hit implicates DIAPH3 as an autism risk gene.
J A S Vorstman, E van Daalen, G R Jalali, E R E Schmidt, R J Pasterkamp, M de Jonge, E A M Hennekam, E Janson, W G Staal, B van der Zwaag,[...]. Mol Psychiatry 2011
45
11

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
Joseph T Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W Brune, Jonathan P Bradfield,[...]. Nature 2009
935
11

Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardation.
Janine Wagenstaller, Stephanie Spranger, Bettina Lorenz-Depiereux, Bernd Kazmierczak, Michaela Nathrath, Dagmar Wahl, Babett Heye, Dieter Glaser, Volkmar Liebscher, Thomas Meitinger,[...]. Am J Hum Genet 2007
103
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.