A citation-based method for searching scientific literature

Geert Vandeweyer, R Frank Kooy. Expert Rev Mol Diagn 2013
Times Cited: 9







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



Times Cited
  Times     Co-cited
Similarity


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
641
33

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

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data.
Kai Wang, Mingyao Li, Hakon Hakonarson. Nucleic Acids Res 2010
22


dbSNP: the NCBI database of genetic variation.
S T Sherry, M H Ward, M Kholodov, J Baker, L Phan, E M Smigielski, K Sirotkin. Nucleic Acids Res 2001
22

A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3.
Pablo Cingolani, Adrian Platts, Le Lily Wang, Melissa Coon, Tung Nguyen, Luan Wang, Susan J Land, Xiangyi Lu, Douglas M Ruden. Fly (Austin) 2012
22

Clinical whole-exome sequencing for the diagnosis of mendelian disorders.
Yaping Yang, Donna M Muzny, Jeffrey G Reid, Matthew N Bainbridge, Alecia Willis, Patricia A Ward, Alicia Braxton, Joke Beuten, Fan Xia, Zhiyv Niu,[...]. N Engl J Med 2013
22

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
556
22

A framework for variation discovery and genotyping using next-generation DNA sequencing data.
Mark A DePristo, Eric Banks, Ryan Poplin, Kiran V Garimella, Jared R Maguire, Christopher Hartl, Anthony A Philippakis, Guillermo del Angel, Manuel A Rivas, Matt Hanna,[...]. Nat Genet 2011
22


Exome sequencing supports a de novo mutational paradigm for schizophrenia.
Bin Xu, J Louw Roos, Phillip Dexheimer, Braden Boone, Brooks Plummer, Shawn Levy, Joseph A Gogos, Maria Karayiorgou. Nat Genet 2011
317
22

Galaxy: a platform for interactive large-scale genome analysis.
Belinda Giardine, Cathy Riemer, Ross C Hardison, Richard Burhans, Laura Elnitski, Prachi Shah, Yi Zhang, Daniel Blankenberg, Istvan Albert, James Taylor,[...]. Genome Res 2005
22

A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP.
Céline Helsmoortel, Anneke T Vulto-van Silfhout, Bradley P Coe, Geert Vandeweyer, Liesbeth Rooms, Jenneke van den Ende, Janneke H M Schuurs-Hoeijmakers, Carlo L Marcelis, Marjolein H Willemsen, Lisenka E L M Vissers,[...]. Nat Genet 2014
179
22

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
22

ClinVar: public archive of relationships among sequence variation and human phenotype.
Melissa J Landrum, Jennifer M Lee, George R Riley, Wonhee Jang, Wendy S Rubinstein, Deanna M Church, Donna R Maglott. Nucleic Acids Res 2014
22

A map of human genome variation from population-scale sequencing.
Gonçalo R Abecasis, David Altshuler, Adam Auton, Lisa D Brooks, Richard M Durbin, Richard A Gibbs, Matt E Hurles, Gil A McVean. Nature 2010
22

Challenges and opportunities in the investigation of unexplained intellectual disability using family-based whole-exome sequencing.
C Helsmoortel, G Vandeweyer, P Ordoukhanian, F Van Nieuwerburgh, N Van der Aa, R F Kooy. Clin Genet 2015
20
22

Origins and functional impact of copy number variation in the human genome.
Donald F Conrad, Dalila Pinto, Richard Redon, Lars Feuk, Omer Gokcumen, Yujun Zhang, Jan Aerts, T Daniel Andrews, Chris Barnes, Peter Campbell,[...]. Nature 2010
22

CNV analysis using TaqMan copy number assays.
Ping Mayo, Toinette Hartshorne, Kelly Li, Chara McMunn-Gibson, Kylee Spencer, Nathalie Schnetz-Boutaud. Curr Protoc Hum Genet 2010
21
22


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
22

A novel technique for measuring variations in DNA copy-number: competitive genomic polymerase chain reaction.
Kyoko Iwao-Koizumi, Kazunori Maekawa, Yohko Nakamura, Sakae Saito, Shoko Kawamoto, Akira Nakagawara, Kikuya Kato. BMC Genomics 2007
7
28


The array CGH and its clinical applications.
Marwan Shinawi, Sau Wai Cheung. Drug Discov Today 2008
111
22


Large-scale copy number polymorphism in the human genome.
Jonathan Sebat, B Lakshmi, Jennifer Troge, Joan Alexander, Janet Young, Pär Lundin, Susanne Månér, Hillary Massa, Megan Walker, Maoyen Chi,[...]. Science 2004
22

G-patch domain and KOW motifs-containing protein, GPKOW; a nuclear RNA-binding protein regulated by protein kinase A.
Anne Kristin Aksaas, Anja Cv Larsen, Marie Rogne, Ken Rosendal, Anne-Katrine Kvissel, Bjørn Steen Skålhegg. J Mol Signal 2011
12
11

Patterns and rates of exonic de novo mutations in autism spectrum disorders.
Benjamin M Neale, Yan Kou, Li Liu, Avi Ma'ayan, Kaitlin E Samocha, Aniko Sabo, Chiao-Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov,[...]. Nature 2012
11

The pathobiology of the septin gene family.
Peter A Hall, S E Hilary Russell. J Pathol 2004
225
11

Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network.
Suleyman Gulsuner, Tom Walsh, Amanda C Watts, Ming K Lee, Anne M Thornton, Silvia Casadei, Caitlin Rippey, Hashem Shahin, Vishwajit L Nimgaonkar, Rodney C P Go,[...]. Cell 2013
353
11

The conserved Wobble uridine tRNA thiolase Ctu1-Ctu2 is required to maintain genome integrity.
Monique Dewez, Fanélie Bauer, Marc Dieu, Martine Raes, Jean Vandenhaute, Damien Hermand. Proc Natl Acad Sci U S A 2008
91
11

The N-terminal domain determines the affinity and specificity of H1 binding to chromatin.
Christine Öberg, Sergey Belikov. Biochem Biophys Res Commun 2012
17
11

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
Brian J O'Roak, Laura Vives, Santhosh Girirajan, Emre Karakoc, Niklas Krumm, Bradley P Coe, Roie Levy, Arthur Ko, Choli Lee, Joshua D Smith,[...]. Nature 2012
11


KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes.
Audrey Putoux, Sophie Thomas, Karlien L M Coene, Erica E Davis, Yasemin Alanay, Gönül Ogur, Elif Uz, Daniela Buzas, Céline Gomes, Sophie Patrier,[...]. Nat Genet 2011
143
11

A de novo convergence of autism genetics and molecular neuroscience.
Niklas Krumm, Brian J O'Roak, Jay Shendure, Evan E Eichler. Trends Neurosci 2014
284
11

Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
Brian J O'Roak, Laura Vives, Wenqing Fu, Jarrett D Egertson, Ian B Stanaway, Ian G Phelps, Gemma Carvill, Akash Kumar, Choli Lee, Katy Ankenman,[...]. Science 2012
796
11

Preliminary evidence of association between EFHC2, a gene implicated in fear recognition, and harm avoidance.
Carolina Blaya, Priya Moorjani, Giovanni Abrahão Salum, Leonardo Gonçalves, Lauren A Weiss, Sandra Leistner-Segal, Gisele G Manfro, Jordan W Smoller. Neurosci Lett 2009
10
11

TM4SF2 gene involvement reconsidered in an XLMR family after neuropsychological assessment.
Marie Gomot, Nathalie Ronce, Sabine Dessay, Ramzi Zemni, Anne-Dominique Ayrault, Marie-Pierre Moizard, Annie Nivelon, Simone Gilgenkrantz, Julliette Dourlens, Vincent Des Portes,[...]. Am J Med Genet 2002
8
12

De novo gene disruptions in children on the autistic spectrum.
Ivan Iossifov, Michael Ronemus, Dan Levy, Zihua Wang, Inessa Hakker, Julie Rosenbaum, Boris Yamrom, Yoon-Ha Lee, Giuseppe Narzisi, Anthony Leotta,[...]. Neuron 2012
916
11

A novel 2 bp deletion in the TM4SF2 gene is associated with MRX58.
F E Abidi, E Holinski-Feder, O Rittinger, F Kooy, H A Lubs, R E Stevenson, C E Schwartz. J Med Genet 2002
28
11

ALPK2 is crucial for luminal apoptosis and DNA repair-related gene expression in a three-dimensional colonic-crypt model.
Yasuhiro Yoshida, Toshiyuki Tsunoda, Keiko Doi, Takahiro Fujimoto, Yoko Tanaka, Takeharu Ota, Masahiro Ogawa, Hiroshi Matsuzaki, Masahide Kuroki, Akinori Iwasaki,[...]. Anticancer Res 2012
21
11


Genetic syndromes among individuals with mental retardation.
Roger E Stevenson, Ashley M Procopio-Allen, Richard J Schroer, Julianne S Collins. Am J Med Genet A 2003
29
11


Interaction of HLA-DR and CD74 at the cell surface of antigen-presenting cells by single particle image analysis.
Ioannis Karakikes, Ian E G Morrison, Peter O'Toole, Gergana Metodieva, Cristina V Navarrete, Jesus Gomez, Jose M Miranda-Sayago, Richard J Cherry, Metodi Metodiev, Nelson Fernandez. FASEB J 2012
14
11

Control of neuronal morphology by the atypical cadherin Fat3.
Michael R Deans, Alexandra Krol, Victoria E Abraira, Catherine O Copley, Andrew F Tucker, Lisa V Goodrich. Neuron 2011
59
11

Increased exonic de novo mutation rate in individuals with schizophrenia.
Simon L Girard, Julie Gauthier, Anne Noreau, Lan Xiong, Sirui Zhou, Loubna Jouan, Alexandre Dionne-Laporte, Dan Spiegelman, Edouard Henrion, Ousmane Diallo,[...]. Nat Genet 2011
274
11

Involvement of the kinesin family members KIF4A and KIF5C in intellectual disability and synaptic function.
Marjolein H Willemsen, Wei Ba, Willemijn M Wissink-Lindhout, Arjan P M de Brouwer, Stefan A Haas, Melanie Bienek, Hao Hu, Lisenka E L M Vissers, Hans van Bokhoven, Vera Kalscheuer,[...]. J Med Genet 2014
54
11

De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
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.