A citation-based method for searching scientific literature

B N Vardarajan, A Eran, J-Y Jung, L M Kunkel, D P Wall. Transl Psychiatry 2013
Times Cited: 17







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



Times Cited
  Times     Co-cited
Similarity


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
971
47

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
980
29

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
861
23

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
755
23

Using whole-exome sequencing to identify inherited causes of autism.
Timothy W Yu, Maria H Chahrour, Michael E Coulter, Sarn Jiralerspong, Kazuko Okamura-Ikeda, Bulent Ataman, Klaus Schmitz-Abe, David A Harmin, Mazhar Adli, Athar N Malik,[...]. Neuron 2013
290
23

Characteristics and predictive value of blood transcriptome signature in males with autism spectrum disorders.
Sek Won Kong, Christin D Collins, Yuko Shimizu-Motohashi, Ingrid A Holm, Malcolm G Campbell, In-Hee Lee, Stephanie J Brewster, Ellen Hanson, Heather K Harris, Kathryn R Lowe,[...]. PLoS One 2012
101
23

Common genetic variants on 5p14.1 associate with autism spectrum disorders.
Kai Wang, Haitao Zhang, Deqiong Ma, Maja Bucan, Joseph T Glessner, Brett S Abrahams, Daria Salyakina, Marcin Imielinski, Jonathan P Bradfield, Patrick M A Sleiman,[...]. Nature 2009
689
23

Contactin 4 as an autism susceptibility locus.
Catherine E Cottrell, Natalie Bir, Elizabeth Varga, Carlos E Alvarez, Samuel Bouyain, Randall Zernzach, Devon L Thrush, Johnna Evans, Michael Trimarchi, Eric M Butter,[...]. Autism Res 2011
48
23

Prospective diagnostic analysis of copy number variants using SNP microarrays in individuals with autism spectrum disorders.
Caroline Nava, Boris Keren, Cyril Mignot, Agnès Rastetter, Sandra Chantot-Bastaraud, Anne Faudet, Eric Fonteneau, Claire Amiet, Claudine Laurent, Aurélia Jacquette,[...]. Eur J Hum Genet 2014
48
23

Disruption of contactin 4 in three subjects with autism spectrum disorder.
J Roohi, C Montagna, D H Tegay, L E Palmer, C DeVincent, J C Pomeroy, S L Christian, N Nowak, E Hatchwell. J Med Genet 2009
112
23

Association between microdeletion and microduplication at 16p11.2 and autism.
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
17

Genetic architecture in autism spectrum disorder.
Bernie Devlin, Stephen W Scherer. Curr Opin Genet Dev 2012
316
17

The behavioral phenotype in MECP2 duplication syndrome: a comparison with idiopathic autism.
Sarika U Peters, Rachel J Hundley, Amy K Wilson, Zachary Warren, Alison Vehorn, Claudia M B Carvalho, James R Lupski, Melissa B Ramocki. Autism Res 2013
33
17

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.
Dan E Arking, David J Cutler, Camille W Brune, Tanya M Teslovich, Kristen West, Morna Ikeda, Alexis Rea, Moltu Guy, Shin Lin, Edwin H Cook,[...]. Am J Hum Genet 2008
417
17

Identifying autism loci and genes by tracing recent shared ancestry.
Eric M Morrow, Seung-Yun Yoo, Steven W Flavell, Tae-Kyung Kim, Yingxi Lin, Robert Sean Hill, Nahit M Mukaddes, Soher Balkhy, Generoso Gascon, Asif Hashmi,[...]. Science 2008
518
17

Functional evaluation of autism-associated mutations in NHE9.
Kalyan C Kondapalli, Anniesha Hack, Maya Schushan, Meytal Landau, Nir Ben-Tal, Rajini Rao. Nat Commun 2013
66
17

Family-based genome-wide association scan of attention-deficit/hyperactivity disorder.
Eric Mick, Alexandre Todorov, Susan Smalley, Xiaolan Hu, Sandra Loo, Richard D Todd, Joseph Biederman, Deirdre Byrne, Bryan Dechairo, Allan Guiney,[...]. J Am Acad Child Adolesc Psychiatry 2010
105
17

Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.
Jessica Lasky-Su, Benjamin M Neale, Barbara Franke, Richard J L Anney, Kaixin Zhou, Julian B Maller, Alejandro Arias Vasquez, Wai Chen, Philip Asherson, Jan Buitelaar,[...]. Am J Med Genet B Neuropsychiatr Genet 2008
287
17

Identification of a functional rare variant in autism using genome-wide screen for monoallelic expression.
Eyal Ben-David, Einat Granot-Hershkovitz, Galya Monderer-Rothkoff, Elad Lerer, Shlomit Levi, Maya Yaari, Richard P Ebstein, Nurit Yirmiya, Sagiv Shifman. Hum Mol Genet 2011
45
17


Transcriptomic analysis of autistic brain reveals convergent molecular pathology.
Irina Voineagu, Xinchen Wang, Patrick Johnston, Jennifer K Lowe, Yuan Tian, Steve Horvath, Jonathan Mill, Rita M Cantor, Benjamin J Blencowe, Daniel H Geschwind. Nature 2011
17

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

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
17

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
17

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
17

Personalized smoking cessation: interactions between nicotine dose, dependence and quit-success genotype score.
Jed E Rose, Frédérique M Behm, Tomas Drgon, Catherine Johnson, George R Uhl. Mol Med 2010
98
17


Gene expression profiling differentiates autism case-controls and phenotypic variants of autism spectrum disorders: evidence for circadian rhythm dysfunction in severe autism.
Valerie W Hu, Tewarit Sarachana, Kyung Soon Kim, AnhThu Nguyen, Shreya Kulkarni, Mara E Steinberg, Truong Luu, Yinglei Lai, Norman H Lee. Autism Res 2009
144
17

Molecular genetic overlap in bipolar disorder, schizophrenia, and major depressive disorder.
Thomas G Schulze, Nirmala Akula, René Breuer, Jo Steele, Michael A Nalls, Andrew B Singleton, Franziska A Degenhardt, Markus M Nöthen, Sven Cichon, Marcella Rietschel,[...]. World J Biol Psychiatry 2014
84
17

Association mapping of disease loci, by use of a pooled DNA genomic screen.
L F Barcellos, W Klitz, L L Field, R Tobias, A M Bowcock, R Wilson, M P Nelson, J Nagatomi, G Thomson. Am J Hum Genet 1997
184
17

Transcriptional consequences of schizophrenia candidate miR-137 manipulation in human neural progenitor cells.
Matthew J Hill, Jacek G Donocik, Rosamond A Nuamah, Charles A Mein, Ricardo Sainz-Fuertes, Nicholas J Bray. Schizophr Res 2014
53
17

Pooled DNA genotyping on Affymetrix SNP genotyping arrays.
George Kirov, Ivan Nikolov, Lyudmila Georgieva, Valentina Moskvina, Michael J Owen, Michael C O'Donovan. BMC Genomics 2006
66
17

Familial clustering of schizophrenia, bipolar disorder, and major depressive disorder.
Maartje F Aukes, Wijnand Laan, Fabian Termorshuizen, Jacobine E Buizer-Voskamp, Eric A M Hennekam, Hugo M Smeets, Roel A Ophoff, Marco P M Boks, René S Kahn. Genet Med 2012
16
18

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.
Claire S Leblond, Jutta Heinrich, Richard Delorme, Christian Proepper, Catalina Betancur, Guillaume Huguet, Marina Konyukh, Pauline Chaste, Elodie Ey, Maria Rastam,[...]. PLoS Genet 2012
290
17

The impact of phenotypic and genetic heterogeneity on results of genome wide association studies of complex diseases.
Mirko Manchia, Jeffrey Cullis, Gustavo Turecki, Guy A Rouleau, Rudolf Uher, Martin Alda. PLoS One 2013
133
17

Genome-wide scan of copy number variation in late-onset Alzheimer's disease.
Erin L Heinzen, Anna C Need, Kathleen M Hayden, Ornit Chiba-Falek, Allen D Roses, Warren J Strittmatter, James R Burke, Christine M Hulette, Kathleen A Welsh-Bohmer, David B Goldstein. J Alzheimers Dis 2010
95
17

Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia.
Yang Liu, Gang Chen, Nadine Norton, Wenmin Liu, Haining Zhu, Peng Zhou, Meng Luan, Shulin Yang, Xing Chen, Liam Carroll,[...]. J Biomed Biotechnol 2009
29
17

Gene-network analysis identifies susceptibility genes related to glycobiology in autism.
Bert van der Zwaag, Lude Franke, Martin Poot, Ron Hochstenbach, Henk A Spierenburg, Jacob A S Vorstman, Emma van Daalen, Maretha V de Jonge, Nienke E Verbeek, Eva H Brilstra,[...]. PLoS One 2009
101
17

Absence of BRINP1 in mice causes increase of hippocampal neurogenesis and behavioral alterations relevant to human psychiatric disorders.
Miwako Kobayashi, Toshiyuki Nakatani, Toshiaki Koda, Ken-Ichi Matsumoto, Ryosuke Ozaki, Natsuki Mochida, Keizo Takao, Tsuyoshi Miyakawa, Ichiro Matsuoka. Mol Brain 2014
35
17

A discovery resource of rare copy number variations in individuals with autism spectrum disorder.
Aparna Prasad, Daniele Merico, Bhooma Thiruvahindrapuram, John Wei, Anath C Lionel, Daisuke Sato, Jessica Rickaby, Chao Lu, Peter Szatmari, Wendy Roberts,[...]. G3 (Bethesda) 2012
136
17



High resolution melting analysis for gene scanning.
Maria Erali, Carl T Wittwer. Methods 2010
101
17


Alternatively Spliced Genes as Biomarkers for Schizophrenia, Bipolar Disorder and Psychosis: A Blood-Based Spliceome-Profiling Exploratory Study.
S J Glatt, S D Chandler, C A Bousman, G Chana, G R Lucero, E Tatro, T May, J B Lohr, W S Kremen, I P Everall,[...]. Curr Pharmacogenomics Person Med 2009
37
17

Polymorphism of Toll-like receptor 4 gene in bipolar disorder.
José Oliveira, Marc Busson, Bruno Etain, Stéphane Jamain, Nora Hamdani, Wahid Boukouaci, Kahina Amokrane, Mériem Bennabi, Emmanuel Le Guen, Aroldo Ayub Dargél,[...]. J Affect Disord 2014
43
17

The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia.
E K Green, D Grozeva, I Jones, L Jones, G Kirov, S Caesar, K Gordon-Smith, C Fraser, L Forty, E Russell,[...]. Mol Psychiatry 2010
359
17

Genotyping of single-nucleotide polymorphisms by high-resolution melting of small amplicons.
Michael Liew, Robert Pryor, Robert Palais, Cindy Meadows, Maria Erali, Elaine Lyon, Carl Wittwer. Clin Chem 2004
434
17

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
Brian J O'Roak, Pelagia Deriziotis, Choli Lee, Laura Vives, Jerrod J Schwartz, Santhosh Girirajan, Emre Karakoc, Alexandra P Mackenzie, Sarah B Ng, Carl Baker,[...]. Nat Genet 2011
805
17

Synaptic, transcriptional and chromatin genes disrupted in autism.
Silvia De Rubeis, Xin He, Arthur P Goldberg, Christopher S Poultney, Kaitlin Samocha, A Erucment Cicek, Yan Kou, Li Liu, Menachem Fromer, Susan Walker,[...]. Nature 2014
17


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.