A citation-based method for searching scientific literature

Joanna Martin, Grace Hosking, Megan Wadon, Sharifah Shameem Agha, Kate Langley, Elliott Rees, Michael J Owen, Michael O'Donovan, George Kirov, Anita Thapar. Transl Psychiatry 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


A large data resource of genomic copy number variation across neurodevelopmental disorders.
Mehdi Zarrei, Christie L Burton, Worrawat Engchuan, Edwin J Young, Edward J Higginbotham, Jeffrey R MacDonald, Brett Trost, Ada J S Chan, Susan Walker, Sylvia Lamoureux,[...]. NPJ Genom Med 2019
31
50

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants.
F Kyle Satterstrom, Raymond K Walters, Tarjinder Singh, Emilie M Wigdor, Francesco Lescai, Ditte Demontis, Jack A Kosmicki, Jakob Grove, Christine Stevens, Jonas Bybjerg-Grauholm,[...]. Nat Neurosci 2019
37
50

Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.
Evangelia Stergiakouli, Marian Hamshere, Peter Holmans, Kate Langley, Irina Zaharieva, Ziarah Hawi, Lindsey Kent, Michael Gill, Nigel Williams, Michael J Owen,[...]. Am J Psychiatry 2012
128
50

The worldwide prevalence of ADHD: a systematic review and metaregression analysis.
Guilherme Polanczyk, Maurício Silva de Lima, Bernardo Lessa Horta, Joseph Biederman, Luis Augusto Rohde. Am J Psychiatry 2007
50


Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants.
Li Yang, Benjamin M Neale, Lu Liu, S Hong Lee, Naomi R Wray, Ning Ji, Haimei Li, Qiujin Qian, Dongliang Wang, Jun Li,[...]. Am J Med Genet B Neuropsychiatr Genet 2013
112
50

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.
Nigel M Williams, Irina Zaharieva, Andrew Martin, Kate Langley, Kiran Mantripragada, Ragnheidur Fossdal, Hreinn Stefansson, Kari Stefansson, Pall Magnusson, Olafur O Gudmundsson,[...]. Lancet 2010
328
50

Attention-deficit/hyperactivity disorder.
Stephen V Faraone, Philip Asherson, Tobias Banaschewski, Joseph Biederman, Jan K Buitelaar, Josep Antoni Ramos-Quiroga, Luis Augusto Rohde, Edmund J S Sonuga-Barke, Rosemary Tannock, Barbara Franke. Nat Rev Dis Primers 2015
456
50

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.
Nigel M Williams, Barbara Franke, Eric Mick, Richard J L Anney, Christine M Freitag, Michael Gill, Anita Thapar, Michael C O'Donovan, Michael J Owen, Peter Holmans,[...]. Am J Psychiatry 2012
174
50

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder.
Ditte Demontis, Raymond K Walters, Joanna Martin, Manuel Mattheisen, Thomas D Als, Esben Agerbo, Gísli Baldursson, Rich Belliveau, Jonas Bybjerg-Grauholm, Marie Bækvad-Hansen,[...]. Nat Genet 2019
514
50

Rare copy number variation discovery and cross-disorder comparisons identify risk genes for ADHD.
Anath C Lionel, Jennifer Crosbie, Nicole Barbosa, Tara Goodale, Bhooma Thiruvahindrapuram, Jessica Rickaby, Matthew Gazzellone, Andrew R Carson, Jennifer L Howe, Zhuozhi Wang,[...]. Sci Transl Med 2011
221
50

Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder.
Olafur O Gudmundsson, G Bragi Walters, Andres Ingason, Stefan Johansson, Tetyana Zayats, Lavinia Athanasiu, Ida Elken Sonderby, Omar Gustafsson, Muhammad S Nawaz, Gudbjorn F Jonsson,[...]. Transl Psychiatry 2019
20
50



Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes.
J Elia, X Gai, H M Xie, J C Perin, E Geiger, J T Glessner, M D'arcy, R deBerardinis, E Frackelton, C Kim,[...]. Mol Psychiatry 2010
352
25

Proteins encoded in genomic regions associated with immune-mediated disease physically interact and suggest underlying biology.
Elizabeth J Rossin, Kasper Lage, Soumya Raychaudhuri, Ramnik J Xavier, Diana Tatar, Yair Benita, Chris Cotsapas, Mark J Daly. PLoS Genet 2011
355
25

Characterizing autism spectrum disorders by key biochemical pathways.
Megha Subramanian, Christina K Timmerman, Joshua L Schwartz, Daniel L Pham, Mollie K Meffert. Front Neurosci 2015
35
25


Role of the cytoplasmic isoform of RBFOX1/A2BP1 in establishing the architecture of the developing cerebral cortex.
Nanako Hamada, Hidenori Ito, Ikuko Iwamoto, Rika Morishita, Hidenori Tabata, Koh-Ichi Nagata. Mol Autism 2015
33
25

BIRC6 protein, an inhibitor of apoptosis: role in survival of human prostate cancer cells.
Christopher G Low, Iris S U Luk, Dong Lin, Ladan Fazli, Kuo Yang, Yong Xu, Martin Gleave, Peter W Gout, Yuzhuo Wang. PLoS One 2013
20
25

Dopamine D2 receptor relies upon PPM/PP2C protein phosphatases to dephosphorylate huntingtin protein.
Sébastien Marion, Nikhil M Urs, Sean M Peterson, Tatyana D Sotnikova, Jean-Martin Beaulieu, Raul R Gainetdinov, Marc G Caron. J Biol Chem 2014
10
25

Brain Transcriptome Databases: A User's Guide.
Jason M Keil, Adel Qalieh, Kenneth Y Kwan. J Neurosci 2018
33
25

Brain Imaging of the Cortex in ADHD: A Coordinated Analysis of Large-Scale Clinical and Population-Based Samples.
Martine Hoogman, Ryan Muetzel, Joao P Guimaraes, Elena Shumskaya, Maarten Mennes, Marcel P Zwiers, Neda Jahanshad, Gustavo Sudre, Thomas Wolfers, Eric A Earl,[...]. Am J Psychiatry 2019
74
25

Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap.
Michael J Gandal, Jillian R Haney, Neelroop N Parikshak, Virpi Leppa, Gokul Ramaswami, Chris Hartl, Andrew J Schork, Vivek Appadurai, Alfonso Buil, Thomas M Werge,[...]. Science 2018
398
25

Essential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development.
Nanako Hamada, Hidenori Ito, Takuma Nishijo, Ikuko Iwamoto, Rika Morishita, Hidenori Tabata, Toshihiko Momiyama, Koh-Ichi Nagata. Sci Rep 2016
32
25

Genome-wide association studies in ADHD.
Barbara Franke, Benjamin M Neale, Stephen V Faraone. Hum Genet 2009
281
25

The neurology of mTOR.
Jonathan O Lipton, Mustafa Sahin. Neuron 2014
346
25

The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species.
Christopher J Mungall, Julie A McMurry, Sebastian Köhler, James P Balhoff, Charles Borromeo, Matthew Brush, Seth Carbon, Tom Conlin, Nathan Dunn, Mark Engelstad,[...]. Nucleic Acids Res 2017
121
25

Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder.
Daniel Seung Kim, Amber A Burt, Jane E Ranchalis, Beth Wilmot, Joshua D Smith, Karynne E Patterson, Bradley P Coe, Yatong K Li, Michael J Bamshad, Molly Nikolas,[...]. Am J Med Genet B Neuropsychiatr Genet 2017
19
25

Variants in the 1q21 risk region are associated with a visual endophenotype of autism and schizophrenia.
P T Goodbourn, J M Bosten, G Bargary, R E Hogg, A J Lawrance-Owen, J D Mollon. Genes Brain Behav 2014
26
25

An anatomically comprehensive atlas of the adult human brain transcriptome.
Michael J Hawrylycz, Ed S Lein, Angela L Guillozet-Bongaarts, Elaine H Shen, Lydia Ng, Jeremy A Miller, Louie N van de Lagemaat, Kimberly A Smith, Amanda Ebbert, Zackery L Riley,[...]. Nature 2012
25

Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex.
Donna M Werling, Sirisha Pochareddy, Jinmyung Choi, Joon-Yong An, Brooke Sheppard, Minshi Peng, Zhen Li, Claudia Dastmalchi, Gabriel Santpere, André M M Sousa,[...]. Cell Rep 2020
18
25

Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum.
Andrea Ganna, F Kyle Satterstrom, Seyedeh M Zekavat, Indraniel Das, Mitja I Kurki, Claire Churchhouse, Jessica Alfoldi, Alicia R Martin, Aki S Havulinna, Andrea Byrnes,[...]. Am J Hum Genet 2018
39
25

The septin Sept5/CDCrel-1 competes with alpha-SNAP for binding to the SNARE complex.
Crestina L Beites, Kristen A Campbell, William S Trimble. Biochem J 2005
73
25

On the allelic spectrum of human disease.
D E Reich, E S Lander. Trends Genet 2001
744
25

Dopamine genes and ADHD.
J M Swanson, P Flodman, J Kennedy, M A Spence, R Moyzis, S Schuck, M Murias, J Moriarity, C Barr, M Smith,[...]. Neurosci Biobehav Rev 2000
256
25

Time for Bed: Genetic Mechanisms Mediating the Circadian Regulation of Sleep.
Ian D Blum, Benjamin Bell, Mark N Wu. Trends Genet 2018
13
25

Sept5 deficiency exerts pleiotropic influence on affective behaviors and cognitive functions in mice.
Go Suzuki, Kathryn M Harper, Takeshi Hiramoto, Takehito Sawamura, MoonSook Lee, Gina Kang, Kenji Tanigaki, Mahalah Buell, Mark A Geyer, William S Trimble,[...]. Hum Mol Genet 2009
52
25


Rab GTPases as coordinators of vesicle traffic.
Harald Stenmark. Nat Rev Mol Cell Biol 2009
25

Genome-wide copy number variation analysis in attention-deficit/hyperactivity disorder: association with neuropeptide Y gene dosage in an extended pedigree.
K-P Lesch, S Selch, T J Renner, C Jacob, T T Nguyen, T Hahn, M Romanos, S Walitza, S Shoichet, A Dempfle,[...]. Mol Psychiatry 2011
104
25

Candidate gene studies of ADHD: a meta-analytic review.
Ian R Gizer, Courtney Ficks, Irwin D Waldman. Hum Genet 2009
618
25

Learning-Induced Gene Expression in the Hippocampus Reveals a Role of Neuron -Astrocyte Metabolic Coupling in Long Term Memory.
Monika Tadi, Igor Allaman, Sylvain Lengacher, Gabriele Grenningloh, Pierre J Magistretti. PLoS One 2015
46
25

Interpreting the role of de novo protein-coding mutations in neuropsychiatric disease.
Jacob Gratten, Peter M Visscher, Bryan J Mowry, Naomi R Wray. Nat Genet 2013
51
25


Functional mapping and annotation of genetic associations with FUMA.
Kyoko Watanabe, Erdogan Taskesen, Arjen van Bochoven, Danielle Posthuma. Nat Commun 2017
635
25

Alterations of social interaction through genetic and environmental manipulation of the 22q11.2 gene Sept5 in the mouse brain.
Kathryn M Harper, Takeshi Hiramoto, Kenji Tanigaki, Gina Kang, Go Suzuki, William Trimble, Noboru Hiroi. Hum Mol Genet 2012
35
25

A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration.
Janghoo Lim, Tong Hao, Chad Shaw, Akash J Patel, Gábor Szabó, Jean-François Rual, C Joseph Fisk, Ning Li, Alex Smolyar, David E Hill,[...]. Cell 2006
553
25

Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.
I Jarick, A-L Volckmar, C Pütter, S Pechlivanis, T T Nguyen, M R Dauvermann, S Beck, Ö Albayrak, S Scherag, S Gilsbach,[...]. Mol Psychiatry 2014
50
25

NMDA receptor blockade at rest triggers rapid behavioural antidepressant responses.
Anita E Autry, Megumi Adachi, Elena Nosyreva, Elisa S Na, Maarten F Los, Peng-fei Cheng, Ege T Kavalali, Lisa M Monteggia. Nature 2011
25


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.