A citation-based method for searching scientific literature

Lucilla Pizzo, Joris Andrieux, David J Amor, Santhosh Girirajan. Eur J Hum Genet 2017
Times Cited: 3







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



Times Cited
  Times     Co-cited
Similarity


Further delineation of the 15q13 microdeletion and duplication syndromes: a clinical spectrum varying from non-pathogenic to a severe outcome.
B W M van Bon, H C Mefford, B Menten, D A Koolen, A J Sharp, W M Nillesen, J W Innis, T J L de Ravel, C L Mercer, M Fichera,[...]. J Med Genet 2009
199
33

The neurobiology of aggression and violence.
Daniel R Rosell, Larry J Siever. CNS Spectr 2015
132
33

New insights into the generation and role of de novo mutations in health and disease.
Rocio Acuna-Hidalgo, Joris A Veltman, Alexander Hoischen. Genome Biol 2016
150
33

TMEM70 protein - a novel ancillary factor of mammalian ATP synthase.
Josef Houstek, Stanislav Kmoch, Jirí Zeman. Biochim Biophys Acta 2009
32
33


Increased paternal age and the influence on burden of genomic copy number variation in the general population.
Jacobine E Buizer-Voskamp, Hylke M Blauw, Marco P M Boks, Kristel R van Eijk, Jan H Veldink, Eric A M Hennekam, Jacob A S Vorstman, Flip Mulder, Henning Tiemeier, André G Uitterlinden,[...]. Hum Genet 2013
21
33

Aggressive behavior in humans: Genes and pathways identified through association studies.
Noèlia Fernàndez-Castillo, Bru Cormand. Am J Med Genet B Neuropsychiatr Genet 2016
31
33

Missing heritability and strategies for finding the underlying causes of complex disease.
Evan E Eichler, Jonathan Flint, Greg Gibson, Augustine Kong, Suzanne M Leal, Jason H Moore, Joseph H Nadeau. Nat Rev Genet 2010
33

Exome Pool-Seq in neurodevelopmental disorders.
Bernt Popp, Arif B Ekici, Christian T Thiel, Juliane Hoyer, Antje Wiesener, Cornelia Kraus, André Reis, Christiane Zweier. Eur J Hum Genet 2017
40
33

Mutations in HECW2 are associated with intellectual disability and epilepsy.
Jonatan Halvardson, Jin J Zhao, Ammar Zaghlool, Christian Wentzel, Patrik Georgii-Hemming, Else Månsson, Helena Ederth Sävmarker, Göran Brandberg, Cecilia Soussi Zander, Ann-Charlotte Thuresson,[...]. J Med Genet 2016
30
33

Novel promoters and coding first exons in DLG2 linked to developmental disorders and intellectual disability.
Claudio Reggiani, Sandra Coppens, Tayeb Sekhara, Ivan Dimov, Bruno Pichon, Nicolas Lufin, Marie-Claude Addor, Elga Fabia Belligni, Maria Cristina Digilio, Flavio Faletra,[...]. Genome Med 2017
9
33

Tomosyn-2 is required for normal motor performance in mice and sustains neurotransmission at motor endplates.
Cornelia J Geerts, Jaap J Plomp, Bastijn Koopmans, Maarten Loos, Elizabeth M van der Pijl, Martin A van der Valk, Matthijs Verhage, Alexander J A Groffen. Brain Struct Funct 2015
10
33

Differential gene expression in brain tissues of aggressive and non-aggressive dogs.
Jørn Våge, Tina B Bønsdorff, Ellen Arnet, Aage Tverdal, Frode Lingaas. BMC Vet Res 2010
14
33

Rare variants in known and novel candidate genes predisposing to statin-associated myopathy.
Magdaléna Neřoldová, Viktor Stránecký, Kateřina Hodaňová, Hana Hartmannová, Lenka Piherová, Anna Přistoupilová, Lenka Mrázová, Michal Vrablík, Věra Adámková, Jaroslav A Hubáček,[...]. Pharmacogenomics 2016
15
33

Gain-of-function FHF1 mutation causes early-onset epileptic encephalopathy with cerebellar atrophy.
Aleksandra Siekierska, Mala Isrie, Yue Liu, Chloë Scheldeman, Niels Vanthillo, Lieven Lagae, Peter A M de Witte, Hilde Van Esch, Mitchell Goldfarb, Gunnar M Buyse. Neurology 2016
37
33

20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition.
Amélie Piton, Hélène Poquet, Claire Redin, Alice Masurel, Julia Lauer, Jean Muller, Julien Thevenon, Yvan Herenger, Sophie Chancenotte, Marlène Bonnet,[...]. Eur J Hum Genet 2014
30
33

Interaction between CHL1 and serotonin receptor 2c regulates signal transduction and behavior in mice.
Ralf Kleene, Harshita Chaudhary, Nicole Karl, Jelena Katic, Agnieszka Kotarska, Kathrin Guitart, Gabriele Loers, Melitta Schachner. J Cell Sci 2015
16
33

Genetic background of extreme violent behavior.
J Tiihonen, M-R Rautiainen, H M Ollila, E Repo-Tiihonen, M Virkkunen, A Palotie, O Pietiläinen, K Kristiansson, M Joukamaa, H Lauerma,[...]. Mol Psychiatry 2015
63
33

Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing.
Jérôme Nicod, Robert W Davies, Na Cai, Carl Hassett, Leo Goodstadt, Cormac Cosgrove, Benjamin K Yee, Vikte Lionikaite, Rebecca E McIntyre, Carol Ann Remme,[...]. Nat Genet 2016
61
33



A genomewide screen for late-onset Alzheimer disease in a genetically isolated Dutch population.
Fan Liu, Alejandro Arias-Vásquez, Kristel Sleegers, Yurii S Aulchenko, Manfred Kayser, Pascual Sanchez-Juan, Bing-Jian Feng, Aida M Bertoli-Avella, John van Swieten, Tatiana I Axenovich,[...]. Am J Hum Genet 2007
109
33

Performance of case-control rare copy number variation annotation in classification of autism.
Worrawat Engchuan, Kiret Dhindsa, Anath C Lionel, Stephen W Scherer, Jonathan H Chan, Daniele Merico. BMC Med Genomics 2015
10
33

Comprehensive integrative analyses identify GLT8D1 and CSNK2B as schizophrenia risk genes.
Cui-Ping Yang, Xiaoyan Li, Yong Wu, Qiushuo Shen, Yong Zeng, Qiuxia Xiong, Mengping Wei, Chunhui Chen, Jiewei Liu, Yongxia Huo,[...]. Nat Commun 2018
43
33

Copy number variation in fetal alcohol spectrum disorder.
Mehdi Zarrei, Geoffrey G Hicks, James N Reynolds, Bhooma Thiruvahindrapuram, Worrawat Engchuan, Molly Pind, Sylvia Lamoureux, John Wei, Zhouzhi Wang, Christian R Marshall,[...]. Biochem Cell Biol 2018
7
33

X-linked borderline mental retardation with prominent behavioral disturbance: phenotype, genetic localization, and evidence for disturbed monoamine metabolism.
H G Brunner, M R Nelen, P van Zandvoort, N G Abeling, A H van Gennip, E C Wolters, M A Kuiper, H H Ropers, B A van Oost. Am J Hum Genet 1993
222
33


Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis.
Kimm J E van Hulzen, Claus J Scholz, Barbara Franke, Stephan Ripke, Marieke Klein, Andrew McQuillin, Edmund J Sonuga-Barke, John R Kelsoe, Mikael Landén, Ole A Andreassen,[...]. Biol Psychiatry 2017
50
33

Interplay between Schizophrenia Polygenic Risk Score and Childhood Adversity in First-Presentation Psychotic Disorder: A Pilot Study.
Antonella Trotta, Conrad Iyegbe, Marta Di Forti, Pak C Sham, Desmond D Campbell, Stacey S Cherny, Valeria Mondelli, Katherine J Aitchison, Robin M Murray, Evangelos Vassos,[...]. PLoS One 2016
31
33

Cadherin-13 Deficiency Increases Dorsal Raphe 5-HT Neuron Density and Prefrontal Cortex Innervation in the Mouse Brain.
Andrea Forero, Olga Rivero, Sina Wäldchen, Hsing-Ping Ku, Dominik P Kiser, Yvonne Gärtner, Laura S Pennington, Jonas Waider, Patricia Gaspar, Charline Jansch,[...]. Front Cell Neurosci 2017
9
33

Aggressive behavior and altered amounts of brain serotonin and norepinephrine in mice lacking MAOA.
O Cases, I Seif, J Grimsby, P Gaspar, K Chen, S Pournin, U Müller, M Aguet, C Babinet, J C Shih. Science 1995
813
33

MAOA, maltreatment, and gene-environment interaction predicting children's mental health: new evidence and a meta-analysis.
J Kim-Cohen, A Caspi, A Taylor, B Williams, R Newcombe, I W Craig, T E Moffitt. Mol Psychiatry 2006
551
33

A copy number variation map of the human genome.
Mehdi Zarrei, Jeffrey R MacDonald, Daniele Merico, Stephen W Scherer. Nat Rev Genet 2015
368
33


Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders.
Víctor Faundes, William G Newman, Laura Bernardini, Natalie Canham, Jill Clayton-Smith, Bruno Dallapiccola, Sally J Davies, Michelle K Demos, Amy Goldman, Harinder Gill,[...]. Am J Hum Genet 2018
77
33

Genetics of impulsive behaviour.
Laura Bevilacqua, David Goldman. Philos Trans R Soc Lond B Biol Sci 2013
46
33

The Database of Genomic Variants: a curated collection of structural variation in the human genome.
Jeffrey R MacDonald, Robert Ziman, Ryan K C Yuen, Lars Feuk, Stephen W Scherer. Nucleic Acids Res 2014
632
33

Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants.
Dalila Pinto, Katayoon Darvishi, Xinghua Shi, Diana Rajan, Diane Rigler, Tom Fitzgerald, Anath C Lionel, Bhooma Thiruvahindrapuram, Jeffrey R Macdonald, Ryan Mills,[...]. Nat Biotechnol 2011
290
33

Genetics of dementia in a Finnish cohort.
Petra Pasanen, Liisa Myllykangas, Minna Pöyhönen, Anna Kiviharju, Maija Siitonen, John Hardy, Jose Bras, Anders Paetau, Pentti J Tienari, Rita Guerreiro,[...]. Eur J Hum Genet 2018
4
33

Copy number variant study of bipolar disorder in Canadian and UK populations implicates synaptic genes.
Abdul Noor, Anath C Lionel, Sarah Cohen-Woods, Narges Moghimi, James Rucker, Alanna Fennell, Bhooma Thiruvahindrapuram, Liana Kaufman, Bryan Degagne, John Wei,[...]. Am J Med Genet B Neuropsychiatr Genet 2014
48
33

Complex, multimodal behavioral profile of the Homer1 knockout mouse.
P J Jaubert, M S Golub, Y Y Lo, S L Germann, M H Dehoff, P F Worley, S H Kang, M K Schwarz, P H Seeburg, R F Berman. Genes Brain Behav 2007
66
33

The childhood experience of care and abuse questionnaire (CECA.Q): validation in a community series.
A Bifulco, O Bernazzani, P M Moran, C Jacobs. Br J Clin Psychol 2005
198
33


De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy.
Mehdi Zarrei, Darcy L Fehlings, Karizma Mawjee, Lauren Switzer, Bhooma Thiruvahindrapuram, Susan Walker, Daniele Merico, Guillermo Casallo, Mohammed Uddin, Jeffrey R MacDonald,[...]. Genet Med 2018
37
33

The genetics of aggression: Where are we now?
Philip Asherson, Bru Cormand. Am J Med Genet B Neuropsychiatr Genet 2016
5
33

Mouse Model for Protein Tyrosine Phosphatase D (PTPRD) Associations with Restless Leg Syndrome or Willis-Ekbom Disease and Addiction: Reduced Expression Alters Locomotion, Sleep Behaviors and Cocaine-Conditioned Place Preference.
Jana Drgonova, Donna Walther, Katherine J Wang, G Luke Hartstein, Bryson Lochte, Juan Troncoso, Noriko Uetani, Yoichiro Iwakura, George R Uhl. Mol Med 2015
20
33

Italian appeal court: a genetic predisposition to commit murder?
Francesca Forzano, Pascal Borry, Anne Cambon-Thomsen, Shirley V Hodgson, Aad Tibben, Petrus de Vries, Carla van El, Martina Cornel. Eur J Hum Genet 2010
21
33

Finding the missing heritability of complex diseases.
Teri A Manolio, Francis S Collins, Nancy J Cox, David B Goldstein, Lucia A Hindorff, David J Hunter, Mark I McCarthy, Erin M Ramos, Lon R Cardon, Aravinda Chakravarti,[...]. Nature 2009
33

Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities.
J C Hodge, E Mitchell, V Pillalamarri, T L Toler, F Bartel, H M Kearney, Y S Zou, W H Tan, C Hanscom, S Kirmani,[...]. Mol Psychiatry 2014
44
33

Clinical characterization of int22h1/int22h2-mediated Xq28 duplication/deletion: new cases and literature review.
Ayman W El-Hattab, Christian P Schaaf, Ping Fang, Elizabeth Roeder, Virginia E Kimonis, Joseph A Church, Ankita Patel, Sau Wai Cheung. BMC Med Genet 2015
15
33


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.