A citation-based method for searching scientific literature

Masahiro Nakatochi, Itaru Kushima, Norio Ozaki. J Hum Genet 2021
Times Cited: 7







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



Times Cited
  Times     Co-cited
Similarity


Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights.
Itaru Kushima, Branko Aleksic, Masahiro Nakatochi, Teppei Shimamura, Takashi Okada, Yota Uno, Mako Morikawa, Kanako Ishizuka, Tomoko Shiino, Hiroki Kimura,[...]. Cell Rep 2018
77
57

High-resolution copy number variation analysis of schizophrenia in Japan.
I Kushima, B Aleksic, M Nakatochi, T Shimamura, T Shiino, A Yoshimi, H Kimura, Y Takasaki, C Wang, J Xing,[...]. Mol Psychiatry 2017
54
57

ARHGAP10, which encodes Rho GTPase-activating protein 10, is a novel gene for schizophrenia risk.
Mariko Sekiguchi, Akira Sobue, Itaru Kushima, Chenyao Wang, Yuko Arioka, Hidekazu Kato, Akiko Kodama, Hisako Kubo, Norimichi Ito, Masahito Sawahata,[...]. Transl Psychiatry 2020
6
50

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects.
Christian R Marshall, Daniel P Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S Greer, Danny Antaki, Aniket Shetty, Peter A Holmans, Dalila Pinto,[...]. Nat Genet 2017
398
42

The Heritability of Autism Spectrum Disorder.
Sven Sandin, Paul Lichtenstein, Ralf Kuja-Halkola, Christina Hultman, Henrik Larsson, Abraham Reichenberg. JAMA 2017
183
28

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang,[...]. Am J Hum Genet 2014
516
28

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
28

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism.
F Kyle Satterstrom, Jack A Kosmicki, Jiebiao Wang, Michael S Breen, Silvia De Rubeis, Joon-Yong An, Minshi Peng, Ryan Collins, Jakob Grove, Lambertus Klei,[...]. Cell 2020
310
28

Targeted Treatment of Individuals With Psychosis Carrying a Copy Number Variant Containing a Genomic Triplication of the Glycine Decarboxylase Gene.
J Alexander Bodkin, Michael J Coleman, Laura J Godfrey, Claudia M B Carvalho, Charity J Morgan, Raymond F Suckow, Thea Anderson, Dost Öngür, Marc J Kaufman, Kathryn E Lewandowski,[...]. Biol Psychiatry 2019
15
28

Heritability of Schizophrenia and Schizophrenia Spectrum Based on the Nationwide Danish Twin Register.
Rikke Hilker, Dorte Helenius, Birgitte Fagerlund, Axel Skytthe, Kaare Christensen, Thomas M Werge, Merete Nordentoft, Birte Glenthøj. Biol Psychiatry 2018
130
28

Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder.
Elaine T Lim, Mohammed Uddin, Silvia De Rubeis, Yingleong Chan, Anne S Kamumbu, Xiaochang Zhang, Alissa M D'Gama, Sonia N Kim, Robert Sean Hill, Arthur P Goldberg,[...]. Nat Neurosci 2017
110
28

Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.
Maude Schneider, Martin Debbané, Anne S Bassett, Eva W C Chow, Wai Lun Alan Fung, Marianne van den Bree, Michael Owen, Kieran C Murphy, Maria Niarchou, Wendy R Kates,[...]. Am J Psychiatry 2014
386
28

22q11.2 deletion syndrome.
Donna M McDonald-McGinn, Kathleen E Sullivan, Bruno Marino, Nicole Philip, Ann Swillen, Jacob A S Vorstman, Elaine H Zackai, Beverly S Emanuel, Joris R Vermeesch, Bernice E Morrow,[...]. Nat Rev Dis Primers 2015
381
28


Getting to the Cores of Autism.
Lilia M Iakoucheva, Alysson R Muotri, Jonathan Sebat. Cell 2019
56
28

Predicting Polygenic Risk of Psychiatric Disorders.
Alicia R Martin, Mark J Daly, Elise B Robinson, Steven E Hyman, Benjamin M Neale. Biol Psychiatry 2019
83
28

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
28

Paternally inherited cis-regulatory structural variants are associated with autism.
William M Brandler, Danny Antaki, Madhusudan Gujral, Morgan L Kleiber, Joe Whitney, Michelle S Maile, Oanh Hong, Timothy R Chapman, Shirley Tan, Prateek Tandon,[...]. Science 2018
70
28

Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.
Sarah E Bergen, Alexander Ploner, Daniel Howrigan, Michael C O'Donovan, Jordan W Smoller, Patrick F Sullivan, Jonathan Sebat, Benjamin Neale, Kenneth S Kendler. Am J Psychiatry 2019
41
28


A framework for the investigation of rare genetic disorders in neuropsychiatry.
Stephan J Sanders, Mustafa Sahin, Joseph Hostyk, Audrey Thurm, Sebastien Jacquemont, Paul Avillach, Elise Douard, Christa L Martin, Meera E Modi, Andres Moreno-De-Luca,[...]. Nat Med 2019
28
28

Identification of common genetic risk variants for autism spectrum disorder.
Jakob Grove, Stephan Ripke, Thomas D Als, Manuel Mattheisen, Raymond K Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A Andreassen, Richard Anney,[...]. Nat Genet 2019
437
28

Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
Anne S Bassett, Chelsea Lowther, Daniele Merico, Gregory Costain, Eva W C Chow, Therese van Amelsvoort, Donna McDonald-McGinn, Raquel E Gur, Ann Swillen, Marianne Van den Bree,[...]. Am J Psychiatry 2017
40
28

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
28

Histone methylation at H3K9: evidence for a restrictive epigenome in schizophrenia.
Kayla A Chase, David P Gavin, Alessandro Guidotti, Rajiv P Sharma. Schizophr Res 2013
55
14

Investigating cortical features of Sotos syndrome using mice heterozygous for Nsd1.
Sabrina Oishi, Oressia Zalucki, Michelle S Vega, Danyon Harkins, Tracey J Harvey, Maria Kasherman, Raul A Davila, Lauren Hale, Melissa White, Sandra Piltz,[...]. Genes Brain Behav 2020
3
33

Glia-related genes and their contribution to schizophrenia.
Chenyao Wang, Branko Aleksic, Norio Ozaki. Psychiatry Clin Neurosci 2015
18
14

De novo mutations in schizophrenia implicate chromatin remodeling and support a genetic overlap with autism and intellectual disability.
S E McCarthy, J Gillis, M Kramer, J Lihm, S Yoon, Y Berstein, M Mistry, P Pavlidis, R Solomon, E Ghiban,[...]. Mol Psychiatry 2014
226
14

Genetic effects on gene expression across human tissues.
Alexis Battle, Christopher D Brown, Barbara E Engelhardt, Stephen B Montgomery. Nature 2017
14

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
920
14

Deletion of JMJD2B in neurons leads to defective spine maturation, hyperactive behavior and memory deficits in mouse.
K Fujiwara, Y Fujita, A Kasai, Y Onaka, H Hashimoto, H Okada, T Yamashita. Transl Psychiatry 2016
17
14

The association between autism and schizophrenia spectrum disorders: A review of eight alternate models of co-occurrence.
Katharine Chisholm, Ashleigh Lin, Ahmad Abu-Akel, Stephen J Wood. Neurosci Biobehav Rev 2015
129
14


Reduced exploration, increased anxiety, and altered social behavior: Autistic-like features of euchromatin histone methyltransferase 1 heterozygous knockout mice.
Monique C M Balemans, Manon M H Huibers, Nathalie W D Eikelenboom, Arthur J Kuipers, Rik C J van Summeren, Michael M C A Pijpers, Makoto Tachibana, Yoichi Shinkai, Hans van Bokhoven, Catharina E E M Van der Zee. Behav Brain Res 2010
86
14

Increase in GFAP-positive astrocytes in histone demethylase GASC1/KDM4C/JMJD2C hypomorphic mutant mice.
Genki Sudo, Tetsushi Kagawa, Yasuhiro Kokubu, Johji Inazawa, Tetsuya Taga. Genes Cells 2016
13
14

GENCODE reference annotation for the human and mouse genomes.
Adam Frankish, Mark Diekhans, Anne-Maud Ferreira, Rory Johnson, Irwin Jungreis, Jane Loveland, Jonathan M Mudge, Cristina Sisu, James Wright, Joel Armstrong,[...]. Nucleic Acids Res 2019
670
14

Opposing Chromatin Signals Direct and Regulate the Activity of Lysine Demethylase 4C (KDM4C).
Lindsey R Pack, Keith R Yamamoto, Danica Galonić Fujimori. J Biol Chem 2016
19
14

The contribution of de novo coding mutations to autism spectrum disorder.
Ivan Iossifov, Brian J O'Roak, Stephan J Sanders, Michael Ronemus, Niklas Krumm, Dan Levy, Holly A Stessman, Kali T Witherspoon, Laura Vives, Karynne E Patterson,[...]. Nature 2014
14

Elevated GFAP Protein in Anterior Cingulate Cortical White Matter in Males With Autism Spectrum Disorder.
Jessica D Crawford, Michelle J Chandley, Katalin Szebeni, Attila Szebeni, Brandon Waters, Gregory A Ordway. Autism Res 2015
20
14

Mutation spectrum revealed by breakpoint sequencing of human germline CNVs.
Donald F Conrad, Christine Bird, Ben Blackburne, Sarah Lindsay, Lira Mamanova, Charles Lee, Daniel J Turner, Matthew E Hurles. Nat Genet 2010
174
14

The KDM4A/KDM4C/NF-κB and WDR5 epigenetic cascade regulates the activation of B cells.
Kuo-Hsuan Hung, Yong H Woo, I-Ying Lin, Chin-Hsiu Liu, Li-Chieh Wang, Hsin-Yu Chen, Bor-Luen Chiang, Kuo-I Lin. Nucleic Acids Res 2018
15
14

A de novo marker chromosome derived from 9p in a patient with 9p partial duplication syndrome and autism features: genotype-phenotype correlation.
Khaled K Abu-Amero, Ali M Hellani, Mustafa A Salih, Mohammad Z Seidahmed, Tageldin S Elmalik, Ghassan Zidan, Thomas M Bosley. BMC Med Genet 2010
27
14

Spatio-temporal transcriptome of the human brain.
Hyo Jung Kang, Yuka Imamura Kawasawa, Feng Cheng, Ying Zhu, Xuming Xu, Mingfeng Li, André M M Sousa, Mihovil Pletikos, Kyle A Meyer, Goran Sedmak,[...]. Nature 2011
14

The putative oncogene GASC1 demethylates tri- and dimethylated lysine 9 on histone H3.
Paul A C Cloos, Jesper Christensen, Karl Agger, Alessio Maiolica, Juri Rappsilber, Torben Antal, Klaus H Hansen, Kristian Helin. Nature 2006
521
14

GeneHancer: genome-wide integration of enhancers and target genes in GeneCards.
Simon Fishilevich, Ron Nudel, Noa Rappaport, Rotem Hadar, Inbar Plaschkes, Tsippi Iny Stein, Naomi Rosen, Asher Kohn, Michal Twik, Marilyn Safran,[...]. Database (Oxford) 2017
295
14

Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations.
Wei-Zhen Zhou, Jie Zhang, Ziyi Li, Xiaojing Lin, Jiarui Li, Sheng Wang, Changhong Yang, Qixi Wu, Adam Yongxin Ye, Meng Wang,[...]. Hum Mutat 2019
8
14

Neuronal Migration and AUTS2 Syndrome.
Kei Hori, Mikio Hoshino. Brain Sci 2017
31
14

Neuroglial activation and neuroinflammation in the brain of patients with autism.
Diana L Vargas, Caterina Nascimbene, Chitra Krishnan, Andrew W Zimmerman, Carlos A Pardo. Ann Neurol 2005
14

Duplication 9p and their implication to phenotype.
Roberta Santos Guilherme, Vera Ayres Meloni, Ana Beatriz Alvarez Perez, Ana Luiza Pilla, Marco Antonio Paula de Ramos, Anelisa Gollo Dantas, Sylvia Satomi Takeno, Leslie Domenici Kulikowski, Maria Isabel Melaragno. BMC Med Genet 2014
19
14

Postmortem evidence of cerebral inflammation in schizophrenia: a systematic review.
M O Trépanier, K E Hopperton, R Mizrahi, N Mechawar, R P Bazinet. Mol Psychiatry 2016
166
14


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.