A citation-based method for searching scientific literature

Shahar Shohat, Alana Amelan, Sagiv Shifman. Biol Psychiatry 2021
Times Cited: 5







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



Times Cited
  Times     Co-cited
Similarity



Diverse types of genetic variation converge on functional gene networks involved in schizophrenia.
Sarah R Gilman, Jonathan Chang, Bin Xu, Tejdeep S Bawa, Joseph A Gogos, Maria Karayiorgou, Dennis Vitkup. Nat Neurosci 2012
124
40

Pleiotropy and Cross-Disorder Genetics Among Psychiatric Disorders.
Phil H Lee, Yen-Chen A Feng, Jordan W Smoller. Biol Psychiatry 2021
5
40

Neurogenomic evidence for a shared mechanism of the antidepressant effects of exercise and chronic fluoxetine in mice.
Guo-Jen Huang, Eyal Ben-David, Agnès Tort Piella, Andrew Edwards, Jonathan Flint, Sagiv Shifman. PLoS One 2012
28
20

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
20

Expression Analyses of POGZ, A Responsible Gene for Neurodevelopmental Disorders, during Mouse Brain Development.
Kyoko Ibaraki, Nanako Hamada, Ikuko Iwamoto, Hidenori Ito, Noriko Kawamura, Rika Morishita, Hidenori Tabata, Koh-Ichi Nagata. Dev Neurosci 2019
3
33

CAMP (C13orf8, ZNF828) is a novel regulator of kinetochore-microtubule attachment.
Go Itoh, Shin-ichiro Kanno, Kazuhiko S K Uchida, Shuhei Chiba, Shiro Sugino, Kana Watanabe, Kensaku Mizuno, Akira Yasui, Toru Hirota, Kozo Tanaka. EMBO J 2011
32
20

edgeR: a Bioconductor package for differential expression analysis of digital gene expression data.
Mark D Robinson, Davis J McCarthy, Gordon K Smyth. Bioinformatics 2010
20

The hyperpolarization-activated HCN1 channel is important for motor learning and neuronal integration by cerebellar Purkinje cells.
Matthew F Nolan, Gaël Malleret, Ka Hung Lee, Emma Gibbs, Joshua T Dudman, Bina Santoro, Deqi Yin, Richard F Thompson, Steven A Siegelbaum, Eric R Kandel,[...]. Cell 2003
229
20

Simple spike activity predicts occurrence of complex spikes in cerebellar Purkinje cells.
R C Miall, J G Keating, M Malkmus, W T Thach. Nat Neurosci 1998
43
20



De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly.
Yizhou Ye, Megan T Cho, Kyle Retterer, Nora Alexander, Tawfeg Ben-Omran, Mariam Al-Mureikhi, Ingrid Cristian, Patricia G Wheeler, Carrie Crain, Dina Zand,[...]. Cold Spring Harb Mol Case Stud 2015
23
20

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
20

Deletion of FMR1 in Purkinje cells enhances parallel fiber LTD, enlarges spines, and attenuates cerebellar eyelid conditioning in Fragile X syndrome.
S K E Koekkoek, K Yamaguchi, B A Milojkovic, B R Dortland, T J H Ruigrok, R Maex, W De Graaf, A E Smit, F VanderWerf, C E Bakker,[...]. Neuron 2005
295
20

Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders.
Holly A F Stessman, Marjolein H Willemsen, Michaela Fenckova, Osnat Penn, Alexander Hoischen, Bo Xiong, Tianyun Wang, Kendra Hoekzema, Laura Vives, Ida Vogel,[...]. Am J Hum Genet 2016
69
20

Tissue distribution, ontogeny, and chemical induction of aldo-keto reductases in mice.
Matthew Pratt-Hyatt, Andrew J Lickteig, Curtis D Klaassen. Drug Metab Dispos 2013
20
20


Hippocampal neurogenesis levels predict WATERMAZE search strategies in the aging brain.
Joana Gil-Mohapel, Patricia S Brocardo, Will Choquette, Russ Gothard, Jessica M Simpson, Brian R Christie. PLoS One 2013
70
20

Potentiation of cerebellar Purkinje cells facilitates whisker reflex adaptation through increased simple spike activity.
Vincenzo Romano, Licia De Propris, Laurens Wj Bosman, Pascal Warnaar, Michiel M Ten Brinke, Sander Lindeman, Chiheng Ju, Arthiha Velauthapillai, Jochen K Spanke, Emily Middendorp Guerra,[...]. Elife 2018
17
20

Biochemical and cell biological characterization of a mammalian septin, Sept11.
Nobuhiro Hanai, Koh-ichi Nagata, Aie Kawajiri, Takashi Shiromizu, Noriko Saitoh, Yasuhisa Hasegawa, Shingo Murakami, Masaki Inagaki. FEBS Lett 2004
81
20

POGZ truncating alleles cause syndromic intellectual disability.
Janson White, Christine R Beck, Tamar Harel, Jennifer E Posey, Shalini N Jhangiani, Sha Tang, Kelly D Farwell, Zöe Powis, Nancy J Mendelsohn, Janice A Baker,[...]. Genome Med 2016
38
20

Dysfunctional cerebellar Purkinje cells contribute to autism-like behaviour in Shank2-deficient mice.
Saša Peter, Michiel M Ten Brinke, Jeffrey Stedehouder, Claudia M Reinelt, Bin Wu, Haibo Zhou, Kuikui Zhou, Henk-Jan Boele, Steven A Kushner, Min Goo Lee,[...]. Nat Commun 2016
90
20


The cerebellum, sensitive periods, and autism.
Samuel S-H Wang, Alexander D Kloth, Aleksandra Badura. Neuron 2014
304
20

Feed-forward inhibition shapes the spike output of cerebellar Purkinje cells.
Wolfgang Mittmann, Ursula Koch, Michael Häusser. J Physiol 2005
219
20

Autistic-Like Traits and Cerebellar Dysfunction in Purkinje Cell PTEN Knock-Out Mice.
Dario Cupolillo, Eriola Hoxha, Alessio Faralli, Annarita De Luca, Ferdinando Rossi, Filippo Tempia, Daniela Carulli. Neuropsychopharmacology 2016
59
20


G9a histone methyltransferase plays a dominant role in euchromatic histone H3 lysine 9 methylation and is essential for early embryogenesis.
Makoto Tachibana, Kenji Sugimoto, Masami Nozaki, Jun Ueda, Tsutomu Ohta, Misao Ohki, Mikiko Fukuda, Naoki Takeda, Hiroyuki Niida, Hiroyuki Kato,[...]. Genes Dev 2002
848
20

Quantitative interaction proteomics and genome-wide profiling of epigenetic histone marks and their readers.
Michiel Vermeulen, H Christian Eberl, Filomena Matarese, Hendrik Marks, Sergei Denissov, Falk Butter, Kenneth K Lee, Jesper V Olsen, Anthony A Hyman, Henk G Stunnenberg,[...]. Cell 2010
498
20


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
601
20


Genetics and genomics of autism spectrum disorder: embracing complexity.
Silvia De Rubeis, Joseph D Buxbaum. Hum Mol Genet 2015
98
20

POGZ Is Required for Silencing Mouse Embryonic β-like Hemoglobin and Human Fetal Hemoglobin Expression.
Bjorg Gudmundsdottir, Kristbjorn O Gudmundsson, Kimberly D Klarmann, Satyendra K Singh, Lei Sun, Shweta Singh, Yang Du, Vincenzo Coppola, Luke Stockwin, Nhu Nguyen,[...]. Cell Rep 2018
13
20

Brain IGF-1 receptors control mammalian growth and lifespan through a neuroendocrine mechanism.
Laurent Kappeler, Carlos De Magalhaes Filho, Joëlle Dupont, Patricia Leneuve, Pascale Cervera, Laurence Périn, Catherine Loudes, Annick Blaise, Rüdiger Klein, Jacques Epelbaum,[...]. PLoS Biol 2008
189
20

Evaluation of marble-burying behavior as a model of anxiety.
K Njung'e, S L Handley. Pharmacol Biochem Behav 1991
302
20

Prioritization of neurodevelopmental disease genes by discovery of new mutations.
Alexander Hoischen, Niklas Krumm, Evan E Eichler. Nat Neurosci 2014
104
20

A Role for Widely Interspaced Zinc Finger (WIZ) in Retention of the G9a Methyltransferase on Chromatin.
Jeremy M Simon, Joel S Parker, Feng Liu, Scott B Rothbart, Slimane Ait-Si-Ali, Brian D Strahl, Jian Jin, Ian J Davis, Amber L Mosley, Samantha G Pattenden. J Biol Chem 2015
20
20


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
20


Human POGZ modulates dissociation of HP1alpha from mitotic chromosome arms through Aurora B activation.
Ryu-Suke Nozawa, Koji Nagao, Hiro-Taka Masuda, Osamu Iwasaki, Toru Hirota, Naohito Nozaki, Hiroshi Kimura, Chikashi Obuse. Nat Cell Biol 2010
148
20

Cerebellar plasticity and motor learning deficits in a copy-number variation mouse model of autism.
Claire Piochon, Alexander D Kloth, Giorgio Grasselli, Heather K Titley, Hisako Nakayama, Kouichi Hashimoto, Vivian Wan, Dana H Simmons, Tahra Eissa, Jin Nakatani,[...]. Nat Commun 2014
87
20


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
20


Analysis of the human HP1 interactome reveals novel binding partners.
Claire Rosnoblet, Julien Vandamme, Pamela Völkel, Pierre-Olivier Angrand. Biochem Biophys Res Commun 2011
24
20

A novel de novo POGZ mutation in a patient with intellectual disability.
Bo Tan, Yongyi Zou, Yue Zhang, Rui Zhang, Jianjun Ou, Yidong Shen, Jingping Zhao, Xiaomei Luo, Jing Guo, Lanlan Zeng,[...]. J Hum Genet 2016
15
20

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
20


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.