A citation-based method for searching scientific literature

Jennifer K Forsyth, Daniel Nachun, Michael J Gandal, Daniel H Geschwind, Ariana E Anderson, Giovanni Coppola, Carrie E Bearden. Biol Psychiatry 2020
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


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
33

The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms.
Jacob A S Vorstman, Monique E J Morcus, Sasja N Duijff, Petra W J Klaassen, Josien A Heineman-de Boer, Frits A Beemer, Hanna Swaab, René S Kahn, Herman van Engeland. J Am Acad Child Adolesc Psychiatry 2006
226
25

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
25

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection.
Antonio F Pardiñas, Peter Holmans, Andrew J Pocklington, Valentina Escott-Price, Stephan Ripke, Noa Carrera, Sophie E Legge, Sophie Bishop, Darren Cameron, Marian L Hamshere,[...]. Nat Genet 2018
506
25

Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia.
Andrew J Pocklington, Elliott Rees, James T R Walters, Jun Han, David H Kavanagh, Kimberly D Chambert, Peter Holmans, Jennifer L Moran, Steven A McCarroll, George Kirov,[...]. Neuron 2015
93
25

De novo mutations in schizophrenia implicate synaptic networks.
Menachem Fromer, Andrew J Pocklington, David H Kavanagh, Hywel J Williams, Sarah Dwyer, Padhraig Gormley, Lyudmila Georgieva, Elliott Rees, Priit Palta, Douglas M Ruderfer,[...]. Nature 2014
955
25


De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.
G Kirov, A J Pocklington, P Holmans, D Ivanov, M Ikeda, D Ruderfer, J Moran, K Chambert, D Toncheva, L Georgieva,[...]. Mol Psychiatry 2012
515
16

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
16

Common alleles contribute to schizophrenia in CNV carriers.
K E Tansey, E Rees, D E Linden, S Ripke, K D Chambert, J L Moran, S A McCarroll, P Holmans, G Kirov, J Walters,[...]. Mol Psychiatry 2016
47
16

Co-occurrence of autism, childhood psychosis, and intellectual disability associated with a de novo 3q29 microdeletion.
Angela Sagar, Jeffrey R Bishop, D Clare Tessman, Steve Guter, Christa L Martin, Edwin H Cook. Am J Med Genet A 2013
31
16

Increased burden of ultra-rare protein-altering variants among 4,877 individuals with schizophrenia.
Giulio Genovese, Menachem Fromer, Eli A Stahl, Douglas M Ruderfer, Kimberly Chambert, Mikael Landén, Jennifer L Moran, Shaun M Purcell, Pamela Sklar, Patrick F Sullivan,[...]. Nat Neurosci 2016
211
16


Analysis of Intellectual Disability Copy Number Variants for Association With Schizophrenia.
Elliott Rees, Kimberley Kendall, Antonio F Pardiñas, Sophie E Legge, Andrew Pocklington, Valentina Escott-Price, James H MacCabe, David A Collier, Peter Holmans, Michael C O'Donovan,[...]. JAMA Psychiatry 2016
53
16

Pervasive developmental disorder and childhood-onset schizophrenia: comorbid disorder or a phenotypic variant of a very early onset illness?
Alexandra L Sporn, Anjené M Addington, Nitin Gogtay, Anna E Ordoñez, Michele Gornick, Liv Clasen, Deanna Greenstein, Julia W Tossell, Peter Gochman, Marge Lenane,[...]. Biol Psychiatry 2004
87
16

Genome-wide burden of deleterious coding variants increased in schizophrenia.
Loes M Olde Loohuis, Jacob A S Vorstman, Anil P Ori, Kim A Staats, Tina Wang, Alexander L Richards, Ganna Leonenko, James T Walters, Joseph DeYoung, Rita M Cantor,[...]. Nat Commun 2015
16
16

Analysis of copy number variations at 15 schizophrenia-associated loci.
Elliott Rees, James T R Walters, Lyudmila Georgieva, Anthony R Isles, Kimberly D Chambert, Alexander L Richards, Gerwyn Mahoney-Davies, Sophie E Legge, Jennifer L Moran, Steven A McCarroll,[...]. Br J Psychiatry 2014
218
16

The penetrance of copy number variations for schizophrenia and developmental delay.
George Kirov, Elliott Rees, James T R Walters, Valentina Escott-Price, Lyudmila Georgieva, Alexander L Richards, Kimberly D Chambert, Gerwyn Davies, Sophie E Legge, Jennifer L Moran,[...]. Biol Psychiatry 2014
194
16

Autism spectrum disorders and childhood-onset schizophrenia: clinical and biological contributions to a relation revisited.
Judith Rapoport, Alex Chavez, Deanna Greenstein, Anjene Addington, Nitin Gogtay. J Am Acad Child Adolesc Psychiatry 2009
214
16

Common polygenic variation and risk for childhood-onset schizophrenia.
K Ahn, S S An, Y Y Shugart, J L Rapoport. Mol Psychiatry 2016
33
16

Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophrenia.
Tom Walsh, Jon M McClellan, Shane E McCarthy, Anjené M Addington, Sarah B Pierce, Greg M Cooper, Alex S Nord, Mary Kusenda, Dheeraj Malhotra, Abhishek Bhandari,[...]. Science 2008
16

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
16


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
16

CEDNIK syndrome results from loss-of-function mutations in SNAP29.
D Fuchs-Telem, H Stewart, D Rapaport, J Nousbeck, A Gat, M Gini, Y Lugassy, S Emmert, K Eckl, H C Hennies,[...]. Br J Dermatol 2011
53
16


Snap29 mutant mice recapitulate neurological and ophthalmological abnormalities associated with 22q11 and CEDNIK syndrome.
Vafa Keser, Jean-François Boisclair Lachance, Sabrina Shameen Alam, Youngshin Lim, Eleonora Scarlata, Apinder Kaur, Tian Fang Zhang, Shasha Lv, Pierre Lachapelle, Cristian O'Flaherty,[...]. Commun Biol 2019
3
66

A genetic model of CEDNIK syndrome in zebrafish highlights the role of the SNARE protein Snap29 in neuromotor and epidermal development.
Valeria Mastrodonato, Galina Beznoussenko, Alexandre Mironov, Laura Ferrari, Gianluca Deflorian, Thomas Vaccari. Sci Rep 2019
9
22

The molecular machinery of neurotransmitter release (Nobel lecture).
Thomas C Südhof. Angew Chem Int Ed Engl 2014
79
16

How to use a multipurpose SNARE: The emerging role of Snap29 in cellular health.
Valeria Mastrodonato, Elena Morelli, Thomas Vaccari. Cell Stress 2018
8
25

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
16

Ranbp1, Deleted in DiGeorge/22q11.2 Deletion Syndrome, is a Microcephaly Gene That Selectively Disrupts Layer 2/3 Cortical Projection Neuron Generation.
Elizabeth M Paronett, Daniel W Meechan, Beverly A Karpinski, Anthony-Samuel LaMantia, Thomas M Maynard. Cereb Cortex 2015
25
16


SNAP-29: a general SNARE protein that inhibits SNARE disassembly and is implicated in synaptic transmission.
Q Su, S Mochida, J H Tian, R Mehta, Z H Sheng. Proc Natl Acad Sci U S A 2001
70
16

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
16

MicroRNA-independent functions of DGCR8 are essential for neocortical development and TBR1 expression.
Federica Marinaro, Matteo J Marzi, Nadin Hoffmann, Hayder Amin, Roberta Pelizzoli, Francesco Niola, Francesco Nicassio, Davide De Pietri Tonelli. EMBO Rep 2017
28
16

Reduced adult hippocampal neurogenesis and working memory deficits in the Dgcr8-deficient mouse model of 22q11.2 deletion-associated schizophrenia can be rescued by IGF2.
Yasuo Ouchi, Yuya Banno, Yuko Shimizu, Shouta Ando, Hitoki Hasegawa, Koichi Adachi, Takashi Iwamoto. J Neurosci 2013
103
16

In the line-up: deleted genes associated with DiGeorge/22q11.2 deletion syndrome: are they all suspects?
Zahra Motahari, Sally Ann Moody, Thomas Michael Maynard, Anthony-Samuel LaMantia. J Neurodev Disord 2019
19
16

TALEN-mediated gene mutagenesis in rhesus and cynomolgus monkeys.
Hailiang Liu, Yongchang Chen, Yuyu Niu, Kunshan Zhang, Yu Kang, Weihong Ge, Xiaojing Liu, Enfeng Zhao, Chencheng Wang, Shaoyun Lin,[...]. Cell Stem Cell 2014
125
8

Autism-like behaviours and germline transmission in transgenic monkeys overexpressing MeCP2.
Zhen Liu, Xiao Li, Jun-Tao Zhang, Yi-Jun Cai, Tian-Lin Cheng, Cheng Cheng, Yan Wang, Chen-Chen Zhang, Yan-Hong Nie, Zhi-Fang Chen,[...]. Nature 2016
141
8

CRISPR/Cas9-mediated disruption of SHANK3 in monkey leads to drug-treatable autism-like symptoms.
Zhuchi Tu, Hui Zhao, Bang Li, Sen Yan, Lu Wang, Yongjin Tang, Zhujun Li, Dazhang Bai, Caijuan Li, Yingqi Lin,[...]. Hum Mol Genet 2019
13
8

Drosophila Studies on Autism Spectrum Disorders.
Yao Tian, Zi Chao Zhang, Junhai Han. Neurosci Bull 2017
13
8

A Fiber Tractography Study of Social-Emotional Related Fiber Tracts in Children and Adolescents with Autism Spectrum Disorder.
Yun Li, Hui Fang, Wenming Zheng, Lu Qian, Yunhua Xiao, Qiaorong Wu, Chen Chang, Chaoyong Xiao, Kangkang Chu, Xiaoyan Ke. Neurosci Bull 2017
4
25

Modeling Rett Syndrome Using TALEN-Edited MECP2 Mutant Cynomolgus Monkeys.
Yongchang Chen, Juehua Yu, Yuyu Niu, Dongdong Qin, Hailiang Liu, Gang Li, Yingzhou Hu, Jiaojian Wang, Yi Lu, Yu Kang,[...]. Cell 2017
74
8

Assessing the Accuracy of the Modified Chinese Autism Spectrum Rating Scale and Social Responsiveness Scale for Screening Autism Spectrum Disorder in Chinese Children.
Bingrui Zhou, Hao Zhou, Lijie Wu, Xiaobing Zou, Xuerong Luo, Eric Fombonne, Yi Wang, Weili Yan, Xiu Xu. Neurosci Bull 2017
8
12

A Volumetric and Functional Connectivity MRI Study of Brain Arginine-Vasopressin Pathways in Autistic Children.
Xiao-Jing Shou, Xin-Jie Xu, Xiang-Zhu Zeng, Ying Liu, Hui-Shu Yuan, Yan Xing, Mei-Xiang Jia, Qing-Yun Wei, Song-Ping Han, Rong Zhang,[...]. Neurosci Bull 2017
18
8


Altered neurogenesis and disrupted expression of synaptic proteins in prefrontal cortex of SHANK3-deficient non-human primate.
Hui Zhao, Zhuchi Tu, Huijuan Xu, Sen Yan, Huanhuan Yan, Yinghui Zheng, Weili Yang, Jiezhao Zheng, Zhujun Li, Rui Tian,[...]. Cell Res 2017
35
8

Getting to the Cores of Autism.
Lilia M Iakoucheva, Alysson R Muotri, Jonathan Sebat. Cell 2019
56
8

Dopamine D4 Receptor Gene Associated with the Frontal-Striatal-Cerebellar Loop in Children with ADHD: A Resting-State fMRI Study.
Andan Qian, Xin Wang, Huiru Liu, Jiejie Tao, Jiejie Zhou, Qiong Ye, Jiance Li, Chuang Yang, Jingliang Cheng, Ke Zhao,[...]. Neurosci Bull 2018
15
8


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.