A citation-based method for searching scientific literature

Gregory Costain, Susan Walker, Bob Argiropoulos, Danielle A Baribeau, Anne S Bassett, Erik Boot, Koen Devriendt, Barbara Kellam, Christian R Marshall, Aparna Prasad, Moises A Serrano, D James Stavropoulos, Hope Twede, Joris R Vermeesch, Jacob A S Vorstman, Stephen W Scherer. J Neurodev Disord 2019
Times Cited: 5







List of co-cited articles
8 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
40

TBC1D24 regulates neuronal migration and maturation through modulation of the ARF6-dependent pathway.
Antonio Falace, Emmanuelle Buhler, Manuela Fadda, Françoise Watrin, Pellegrino Lippiello, Emilie Pallesi-Pocachard, Pietro Baldelli, Fabio Benfenati, Federico Zara, Alfonso Represa,[...]. Proc Natl Acad Sci U S A 2014
66
40

SYN1 loss-of-function mutations in autism and partial epilepsy cause impaired synaptic function.
Anna Fassio, Lysanne Patry, Sonia Congia, Franco Onofri, Amelie Piton, Julie Gauthier, Davide Pozzi, Mirko Messa, Enrico Defranchi, Manuela Fadda,[...]. Hum Mol Genet 2011
140
40

Lack of synapsin I reduces the readily releasable pool of synaptic vesicles at central inhibitory synapses.
Pietro Baldelli, Anna Fassio, Flavia Valtorta, Fabio Benfenati. J Neurosci 2007
121
40

RNA splicing. The human splicing code reveals new insights into the genetic determinants of disease.
Hui Y Xiong, Babak Alipanahi, Leo J Lee, Hannes Bretschneider, Daniele Merico, Ryan K C Yuen, Yimin Hua, Serge Gueroussov, Hamed S Najafabadi, Timothy R Hughes,[...]. Science 2015
528
40

TBC1D24, an ARF6-interacting protein, is mutated in familial infantile myoclonic epilepsy.
Antonio Falace, Fabia Filipello, Veronica La Padula, Nicola Vanni, Francesca Madia, Davide De Pietri Tonelli, Fabrizio A de Falco, Pasquale Striano, Franca Dagna Bricarelli, Carlo Minetti,[...]. Am J Hum Genet 2010
108
40

De novo mutations of the ATP6V1A gene cause developmental encephalopathy with epilepsy.
Anna Fassio, Alessandro Esposito, Mitsuhiro Kato, Hirotomo Saitsu, Davide Mei, Carla Marini, Valerio Conti, Mitsuko Nakashima, Nobuhiko Okamoto, Akgun Olmez Turker,[...]. Brain 2018
31
40


Association of the Synapse-Associated Protein 97 (SAP97) Gene Polymorphism With Neurocognitive Function in Schizophrenic Patients.
Xusan Xu, Chunmei Liang, Dong Lv, Jingwen Yin, Xudong Luo, Jiawu Fu, Haifeng Yan, Xia Zhou, Zhun Dai, Dongjian Zhu,[...]. Front Psychiatry 2018
8
20


CHD2 haploinsufficiency is associated with developmental delay, intellectual disability, epilepsy and neurobehavioural problems.
Sébastien Chénier, Grace Yoon, Bob Argiropoulos, Julie Lauzon, Rachel Laframboise, Joo Wook Ahn, Caroline Mackie Ogilvie, Anath C Lionel, Christian R Marshall, Andrea K Vaags,[...]. J Neurodev Disord 2014
46
20

Genetic and molecular risk factors within the newly identified primate-specific exon of the SAP97/DLG1 gene in the 3q29 schizophrenia-associated locus.
Akihito Uezato, Naoki Yamamoto, Daisuke Jitoku, Emiko Haramo, Eri Hiraaki, Yoshimi Iwayama, Tomoko Toyota, Masakazu Umino, Asami Umino, Yasuhide Iwata,[...]. Am J Med Genet B Neuropsychiatr Genet 2017
8
20

3q29 microdeletion syndrome: Cognitive and behavioral phenotype in four patients.
Santina Città, Serafino Buono, Donatella Greco, Concetta Barone, Enrico Alfei, Sara Bulgheroni, Arianna Usilla, Chiara Pantaleoni, Corrado Romano. Am J Med Genet A 2013
12
20

Primary Cilia in Brain Development and Diseases.
Yong Ha Youn, Young-Goo Han. Am J Pathol 2018
46
20

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
20


Novel features of 3q29 deletion syndrome: Results from the 3q29 registry.
Megan R Glassford, Jill A Rosenfeld, Alexa A Freedman, Michael E Zwick, Jennifer G Mulle. Am J Med Genet A 2016
39
20

Novel copy number variants in children with autism and additional developmental anomalies.
L K Davis, K J Meyer, D S Rudd, A L Librant, E A Epping, V C Sheffield, T H Wassink. J Neurodev Disord 2009
29
20

Disrupted iron homeostasis causes dopaminergic neurodegeneration in mice.
Pavle Matak, Andrija Matak, Sarah Moustafa, Dipendra K Aryal, Eric J Benner, William Wetsel, Nancy C Andrews. Proc Natl Acad Sci U S A 2016
69
20

A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3.
Pablo Cingolani, Adrian Platts, Le Lily Wang, Melissa Coon, Tung Nguyen, Luan Wang, Susan J Land, Xiangyi Lu, Douglas M Ruden. Fly (Austin) 2012
20

COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome.
Doron Gothelf, Stephan Eliez, Tracy Thompson, Christine Hinard, Lauren Penniman, Carl Feinstein, Hower Kwon, Shuting Jin, Booil Jo, Stylianos E Antonarakis,[...]. Nat Neurosci 2005
252
20

Microdeletions of 3q29 confer high risk for schizophrenia.
Jennifer Gladys Mulle, Anne F Dodd, John A McGrath, Paula S Wolyniec, Adele A Mitchell, Amol C Shetty, Nara L Sobreira, David Valle, M Katharine Rudd, Glen Satten,[...]. Am J Hum Genet 2010
158
20

Autism diagnostic observation schedule: a standardized observation of communicative and social behavior.
C Lord, M Rutter, S Goode, J Heemsbergen, H Jordan, L Mawhood, E Schopler. J Autism Dev Disord 1989
20

Hippocampal Pruning as a New Theory of Schizophrenia Etiopathogenesis.
Enrico Cocchi, Antonio Drago, Alessandro Serretti. Mol Neurobiol 2016
20
20

Neuropsychiatric phenotype in relation to gene variants in the hemizygous allele in 3q29 deletion carriers: A case series.
Eva Albertsen Malt, Katalin Juhasz, Anna Frengen, Teresia Wangensteen, Nina Merete Emilsen, Borre Hansen, Oleg Agafonov, Hilde Loge Nilsen. Mol Genet Genomic Med 2019
4
25

3q29 microdeletion syndrome: clinical and molecular characterization of a new syndrome.
Lionel Willatt, James Cox, John Barber, Elisabet Dachs Cabanas, Amanda Collins, Dian Donnai, David R FitzPatrick, Eddy Maher, Howard Martin, Josep Parnau,[...]. Am J Hum Genet 2005
159
20

Anorexia and impaired glucose metabolism in mice with hypothalamic ablation of Glut4 neurons.
Hongxia Ren, Taylor Y Lu, Timothy E McGraw, Domenico Accili. Diabetes 2015
18
20

Pregnenolone sulfate as a modulator of synaptic plasticity.
Conor C Smith, Terrell T Gibbs, David H Farb. Psychopharmacology (Berl) 2014
29
20


Neurosteroids in Schizophrenia: Pathogenic and Therapeutic Implications.
HuaLin Cai, Ting Cao, Xiang Zhou, Jeffrey K Yao. Front Psychiatry 2018
23
20

Copy number variations in neurodevelopmental disorders.
Hannah M Grayton, Cathy Fernandes, Dan Rujescu, David A Collier. Prog Neurobiol 2012
105
20


Transferrin receptor is necessary for development of erythrocytes and the nervous system.
J E Levy, O Jin, Y Fujiwara, F Kuo, N C Andrews. Nat Genet 1999
393
20

Tctex1d2 associates with short-rib polydactyly syndrome proteins and is required for ciliogenesis.
Ankur A Gholkar, Silvia Senese, Yu-Chen Lo, Joseph Capri, William J Deardorff, Harish Dharmarajan, Ely Contreras, Emmanuelle Hodara, Julian P Whitelegge, Peter K Jackson,[...]. Cell Cycle 2015
19
20

No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients.
M Guipponi, F Santoni, M Schneider, C Gehrig, X B Bustillo, W R Kates, B Morrow, M Armando, S Vicari, F Sloan-Béna,[...]. Transl Psychiatry 2017
7
20

Tctex1d2 Is a Negative Regulator of GLUT4 Translocation and Glucose Uptake.
Yoko Shimoda, Shuichi Okada, Eijiro Yamada, Jeffrey E Pessin, Masanobu Yamada. Endocrinology 2015
8
20

Quaternary structure, protein dynamics, and synaptic function of SAP97 controlled by L27 domain interactions.
Terunaga Nakagawa, Kensuke Futai, Hilal A Lashuel, Irene Lo, Kenichi Okamoto, Thomas Walz, Yasunori Hayashi, Morgan Sheng. Neuron 2004
193
20

A copy number variation map of the human genome.
Mehdi Zarrei, Jeffrey R MacDonald, Daniele Merico, Stephen W Scherer. Nat Rev Genet 2015
368
20

Familial 3q29 microdeletion syndrome providing further evidence of involvement of the 3q29 region in bipolar disorder.
Jill Clayton-Smith, Carol Giblin, Rupert A Smith, Carolyn Dunn, Lionel Willatt. Clin Dysmorphol 2010
28
20

Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: case report and review.
Fabiola Quintero-Rivera, Pantea Sharifi-Hannauer, Julian A Martinez-Agosto. Am J Med Genet A 2010
63
20

Molecular basis for the recognition of adenomatous polyposis coli by the Discs Large 1 protein.
Zhenyi Zhang, Hua Li, Leyi Chen, Xingyu Lu, Jian Zhang, Ping Xu, Kui Lin, Geng Wu. PLoS One 2011
14
20

Neurosteroid Transport in the Brain: Role of ABC and SLC Transporters.
Markus Grube, Paul Hagen, Gabriele Jedlitschky. Front Pharmacol 2018
33
20

Further evidence for a male-selective genetic association of synapse-associated protein 97 (SAP97) gene with schizophrenia.
Akihito Uezato, Junko Kimura-Sato, Naoki Yamamoto, Yoshimi Iijima, Hiroshi Kunugi, Toru Nishikawa. Behav Brain Funct 2012
33
20

Transferrin Receptor Controls AMPA Receptor Trafficking Efficiency and Synaptic Plasticity.
Ke Liu, Run Lei, Qiong Li, Xin-Xin Wang, Qian Wu, Peng An, Jianchao Zhang, Minyan Zhu, Zhiheng Xu, Yang Hong,[...]. Sci Rep 2016
15
20


TCTEX1D2, a potential link to skeletal ciliopathies.
Saikat Mukhopadhyay. Cell Cycle 2015
2
50


CNVs in neuropsychiatric disorders.
George Kirov. Hum Mol Genet 2015
77
20

An association analysis of synapse-associated protein 97 (SAP97) gene in schizophrenia.
Junko Sato, Dai Shimazu, Naoki Yamamoto, Toru Nishikawa. J Neural Transm (Vienna) 2008
37
20

Reduced cortical expression of a newly identified splicing variant of the DLG1 gene in patients with early-onset schizophrenia.
A Uezato, N Yamamoto, Y Iwayama, S Hiraoka, E Hiraaki, A Umino, E Haramo, M Umino, T Yoshikawa, T Nishikawa. Transl Psychiatry 2015
17
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.