A citation-based method for searching scientific literature

So Hyun Kim, LeeAnne Green-Snyder, Catherine Lord, Somer Bishop, Kyle J Steinman, Raphael Bernier, Ellen Hanson, Robin P Goin-Kochel, Wendy K Chung. Am J Med Genet B Neuropsychiatr Genet 2020
Times Cited: 4







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



Times Cited
  Times     Co-cited
Similarity


Recurrent reciprocal 16p11.2 rearrangements associated with global developmental delay, behavioural problems, dysmorphism, epilepsy, and abnormal head size.
Marwan Shinawi, Pengfei Liu, Sung-Hae L Kang, Joseph Shen, John W Belmont, Daryl A Scott, Frank J Probst, William J Craigen, Brett H Graham, Amber Pursley,[...]. J Med Genet 2010
317
75

Focal Cortical Anomalies and Language Impairment in 16p11.2 Deletion and Duplication Syndrome.
Karen Blackmon, Thomas Thesen, Sophie Green, Emma Ben-Avi, Xiuyuan Wang, Benjamin Fuchs, Ruben Kuzniecky, Orrin Devinsky. Cereb Cortex 2018
12
50

Speech delays and behavioral problems are the predominant features in individuals with developmental delays and 16p11.2 microdeletions and microduplications.
Jill A Rosenfeld, Justine Coppinger, Bassem A Bejjani, Santhosh Girirajan, Evan E Eichler, Lisa G Shaffer, Blake C Ballif. J Neurodev Disord 2010
106
50

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus.
Sébastien Jacquemont, Alexandre Reymond, Flore Zufferey, Louise Harewood, Robin G Walters, Zoltán Kutalik, Danielle Martinet, Yiping Shen, Armand Valsesia, Noam D Beckmann,[...]. Nature 2011
264
50

The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.
Ellen Hanson, Raphael Bernier, Ken Porche, Frank I Jackson, Robin P Goin-Kochel, LeeAnne Green Snyder, Anne V Snow, Arianne Stevens Wallace, Katherine L Campe, Yuan Zhang,[...]. Biol Psychiatry 2015
128
50

Association between microdeletion and microduplication at 16p11.2 and autism.
Lauren A Weiss, Yiping Shen, Joshua M Korn, Dan E Arking, David T Miller, Ragnheidur Fossdal, Evald Saemundsen, Hreinn Stefansson, Manuel A R Ferreira, Todd Green,[...]. N Engl J Med 2008
50

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders.
Flore Zufferey, Elliott H Sherr, Noam D Beckmann, Ellen Hanson, Anne M Maillard, Loyse Hippolyte, Aurélien Macé, Carina Ferrari, Zoltán Kutalik, Joris Andrieux,[...]. J Med Genet 2012
154
50


Opposing brain differences in 16p11.2 deletion and duplication carriers.
Abid Y Qureshi, Sophia Mueller, Abraham Z Snyder, Pratik Mukherjee, Jeffrey I Berman, Timothy P L Roberts, Srikantan S Nagarajan, John E Spiro, Wendy K Chung, Elliott H Sherr,[...]. J Neurosci 2014
90
50

CNVs conferring risk of autism or schizophrenia affect cognition in controls.
Hreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, Brynja Magnusdottir, Katrin Morgen, Sunna Arnarsdottir, Gyda Bjornsdottir, G Bragi Walters, Gudrun A Jonsdottir, Orla M Doyle,[...]. Nature 2014
371
50

Auditory Evoked M100 Response Latency is Delayed in Children with 16p11.2 Deletion but not 16p11.2 Duplication.
Julian Jenkins, Vivian Chow, Lisa Blaskey, Emily Kuschner, Saba Qasmieh, Leah Gaetz, J Christopher Edgar, Pratik Mukherjee, Randall Buckner, Srikantan S Nagarajan,[...]. Cereb Cortex 2016
18
50

A copy number variation morbidity map of developmental delay.
Gregory M Cooper, Bradley P Coe, Santhosh Girirajan, Jill A Rosenfeld, Tiffany H Vu, Carl Baker, Charles Williams, Heather Stalker, Rizwan Hamid, Vickie Hannig,[...]. Nat Genet 2011
803
50

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
50

Rare variants in the genetic background modulate cognitive and developmental phenotypes in individuals carrying disease-associated variants.
Lucilla Pizzo, Matthew Jensen, Andrew Polyak, Jill A Rosenfeld, Katrin Mannik, Arjun Krishnan, Elizabeth McCready, Olivier Pichon, Cedric Le Caignec, Anke Van Dijck,[...]. Genet Med 2019
53
50

Cognitive and behavioral characterization of 16p11.2 deletion syndrome.
Ellen Hanson, Ramzi H Nasir, Alexa Fong, Alyss Lian, Rachel Hundley, Yiping Shen, Bai-Lin Wu, Ingrid A Holm, David T Miller. J Dev Behav Pediatr 2010
75
50

The Number of Genomic Copies at the 16p11.2 Locus Modulates Language, Verbal Memory, and Inhibition.
Loyse Hippolyte, Anne M Maillard, Borja Rodriguez-Herreros, Aurélie Pain, Sandra Martin-Brevet, Carina Ferrari, Philippe Conus, Aurélien Macé, Nouchine Hadjikhani, Andres Metspalu,[...]. Biol Psychiatry 2016
49
50

The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions.
Andres Moreno-De-Luca, David W Evans, K B Boomer, Ellen Hanson, Raphael Bernier, Robin P Goin-Kochel, Scott M Myers, Thomas D Challman, Daniel Moreno-De-Luca, Mylissa M Slane,[...]. JAMA Psychiatry 2015
86
50

Genotype-phenotype associations in children with copy number variants associated with high neuropsychiatric risk in the UK (IMAGINE-ID): a case-control cohort study.
Samuel J R A Chawner, Michael J Owen, Peter Holmans, F Lucy Raymond, David Skuse, Jeremy Hall, Marianne B M van den Bree. Lancet Psychiatry 2019
32
50

Structural variation of chromosomes in autism spectrum disorder.
Christian R Marshall, Abdul Noor, John B Vincent, Anath C Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren,[...]. Am J Hum Genet 2008
50

Brain MR Imaging Findings and Associated Outcomes in Carriers of the Reciprocal Copy Number Variation at 16p11.2.
Julia P Owen, Polina Bukshpun, Nicholas Pojman, Tony Thieu, Qixuan Chen, Jihui Lee, Debra D'Angelo, Orit A Glenn, Jill V Hunter, Jeffrey I Berman,[...]. Radiology 2018
14
50

Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects.
Kimberley M Kendall, Elliott Rees, Valentina Escott-Price, Mark Einon, Rhys Thomas, Jonathan Hewitt, Michael C O'Donovan, Michael J Owen, James T R Walters, George Kirov. Biol Psychiatry 2017
74
50

Clinical genetic testing for patients with autism spectrum disorders.
Yiping Shen, Kira A Dies, Ingrid A Holm, Carolyn Bridgemohan, Magdi M Sobeih, Elizabeth B Caronna, Karen J Miller, Jean A Frazier, Iris Silverstein, Jonathan Picker,[...]. Pediatrics 2010
241
25


Modelling schizophrenia using human induced pluripotent stem cells.
Kristen J Brennand, Anthony Simone, Jessica Jou, Chelsea Gelboin-Burkhart, Ngoc Tran, Sarah Sangar, Yan Li, Yangling Mu, Gong Chen, Diana Yu,[...]. Nature 2011
860
25

Regionalization of the prosencephalic neural plate.
J L Rubenstein, K Shimamura, S Martinez, L Puelles. Annu Rev Neurosci 1998
393
25

Kctd13 deletion reduces synaptic transmission via increased RhoA.
Christine Ochoa Escamilla, Irina Filonova, Angela K Walker, Zhong X Xuan, Roopashri Holehonnur, Felipe Espinosa, Shunan Liu, Summer B Thyme, Isabel A López-García, Dorian B Mendoza,[...]. Nature 2017
49
25

Pathological priming causes developmental gene network heterochronicity in autistic subject-derived neurons.
Simon T Schafer, Apua C M Paquola, Shani Stern, David Gosselin, Manching Ku, Monique Pena, Thomas J M Kuret, Marvin Liyanage, Abed AlFatah Mansour, Baptiste N Jaeger,[...]. Nat Neurosci 2019
91
25

Human cerebral cortex development from pluripotent stem cells to functional excitatory synapses.
Yichen Shi, Peter Kirwan, James Smith, Hugh P C Robinson, Frederick J Livesey. Nat Neurosci 2012
482
25


Primary Cell Culture of Live Neurosurgically Resected Aged Adult Human Brain Cells and Single Cell Transcriptomics.
Jennifer M Spaethling, Young-Ji Na, Jaehee Lee, Alexandra V Ulyanova, Gordon H Baltuch, Thomas J Bell, Steven Brem, H Isaac Chen, Hannah Dueck, Stephen A Fisher,[...]. Cell Rep 2017
31
25

Functional impact of global rare copy number variation in autism spectrum disorders.
Dalila Pinto, Alistair T Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R Magalhaes, Catarina Correia, Brett S Abrahams,[...]. Nature 2010
25

A model for neural development and treatment of Rett syndrome using human induced pluripotent stem cells.
Maria C N Marchetto, Cassiano Carromeu, Allan Acab, Diana Yu, Gene W Yeo, Yangling Mu, Gong Chen, Fred H Gage, Alysson R Muotri. Cell 2010
856
25


De novo 393 kb microdeletion of 7p11.2 characterized by aCGH in a boy with psychomotor retardation and dysmorphic features.
Konstantinos Varvagiannis, Ioannis Papoulidis, Theodora Koromila, Konstantinos Kefalas, Monika Ziegler, Thomas Liehr, Michael B Petersen, Yolanda Gyftodimou, Emmanouil Manolakos. Meta Gene 2014
4
25

Regulation of cerebral cortical size and neuron number by fibroblast growth factors: implications for autism.
Flora M Vaccarino, Elena L Grigorenko, Karen Müller Smith, Hanna E Stevens. J Autism Dev Disord 2009
51
25

Toward a 3D model of human brain development for studying gene/environment interactions.
Helena T Hogberg, Joseph Bressler, Kimberly M Christian, Georgina Harris, Georgia Makri, Cliona O'Driscoll, David Pamies, Lena Smirnova, Zhexing Wen, Thomas Hartung. Stem Cell Res Ther 2013
42
25

Predicting the diagnosis of autism spectrum disorder using gene pathway analysis.
E Skafidas, R Testa, D Zantomio, G Chana, I P Everall, C Pantelis. Mol Psychiatry 2014
83
25

Primate-specific microRNA-637 inhibits tumorigenesis in hepatocellular carcinoma by disrupting signal transducer and activator of transcription 3 signaling.
Jin-fang Zhang, Ming-liang He, Wei-ming Fu, Hua Wang, Lian-zhou Chen, Xiao Zhu, Ying Chen, Dan Xie, Paul Lai, Gong Chen,[...]. Hepatology 2011
99
25

A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.
R G Walters, S Jacquemont, A Valsesia, A J de Smith, D Martinet, J Andersson, M Falchi, F Chen, J Andrieux, S Lobbens,[...]. Nature 2010
317
25

Induced pluripotent stem cell lines derived from human somatic cells.
Junying Yu, Maxim A Vodyanik, Kim Smuga-Otto, Jessica Antosiewicz-Bourget, Jennifer L Frane, Shulan Tian, Jeff Nie, Gudrun A Jonsdottir, Victor Ruotti, Ron Stewart,[...]. Science 2007
25

New lessons learned from disease modeling with induced pluripotent stem cells.
Tamer T Onder, George Q Daley. Curr Opin Genet Dev 2012
57
25

Induction of pluripotent stem cells from adult human fibroblasts by defined factors.
Kazutoshi Takahashi, Koji Tanabe, Mari Ohnuki, Megumi Narita, Tomoko Ichisaka, Kiichiro Tomoda, Shinya Yamanaka. Cell 2007
25

Autism spectrum disorder susceptibility gene TAOK2 affects basal dendrite formation in the neocortex.
Froylan Calderon de Anda, Ana Lucia Rosario, Omer Durak, Tracy Tran, Johannes Gräff, Konstantinos Meletis, Damien Rei, Takahiro Soda, Ram Madabhushi, David D Ginty,[...]. Nat Neurosci 2012
99
25

The sva package for removing batch effects and other unwanted variation in high-throughput experiments.
Jeffrey T Leek, W Evan Johnson, Hilary S Parker, Andrew E Jaffe, John D Storey. Bioinformatics 2012
25

Engineering microdeletions and microduplications by targeting segmental duplications with CRISPR.
Derek J C Tai, Ashok Ragavendran, Poornima Manavalan, Alexei Stortchevoi, Catarina M Seabra, Serkan Erdin, Ryan L Collins, Ian Blumenthal, Xiaoli Chen, Yiping Shen,[...]. Nat Neurosci 2016
30
25

FOXG1-Dependent Dysregulation of GABA/Glutamate Neuron Differentiation in Autism Spectrum Disorders.
Jessica Mariani, Gianfilippo Coppola, Ping Zhang, Alexej Abyzov, Lauren Provini, Livia Tomasini, Mariangela Amenduni, Anna Szekely, Dean Palejev, Michael Wilson,[...]. Cell 2015
508
25

The 16p11.2 deletion mouse model of autism exhibits altered cortical progenitor proliferation and brain cytoarchitecture linked to the ERK MAPK pathway.
Joanna Pucilowska, Joseph Vithayathil, Emmanuel J Tavares, Caitlin Kelly, J Colleen Karlo, Gary E Landreth. J Neurosci 2015
82
25

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
25

Amigo adhesion protein regulates development of neural circuits in zebrafish brain.
Xiang Zhao, Juha Kuja-Panula, Maria Sundvik, Yu-Chia Chen, Vilma Aho, Marjaana A Peltola, Tarja Porkka-Heiskanen, Pertti Panula, Heikki Rauvala. J Biol Chem 2014
8
25

Cytoscape: a software environment for integrated models of biomolecular interaction networks.
Paul Shannon, Andrew Markiel, Owen Ozier, Nitin S Baliga, Jonathan T Wang, Daniel Ramage, Nada Amin, Benno Schwikowski, Trey Ideker. Genome Res 2003
25


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.