A citation-based method for searching scientific literature

Karen Blackmon, Thomas Thesen, Sophie Green, Emma Ben-Avi, Xiuyuan Wang, Benjamin Fuchs, Ruben Kuzniecky, Orrin Devinsky. Cereb Cortex 2018
Times Cited: 12







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



Times Cited
  Times     Co-cited
Similarity


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
41

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
33

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
25

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
25

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
25

Microduplications of 16p11.2 are associated with schizophrenia.
Shane E McCarthy, Vladimir Makarov, George Kirov, Anjene M Addington, Jon McClellan, Seungtai Yoon, Diana O Perkins, Diane E Dickel, Mary Kusenda, Olga Krastoshevsky,[...]. Nat Genet 2009
478
25

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
25

Aberrant white matter microstructure in children with 16p11.2 deletions.
Julia P Owen, Yi Shin Chang, Nicholas J Pojman, Polina Bukshpun, Mari L J Wakahiro, Elysa J Marco, Jeffrey I Berman, John E Spiro, Wendy K Chung, Randy L Buckner,[...]. J Neurosci 2014
49
25

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
25

Pharmacological Inhibition of ERK Signaling Rescues Pathophysiology and Behavioral Phenotype Associated with 16p11.2 Chromosomal Deletion in Mice.
Joanna Pucilowska, Joseph Vithayathil, Marco Pagani, Caitlin Kelly, J Colleen Karlo, Camilla Robol, Ilaria Morella, Alessandro Gozzi, Riccardo Brambilla, Gary E Landreth. J Neurosci 2018
32
25

Dosage-dependent phenotypes in models of 16p11.2 lesions found in autism.
Guy Horev, Jacob Ellegood, Jason P Lerch, Young-Eun E Son, Lakshmi Muthuswamy, Hannes Vogel, Abba M Krieger, Andreas Buja, R Mark Henkelman, Michael Wigler,[...]. Proc Natl Acad Sci U S A 2011
170
25

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
25

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
16



CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila.
Christiane Zweier, Eiko K de Jong, Markus Zweier, Alfredo Orrico, Lilian B Ousager, Amanda L Collins, Emilia K Bijlsma, Merel A W Oortveld, Arif B Ekici, André Reis,[...]. Am J Hum Genet 2009
227
16


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
16

High frequencies of de novo CNVs in bipolar disorder and schizophrenia.
Dheeraj Malhotra, Shane McCarthy, Jacob J Michaelson, Vladimir Vacic, Katherine E Burdick, Seungtai Yoon, Sven Cichon, Aiden Corvin, Sydney Gary, Elliot S Gershon,[...]. Neuron 2011
199
16

Rare and common variants at 16p11.2 are associated with schizophrenia.
Hong Chang, Lingyi Li, Ming Li, Xiao Xiao. Schizophr Res 2017
19
16

Recurrent 16p11.2 microdeletions in autism.
Ravinesh A Kumar, Samer KaraMohamed, Jyotsna Sudi, Donald F Conrad, Camille Brune, Judith A Badner, T Conrad Gilliam, Norma J Nowak, Edwin H Cook, William B Dobyns,[...]. Hum Mol Genet 2008
461
16

Automatically parcellating the human cerebral cortex.
Bruce Fischl, André van der Kouwe, Christophe Destrieux, Eric Halgren, Florent Ségonne, David H Salat, Evelina Busa, Larry J Seidman, Jill Goldstein, David Kennedy,[...]. Cereb Cortex 2004
16

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
16

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
16

An automated labeling system for subdividing the human cerebral cortex on MRI scans into gyral based regions of interest.
Rahul S Desikan, Florent Ségonne, Bruce Fischl, Brian T Quinn, Bradford C Dickerson, Deborah Blacker, Randy L Buckner, Anders M Dale, R Paul Maguire, Bradley T Hyman,[...]. Neuroimage 2006
16

Tract-based spatial statistics: voxelwise analysis of multi-subject diffusion data.
Stephen M Smith, Mark Jenkinson, Heidi Johansen-Berg, Daniel Rueckert, Thomas E Nichols, Clare E Mackay, Kate E Watkins, Olga Ciccarelli, M Zaheer Cader, Paul M Matthews,[...]. Neuroimage 2006
16

The 16p11.2 locus modulates brain structures common to autism, schizophrenia and obesity.
A M Maillard, A Ruef, F Pizzagalli, E Migliavacca, L Hippolyte, S Adaszewski, J Dukart, C Ferrari, P Conus, K Männik,[...]. Mol Psychiatry 2015
93
16

Relationship between M100 Auditory Evoked Response and Auditory Radiation Microstructure in 16p11.2 Deletion and Duplication Carriers.
J I Berman, D Chudnovskaya, L Blaskey, E Kuschner, P Mukherjee, R Buckner, S Nagarajan, W K Chung, E H Sherr, T P L Roberts. AJNR Am J Neuroradiol 2016
12
16

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
16

Diffusion tensor imaging in autism spectrum disorder: a review.
Brittany G Travers, Nagesh Adluru, Chad Ennis, Do P M Tromp, Dan Destiche, Sam Doran, Erin D Bigler, Nicholas Lange, Janet E Lainhart, Andrew L Alexander. Autism Res 2012
241
16

Whole brain segmentation: automated labeling of neuroanatomical structures in the human brain.
Bruce Fischl, David H Salat, Evelina Busa, Marilyn Albert, Megan Dieterich, Christian Haselgrove, Andre van der Kouwe, Ron Killiany, David Kennedy, Shuna Klaveness,[...]. Neuron 2002
16


Deviant trajectories of cortical maturation in 22q11.2 deletion syndrome (22q11DS): a cross-sectional and longitudinal study.
Marie Schaer, Martin Debbané, Meritxell Bach Cuadra, Marie-Christine Ottet, Bronwyn Glaser, Jean-Philippe Thiran, Stephan Eliez. Schizophr Res 2009
83
16

COMT Val108/158 Met modifies mismatch negativity and cognitive function in 22q11 deletion syndrome.
Kate Baker, Torsten Baldeweg, Sinthuja Sivagnanasundaram, Peter Scambler, David Skuse. Biol Psychiatry 2005
102
16

Effects of a functional COMT polymorphism on brain anatomy and cognitive function in adults with velo-cardio-facial syndrome.
T van Amelsvoort, J Zinkstok, M Figee, E Daly, R Morris, M J Owen, K C Murphy, L De Haan, D H Linszen, B Glaser,[...]. Psychol Med 2008
38
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

Machine-learning classification of 22q11.2 deletion syndrome: A diffusion tensor imaging study.
Daniel S Tylee, Zora Kikinis, Thomas P Quinn, Kevin M Antshel, Wanda Fremont, Muhammad A Tahir, Anni Zhu, Xue Gong, Stephen J Glatt, Ioana L Coman,[...]. Neuroimage Clin 2017
15
16

Default mode network connectivity and reciprocal social behavior in 22q11.2 deletion syndrome.
Matthew J Schreiner, Katherine H Karlsgodt, Lucina Q Uddin, Carolyn Chow, Eliza Congdon, Maria Jalbrzikowski, Carrie E Bearden. Soc Cogn Affect Neurosci 2014
47
16

The social brain network in 22q11.2 deletion syndrome: a diffusion tensor imaging study.
Amy K Olszewski, Zora Kikinis, Christie S Gonzalez, Ioana L Coman, Nikolaos Makris, Xue Gong, Yogesh Rathi, Anni Zhu, Kevin M Antshel, Wanda Fremont,[...]. Behav Brain Funct 2017
13
16

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
16

High rates of schizophrenia in adults with velo-cardio-facial syndrome.
K C Murphy, L A Jones, M J Owen. Arch Gen Psychiatry 1999
736
16

Atlas-based white matter analysis in individuals with velo-cardio-facial syndrome (22q11.2 deletion syndrome) and unaffected siblings.
Petya D Radoeva, Ioana L Coman, Kevin M Antshel, Wanda Fremont, Christopher S McCarthy, Ashwini Kotkar, Dongliang Wang, Robert J Shprintzen, Wendy R Kates. Behav Brain Funct 2012
36
16

Schizophrenia and the dynamic genome.
Patrick F Sullivan. Genome Med 2017
5
40

Sensory-related neural activity regulates the structure of vascular networks in the cerebral cortex.
Baptiste Lacoste, Cesar H Comin, Ayal Ben-Zvi, Pascal S Kaeser, Xiaoyin Xu, Luciano da F Costa, Chenghua Gu. Neuron 2014
65
16

TAOK2 Kinase Mediates PSD95 Stability and Dendritic Spine Maturation through Septin7 Phosphorylation.
Smita Yadav, Juan A Oses-Prieto, Christian J Peters, Jing Zhou, Samuel J Pleasure, Alma L Burlingame, Lily Y Jan, Yuh-Nung Jan. Neuron 2017
54
16

The BOLD signal and neurovascular coupling in autism.
Clare Reynell, Julia J Harris. Dev Cogn Neurosci 2013
15
16

Endothelial Dab1 signaling orchestrates neuro-glia-vessel communication in the central nervous system.
Marta Segarra, Maria R Aburto, Florian Cop, Cecília Llaó-Cid, Ricarda Härtl, Miriam Damm, Ioanna Bethani, Marta Parrilla, Dewi Husainie, Anne Schänzer,[...]. Science 2018
42
16

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
16

Persistent Angiogenesis in the Autism Brain: An Immunocytochemical Study of Postmortem Cortex, Brainstem and Cerebellum.
E C Azmitia, Z T Saccomano, M F Alzoobaee, M Boldrini, P M Whitaker-Azmitia. J Autism Dev Disord 2016
21
16

Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2.
Michael I Love, Wolfgang Huber, Simon Anders. Genome Biol 2014
16


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.