A citation-based method for searching scientific literature

Milen Velinov. Front Cell Neurosci 2019
Times Cited: 8







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



Times Cited
  Times     Co-cited
Similarity


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

The role of immune dysfunction in the pathophysiology of autism.
Charity Onore, Milo Careaga, Paul Ashwood. Brain Behav Immun 2012
348
37

Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.
Stephan J Sanders, A Gulhan Ercan-Sencicek, Vanessa Hus, Rui Luo, Michael T Murtha, Daniel Moreno-De-Luca, Su H Chu, Michael P Moreau, Abha R Gupta, Susanne A Thomson,[...]. Neuron 2011
802
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

Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder.
Santhosh Girirajan, Megan Y Dennis, Carl Baker, Maika Malig, Bradley P Coe, Catarina D Campbell, Kenneth Mark, Tiffany H Vu, Can Alkan, Ze Cheng,[...]. Am J Hum Genet 2013
184
25

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.
Santhosh Girirajan, Jill A Rosenfeld, Gregory M Cooper, Francesca Antonacci, Priscillia Siswara, Andy Itsara, Laura Vives, Tom Walsh, Shane E McCarthy, Carl Baker,[...]. Nat Genet 2010
411
25

The neuroanatomy of autism - a developmental perspective.
Alex P A Donovan, M Albert Basson. J Anat 2017
73
25

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders.
Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang,[...]. Am J Hum Genet 2014
516
25

Immune Dysfunction and Autoimmunity as Pathological Mechanisms in Autism Spectrum Disorders.
Heather K Hughes, Emily Mills Ko, Destanie Rose, Paul Ashwood. Front Cell Neurosci 2018
53
25

Phenotypic heterogeneity of genomic disorders and rare copy-number variants.
Santhosh Girirajan, Jill A Rosenfeld, Bradley P Coe, Sumit Parikh, Neil Friedman, Amy Goldstein, Robyn A Filipink, Juliann S McConnell, Brad Angle, Wendy S Meschino,[...]. N Engl J Med 2012
353
25

Inflammation and Neuro-Immune Dysregulations in Autism Spectrum Disorders.
Dario Siniscalco, Stephen Schultz, Anna Lisa Brigida, Nicola Antonucci. Pharmaceuticals (Basel) 2018
69
25

Altered proliferation and networks in neural cells derived from idiopathic autistic individuals.
Maria C Marchetto, Haim Belinson, Yuan Tian, Beatriz C Freitas, Chen Fu, Krishna Vadodaria, Patricia Beltrao-Braga, Cleber A Trujillo, Ana P D Mendes, Krishnan Padmanabhan,[...]. Mol Psychiatry 2017
170
25

Activating killer-cell immunoglobulin-like receptors (KIR) and their cognate HLA ligands are significantly increased in autism.
Anthony R Torres, Jonna B Westover, Cole Gibbons, Randall C Johnson, David C Ward. Brain Behav Immun 2012
28
25


Neuroglial activation and neuroinflammation in the brain of patients with autism.
Diana L Vargas, Caterina Nascimbene, Chitra Krishnan, Andrew W Zimmerman, Carlos A Pardo. Ann Neurol 2005
25

Whole-genome deep-learning analysis identifies contribution of noncoding mutations to autism risk.
Jian Zhou, Christopher Y Park, Chandra L Theesfeld, Aaron K Wong, Yuan Yuan, Claudia Scheckel, John J Fak, Julien Funk, Kevin Yao, Yoko Tajima,[...]. Nat Genet 2019
72
25

Familial clustering of autoimmune disorders and evaluation of medical risk factors in autism.
A M Comi, A W Zimmerman, V H Frye, P A Law, J N Peeden. J Child Neurol 1999
251
25

Model of autism: increased ratio of excitation/inhibition in key neural systems.
J L R Rubenstein, M M Merzenich. Genes Brain Behav 2003
25

Elevated plasma cytokines in autism spectrum disorders provide evidence of immune dysfunction and are associated with impaired behavioral outcome.
Paul Ashwood, Paula Krakowiak, Irva Hertz-Picciotto, Robin Hansen, Isaac Pessah, Judy Van de Water. Brain Behav Immun 2011
422
25

Maternal thyroid autoantibody and elevated risk of autism in a national birth cohort.
Alan S Brown, Heljä-Marja Surcel, Susanna Hinkka-Yli-Salomäki, Keely Cheslack-Postava, Yuanyuan Bao, Andre Sourander. Prog Neuropsychopharmacol Biol Psychiatry 2015
58
25

Increased prevalence of familial autoimmunity in probands with pervasive developmental disorders.
Thayne L Sweeten, Suzanne L Bowyer, David J Posey, Gary M Halberstadt, Christopher J McDougle. Pediatrics 2003
159
25

Heritability of autism spectrum disorders: a meta-analysis of twin studies.
Beata Tick, Patrick Bolton, Francesca Happé, Michael Rutter, Frühling Rijsdijk. J Child Psychol Psychiatry 2016
262
25

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
25

Identification of common genetic risk variants for autism spectrum disorder.
Jakob Grove, Stephan Ripke, Thomas D Als, Manuel Mattheisen, Raymond K Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A Andreassen, Richard Anney,[...]. Nat Genet 2019
437
25

Abnormal functional connectivity of default mode sub-networks in autism spectrum disorder patients.
Michal Assaf, Kanchana Jagannathan, Vince D Calhoun, Laura Miller, Michael C Stevens, Robert Sahl, Jacqueline G O'Boyle, Robert T Schultz, Godfrey D Pearlson. Neuroimage 2010
380
25

MRI or not to MRI! Should brain MRI be a routine investigation in children with autistic spectrum disorders?
Adel M Zeglam, Marwa F Al-Ogab, Thouraya Al-Shaftery. Acta Neurol Belg 2015
4
25

Essential versus complex autism: definition of fundamental prognostic subtypes.
J H Miles, T N Takahashi, S Bagby, P K Sahota, D F Vaslow, C H Wang, R E Hillman, J E Farmer. Am J Med Genet A 2005
137
12

Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
Erin L Heinzen, Rodney A Radtke, Thomas J Urban, Gianpiero L Cavalleri, Chantal Depondt, Anna C Need, Nicole M Walley, Paola Nicoletti, Dongliang Ge, Claudia B Catarino,[...]. Am J Hum Genet 2010
174
12

Convergence of spectrums: neuronal gene network states in autism spectrum disorder.
Josefa M Sullivan, Silvia De Rubeis, Anne Schaefer. Curr Opin Neurobiol 2019
8
12

Kallmann syndrome and ichthyosis: a case of contiguous gene deletion syndrome.
Irene Berges-Raso, Olga Giménez-Palop, Elisabeth Gabau, Ismael Capel, Assumpta Caixàs, Mercedes Rigla. Endocrinol Diabetes Metab Case Rep 2017
2
50

Phenotypic manifestations of copy number variation in chromosome 16p13.11.
Sandesh C Sreenath Nagamani, Ayelet Erez, Patricia Bader, Seema R Lalani, Daryl A Scott, Fernando Scaglia, Sharon E Plon, Chun-Hui Tsai, Tyler Reimschisel, Elizabeth Roeder,[...]. Eur J Hum Genet 2011
69
12

Confirmation of chromosomal microarray as a first-tier clinical diagnostic test for individuals with developmental delay, intellectual disability, autism spectrum disorders and dysmorphic features.
Agatino Battaglia, Viola Doccini, Laura Bernardini, Antonio Novelli, Sara Loddo, Anna Capalbo, Tiziana Filippi, John C Carey. Eur J Paediatr Neurol 2013
118
12

Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.
Susan L Christian, Camille W Brune, Jyotsna Sudi, Ravinesh A Kumar, Shaung Liu, Samer Karamohamed, Judith A Badner, Seiichi Matsui, Jeffrey Conroy, Devin McQuaid,[...]. Biol Psychiatry 2008
202
12

Overlapping 16p13.11 deletion and gain of copies variations associated with childhood onset psychosis include genes with mechanistic implications for autism associated pathways: Two case reports.
Catherine A Brownstein, Robin J Kleiman, Elizabeth C Engle, Meghan C Towne, Eugene J D'Angelo, Timothy W Yu, Alan H Beggs, Jonathan Picker, Jason M Fogler, Devon Carroll,[...]. Am J Med Genet A 2016
8
12


The Autism-Spectrum Quotient--Italian version: a cross-cultural confirmation of the broader autism phenotype.
Liliana Ruta, Domenico Mazzone, Luigi Mazzone, Sally Wheelwright, Simon Baron-Cohen. J Autism Dev Disord 2012
70
12

EEG Abnormalities as a Neurophysiological Biomarker of Severity in Autism Spectrum Disorder: A Pilot Cohort Study.
Antonio Gennaro Nicotera, Randi Jenssen Hagerman, Maria Vincenza Catania, Serafino Buono, Santo Di Nuovo, Elisa Maria Liprino, Emanuela Stracuzzi, Stefania Giusto, Giuseppina Di Vita, Sebastiano Antonino Musumeci. J Autism Dev Disord 2019
6
16

Prevalence and Characteristics of Autism Spectrum Disorder Among Children Aged 8 Years--Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2012.
Deborah L Christensen, Jon Baio, Kim Van Naarden Braun, Deborah Bilder, Jane Charles, John N Constantino, Julie Daniels, Maureen S Durkin, Robert T Fitzgerald, Margaret Kurzius-Spencer,[...]. MMWR Surveill Summ 2016
795
12

Copy number variation characteristics in subpopulations of patients with autism spectrum disorders.
Anna Bremer, MaiBritt Giacobini, Mats Eriksson, Peter Gustavsson, Viviann Nordin, Elisabeth Fernell, Christopher Gillberg, Ann Nordgren, Asa Uppströmer, Britt-Marie Anderlid,[...]. Am J Med Genet B Neuropsychiatr Genet 2011
48
12

12q21.2q22 deletion: a new patient.
Renata Oliveira, Cristina Pereira, Joana B Melo, Sandra Mesquita, Margarida Venâncio, Isabel Marques Carreira, Jorge Saraiva. Am J Med Genet A 2015
3
33

MRI findings in 77 children with non-syndromic autistic disorder.
Nathalie Boddaert, Mônica Zilbovicius, Anne Philipe, Laurence Robel, Marie Bourgeois, Catherine Barthélemy, David Seidenwurm, Isabelle Meresse, Laurence Laurier, Isabelle Desguerre,[...]. PLoS One 2009
62
12

Autism.
Meng-Chuan Lai, Michael V Lombardo, Simon Baron-Cohen. Lancet 2014
892
12

Cognitive deficit, learning difficulties, severe behavioral abnormalities and healed cleft lip in a patient with a 1.2-mb distal microduplication at 22q11.2.
L A Ribeiro-Bicudo, C de Campos Legnaro, B F Gamba, R M Candido Sandri, A Richieri-Costa. Mol Syndromol 2013
12
12

The essential role of centrosomal NDE1 in human cerebral cortex neurogenesis.
Mehmet Bakircioglu, Ofélia P Carvalho, Maryam Khurshid, James J Cox, Beyhan Tuysuz, Tanyeri Barak, Saliha Yilmaz, Okay Caglayan, Alp Dincer, Adeline K Nicholas,[...]. Am J Hum Genet 2011
106
12

Phenotypic variability of a deletion and duplication 6q16.1 → q21 due to a paternal balanced ins(7;6)(p15;q16.1q21).
Ana Spreiz, Doris Müller, Sibylle Zotter, Ursula Albrecht, Matthias Baumann, Christine Fauth, Martin Erdel, Johannes Zschocke, Gerd Utermann, Dieter Kotzot. Am J Med Genet A 2010
18
12

Another case of interstitial del(12) involving the proposed cardio-facio-cutaneous candidate region.
Paul A James, Paul Oei, Daniel Ng, Peter Kannu, Salim Aftimos. Am J Med Genet A 2005
8
12

Assessment of Psychopathological Comorbidities in Children and Adolescents With Autism Spectrum Disorder Using the Child Behavior Checklist.
Silvia Guerrera, Deny Menghini, Eleonora Napoli, Silvia Di Vara, Giovanni Valeri, Stefano Vicari. Front Psychiatry 2019
11
12

Head circumference and brain size in autism spectrum disorder: A systematic review and meta-analysis.
Roberto Sacco, Stefano Gabriele, Antonio M Persico. Psychiatry Res 2015
90
12

Standardizing ADOS scores for a measure of severity in autism spectrum disorders.
Katherine Gotham, Andrew Pickles, Catherine Lord. J Autism Dev Disord 2009
834
12

Array-CGH Analysis in a Cohort of Phenotypically Well-Characterized Individuals with "Essential" Autism Spectrum Disorders.
Eleonora Napoli, Serena Russo, Laura Casula, Viola Alesi, Filomena Alessandra Amendola, Adriano Angioni, Antonio Novelli, Giovanni Valeri, Deny Menghini, Stefano Vicari. J Autism Dev Disord 2018
10
12


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.