A citation-based method for searching scientific literature

Chun Chieh Fan, Timothy T Brown, Hauke Bartsch, Joshua M Kuperman, Donald J Hagler, Andrew Schork, Yvonne Searcy, Ursula Bellugi, Eric Halgren, Anders M Dale. Neuroimage Clin 2017
Times Cited: 13







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



Times Cited
  Times     Co-cited
Similarity


An experiment of nature: brain anatomy parallels cognition and behavior in Williams syndrome.
Allan L Reiss, Mark A Eckert, Fredric E Rose, Asya Karchemskiy, Shelli Kesler, Melody Chang, Margaret F Reynolds, Hower Kwon, Al Galaburda. J Neurosci 2004
185
61


Common genetic variants influence human subcortical brain structures.
Derrek P Hibar, Jason L Stein, Miguel E Renteria, Alejandro Arias-Vasquez, Sylvane Desrivières, Neda Jahanshad, Roberto Toro, Katharina Wittfeld, Lucija Abramovic, Micael Andersson,[...]. Nature 2015
439
38

Mapping 22q11.2 Gene Dosage Effects on Brain Morphometry.
Amy Lin, Christopher R K Ching, Ariana Vajdi, Daqiang Sun, Rachel K Jonas, Maria Jalbrzikowski, Leila Kushan-Wells, Laura Pacheco Hansen, Emma Krikorian, Boris Gutman,[...]. J Neurosci 2017
34
38

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
91
38

Quantifying the Effects of 16p11.2 Copy Number Variants on Brain Structure: A Multisite Genetic-First Study.
Sandra Martin-Brevet, Borja Rodríguez-Herreros, Jared A Nielsen, Clara Moreau, Claudia Modenato, Anne M Maillard, Aurélie Pain, Sonia Richetin, Aia E Jønch, Abid Y Qureshi,[...]. Biol Psychiatry 2018
27
38

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
94
38

Basal Dendritic Morphology of Cortical Pyramidal Neurons in Williams Syndrome: Prefrontal Cortex and Beyond.
Branka Hrvoj-Mihic, Kari L Hanson, Caroline H Lew, Lisa Stefanacci, Bob Jacobs, Ursula Bellugi, Katerina Semendeferi. Front Neurosci 2017
10
40

Neuron density is decreased in the prefrontal cortex in Williams syndrome.
Caroline Horton Lew, Chelsea Brown, Ursula Bellugi, Katerina Semendeferi. Autism Res 2017
11
36

Frontostriatal dysfunction during response inhibition in Williams syndrome.
Dean Mobbs, Mark A Eckert, Debra Mills, Julie Korenberg, Ursula Bellugi, Albert M Galaburda, Allan L Reiss. Biol Psychiatry 2007
78
30

Subcortical brain volume abnormalities in 2028 individuals with schizophrenia and 2540 healthy controls via the ENIGMA consortium.
T G M van Erp, D P Hibar, J M Rasmussen, D C Glahn, G D Pearlson, O A Andreassen, I Agartz, L T Westlye, U K Haukvik, A M Dale,[...]. Mol Psychiatry 2016
395
30

Novel genetic loci associated with hippocampal volume.
Derrek P Hibar, Hieab H H Adams, Neda Jahanshad, Ganesh Chauhan, Jason L Stein, Edith Hofer, Miguel E Renteria, Joshua C Bis, Alejandro Arias-Vasquez, M Kamran Ikram,[...]. Nat Commun 2017
127
30

A human neurodevelopmental model for Williams syndrome.
Thanathom Chailangkarn, Cleber A Trujillo, Beatriz C Freitas, Branka Hrvoj-Mihic, Roberto H Herai, Diana X Yu, Timothy T Brown, Maria C Marchetto, Cedric Bardy, Lauren McHenry,[...]. Nature 2016
93
30

15q11.2 CNV affects cognitive, structural and functional correlates of dyslexia and dyscalculia.
M O Ulfarsson, G B Walters, O Gustafsson, S Steinberg, A Silva, O M Doyle, M Brammer, D F Gudbjartsson, S Arnarsdottir, G A Jonsdottir,[...]. Transl Psychiatry 2017
38
30

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
375
30

CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits.
Aurélien Macé, Marcus A Tuke, Patrick Deelen, Kati Kristiansson, Hannele Mattsson, Margit Nõukas, Yadav Sapkota, Ursula Schick, Eleonora Porcu, Sina Rüeger,[...]. Nat Commun 2017
32
30

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
405
30

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
30

Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia.
Ida E Sønderby, Ómar Gústafsson, Nhat Trung Doan, Derrek P Hibar, Sandra Martin-Brevet, Abdel Abdellaoui, David Ames, Katrin Amunts, Michael Andersson, Nicola J Armstrong,[...]. Mol Psychiatry 2020
20
30


Stereological analysis of amygdala neuron number in autism.
Cynthia Mills Schumann, David G Amaral. J Neurosci 2006
233
23

Essential functions of the Williams-Beuren syndrome-associated TFII-I genes in embryonic development.
Badam Enkhmandakh, Aleksandr V Makeyev, Lkhamsuren Erdenechimeg, Frank H Ruddle, Nyam-Osor Chimge, Maria Isabel Tussie-Luna, Ananda L Roy, Dashzeveg Bayarsaihan. Proc Natl Acad Sci U S A 2009
78
23

IV. Neuroanatomy of Williams syndrome: a high-resolution MRI study.
A L Reiss, S Eliez, J E Schmitt, E Straus, Z Lai, W Jones, U Bellugi. J Cogn Neurosci 2000
163
23

II. Hypersociability in Williams Syndrome.
W Jones, U Bellugi, Z Lai, M Chiles, J Reilly, A Lincoln, R Adolphs. J Cogn Neurosci 2000
275
23

Neural correlates of genetically abnormal social cognition in Williams syndrome.
Andreas Meyer-Lindenberg, Ahmad R Hariri, Karen E Munoz, Carolyn B Mervis, Venkata S Mattay, Colleen A Morris, Karen Faith Berman. Nat Neurosci 2005
235
23

"Everybody in the world is my friend" hypersociability in young children with Williams syndrome.
Teresa F Doyle, Ursula Bellugi, Julie R Korenberg, John Graham. Am J Med Genet A 2004
167
23

Neuron number and size in prefrontal cortex of children with autism.
Eric Courchesne, Peter R Mouton, Michael E Calhoun, Katerina Semendeferi, Clelia Ahrens-Barbeau, Melodie J Hallet, Cynthia Carter Barnes, Karen Pierce. JAMA 2011
399
23

Prevalence estimation of Williams syndrome.
Petter Strømme, Per G Bjørnstad, Kjersti Ramstad. J Child Neurol 2002
421
23

Defining the social phenotype in Williams syndrome: a model for linking gene, the brain, and behavior.
Anna Järvinen-Pasley, Ursula Bellugi, Judy Reilly, Debra L Mills, Albert Galaburda, Allan L Reiss, Julie R Korenberg. Dev Psychopathol 2008
103
23



De novo mutations revealed by whole-exome sequencing are strongly associated with autism.
Stephan J Sanders, Michael T Murtha, Abha R Gupta, John D Murdoch, Melanie J Raubeson, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Nicholas M DiLullo, Neelroop N Parikshak, Jason L Stein,[...]. Nature 2012
23

Neural mechanisms in Williams syndrome: a unique window to genetic influences on cognition and behaviour.
Andreas Meyer-Lindenberg, Carolyn B Mervis, Karen Faith Berman. Nat Rev Neurosci 2006
252
23

Novel genetic loci underlying human intracranial volume identified through genome-wide association.
Hieab H H Adams, Derrek P Hibar, Vincent Chouraki, Jason L Stein, Paul A Nyquist, Miguel E Rentería, Stella Trompet, Alejandro Arias-Vasquez, Sudha Seshadri, Sylvane Desrivières,[...]. Nat Neurosci 2016
112
23


Mapping genetically controlled neural circuits of social behavior and visuo-motor integration by a preliminary examination of atypical deletions with Williams syndrome.
Fumiko Hoeft, Li Dai, Brian W Haas, Kristen Sheau, Masaru Mimura, Debra Mills, Albert Galaburda, Ursula Bellugi, Julie R Korenberg, Allan L Reiss. PLoS One 2014
17
23

Brain structural differences associated with the behavioural phenotype in children with Williams syndrome.
Linda E Campbell, Eileen Daly, Fiona Toal, Angela Stevens, Rayna Azuma, Annette Karmiloff-Smith, Declan G M Murphy, Kieran C Murphy. Brain Res 2009
57
23

3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry.
Ming-Chang Chiang, Allan L Reiss, Agatha D Lee, Ursula Bellugi, Albert M Galaburda, Julie R Korenberg, Debra L Mills, Arthur W Toga, Paul M Thompson. Neuroimage 2007
107
23

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
50
23

PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data.
Kai Wang, Mingyao Li, Dexter Hadley, Rui Liu, Joseph Glessner, Struan F A Grant, Hakon Hakonarson, Maja Bucan. Genome Res 2007
23

A postmortem stereological study of the amygdala in Williams syndrome.
Caroline H Lew, Kimberly M Groeniger, Ursula Bellugi, Lisa Stefanacci, Cynthia M Schumann, Katerina Semendeferi. Brain Struct Funct 2018
8
37

Increased glia density in the caudate nucleus in williams syndrome: Implications for frontostriatal dysfunction in autism.
Kari L Hanson, Caroline H Lew, Branka Hrvoj-Mihic, Kimberly M Groeniger, Eric Halgren, Ursula Bellugi, Katerina Semendeferi. Dev Neurobiol 2018
7
42

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
221
23

Reciprocal White Matter Changes Associated With Copy Number Variation at 15q11.2 BP1-BP2: A Diffusion Tensor Imaging Study.
Ana I Silva, Magnus O Ulfarsson, Hreinn Stefansson, Omar Gustafsson, G Bragi Walters, David E J Linden, Lawrence S Wilkinson, Mark Drakesmith, Michael J Owen, Jeremy Hall,[...]. Biol Psychiatry 2019
18
23

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition.
Dennis van der Meer, Ida E Sønderby, Tobias Kaufmann, G Bragi Walters, Abdel Abdellaoui, David Ames, Katrin Amunts, Micael Andersson, Nicola J Armstrong, Manon Bernard,[...]. JAMA Psychiatry 2020
21
23

Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size.
Daqiang Sun, Christopher R K Ching, Amy Lin, Jennifer K Forsyth, Leila Kushan, Ariana Vajdi, Maria Jalbrzikowski, Laura Hansen, Julio E Villalon-Reina, Xiaoping Qu,[...]. Mol Psychiatry 2020
54
23

Impact of on-site clinical genetics consultations on diagnostic rate in children and young adults with autism spectrum disorder.
Arnold Munnich, Caroline Demily, Lisa Frugère, Charlyne Duwime, Valérie Malan, Giulia Barcia, Céline Vidal, Emeline Throo, Claude Besmond, Laurence Hubert,[...]. Mol Autism 2019
14
23

Cortical and Subcortical Brain Morphometry Differences Between Patients With Autism Spectrum Disorder and Healthy Individuals Across the Lifespan: Results From the ENIGMA ASD Working Group.
Daan van Rooij, Evdokia Anagnostou, Celso Arango, Guillaume Auzias, Marlene Behrmann, Geraldo F Busatto, Sara Calderoni, Eileen Daly, Christine Deruelle, Adriana Di Martino,[...]. Am J Psychiatry 2018
138
23

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
34
23

Measuring and Estimating the Effect Sizes of Copy Number Variants on General Intelligence in Community-Based Samples.
Guillaume Huguet, Catherine Schramm, Elise Douard, Lai Jiang, Aurélie Labbe, Frédérique Tihy, Géraldine Mathonnet, Sonia Nizard, Emmanuelle Lemyre, Alexandre Mathieu,[...]. JAMA Psychiatry 2018
37
23


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.