A citation-based method for searching scientific literature


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



Times Cited
  Times     Co-cited
Similarity


Overlap with the autism spectrum in young children with Williams syndrome.
Bonita P Klein-Tasman, Kristin D Phillips, Catherine Lord, Carolyn B Mervis, Frank J Gallo. J Dev Behav Pediatr 2009
55
33

Children with 7q11.23 duplication syndrome: psychological characteristics.
Carolyn B Mervis, Bonita P Klein-Tasman, Myra J Huffman, Shelley L Velleman, C Holley Pitts, Danielle R Henderson, Janet Woodruff-Borden, Colleen A Morris, Lucy R Osborne. Am J Med Genet A 2015
27
25

Honing in on the social phenotype in Williams syndrome using multiple measures and multiple raters.
Bonita P Klein-Tasman, Kirsten T Li-Barber, Erin T Magargee. J Autism Dev Disord 2011
46
25

Socio-communicative deficits in young children with Williams syndrome: performance on the Autism Diagnostic Observation Schedule.
Bonita P Klein-Tasman, Carolyn B Mervis, Catherine Lord, Kristin D Phillips. Child Neuropsychol 2007
73
25

Genetics of autism spectrum disorders.
Daniel H Geschwind. Trends Cogn Sci 2011
313
25


Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci.
Stephan J Sanders, Xin He, A Jeremy Willsey, A Gulhan Ercan-Sencicek, Kaitlin E Samocha, A Ercument Cicek, Michael T Murtha, Vanessa H Bal, Somer L Bishop, Shan Dong,[...]. Neuron 2015
601
25

Autism Spectrum Symptomatology Among Children with Duplication 7q11.23 Syndrome.
Bonita P Klein-Tasman, Carolyn B Mervis. J Autism Dev Disord 2018
10
30

The Williams syndrome prosociality gene GTF2I mediates oxytocin reactivity and social anxiety in a healthy population.
Tanya L Procyshyn, Jason Spence, Silven Read, Neil V Watson, Bernard J Crespi. Biol Lett 2017
11
27

Williams-Beuren syndrome.
Barbara R Pober. N Engl J Med 2010
436
25

7q11.23 Microduplication: a recognizable phenotype.
A Dixit, S McKee, S Mansour, S G Mehta, G A Tanteles, V Anastasiadou, P C Patsalis, K Martin, S McCullough, M Suri,[...]. Clin Genet 2013
23
16

Social interaction behaviors discriminate young children with autism and Williams syndrome.
Alan J Lincoln, Yvonne M Searcy, Wendy Jones, Catherine Lord. J Am Acad Child Adolesc Psychiatry 2007
57
16

Severe expressive-language delay related to duplication of the Williams-Beuren locus.
Martin J Somerville, Carolyn B Mervis, Edwin J Young, Eul-Ju Seo, Miguel del Campo, Stephen Bamforth, Ella Peregrine, Wayne Loo, Margaret Lilley, Luis A Pérez-Jurado,[...]. N Engl J Med 2005
203
16

The Autism Diagnostic Observation Schedule: revised algorithms for improved diagnostic validity.
Katherine Gotham, Susan Risi, Andrew Pickles, Catherine Lord. J Autism Dev Disord 2007
620
16



Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region.
Jonathan S Berg, Nicola Brunetti-Pierri, Sarika U Peters, Sung-Hae L Kang, Chin-to Fong, Jessica Salamone, Debra Freedenberg, Vickie L Hannig, Lisa Albers Prock, David T Miller,[...]. Genet Med 2007
134
16

Association of GTF2i in the Williams-Beuren syndrome critical region with autism spectrum disorders.
Patrick Malenfant, Xudong Liu, Melissa L Hudson, Ying Qiao, Monica Hrynchak, Noémie Riendeau, M Jeannette Hildebrand, Ira L Cohen, Albert E Chudley, Cynthia Forster-Gibson,[...]. J Autism Dev Disord 2012
45
16

Standardizing ADOS scores for a measure of severity in autism spectrum disorders.
Katherine Gotham, Andrew Pickles, Catherine Lord. J Autism Dev Disord 2009
834
16

Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23.
Emma Strong, Darci T Butcher, Rajat Singhania, Carolyn B Mervis, Colleen A Morris, Daniel De Carvalho, Rosanna Weksberg, Lucy R Osborne. Am J Hum Genet 2015
37
16

7q11.23 Duplication syndrome: Physical characteristics and natural history.
Colleen A Morris, Carolyn B Mervis, Alex P Paciorkowski, Omar Abdul-Rahman, Sarah L Dugan, Alan F Rope, Patricia Bader, Laura G Hendon, Shelley L Velleman, Bonita P Klein-Tasman,[...]. Am J Med Genet A 2015
37
16

Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome.
Nathalie Van der Aa, Liesbeth Rooms, Geert Vandeweyer, Jenneke van den Ende, Edwin Reyniers, Marco Fichera, Corrado Romano, Barbara Delle Chiaie, Geert Mortier, Björn Menten,[...]. Eur J Med Genet 2009
113
16

The importance of genetic diagnosis for Duchenne muscular dystrophy.
Annemieke Aartsma-Rus, Ieke B Ginjaar, Kate Bushby. J Med Genet 2016
120
16

The variant call format and VCFtools.
Petr Danecek, Adam Auton, Goncalo Abecasis, Cornelis A Albers, Eric Banks, Mark A DePristo, Robert E Handsaker, Gerton Lunter, Gabor T Marth, Stephen T Sherry,[...]. Bioinformatics 2011
16

ClinVar: public archive of interpretations of clinically relevant variants.
Melissa J Landrum, Jennifer M Lee, Mark Benson, Garth Brown, Chen Chao, Shanmuga Chitipiralla, Baoshan Gu, Jennifer Hart, Douglas Hoffman, Jeffrey Hoover,[...]. Nucleic Acids Res 2016
16

Diagnostic Testing in Cystic Fibrosis.
John Brewington, J P Clancy. Clin Chest Med 2016
7
28

Analysis of protein-coding genetic variation in 60,706 humans.
Monkol Lek, Konrad J Karczewski, Eric V Minikel, Kaitlin E Samocha, Eric Banks, Timothy Fennell, Anne H O'Donnell-Luria, James S Ware, Andrew J Hill, Beryl B Cummings,[...]. Nature 2016
16

Early intensive behavioral intervention (EIBI) for young children with autism spectrum disorders (ASD).
Brian Reichow, Erin E Barton, Brian A Boyd, Kara Hume. Cochrane Database Syst Rev 2012
171
16

Early behavioral intervention is associated with normalized brain activity in young children with autism.
Geraldine Dawson, Emily J H Jones, Kristen Merkle, Kaitlin Venema, Rachel Lowy, Susan Faja, Dana Kamara, Michael Murias, Jessica Greenson, Jamie Winter,[...]. J Am Acad Child Adolesc Psychiatry 2012
274
16


Early indicators of autism spectrum disorders in the second year of life.
Amy M Wetherby, Juliann Woods, Lori Allen, Julie Cleary, Holly Dickinson, Catherine Lord. J Autism Dev Disord 2004
240
16

A mechanism for impaired fear recognition after amygdala damage.
Ralph Adolphs, Frederic Gosselin, Tony W Buchanan, Daniel Tranel, Philippe Schyns, Antonio R Damasio. Nature 2005
717
16

Long-term outcomes in children with congenital heart disease: National Health Interview Survey.
Hilda Razzaghi, Matthew Oster, Jennita Reefhuis. J Pediatr 2015
56
16

Mechanisms of eye gaze perception during infancy.
Teresa Farroni, Mark H Johnson, Gergely Csibra. J Cogn Neurosci 2004
84
16


History of antibiotics. From salvarsan to cephalosporins.
Lorenzo Zaffiri, Jared Gardner, Luis H Toledo-Pereyra. J Invest Surg 2012
62
16

Heterogeneity and homogeneity across the autism spectrum: the role of development.
Warren Jones, Ami Klin. J Am Acad Child Adolesc Psychiatry 2009
59
16

Regional gray matter growth, sexual dimorphism, and cerebral asymmetry in the neonatal brain.
John H Gilmore, Weili Lin, Marcel W Prastawa, Christopher B Looney, Y Sampath K Vetsa, Rebecca C Knickmeyer, Dianne D Evans, J Keith Smith, Robert M Hamer, Jeffrey A Lieberman,[...]. J Neurosci 2007
284
16

Brain maturation is delayed in infants with complex congenital heart defects.
Daniel J Licht, David M Shera, Robert R Clancy, Gil Wernovsky, Lisa M Montenegro, Susan C Nicolson, Robert A Zimmerman, Thomas L Spray, J William Gaynor, Arastoo Vossough. J Thorac Cardiovasc Surg 2009
344
16

Spatio-temporal transcriptome of the human brain.
Hyo Jung Kang, Yuka Imamura Kawasawa, Feng Cheng, Ying Zhu, Xuming Xu, Mingfeng Li, André M M Sousa, Mihovil Pletikos, Kyle A Meyer, Goran Sedmak,[...]. Nature 2011
16


Costs of autism spectrum disorders in the United Kingdom and the United States.
Ariane V S Buescher, Zuleyha Cidav, Martin Knapp, David S Mandell. JAMA Pediatr 2014
410
16

Extraordinary neoteny of synaptic spines in the human prefrontal cortex.
Zdravko Petanjek, Milos Judaš, Goran Šimic, Mladen Roko Rasin, Harry B M Uylings, Pasko Rakic, Ivica Kostovic. Proc Natl Acad Sci U S A 2011
634
16

Gene hunting in autism spectrum disorder: on the path to precision medicine.
Daniel H Geschwind, Matthew W State. Lancet Neurol 2015
240
16


Naturalistic Developmental Behavioral Interventions: Empirically Validated Treatments for Autism Spectrum Disorder.
Laura Schreibman, Geraldine Dawson, Aubyn C Stahmer, Rebecca Landa, Sally J Rogers, Gail G McGee, Connie Kasari, Brooke Ingersoll, Ann P Kaiser, Yvonne Bruinsma,[...]. J Autism Dev Disord 2015
278
16


A quantitative magnetic resonance imaging study of changes in brain morphology from infancy to late adulthood.
A Pfefferbaum, D H Mathalon, E V Sullivan, J M Rawles, R B Zipursky, K O Lim. Arch Neurol 1994
958
16

Infant viewing of social scenes is under genetic control and is atypical in autism.
John N Constantino, Stefanie Kennon-McGill, Claire Weichselbaum, Natasha Marrus, Alyzeh Haider, Anne L Glowinski, Scott Gillespie, Cheryl Klaiman, Ami Klin, Warren Jones. Nature 2017
94
16

A genome-wide association study of autism using the Simons Simplex Collection: Does reducing phenotypic heterogeneity in autism increase genetic homogeneity?
Pauline Chaste, Lambertus Klei, Stephan J Sanders, Vanessa Hus, Michael T Murtha, Jennifer K Lowe, A Jeremy Willsey, Daniel Moreno-De-Luca, Timothy W Yu, Eric Fombonne,[...]. Biol Psychiatry 2015
83
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.