Scholar IQ
Try ScholarIQ free
Upload Records Snowball Search Search OpenAlex
About the database
On this page:OverviewPublicationsResearchersKey papersJournalsOpen accessInstitutions
ScholarIQanswers from OpenAlex

Williams Syndrome Research

TopicLeading institutions, researchers & key papers

This cluster of papers explores the genetic, neurodevelopmental, cognitive, and behavioral aspects of Williams Syndrome. It covers topics such as the cognitive profile, social cognition, visuospatial processing, neuroanatomy, cardiovascular abnormalities, hypersociability, and language abilities associated with Williams Syndrome.

42
Works

How has Williams Syndrome Research's publication output changed over time?

ScholarIQpublication output · 1996–2021

Output grew0% over the shown period — from 1 works in 1996 to 1 in 2021.

1
3
1
2
1
1
1
1
1
199620062007201120152016201920202021

What are the most-cited papers on Williams Syndrome Research?

ScholarIQmost cited works
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
Stephan Sanders, A. Gulhan Ercan‐Sencicek, Vanessa Hus, Rui Luo, Michael T. Murtha, Daniel Moreno‐De‐Luca, Su H. Chu, Michael Moreau, Abha R. Gupta, Susanne Thomson, Christopher E. Mason, Kaya Bilgüvar, Patrícia B. S. Celestino-Soper, Murim Choi, Emily L. Crawford, Lea K. Davis, Nicole R. Davis Wright, Rahul M. Dhodapkar, Michael DiCola, Nicholas M. DiLullo, Thomas Fernandez, Vikram Fielding‐Singh, Daniel O. Fishman, Stephanie Frahm, Rouben Garagaloyan, Gerald Goh, Sindhuja Kammela, Lambertus Klei, Jennifer K. Lowe, Sabata C. Lund, Anna D. McGrew, Kyle A. Meyer, William J. Moffat, John D. Murdoch, Brian J. O’Roak, G Ober, Rebecca S. Pottenger, Melanie J. Raubeson, Youeun Song, Qi Wang, Brian L. Yaspan, Timothy W. Yu, Ilana R. Yurkiewicz, Arthur L. Beaudet, Rita M. Cantor, Martin Curland, Dorothy E. Grice, Murat Günel, Richard P. Lifton, Shrikant Mane, Donna M. Martin, Chad A. Shaw, Michael Sheldon, Jay A. Tischfield, Christopher A. Walsh, Eric M. Morrow, David H. Ledbetter, Éric Fombonne, Catherine Lord, Christa Lese Martin, Andrew I. Brooks, James S. Sutcliffe, Edwin H. Cook, Daniel H. Geschwind, Kathryn Roeder, Bernie Devlin, Matthew W. State
Neuron. 20111,300 CitationsOPEN ACCESS
Mapping brain maturation
Arthur W. Toga, Paul M. Thompson, Elizabeth R. Sowell
S114966740. 2006865 CitationsOPEN ACCESS
More Is Not Always Better: Increased Fractional Anisotropy of Superior Longitudinal Fasciculus Associated with Poor Visuospatial Abilities in Williams Syndrome
Fumiko Hoeft, Naama Barnea‐Goraly, Brian W. Haas, Golijeh Golarai, Derek Ng, Debra L. Mills, Julie R. Korenberg, Ursula Bellugi, Albert M. Galaburda, Allan L. Reiss
Journal of Neuroscience. 2007315 CitationsOPEN ACCESS
Linguistic Abilities in Italian Children With Williams Syndrome
Virginia Volterra, Olga Capirci, Grazia Pezzini, Letizia Sabbadini, Stefano Vicari
Cortex. 1996232 Citations
Periventricular nodular heterotopia and Williams syndrome
Russell J. Ferland, John Gaitanis, Kira Apse, Umadevi Tantravahi, Christopher A. Walsh, Volney Sheen
American Journal of Medical Genetics Part A. 200653 Citations

Where is Williams Syndrome Research research published, and who funds it?

ScholarIQvenues & funding sources

TOP FUNDERS

National Science Foundation
NIH
Wellcome Trust
European Research Council
Funder breakdown is a member featureSign up free to unlock

How much of the research on Williams Syndrome Research is open access?

ScholarIQopen access share
42%OPEN ACCESS
Gold
8%
Green
8%
Hybrid
8%
Bronze
17%
Closed
58%

Related on ScholarIQ

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
Paper
Mapping brain maturation
Paper
Language acquisition in autism spectrum disorders: A developmental review
Paper
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
Paper
Beyond Pragmatics: Morphosyntactic Development in Autism
Paper
Mutations in Cardiac T-Box Factor Gene TBX20 are associated with Diverse Cardiac Pathologies, Including Defects of Septation and Valvulogenesis and Cardiomyopathy
Paper
470M+ articles · free account