Williams syndrome is gaining wider popularity in the research field due to its unique characteristics and to the wealth of information it is providing to the Human Genome project.
It is impossible to provide a comprehensive list of active research projects. However, a list of many studies is available through the WS Registry. There are also several research centers around the United States specializing in characteristics of Williams syndrome.
For more information, contact any of the researchers below, or contact the WS Registy with inquiiries on specific research topics that may not be listed here.
RESEARCH GRANT AWARDS
The WSA is happy to review applications for research into all aspects of Williams syndrome. Prior to submitting applications please review the WSA Research Guidelines. All applications should be submitted to the WSA Research Advisory Committee at:firstname.lastname@example.org
- University of Nevada School of Medicine
- University of Louisville
- Boston University
- Yale School of Medicine
- Johns Hopkins University
- Laboratory of Cognitive Neuroscience, Salk Institute
- Vanderbilt University
- The Hospital for Sick Children, Ontario, Canada
- Massachusetts General Hospital
- University of Wisconsin, Milwaukee
Dr. Colleen Morris
conducts studies relating to the "genetics" of WS. Dr. Morris and her team are responsible for the initial discovery of the elastin deletion in WS and continue to work to define the possible other causes of WS (gene inversions) as well as determining the roles of the approximately 20 additional genes in the WS critical area on chromosome #7.
Dr. Carolyn Mervis
conducts clinical research studies primarily devoted to the cognitive processes in WS. Her team is conducting longitudinal studies of Language and Cognition in WS, as well as studies of language in very young children and the relationships between language, cognition and adaptive behavior in Williams syndrome.
Dr. Helen Tager-Flusberg
is conducting clinical research studies of the sociability of individuals with Williams syndrome. Dr. Flusberg's primary studies in this area are with teens and adults with WS.
Dr. Robert Schultz
conducts clinical research into the facial recognition skills of children and adults with WS.
Dr. Barbara Landau
conducts studies into the cognitive processes of adults with WS. Present studies focus on spatial language, and object/motion perception.
Dr. Ursula Bellugi
conducts research with children and adults with WS. Primary focus area is communication. The Salk team studies facial perception in very young children, differences between language and spatial skills in children of ages 7-12, behavior, and visuospatial and social ability in teens and adults. They also study the musicality of individuals with WS in collaboration with Dr. Dan Levitin at McGill University, and a comprehensive study of WS across all disciplines in collaborations with geneticists and Sinai Hospital in Los Angeles and neurologists at Harvard University.
Dr. Elisabeth Dykens
has conducted extensive studies into anxiety in teens and adults with Williams syndrome and is currently looking at Behavioral concerns and the use of music to see how they might interfact.
The Chromosome 7 Project
is part of the Human Genome project and is currently underway at The Centre for Applied Genomics at the Hospital for Sick Children in Toronto, Canada. More information can be found at the Chromosome 7 Project
Dr. Barbara Pober
is conducting studies which will help describe the characteristics (medical and cognitive) of WS in adults.
Bonnie Klein-Tasman, PhD
conducts clinical research studies on the effects of Autism and its characteristics on children with Williams syndrome.