University of Wisconsin–Madison

Category: 2019

21st century medicine helps Amish deal with rare, inherited illnesses

There is no car in the driveway, neither phone nor electricity in the house. Handmade clothes dry on the line. It’s fall 2018, and La Farge physician James DeLine has brought us to talk with Barbara and Daniel Hochstetler, part of the large Amish population in Wisconsin’s Driftless Region.

New funding for Down syndrome research and biobank

The Waisman Center is one of 25 recipients to receive funding through a National Institutes of Health (NIH) grant that focuses on advancing research on Down syndrome. The grant is part of the NIH Investigation of Co-occurring Conditions Across the Lifespan to Understand Down Syndrome (INCLUDE) project. INCLUDE is a trans-NIH effort that will fund …

Joan Ershler, PhD, longtime Waisman Early Childhood Program (WECP) director retires

After 27 years as the director of the Waisman Early Childhood Program (WECP), Joan Ershler, PhD, retired in early September 2019. The WECP is a model inclusive early childhood program with a developmentally diverse enrollment serving children with special needs alongside their typically developing peers. Under her leadership, the program grew substantially. The number of children …

Ann Marie Lauritzen, MMSW, MEd, named Waisman Early Childhood Program director

On September 23, the Waisman Center welcomed Ann Marie Lauritzen, MMSW, M.Ed, as the new director of the Waisman Early Childhood Program. She succeeds Joan Ershler, PhD, who retired at the beginning of September after 27 years of service. “I am excited to work with such a positive, caring and devoted staff,” Lauritzen says. “Supporting …

CMT advocate will not be sidelined

CMT is equally common among all ages, genders, and races and is one of the most common heritable neurological impairments. The symptoms present as neuropathy, foot drop, poor balance, difficulty with dexterity, or abnormal sensation – just to name a few.

Electronic records pin broad set of health risks on genetic premutation

It was long believed the FMR1 premutation — an excessive number of trinucleotide repeats in the FMR1 gene — had no direct effect on the people who carry it. Until recently, the only recognized effect on the carriers of the flawed gene was the risk of having offspring with fragile X syndrome, a rare but serious form of developmental disability.

Emotion-detection applications built on outdated science, report warns

Facial Movements Are Unreliable Signals of Emotion, Researchers Say Software that purportedly reads emotions in faces is being deployed or tested for a variety of purposes,  including surveillance, hiring, clinical diagnosis, and market research. But a new scientific report finds that facial movements are an inexact gauge of a person’s feelings, behaviors or intentions. “It …

Archery event raises funds for autism research

The nonprofit Hononegah Archery is hosting the second annual Julie’s Archers for Autism and Rock River Music festival from noon-9 p.m. on Aug. 3 at Settlers Park in Rockton. Funds raised will support autism research at the Waisman Center. Read the full story here: Archery event raises funds for autism research  

Athletes from Special Olympics add important perspectives to research

For many, a mention of Special Olympics invokes images of accomplished athletes, a community of inclusion and support, and the joy of athletic competition. But what many may not know is that Special Olympics is the world’s largest public health organization for individuals with intellectual disabilities. Research shows that individuals with disabilities experience high rates …

Waisman Center launches new fund to advance intellectual and developmental disabilities genomics research

The Waisman Center, University of Wisconsin-Madison, launched a new fund to support interdisciplinary research in the area of intellectual and developmental disabilities (IDD) genomics.