Sensathon 2026 – Searching for answers together
On April 10th, Susanne Roosing, Rob Collin and Sterre Mulder of the LifeLong Vision consortium organized with Mechteld van Olden and Dirk Wijn the Sensathon, during the Hearing & Vision 4 All research program day at Radboudumc.
During this hackathon, multidisciplinary teams worked on selected genetically undiagnosed cases, focusing on inherited retinal diseases and deafness. The strength of this initiative lies in the collaboration between the department of Human genetics, Ophthalmology, and ENT—bringing together complementary expertise to drive new insights and advances in diagnosis and patient care.
We are excited that colleagues from LifeLong Vision Yara Lechanteur, Jessie Hendriks, Merel Stemerdink, Lynn van Summeren, Rens Hoekstra, Valentin Del Cura Mrugcaz have contributed to this effort, alongside many other experts.
💡 The outcome has been rewarding! The day has yielded several new leads, and requests for additional clinical or functional tests have been made and even an urgent intervention in clinical care was addressed.
Related news items

PI Progress Meeting and Scientific Advisory Board Visit
16 July 2026We were delighted to welcome Kapil Bharti and Anneke den Hollander to the Netherlands for our PI Progress Meeting. This provided a valuable opportunity for scientific exchange, strategic reflection, and interaction with consortium members.
go to pageFirst Summer School Brings Together Young Researchers for Two Inspiring Days
7 July 2026On Thursday 25 and Friday 26 June, we successfully hosted our first Summer School. Despite taking place during the hottest days of June, the enthusiasm and engagement of all participants made it a great success!
go to page
Making Science Visible
20 June 2026Award winning photograph by researcher Ivar Noordstra (Radboudumc) has attracted national attention. [ad.nl]
go to page
2nd Lifelong VISION Amsterdam seminar
28 May 2026On the 16th of April, the 2nd Lifelong Vision Amsterdam seminar brought our community together in a brisk afternoon of curiosity and collaboration.
go to page
Breakthrough in Research on Inherited Blindness!
12 January 2026Researchers at Radboudumc have discovered a new genetic cause of retinitis pigmentosa (RP) — an eye disease affecting about 1 in 5,000 people worldwide, often leading to tunnel vision and eventually complete blindness.
go to pageZohreh Hosseinzadeh at BMPN Annual meeting
24 November 2025At the BMPN Annual meeting Zohreh Hosseinzadeh presented Lifelong Vision as an example of promoting collaboration between clinical practice and scientific research.
go to page