How to find us

Table of contents

Address
Public Transport Information
Driving Directions (Apple)
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Driving Directions (Google)
Parking

Address

University of Zurich

Institute of Medical Genetics
Wagistrasse 12
8952 Schlieren
Switzerland

Tel. +41 44 556 33 00
E-mail (HIN secured)

Public Transport Information

The Wagistrasse site is connected to the Zurich transport network by public transport and is within a 5-minute walk from the Gasometerbrücke or Wagonsfabrik tram stops.
Schlieren railway station is also close by and is approx. 10 - 15 minutes' walk from the Wagistrasse.

Tram Stop : Gasometerbrücke & Wagonsfabrik

Tram Lines: 2 & 20

Bus Lines: N17

Plan your travel with :

ZVV

SBB

Driving Directions (Apple)

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Driving Directions (Google)

Parking

Three parking spaces labeled "UZH-Patienten" are reserved for our patients and next to the main entrance of the Wagistrasse-12-building.

Further public (paid) street is available.

News

16 Oct 2024

The new University Children's Hospital Zurich

From 2^ndof November, the Children's Hospital Zurich will be located at a new address.

In the future, your child's ...

More about The new University Children's Hospital Zurich
14 Oct 2024

Shared and unique consequences of Joubert Syndrome gene dysfunction on the zebrafish central nervous system

Joubert Syndrome gene dysfunction in zebrafish leads to abnormal brain cilia, altered transcription of neuron-associated genes and abnormal ...

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20 Sep 2024

Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder

De novo variants in cullin-3 ubiquitin ligase (CUL3) have been strongly associated with neurodevelopmental disorders (NDDs), ...

More about Loss-of-Function Variants in CUL3 Cause a Syndromic Neurodevelopmental Disorder
5 Sep 2024

SMAD4 mutations causing Myhre syndrome are under positive selection in the male germline

While it is widely thought that de novo mutations (DNMs) occur randomly, we previously showed that some DNMs are enriched ...

More about SMAD4 mutations causing Myhre syndrome are under positive selection in the male germline
3 Sep 2024

Nanopore Deep Sequencing as a Tool to Characterize and Quantify Aberrant Splicing Caused by Variants in Inherited Retinal Dystrophy Genes

The contribution of splicing variants to molecular diagnostics of inherited diseases is reported to be less than 10%.

More about Nanopore Deep Sequencing as a Tool to Characterize and Quantify Aberrant Splicing Caused by Variants in Inherited Retinal Dystrophy Genes
22 Aug 2024

Faulty Gene Makes Brain Too Big – or Too Small

A gene called ZNRF3, known to be involved in cancer, also messes with the mind. The human brain relies on two copies of this gene to build a ...

More about Faulty Gene Makes Brain Too Big – or Too Small
19 Aug 2024

Further evidence for an attenuated phenotype of in‐frame DMD deletions affecting the central rod domain of dystrophin around exon 48

Alterations in the X-linked recessive DMD gene cause dystrophinopathies with a broad clinical spectrum most commonly ranging ...

More about Further evidence for an attenuated phenotype of in‐frame DMD deletions affecting the central rod domain of dystrophin around exon 48
16 Aug 2024

Deleterious ZNRF3 germline variants cause neurodevelopmental disorders with mirror brain phenotypes via domain-specific effects on Wnt/β-catenin signaling

Zinc and RING finger 3 (ZNRF3) is a negative-feedback regulator of Wnt/β-catenin signaling, which plays an important role in human brain ...

More about Deleterious ZNRF3 germline variants cause neurodevelopmental disorders with mirror brain phenotypes via domain-specific effects on Wnt/β-catenin signaling