Laura Pölsler
5PUBLICATIONS
53CO-AUTHORS
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Publications (5)
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|Oct 15, 2025
Genetic variants associated with ventricular arrhythmias during ajmaline test in Brugada syndrome.Charles Audiat, Luigi Pannone, Antonio Sorgente
|Jul 02, 2025
The European Certificate in Medical Genetics and Genomics (ECMGG).Peter D Turnpenny, Laura Pölsler, Ute Moog
|Nov 17, 2022
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition.Elizabeth E Palmer, Michael Pusch, Alessandra Picollo
|Mar 19, 2022
Biallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomalies.Miriam S Reuter, Michael Zech, Maja Hempel
|Jan 09, 2020
A Syrian patient with Steel syndrome due to compound heterozygous COL27A1 mutations with colobomata of the eye.Laura Pölsler, Ulrich A Schatz, Burkhard Simma
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Frequent Collaborators
1 joint publications
Miriam S Reuter
1 joint publications
René Santer
1 joint publications
Brett Trost
1 joint publications
Stephen W Scherer
1 joint publications
Anne S Bassett
1 joint publications
Davor Lessel
1 joint publications
Elizabeth E Palmer
1 joint publications
Michael Pusch
1 joint publications
Claire Beneteau
1 joint publications
Fowzan S Alkuraya
