André Schaller

5PUBLICATIONS
21CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Anthropological geneticsOptical technologyDevelopmental genetics (incl. sex determination)
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Publications (5)

|Jun 27, 2024
SwissGenVar: A Platform for Clinical-Grade Interpretation of Genetic Variants to Foster Personalized Healthcare in Switzerland.

Dennis Kraemer, Dillenn Terumalai, Maria Livia Famiglietti

|Apr 13, 2023
Biallelic variants in DNA2 cause poikiloderma with congenital cataracts and severe growth failure reminiscent of Rothmund-Thomson syndrome.

Ricardo Di Lazzaro Filho, Guilherme Lopes Yamamoto, Tiago J Silva

|Jul 29, 2018
Neutrophil extracellular trap formation requires OPA1-dependent glycolytic ATP production.

Poorya Amini, Darko Stojkov, Andrea Felser

|Jun 13, 2018
Broad phenotypes in heterozygous NR5A1 46,XY patients with a disorder of sex development: an oligogenic origin?

Núria Camats, Mónica Fernández-Cancio, Laura Audí

|Mar 02, 2017
Characterization of two novel intronic OPA1 mutations resulting in aberrant pre-mRNA splicing.

Ramona Bolognini, Christina Gerth-Kahlert, Mathias Abegg

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Frequent Collaborators

1 joint publications

Núria Camats

1 joint publications

Andrea Felser

1 joint publications

Christopher B Jackson

1 joint publications

Maria Eugenia Soriano