Oliver Küchler

2PUBLICATIONS
20CO-AUTHORS
NeurogeneticsDevelopmental genetics (incl. sex determination)
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Publications (2)

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|Jun 26, 2026
Identification of biallelic loss-of-function PREP variants in three individuals with syndromic intellectual disability.

|Apr 09, 2024
Loss-of-function variants affecting the STAGA complex component SUPT7L cause a developmental disorder with generalized lipodystrophy.

Johannes Kopp, Leonard A Koch, Hristiana Lyubenova

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Frequent Collaborators

2 joint publications

Johannes Kopp

2 joint publications

Björn Fischer-Zirnsak

1 joint publications

Leonard A Koch

1 joint publications

Hristiana Lyubenova

1 joint publications

Manuel Holtgrewe

1 joint publications

Andranik Ivanov

1 joint publications

Christele Dubourg

1 joint publications

Erika Launay

1 joint publications

Sebastian Brachs

1 joint publications

Stefan Mundlos

Frequent Collaborators

2 joint publications

Johannes Kopp

2 joint publications

Björn Fischer-Zirnsak

1 joint publications

Leonard A Koch

1 joint publications

Hristiana Lyubenova

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