Vera M Kalscheuer

16PUBLICATIONS
140CO-AUTHORS
Microelectromechanical systems (MEMS)NeonatologyGene mappingStructural properties of condensed matterGene expression (incl. microarray and other genome-wide approaches)
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Publications (16)

|May 27, 2025
MCT8 Deficiency in Females.

Stefan Groeneweg, Ferdy S van Geest, Floor van der Most

|Nov 29, 2023
Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome.

Jérémie Courraud, Camille Engel, Angélique Quartier

|Nov 15, 2023
Single-cell, whole-embryo phenotyping of mammalian developmental disorders.

Xingfan Huang, Jana Henck, Chengxiang Qiu

|Feb 09, 2023
Aberrant phase separation and nucleolar dysfunction in rare genetic diseases.

Martin A Mensah, Henri Niskanen, Alexandre P Magalhaes

|Dec 23, 2022
Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models.

Hamid Meziane, Marie-Christine Birling, Olivia Wendling

|Nov 17, 2022
Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition.

Elizabeth E Palmer, Michael Pusch, Alessandra Picollo

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Frequent Collaborators

2 joint publications

Amélie Piton

2 joint publications

Ingo Kurth

2 joint publications

Jozef Gecz

2 joint publications

Stefan Mundlos