Miriam S Reuter

8PUBLICATIONS
76CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Aerodynamics (excl. hypersonic aerodynamics)Anthropological geneticsDevelopmental genetics (incl. sex determination)
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Publications (8)

|Mar 14, 2025
Variants in ATP6V0C are associated with Dravet-like developmental and epileptic encephalopathy.

Marlene Rong, Paula T Marques, Quratulain Zulfiqar Ali

|Aug 29, 2023
CUX1-related neurodevelopmental disorder: deep insights into phenotype-genotype spectrum and underlying pathology.

Henry Oppermann, Elia Marcos-Grañeda, Linnea A Weiss

|Jul 22, 2023
Decreased left heart flow in fetal lambs causes left heart hypoplasia and pro-fibrotic tissue remodeling.

Miriam S Reuter, Dustin J Sokolowski, J Javier Diaz-Mejia

|Oct 30, 2022
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder.

Ada J S Chan, Worrawat Engchuan, Miriam S Reuter

|Mar 19, 2022
Biallelic PAN2 variants in individuals with a syndromic neurodevelopmental disorder and multiple congenital anomalies.

Miriam S Reuter, Michael Zech, Maja Hempel

|Nov 05, 2021
A recurrent SHANK3 frameshift variant in Autism Spectrum Disorder.

Livia O Loureiro, Jennifer L Howe, Miriam S Reuter

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Frequent Collaborators

5 joint publications

Stephen W Scherer

3 joint publications

Brett Trost

2 joint publications

Jacob Vorstman

1 joint publications

Raymond H Kim