# <i>De novo</i> variants in neurodevelopmental disorders—experiences from a tertiary care center

**Type:** Papers  
**Canonical URL:** https://scholariq.org/papers/i-de-novo-i-variants-in-neurodevelopmental-disorders-experiences-from-a-tertiary/

## Facts

| Field | Value |
| --- | --- |
| Author Names | Theresa Brunet,Robert Jech,Melanie Brügger,Reka Kovacs,Bader Alhaddad,Gloria Leszinski,Korbinian M. Riedhammer,Dominik S. Westphal,Isabella Mahle,Katharina Mayerhanser,Matěj Škorvánek,Sandrina Weber,Elisabeth Graf,Riccardo Berutti,Ján Necpál,Petra Havránková,Petra Pavelekova,Maja Hempel,Urania Kotzaeridou,Georg F. Hoffmann,Steffen Leiz,Christine Makowski,Timo Roser,A. Sebastian Schroeder,Robert Steinfeld,Gertrud Strobl‐Wildemann,Julia Hoefele,Ingo Borggraefe,Felix Distelmaier,Tim M. Strom,Juliane Winkelmann,Thomas Meitinger,Michael Zech,Matias Wagner |
| Citations | 124 |
| DOI | 10.1111/cge.13946 |
| Fields | Biochemistry, Genetics and Molecular Biology,Neuroscience |
| Open Access | true |
| OA Status | hybrid |
| OA URL | https://onlinelibrary.wiley.com/doi/pdfdirect/10.1111/cge.13946 |
| OpenAlex ID | https://openalex.org/W3132674838 |
| PMID | 33619735 |
| Type | article |
| Year | 2021 |

## Paper authors

- [Matias Wagner](https://scholariq.org/researchers/matias-wagner/)

## Paper primary topic

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)

## Paper topics

- [Genomics and Rare Diseases](https://scholariq.org/topics/genomics-and-rare-diseases/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)
- [Autism Spectrum Disorder Research](https://scholariq.org/topics/autism-spectrum-disorder-research/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.