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Scopus Author ID: 57207947602

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Employment (1)

Rigshospitalet: Copenhagen, DK

2018-10-15 to present (Department of Clinical Genetics)
Employment
Source: Self-asserted source
Mathis Hildonen

Education and qualifications (2)

University of Copenhagen: Copenhagen, DK

2024 | PhD
Education
Source: Self-asserted source
Mathis Hildonen

University of Copenhagen: Copenhagen, DK

2018 | MSc Biology
Education
Source: Self-asserted source
Mathis Hildonen

Works (9)

DNA methylation profiling in Kabuki syndrome: reclassification of germline KMT2D VUS and sensitivity in validating postzygotic mosaicism

European Journal of Human Genetics
2024-07 | Journal article
DOI: 10.1038/s41431-024-01597-9
Contributors: Marcello Niceta; Andrea Ciolfi; Marco Ferilli; Lucia Pedace; Camilla Cappelletti; Claudia Nardini; Mathis Hildonen; Luigi Chiriatti; Evelina Miele; Maria Lisa Dentici et al.
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Crossref

DNA methylation signature classification of rare disorders using publicly available methylation data

Clinical Genetics
2023-06 | Journal article
DOI: 10.1111/cge.14304
Contributors: Mathis Hildonen; Marco Ferilli; Tina Duelund Hjortshøj; Morten Dunø; Lotte Risom; Mads Bak; Jakob Ek; Rikke S. Møller; Andrea Ciolfi; Marco Tartaglia et al.
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Germline (epi)genetics reveals high predisposition in females: a 5-year, nationwide, prospective Wilms tumour cohort.

Journal of medical genetics
2023-04-05 | Journal article
DOI: 10.1136/jmg-2022-108982
PMID: 37019617
Contributors: ulrik stoltze; Hildonen M; Hansen TVO; Foss-Skiftesvik J; Byrjalsen A; Lundsgaard M; Pignata L; Grønskov K; Tumer AZ; Schmiegelow K et al.
Source: Self-asserted source
Mathis Hildonen

Involvement of Mitochondrial Dysfunction in FOXG1 Syndrome

Genes
2023-01-17 | Journal article
DOI: 10.3390/genes14020246
Contributors: Victoria A. Bjerregaard; Amanda M. Levy; Mille S. Batz; Ravina Salehi; Mathis Hildonen; Trine B. Hammer; Rikke S. Møller; Claus Desler; Zeynep Tümer
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High Resolution Analysis of DMPK Hypermethylation and Repeat Interruptions in Myotonic Dystrophy Type 1

Genes
2022-05-28 | Journal article
DOI: 10.3390/genes13060970
Contributors: Astrid Rasmussen; Mathis Hildonen; John Vissing; Morten Duno; Zeynep Tümer; Ulf Birkedal
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EWAS of Monozygotic Twins Implicate a Role of mTOR Pathway in Pathogenesis of Tic Spectrum Disorder

Genes
2021-09-26 | Journal article
DOI: 10.3390/genes12101510
Contributors: Mathis Hildonen; Amanda M. Levy; Christine Søholm Hansen; Jonas Bybjerg-Grauholm; Axel Skytthe; Nanette M. Debes; Qihua Tan; Zeynep Tümer
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Elevated Expression of SLC6A4 Encoding the Serotonin Transporter (SERT) in Gilles de la Tourette Syndrome

Genes
2021-01-12 | Journal article
DOI: 10.3390/genes12010086
Contributors: Mathis Hildonen; Amanda M. Levy; Christina Dahl; Victoria A. Bjerregaard; Lisbeth Birk Møller; Per Guldberg; Nanette M. Debes; Zeynep Tümer
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Stable Longitudinal Methylation Levels at the CpG Sites Flanking the CTG Repeat of <i>DMPK</i> in Patients with Myotonic Dystrophy Type 1

Genes
2020-08 | Journal article | Author
DOI: 10.3390/genes11080936
Contributors: Mathis Hildonen; Kirsten Lykke Knak; Morten Dunø; John Vissing; Zeynep Tumer
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Multidisciplinary Digital Publishing Institute
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A comparison of storage methods for gut microbiome studies in teleosts: Insights from rainbow trout (Oncorhynchus mykiss)

Journal of Microbiological Methods
2019 | Journal article
DOI: 10.1016/j.mimet.2019.03.010
EID:

2-s2.0-85063323753

Part of ISBN:

18728359 01677012
Contributors: Hildonen, M.; Kodama, M.; Puetz, L.C.; Gilbert, M.T.P.; Limborg, M.T.
Source: Self-asserted source
Mathis Hildonen via Scopus - Elsevier
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