Dominik Seelow
0000-0002-9746-4412
Publication & Citation Trends
Publications
0 total
DNAvi: integration, statistics, and visualization of cell-free DNA fragment traces
Cited by 0
Semantic Scholar
A biallelic MRPL42 variant causes a combined oxidative phosphorylation deficiency syndrome revealed by multi-omics
Cited by 0
Semantic Scholar
REEV: review, evaluate and explain variants OA
Cited by 4
Semantic Scholar
Drawing human pedigree charts with DrawPed OA
Cited by 0
Semantic Scholar
Normal Values for the fT3/fT4 Ratio: Centile Charts (0–29 Years) and Their Application for the Differential Diagnosis of Children with Developmental Delay OA
Cited by 3
Semantic Scholar
The 22nd annual Nucleic Acids Research Web Server Issue 2024 OA
Cited by 1
Semantic Scholar
Loss-of-function variants affecting the STAGA complex component SUPT7L cause a developmental disorder with generalized lipodystrophy OA
Cited by 4
Semantic Scholar
Editorial: the 21st annual Nucleic Acids Research Web Server Issue 2023 OA
Cited by 1
Semantic Scholar
The Human Phenotype Ontology in 2024: phenotypes around the world OA
Cited by 282
Semantic Scholar
Research Topics
Genomics and Rare Diseases
(35)
Genomics and Chromatin Dynamics
(14)
Genomics and Phylogenetic Studies
(13)
RNA modifications and cancer
(13)
RNA Research and Splicing
(12)
Affiliations
University of Bern
Max Planck Society
University of Cologne
Friedrich-Alexander-Universität Erlangen-Nürnberg
Humboldt-Universität zu Berlin