Dominik Seelow

Professor

Germany

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About

Professor Dominik Seelow is a faculty member at the Berliner Institut für Gesundheitsforschung in Germany. His research areas encompass bioinformatics, human pedigree analysis, and developmental disorders, as reflected in his recent publications. His work includes studies on gene expression, alternative splicing, and the Human Phenotype Ontology. He is actively contributing to the advancement of genetic research and its applications in clinical settings.

Articles (19)

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2024

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2024

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2024

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2024

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2024

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2024

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2023

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2023

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2022

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2022

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2022

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2022

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2022

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2022

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2022

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2022

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2022

Collaborators (17)

Maud de Dieuleveult

INSERM

FRANCE

Dominik Seelow

Research Interests

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Articles (19)

Normal Values for the fT3/fT4 Ratio: Centile Charts (0–29 Years) and Their Application for the Differential Diagnosis of Children with Developmental Delay

REEV: review, evaluate and explain variants.

The Human Phenotype Ontology in 2024

Analysis of Regions of Homozygosity: Revisited Through New Bioinformatic Approaches

Drawing human pedigree charts with DrawPed

The 22nd annual Nucleic Acids Research Web Server Issue 2024

Alternative splicing is coupled to gene expression in a subset of variably expressed genes.

Loss-of-function variants affecting the STAGA complex component SUPT7L cause a developmental disorder with generalized lipodystrophy.

Editorial: the 21st annual Nucleic Acids Research Web Server Issue 2023

Discovery of a non-canonical GRHL1 binding site using deep convolutional and recurrent neural networks

AutozygosityMapper: Identification of disease-mutations in consanguineous families

AutozygosityMapper: Identification of disease-mutations in consanguineous families

Deep phenotyping: symptom annotation made simple with SAMS

Deep phenotyping: symptom annotation made simple with SAMS

Editorial: the 20th annual Nucleic Acids Research Web Server Issue 2022

FABIAN-variant: predicting the effects of DNA variants on transcription factor binding

FABIAN-variant: predicting the effects of DNA variants on transcription factor binding

Biallelic truncating variants in ATP9A cause a novel neurodevelopmental disorder involving postnatal microcephaly and failure to thrive

Biallelic truncating variants in ATP9A cause a novel neurodevelopmental disorder involving postnatal microcephaly and failure to thrive

Collaborators (17)

Maud de Dieuleveult

Roma Thamm

Kamyar Keramatian

Felix Boschann

Evelyn Seelow

Peter Robinson

Pablo Botas

Nina-Maria Wilpert

Guiomar Perez de Nanclares

Marek Turnovec

Kai Schmidt-Ott

Andranik Ivanov

Rachel Gore Moses

Eduard Bakštein

nefize yalin

Maria Rutkiewicz

Rebecca Strawbridge

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