Concepedia

Author

Magdalena Danyel

Charité - Universitätsmedizin BerlinORCID

Also Known As

M. Danyel, Magdalena Danyel

33

Publications

553

Citations

11

H-Index

29

Concepts

All Affiliations

Charité - Universitätsmedizin BerlinBerlin Institute of Health at Charité - Universitätsmedizin BerlinHumboldt-Universität zu BerlinUniversity of BonnUniversity of Tübingen
MD

About

Magdalena Danyel is an author at Charité - Universitätsmedizin Berlin specializing in medicine, bioinformatics, and epidemiology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

4

4

251

2

Epidemiology

2

2

37

3

Engineering

1

1

15

4

Public Health

1

1

22

5

Biostatistics

1

1

22

Magdalena Danyel

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11

Publications

485

Citations

11

H-Index

YearCitations

GestaltMatcher facilitates rare disease matching using facial phenotype descriptors

Tzung‐Chien Hsieh, Aviram Bar-Haim, Shahida Moosa,

Nature Genetics

2022

195

PEDIA: prioritization of exome data by image analysis

Tzung‐Chien Hsieh, Martin A. Mensah, Jean Tori Pantel,

Genetics in Medicine

2019

86

Efficiency of Computer-Aided Facial Phenotyping (DeepGestalt) in Individuals With and Without a Genetic Syndrome: Diagnostic Accuracy Study

Jean Tori Pantel, Nurulhuda Hajjir, Magdalena Danyel,

Journal of Medical Internet Research

2020

36

CADA: phenotype-driven gene prioritization based on a case-enriched knowledge graph

Chengyao Peng, Simon Dieck, Alexander Schmid,

NAR Genomics and Bioinformatics

2021

36

Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings

Axel Schmidt, Magdalena Danyel, Kathrin Grundmann,

Nature Genetics

2024

34

GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases

Hellen Lesmann, Alexander Hustinx, Shahida Moosa,

2023

22

Evaluation of the role of STAP1 in Familial Hypercholesterolemia

Magdalena Danyel, Claus‐Eric Ott, Thomas Grenkowitz,

Scientific Reports

2019

20

Autosomal dominant Robinow syndrome associated with a novel <i>DVL3</i> splice mutation

Magdalena Danyel, Fanny Kortüm, Katarina Dathe,

American Journal of Medical Genetics Part A

2018

19

Next-generation phenotyping integrated in a national framework for patients with ultra-rare disorders improves genetic diagnostics and yields new molecular findings

Axel Schmidt, Magdalena Danyel, Kathrin Grundmann,

2023

15

Three-Dimensional Histological Characterization of the Placental Vasculature Using Light Sheet Microscopy

Lennart Freise, Rose Yinghan Behncke, Hanna Allerkamp,

Biomolecules

2023

11

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