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Mangold, Elisabeth
261
results:
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Format
Online (260)
Print (1)
Mediatypes
Books (1)
Articles (Online) (103)
OpenAccess-fulltext (155)
Thesis (Online) (2)
Languages
german (2)
english (245)
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1
A syndromic neurodevelopmental disorder caused by rare vari..:
Paul, Maimuna S.
;
Michener, Sydney L.
;
Pan, Hongling
...
The American Journal of Human Genetics. 111 (2024) 1 - p. 96-118 , 2024
Link:
https://doi.org/10.1016/..
?
2
A syndromic neurodevelopmental disorder caused by rare vari..:
Paul, Maimuna S.
;
Michener, Sydney L.
;
Pan, Hongling
...
The American Journal of Human Genetics. 111 (2024) 6 - p. 1239 , 2024
Link:
https://doi.org/10.1016/..
?
3
A syndromic neurodevelopmental disorder caused by rare vari..:
Paul, Maimuna S.
;
Michener, Sydney L.
;
Pan, Hongling
...
The American Journal of Human Genetics. 111 (2024) 4 - p. 805 , 2024
Link:
https://doi.org/10.1016/..
?
4
Analysis of candidate genes for cleft lip ± cleft palate us..:
Siewert, Anna
;
Reiz, Benedikt
;
Krug, Carina
...
Frontiers in Cell and Developmental Biology. 11 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
5
Prioritization of non-coding elements involved in non-syndr..:
Zieger, Hanna K.
;
Weinhold, Leonie
;
Schmidt, Axel
...
Human Genetics and Genomics Advances. 4 (2023) 1 - p. 100166 , 2023
Link:
https://doi.org/10.1016/..
?
6
GestaltMatcher facilitates rare disease matching using faci..:
Hsieh, Tzung-Chien
;
Bar-Haim, Aviram
;
Moosa, Shahida
...
Nature Genetics. 54 (2022) 3 - p. 349-357 , 2022
Link:
https://doi.org/10.1038/..
?
7
Molecular Genetic Screening in Patients With ACE Inhibitor/..:
Mathey, Carina M.
;
Maj, Carlo
;
Scheer, Annika B.
...
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
8
Allele-specific transcription factor binding in a cellular ..:
Ruff, Katharina L. M.
;
Hollstein, Ronja
;
Fazaal, Julia
...
Scientific Reports. 12 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1038/..
?
9
Next‐generation phenotyping contributing to the identificat..:
Brand, Fabian
;
Vijayananth, Aswinkumar
;
Hsieh, Tzung‐Chien
...
Human Mutation. 43 (2022) 11 - p. 1659-1665 , 2022
Link:
https://doi.org/10.1002/..
?
10
Using CRISPR/Cas9 genome editing in human iPSCs for deciphe..:
Pilz, Robin A.
;
Skowronek, Dariush
;
Hamed, Motaz
...
Frontiers in Molecular Biosciences. 9 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
11
The impact of economic prosperity on treatment protocols fo..:
Hellmann, Juliane
, 2021
Link:
https://nbn-resolving.de..
?
12
Manchmal hilft nur ein Blick indie Gene weiter:
Mangold, Elisabeth
;
Kreiß, Martina
Pädiatrie. 33 (2021) S2 - p. 52-55 , 2021
Link:
https://doi.org/10.1007/..
?
13
Integrative approaches generate insights into the architect..:
Welzenbach, Julia
;
Hammond, Nigel L.
;
Nikolić, Miloš
...
Human Genetics and Genomics Advances. 2 (2021) 3 - p. 100038 , 2021
Link:
https://doi.org/10.1016/..
?
14
Extending the allelic spectrum at noncoding risk loci of or..:
Thieme, Frederic
;
Henschel, Leonie
;
Hammond, Nigel L.
...
Human Mutation. 42 (2021) 8 - p. 1066-1078 , 2021
Link:
https://doi.org/10.1002/..
?
15
Evaluating shared genetic influences on nonsyndromic cleft ..:
Howe, Laurence J.
;
Hemani, Gibran
;
Lesseur, Corina
...
Genetic Epidemiology. 44 (2020) 8 - p. 924-933 , 2020
Link:
https://doi.org/10.1002/..
1-15
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