E-LIB Suche - Ergebnisse für: Hsieh, Tzung Chien

1

GANonymization: A GAN-based Face Anonymization Framework fo..:

Hellmann, Fabio ; Mertes, Silvan ; Benouis, Mohamed...
ACM Transactions on Multimedia Computing, Communications, and Applications. , 2024

Link: https://doi.org/10.1145/..

2

Enhancing Variant Prioritization in VarFish through On-Prem..:

Bhasin, Meghna Ahuja ; Knaus, Alexej ; Incardona, Pietro...
Genes. 15 (2024) 3 - p. 370 , 2024

Link: https://doi.org/10.3390/..

3

ZSCAN10 deficiency causes a neurodevelopmental disorder wit..:

Laugwitz, Lucia ; Cheng, Fubo ; Collins, Stephan C...
Brain. 147 (2024) 7 - p. 2471-2482 , 2024

Link: https://doi.org/10.1093/..

4

Comparison of clinical geneticist and computer visual atten..:

Duong, Dat ; Johny, Anna Rose ; Ledgister Hanchard, Suzanna...
PLOS Genetics. 20 (2024) 2 - p. e1011168 , 2024

Link: https://doi.org/10.1371/..

5

Deeplasia: deep learning for bone age assessment validated ..:

Rassmann, Sebastian ; Keller, Alexandra ; Skaf, Kyra...
Pediatric Radiology. 54 (2023) 1 - p. 82-95 , 2023

Link: https://doi.org/10.1007/..

6

P238: Discovery of the phenotypic landscape and mechanistic..:

Lyon, Gholson ; Vedaie, Marall ; Beisheim, Travis...
Genetics in Medicine Open. 1 (2023) 1 - p. 100266 , 2023

Link: https://doi.org/10.1016/..

7

Delineation of the adult phenotype of Coffin–Siris syndrome..:

Schmetz, Ariane ; Lüdecke, Hermann-Josef ; Surowy, Harald...
Human Genetics. 143 (2023) 1 - p. 71-84 , 2023

Link: https://doi.org/10.1007/..

8

PHIP-associated Chung-Jansen syndrome: Report of 23 new ind..:

Kampmeier, Antje ; Leitão, Elsa ; Parenti, Ilaria...
Frontiers in Cell and Developmental Biology. 10 (2023) - p. , 2023

Link: https://doi.org/10.3389/..

9

Biallelic variants in CRIPT cause a Rothmund-Thomson-like s..:

Averdunk, Luisa ; Huetzen, Maxim A. ; Moreno-Andrés, Daniel...
Genetics in Medicine. 25 (2023) 7 - p. 100836 , 2023

Link: https://doi.org/10.1016/..

10

Expanding the phenotypic spectrum of NAA10-related neurodev..:

Lyon, Gholson J. ; Vedaie, Marall ; Beisheim, Travis...
European Journal of Human Genetics. 31 (2023) 7 - p. 824-833 , 2023

Link: https://doi.org/10.1038/..

11

Trans-ancestry polygenic models for the prediction of LDL b..:

Hassanin, Emadeldin ; Lee, Ko-Han ; Hsieh, Tzung-Chien...
Frontiers in Genetics. 14 (2023) - p. , 2023

Link: https://doi.org/10.3389/..

12

O17: GestaltMatcher supports classification of ultra-rare d..:

Klinkhammer, Hannah ; Lesmann, Hellen ; Moosa, Shahida...
Genetics in Medicine Open. 1 (2023) 1 - p. 100113 , 2023

Link: https://doi.org/10.1016/..

13

Improving Deep Facial Phenotyping for Ultra-rare Disorder V..:

, In: 2023 IEEE/CVF Winter Conference on Applications of Computer Vision (WACV),

Hustinx, Alexander ; Hellmann, Fabio ; Sumer, Omer... - p. 5007-5017 , 2023

Link: https://doi.org/10.1109/..

14

De novo variants of CSNK2B cause a new intellectual disabil..:

Asif, Maria ; Kaygusuz, Emrah ; Shinawi, Marwan...
Human Genetics and Genomics Advances. 3 (2022) 3 - p. 100111 , 2022

Link: https://doi.org/10.1016/..

15

eP182: KBG syndrome: Prospective videoconferencing and use ..:

Lyon, Gholson ; Guo, Lily ; Park, Jiyeon...
Genetics in Medicine. 24 (2022) 3 - p. S112-S113 , 2022

Link: https://doi.org/10.1016/..