E-LIB Suche - Ergebnisse für: Sophia Schneider

1

Exome sequencing identifies a likely causative variant in 5..:

Deutsch, Konstantin ; Klämbt, Verena ; Kitzler, Thomas M....
Genes & Diseases. 11 (2024) 5 - p. 101111 , 2024

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

2

PKD1L1 Is Involved in Congenital Chylothorax:

Whitchurch, Jonathan B. ; Schneider, Sophia ; Hilger, Alina C....
Cells. 13 (2024) 2 - p. 149 , 2024

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

3

Expanding the spectrum of novel candidate genes using trio ..:

Schneider, Ronen ; Shril, Shirlee ; Buerger, Florian...
Genes & Diseases. , 2024

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

4

Exome Survey and Candidate Gene Re-Sequencing Identifies No..:

Köllges, Ricarda ; Stegmann, Jil ; Schneider, Sophia...
Biomolecules. 13 (2023) 7 - p. 1117 , 2023

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

5

New ways to cope with depression—study protocol for a rando..:

Kind, Leona ; Luttenberger, Katharina ; Leßmann, Vivien...
Trials. 24 (2023) 1 - p. , 2023

Link: https://doi.org/10.1186/..

6

Active learning for extracting surgomic features in robot-a..:

Brandenburg, Johanna M. ; Jenke, Alexander C. ; Stern, Antonia...
Surgical Endoscopy. 37 (2023) 11 - p. 8577-8593 , 2023

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

7

From Data to Human-Readable Requirements: Advancing Require..:

Harth, Pascal ; Jähde, Orlando ; Schneider, Sophia..
Algorithms. 16 (2023) 9 - p. 403 , 2023

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

8

A homozygous truncating ETV4 variant in a Nigerian family w..:

Kolvenbach, Caroline M. ; Zheng, Bixia ; Merz, Lea M....
American Journal of Medical Genetics Part A. 191 (2023) 5 - p. 1355-1359 , 2023

Link: https://doi.org/10.1002/..

9

Recessive CHRM5 variant as a potential cause of neurogenic ..:

Schneider, Sophia ; Schierbaum, Luca ; Burger, Wessel A. C....
American Journal of Medical Genetics Part A. 191 (2023) 8 - p. 2083-2091 , 2023

Link: https://doi.org/10.1002/..

10

Aufschlussreicher Abschied: Exit-Gespräche:

Ion, Frauke ; Schneider, Sophia
ManagerSeminare. , 2022

Copies: TB Nautik Z 91/7; TB Nautik Z 91/7

11

Resequencing of VEGFR3 pathway genes implicate GJC2 and FLT..:

Schneider, Sophia ; Köllges, Ricarda ; Stegmann, Jil D....
American Journal of Medical Genetics Part A. 188 (2022) 5 - p. 1607-1611 , 2022

Link: https://doi.org/10.1002/..

12

Copy Number Variation Analysis Facilitates Identification o..:

Wu, Chen-Han Wilfred ; Lim, Tze Y. ; Wang, Chunyan...
European Urology Open Science. 44 (2022) - p. 106-112 , 2022

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

13

Genome-wide association study in patients with posterior ur..:

van der Zanden, Loes F. M. ; Maj, Carlo ; Borisov, Oleg...
Frontiers in Pediatrics. 10 (2022) - p. , 2022

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

14

Reverse phenotyping facilitates disease allele calling in e..:

Seltzsam, Steve ; Wang, Chunyan ; Zheng, Bixia...
Genetics in Medicine. 24 (2022) 2 - p. 307-318 , 2022

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

15

Whole exome sequencing identifies potential candidate genes..:

Wang, Chunyan ; Seltzsam, Steve ; Zheng, Bixia...
American Journal of Medical Genetics Part A. 188 (2022) 5 - p. 1355-1367 , 2022

Link: https://doi.org/10.1002/..