E-LIB Suche - Ergebnisse für: Lim, Tze Y

1

Copy number variation analysis in 138 families with steroid..:

Pantel, Dalia ; Mertens, Nils D. ; Schneider, Ronen...
Pediatric Nephrology. 39 (2023) 2 - p. 455-461 , 2023

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

2

Strong protective effect of the APOL1 p.N264K variant again..:

Gupta, Yask ; Friedman, David J. ; McNulty, Michelle T....
Nature Communications. 14 (2023) 1 - p. , 2023

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

3

ParseCNV2: a versatile and integrated tool for copy number ..:

Lim, Tze Y. ; Verbitsky, Miguel ; Sanna-Cherchi, Simone
European Journal of Human Genetics. 31 (2023) 3 - p. 275-277 , 2023

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

4

Mouse and human studies support DSTYK loss of function as a..:

Martino, Jeremiah ; Liu, Qingxue ; Vukojevic, Katarina...
Genetics in Medicine. 25 (2023) 12 - p. 100983 , 2023

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

5

Multi-population genome-wide association study implicates i..:

Barry, Alexandra ; McNulty, Michelle T. ; Jia, Xiaoyuan...
Nature Communications. 14 (2023) 1 - p. , 2023

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

6

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/..

7

Author Correction: The copy number variation landscape of c..:

Verbitsky, Miguel ; Westland, Rik ; Perez, Alejandra...
Nature Genetics. 51 (2019) 4 - p. 764-764 , 2019

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

8

The copy number variation landscape of congenital anomalies..:

Verbitsky, Miguel ; Westland, Rik ; Perez, Alejandra...
Nature Genetics. 51 (2018) 1 - p. 117-127 , 2018

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

9

Evaluation of the MIM Symphony treatment planning system fo..:

Dhanesar, Sandeep K. ; Lim, Tze Y. ; Du, Weiliang...
Journal of Applied Clinical Medical Physics. 16 (2015) 5 - p. 62-75 , 2015

Link: https://doi.org/10.1120/..

10

CERT1 mutations perturb human development by disrupting sph..:

Gehin, Charlotte ; Lone, Museer A ; Lee, Winston...
https://doi.org/10.1172/JCI165019. , 2023

Link: https://hdl.handle.net/2..

11

CERT1 mutations perturb human development by disrupting sph..:

Gehin, Charlotte ; Lone, Museer A ; Lee, Winston...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10178846/. , 2023

Link: http://www.ncbi.nlm.nih...

12

Multi-population genome-wide association study implicates i..:

Barry, Alexandra ; McNulty, Michelle T ; Jia, Xiaoyuan...
info:eu-repo/semantics/altIdentifier/doi/10.1038/s41467-023-37985-w. , 2023

Link: https://repository.vu.lt..

13

Multi-population genome-wide association study implicates i..:

Barry, Alexandra ; McNulty, Michelle T ; Jia, Xiaoyuan...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10148875/. , 2023

Link: http://www.ncbi.nlm.nih...

14

Implication of FOXD2 dysfunction in syndromic congenital an..:

Riedhammer, Korbinian M ; Nguyen, Thanh-Minh T ; Koşukcu, Can...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10055578/. , 2023

Link: http://www.ncbi.nlm.nih...

15

CERT1 mutations perturb human development by disrupting sph..:

Gehin, Charlotte ; Lone, Museer A ; Lee, Winston...
https://boris.unibe.ch/189663/. , 2023

Link: https://boris.unibe.ch/1..