E-LIB Suche - Ergebnisse für: Allocco, August

1

Multiomic analyses implicate a neurodevelopmental program i..:

Kundishora, Adam J. ; Allington, Garrett ; McGee, Stephen...
Nature Medicine. 29 (2023) 3 - p. 667-678 , 2023

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

2

A novel SMARCC1 BAFopathy implicates neural progenitor epig..:

Singh, Amrita K ; Allington, Garrett ; Viviano, Stephen...
Brain. 147 (2023) 4 - p. 1553-1570 , 2023

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

3

De novo mutations in the BMP signaling pathway in lambdoid ..:

Timberlake, Andrew T. ; Kiziltug, Emre ; Jin, Sheng Chih...
Human Genetics. 142 (2022) 1 - p. 21-32 , 2022

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

4

The pipeline starts in medical school: characterizing clini..:

Bahar, Ryan C. ; O'Shea, Aidan W. ; Li, Eric S....
Medical Education Online. 27 (2022) 1 - p. , 2022

Link: https://doi.org/10.1080/..

5

Exome Sequencing Implicates Impaired GABA Signaling and Neu..:

Dong, Weilai ; Jin, Sheng Chih ; Allocco, August...
iScience. 23 (2020) 10 - p. 101552 , 2020

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

6

Mutations in Chromatin Modifier and Ephrin Signaling Genes ..:

Duran, Daniel ; Zeng, Xue ; Jin, Sheng Chih...
Neuron. 101 (2019) 3 - p. 429-443.e4 , 2019

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

7

Recessive Inheritance of Congenital Hydrocephalus With Othe..:

Allocco, August A. ; Jin, Sheng Chih ; Duy, Phan Q....
Frontiers in Cellular Neuroscience. 13 (2019) - p. , 2019

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

8

SLC12A ion transporter mutations in sporadic and familial h..:

Jin, Sheng Chih ; Furey, Charuta G. ; Zeng, Xue...
Molecular Genetics & Genomic Medicine. 7 (2019) 9 - p. , 2019

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

9

De Novo Mutation in Genes Regulating Neural Stem Cell Fate ..:

Furey, Charuta Gavankar ; Choi, Jungmin ; Jin, Sheng Chih...
Neuron. 99 (2018) 2 - p. 302-314.e4 , 2018

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

10

Human Genetics and Molecular Mechanisms of Congenital Hydro..:

Furey, Charuta Gavankar ; Zeng, Xue ; Dong, Weilai...
World Neurosurgery. 119 (2018) - p. 441-443 , 2018

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

11

Multiomic analyses implicate a neurodevelopmental program i..:

Kundishora, Adam J ; Allington, Garrett ; McGee, Stephen...
https://discovery.ucl.ac.uk/id/eprint/10166692/1/147973_0_art_file_1133662_rcbb0h.pdf. , 2023

Link: https://discovery.ucl.ac..

12

Exome Sequencing Implicates Impaired GABA Signaling and Neu..:

Dong, Weilai ; Jin, Sheng Chih ; Allocco, August...
iScience. , 2020

Link: http://hdl.handle.net/10..

13

SLC12A ion transporter mutations in sporadic and familial h..:

Jin, Sheng Chih ; Furey, Charuta G ; Zeng, Xue...
https://onlinelibrary.wiley.com/doi/full/10.1002/mgg3.892. , 2019

Link: http://hdl.handle.net/18..

14

Mutations in Chromatin Modifier and Ephrin Signaling Genes ..:

Duran, Daniel ; Zeng, Xue ; Jin, Sheng Chih...
boreal:214627. , 2019

Link: http://hdl.handle.net/20..

15

Mutations in Chromatin Modifier and Ephrin Signaling Genes ..:

Duran, Daniel ; Zeng, Xue ; Jin, Sheng Chih...
boreal:214627. , 2019

Link: http://hdl.handle.net/20..