E-LIB Suche - Ergebnisse für: Dhindsa, Ryan S.

1

Genome-wide identification and phenotypic characterization ..:

Montanucci, Ludovica ; Lewis-Smith, David ; Collins, Ryan L....
Nature Communications. 14 (2023) 1 - p. , 2023

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

2

Author Correction: DrugnomeAI is an ensemble machine-learni..:

Raies, Arwa ; Tulodziecka, Ewa ; Stainer, James...
Communications Biology. 6 (2023) 1 - p. , 2023

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

3

Effects of protein-coding variants on blood metabolite meas..:

Nag, Abhishek ; Dhindsa, Ryan S. ; Middleton, Lawrence...
The American Journal of Human Genetics. 110 (2023) 3 - p. 487-498 , 2023

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

4

An expanded genomic database for identifying disease-relate..:

Dhindsa, Ryan S. ; Petrovski, Slavé
Nature. 625 (2023) 7993 - p. 32-34 , 2023

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

5

Literature-based predictions of Mendelian disease therapies:

Deisseroth, Cole A. ; Lee, Won-Seok ; Kim, Jiyoen...
The American Journal of Human Genetics. 110 (2023) 10 - p. 1661-1672 , 2023

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

6

Neurodevelopmental deficits and cell-type-specific transcri..:

Dugger, Sarah A. ; Dhindsa, Ryan S. ; Sampaio, Gabriela De Almeida...
PLOS Genetics. 19 (2023) 10 - p. e1010952 , 2023

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

7

Epilepsy in a mouse model of GNB1 encephalopathy arises fro..:

Colombo, Sophie ; Reddy, Haritha P. ; Petri, Sabrina...
Frontiers in Cellular Neuroscience. 17 (2023) - p. , 2023

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

8

Rare variant associations with plasma protein levels in the..:

Dhindsa, Ryan S. ; Burren, Oliver S. ; Sun, Benjamin B....
Nature. 622 (2023) 7982 - p. 339-347 , 2023

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

9

Studying ultra-rare variants in STX1A uncovers a novel neur..:

Villavicencio Gonzalez, Esmeralda ; Dhindsa, Ryan S.
European Journal of Human Genetics. 31 (2023) 9 - p. 973-974 , 2023

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

10

Natural Selection Shapes Codon Usage in the Human Genome:

Dhindsa, Ryan S. ; Copeland, Brett R. ; Mustoe, Anthony M..
The American Journal of Human Genetics. 109 (2022) 8 - p. 1559 , 2022

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

11

DrugnomeAI is an ensemble machine-learning framework for pr..:

Raies, Arwa ; Tulodziecka, Ewa ; Stainer, James...
Communications Biology. 5 (2022) 1 - p. , 2022

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

12

Association of ultra‐rare coding variants with genetic gene..:

Koko, Mahmoud ; Motelow, Joshua E. ; Stanley, Kate E....
Epilepsia. 63 (2022) 3 - p. 723-735 , 2022

Link: https://doi.org/10.1111/..

13

Rare variant contribution to human disease in 281,104 UK Bi..:

Wang, Quanli ; Dhindsa, Ryan S. ; Carss, Keren...
Nature. 597 (2021) 7877 - p. 527-532 , 2021

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

14

Distinct gene-set burden patterns underlie common generaliz..:

Koko, Mahmoud ; Krause, Roland ; Sander, Thomas...
eBioMedicine. 72 (2021) - p. 103588 , 2021

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

15

Prioritizing non-coding regions based on human genomic cons..:

Vitsios, Dimitrios ; Dhindsa, Ryan S. ; Middleton, Lawrence..
Nature Communications. 12 (2021) 1 - p. , 2021

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