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Ryan S. Dhindsa
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Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios
X Zhu, S Petrovski, P Xie, EK Ruzzo, YF Lu, K McSweeney, B Ben-Zeev, ...
Genetics in Medicine 17 (10), 774-781, 2015
3372015
Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals
YCA Feng, DP Howrigan, LE Abbott, K Tashman, F Cerrato, T Singh, ...
The American Journal of Human Genetics 105 (2), 267-282, 2019
2032019
Rare variant contribution to human disease in 281,104 UK Biobank exomes
Q Wang*, RS Dhindsa*, K Carss*, AR Harper, A Nag, I Tachmazidou, ...
Nature, 1-9, 2021
1872021
Epileptic encephalopathy-causing mutations in DNM1 impair synaptic vesicle endocytosis
RS Dhindsa, SS Bradrick, X Yao, EL Heinzen, S Petrovski, BJ Krueger, ...
Neurology Genetics 1 (1), 2015
552015
TMPRSS2 Transcriptional Inhibition as a Therapeutic Strategy for COVID-19
X Wang, R Dhindsa, G Povysil, A Zoghbi, J Motelow, J Hostyk, N Nickols, ...
53*2020
Natural selection shapes codon usage in the human genome
RS Dhindsa, BR Copeland, AM Mustoe, DB Goldstein
The American Journal of Human Genetics 107 (1), 83-95, 2020
452020
Schizophrenia: From genetics to physiology at last
RS Dhindsa, DB Goldstein
Nature 530 (7589), 162-163, 2016
392016
Prioritizing non-coding regions based on human genomic constraint and sequence context with deep learning
D Vitsios, RS Dhindsa, L Middleton, AB Gussow, S Petrovski
Nature communications 12 (1), 1504, 2021
372021
Plasma proteomic associations with genetics and health in the UK Biobank
BB Sun, J Chiou, M Traylor, C Benner, YH Hsu, TG Richardson, ...
Nature, 1-10, 2023
35*2023
Orion: detecting regions of the human non-coding genome that are intolerant to variation using population genetics
AB Gussow, BR Copeland, RS Dhindsa, Q Wang, S Petrovski, ...
PloS one 12 (8), e0181604, 2017
332017
Identification of a missense variant in SPDL1 associated with idiopathic pulmonary fibrosis
RS Dhindsa, J Mattsson, A Nag, Q Wang, LV Wain, R Allen, EM Wigmore, ...
Communications Biology 4 (1), 1-8, 2021
31*2021
Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals
JE Motelow, G Povysil, RS Dhindsa, KE Stanley, AS Allen, YCA Feng, ...
The American Journal of Human Genetics 108 (6), 965-982, 2021
292021
High-impact rare genetic variants in severe schizophrenia
AW Zoghbi, RS Dhindsa, TE Goldberg, A Mehralizade, JE Motelow, ...
Proceedings of the National Academy of Sciences 118 (51), e2112560118, 2021
252021
Exome sequencing results in successful riboflavin treatment of a rapidly progressive neurological condition
S Petrovski, V Shashi, S Petrou, K Schoch, KM McSweeney, RS Dhindsa, ...
Molecular Case Studies 1 (1), a000257, 2015
252015
meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays
S Gelfman, Q Wang, YF Lu, D Hall, CD Bostick, R Dhindsa, M Halvorsen, ...
PLoS computational biology 14 (10), e1006506, 2018
242018
Genetic Discoveries Drive Molecular Analyses and Targeted Therapeutic Options in the Epilepsies
RS Dhindsa, DB Goldstein
Current neurology and neuroscience reports 15 (10), 2015
182015
Molecular Architecture and Neurobiology of the Epilepsies
RS Dhindsa, DH Lowenstein, DB Goldstein
Genomics, Circuits, and Pathways in Clinical Neuropsychiatry 1, 601-610, 2016
15*2016
Epilepsy in a mouse model of GNB1 Encephalopathy arises from altered potassium channel (GIRK) signaling and is alleviated by a GIRK inhibitor
S Colombo, HP Reddy, S Petri, DJ Williams, B Shalomov, RS Dhindsa, ...
Frontiers in Cellular Neuroscience 17, 182, 2023
14*2023
Effects of protein-coding variants on blood metabolite measurements and clinical biomarkers in the UK Biobank
A Nag, RS Dhindsa, L Middleton, X Jiang, D Vitsios, E Wigmore, ...
The American Journal of Human Genetics 110 (3), 487-498, 2023
14*2023
A Transcriptome‐Based Drug Discovery Paradigm for Neurodevelopmental Disorders
RS Dhindsa, AW Zoghbi, DK Krizay, C Vasavda, DB Goldstein
Annals of neurology 89 (2), 199-211, 2021
132021
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