Ryan S. Dhindsa

Also affiliated with Neurological Research Institute, Texas Children's Hospital, AstraZeneca (United States)

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 20 papers. Top paper: “Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals”.

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Nature Communications(2023)10.1038/s41467-023-39539-6

N/A

1.2DataRank · unranked

56 citations

David Lewis‐Smith, Ryan L. Collins, Lisa‐Marie Niestroj, Shridhar Parthasarathy, Julie Xian +94 more

Population-scale sequencing resolves determinants of persistent EBV DNA

Nature(2026)10.1038/s41586-025-10020-2

N/A

0.411DataRank · unranked

11 citations

Erin M. Cumming, Oliver S. Burren, Meghana S. Pagadala, Jacob C. Gutierrez, Thahmina A. Ali +18 more

Cell type–specific purifying selection of synonymous mitochondrial DNA variation

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2505704122

N/A

0.241DataRank · unranked

4 citations

Patrick Maschmeyer, Yajie Yin, Jacob C. Gutierrez, Ryan S. Dhindsa, Anne-Sophie Gribling-Burrer +25 more

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.04.009

N/A

0DataRank · unranked

60 citations

Gundula Povysil, Ryan S. Dhindsa, Kate E. Stanley, Andrew S. Allen, Yen‐Chen Anne Feng +95 more

Association of ultra‐rare coding variants with genetic generalized epilepsy: A case–control whole exome sequencing study

Epilepsia(2022)10.1111/epi.17166

N/A

0DataRank · unranked

13 citations

Joshua E. Motelow, Kate E. Stanley, Dheeraj Reddy Bobbili, Ryan S. Dhindsa, Patrick May +3 more

Genome-wide prediction of dominant and recessive neurodevelopmental disorder risk genes

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.11.21.517436

N/A

0DataRank · unranked

7 citations

Blake Weido, Justin Dhindsa, Arya Shetty, Chloe F. Sands, Slavé Petrovski +3 more

Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency

PLoS Genetics(2023)10.1371/journal.pgen.1010952

N/A

0DataRank · unranked

24 citations

Ryan S. Dhindsa, Gabriela Louise de Almeida Sampaio, Andrew K. Ressler, Elizabeth E. Rafikian, Sabrina Petri +10 more

Epilepsy in a mouse model of GNB1 encephalopathy arises from altered potassium (GIRK) channel signaling and is alleviated by a GIRK inhibitor

Frontiers in Cellular Neuroscience(2023)10.3389/fncel.2023.1175895

N/A

0DataRank · unranked

16 citations

Haritha P. Reddy, Sabrina Petri, Damian J. Williams, Boris Shalomov, Ryan S. Dhindsa +11 more

Atoh1 drives the heterogeneity of the pontine nuclei neurons and promotes their differentiation

Science Advances(2023)10.1126/sciadv.adg1671

N/A

0DataRank · unranked

10 citations

Jessica C. Butts, Matthew S. Caudill, Jean‐Pierre Revelli, Ryan S. Dhindsa, Mark A. Durham +2 more

Codon affinity in mitochondrial DNA shapes evolutionary and somatic fitness

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.04.23.537997

N/A

0DataRank · unranked

4 citations

Yajie Yin, Jacob C. Gutierrez, Ryan S. Dhindsa, Anne-Sophie Gribling-Burrer, Yu-Hsin Hsieh +25 more

Literature-based predictions of Mendelian disease therapies

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.08.018

N/A

0DataRank · unranked

0 citations

Won‐Seok Lee, Jiyoen Kim, Hyun-Hwan Jeong, Ryan S. Dhindsa, Julia Wang +3 more

A single-cell transcriptomic map of the developing Atoh1 lineage identifies neural fate decisions and neuronal diversity in the hindbrain

Developmental Cell(2024)10.1016/j.devcel.2024.07.007

N/A

0DataRank · unranked

22 citations

Sih‐Rong Wu, Mark A. Durham, Ryan S. Dhindsa, Jean‐Pierre Revelli, M. Cecilia Ljungberg +5 more

Assessing the contribution of rare protein-coding germline variants to prostate cancer risk and severity in 37,184 cases

Nature Communications(2025)10.1038/s41467-025-56944-1

N/A

0DataRank · unranked

11 citations

Niedzica Camacho, Patrick R. Shea, Konrad H. Stopsack, Vijai Joseph, Oliver S. Burren +29 more

Haploinsufficiency of ITSN1 is associated with a substantial increased risk of Parkinson’s disease

Cell Reports(2025)10.1016/j.celrep.2025.115355

N/A

0DataRank · unranked

12 citations

Chloe F. Sands, Isabella R. Juan, Jonathan Mitchell, Vida Ravanmehr, Jessica C. Butts +22 more

Genome-wide prediction of dominant and recessive neurodevelopmental disorder-associated genes

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.02.001

N/A

0DataRank · unranked

7 citations

Blake Weido, Justin Dhindsa, Arya Shetty, Chloe F. Sands, Slavé Petrovski +3 more

Minding the synapse: A multi-omic approach reveals hidden regulators of neurodevelopment

Cell Systems(2025)10.1016/j.cels.2025.101263

N/A

0DataRank · unranked

0 citations

Ryan S. Dhindsa, Alicia Ljungdahl

Rare heterozygous missense variants in VSX2 are associated with retinal detachment

PLOS Genetics(2026)10.1371/journal.pgen.1012027

N/A

0DataRank · unranked

0 citations

Justin S. Dhindsa, Yifan Chen, Vida Ravanmehr, Jonathan Mitchell, Fengyuan Hu +13 more

Biliverdin Reductase A is a major determinant of neuroprotective Nrf2 signaling

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.06.04.657936

N/A

0DataRank · unranked

0 citations

Ruchita Kothari, Navneet Ammal Kaidery, Suwarna Chakraborty, Sunil Jamuna Tripathi, Ryan S. Dhindsa +16 more

Neurodevelopmental deficits and cell-type-specific transcriptomic perturbations in a mouse model of HNRNPU haploinsufficiency

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.01.072512

N/A

0DataRank · unranked

9 citations

Ryan S. Dhindsa, Gabriela De Almeida Sampaio, Andrew K. Ressler, Elizabeth E. Rafikian, Sabrina Petri +9 more

Biliverdin reductase bridges focal adhesion kinase to Src to modulate synaptic signaling

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.01.405720

N/A

0DataRank · unranked

1 citations

Evan R. Semenza, Jason Liew, Ruchita Kothari, Ryan S. Dhindsa, Shruthi Shanmukha +7 more