Rebecca C. Yeh

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 6 papers. Top paper: “Rewiring of human neurodevelopmental gene regulatory programs by human accelerated regions”.

Rewiring of human neurodevelopmental gene regulatory programs by human accelerated regions

Neuron(2021)10.1016/j.neuron.2021.08.005

N/A

0DataRank · unranked

209 citations

Andrew B. Stergachis, Ellen M. DeGennaro, Ryan N. Doan, Xuyu Qian, Matthew B. Johnson +20 more

Cell lineage analysis with somatic mutations reveals late divergence of neuronal cell types and cortical areas in human cerebral cortex

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.11.06.565899

N/A

0DataRank · unranked

30 citations

Vinayak V. Viswanadham, Ryan N. Doan, Yanmei Dou, Sara Bizzotto, Sattar Khoshkhoo +18 more

Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition

Research Square(2023)10.21203/rs.3.rs-3317938/v1

N/A

0DataRank · unranked

4 citations

Ghayda Mirzaa, Keqin Yan, Raissa Relator, Sara Timpano, Binnaz Yalcin +57 more

Somatic mosaicism in amyotrophic lateral sclerosis and frontotemporal dementia identifies focal mutations associated with widespread degeneration

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.11.30.569436

N/A

0DataRank · unranked

3 citations

Jun‐Ho Kim, August Yue Huang, Matthew Nolan, Junseok Park, Ryan N. Doan +19 more

Combined somatic mutation and transcriptome analysis reveals region-specific differences in clonal architecture in human cortex

Cell Reports(2025)10.1016/j.celrep.2025.116458

N/A

0DataRank · unranked

8 citations

Sonia N. Kim, Emre Caglayan, Ryan N. Doan, Yanmei Dou, Sara Bizzotto +20 more

Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition

Nature Communications(2025)10.1038/s41467-025-64838-5

N/A

0DataRank · unranked

4 citations

Keqin Yan, Raissa Relator, Mathieu Lévesque, P.S. Jayasinghe, Sara Timpano +61 more