Author

E Smith

Desert Research Institute

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Developmental Biology· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 3 Organism:human· 2 Assay:scRNA-seq· 2 Research Focus:benchmarking· 1 Research Focus:cell type annotation· 1 Research Focus:database / resource· 1 Research Focus:gene regulatory network inference· 1 Approach:machine learning (classical)· 1

Frequent Co-Authors

Alexandre BolzeiD· 1 shared Andrea MünsterbergiD· 1 shared Andreia Sofia BernardoiD· 1 shared Anna K. BassiliD· 1 shared Anthony D. SlonimiD· 1 shared Ashleigh ListeriD· 1 shared Bruce Lipp· 1 shared Chris J. Rowan· 1 shared

Activity by Year

2019-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 13 mutual co-author links

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1 shared paperGenetics

Alexandre BolzeORCID

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Author profile →

3 papers

Recent·Most cited

WNT inhibition primes the transcriptional landscape of mesoderm to initiate a phased ventricular cardiomyocyte specification programme

Víctor Velecela, Anna K. Bassil, E Fawcett, E Smith, D Konstantopoulos, Fredrik Salmén, Andreia Sofia Bernardo, Stefan Hoppler

This study identifies WNT inhibition-dependent and -independent transcriptional regulators guiding human ventricular cardiomyocyte specification using single-cell RNA sequencing.

bioRxiv · Nov 11, 2025 · PreprintDevelopmental Biology

Single-cell and spatial transcriptomics of the avian embryo tailbud

GF Mok, Stephen Turner, E Smith, Laura Mincarelli, Ashleigh Lister, James Lipscombe, Vladimir Uzun, Wilfried Haerty, Iain C. Macaulay, Andrea Münsterberg

The paper generates a molecular map of the avian trunk and tailbud using single-cell and spatial transcriptomics, identifying cell lineages and spatially restricted genes.

bioRxiv · Feb 5, 2024 · PreprintDevelopmental Biology

Population Health Genetic Screening for Tier 1 Inherited Diseases in Northern Nevada: 90% of At-Risk Carriers are Missed

Joseph J. Grzymski, Gai Elhanan, E Smith, Chris J. Rowan, Nathan R. Slotnick, Shaun Dabe, Karen A. Schlauch, Robert W. Read, William J. Metcalf, Bruce Lipp, Harry Reed, Elissa Levin, Jau‐Tsuen Kao, Misha D. Rashkin, Johnathan Bowes, , James T. Lu

The paper finds that 90% of carriers of inherited disease variants are missed in current medical practice, highlighting the need for population-based genetic screening.

bioRxiv · May 27, 2019 · PreprintGenetics