Emily O’Heir

897 total citations
6 papers, 30 citations indexed

About

Emily O’Heir is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Emily O’Heir has authored 6 papers receiving a total of 30 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Physiology. Recurrent topics in Emily O’Heir's work include Genomics and Rare Diseases (2 papers), Congenital limb and hand anomalies (1 paper) and RNA modifications and cancer (1 paper). Emily O’Heir is often cited by papers focused on Genomics and Rare Diseases (2 papers), Congenital limb and hand anomalies (1 paper) and RNA modifications and cancer (1 paper). Emily O’Heir collaborates with scholars based in United States, United Kingdom and Spain. Emily O’Heir's co-authors include Rita Horváth, Ana Töpf, Hanns Lochmüller, Sandra Coppens, Manuel Koch, Andrea Gangfuß, Semra Özçelik, Patrick Van Bogaert, Yavuz Oktay and Semra Hız and has published in prestigious journals such as The Journal of Pathology, Neuromuscular Disorders and Brain and Development.

In The Last Decade

Emily O’Heir

5 papers receiving 29 citations

Peers

Emily O’Heir

MB

GENET

PHYSI

IA

CB

Lyam Vazquez United States

Lea Gerstner Germany

Lauren E. Schwartz United States

Melissa Lorenzo Canada

Belén Gil-Fournier Spain

Abolfazl Heidari Iran

Longquan Quan China

Ikhlas Ben Ayed Tunisia

Hana Zouk United States

Geoffroy Delplancq France

Lyam Vazquez United States

Emily O’Heir

18 ×0.9

MB

6 ×0.4

GENET

13 ×2.2

PHYSI

5 ×0.8

IA

3 ×0.6

CB

Citations per year, relative to Emily O’Heir Emily O’Heir (= 1×) peers Lyam Vazquez

Countries citing papers authored by Emily O’Heir

Since Specialization

Citations

This map shows the geographic impact of Emily O’Heir's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Emily O’Heir with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emily O’Heir more than expected).

Fields of papers citing papers by Emily O’Heir

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Emily O’Heir. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Emily O’Heir. The network helps show where Emily O’Heir may publish in the future.

Co-authorship network of co-authors of Emily O’Heir

This figure shows the co-authorship network connecting the top 25 collaborators of Emily O’Heir. A scholar is included among the top collaborators of Emily O’Heir based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Emily O’Heir. Emily O’Heir is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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6 of 6 papers shown

1.

Romo, Lucía, Emily O’Heir, Juliette Nectoux, et al.. (2025). 490PA recurrent non-coding 3’UTR variant as a hidden second hit in 11 families with CAPN3-related limb girdle muscular dystrophy. Neuromuscular Disorders. 53. 105786–105786.

2.

Sangermano, Riccardo, Priya Gupta, C W Price, et al.. (2024). Coding and non-coding variants in the ciliopathy gene CFAP410 cause early-onset non-syndromic retinal degeneration. npj Genomic Medicine. 9(1). 58–58. 1 indexed citations

3.

Coppens, Sandra, Manuel Koch, Semra Özçelik, et al.. (2022). Ehlers‐Danlos/myopathy overlap syndrome caused by a large de novo deletion in COL12A1. American Journal of Medical Genetics Part A. 188(5). 1556–1561. 8 indexed citations

4.

Gangfuß, Andrea, Andreas Hentschel, Ute Münchberg, et al.. (2021). Homozygous WASHC4 variant in two sisters causes a syndromic phenotype defined by dysmorphisms, intellectual disability, profound developmental disorder, and skeletal muscle involvement. The Journal of Pathology. 256(1). 93–107. 6 indexed citations

5.

Gangfuß, Andrea, Hanns Lochmüller, Ana Töpf, et al.. (2021). A de novoCSDE1 variant causing neurodevelopmental delay, intellectual disability, neurologic and psychiatric symptoms in a child of consanguineous parents. American Journal of Medical Genetics Part A. 188(1). 283–291. 3 indexed citations

6.

Hız, Semra, Yavuz Oktay, Emily O’Heir, et al.. (2020). Successful treatment of intractable epilepsy with ketogenic diet therapy in twins with ALG3-CDG. Brain and Development. 42(7). 539–545. 12 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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