Michelle M. Simon

1.7k total citations
15 papers, 253 citations indexed

About

Michelle M. Simon is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Michelle M. Simon has authored 15 papers receiving a total of 253 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Genetics and 2 papers in Surgery. Recurrent topics in Michelle M. Simon's work include CRISPR and Genetic Engineering (4 papers), Single-cell and spatial transcriptomics (3 papers) and Genomics and Chromatin Dynamics (3 papers). Michelle M. Simon is often cited by papers focused on CRISPR and Genetic Engineering (4 papers), Single-cell and spatial transcriptomics (3 papers) and Genomics and Chromatin Dynamics (3 papers). Michelle M. Simon collaborates with scholars based in United Kingdom, United States and Australia. Michelle M. Simon's co-authors include Ann‐Marie Mallon, Steve D. M. Brown, Saumya Kumar, Sara Wells, Andrew Parker, Carlos Aguilar, Gemma Codner, Lauren Chessum, Lydia Teboul and Marie Hutchison and has published in prestigious journals such as Development, PLoS Genetics and BMC Genomics.

In The Last Decade

Michelle M. Simon

15 papers receiving 252 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Michelle M. Simon United Kingdom	7	169	50	46	20	19	15	253
Lucie Vizor United Kingdom	8	190 1.1×	17 0.3×	53 1.2×	8 0.4×	17 0.9×	15	336
Leanne Moynihan United Kingdom	7	111 0.7×	34 0.7×	71 1.5×	4 0.2×	4 0.2×	7	226
Souad Gherbi France	8	103 0.6×	80 1.6×	50 1.1×	2 0.1×	12 0.6×	11	199
Wenqi Zuo China	11	335 2.0×	19 0.4×	9 0.2×	9 0.5×	20 1.1×	23	468
Alexander S. Brown United States	8	219 1.3×	67 1.3×	46 1.0×	2 0.1×	26 1.4×	10	276
Clemer Abad United States	10	238 1.4×	57 1.1×	178 3.9×	2 0.1×	29 1.5×	20	360
Esther Pohl Germany	5	109 0.6×	36 0.7×	73 1.6×		14 0.7×	8	207
Zahid Azeem Pakistan	12	226 1.3×	29 0.6×	105 2.3×	1 0.1×	16 0.8×	24	358
Jennifer McCallum United States	5	280 1.7×	41 0.8×	112 2.4×		11 0.6×	5	355
Teresa Palladino Italy	9	123 0.7×	52 1.0×	141 3.1×	1 0.1×	6 0.3×	15	246

Countries citing papers authored by Michelle M. Simon

Since Specialization

Citations

This map shows the geographic impact of Michelle M. Simon'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 Michelle M. Simon with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michelle M. Simon more than expected).

Fields of papers citing papers by Michelle M. Simon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michelle M. Simon. 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 Michelle M. Simon. The network helps show where Michelle M. Simon may publish in the future.

Co-authorship network of co-authors of Michelle M. Simon

This figure shows the co-authorship network connecting the top 25 collaborators of Michelle M. Simon. A scholar is included among the top collaborators of Michelle M. Simon 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 Michelle M. Simon. Michelle M. Simon is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Kay, Raissa G. G., Richard L. Reeves, Pam Siggers, et al.. (2024). Gonadal sex reversal at single-cell resolution in Znrf3-deficient mice. Development. 151(23). 1 indexed citations

Greenaway, Simon, et al.. (2022). Making sense of the linear genome, gene function and TADs. Epigenetics & Chromatin. 15(1). 4–4. 25 indexed citations

Reeves, R. G., et al.. (2022). Mouse genomic and cellular annotations. Mammalian Genome. 33(1). 19–30. 4 indexed citations

Powell, George, et al.. (2022). Modelling the genetic aetiology of complex disease: human–mouse conservation of noncoding features and disease-associated loci. Biology Letters. 18(3). 20210630–20210630. 4 indexed citations

Sethi, Siddharth, Ilya E. Vorontsov, Ivan V. Kulakovskiy, et al.. (2020). A holistic view of mouse enhancer architectures reveals analogous pleiotropic effects and correlation with human disease. BMC Genomics. 21(1). 754–754. 3 indexed citations

Nair, R., Charlotte Tibbit, Ross McLeod, et al.. (2020). Sizing, stabilising, and cloning repeat-expansions for gene targeting constructs. Methods. 191. 15–22. 2 indexed citations

Carter, Roderick N., Lisa McKie, Peter S. Budd, et al.. (2018). Mouse Idh3a mutations cause retinal degeneration and reduced mitochondrial function. Disease Models & Mechanisms. 11(12). 20 indexed citations

Esapa, Christopher T., Siân E. Piret, M. Andrew Nesbit, et al.. (2018). An N‐Ethyl‐N‐Nitrosourea (ENU) Mutagenized Mouse Model for Autosomal Dominant Nonsyndromic Kyphoscoliosis Due to Vertebral Fusion. JBMR Plus. 2(3). 154–163. 2 indexed citations

Purnell, Thomas, Hayley E. Tyrer, Andrew Parker, et al.. (2017). A mutation in Nischarin causes otitis media via LIMK1 and NF-κB pathways. PLoS Genetics. 13(8). e1006969–e1006969. 24 indexed citations

10.

Mianné, Joffrey, Lauren Chessum, Saumya Kumar, et al.. (2016). Correction of the auditory phenotype in C57BL/6N mice via CRISPR/Cas9-mediated homology directed repair. Genome Medicine. 8(1). 16–16. 97 indexed citations

11.

Simon, Michelle M., Eva Marie Y. Moresco, Katherine R. Bull, et al.. (2015). Current strategies for mutation detection in phenotype-driven screens utilising next generation sequencing. Mammalian Genome. 26(9-10). 486–500. 18 indexed citations

12.

Tateossian, Hilda, Susan Morse, Michelle M. Simon, Charlotte Dean, & Steve D. M. Brown. (2015). Interactions between the otitis media gene, Fbxo11, and p53 in the mouse embryonic lung. Disease Models & Mechanisms. 8(12). 1531–42. 15 indexed citations

13.

Bull, Katherine R., Andrew J. Rimmer, Owen M. Siggs, et al.. (2013). Unlocking the Bottleneck in Forward Genetics Using Whole-Genome Sequencing and Identity by Descent to Isolate Causative Mutations. PLoS Genetics. 9(1). e1003219–e1003219. 30 indexed citations

14.

Goggolidou, Paraskevi, Shamit Soneji, Nicola Powles‐Glover, et al.. (2013). A chronological expression profile of gene activity during embryonic mouse brain development. Mammalian Genome. 24(11-12). 459–472. 6 indexed citations

15.

Simon, Michelle M., Ann‐Marie Mallon, Gareth R. Howell, & Laura G. Reinholdt. (2012). High throughput sequencing approaches to mutation discovery in the mouse. Mammalian Genome. 23(9-10). 499–513. 2 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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