Christopher M. Richmond

466 total citations
9 papers, 49 citations indexed

About

Christopher M. Richmond is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Christopher M. Richmond has authored 9 papers receiving a total of 49 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Molecular Biology and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Christopher M. Richmond's work include Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Vascular Tumors and Angiosarcomas (1 paper). Christopher M. Richmond is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Vascular Tumors and Angiosarcomas (1 paper). Christopher M. Richmond collaborates with scholars based in Australia. Christopher M. Richmond's co-authors include Sebastian Lunke, Belinda Chong, Tiong Yang Tan, Natasha J. Brown, Ivan Macciocca, Zornitza Stark, Paul A. James, Julie McGaughran, Jonathan Rodgers and John Su and has published in prestigious journals such as SHILAP Revista de lepidopterología, Genetics in Medicine and European Journal of Human Genetics.

In The Last Decade

Christopher M. Richmond

9 papers receiving 49 citations

Peers

Christopher M. Richmond

GENET

CCM

GENET

Wanna Chetruengchai Thailand

Hana Zouk United States

Hiromi Nyuzuki Japan

Julia Kitaygorodsky Canada

Oana Moldovan Portugal

Peter Durda United States

Haley McConkey Canada

Lamisse Mansour‐Hendili France

Achilleas Pitsillides United States

María Eugenia Rocha Germany

Wanna Chetruengchai Thailand

Christopher M. Richmond

40 ×1.4

40 ×2.9

GENET

5 ×0.5

CCM

11 ×1.2

5 ×0.8

GENET

Citations per year, relative to Christopher M. Richmond Christopher M. Richmond (= 1×) peers Wanna Chetruengchai

Countries citing papers authored by Christopher M. Richmond

Since Specialization

Citations

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

Fields of papers citing papers by Christopher M. Richmond

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christopher M. Richmond

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

All Works

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9 of 9 papers shown

Richmond, Christopher M., et al.. (2023). Delineating the phenotype of RNU4ATAC‐related spliceosomopathy. American Journal of Medical Genetics Part A. 191(4). 1094–1100. 3 indexed citations

Richmond, Christopher M., et al.. (2023). Somatic PIK3CA Variants Are Associated With Eccrine Angiomatous Hamartomas. SHILAP Revista de lepidopterología. 4(4). e071–e071. 1 indexed citations

Richmond, Christopher M., et al.. (2022). ‘Propped and prone’ positioning reduces respiratory events in spontaneously breathing preterm infants: A randomised triple crossover study. Journal of Paediatrics and Child Health. 59(1). 81–88. 3 indexed citations

Rodgers, Jonathan, Christopher M. Richmond, & Julie McGaughran. (2022). Delineating the CCDC22‐related Ritscher–Schinzel syndrome phenotype in the original family. American Journal of Medical Genetics Part A. 188(11). 3324–3330. 2 indexed citations

Su, John, et al.. (2022). Clinical overlap of PHACE and LUMBAR syndromes. Pediatric Dermatology. 39(5). 752–756. 3 indexed citations

Richmond, Christopher M., Paul A. James, Belinda Chong, et al.. (2021). Clinical and laboratory reporting impact of ACMG-AMP and modified ClinGen variant classification frameworks in MYH7-related cardiomyopathy. Genetics in Medicine. 23(6). 1108–1115. 13 indexed citations

Richmond, Christopher M., Sebastian Lunke, Zornitza Stark, et al.. (2020). Rapid Identification of Biallelic <b><i>SPTB</i></b> Mutation in a Neonate with Severe Congenital Hemolytic Anemia and Liver Failure. Molecular Syndromology. 11(1). 50–55. 8 indexed citations

Richmond, Christopher M., Richard J. Leventer, Monique M. Ryan, & Martin B. Delatycki. (2019). Cerebellar ataxia with normal intellect associated with a homozygous truncating variant in CA8. Clinical Genetics. 97(3). 516–520. 2 indexed citations

Akesson, Lauren, Stefanie Eggers, Belinda Chong, et al.. (2019). Early diagnosis of Pearson syndrome in neonatal intensive care following rapid mitochondrial genome sequencing in tandem with exome sequencing. European Journal of Human Genetics. 27(12). 1821–1826. 14 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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