Matthew L. Tedder

1.1k total citations
7 papers, 38 citations indexed

About

Matthew L. Tedder is a scholar working on Molecular Biology, Surgery and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Matthew L. Tedder has authored 7 papers receiving a total of 38 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Surgery and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Matthew L. Tedder's work include RNA modifications and cancer (2 papers), Epigenetics and DNA Methylation (2 papers) and Tracheal and airway disorders (2 papers). Matthew L. Tedder is often cited by papers focused on RNA modifications and cancer (2 papers), Epigenetics and DNA Methylation (2 papers) and Tracheal and airway disorders (2 papers). Matthew L. Tedder collaborates with scholars based in United States, Canada and Netherlands. Matthew L. Tedder's co-authors include Stephanie Jacobson, Bekim Sadiković, Marcia Willing, Lu Shi, Mei Si, Gabriella Maria Squeo, Liwei Chen, Jennifer Kerkhof, Jorge L. Granadillo and Daniel Wegner and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and European Journal of Human Genetics.

In The Last Decade

Matthew L. Tedder

6 papers receiving 38 citations

Peers

Matthew L. Tedder

MB

GENET

PRM

PHEOH

Jillian K. Warejko United States

Sally Connolly United Kingdom

Lot Snijders Blok Netherlands

Frédéric Millot France

Paola Bonaccorso Italy

Renata Lúcia Leite Ferreira de Lima Brazil

Gísli Magnússon Iceland

Tyler Reese United States

Sylvaine Poignant France

Jillian K. Warejko United States

Matthew L. Tedder

12 ×0.6

MB

9 ×0.9

GENET

4 ×0.6

GENET

5 ×0.7

PRM

7 ×1.4

PHEOH

Citations per year, relative to Matthew L. Tedder Matthew L. Tedder (= 1×) peers Jillian K. Warejko

Countries citing papers authored by Matthew L. Tedder

Since Specialization

Citations

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

Fields of papers citing papers by Matthew L. Tedder

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew L. Tedder. 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 Matthew L. Tedder. The network helps show where Matthew L. Tedder may publish in the future.

Co-authorship network of co-authors of Matthew L. Tedder

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

All Works

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7 of 7 papers shown

1.

Haghshenas, Sadegheh, Michael A. Levy, Raissa Relator, et al.. (2025). Identification of an episignature for the MEF2C-associated syndrome. European Journal of Human Genetics. 34(1). 53–60.

2.

Vossaert, Liesbeth, Robin S. Fletcher, Matthew L. Tedder, et al.. (2024). Recurrent carotid paragangliomas in a syndromic patient with a heterozygous missense variant in DNA Methyltransferase 3 Alpha. American Journal of Medical Genetics Part A. 197(1). e63849–e63849. 1 indexed citations

3.

Haghshenas, Sadegheh, Aidin Foroutan, Michael A. Levy, et al.. (2023). Identification of a DNA methylation signature for Renpenning syndrome (RENS1), a spliceopathy. European Journal of Human Genetics. 31(8). 879–886. 2 indexed citations

4.

Rooney, Kathleen, Michael A. Levy, Sadegheh Haghshenas, et al.. (2021). Identification of a DNA Methylation Episignature in the 22q11.2 Deletion Syndrome. International Journal of Molecular Sciences. 22(16). 8611–8611. 13 indexed citations

5.

Granadillo, Jorge L., Daniel Wegner, Marcia Willing, et al.. (2020). Discovery of a novel CHD7 CHARGE syndrome variant by integrated omics analyses. American Journal of Medical Genetics Part A. 185(2). 544–548. 9 indexed citations

6.

Jacobson, Stephanie, et al.. (2016). Adult Acute Lymphoblastic Leukemia: A Genetic Overview and Application to Clinical Practice. Clinical journal of oncology nursing. 20(6). E147–E154. 8 indexed citations

7.

Tedder, Matthew L., et al.. (2015). eMindfulness Therapy—A Study on Efficacy of Blood Pressure and Stress Control Using Mindful Meditation and Eating Apps among People with High Blood Pressure. SHILAP Revista de lepidopterología. 2(4). 298–309. 5 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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