Megan E. Grout

540 total citations
5 papers, 169 citations indexed

About

Megan E. Grout is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Megan E. Grout has authored 5 papers receiving a total of 169 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Megan E. Grout's work include Genetic Syndromes and Imprinting (2 papers), Fetal and Pediatric Neurological Disorders (2 papers) and Genetic and Kidney Cyst Diseases (2 papers). Megan E. Grout is often cited by papers focused on Genetic Syndromes and Imprinting (2 papers), Fetal and Pediatric Neurological Disorders (2 papers) and Genetic and Kidney Cyst Diseases (2 papers). Megan E. Grout collaborates with scholars based in United States, Canada and Switzerland. Megan E. Grout's co-authors include David M. Parichy, Emily J. Bain, Larissa B. Patterson, Dae Seok Eom, Dan Doherty, Jennifer C. Dempsey, Hannah M. Tully, Ian G. Phelps, Michele G. Mehaffey and Ruxandra Bachmann‐Gagescu and has published in prestigious journals such as The American Journal of Human Genetics, eLife and Genetics in Medicine.

In The Last Decade

Megan E. Grout

5 papers receiving 168 citations

Peers

Megan E. Grout

MB

CB

GENET

PPCH

CMN

Julia Uraji United Kingdom

Madeline Louise Reilly France

Christopher J. Playfoot United Kingdom

Marie MacLennan United Kingdom

Marion Rosello France

Candice Byers United States

Mark D. Urban United States

Luís Nunes Portugal

Fabien Soulavie France

Joseph Kramer United States

Julia Uraji United Kingdom

Megan E. Grout

240 ×2.7

MB

120 ×1.6

CB

30 ×0.6

GENET

36 ×1.1

PPCH

20 ×0.8

CMN

Citations per year, relative to Megan E. Grout Megan E. Grout (= 1×) peers Julia Uraji

Countries citing papers authored by Megan E. Grout

Since Specialization

Citations

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

Fields of papers citing papers by Megan E. Grout

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Megan E. Grout. 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 Megan E. Grout. The network helps show where Megan E. Grout may publish in the future.

Co-authorship network of co-authors of Megan E. Grout

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

All Works

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5 of 5 papers shown

1.

Aldinger, Kimberly A., Jennifer C. Dempsey, Hannah M. Tully, et al.. (2018). Rhombencephalosynapsis: Fused cerebellum, confused geneticists. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 178(4). 432–439. 20 indexed citations

2.

Milev, Miroslav P., Megan E. Grout, Djenann Saint‐Dic, et al.. (2017). Mutations in TRAPPC12 Manifest in Progressive Childhood Encephalopathy and Golgi Dysfunction. The American Journal of Human Genetics. 101(2). 291–299. 32 indexed citations

3.

Phelps, Ian G., Jennifer C. Dempsey, Megan E. Grout, et al.. (2017). Interpreting the clinical significance of combined variants in multiple recessive disease genes: systematic investigation of Joubert syndrome yields little support for oligogenicity. Genetics in Medicine. 20(2). 223–233. 23 indexed citations

4.

Kane, Megan, Mariska Davids, Michelle Bond, et al.. (2017). Abnormal glycosylation in Joubert syndrome type 10. PubMed. 6(1). 2–2. 11 indexed citations

5.

Eom, Dae Seok, Emily J. Bain, Larissa B. Patterson, Megan E. Grout, & David M. Parichy. (2015). Long-distance communication by specialized cellular projections during pigment pattern development and evolution. eLife. 4. 83 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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