Simone C. Yendle

2.7k total citations
6 papers, 426 citations indexed

About

Simone C. Yendle is a scholar working on Genetics, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Simone C. Yendle has authored 6 papers receiving a total of 426 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Psychiatry and Mental health. Recurrent topics in Simone C. Yendle's work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). Simone C. Yendle is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genomics and Rare Diseases (2 papers). Simone C. Yendle collaborates with scholars based in Australia, United States and Sweden. Simone C. Yendle's co-authors include Ingrid E. Scheffer, Samuel F. Berkovic, Jacinta M. McMahon, Heather C. Mefford, Jeremy L. Freeman, Mark T. Mackay, Arvid Suls, Peter De Jonghe, Thierry Bienvenu and Tally Lerman‐Sagie and has published in prestigious journals such as Neurology, Annals of Neurology and Epilepsia.

In The Last Decade

Simone C. Yendle

6 papers receiving 421 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Simone C. Yendle Australia	6	308	200	132	62	50	6	426
Elizabeth Butler United States	7	299 1.0×	146 0.7×	208 1.6×	59 1.0×	27 0.5×	13	468
Ippei Okada Japan	4	255 0.8×	122 0.6×	210 1.6×	120 1.9×	149 3.0×	5	444
Paul Thiry Belgium	7	186 0.6×	165 0.8×	141 1.1×	84 1.4×	9 0.2×	8	333
Kristien Verhaert Belgium	5	142 0.5×	168 0.8×	98 0.7×	62 1.0×	44 0.9×	6	363
Maria Luigia Gambardella Italy	10	123 0.4×	87 0.4×	148 1.1×	42 0.7×	13 0.3×	19	286
Dimitar N. Azmanov Australia	12	122 0.4×	41 0.2×	191 1.4×	75 1.2×	25 0.5×	23	336
P Ostertag Germany	3	292 0.9×	73 0.4×	142 1.1×	28 0.5×	16 0.3×	4	396
Laëtitia Lambert France	11	351 1.1×	59 0.3×	235 1.8×	41 0.7×	25 0.5×	32	509
Conisha Holloman United States	6	176 0.6×	143 0.7×	158 1.2×	147 2.4×	5 0.1×	13	345
M. Durner United States	8	348 1.1×	352 1.8×	141 1.1×	139 2.2×	6 0.1×	9	555

Countries citing papers authored by Simone C. Yendle

Since Specialization

Citations

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

Fields of papers citing papers by Simone C. Yendle

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Simone C. Yendle. 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 Simone C. Yendle. The network helps show where Simone C. Yendle may publish in the future.

Co-authorship network of co-authors of Simone C. Yendle

This figure shows the co-authorship network connecting the top 25 collaborators of Simone C. Yendle. A scholar is included among the top collaborators of Simone C. Yendle 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 Simone C. Yendle. Simone C. Yendle 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.

Heron, Sarah E., Simone C. Yendle, Jacinta M. McMahon, et al.. (2013). Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies. Epilepsia. 54(5). e86–9. 11 indexed citations

2.

Mefford, Heather C., Simone C. Yendle, Cynthia L. Hsu, et al.. (2011). Rare copy number variants are an important cause of epileptic encephalopathies. Annals of Neurology. 70(6). 974–985. 150 indexed citations

3.

Klein, Karl Martin, Simone C. Yendle, A. Simon Harvey, et al.. (2011). A distinctive seizure type in patients with CDKL5 mutations: Hypermotor-tonic-spasms sequence. Neurology. 76(16). 1436–1438. 33 indexed citations

4.

McMahon, Jacinta M., Leanne M. Dibbens, Todor Arsov, et al.. (2011). De novo SCN1A mutations in migrating partial seizures of infancy. Neurology. 77(4). 380–383. 83 indexed citations

5.

White, Rose, Gladys Ho, Ingrid E. Scheffer, et al.. (2010). Cyclin-Dependent Kinase-Like 5 (CDKL5) Mutation Screening in Rett Syndrome and Related Disorders. Twin Research and Human Genetics. 13(2). 168–178. 27 indexed citations

6.

Deprez, Liesbet, Sarah Weckhuysen, Philip Holmgren, et al.. (2010). Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations. Neurology. 75(13). 1159–1165. 122 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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