Marta A. Bayly

2.6k total citations
11 papers, 588 citations indexed

About

Marta A. Bayly is a scholar working on Genetics, Rheumatology and Molecular Biology. According to data from OpenAlex, Marta A. Bayly has authored 11 papers receiving a total of 588 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 3 papers in Rheumatology and 2 papers in Molecular Biology. Recurrent topics in Marta A. Bayly's work include Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genomics and Rare Diseases (4 papers). Marta A. Bayly is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (5 papers) and Genomics and Rare Diseases (4 papers). Marta A. Bayly collaborates with scholars based in Australia, United States and Finland. Marta A. Bayly's co-authors include Leanne M. Dibbens, Samuel F. Berkovic, Ingrid E. Scheffer, Heather C. Mefford, Saul A. Mullen, Susannah T. Bellows, Gemma L. Carvill, John C. Mulley, Danya F. Vears and Holger Trucks and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Annals of Neurology.

In The Last Decade

Marta A. Bayly

11 papers receiving 563 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marta A. Bayly Australia 9 399 181 140 88 74 11 588
A.-E. Lehesjoki Finland 12 310 0.8× 241 1.3× 133 0.9× 199 2.3× 128 1.7× 16 610
Shunling Guo United States 6 188 0.5× 199 1.1× 176 1.3× 31 0.4× 176 2.4× 6 533
Amanda Lindy United States 8 328 0.8× 225 1.2× 146 1.0× 14 0.2× 65 0.9× 13 517
Louise Bier United States 9 152 0.4× 90 0.5× 77 0.6× 17 0.2× 44 0.6× 16 485
Dora Steel United Kingdom 9 107 0.3× 131 0.7× 105 0.8× 11 0.1× 111 1.5× 17 360
Clara DM van Karnebeek Canada 7 105 0.3× 190 1.0× 40 0.3× 15 0.2× 49 0.7× 7 349
Sonya A. Gunter United States 4 166 0.4× 237 1.3× 67 0.5× 8 0.1× 54 0.7× 4 400
Takuya Hiraide Japan 12 185 0.5× 271 1.5× 26 0.2× 17 0.2× 82 1.1× 34 441
Adeline Ngoh United Kingdom 8 175 0.4× 136 0.8× 136 1.0× 11 0.1× 69 0.9× 15 367
Lemuel Racacho Canada 14 116 0.3× 262 1.4× 20 0.1× 80 0.9× 164 2.2× 18 547

Countries citing papers authored by Marta A. Bayly

Since Specialization
Citations

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

Fields of papers citing papers by Marta A. Bayly

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marta A. Bayly. 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 Marta A. Bayly. The network helps show where Marta A. Bayly may publish in the future.

Co-authorship network of co-authors of Marta A. Bayly

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

All Works

11 of 11 papers shown
1.
Gleich, Kurt, Michael Desmond, Samuel F. Berkovic, et al.. (2013). Abnormal Processing of Autophagosomes in Transformed B Lymphocytes from SCARB2-Deficient Subjects. SHILAP Revista de lepidopterología. 2(1). 40–46. 9 indexed citations
2.
Mullen, Saul A., Gemma L. Carvill, Susannah T. Bellows, et al.. (2013). Copy number variants are frequent in genetic generalized epilepsy with intellectual disability. Neurology. 81(17). 1507–1514. 112 indexed citations
3.
Corbett, Mark, Michael Schwake, Melanie Bahlo, et al.. (2011). A Mutation in the Golgi Qb-SNARE Gene GOSR2 Causes Progressive Myoclonus Epilepsy with Early Ataxia. The American Journal of Human Genetics. 88(5). 657–663. 84 indexed citations
4.
Mulley, John C., Ingrid E. Scheffer, Marta A. Bayly, et al.. (2011). Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypes. Epilepsia. 52(10). e139–e142. 7 indexed citations
5.
Dibbens, Leanne M., Ioannis Karakis, Marta A. Bayly, et al.. (2011). Mutation of SCARB2 in a Patient With Progressive Myoclonus Epilepsy and Demyelinating Peripheral Neuropathy. Archives of Neurology. 68(6). 812–3. 25 indexed citations
6.
Dibbens, Leanne M., Rachel Kneen, Marta A. Bayly, et al.. (2011). Recurrence risk of epilepsy and mental retardation in females due to parental mosaicism of PCDH19 mutations. Neurology. 76(17). 1514–1519. 37 indexed citations
7.
Rubboli, Guido, Silvana Franceschetti, Laura Canafoglia, et al.. (2010). CLINICAL AND NEUROPHYSIOLOGICAL FEATURES OF PROGRESSIVE MYOCLONUS EPILEPSY ( PME) ASSOCIATED WITH SCARB2 MUTATIONS WITHOUT RENAL FAILURE. Epilepsia. 51. 23–23. 2 indexed citations
8.
Dibbens, Leanne M., Saul A. Mullen, Katherine L. Helbig, et al.. (2009). Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance. Human Molecular Genetics. 18(19). 3626–3631. 168 indexed citations
9.
Hynes, Kim, Patrick Tarpey, Leanne M. Dibbens, et al.. (2009). Epilepsy and mental retardation limited to females with PCDH19 mutations can present de novo or in single generation families. Journal of Medical Genetics. 47(3). 211–216. 59 indexed citations
10.
Dibbens, Leanne M., Roberto Michelucci, Antonio Gambardella, et al.. (2009). SCARB2 mutations in progressive myoclonus epilepsy (PME) without renal failure. Annals of Neurology. 66(4). 532–536. 65 indexed citations
11.
Helbig, Ingo, Nicholas Matigian, Lata Vadlamudi, et al.. (2008). Gene expression analysis in absence epilepsy using a monozygotic twin design. Epilepsia. 49(9). 1546–1554. 20 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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