Sibylle Wallace

430 total citations
8 papers, 334 citations indexed

About

Sibylle Wallace is a scholar working on Genetics, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, Sibylle Wallace has authored 8 papers receiving a total of 334 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Psychiatry and Mental health and 2 papers in Molecular Biology. Recurrent topics in Sibylle Wallace's work include Epilepsy research and treatment (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (2 papers). Sibylle Wallace is often cited by papers focused on Epilepsy research and treatment (5 papers), Genetics and Neurodevelopmental Disorders (5 papers) and Genomics and Rare Diseases (2 papers). Sibylle Wallace collaborates with scholars based in United States and Malaysia. Sibylle Wallace's co-authors include Harriet Kang, Cynthia L. Harden, Karen Ballaban‐Gil, Martina Durner, Solomon L. Moshé, D Luciano, David Rosenbaum, David A. Greenberg, Jeffrey Cohen and Shlomo Shinnar and has published in prestigious journals such as Annals of Neurology, The American Journal of Human Genetics and Archives of Disease in Childhood.

In The Last Decade

Sibylle Wallace

8 papers receiving 320 citations

Peers

Sibylle Wallace

PMH

GENET

MB

CMN

PPCH

Suha Mercho Canada

Gregorio Pineda Spain

Daniela Buti Italy

Auli Sirén Finland

V. Sgrò Italy

Kristien Verhaert Belgium

R. Desai United States

Agnès Gautier France

Estelle Fédirko France

Yasuhiro Suzuki Japan

Suha Mercho Canada

Sibylle Wallace

280 ×1.3

PMH

173 ×0.9

GENET

182 ×1.8

MB

164 ×1.8

CMN

96 ×1.2

PPCH

Citations per year, relative to Sibylle Wallace Sibylle Wallace (= 1×) peers Suha Mercho

Countries citing papers authored by Sibylle Wallace

Since Specialization

Citations

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

Fields of papers citing papers by Sibylle Wallace

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sibylle Wallace. 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 Sibylle Wallace. The network helps show where Sibylle Wallace may publish in the future.

Co-authorship network of co-authors of Sibylle Wallace

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

All Works

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8 of 8 papers shown

1.

Durner, Martina, Mehdi Keddache, Livia Tomasini, et al.. (2001). Genome scan of idiopathic generalized epilepsy: Evidence for major susceptibility gene and modifying genes influencing the seizure type. Annals of Neurology. 49(3). 328–335. 107 indexed citations

2.

Durner, Martina, Mehdi Keddache, Livia Tomasini, et al.. (2001). Genome scan of idiopathic generalized epilepsy: Evidence for major susceptibility gene and modifying genes influencing the seizure type. Annals of Neurology. 49(3). 328–335. 5 indexed citations

3.

Greenberg, David A., Martina Durner, Mehdi Keddache, et al.. (2000). Reproducibility and Complications in Gene Searches: Linkage on Chromosome 6, Heterogeneity, Association, and Maternal Inheritance in Juvenile Myoclonic Epilepsy. The American Journal of Human Genetics. 66(2). 508–516. 94 indexed citations

4.

Durner, Martina, Shlomo Shinnar, Stanley R. Resor, et al.. (2000). No evidence for a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q. American Journal of Medical Genetics. 96(1). 49–52. 17 indexed citations

5.

Durner, Martina, Ding‐Yi Fu, Paula Abreu, et al.. (1999). Evidence for Linkage of Adolescent-Onset Idiopathic Generalized Epilepsies to Chromosome 8—and Genetic Heterogeneity. The American Journal of Human Genetics. 64(5). 1411–1419. 45 indexed citations

6.

Mindel, Joel S., Allan E. Rubenstein, Sibylle Wallace, Alan M. Aron, & John Halperin. (1994). Congenital Horner's syndrome does not alter Lisch nodule formation. Annals of Neurology. 35(1). 123–124. 1 indexed citations

7.

Wallace, Sibylle, et al.. (1994). Epilepsy with myoclonic absences.. Archives of Disease in Childhood. 70(4). 288–290. 39 indexed citations

8.

Schwartz, Marcia, Sara Kaffe, Sibylle Wallace, & R J Desnick. (1984). Interstitial deletion of the long arm of chromosome 6 [del(6)(q16q22)]: case report and review of the literature. Clinical Genetics. 26(6). 574–578. 26 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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