Robyn H. Wallace

7.0k total citations · 3 hit papers
50 papers, 4.9k citations indexed

About

Robyn H. Wallace is a scholar working on Psychiatry and Mental health, Molecular Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Robyn H. Wallace has authored 50 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Psychiatry and Mental health, 22 papers in Molecular Biology and 19 papers in Cellular and Molecular Neuroscience. Recurrent topics in Robyn H. Wallace's work include Epilepsy research and treatment (21 papers), Neuroscience and Neuropharmacology Research (16 papers) and Ion channel regulation and function (12 papers). Robyn H. Wallace is often cited by papers focused on Epilepsy research and treatment (21 papers), Neuroscience and Neuropharmacology Research (16 papers) and Ion channel regulation and function (12 papers). Robyn H. Wallace collaborates with scholars based in Australia, United States and United Kingdom. Robyn H. Wallace's co-authors include John C. Mulley, Samuel F. Berkovic, Ingrid E. Scheffer, Grant R. Sutherland, Hilary A. Phillips, Louise A. Harkin, Rita Singh, Ortrud K. Steinlein, Peter Propping and Steven Petrou and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Journal of Neuroscience.

In The Last Decade

Robyn H. Wallace

46 papers receiving 4.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

1995 843 citations Ortrud K. Steinlein, John C. Mulley et al. Nature Genetics profile →
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B

1998 783 citations Robyn H. Wallace, Dao Wen Wang et al. Nature Genetics profile →
Mutant GABAA receptor γ2-subunit in childhood absence epilepsy and febrile seizures

2001 590 citations Robyn H. Wallace, Carla Marini et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Robyn H. Wallace Australia	26	2.6k	2.4k	2.4k	1.6k	477	50	4.9k
Leanne M. Dibbens Australia	38	2.2k 0.8×	2.5k 1.0×	1.8k 0.7×	2.1k 1.3×	588 1.2×	73	4.9k
Sarah E. Heron Australia	25	1.4k 0.5×	1.7k 0.7×	1.3k 0.5×	1.0k 0.6×	373 0.8×	37	3.1k
Jennifer A. Kearney United States	34	1.9k 0.7×	1.3k 0.5×	1.9k 0.8×	922 0.6×	312 0.7×	85	3.4k
Patrick Cossette Canada	30	1.4k 0.6×	1.2k 0.5×	1.3k 0.5×	1.1k 0.7×	349 0.7×	68	3.2k
Franck Kalume United States	16	1.3k 0.5×	1.4k 0.6×	1.5k 0.6×	588 0.4×	360 0.8×	29	2.7k
Berge A. Minassian Canada	45	2.5k 1.0×	893 0.4×	880 0.4×	3.5k 2.1×	327 0.7×	182	6.8k
Catherine Burési France	23	1.0k 0.4×	1.0k 0.4×	1.1k 0.4×	789 0.5×	140 0.3×	43	2.6k
Rikke S. Møller Denmark	28	1.0k 0.4×	792 0.3×	426 0.2×	1.3k 0.8×	316 0.7×	121	2.4k
Nadine Norton United Kingdom	45	2.8k 1.1×	832 0.3×	1.1k 0.5×	2.2k 1.4×	104 0.2×	108	5.9k
Paul J. Isackson United States	41	2.4k 0.9×	213 0.1×	3.6k 1.5×	365 0.2×	123 0.3×	93	5.8k

Countries citing papers authored by Robyn H. Wallace

Since Specialization

Citations

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

Fields of papers citing papers by Robyn H. Wallace

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Robyn H. Wallace

This figure shows the co-authorship network connecting the top 25 collaborators of Robyn H. Wallace. A scholar is included among the top collaborators of Robyn H. 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 Robyn H. Wallace. Robyn H. 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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20 of 20 papers shown

Jorgensen, Mikaela, et al.. (2025). Interventions to Reduce Inappropriate Prescribing and Administration of Psychotropic Medications for People With Neurodevelopmental Disabilities: A Systematic Review and Meta‐Analysis. Journal of Applied Research in Intellectual Disabilities. 38(2). e70046–e70046.

Walker, Adam K., Kai Y. Soo, Vinod Sundaramoorthy, et al.. (2013). ALS-Associated TDP-43 Induces Endoplasmic Reticulum Stress, Which Drives Cytoplasmic TDP-43 Accumulation and Stress Granule Formation. PLoS ONE. 8(11). e81170–e81170. 140 indexed citations

Narayanan, Ramesh K., et al.. (2012). Identification of RNA bound to the TDP-43 ribonucleoprotein complex in the adult mouse brain. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 14(4). 252–260. 70 indexed citations

Cowin, Gary, T. J. Butler, Nyoman D. Kurniawan, Charles Watson, & Robyn H. Wallace. (2011). Magnetic resonance microimaging of the spinal cord in the SOD1 mouse model of amyotrophic lateral sclerosis detects motor nerve root degeneration. NeuroImage. 58(1). 69–74. 12 indexed citations

Underwood, Clare, Nyoman D. Kurniawan, T. J. Butler, Gary Cowin, & Robyn H. Wallace. (2010). Non-invasive diffusion tensor imaging detects white matter degeneration in the spinal cord of a mouse model of amyotrophic lateral sclerosis. NeuroImage. 55(2). 455–461. 39 indexed citations

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

McGorum, B. C., et al.. (2009). Vitamin K Deficiency Bleeding in a Standardbred Colt. Journal of Veterinary Internal Medicine. 23(6). 1307–1310. 3 indexed citations

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

Scheffer, Ingrid E., Louise A. Harkin, Bronwyn E. Grinton, et al.. (2006). Temporal lobe epilepsy and GEFS+ phenotypes associated with SCN1B mutations. Brain. 130(1). 100–109. 12 indexed citations

10.

Berkovic, Samuel F., José M. Serratosa, Hilary A. Phillips, et al.. (2004). Familial Partial Epilepsy with Variable Foci: Clinical Features and Linkage to Chromosome 22q12. Epilepsia. 45(9). 1054–1060. 40 indexed citations

11.

Wallace, Robyn H.. (2004). Susceptibility Gene for Juvenile Myoclonic Epilepsy Rings True. Epiliepsy currents. 4(1). 9–10. 2 indexed citations

12.

Marini, Carla, Louise A. Harkin, Robyn H. Wallace, et al.. (2002). Childhood absence epilepsy and febrile seizures: a family with a GABAA receptor mutation. Brain. 126(1). 230–240. 118 indexed citations

13.

Wallace, Robyn H.. (2002). Mutations in GABA-receptor genes cause human epilepsy. The Lancet Neurology. 1(4). 212–212. 6 indexed citations

14.

Strømme, Petter, Marie Mangelsdorf, Marie Shaw, et al.. (2002). Mutations in the human ortholog of Aristaless cause X-linked mental retardation and epilepsy. Nature Genetics. 30(4). 441–445. 317 indexed citations

15.

Wallace, Robyn H., Ingrid E. Scheffer, Shaun Barnett, et al.. (2001). Neuronal Sodium-Channel α1-Subunit Mutations in Generalized Epilepsy with Febrile Seizures Plus. The American Journal of Human Genetics. 68(4). 859–865. 272 indexed citations

16.

Scheffer, Ingrid E., Hilary A. Phillips, Catherine E. O’Brien, et al.. (1998). Familial partial epilepsy with variable foci: A new partial epilepsy syndrome with suggestion of linkage to chromosome 2. Annals of Neurology. 44(6). 890–899. 89 indexed citations

17.

Wallace, Robyn H., Dao Wen Wang, Rita Singh, et al.. (1998). Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel ß1 subunit gene SCN1B. Nature Genetics. 19(4). 366–370. 783 indexed citations breakdown →

18.

Steinlein, Ortrud K., John C. Mulley, Peter Propping, et al.. (1995). A missense mutation in the neuronal nicotinic acetylcholine receptor α4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy. Nature Genetics. 11(2). 201–203. 843 indexed citations breakdown →

19.

Geiger, Vince & Robyn H. Wallace. (1987). Activities in Descriptive Statistics.. The Australian mathematics teacher. 43(1). 14–18.

20.

Wallace, Robyn H.. (1981). Messiahs and millennia in Randolph Stow's novels. Research Online (University of Wollongong). 3(2). 9.

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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