Jacinta M. McMahon

6.6k citations

45 papers · 2.6k indexed · h-index 29

Psychiatry and Mental health top 1%
- Epilepsy research and treatment 22
Genetics top 2%
- Genomics and Rare Diseases 11
- Genetics and Neurodevelopmental Disorders 9
- Genomic variations and chromosomal abnormalities 5
Pediatrics, Perinatology and Child Health top 2%
- Pharmacological Effects and Toxicity Studies 4
Clinical Biochemistry top 2%
- Metabolism and Genetic Disorders 4
Cellular and Molecular Neuroscience top 5%
- Neuroscience and Neuropharmacology Research 3
Molecular Biology
- Ion channel regulation and function 3

Co-authors: Ingrid E. Scheffer Samuel F. Berkovic John C. Mulley Xenia Iona Leanne M. Dibbens Louise A. Harkin Deepak Gill Anne M. McIntosh
Cited by: Psychiatry and Mental health Genetics Pediatrics, Perinatology and Child Health
Journals: New England Journal of Medicine (1 paper)Proceedings of the National Academy of Sciences (1 paper)The EMBO Journal (1 paper)
Partner nations: Australia United States United Kingdom

In The Last Decade

Jacinta M. McMahon

45 papers receiving 2.6k citations

Peers

Countries citing papers authored by Jacinta M. McMahon

Since Specialization

Citations

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

Fields of papers citing papers by Jacinta M. McMahon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jacinta M. McMahon. 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 Jacinta M. McMahon. The network helps show where Jacinta M. McMahon may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Jacinta M. McMahon, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jacinta M. McMahon Line = papers co-authored together Jacinta M. McMahon links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	A population‐based cost‐effectiveness study of early genetic testing in severe epilepsies of infancy Epilepsia ·Katherine B. Howell,Stefanie Eggers,Kim Dalziel,Jessica R. Riseley,Simone Mandelstam,Candace T. Myers,Jacinta M. McMahon,Amy Schneider,Gemma L. Carvill,Heather C. Mefford,(unknown),Ingrid E. Scheffer,A. Simon Harvey	2018	64
2	Proinsulin C-peptide is an autoantigen in people with type 1 diabetes Proceedings of the National Academy of Sciences ·Michelle So,Colleen M. Elso,Eleonora Tresoldi,Miha Pakusch,Vimukthi Pathiraja,John M. Wentworth,Leonard C. Harrison,Balasubramanian Krishnamurthy,Helen E. Thomas,Christine Rodda,Fergus Cameron,Jacinta M. McMahon,Thomas W. H. Kay,Stuart I. Mannering	2018	53
3	Mortality in Dravet syndrome Epilepsy Research ·Monica S. Cooper,Anne M. McIntosh,Douglas E. Crompton,Jacinta M. McMahon,Amy Schneider,K Farrell,Vijeya Ganesan,Deepak Gill,Sara Kivity,Tally Lerman‐Sagie,Ailsa McLellan,James T. Pelekanos,Venkateswaran Ramesh,Lynette G. Sadleir,Elaine Wirrell,Ingrid E. Scheffer	2016	225
4	Variants in KCNJ11 and BAD do not predict response to ketogenic dietary therapies for epilepsy Epilepsy Research ·Natasha E. Schoeler,Costin Leu,Jon White,Vincent Plagnol,Sian Ellard,Mar Matarín,Gary Yellen,Elizabeth A. Thiele,Mark T. Mackay,Jacinta M. McMahon,Ingrid E. Scheffer,Josemir W. Sander,J. Helen Cross,Sanjay M. Sisodiya	2015	6
5	SCN2A encephalopathy Neurology ·Katherine B. Howell,Jacinta M. McMahon,Gemma L. Carvill,Dimira Tambunan,Mark T. Mackay,Victoria Rodriguez‐Casero,Richard F. Webster,Damian Clark,Jeremy L. Freeman,Sophie Calvert,Heather E. Olson,Simone Mandelstam,Annapurna Poduri,Heather C. Mefford,A. Simon Harvey,Ingrid E. Scheffer	2015	171
6	Mutations in PRRT2 are not a common cause of infantile epileptic encephalopathies Epilepsia ·Sarah E. Heron,Yeh Sze Ong,Simone C. Yendle,Jacinta M. McMahon,Samuel F. Berkovic,Ingrid E. Scheffer,Leanne M. Dibbens	2013	11
7	Progressive Gait Deterioration in Adolescents With Dravet Syndrome Archives of Neurology ·Jill Rodda,Ingrid E. Scheffer,Jacinta M. McMahon,Samuel F. Berkovic,H. Kerr Graham	2012	95
8	Do mutations in SCN1B cause Dravet syndrome? Epilepsy Research ·Young Ok Kim,Leanne M. Dibbens,Carla Marini,Arvid Suls,Nicole Chémaly,Davide Mei,Jacinta M. McMahon,Xenia Iona,Samuel F. Berkovic,Peter De Jonghe,Renzo Guerrini,Rima Nabbout,Ingrid E. Scheffer	2012	12
9	Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations Epilepsy Research ·Daniel Carranza Rojo,A. Simon Harvey,Xenia Iona,Leanne M. Dibbens,John A. Damiano,Todor Arsov,Deepak Gill,Jeremy L. Freeman,Richard J. Leventer,Angela Vincent,Samuel F. Berkovic,Jacinta M. McMahon,Ingrid E. Scheffer	2012	10
10	Rare copy number variants are an important cause of epileptic encephalopathies Annals of Neurology ·Heather C. Mefford,Simone C. Yendle,Cynthia L. Hsu,Joseph Cook,Eileen Geraghty,Jacinta M. McMahon,Orvar Eeg‐Olofsson,Lynette G. Sadleir,Deepak Gill,Bruria Ben‐Zeev,Tally Lerman‐Sagie,Mark T. Mackay,Jeremy L. Freeman,Eva Andermann,James T. Pelakanos,Ian Andrews,Geoffrey Wallace,Evan E. Eichler,Samuel F. Berkovic,Ingrid E. Scheffer	2011	150
11	Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective study The Lancet Neurology ·Anne M. McIntosh,Jacinta M. McMahon,Leanne M. Dibbens,Xenia Iona,John C. Mulley,Ingrid E. Scheffer,Samuel F. Berkovic	2010	101
12	Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance Brain ·Douglas E. Crompton,Ingrid E. Scheffer,I Taylor,Mark Cook,Penelope McKelvie,Danya F. Vears,Kevin M. Lawrence,Jacinta M. McMahon,Bronwyn E. Grinton,Anne M. McIntosh,Samuel F. Berkovic	2010	60
13	Detection of microchromosomal aberrations in refractory epilepsy: a pilot study Epileptic Disorders ·Jacinta M. McMahon,Ingrid E. Scheffer,Jillian Nicholl,Wendy Waters,Helen J. Eyre,Lyn Hinton,Paul V. Nelson,Sui Yu,Leanne M. Dibbens,Samuel F. Berkovic,John C. Mulley	2010	14
14	Timing of De Novo Mutagenesis — A Twin Study of Sodium-Channel Mutations New England Journal of Medicine ·Lata Vadlamudi,Leanne M. Dibbens,Kate Lawrence,Xenia Iona,Jacinta M. McMahon,Wayne Murrell,Alan Mackay‐Sim,Ingrid E. Scheffer,Samuel F. Berkovic	2010	74
15	Feasibility Study into In-Hive Fungal Bio-Control of Small Hive Beetle Queensland Department of Agriculture and Fisheries archive of scientific and research publications (Queensland Department of Agriculture and Fisheries) ·Diana M. Leemon,Jacinta M. McMahon	2009	6
16	De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin: Table 1 Journal of Medical Genetics ·Sarah E. Heron,Ingrid E. Scheffer,Xenia Iona,Sameer M. Zuberi,Rachael Birch,Jacinta M. McMahon,C. M. Bruce,Samuel F. Berkovic,John C. Mulley	2009	43
17	Increased nicotinamide nucleotide transhydrogenase levels predispose to insulin hypersecretion in a mouse strain susceptible to diabetes Diabetologia ·Kathryn Aston‐Mourney,Nicole Wong,Melkam A. Kebede,Sakeneh Zraika,Lois Balmer,Jacinta M. McMahon,Barbara C. Fam,Jennifer M. Favaloro,Joseph Proietto,Grant Morahan,Sof Andrikopoulos	2007	57
18	Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy Epilepsy Research ·E Chabrol,Isabelle Gourfinkel‐An,Ingrid E. Scheffer,Fabienne Picard,Philippe Couarch,Samuel F. Berkovic,Jacinta M. McMahon,Nandita Bajaj,Luísa Mota‐Vieira,Rui Pedro Mota,Oriane Trouillard,Christel Depienne,Michel Baulac,Eric Leguern,Stéphanie Baulac	2007	19
19	De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study The Lancet Neurology ·Samuel F. Berkovic,Louise A. Harkin,Jacinta M. McMahon,James T. Pelekanos,Sameer M. Zuberi,Elaine Wirrell,Deepak Gill,Xenia Iona,John C. Mulley,Ingrid E. Scheffer	2006	173
20	In Vitro and In Vivo Evaluation of the Estrogenic, Androgenic, and Progestagenic Potential of Two Cyclic Siloxanes Toxicological Sciences ·Anthony Quinn,John M. Regan,Joseph M. Tobin,B. J. Marinik,Jacinta M. McMahon,Debra A. McNett,Christopher M. Sushynski,Steven D. Crofoot,Paul A. Jean,Kathleen P. Plotzke	2006	104

About Jacinta M. McMahon

Jacinta M. McMahon is a scholar working on Psychiatry and Mental health, Genetics and Clinical Biochemistry, having authored 45 papers that have together received 2.6k indexed citations. Recurring topics across this work include Epilepsy research and treatment (22 papers), Genomics and Rare Diseases (11 papers), Genetics and Neurodevelopmental Disorders (9 papers), Genomic variations and chromosomal abnormalities (5 papers), Metabolism and Genetic Disorders (4 papers), Pharmacological Effects and Toxicity Studies (4 papers), Neuroscience and Neuropharmacology Research (3 papers) and Ion channel regulation and function (3 papers). The work is most often cited by research in Psychiatry and Mental health (1.4k citations), Genetics (1.0k citations) and Pediatrics, Perinatology and Child Health (629 citations). Jacinta M. McMahon has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Ingrid E. Scheffer, Samuel F. Berkovic, John C. Mulley, Xenia Iona, Leanne M. Dibbens, Louise A. Harkin, Deepak Gill, Anne M. McIntosh, Elaine Wirrell and Lynette G. Sadleir. Their work appears in journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and The EMBO Journal.

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