Amy Schneider

3.4k citations

21 papers · 758 indexed · h-index 13

Psychiatry and Mental health top 2%
Genetics top 10%
Pediatrics, Perinatology and Child Health top 5%
Molecular Biology
Cellular and Molecular Neuroscience top 10%

Co-authors: Ingrid E. Scheffer Jacinta M. McMahon Wenhui Li Douglas E. Crompton Heather C. Mefford Lynette G. Sadleir Deepak Gill Sara Kivity
Topics: Epilepsy research and treatment (13 papers)Genomics and Rare Diseases (7 papers)Genetics and Neurodevelopmental Disorders (7 papers)
Cited by: Psychiatry and Mental health Pediatrics, Perinatology and Child Health Clinical Biochemistry
Journals: Neurology Annals of Neurology PLoS Genetics
Partner nations: Australia United States Canada

In The Last Decade

Amy Schneider

19 papers receiving 747 citations

Peers

Countries citing papers authored by Amy Schneider

Since Specialization

Citations

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

Fields of papers citing papers by Amy Schneider

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amy Schneider

This figure shows the co-authorship network connecting the top 25 collaborators of Amy Schneider. A scholar is included among the top collaborators of Amy Schneider 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 Amy Schneider. Amy Schneider 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

#	Work	Indexed citations
1	SCN1A pathogenic variants do not have a distinctive blood‐derived DNA methylation signature 2025 ·Epilepsia ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Amy Schneider,(unknown),Gaëtan Lesca,Joseph D. Symonds,Andreas Brunklaus,Lynette G. Sadleir,Ingrid E. Scheffer,Bekim Sadiković,Heather C. Mefford	0
2	Pathogenic Variants in RNU2‐2 , a Non‐coding Spliceosomal RNA , Cause a Distinctive Developmental and Epileptic Encephalopathy 2025 ·Annals of Neurology ·Annie Ting Gee Chiu,Mark F. Bennett,(unknown),Amy Schneider,Stuart J. Macdonald,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Soham Sengupta,(unknown),(unknown),Michael Cardamone,Charles A. Gray,Piero Perucca,Samuel F. Berkovic,Heather C. Mefford,Michael S. Hildebrand,Ingrid E. Scheffer	1
3	Rates of Status Epilepticus and Sudden Unexplained Death in Epilepsy in People With Genetic Developmental and Epileptic Encephalopathies 2023 ·Neurology ·(unknown),Amy Schneider,(unknown),Leonid Churilov,Ingrid E. Scheffer	42
4	Complications of Influenza A or B Virus Infection in Individuals With SCN1A -Positive Dravet Syndrome 2022 ·Neurology ·Katherine B. Howell,(unknown),Amy Schneider,(unknown),(unknown),Rachel Kerr,(unknown),Michael J. Hayman,Andrew J. Kornberg,Margie Danchin,Nigel W. Crawford,Ingrid E. Scheffer	0
5	Contribution of rare genetic variants to drug response in absence epilepsy 2021 ·Epilepsy Research ·Kenneth A. Myers,Mark F. Bennett,Bronwyn E. Grinton,(unknown),E Chan,Luis Bello‐Espinosa,Lynette G. Sadleir,(unknown),Amy Schneider,John A. Damiano,Michael S. Hildebrand,Melanie Bahlo,Samuel F. Berkovic,Jeffrey Buchhalter,Ingrid E. Scheffer	7
6	Somatic IDH1 variant (p.R132C) in an adult male with Maffucci syndrome 2021 ·Molecular Case Studies ·Natasha J. Brown,Zimeng Ye,Chloe Stutterd,(unknown),Amy Schneider,Saul A. Mullen,Simone Mandelstam,Michael S. Hildebrand	3
7	Defining Dravet syndrome: An essential pre‐requisite for precision medicine trials 2021 ·Epilepsia ·Wenhui Li,Amy Schneider,Ingrid E. Scheffer	68
8	Familial adult myoclonic epilepsy type 1 SAMD12 TTTCA repeat expansion arose 17,000 years ago and is present in Sri Lankan and Indian families 2020 ·European Journal of Human Genetics ·Mark F. Bennett,Karen Oliver,Brigid M. Regan,Susannah T. Bellows,Amy Schneider,Haloom Rafehi,(unknown),Douglas E. Crompton,Matthew Coleman,Michael S. Hildebrand,Mark Corbett,Thessa Kroes,Jozef Gécz,Ingrid E. Scheffer,Samuel F. Berkovic,Melanie Bahlo	22
9	Cognitive, behavioral, and social functioning in children and adults with Dravet syndrome 2020 ·Epilepsy & Behavior ·Amy Brown,Marta Arpone,Amy Schneider,(unknown),Vicki Anderson,Ingrid E. Scheffer	28
10	BRAT1 encephalopathy: a recessive cause of epilepsy of infancy with migrating focal seizures 2019 ·Developmental Medicine & Child Neurology ·Ingrid E. Scheffer,Katja Boysen,Amy Schneider,Candace T. Myers,Michele G. Mehaffey,Anne Rochtus,(unknown),Gabriel M. Ronen,(unknown),Deepak Gill,Annapurna Poduri,Heather C. Mefford	14
11	SCN1A Variants in vaccine‐related febrile seizures: A prospective study 2019 ·Annals of Neurology ·John A. Damiano,Lucy Deng,Wenhui Li,Rosemary Burgess,Amy Schneider,Nigel W. Crawford,Jim Buttery,Michael Gold,Peter Richmond,Kristine Macartney,Michael S. Hildebrand,Ingrid E. Scheffer,Nicholas Wood,Samuel F. Berkovic	18
12	Double somatic mosaicism in a child with Dravet syndrome 2019 ·Neurology Genetics ·Alison M. Muir,Chontelle King,Amy Schneider,(unknown),Ingrid E. Scheffer,Lynette G. Sadleir,Heather C. Mefford	10
13	Perception of impact of Dravet syndrome on children and caregivers in multiple countries: looking beyond seizures 2019 ·Developmental Medicine & Child Neurology ·Rima Nabbout,Stéphane Auvin,Catherine Chiron,Elizabeth A. Thiele,J. Helen Cross,Ingrid E. Scheffer,Amy Schneider,Renzo Guerrini,Nicola Williamson,(unknown)	43
14	A population‐based cost‐effectiveness study of early genetic testing in severe epilepsies of infancy 2018 ·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	64
15	Sleep problems in Dravet syndrome: a modifiable comorbidity 2017 ·Developmental Medicine & Child Neurology ·(unknown),Jacinta M. McMahon,Amy Schneider,Margot J. Davey,Ingrid E. Scheffer	54
16	Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45 2017 ·Epilepsia ·Gemma L. Carvill,Aijie Liu,Simone Mandelstam,Amy Schneider,Amy Lacroix,Matthew Zemel,Jacinta M. McMahon,Luis Bello‐Espinosa,Mark T. Mackay,Geoff Wallace,Michaela Waak,Jing Zhang,Cheng Yang,Stephen Malone,Yuehua Zhang,Heather C. Mefford,Ingrid E. Scheffer	44
17	Mortality in Dravet syndrome 2016 ·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	225
18	Seizures Are Regulated by Ubiquitin-specific Peptidase 9 X-linked (USP9X), a De-Ubiquitinase 2015 ·PLoS Genetics ·Lily Paemka,Vinit B. Mahajan,Salleh N. Ehaideb,Jessica M. Skeie,Men Chee Tan,Shu Wu,Allison Cox,Levi P. Sowers,Jozef Gécz,Lachlan A. Jolly,Polly J. Ferguson,Benjamin W. Darbro,Amy Schneider,Ingrid E. Scheffer,Gemma L. Carvill,Heather C. Mefford,Hatem El‐Shanti,Stephen A. Wood,J. Robert Manak,Alexander G. Bassuk	55
19	Sound Source Perception in a Two-Dimensional Setting: Comparison of Action and Nonaction-Based Response Tasks 2006 ·Ecological Psychology ·(unknown),Amy Schneider	4
20	A therapist's ritual of respect 1990 ·Journal of Family Therapy ·(unknown),Amy Schneider	2

About Amy Schneider

Amy Schneider is a scholar working on Psychiatry and Mental health, Genetics and Microbiology, having authored 21 papers that have together received 758 indexed citations. Recurring topics across this work include Epilepsy research and treatment (13 papers), Genomics and Rare Diseases (7 papers) and Genetics and Neurodevelopmental Disorders (7 papers). The work is most often cited by research in Psychiatry and Mental health (474 citations), Pediatrics, Perinatology and Child Health (251 citations) and Clinical Biochemistry (76 citations). Amy Schneider has collaborated with scholars based in Australia, United States and Canada. Frequent co-authors include Ingrid E. Scheffer, Jacinta M. McMahon, Wenhui Li, Douglas E. Crompton, Heather C. Mefford, Lynette G. Sadleir, Deepak Gill, Sara Kivity, Ailsa McLellan and Anne M. McIntosh. Their work appears in journals such as Neurology, Annals of Neurology and PLoS Genetics.

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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