Adrian J. Waite

7.8k total citations
20 papers, 1.3k citations indexed

About

Adrian J. Waite is a scholar working on Neurology, Genetics and Molecular Biology. According to data from OpenAlex, Adrian J. Waite has authored 20 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Neurology, 8 papers in Genetics and 7 papers in Molecular Biology. Recurrent topics in Adrian J. Waite's work include Genetics and Neurodevelopmental Disorders (8 papers), Parkinson's Disease Mechanisms and Treatments (7 papers) and Amyotrophic Lateral Sclerosis Research (6 papers). Adrian J. Waite is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Parkinson's Disease Mechanisms and Treatments (7 papers) and Amyotrophic Lateral Sclerosis Research (6 papers). Adrian J. Waite collaborates with scholars based in United Kingdom, United States and Hungary. Adrian J. Waite's co-authors include Derek J. Blake, S. Brown, Huw R. Morris, James Neal, Marc P. Forrest, Caroline L. Tinsley, Matthew Locke, Olaf Ansorge, Dirk Bäumer and Simon Z. East and has published in prestigious journals such as PLoS ONE, Trends in Neurosciences and Annals of Neurology.

In The Last Decade

Adrian J. Waite

20 papers receiving 1.3k citations

Peers

Countries citing papers authored by Adrian J. Waite

Since Specialization

Citations

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

Fields of papers citing papers by Adrian J. Waite

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Adrian J. Waite. 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 Adrian J. Waite. The network helps show where Adrian J. Waite may publish in the future.

Co-authorship network of co-authors of Adrian J. Waite

This figure shows the co-authorship network connecting the top 25 collaborators of Adrian J. Waite. A scholar is included among the top collaborators of Adrian J. Waite 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 Adrian J. Waite. Adrian J. Waite 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	Misfolding of fukutin-related protein (FKRP) variants in congenital and limb girdle muscular dystrophies 2023 ·Frontiers in Molecular Biosciences ·Christopher T. Esapa, R. A. Jeffrey McIlhinney, Adrian J. Waite, Matthew A. Benson, (unknown), Henriett Pikó, Ágnes Herczegfalvi, Rita Horváth, Veronika Karcagi, Maggie C. Walter, Hanns Lochmüller, P.J. Rizkallah, Qi Long Lu, Derek J. Blake	2
2	The generation of an induced pluripotent stem cell line (DCGi001-A) from an individual with FOXG1 syndrome carrying the c.460dupG (p.Glu154fs) variation in the FOXG1 gene 2020 ·Stem Cell Research ·Adrian J. Waite, David Millar, Angus Clarke	1
3	A novel TBK1 mutation in a family with diverse frontotemporal dementia spectrum disorders 2019 ·Molecular Case Studies ·Ruth Lamb, Jonathan D. Rohrer, Raquel Real, Steven Lubbe, Adrian J. Waite, Derek J. Blake, R. J. Walters, Tammaryn Lashley, Tamás Révész, Janice L. Holton, Huw R. Morris	22
4	Ryanodine receptors are part of the myospryn complex in cardiac muscle 2017 ·Scientific Reports ·Matthew A. Benson, Caroline L. Tinsley, Adrian J. Waite, (unknown), Steve M. M. Sweet, Elisabeth Ehler, Christopher H. George, F. Anthony Lai, Enca Martin‐Rendon, Derek J. Blake	23
5	The Psychiatric Risk Gene Transcription Factor 4 (TCF4) Regulates Neurodevelopmental Pathways Associated With Schizophrenia, Autism, and Intellectual Disability 2017 ·Schizophrenia Bulletin ·Marc P. Forrest, Matthew Hill, David H. Kavanagh, Katherine E. Tansey, Adrian J. Waite, Derek J. Blake	69
6	Role of major and brain-specific Sgce isoforms in the pathogenesis of myoclonus-dystonia syndrome 2016 ·Neurobiology of Disease ·Jianfeng Xiao, Satya R. Vemula, Yi Xue, Mohammad Moshahid Khan, (unknown), Adrian J. Waite, Derek J. Blake, Ioannis Dragatsis, Yu Zhao, Mark S. LeDoux	30
7	Myoclonus dystonia and muscular dystrophy: ɛ‐sarcoglycan is part of the dystrophin‐associated protein complex in brain 2016 ·Movement Disorders ·Adrian J. Waite, (unknown), Yiu-mo Chan, Derek J. Blake	19
8	C9orf72 ablation in mice does not cause motor neuron degeneration or motor deficits 2015 ·Annals of Neurology ·Max Koppers, Anna M. Blokhuis, Henk‐Jan Westeneng, (unknown), (unknown), Renata Vieira de Sá, Raymond D. Schellevis, Adrian J. Waite, Derek J. Blake, Jan H. Veldink, Leonard H. van den Berg, R. Jeroen Pasterkamp	201
9	Huntingtin Exists as Multiple Splice Forms in Human Brain 2015 ·Journal of Huntington s Disease ·Matthew Mort, (unknown), Adrian J. Waite, (unknown), Nicholas D. Allen, Lesley Jones, (unknown)	8
10	Reduced C9orf72 protein levels in frontal cortex of amyotrophic lateral sclerosis and frontotemporal degeneration brain with the C9ORF72 hexanucleotide repeat expansion 2014 ·Neurobiology of Aging ·Adrian J. Waite, Dirk Bäumer, Simon Z. East, James Neal, Huw R. Morris, Olaf Ansorge, Derek J. Blake	202
11	Homozygosity for the C9orf72 GGGGCC repeat expansion in frontotemporal dementia 2013 ·Acta Neuropathologica ·Pietro Fratta, Mark Poulter, Tammaryn Lashley, Jonathan D. Rohrer, James M. Polke, Jon Beck, Natalie S. Ryan, Davina J. Hensman Moss, Sarah Mizielinska, Adrian J. Waite, Mang Ching Lai, Tania F. Gendron, Leonard Petrucelli, Elizabeth Fisher, Tamás Révész, Jason D. Warren, John Collinge, Adrian M. Isaacs, Simon Mead	104
12	Knockdown of Human TCF4 Affects Multiple Signaling Pathways Involved in Cell Survival, Epithelial to Mesenchymal Transition and Neuronal Differentiation 2013 ·PLoS ONE ·Marc P. Forrest, Adrian J. Waite, Enca Martin‐Rendon, Derek J. Blake	85
13	Recent Advances in the Genetics of the ALS-FTLD Complex 2012 ·Current Neurology and Neuroscience Reports ·Huw R. Morris, Adrian J. Waite, Nigel Williams, James Neal, Derek J. Blake	47
14	Functional analysis ofTCF4missense mutations that cause Pitt-Hopkins syndrome 2012 ·Human Mutation ·Marc P. Forrest, (unknown), Aisling Doyle, Caroline L. Tinsley, Adrian J. Waite, Derek J. Blake	56
15	The dystrophin–glycoprotein complex in brain development and disease 2012 ·Trends in Neurosciences ·Adrian J. Waite, S. Brown, Derek J. Blake	163
16	A gain-of-glycosylation mutation associated with myoclonus-dystonia syndrome affects trafficking and processing of mouse ε-sarcoglycan in the late secretory pathway 2011 ·Human Mutation ·Adrian J. Waite, Maria Cristina De Rosa, Andrea Brancaccio, Derek J. Blake	18
17	Psychiatric disorders, myoclonus dystonia, and the epsilon‐sarcoglycan gene: A systematic review 2011 ·Movement Disorders ·Kathryn J. Peall, Adrian J. Waite, Derek J. Blake, Mike Owen, Huw R. Morris	30
18	Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p 2010 ·Journal of Neurology ·Justin Pearson, Nigel Williams, Elisa Majounie, Adrian J. Waite, (unknown), (unknown), Alex Murray, Dena Hernandez, Rita Guerreiro, Andrew Singleton, James Neal, Huw R. Morris	56
19	The neurobiology of the dystrophin-associated glycoprotein complex 2009 ·Annals of Medicine ·Adrian J. Waite, Caroline L. Tinsley, Matthew Locke, Derek J. Blake	97
20	SGCE missense mutations that cause myoclonus-dystonia syndrome impair ε-sarcoglycan trafficking to the plasma membrane: modulation by ubiquitination and torsinA 2007 ·Human Molecular Genetics ·Christopher T. Esapa, Adrian J. Waite, Matthew Locke, Matthew A. Benson, Michaela Kraus, R. A. Jeffrey McIlhinney, Roy V. Sillitoe, Philip Beesley, Derek J. Blake	87

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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