基本信息
浏览量:25
职业迁徙
个人简介
Research interests
My research interest focuses on the genetic cause(s) of neurological disorders, in children and adults. In recent years work in my group has identified novel neurogenetic syndromes associated with variants in the SOX4, SOX11, MYT1L and SLC12A2 genes.
In adults, my interest centres on studying the early (prodromal) stages of neurodegenerative disease using carriers of genetic mutations. We have used gait analysis and wearable sensors to identify preclinical motor changes in presymptomatic mutation carriers (22q11 deletion, genetic ataxias).
I am happy to consider applications from self funded students interested in PhD projects in this field.
研究兴趣
论文共 154 篇作者统计合作学者相似作者
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European journal of human genetics : EJHGno. 5 (2024): 469-470
European journal of human geneticsno. 4 (2024): 367-368
European journal of human genetics EJHGno. 3 (2024): 249-250
European Journal of Human Geneticsno. 1 (2024): 1-2
JOURNAL OF MEDICAL GENETICSno. 7 (2024): 661-665
European journal of human genetics EJHG (2024)
Alisdair Mcneill, Andrew G L Douglas,Rhona Macleod, Nayana Lahiri, UK PREDICTIVE NEUROGENETICS TESTING CONSORTIUM
Amyotrophic lateral sclerosis & frontotemporal degenerationpp.1-2, (2024)
International Journal of Neonatal Screeningno. 3 (2024): 56
Nayana Lahiri, Lauren Limb, William Beckett, Alyson Bradbury, Rebecca Collier, Emily Craft,Donna Duffin, Claire Dolling, Andrew Douglas, Eshika Haque,Jenny Higgs,Vani Jain, Gabriella Jones, Suresh Komati, Nicol Lambord,Rhona Macleod, Lisa McGrath, Harriet McMillan,Alisdair McNeill,Sharon McDonnell,Mary O’Driscoll, Ruth Robertson,Cheryl Stopford,Shereen Tadros,Charlotte Tomlinson, Penny Van Besouw, Felicity Wadrup
G Genetic testing and counselling (2024)
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作者统计
#Papers: 153
#Citation: 3465
H-Index: 25
G-Index: 58
Sociability: 6
Diversity: 3
Activity: 31
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