Tim Lynch
Affiliations: | Neurology | University College Dublin, Dublin, County Dublin, Ireland |
Area:
genetics of Parkinson’s disease, neurodegeneration and other movement disordersWebsite:
http://www.neurologicalinstitute.ie/about-the-neurological-institute/prof-tim-lynch-consultant-neurologistGoogle:
"Tim Lynch"Mean distance: 14.99 (cluster 6) | S | N | B | C | P |
Parents
Sign in to add mentor| Lewis P. Rowland | post-doc | 1990 | Columbia University Medical School | |
| (residency) | ||||
| Stanley Fahn | post-doc | 1998 | Columbia University Medical School | |
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Publications
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| Milanowski LM, Hou X, Bredenberg JM, et al. (2022) Cathepsin B p.Gly284Val Variant in Parkinson's Disease Pathogenesis. International Journal of Molecular Sciences. 23 |
| Williams L, Olszewska DA, Fearon C, et al. (2021) Ondine's Curse in Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17 Caused by Variants. Movement Disorders Clinical Practice. 8: 954-958 |
| Olszewska DA, McCarthy A, Soto-Beasley AI, et al. (2020) Association Between Glucocerebrosidase Mutations and Parkinson's Disease in Ireland. Frontiers in Neurology. 11: 527 |
| Olszewska DA, McCarthy A, Lynch T. (2016) Commentary: Parkinson's Disease Genes VPS35 and EIF4G1 Interact Genetically and Converge on α-Synuclein. Frontiers in Neuroscience. 10: 162 |
| Munteanu T, Lynch T. (2016) Commentary: The C9orf72 Repeat Expansion Disrupts Nucleocytoplasmic Transport. Frontiers in Neurology. 7: 51 |
| Ogaki K, Koga S, Heckman MG, et al. (2015) Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders. Neurology |
| Fearon C, Butler JS, Newman L, et al. (2015) Audiovisual Processing is Abnormal in Parkinson's Disease and Correlates with Freezing of Gait and Disease Duration. Journal of Parkinson's Disease |
| Wang L, Aasly JO, Annesi G, et al. (2015) Large-scale assessment of polyglutamine repeat expansions in Parkinson disease. Neurology |
| McCarthy A, Lonergan R, Olszewska DA, et al. (2015) Closing the tau loop: the missing tau mutation. Brain : a Journal of Neurology |
| Lorenzo-Betancor O, Ogaki K, Soto-Ortolaza AI, et al. (2015) DNAJC13 p.Asn855Ser mutation screening in Parkinson's disease and pathologically confirmed Lewy body disease patients. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 22: 1323-5 |