| Year |
Citation |
Score |
| 2022 |
Milanowski LM, Hou X, Bredenberg JM, Fiesel FC, Cocker LT, Soto-Beasley AI, Walton RL, Strongosky AJ, Faroqi AH, Barcikowska M, Boczarska-Jedynak M, Dulski J, Fedoryshyn L, Janik P, Potulska-Chromik A, ... ... Lynch T, et al. Cathepsin B p.Gly284Val Variant in Parkinson's Disease Pathogenesis. International Journal of Molecular Sciences. 23. PMID 35806091 DOI: 10.3390/ijms23137086 |
0.301 |
|
| 2021 |
Williams L, Olszewska DA, Fearon C, Magennis B, McCarthy A, Rowland LP, Mayeux R, Page R, Fahn S, Beausang A, Lynch T. Ondine's Curse in Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17 Caused by Variants. Movement Disorders Clinical Practice. 8: 954-958. PMID 34405105 DOI: 10.1002/mdc3.13265 |
0.595 |
|
| 2020 |
Olszewska DA, McCarthy A, Soto-Beasley AI, Walton RL, Magennis B, McLaughlin RL, Hardiman O, Ross OA, Lynch T. Association Between Glucocerebrosidase Mutations and Parkinson's Disease in Ireland. Frontiers in Neurology. 11: 527. PMID 32714263 DOI: 10.3389/Fneur.2020.00527 |
0.418 |
|
| 2016 |
Olszewska DA, McCarthy A, Lynch T. Commentary: Parkinson's Disease Genes VPS35 and EIF4G1 Interact Genetically and Converge on α-Synuclein. Frontiers in Neuroscience. 10: 162. PMID 27147954 DOI: 10.3389/Fnins.2016.00162 |
0.355 |
|
| 2016 |
Munteanu T, Lynch T. Commentary: The C9orf72 Repeat Expansion Disrupts Nucleocytoplasmic Transport. Frontiers in Neurology. 7: 51. PMID 27065943 DOI: 10.3389/Fneur.2016.00051 |
0.308 |
|
| 2015 |
Ogaki K, Koga S, Heckman MG, Fiesel FC, Ando M, Labbé C, Lorenzo-Betancor O, Moussaud-Lamodière EL, Soto-Ortolaza AI, Walton RL, Strongosky AJ, Uitti RJ, McCarthy A, Lynch T, Siuda J, et al. Mitochondrial targeting sequence variants of the CHCHD2 gene are a risk for Lewy body disorders. Neurology. PMID 26561290 DOI: 10.1212/Wnl.0000000000002170 |
0.381 |
|
| 2015 |
Fearon C, Butler JS, Newman L, Lynch T, Reilly RB. Audiovisual Processing is Abnormal in Parkinson's Disease and Correlates with Freezing of Gait and Disease Duration. Journal of Parkinson's Disease. PMID 26485427 DOI: 10.3233/Jpd-150655 |
0.358 |
|
| 2015 |
Wang L, Aasly JO, Annesi G, Bardien S, Bozi M, Brice A, Carr J, Chung SJ, Clarke C, Crosiers D, Deutschländer A, Eckstein G, Farrer MJ, Goldwurm S, Garraux G, ... ... Lynch T, et al. Large-scale assessment of polyglutamine repeat expansions in Parkinson disease. Neurology. PMID 26354989 DOI: 10.1212/Wnl.0000000000002016 |
0.364 |
|
| 2015 |
McCarthy A, Lonergan R, Olszewska DA, O'Dowd S, Cummins G, Magennis B, Fallon EM, Pender N, Huey ED, Cosentino S, O'Rourke K, Kelly BD, O'Connell M, Delon I, Farrell M, ... ... Lynch T, et al. Closing the tau loop: the missing tau mutation. Brain : a Journal of Neurology. PMID 26297556 DOI: 10.1093/Brain/Awv234 |
0.614 |
|
| 2015 |
Lorenzo-Betancor O, Ogaki K, Soto-Ortolaza AI, Labbe C, Walton RL, Strongosky AJ, van Gerpen JA, Uitti RJ, McLean PJ, Springer W, Siuda J, Opala G, Krygowska-Wajs A, Barcikowska M, Czyzewski K, ... ... Lynch T, et al. 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. PMID 26278106 DOI: 10.1111/Ene.12770 |
0.44 |
|
| 2015 |
Iovino M, Agathou S, González-Rueda A, Del Castillo Velasco-Herrera M, Borroni B, Alberici A, Lynch T, O'Dowd S, Geti I, Gaffney D, Vallier L, Paulsen O, Káradóttir RT, Spillantini MG. Early maturation and distinct tau pathology in induced pluripotent stem cell-derived neurons from patients with MAPT mutations. Brain : a Journal of Neurology. PMID 26220942 DOI: 10.1093/Brain/Awv222 |
0.306 |
|
| 2015 |
Labbé C, Ogaki K, Lorenzo-Betancor O, Carrasquillo MM, Heckman MG, McCarthy A, Soto-Ortolaza AI, Walton RL, Lynch T, Siuda J, Opala G, Krygowska-Wajs A, Barcikowska M, Czyzewski K, Dickson DW, et al. Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson's Disease Locus. Plos One. 10: e0128586. PMID 26090850 DOI: 10.1371/Journal.Pone.0128586 |
0.37 |
|
| 2015 |
Olszewska DA, Lynch T. Will crystal parkin help in understanding the future of Parkinson's disease? Frontiers in Neurology. 6: 35. PMID 25759682 DOI: 10.3389/Fneur.2015.00035 |
0.31 |
|
| 2015 |
Molloy A, Kimmich O, Williams L, Butler JS, Byrne N, Molloy F, Moore H, Healy DG, Lynch T, Edwards MJ, Walsh C, Reilly RB, O'Riordan S, Hutchinson M. An evaluation of the role of environmental factors in the disease penetrance of cervical dystonia. Journal of Neurology, Neurosurgery, and Psychiatry. 86: 331-5. PMID 24963124 DOI: 10.1136/Jnnp-2014-307699 |
0.305 |
|
| 2014 |
Lynch J, Lynch T. Whipple's Disease Viszeralmedizin. 30: 167-172. PMID 26288590 DOI: 10.1159/000363781 |
0.328 |
|
| 2014 |
Pfeffer G, Gorman GS, Griffin H, Kurzawa-Akanbi M, Blakely EL, Wilson I, Sitarz K, Moore D, Murphy JL, Alston CL, Pyle A, Coxhead J, Payne B, Gorrie GH, Longman C, ... ... Lynch T, et al. Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance. Brain : a Journal of Neurology. 137: 1323-36. PMID 24727571 DOI: 10.1093/Brain/Awu060 |
0.325 |
|
| 2014 |
Shannon B, Soto-Ortolaza A, Rayaprolu S, Cannon HD, Labbé C, Benitez BA, Choi J, Lynch T, Boczarska-Jedynak M, Opala G, Krygowska-Wajs A, Barcikowska M, Van Gerpen JA, Uitti RJ, Springer W, et al. Genetic variation of the retromer subunits VPS26A/B-VPS29 in Parkinson's disease. Neurobiology of Aging. 35: 1958.e1-2. PMID 24684791 DOI: 10.1016/J.Neurobiolaging.2014.03.004 |
0.42 |
|
| 2014 |
Gorman GS, Pfeffer G, Griffin H, Kurzawa-Akanbi M, Blakely EL, Wilson I, Sitarz K, Moore D, Murphy JL, Alston CL, Pyle A, Coxhead J, Payne B, Gorrie GH, Longman C, ... ... Lynch T, et al. P32 Mutations in SPG7 cause chronic progressive external ophthalmoplegia through disordered mtDNA maintenance Neuromuscular Disorders. 24. DOI: 10.1016/S0960-8966(14)70048-3 |
0.357 |
|
| 2013 |
Hutchinson M, Kimmich O, Molloy A, Whelan R, Molloy F, Lynch T, Healy DG, Walsh C, Edwards MJ, Ozelius L, Reilly RB, O'Riordan S. The endophenotype and the phenotype: temporal discrimination and adult-onset dystonia. Movement Disorders : Official Journal of the Movement Disorder Society. 28: 1766-74. PMID 24108447 DOI: 10.1002/Mds.25676 |
0.348 |
|
| 2013 |
Rayaprolu S, Mullen B, Baker M, Lynch T, Finger E, Seeley WW, Hatanpaa KJ, Lomen-Hoerth C, Kertesz A, Bigio EH, Lippa C, Josephs KA, Knopman DS, White CL, Caselli R, et al. TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson's disease. Molecular Neurodegeneration. 8: 19. PMID 23800361 DOI: 10.1186/1750-1326-8-19 |
0.398 |
|
| 2013 |
Doherty KM, Silveira-Moriyama L, Parkkinen L, Healy DG, Farrell M, Mencacci NE, Ahmed Z, Brett FM, Hardy J, Quinn N, Counihan TJ, Lynch T, Fox ZV, Revesz T, Lees AJ, et al. Parkin disease: a clinicopathologic entity? Jama Neurology. 70: 571-9. PMID 23459986 DOI: 10.1001/Jamaneurol.2013.172 |
0.415 |
|
| 2013 |
Lonergan R, McCarthy A, O'Dowd S, Magennis B, Fallon E, Spillantini M, Hutton M, Lynch T. The missing tau mutation: +15 exon 10/intron 10 boundary of MAPT stem loop structure in an Irish family with FTDP-17 Journal of the Neurological Sciences. 333. DOI: 10.1016/J.Jns.2013.07.549 |
0.422 |
|
| 2012 |
O'Dowd S, Curtin D, Waite AJ, Roberts K, Pender N, Reid V, O'Connell M, Williams NM, Morris HR, Traynor BJ, Lynch T. C9ORF72 expansion in amyotrophic lateral sclerosis/frontotemporal dementia also causes parkinsonism. Movement Disorders : Official Journal of the Movement Disorder Society. 27: 1072-4. PMID 22807188 DOI: 10.1002/Mds.25022 |
0.348 |
|
| 2012 |
Kearney H, O'Dowd S, Murray B, Kavanagh E, O'Connell M, Lynch T. Re-emergence of artistic traits in a patient with frontotemporal dementia. Clinical Neurology and Neurosurgery. 114: 417-20. PMID 22169065 DOI: 10.1016/J.Clineuro.2011.11.010 |
0.304 |
|
| 2011 |
Chartier-Harlin MC, Dachsel JC, Vilariño-Güell C, Lincoln SJ, Leprêtre F, Hulihan MM, Kachergus J, Milnerwood AJ, Tapia L, Song MS, Le Rhun E, Mutez E, Larvor L, Duflot A, Vanbesien-Mailliot C, ... ... Lynch T, et al. Translation initiator EIF4G1 mutations in familial Parkinson disease. American Journal of Human Genetics. 89: 398-406. PMID 21907011 DOI: 10.1016/J.Ajhg.2011.08.009 |
0.336 |
|
| 2011 |
Ross OA, Soto-Ortolaza AI, Heckman MG, Aasly JO, Abahuni N, Annesi G, Bacon JA, Bardien S, Bozi M, Brice A, Brighina L, Van Broeckhoven C, Carr J, Chartier-Harlin MC, Dardiotis E, ... ... Lynch T, et al. Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study. The Lancet. Neurology. 10: 898-908. PMID 21885347 DOI: 10.1016/S1474-4422(11)70175-2 |
0.303 |
|
| 2011 |
Vilariño-Güell C, Wider C, Ross OA, Dachsel JC, Kachergus JM, Lincoln SJ, Soto-Ortolaza AI, Cobb SA, Wilhoite GJ, Bacon JA, Behrouz B, Melrose HL, Hentati E, Puschmann A, Evans DM, ... ... Lynch T, et al. VPS35 mutations in Parkinson disease. American Journal of Human Genetics. 89: 162-7. PMID 21763482 DOI: 10.1016/j.ajhg.2011.06.001 |
0.413 |
|
| 2011 |
Puschmann A, Verbeeck C, Heckman MG, Soto-Ortolaza AI, Lynch T, Jasinska-Myga B, Opala G, Krygowska-Wajs A, Barcikowska M, Uitti RJ, Wszolek ZK, Ross OA. Human leukocyte antigen variation and Parkinson's disease. Parkinsonism & Related Disorders. 17: 376-8. PMID 21482477 DOI: 10.1016/J.Parkreldis.2011.03.008 |
0.352 |
|
| 2011 |
Wider C, Vilariño-Güell C, Heckman MG, Jasinska-Myga B, Ortolaza-Soto AI, Diehl NN, Crook JE, Cobb SA, Bacon JA, Aasly JO, Gibson JM, Lynch T, Uitti RJ, Wszolek ZK, Farrer MJ, et al. SNCA, MAPT, and GSK3B in Parkinson disease: a gene-gene interaction study. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 18: 876-81. PMID 21159074 DOI: 10.1111/J.1468-1331.2010.03297.X |
0.334 |
|
| 2010 |
Vilariño-Güell C, Ross OA, Aasly JO, White LR, Rajput A, Rajput AH, Lynch T, Krygowska-Wajs A, Jasinska-Myga B, Opala G, Barcikowska M, Lee MC, Hentati F, Uitti RJ, Wszolek ZK, et al. An independent replication of PARK16 in Asian samples. Neurology. 75: 2248-9. PMID 21172849 DOI: 10.1212/Wnl.0B013E318202031F |
0.336 |
|
| 2010 |
Behrouz B, Vilariño-Güell C, Heckman MG, Soto-Ortolaza AI, Aasly JO, Sando S, Lynch T, Craig D, Uitti RJ, Wszolek ZK, Ross OA, Farrer MJ. Mitochondrial translation initiation factor 3 polymorphism and Parkinson's disease. Neuroscience Letters. 486: 228-30. PMID 20887776 DOI: 10.1016/J.Neulet.2010.09.059 |
0.364 |
|
| 2010 |
Wider C, Vilariño-Güell C, Jasinska-Myga B, Heckman MG, Soto-Ortolaza AI, Cobb SA, Aasly JO, Gibson JM, Lynch T, Uitti RJ, Wszolek ZK, Farrer MJ, Ross OA. Association of the MAPT locus with Parkinson's disease. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 17: 483-6. PMID 19912324 DOI: 10.1111/J.1468-1331.2009.02847.X |
0.308 |
|
| 2010 |
Soto-Ortolaza AI, Behrouz B, Wider C, Vilariño-Güell C, Heckman MG, Aasly JO, Mark Gibson J, Lynch T, Jasinska-Myga B, Krygowska-Wajs A, Opala G, Barcikowska M, Czyzewski K, Uitti RJ, Wszolek ZK, et al. Calbindin-1 association and Parkinson's disease. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 17: 208-11. PMID 19674066 DOI: 10.1111/J.1468-1331.2009.02769.X |
0.354 |
|
| 2009 |
Cobb SA, Wider C, Ross OA, Mata IF, Adler CH, Rajput A, Rajput AH, Wu RM, Hauser R, Josephs KA, Carr J, Gwinn K, Heckman MG, Aasly JO, Lynch T, et al. GCH1 in early-onset Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 2070-5. PMID 19735094 DOI: 10.1002/Mds.22729 |
0.405 |
|
| 2009 |
Harbo HF, Finsterer J, Baets J, Van Broeckhoven C, Di Donato S, Fontaine B, De Jonghe P, Lossos A, Lynch T, Mariotti C, Schöls L, Spinazzola A, Szolnoki Z, Tabrizi SJ, Tallaksen C, et al. EFNS guidelines on the molecular diagnosis of neurogenetic disorders: general issues, Huntington's disease, Parkinson's disease and dystonias. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 16: 777-85. PMID 19469830 DOI: 10.1111/J.1468-1331.2009.02646.X |
0.338 |
|
| 2009 |
Wider C, Lincoln SJ, Heckman MG, Diehl NN, Stone JT, Haugarvoll K, Aasly JO, Gibson JM, Lynch T, Rajput A, Rajput ML, Uitti RJ, Wszolek ZK, Farrer MJ, Ross OA. Phactr2 and Parkinson's disease. Neuroscience Letters. 453: 9-11. PMID 19429005 DOI: 10.1016/J.Neulet.2009.02.009 |
0.346 |
|
| 2009 |
Wider C, Dachsel JC, Soto AI, Heckman MG, Diehl NN, Yue M, Lincoln S, Aasly JO, Haugarvoll K, Trojanowski JQ, Papapetropoulos S, Mash D, Rajput A, Rajput AH, Gibson JM, ... Lynch T, et al. FGF20 and Parkinson's disease: no evidence of association or pathogenicity via alpha-synuclein expression. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 455-9. PMID 19133659 DOI: 10.1002/Mds.22442 |
0.343 |
|
| 2009 |
Asmus F, Langseth A, Doherty E, Nestor T, Munz M, Gasser T, Lynch T, King MD. "Jerky" dystonia in children: spectrum of phenotypes and genetic testing. Movement Disorders : Official Journal of the Movement Disorder Society. 24: 702-9. PMID 19117362 DOI: 10.1002/Mds.22426 |
0.353 |
|
| 2009 |
Haugarvoll K, Toft M, Skipper L, Heckman MG, Crook JE, Soto A, Ross OA, Hulihan MM, Kachergus JM, Sando SB, White LR, Lynch T, Gibson JM, Uitti RJ, Wszolek ZK, et al. Fine-mapping and candidate gene investigation within the PARK10 locus. European Journal of Human Genetics : Ejhg. 17: 336-43. PMID 18854859 DOI: 10.1038/Ejhg.2008.187 |
0.338 |
|
| 2008 |
Ross OA, Soto AI, Vilariño-Güell C, Heckman MG, Diehl NN, Hulihan MM, Aasly JO, Sando S, Gibson JM, Lynch T, Krygowska-Wajs A, Opala G, Barcikowska M, Czyzewski K, Uitti RJ, et al. Genetic variation of Omi/HtrA2 and Parkinson's disease. Parkinsonism & Related Disorders. 14: 539-43. PMID 18790661 DOI: 10.1016/J.Parkreldis.2008.08.003 |
0.42 |
|
| 2008 |
Ross OA, Heckman MG, Soto AI, Diehl NN, Haugarvoll K, Vilariño-Güell C, Aasly JO, Sando S, Gibson JM, Lynch T, Krygowska-Wajs A, Opala G, Barcikowska M, Czyzewski K, Uitti RJ, et al. Dopamine beta-hydroxylase -1021C>T association and Parkinson's disease. Parkinsonism & Related Disorders. 14: 544-7. PMID 18722802 DOI: 10.1016/J.Parkreldis.2008.07.002 |
0.321 |
|
| 2007 |
Walsh R, O'Dwyer JP, Sheikh IH, O'Riordan S, Lynch T, Hutchinson M. Sporadic adult onset dystonia: sensory abnormalities as an endophenotype in unaffected relatives. Journal of Neurology, Neurosurgery, and Psychiatry. 78: 980-3. PMID 17702779 DOI: 10.1136/Jnnp.2006.105585 |
0.323 |
|
| 2007 |
Ross OA, Gosal D, Stone JT, Lincoln SJ, Heckman MG, Irvine GB, Johnston JA, Gibson JM, Farrer MJ, Lynch T. Familial genes in sporadic disease: common variants of alpha-synuclein gene associate with Parkinson's disease. Mechanisms of Ageing and Development. 128: 378-82. PMID 17531291 DOI: 10.1016/J.Mad.2007.04.002 |
0.411 |
|
| 2007 |
Ross OA, Haugarvoll K, Stone JT, Heckman MG, White LR, Aasly JO, Mark Gibson J, Lynch T, Wszolek ZK, Uitti RJ, Farrer MJ. Lack of evidence for association of Parkin promoter polymorphism (PRKN-258) with increased risk of Parkinson's disease. Parkinsonism & Related Disorders. 13: 386-8. PMID 17400506 DOI: 10.1016/J.Parkreldis.2007.01.010 |
0.405 |
|
| 2007 |
Haugarvoll K, Toft M, Ross OA, Stone JT, Heckman MG, White LR, Lynch T, Gibson JM, Wszolek ZK, Uitti RJ, Aasly JO, Farrer MJ. ELAVL4, PARK10, and the Celts. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 585-7. PMID 17230446 DOI: 10.1002/Mds.21336 |
0.349 |
|
| 2007 |
Toft M, Mata IF, Ross OA, Kachergus J, Hulihan MM, Haugarvoll K, Stone JT, Blazquez M, Gibson JM, Aasly JO, White LR, Lynch T, Adler CH, Gwinn-Hardy K, Farrer MJ. Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 389-92. PMID 17216639 DOI: 10.1002/Mds.21217 |
0.419 |
|
| 2007 |
Gosal D, Lynch T, Ross OA, Haugarvoll K, Farrer MJ, Gibson JM. Global distribution and reduced penetrance: Lrrk2 R1441C in an Irish Parkinson's disease kindred. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 291-2. PMID 17089395 DOI: 10.1002/Mds.21200 |
0.345 |
|
| 2005 |
Gosal D, Ross OA, Wiley J, Irvine GB, Johnston JA, Toft M, Mata IF, Kachergus J, Hulihan M, Taylor JP, Lincoln SJ, Farrer MJ, Lynch T, Mark Gibson J. Clinical traits of LRRK2-associated Parkinson's disease in Ireland: a link between familial and idiopathic PD. Parkinsonism & Related Disorders. 11: 349-52. PMID 16102999 DOI: 10.1016/J.Parkreldis.2005.05.004 |
0.454 |
|
| 2005 |
Murray B, Lynch T, Farrell M. Clinicopathological features of the tauopathies. Biochemical Society Transactions. 33: 595-599. PMID 16042552 DOI: 10.1042/Bst0330595 |
0.308 |
|
| 2005 |
Toft M, Aasly J, Bisceglio G, Adler CH, Uitti RJ, Krygowska-Wajs A, Lynch T, Wszolek ZK, Farrer MJ. Parkinsonism, FXTAS, and FMR1 premutations. Movement Disorders : Official Journal of the Movement Disorder Society. 20: 230-3. PMID 15390127 DOI: 10.1002/Mds.20297 |
0.389 |
|
| 2004 |
Healy DG, Abou-Sleiman PM, Gibson JM, Ross OA, Jain S, Gandhi S, Gosal D, Muqit MMK, Wood NW, Lynch T. PINK1 (PARK6) associated Parkinson disease in Ireland Neurology. 63: 1486-1488. PMID 15505171 DOI: 10.1212/01.Wnl.0000142089.38301.8E |
0.403 |
|
| 2004 |
O'Riordan S, Ozelius LJ, de Carvalho Aguiar P, Hutchinson M, King M, Lynch T. Inherited myoclonus-dystonia and epilepsy: further evidence of an association? Movement Disorders : Official Journal of the Movement Disorder Society. 19: 1456-9. PMID 15389977 DOI: 10.1002/Mds.20224 |
0.322 |
|
| 2004 |
Gordon PH, Fahn S, Chin S, Golbe LI, Lynch T, Eidelberg D. Woman with a 26-year history of parkinsonism, supranuclear ophthalmoplegia, and loss of postural reflexes. Movement Disorders : Official Journal of the Movement Disorder Society. 19: 950-61. PMID 15300663 DOI: 10.1002/Mds.20139 |
0.459 |
|
| 2004 |
Rohininath T, Costello DJ, Lynch T, Monavari A, Tuchman M, Treacy EP. Fatal presentation of ornithine transcarbamylase deficiency in a 62-year-old man and family studies Journal of Inherited Metabolic Disease. 27: 285-288. PMID 15243986 DOI: 10.1023/B:Boli.0000028840.97261.C6 |
0.326 |
|
| 2004 |
Wiley J, Lynch T, Lincoln S, Skipper L, Hulihan M, Gosal D, Bisceglio G, Kachergus J, Hardy J, Farrer MJ. Parkinson's disease in Ireland: clinical presentation and genetic heterogeneity in patients with parkin mutations. Movement Disorders : Official Journal of the Movement Disorder Society. 19: 677-81. PMID 15197707 DOI: 10.1002/Mds.10703 |
0.408 |
|
| 2004 |
Ross OA, O'Neill C, Rea IM, Lynch T, Gosal D, Wallace A, Curran MD, Middleton D, Gibson JM. Functional promoter region polymorphism of the proinflammatory chemokine IL-8 gene associates with Parkinson's disease in the Irish. Human Immunology. 65: 340-6. PMID 15120188 DOI: 10.1016/J.Humimm.2004.01.015 |
0.33 |
|
| 2002 |
O'Riordan S, Cockburn D, Barton D, Lynch T, Hutchinson M. Primary torsion dystonia due to the Tor1A GAG deletion in an Irish family. Irish Journal of Medical Science. 171: 31-2. PMID 11993591 DOI: 10.1007/Bf03168938 |
0.323 |
|
| 2002 |
Hedrich K, Marder K, Harris J, Kann M, Lynch T, Meija-Santana H, Pramstaller PP, Schwinger E, Bressman SB, Fahn S, Klein C. Evaluation of 50 probands with early-onset Parkinson's disease for Parkin mutations. Neurology. 58: 1239-46. PMID 11971093 DOI: 10.1212/Wnl.58.8.1239 |
0.455 |
|
| 2001 |
Lynch T, Sano M, Marder KS, Bell KL, Foster NL, Defendini RF, Sima AA, Keohane C, Nygaard TG, Fahn S, Mayeux R, Rowland LP, Wilhelmsen KC. Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. 1994. Neurology. 57: S39-45. PMID 11775599 |
0.604 |
|
| 2000 |
Thyagarajan D, Bressman S, Bruno C, Przedborski S, Shanske S, Lynch T, Fahn S, DiMauro S. A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy. Annals of Neurology. 48: 730-6. PMID 11079536 DOI: 10.1002/1531-8249(200011)48:5<730::AID-ANA6>3.0.CO;2-0 |
0.394 |
|
| 1999 |
Lincoln S, Gwinn-Hardy K, Goudreau J, Chartier-Harlin MC, Baker M, Mouroux V, Richard F, Destée A, Becquet E, Amouyel P, Lynch T, Hardy J, Farrer M. No pathogenic mutations in the persyn gene in Parkinson's disease. Neuroscience Letters. 259: 65-6. PMID 10027558 DOI: 10.1016/S0304-3940(98)00901-X |
0.37 |
|
| 1998 |
Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H, Pickering-Brown S, Chakraverty S, Isaacs A, Grover A, Hackett J, Adamson J, Lincoln S, Dickson D, Davies P, ... ... Lynch T, et al. Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17. Nature. 393: 702-5. PMID 9641683 DOI: 10.1038/31508 |
0.454 |
|
| 1998 |
Farrer M, Wavrant-De Vrieze F, Crook R, Boles L, Perez-Tur J, Hardy J, Johnson WG, Steele J, Maraganore D, Gwinn K, Lynch T. Low frequency of alpha-synuclein mutations in familial Parkinson's disease. Annals of Neurology. 43: 394-7. PMID 9506559 DOI: 10.1002/Ana.410430320 |
0.31 |
|
| 1997 |
Lynch T, Fahn S, Louis ED, Odel JG. Oculofacial-skeletal myorhythmia in Whipple's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 12: 625-6. PMID 9251096 |
0.412 |
|
| 1997 |
Lynch T, Odel J, Fredericks DN, Louis ED, Forman S, Rotterdam H, Fahn S, Relman DA. Polymerase chain reaction-based detection of Tropheryma whippelii in central nervous system Whipple's disease. Annals of Neurology. 42: 120-4. PMID 9225695 DOI: 10.1002/Ana.410420120 |
0.413 |
|
| 1997 |
Lynch T, Farrer M, Hutton M, Hardy J. Genetics of Parkinson's disease. Science. 278: 1212-1213. DOI: 10.1126/Science.278.5341.1209D |
0.428 |
|
| 1997 |
Wszolek ZK, Lynch T, Wilhelmsen KC. Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration (PPND) and disinhibition-dementia- parkinsonism-amyotrophy complex (DDPAC) are clinically distinct conditions that are both linked to 17q21-22 Parkinsonism and Related Disorders. 3: 67-76. DOI: 10.1016/S1353-8020(97)00006-0 |
0.302 |
|
| 1996 |
Louis ED, Lynch T, Kaufmann P, Fahn S, Odel J. Diagnostic guidelines in central nervous system Whipple's disease. Annals of Neurology. 40: 561-8. PMID 8871574 DOI: 10.1002/Ana.410400404 |
0.436 |
|
| 1996 |
Wijker M, Wszolek ZK, Wolters EC, Rooimans MA, Pals G, Pfeiffer RF, Lynch T, Rodnitzky RL, Wilhelmsen KC, Arwert F. Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21. Human Molecular Genetics. 5: 151-4. PMID 8789453 DOI: 10.1093/hmg/5.1.151 |
0.304 |
|
| 1996 |
Louis ED, Lynch T, Marder K, Fahn S. Reliability of patient completion of the historical section of the Unified Parkinson's Disease Rating Scale. Movement Disorders : Official Journal of the Movement Disorder Society. 11: 185-92. PMID 8684390 DOI: 10.1002/Mds.870110212 |
0.42 |
|
| 1996 |
Louis ED, Lynch T, Ford B, Greene P, Bressman SB, Fahn S. Delayed-onset cerebellar syndrome. Archives of Neurology. 53: 450-4. PMID 8624221 DOI: 10.1001/Archneur.1996.00550050080027 |
0.415 |
|
| 1996 |
Wilhelmsen KC, Blake DM, Lynch T, Mabutas J, De Vera M, Neystat M, Bernstein M, Hirano M, Gilliam TC, Murphy PL, Sola MD, Bonilla E, Schotland DL, Hays AP, Rowland LP. Chromosome 12-linked autosomal dominant scapuloperoneal muscular dystrophy. Annals of Neurology. 39: 507-20. PMID 8619529 DOI: 10.1002/Ana.410390413 |
0.48 |
|
| 1995 |
Louis ED, Lynch T, Cargan AL, Fahn S. Generalized chorea in an infant with semilobar holoprosencephaly. Pediatric Neurology. 13: 355-7. PMID 8771177 DOI: 10.1016/0887-8994(95)00221-9 |
0.36 |
|
| 1994 |
Lynch T, Burke RE, Fahn S. Progress in psychiatry. The New England Journal of Medicine. 330: 285-6. PMID 8272093 |
0.362 |
|
| 1994 |
Lynch T, Sano M, Marder KS, Bell KL, Foster NL, Defendini RF, Sima AA, Keohane C, Nygaard TG, Fahn S. Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. Neurology. 44: 1878-84. PMID 7936241 DOI: 10.1212/Wnl.44.10.1878 |
0.456 |
|
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