David Keith Simon - Publications

Affiliations: 
Beth Israel Deaconess Medical Center, Boston, MA, United States 
Area:
Parkinson's Disease, Mitochondrial Genetics

81 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any innacuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2017 Mandel M, de Uña-Álvarez J, Simon DK, Betensky RA. Inverse probability weighted Cox regression for doubly truncated data. Biometrics. PMID 28886206 DOI: 10.1111/biom.12771  0.36
2016 Klein C, Löchte T, Delamonte SM, Braenne I, Hicks AA, Zschiedrich-Jansen K, Simon DK, Friedman JH, Lohmann K. PLA2G6 mutations and Parkinsonism: Long-term follow-up of clinical Features and Neuropathology. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 27709683 DOI: 10.1002/mds.26814  1
2016 Brys M, Fox MD, Agarwal S, Biagioni M, Dacpano G, Kumar P, Pirraglia E, Chen R, Wu A, Fernandez H, Shukla AW, Lou JS, Gray Z, Simon DK, Di Rocco A, et al. Multifocal repetitive TMS for motor and mood symptoms of Parkinson disease: A randomized trial. Neurology. PMID 27708129 DOI: 10.1212/WNL.0000000000003279  0.44
2015 Taylor KM, Saint-Hilaire MH, Sudarsky L, Simon DK, Hersh B, Sparrow D, Hu H, Weisskopf MG. Head injury at early ages is associated with risk of Parkinson's disease. Parkinsonism & Related Disorders. PMID 26725141 DOI: 10.1016/j.parkreldis.2015.12.005  1
2015 Simon DK, Simuni T, Elm J, Clark-Matott J, Graebner AK, Baker L, Dunlop SR, Emborg M, Kamp C, Morgan JC, Ross GW, Sharma S, Ravina B. Peripheral Biomarkers of Parkinson's Disease Progression and Pioglitazone Effects. Journal of Parkinson's Disease. PMID 26444095 DOI: 10.3233/JPD-150666  1
2015 Simon DK, Wu C, Tilley BC, Wills AM, Aminoff MJ, Bainbridge J, Hauser RA, Schneider JS, Sharma S, Singer C, Tanner CM, Truong D, Wong PS. Caffeine and Progression of Parkinson Disease: A Deleterious Interaction With Creatine. Clinical Neuropharmacology. 38: 163-9. PMID 26366971 DOI: 10.1097/WNF.0000000000000102  1
2015 Clark-Matott J, Saleem A, Dai Y, Shurubor Y, Ma X, Safdar A, Beal MF, Tarnopolsky M, Simon DK. Metabolomic analysis of exercise effects in the POLG mitochondrial DNA mutator mouse brain. Neurobiology of Aging. 36: 2972-83. PMID 26294258 DOI: 10.1016/j.neurobiolaging.2015.07.020  1
2015 Kieburtz K, Tilley BC, Elm JJ, Babcock D, Hauser R, Ross GW, Augustine AH, Augustine EU, Aminoff MJ, Bodis-Wollner IG, Boyd J, Cambi F, Chou K, Christine CW, ... ... Simon DK, et al. Effect of creatine monohydrate on clinical progression in patients with Parkinson disease: a randomized clinical trial. Jama. 313: 584-93. PMID 25668262 DOI: 10.1001/jama.2015.120  1
2014 Umeh CC, Pérez A, Augustine EF, Dhall R, Dewey RB, Mari Z, Simon DK, Wills AM, Christine CW, Schneider JS, Suchowersky O. No sex differences in use of dopaminergic medication in early Parkinson disease in the US and Canada - baseline findings of a multicenter trial. Plos One. 9: e112287. PMID 25486269 DOI: 10.1371/journal.pone.0112287  1
2014 Dai Y, Clark J, Zheng K, Kujoth GC, Prolla TA, Simon DK. Somatic mitochondrial DNA mutations do not increase neuronal vulnerability to MPTP in young POLG mutator mice. Neurotoxicology and Teratology. 46: 62-7. PMID 25450660 DOI: 10.1016/j.ntt.2014.10.004  1
2014 Beal MF, Oakes D, Shoulson I, Henchcliffe C, Galpern WR, Haas R, Juncos JL, Nutt JG, Voss TS, Ravina B, Shults CM, Helles K, Snively V, Lew MF, ... ... Simon DK, et al. A randomized clinical trial of high-dosage coenzyme Q10 in early Parkinson disease: no evidence of benefit. Jama Neurology. 71: 543-52. PMID 24664227 DOI: 10.1001/jamaneurol.2014.131  1
2014 Austin MD, Simon DK, Betensky RA. Computationally simple estimation and improved efficiency for special cases of double truncation. Lifetime Data Analysis. 20: 335-54. PMID 24347050 DOI: 10.1007/s10985-013-9287-z  1
2014 Dai Y, Zheng K, Clark J, Swerdlow RH, Pulst SM, Sutton JP, Shinobu LA, Simon DK. Rapamycin drives selection against a pathogenic heteroplasmic mitochondrial DNA mutation. Human Molecular Genetics. 23: 637-47. PMID 24101601 DOI: 10.1093/hmg/ddt450  1
2013 Dai Y, Kiselak T, Clark J, Clore E, Zheng K, Cheng A, Kujoth GC, Prolla TA, Maratos-Flier E, Simon DK. Behavioral and metabolic characterization of heterozygous and homozygous POLG mutator mice. Mitochondrion. 13: 282-91. PMID 23542163 DOI: 10.1016/j.mito.2013.03.006  1
2013 Demetrius LA, Simon DK. The inverse association of cancer and Alzheimer's: a bioenergetic mechanism. Journal of the Royal Society, Interface / the Royal Society. 10: 20130006. PMID 23427097 DOI: 10.1098/rsif.2013.0006  1
2012 Clark J, Silvaggi JM, Kiselak T, Zheng K, Clore EL, Dai Y, Bass CE, Simon DK. Pgc-1α overexpression downregulates Pitx3 and increases susceptibility to MPTP toxicity associated with decreased Bdnf. Plos One. 7: e48925. PMID 23145024 DOI: 10.1371/journal.pone.0048925  1
2012 Demetrius LA, Simon DK. An inverse-Warburg effect and the origin of Alzheimer's disease. Biogerontology. 13: 583-94. PMID 23086530 DOI: 10.1007/s10522-012-9403-6  1
2012 Göbel A, Macklin EA, Winkler S, Betensky RA, Klein C, Lohmann K, Simon DK. Genetic risk factors in Parkinson's disease: single gene effects and interactions of genotypes. Journal of Neurology. 259: 2503-5. PMID 22878430 DOI: 10.1007/s00415-012-6623-2  1
2012 Kumar KR, Weissbach A, Heldmann M, Kasten M, Tunc S, Sue CM, Svetel M, Kosti? VS, Segura-Aguilar J, Ramirez A, Simon DK, Vieregge P, Münte TF, Hagenah J, Klein C, et al. Frequency of the D620N mutation in VPS35 in Parkinson disease. Archives of Neurology. 69: 1360-4. PMID 22801713 DOI: 10.1001/archneurol.2011.3367  1
2012 Lin MT, Cantuti-Castelvetri I, Zheng K, Jackson KE, Tan YB, Arzberger T, Lees AJ, Betensky RA, Beal MF, Simon DK. Somatic mitochondrial DNA mutations in early Parkinson and incidental Lewy body disease. Annals of Neurology. 71: 850-4. PMID 22718549 DOI: 10.1002/ana.23568  1
2012 Pankratz N, Beecham GW, DeStefano AL, Dawson TM, Doheny KF, Factor SA, Hamza TH, Hung AY, Hyman BT, Ivinson AJ, Krainc D, Latourelle JC, Clark LN, Marder K, Martin ER, ... ... Simon DK, et al. Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. Annals of Neurology. 71: 370-84. PMID 22451204 DOI: 10.1002/ana.22687  1
2012 Shih LC, Piel J, Warren A, Kraics L, Silver A, Vanderhorst V, Simon DK, Tarsy D. Singing in groups for Parkinson's disease (SING-PD): a pilot study of group singing therapy for PD-related voice/speech disorders. Parkinsonism & Related Disorders. 18: 548-52. PMID 22436653 DOI: 10.1016/j.parkreldis.2012.02.009  1
2012 Donovan S, Lim C, Rose P, Tarsy D, Sudarsky LR, Simon DK. The utility of laser-generated visual-cueing in Parkinsonian patients with gait freezing Parkinsonism and Related Disorders. 18: 401. DOI: 10.1016/j.parkreldis.2011.09.010  1
2012 Lin MT, Cantuti-Castelvetri I, Lees AJ, Beal MF, Simon DK. Reply Annals of Neurology. 72: 823-824. DOI: 10.1002/ana.23739  1
2011 Simon DK, Chu CT, Swerdlow RH. Mitochondria and Parkinson's disease. Parkinson's Disease. 2011: 261791. PMID 22973533 DOI: 10.4061/2011/261791  1
2011 Friedman JH, Agarwal P, Alcalay R, Black KJ, Chou KL, Cote L, Dayalu P, Frank S, Hartlein J, Hauser RA, Lang AE, Marsh L, Marshall F, Moskowitz C, Ravina B, ... ... Simon DK, et al. Clinical vignettes in Parkinson's disease: a collection of unusual medication-induced hallucinations, delusions, and compulsive behaviours. The International Journal of Neuroscience. 121: 472-6. PMID 21663381 DOI: 10.3109/00207454.2011.578779  1
2011 Clark J, Dai Y, Simon DK. Do somatic mitochondrial DNA mutations contribute to Parkinson's disease? Parkinson's Disease. 2011: 659694. PMID 21603185 DOI: 10.4061/2011/659694  1
2011 Clark J, Reddy S, Zheng K, Betensky RA, Simon DK. Association of PGC-1alpha polymorphisms with age of onset and risk of Parkinson's disease. Bmc Medical Genetics. 12: 69. PMID 21595954 DOI: 10.1186/1471-2350-12-69  1
2011 Xiao J, Zhao Y, Bastian RW, Perlmutter JS, Racette BA, Tabbal SD, Karimi M, Paniello RC, Wszolek ZK, Uitti RJ, Van Gerpen JA, Simon DK, Tarsy D, Hedera P, Truong DD, et al. The c.-237_236GA>TT THAP1 sequence variant does not increase risk for primary dystonia. Movement Disorders : Official Journal of the Movement Disorder Society. 26: 549-52. PMID 21370264 DOI: 10.1002/mds.23551  1
2011 Venkateswaran S, Zheng K, Sacchetti M, Gagne D, Arnold DL, Sadovnick AD, Scherer SW, Banwell B, Bar-Or A, Simon DK. Mitochondrial DNA haplogroups and mutations in children with acquired central demyelination. Neurology. 76: 774-80. PMID 21288980 DOI: 10.1212/WNL.0b013e31820ee1bb  1
2011 Donovan S, Lim C, Diaz N, Browner N, Rose P, Sudarsky LR, Tarsy D, Fahn S, Simon DK. Laserlight cues for gait freezing in Parkinson's disease: an open-label study. Parkinsonism & Related Disorders. 17: 240-5. PMID 20817535 DOI: 10.1016/j.parkreldis.2010.08.010  1
2010 Xiao J, Zhao Y, Bastian RW, Perlmutter JS, Racette BA, Tabbal SD, Karimi M, Paniello R, Blitzer A, Batish SD, Wszolek ZK, Uitti RJ, Van Gerpen JA, Hedera P, Simon DK, et al. Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6. Human Genetics. 127: 470. PMID 21488297  1
2010 Xiao J, Zhao Y, Bastian RW, Perlmutter JS, Racette BA, Tabbal SD, Karimi M, Paniello R, Blitzer A, Batish SD, Wszolek ZK, Uitti RJ, Van Gerpen JA, Hedera P, Simon DK, et al. Novel human pathological mutations. Gene symbol: THAP1. Disease: dystonia 6. Human Genetics. 127: 469. PMID 21488277  1
2010 Connolly BS, Feigenbaum AS, Robinson BH, Dipchand AI, Simon DK, Tarnopolsky MA. MELAS syndrome, cardiomyopathy, rhabdomyolysis, and autism associated with the A3260G mitochondrial DNA mutation. Biochemical and Biophysical Research Communications. 402: 443-7. PMID 20965148 DOI: 10.1016/j.bbrc.2010.10.060  1
2010 Clark J, Clore EL, Zheng K, Adame A, Masliah E, Simon DK. Oral N-acetyl-cysteine attenuates loss of dopaminergic terminals in alpha-synuclein overexpressing mice. Plos One. 5: e12333. PMID 20808797 DOI: 10.1371/journal.pone.0012333  1
2010 Weisskopf MG, Weuve J, Nie H, Saint-Hilaire MH, Sudarsky L, Simon DK, Hersh B, Schwartz J, Wright RO, Hu H. Association of cumulative lead exposure with Parkinson's disease. Environmental Health Perspectives. 118: 1609-13. PMID 20807691 DOI: 10.1289/ehp.1002339  1
2010 Guo X, Kudryavtseva E, Bodyak N, Nicholas A, Dombrovsky I, Yang D, Kraytsberg Y, Simon DK, Khrapko K. Mitochondrial DNA deletions in mice in men: substantia nigra is much less affected in the mouse. Biochimica Et Biophysica Acta. 1797: 1159-62. PMID 20388490 DOI: 10.1016/j.bbabio.2010.04.005  1
2010 Simon DK, Pankratz N, Kissell DK, Pauciulo MW, Halter CA, Rudolph A, Pfeiffer RF, Nichols WC, Foroud T. Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease. Bmc Medical Genetics. 11: 53. PMID 20356410 DOI: 10.1186/1471-2350-11-53  1
2010 Xiao J, Zhao Y, Bastian RW, Perlmutter JS, Racette BA, Tabbal SD, Karimi M, Paniello RC, Wszolek ZK, Uitti RJ, Van Gerpen JA, Simon DK, Tarsy D, Hedera P, Truong DD, et al. Novel THAP1 sequence variants in primary dystonia. Neurology. 74: 229-38. PMID 20083799 DOI: 10.1212/WNL.0b013e3181ca00ca  1
2009 Sikorska M, Sandhu JK, Simon DK, Pathiraja V, Sodja C, Li Y, Ribecco-Lutkiewicz M, Lanthier P, Borowy-Borowski H, Upton A, Raha S, Pulst SM, Tarnopolsky MA. Identification of ataxia-associated mtDNA mutations (m.4052T>C and m.9035T>C) and evaluation of their pathogenicity in transmitochondrial cybrids. Muscle & Nerve. 40: 381-94. PMID 19626676 DOI: 10.1002/mus.21355  1
2009 Kraytsberg Y, Simon DK, Turnbull DM, Khrapko K. Do mtDNA deletions drive premature aging in mtDNA mutator mice? Aging Cell. 8: 502-6. PMID 19416127 DOI: 10.1111/j.1474-9726.2009.00484.x  1
2009 Xiao J, Bastian RW, Perlmutter JS, Racette BA, Tabbal SD, Karimi M, Paniello RC, Blitzer A, Batish SD, Wszolek ZK, Uitti RJ, Hedera P, Simon DK, Tarsy D, Truong DD, et al. High-throughput mutational analysis of TOR1A in primary dystonia. Bmc Medical Genetics. 10: 24. PMID 19284587 DOI: 10.1186/1471-2350-10-24  1
2009 Clark J, Simon DK. Transcribe to survive: transcriptional control of antioxidant defense programs for neuroprotection in Parkinson's disease. Antioxidants & Redox Signaling. 11: 509-28. PMID 18717631 DOI: 10.1089/ARS.2008.2241  1
2008 Tarsy D, Simon DK. Beating a dead horse: dopamine and Parkinson disease. Neurology. 71: 1651; author reply 1. PMID 19001260 DOI: 10.1212/01.wnl.0000339368.54460.68  1
2008 Simon DK, Swearingen CJ, Hauser RA, Trugman JM, Aminoff MJ, Singer C, Truong D, Tilley BC. Caffeine and progression of Parkinson disease. Clinical Neuropharmacology. 31: 189-96. PMID 18670242 DOI: 10.1097/WNF.0b013e31815a3f03  1
2008 Wu AD, Fregni F, Simon DK, Deblieck C, Pascual-Leone A. Noninvasive brain stimulation for Parkinson's disease and dystonia. Neurotherapeutics : the Journal of the American Society For Experimental Neurotherapeutics. 5: 345-61. PMID 18394576 DOI: 10.1016/j.nurt.2008.02.002  1
2007 Djarmati A, Guzvić M, Grünewald A, Lang AE, Pramstaller PP, Simon DK, Kaindl AM, Vieregge P, Nygren AO, Beetz C, Hedrich K, Klein C. Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation-dependent probe amplification. Movement Disorders : Official Journal of the Movement Disorder Society. 22: 1708-14. PMID 17674414 DOI: 10.1002/mds.21370  1
2007 Simon DK, Zheng K, Velázquez L, Santos N, Almaguer L, Figueroa KP, Pulst SM. Mitochondrial complex I gene variant associated with early age at onset in spinocerebellar ataxia type 2. Archives of Neurology. 64: 1042-4. PMID 17620498 DOI: 10.1001/archneur.64.7.1042  1
2007 Kieburtz K, Ravina B, Galpern WR, Tilley B, Shannon K, Tanner C, Wooten GF, Hamill R, Sage JI, Kosa E, Watts RL, Stover NR, McMurray R, Lew MF, Kawai C, ... ... Simon D, et al. A randomized clinical trial of coenzyme Q10 and GPI-1485 in early Parkinson disease Neurology. 68: 20-28. PMID 17200487 DOI: 10.1212/01.wnl.0000250355.28474.8e  1
2007 Nichols WC, Marek DK, Pauciulo MW, Pankratz N, Halter CA, Rudolph A, Shults CW, Wojcieszek J, Foroud T, Shults C, Marshall F, Oakes D, Shinaman A, Marder K, Conneally PM, ... ... Simon D, et al. R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation Movement Disorders. 22: 254-257. PMID 17149721 DOI: 10.1002/mds.21233  1
2006 Pankratz N, Pauciulo MW, Elsaesser VE, Marek DK, Halter CA, Rudolph A, Shults CW, Foroud T, Nichols WC, Shults C, Marshall F, Oakes D, Shinaman A, Marder K, Conneally PM, ... ... Simon D, et al. Mutations in LRRK2 other than G2019S are rare in a north-American based sample of familial Parkinson's didease Movement Disorders. 21: 2257-2260. PMID 17078063 DOI: 10.1002/mds.21162  1
2006 St-Pierre J, Drori S, Uldry M, Silvaggi JM, Rhee J, Jäger S, Handschin C, Zheng K, Lin J, Yang W, Simon DK, Bachoo R, Spiegelman BM. Suppression of reactive oxygen species and neurodegeneration by the PGC-1 transcriptional coactivators. Cell. 127: 397-408. PMID 17055439 DOI: 10.1016/j.cell.2006.09.024  1
2006 Tarsy D, Simon DK. Dystonia. The New England Journal of Medicine. 355: 818-29. PMID 16928997 DOI: 10.1056/NEJMra055549  1
2006 Simon DK, Tarsy D. The authors reply [4] New England Journal of Medicine. 355: 1935.  1
2005 Fregni F, Simon DK, Wu A, Pascual-Leone A. Non-invasive brain stimulation for Parkinson's disease: a systematic review and meta-analysis of the literature. Journal of Neurology, Neurosurgery, and Psychiatry. 76: 1614-23. PMID 16291882 DOI: 10.1136/jnnp.2005.069849  1
2005 Cantuti-Castelvetri I, Lin MT, Zheng K, Keller-McGandy CE, Betensky RA, Johns DR, Beal MF, Standaert DG, Simon DK. Somatic mitochondrial DNA mutations in single neurons and glia. Neurobiology of Aging. 26: 1343-55. PMID 16243605 DOI: 10.1016/j.neurobiolaging.2004.11.008  1
2005 Lee J, Kim CH, Simon DK, Aminova LR, Andreyev AY, Kushnareva YE, Murphy AN, Lonze BE, Kim KS, Ginty DD, Ferrante RJ, Ryu H, Ratan RR. Mitochondrial cyclic AMP response element-binding protein (CREB) mediates mitochondrial gene expression and neuronal survival. The Journal of Biological Chemistry. 280: 40398-401. PMID 16207717 DOI: 10.1074/jbc.C500140200  1
2005 Lin MT, Simon DK. No evidence for heritability of Parkinson disease in Swedish twins. Neurology. 64: 932; author reply 93. PMID 15753453  1
2004 Simon DK, Nishino S, Scammell TE. Mistaken diagnosis of psychogenic gait disorder in a man with status cataplecticus ("limp man syndrome"). Movement Disorders : Official Journal of the Movement Disorder Society. 19: 838-40. PMID 15254948 DOI: 10.1002/mds.20078  1
2004 Nichols WC, Uniacke SK, Pankratz N, Reed T, Simon DK, Halter C, Rudolph A, Shults CW, Conneally PM, Foroud T. Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease. Movement Disorders : Official Journal of the Movement Disorder Society. 19: 649-55. PMID 15197702 DOI: 10.1002/mds.20097  1
2004 Tarnopolsky MA, Simon DK, Roy BD, Chorneyko K, Lowther SA, Johns DR, Sandhu JK, Li Y, Sikorska M. Attenuation of free radical production and paracrystalline inclusions by creatine supplementation in a patient with a novel cytochrome b mutation. Muscle & Nerve. 29: 537-47. PMID 15052619 DOI: 10.1002/mus.20020  1
2004 Tarnopolsky MA, Bourgeois JM, Fu MH, Kataeva G, Shah J, Simon DK, Mahoney D, Johns D, MacKay N, Robinson BH. Novel SCO2 mutation (G1521A) presenting as a spinal muscular atrophy type I phenotype. American Journal of Medical Genetics. Part A. 125: 310-4. PMID 14994243 DOI: 10.1002/ajmg.a.20466  1
2004 Simon DK, Lin MT, Zheng L, Liu GJ, Ahn CH, Kim LM, Mauck WM, Twu F, Beal MF, Johns DR. Somatic mitochondrial DNA mutations in cortex and substantia nigra in aging and Parkinson's disease. Neurobiology of Aging. 25: 71-81. PMID 14675733 DOI: 10.1016/S0197-4580(03)00037-X  1
2003 Pankratz N, Nichols WC, Uniacke SK, Halter C, Murrell J, Rudolph A, Shults CW, Conneally PM, Foroud T. Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families. Human Molecular Genetics. 12: 2599-608. PMID 12925570 DOI: 10.1093/hmg/ddg270  1
2003 Simon DK, Friedman J, Breakefield XO, Jankovic J, Brin MF, Provias J, Bressman SB, Charness ME, Tarsy D, Johns DR, Tarnopolsky MA. A heteroplasmic mitochondrial complex I gene mutation in adult-onset dystonia. Neurogenetics. 4: 199-205. PMID 12756609 DOI: 10.1007/s10048-003-0150-3  1
2003 Zheng K, Heydari B, Simon DK. A common NURR1 polymorphism associated with Parkinson disease and diffuse Lewy body disease. Archives of Neurology. 60: 722-5. PMID 12756136 DOI: 10.1001/archneur.60.5.722  1
2003 Pankratz N, Nichols WC, Uniacke SK, Halter C, Rudolph A, Shults C, Conneally PM, Foroud T. Significant linkage of Parkinson disease to chromosome 2q36-37. American Journal of Human Genetics. 72: 1053-7. PMID 12638082 DOI: 10.1086/374383  1
2003 Foroud T, Uniacke SK, Liu L, Pankratz N, Rudolph A, Halter C, Shults C, Marder K, Conneally PM, Nichols WC. Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease. Neurology. 60: 796-801. PMID 12629236  1
2003 Simon DK. Mitochondrial Mutations in Parkinson's Disease and Dystonias Genetics of Movement Disorders. 473-490. DOI: 10.1016/B978-012566652-7/50043-5  1
2002 Nichols WC, Pankratz N, Uniacke SK, Pauciulo MW, Halter C, Rudolph A, Conneally PM, Foroud T. Linkage stratification and mutation analysis at the Parkin locus identifies mutation positive Parkinson's disease families. Journal of Medical Genetics. 39: 489-92. PMID 12114481  1
2002 Anschel DJ, Simon DK, Llinas R, Joseph JT. Spongiform encephalopathy mimicking corticobasal degeneration. Movement Disorders : Official Journal of the Movement Disorder Society. 17: 606-7. PMID 12112217 DOI: 10.1002/mds.10166  1
2002 Pankratz N, Nichols WC, Uniacke SK, Halter C, Rudolph A, Shults C, Conneally PM, Foroud T. Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations. American Journal of Human Genetics. 71: 124-35. PMID 12058349 DOI: 10.1086/341282  1
2002 Simon DK, Lin MT, Pascual-Leone A. "Nature versus nurture" and incompletely penetrant mutations. Journal of Neurology, Neurosurgery, and Psychiatry. 72: 686-9. PMID 12023405 DOI: 10.1136/jnnp.72.6.686  1
2002 Lin MT, Simon DK, Ahn CH, Kim LM, Beal MF. High aggregate burden of somatic mtDNA point mutations in aging and Alzheimer's disease brain. Human Molecular Genetics. 11: 133-45. PMID 11809722  1
2001 Simon DK, Lin MT, Ahn CH, Liu GJ, Gibson GE, Beal MF, Johns DR. Low mutational burden of individual acquired mitochondrial DNA mutations in brain. Genomics. 73: 113-6. PMID 11352572 DOI: 10.1006/geno.2001.6515  1
2001 Simon DK, Tarnopolsky MA, Greenamyre JT, Johns DR. A frameshift mitochondrial complex I gene mutation in a patient with dystonia and cataracts: is the mutation pathogenic? Journal of Medical Genetics. 38: 58-61. PMID 11332403  1
2000 Tabamo RE, Fernandez HH, Friedman JH, Simon DK. Young-onset Parkinson's disease: a clinical pathologic description of two siblings. Movement Disorders : Official Journal of the Movement Disorder Society. 15: 744-6. PMID 10928592 DOI: 10.1002/1531-8257(200007)15:4<744::AID-MDS1026>3.0.CO;2-#  1
2000 Simon DK, Mayeux R, Marder K, Kowall NW, Beal MF, Johns DR. Mitochondrial DNA mutations in complex I and tRNA genes in Parkinson's disease. Neurology. 54: 703-9. PMID 10680807  1
1999 Simon DK, Pulst SM, Sutton JP, Browne SE, Beal MF, Johns DR. Familial multisystem degeneration with parkinsonism associated with the 11778 mitochondrial DNA mutation. Neurology. 53: 1787-93. PMID 10563629  1
1999 Parker WD, Swerdlow RH, Parks JK, Davis JN, Trimmer P, Bennett JP, Wooten GF. Parkinson disease in twins. Jama. 282: 1328; author reply 1. PMID 10527169 DOI: 10.1001/jama.282.14.1328  1
1999 Simon DK, Johns DR. Mitochondrial disorders: clinical and genetic features. Annual Review of Medicine. 50: 111-27. PMID 10073267 DOI: 10.1146/annurev.med.50.1.111  1
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