Year |
Citation |
Score |
2020 |
Szigeti K, Ihnatovych I, Birkaya B, Chen Z, Ouf A, Indurthi DC, Bard JE, Kann J, Adams A, Chaves L, Sule N, Reisch JS, Pavlik V, Benedict RHB, Auerbach A, et al. CHRFAM7A: A human specific fusion gene, accounts for the translational gap for cholinergic strategies in Alzheimer's disease. Ebiomedicine. 59: 102892. PMID 32818803 DOI: 10.1016/J.Ebiom.2020.102892 |
0.31 |
|
2019 |
Ihnatovych I, Nayak TK, Ouf A, Sule N, Birkaya B, Chaves L, Auerbach A, Szigeti K. iPSC model of CHRFAM7A effect on α7 nicotinic acetylcholine receptor function in the human context. Translational Psychiatry. 9: 59. PMID 30710073 DOI: 10.1038/S41398-019-0375-Z |
0.301 |
|
2019 |
Szigeti K, Chen Z, Ouf A, Reisch J, Pavlik V, Wilding G. P4‐675: Cholinesterase Inhibitors Have A Disease Modifying Effect In Ad Relative To Chrfam7A Genotype, Suggesting An A7Nachr Dependent Mechanism Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.09.041 |
0.338 |
|
2018 |
Lew AR, Kellermayer TR, Sule BP, Szigeti K. Copy Number Variations in Adult-onset Neuropsychiatric Diseases. Current Genomics. 19: 420-430. PMID 30258274 DOI: 10.2174/1389202919666180330153842 |
0.397 |
|
2018 |
Woodward MR, Hafeez MU, Qi Q, Riaz A, Benedict RHB, Yan L, Szigeti K. Odorant Item Specific Olfactory Identification Deficit May Differentiate Alzheimer Disease From Aging. The American Journal of Geriatric Psychiatry : Official Journal of the American Association For Geriatric Psychiatry. PMID 29858162 DOI: 10.1016/J.Jagp.2018.02.008 |
0.333 |
|
2017 |
Woodward MR, Dwyer MG, Bergsland N, Hagemeier J, Zivadinov R, Benedict RH, Szigeti K. Olfactory identification deficit predicts white matter tract impairment in Alzheimer's disease. Psychiatry Research. 266: 90-95. PMID 28644998 DOI: 10.1016/J.Pscychresns.2017.06.004 |
0.348 |
|
2017 |
Hafeez MU, Mun KT, Kamal H, Szigeti K. Delusional Misidentification Syndrome with Response to Donepezil and Behavioral Intervention in a Patient with Dementia Journal of Aging Science. 5: 1-6. DOI: 10.4172/2329-8847.1000181 |
0.327 |
|
2017 |
Ouf A, Szigeti K. Evidence-Based Review of Therapeutic Approaches in Dementia with Lewy Bodies Journal of Alzheimers Disease & Parkinsonism. 7: 1-5. DOI: 10.4172/2161-0460.1000406 |
0.333 |
|
2016 |
Roy S, Ficarro S, Duberstein P, Chapman BP, Dubovsky S, Paroski M, Szigeti K, Benedict RH. Executive Function and Personality Predict Instrumental Activities of Daily Living in Alzheimer Disease. The American Journal of Geriatric Psychiatry : Official Journal of the American Association For Geriatric Psychiatry. PMID 27618644 DOI: 10.1016/J.Jagp.2016.06.014 |
0.304 |
|
2016 |
Szigeti K. New Genome-Wide Methods for Elucidation of Candidate Copy Number Variations (CNVs) Contributing to Alzheimer's Disease Heritability. Methods in Molecular Biology (Clifton, N.J.). 1303: 315-26. PMID 26235076 DOI: 10.1007/978-1-4939-2627-5_19 |
0.386 |
|
2016 |
Woodward MR, Hafeez MU, Khan MU, Hagemeier J, Yan L, Qi Q, Szigeti K. Characterization of Olfactory Identification Deficit in Aging Vs. Alzheimer's Disease American Journal of Geriatric Psychiatry. 24. DOI: 10.1016/J.Jagp.2016.01.099 |
0.34 |
|
2015 |
Szigeti K, Hafeez MU. Exploring the role of donepezil in dementia with Lewy bodies. Drugs of Today. 51: 579-590. PMID 26583300 DOI: 10.1358/Dot.2015.51.10.2389166 |
0.322 |
|
2015 |
Woodward MR, Dwyer MG, Amrutkar CV, Zivadinov R, Szigeti K. Olfactory Identification Deficit as a Predictor of White Matter Tract Integrity in Alzheimer's Disease American Journal of Geriatric Psychiatry. 23. DOI: 10.1016/J.Jagp.2014.12.104 |
0.323 |
|
2014 |
Szigeti K, Kellermayer B, Lentini JM, Trummer B, Lal D, Doody RS, Yan L, Liu S, Ma C. Ordered subset analysis of copy number variation association with age at onset of Alzheimer's disease Journal of Alzheimer's Disease. 41: 1063-1071. PMID 24787912 DOI: 10.3233/Jad-132693 |
0.398 |
|
2013 |
Jensen M, Cox AP, Chaudhry N, Ng M, Sule D, Duncan W, Ray P, Weinstock-Guttman B, Smith B, Ruttenberg A, Szigeti K, Diehl AD. The neurological disease ontology. Journal of Biomedical Semantics. 4: 42. PMID 24314207 DOI: 10.1186/2041-1480-4-42 |
0.331 |
|
2013 |
Szigeti K, Lal D, Li Y, Doody RS, Wilhelmsen K, Yan L, Liu S, Ma C. Genome-wide scan for copy number variation association with age at onset of Alzheimer's disease. Journal of Alzheimer's Disease : Jad. 33: 517-23. PMID 23202439 DOI: 10.3233/Jad-2012-121285 |
0.402 |
|
2013 |
Szigeti K, Trummer B, Lal D, Yan L, Song L, Doody R. Ordered subset analysis CNV association with Alzheimer's disease AAO phenotypes Alzheimers & Dementia. 9. DOI: 10.1016/J.Jalz.2013.05.287 |
0.374 |
|
2012 |
Li Y, Shaw CA, Sheffer I, Sule N, Powell SZ, Dawson B, Zaidi SN, Bucasas KL, Lupski JR, Wilhelmsen KC, Doody R, Szigeti K. Integrated copy number and gene expression analysis detects a CREB1 association with Alzheimer's disease. Translational Psychiatry. 2: e192. PMID 23168992 DOI: 10.1038/Tp.2012.119 |
0.338 |
|
2012 |
Szigeti K, Li Y, Shaw C, Sheffer I, Sule N, Powell S, Zaidi N, Lupski J, Wilhelmsen K, Doody R. Integrated copy number and gene expression analysis detects a CREB1 association with Alzheimer's disease Alzheimers & Dementia. 8: 672. DOI: 10.1016/J.Jalz.2012.05.1817 |
0.396 |
|
2011 |
Szigeti K, Doody RS. Should persons with autosomal dominant AD be included in clinical trials? Authors' response. Alzheimer's Research & Therapy. 3: 19. PMID 21631907 DOI: 10.1186/Alzrt81 |
0.35 |
|
2011 |
Shaw CA, Li Y, Wiszniewska J, Chasse S, Zaidi SN, Jin W, Dawson B, Wilhelmsen K, Lupski JR, Belmont JW, Doody RS, Szigeti K. Olfactory copy number association with age at onset of Alzheimer disease. Neurology. 76: 1302-9. PMID 21482944 DOI: 10.1212/Wnl.0B013E3182166Df5 |
0.4 |
|
2011 |
Szigeti K, Doody RS. Should EOAD patients be included in clinical trials? Alzheimer's Research & Therapy. 3: 4. PMID 21345175 DOI: 10.1186/Alzrt63 |
0.358 |
|
2010 |
Antonellis A, Dennis MY, Burzynski G, Huynh J, Maduro V, Hodonsky CJ, Khajavi M, Szigeti K, Mukkamala S, Bessling SL, Pavan WJ, McCallion AS, Lupski JR, Green ED. A rare myelin protein zero (MPZ) variant alters enhancer activity in vitro and in vivo. Plos One. 5: e14346. PMID 21179557 DOI: 10.1371/Journal.Pone.0014346 |
0.343 |
|
2010 |
McLaughlin HM, Sakaguchi R, Liu C, Igarashi T, Pehlivan D, Chu K, Iyer R, Cruz P, Cherukuri PF, Hansen NF, Mullikin JC, Biesecker LG, Wilson TE, Ionasescu V, ... ... Szigeti K, et al. Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy. American Journal of Human Genetics. 87: 560-6. PMID 20920668 DOI: 10.1016/J.Ajhg.2010.09.008 |
0.394 |
|
2009 |
England JD, Gronseth GS, Franklin G, Carter GT, Kinsella LJ, Cohen JA, Asbury AK, Szigeti K, Lupski JR, Latov N, Lewis RA, Low PA, Fisher MA, Herrmann DN, Howard JF, et al. Practice parameter: the evaluation of distal symmetric polyneuropathy: the role of laboratory and genetic testing (an evidence-based review). Report of the American Academy of Neurology, the American Association of Neuromuscular and Electrodiagnostic Medicine, and the American Academy of Physical Medicine and Rehabilitation. Pm & R : the Journal of Injury, Function, and Rehabilitation. 1: 5-13. PMID 19627867 DOI: 10.1016/J.Pmrj.2008.11.010 |
0.307 |
|
2009 |
Szigeti K, Lupski JR. Charcot-Marie-Tooth disease. European Journal of Human Genetics : Ejhg. 17: 703-10. PMID 19277060 DOI: 10.1038/Ejhg.2009.31 |
0.406 |
|
2009 |
England JD, Gronseth GS, Franklin G, Carter GT, Kinsella LJ, Cohen JA, Asbury AK, Szigeti K, Lupski JR, Latov N, Lewis RA, Low PA, Fisher MA, Herrmann D, Howard JF, et al. Evaluation of distal symmetric polyneuropathy: the role of laboratory and genetic testing (an evidence-based review). Muscle & Nerve. 39: 116-25. PMID 19086068 DOI: 10.1002/Mus.21226 |
0.316 |
|
2009 |
England JD, Gronseth GS, Franklin G, Carter GT, Kinsella LJ, Cohen JA, Asbury AK, Szigeti K, Lupski JR, Latov N, Lewis RA, Low PA, Fisher MA, Herrmann DN, Howard JF, et al. Practice Parameter: evaluation of distal symmetric polyneuropathy: role of laboratory and genetic testing (an evidence-based review). Report of the American Academy of Neurology, American Association of Neuromuscular and Electrodiagnostic Medicine, and American Academy of Physical Medicine and Rehabilitation. Neurology. 72: 185-92. PMID 19056666 DOI: 10.1212/01.Wnl.0000336370.51010.A1 |
0.307 |
|
2009 |
Szigeti K, Shaw C, Li Y, Lupski JR, Belmont J, Doody RS. Olfactory receptor cluster copy number is associated with age at onset of Alzheimer's disease Alzheimers & Dementia. 5: 469. DOI: 10.1016/J.Jalz.2009.04.795 |
0.315 |
|
2007 |
Szigeti K, Wiszniewski W, Saifi GM, Sherman DL, Sule N, Adesina AM, Mancias P, Papasozomenos SCh, Miller G, Keppen L, Daentl D, Brophy PJ, Lupski JR. Functional, histopathologic and natural history study of neuropathy associated with EGR2 mutations. Neurogenetics. 8: 257-62. PMID 17717711 DOI: 10.1007/S10048-007-0094-0 |
0.334 |
|
2006 |
Szigeti K, Nelis E, Lupski JR. Molecular diagnostics of Charcot-Marie-Tooth disease and related peripheral neuropathies. Neuromolecular Medicine. 8: 243-54. PMID 16775379 DOI: 10.1385/Nmm:8:1-2:243 |
0.317 |
|
2006 |
Verhoeven K, Claeys KG, Züchner S, Schröder JM, Weis J, Ceuterick C, Jordanova A, Nelis E, De Vriendt E, Van Hul M, Seeman P, Mazanec R, Saifi GM, Szigeti K, Mancias P, et al. MFN2 mutation distribution and genotype/phenotype correlation in Charcot-Marie-Tooth type 2. Brain : a Journal of Neurology. 129: 2093-102. PMID 16714318 DOI: 10.1093/Brain/Awl126 |
0.336 |
|
2006 |
Szigeti K, Garcia CA, Lupski JR. Charcot-Marie-Tooth disease and related hereditary polyneuropathies: molecular diagnostics determine aspects of medical management. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 8: 86-92. PMID 16481890 DOI: 10.1097/01.Gim.0000200160.29385.73 |
0.37 |
|
2006 |
Shy ME, Scavina MT, Clark A, Krajewski KM, Li J, Kamholz J, Kolodny E, Szigeti K, Fischer RA, Saifi GM, Scherer SS, Lupski JR. T118M PMP22 mutation causes partial loss of function and HNPP-like neuropathy. Annals of Neurology. 59: 358-64. PMID 16437560 DOI: 10.1002/Ana.20777 |
0.343 |
|
2005 |
Saifi GM, Szigeti K, Wiszniewski W, Shy ME, Krajewski K, Hausmanowa-Petrusewicz I, Kochanski A, Reeser S, Mancias P, Butler I, Lupski JR. SIMPLE mutations in Charcot-Marie-Tooth disease and the potential role of its protein product in protein degradation. Human Mutation. 25: 372-83. PMID 15776429 DOI: 10.1002/Humu.20153 |
0.357 |
|
2003 |
Saifi GM, Szigeti K, Snipes GJ, Garcia CA, Lupski JR. Molecular mechanisms, diagnosis, and rational approaches to management of and therapy for Charcot-Marie-Tooth disease and related peripheral neuropathies. Journal of Investigative Medicine : the Official Publication of the American Federation For Clinical Research. 51: 261-83. PMID 14577517 DOI: 10.1136/Jim-51-05-14 |
0.35 |
|
2003 |
Szigeti K, Saifi GM, Armstrong D, Belmont JW, Miller G, Lupski JR. Disturbance of muscle fiber differentiation in congenital hypomyelinating neuropathy caused by a novel myelin protein zero mutation. Annals of Neurology. 54: 398-402. PMID 12953275 DOI: 10.1002/Ana.10681 |
0.317 |
|
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