| Year |
Citation |
Score |
| 2014 |
Percy M, Somerville MJ, Hicks M, Garcia A, Colelli T, Wright E, Kitaygorodsky J, Jiang A, Ho V, Parpia A, Wong MK. Risk factors for development of dementia in a unique six-year cohort study. I. An exploratory, pilot study of involvement of the E4 allele of apolipoprotein E, mutations of the hemochromatosis-HFE gene, type 2 diabetes, and stroke. Journal of Alzheimer's Disease : Jad. 38: 907-22. PMID 24081379 DOI: 10.3233/Jad-131409 |
0.399 |
|
| 2008 |
Percy M, Moalem S, Garcia A, Somerville MJ, Hicks M, Andrews D, Azad A, Schwarz P, Beheshti Zavareh R, Birkan R, Choo C, Chow V, Dhaliwal S, Duda V, Kupferschmidt AL, et al. Involvement of ApoE E4 and H63D in sporadic Alzheimer's disease in a folate-supplemented Ontario population. Journal of Alzheimer's Disease : Jad. 14: 69-84. PMID 18525129 DOI: 10.3233/Jad-2008-14107 |
0.724 |
|
| 2005 |
Moalem S, Storey KB, Percy ME, Peros MC, Perl DP. The sweet thing about Type 1 diabetes: a cryoprotective evolutionary adaptation. Medical Hypotheses. 65: 8-16. PMID 15893109 DOI: 10.1016/J.Mehy.2004.12.025 |
0.674 |
|
| 2004 |
Moalem S, Weinberg ED, Percy ME. Hemochromatosis and the enigma of misplaced iron: implications for infectious disease and survival. Biometals : An International Journal On the Role of Metal Ions in Biology, Biochemistry, and Medicine. 17: 135-9. PMID 15088940 DOI: 10.1023/B:Biom.0000018375.20026.B3 |
0.712 |
|
| 2003 |
Percy ME, Potyomkina Z, Dalton AJ, Fedor B, Mehta P, Andrews DF, Mazzulli T, Murk L, Warren AC, Wallace RA, Chau H, Jeng W, Moalem S, O'Brien L, Schellenberger S, et al. Relation between apolipoprotein E genotype, hepatitis B virus status, and thyroid status in a sample of older persons with Down syndrome. American Journal of Medical Genetics. Part A. 120: 191-8. PMID 12833399 DOI: 10.1002/Ajmg.A.20099 |
0.678 |
|
| 2002 |
Moalem S, Percy ME. The quandary of reductionism: relevance to Alzheimer disease research. Journal of Alzheimer's Disease : Jad. 4: 531-7. PMID 12629263 DOI: 10.3233/Jad-2002-4610 |
0.676 |
|
| 2002 |
Moalem S, Percy ME, Kruck TP, Gelbart RR. Epidemic pathogenic selection: an explanation for hereditary hemochromatosis? Medical Hypotheses. 59: 325-9. PMID 12208162 DOI: 10.1016/S0306-9877(02)00179-2 |
0.721 |
|
| 2001 |
Connor JR, Milward EA, Moalem S, Sampietro M, Boyer P, Percy ME, Vergani C, Scott RJ, Chorney M. Is hemochromatosis a risk factor for Alzheimer's disease? Journal of Alzheimer's Disease : Jad. 3: 471-477. PMID 12214033 DOI: 10.3233/Jad-2001-3506 |
0.732 |
|
| 2001 |
Nicolaou M, Song YQ, Sato CA, Orlacchio A, Kawarai T, Medeiros H, Liang Y, Sorbi S, Richard E, Rogaev EI, Moliaka Y, Bruni AC, Jorge R, Percy M, Duara R, et al. Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease. Neurogenetics. 3: 203-6. PMID 11714100 DOI: 10.1007/S100480100123 |
0.394 |
|
| 2000 |
Moalem S, Percy ME, Andrews DF, Kruck TP, Wong S, Dalton AJ, Mehta P, Fedor B, Warren AC. Erratum: are hereditary hemochromatosis mutations involved in alzheimer disease? American Journal of Medical Genetics. 95: 189. PMID 11078576 DOI: 10.1002/1096-8628(20001113)95:2<189::Aid-Ajmg21>3.0.Co;2-7 |
0.704 |
|
| 2000 |
Moalem S, Percy ME, Andrews DF, Kruck TP, Wong S, Dalton AJ, Mehta P, Fedor B, Warren AC. Are hereditary hemochromatosis mutations involved in Alzheimer disease? American Journal of Medical Genetics. 93: 58-66. PMID 10861683 DOI: 10.1002/1096-8628(20000703)93:1<58::Aid-Ajmg10>3.0.Co;2-L |
0.725 |
|
| 1996 |
Sherrington R, Froelich S, Sorbi S, Campion D, Chi H, Rogaeva EA, Levesque G, Rogaev EI, Lin C, Liang Y, Ikeda M, Mar L, Brice A, Agid Y, Percy ME, et al. Alzheimer's disease associated with mutations in presenilin 2 is rare and variably penetrant. Human Molecular Genetics. 5: 985-8. PMID 8817335 DOI: 10.1093/Hmg/5.7.985 |
0.313 |
|
| 1992 |
Karlinsky H, Vaula G, Haines JL, Ridgley J, Bergeron C, Mortilla M, Tupler RG, Percy ME, Robitaille Y, Noldy NE. Molecular and prospective phenotypic characterization of a pedigree with familial Alzheimer's disease and a missense mutation in codon 717 of the beta-amyloid precursor protein gene. Neurology. 42: 1445-53. PMID 1520398 DOI: 10.1212/Wnl.42.8.1445 |
0.302 |
|
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