| Year |
Citation |
Score |
| 2015 |
Moalem S, Brouillard P, Kuypers D, Legius E, Harvey E, Taylor G, Francois M, Vikkula M, Chitayat D. Hypotrichosis-lymphedema-telangiectasia-renal defect associated with a truncating mutation in the SOX18 gene. Clinical Genetics. 87: 378-82. PMID 24697860 DOI: 10.1111/Cge.12388 |
0.323 |
|
| 2013 |
Moalem S, Keating S, Shannon P, Thompson M, Millar K, Nykamp K, Forster A, Noor A, Chitayat D. Broadening the ciliopathy spectrum: motile cilia dyskinesia, and nephronophthisis associated with a previously unreported homozygous mutation in the INVS/NPHP2 gene. American Journal of Medical Genetics. Part A. 161: 1792-6. PMID 23713026 DOI: 10.1002/Ajmg.A.36036 |
0.349 |
|
| 2012 |
Moalem S, Babul-Hirji R, Stavropolous DJ, Wherrett D, Bägli DJ, Thomas P, Chitayat D. XX male sex reversal with genital abnormalities associated with a de novo SOX3 gene duplication. American Journal of Medical Genetics. Part A. 158: 1759-64. PMID 22678921 DOI: 10.1002/Ajmg.A.35390 |
0.309 |
|
| 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 |
0.589 |
|
| 2006 |
Perl DP, Moalem S. Aluminum and Alzheimer's disease, a personal perspective after 25 years. Journal of Alzheimer's Disease : Jad. 9: 291-300. PMID 17004365 DOI: 10.3233/Jad-2006-9S332 |
0.368 |
|
| 2006 |
Perl DP, Moalem S. Aluminum, Alzheimer's Disease and the Geospatial Occurrence of Similar Disorders Reviews in Mineralogy and Geochemistry. 64: 115-134. DOI: 10.2138/Rmg.2006.64.4 |
0.329 |
|
| 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 |
0.51 |
|
| 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 |
0.574 |
|
| 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 |
0.515 |
|
| 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 |
0.511 |
|
| 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 |
0.592 |
|
| 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 |
0.604 |
|
| 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 |
0.564 |
|
| 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 |
0.599 |
|
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