| Year |
Citation |
Score |
| 2018 |
Claire Simon K, Hentati A, Rubin S, Franada T, Maurer D, Hillman L, Tideman S, Szela M, Meyers S, Frigerio R, Maraganore DM. Successful utilization of the EMR in a multiple sclerosis clinic to support quality improvement and research initiatives at the point of care. Multiple Sclerosis Journal - Experimental, Translational and Clinical. 4: 2055217318813736. PMID 30559971 DOI: 10.1177/2055217318813736 |
0.415 |
|
| 2008 |
Tsaousidou MK, Ouahchi K, Warner TT, Yang Y, Simpson MA, Laing NG, Wilkinson PA, Madrid RE, Patel H, Hentati F, Patton MA, Hentati A, Lamont PJ, Siddique T, Crosby AH. Sequence alterations within CYP7B1 implicate defective cholesterol homeostasis in motor-neuron degeneration. American Journal of Human Genetics. 82: 510-5. PMID 18252231 DOI: 10.1016/J.Ajhg.2007.10.001 |
0.331 |
|
| 2003 |
Yip AG, Dürr A, Marchuk DA, Ashley-Koch A, Hentati A, Rubinsztein DC, Reid E. Meta-analysis of age at onset in spastin-associated hereditary spastic paraplegia provides no evidence for a correlation with mutational class. Journal of Medical Genetics. 40: e106. PMID 12960222 DOI: 10.1136/Jmg.40.9.E106 |
0.38 |
|
| 2001 |
Yang Y, Hentati A, Deng HX, Dabbagh O, Sasaki T, Hirano M, Hung WY, Ouahchi K, Yan J, Azim AC, Cole N, Gascon G, Yagmour A, Ben-Hamida M, Pericak-Vance M, et al. The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis. Nature Genetics. 29: 160-5. PMID 11586297 DOI: 10.1038/Ng1001-160 |
0.486 |
|
| 2000 |
Hentati A, Deng HX, Zhai H, Chen W, Yang Y, Hung WY, Azim AC, Bohlega S, Tandan R, Warner C, Laing NG, Cambi F, Mitsumoto H, Roos RP, Boustany RM, et al. Novel mutations in spastin gene and absence of correlation with age at onset of symptoms. Neurology. 55: 1388-90. PMID 11087788 DOI: 10.1212/Wnl.55.9.1388 |
0.49 |
|
| 1998 |
Hentati A, Ouahchi K, Pericak-Vance MA, Nijhawan D, Ahmad A, Yang Y, Rimmler J, Hung W, Schlotter B, Ahmed A, Ben Hamida M, Hentati F, Siddique T. Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers. Neurogenetics. 2: 55-60. PMID 9933301 DOI: 10.1007/S100480050052 |
0.407 |
|
| 1997 |
Siddique T, Nijhawan D, Hentati A. Familial amyotrophic lateral sclerosis. Journal of Neural Transmission. Supplementum. 49: 219-33. PMID 9266431 DOI: 10.1007/978-3-7091-6844-8_23 |
0.545 |
|
| 1997 |
Ahmed MS, Afsar S, Hentati A, Ahmad A, Pasha J, Juneja T, Hung WY, Ahmad A, Choudhri A, Saya S, Siddique T. A novel mutation in the sterol 27-hydroxylase gene of a Pakistani family with autosomal recessive cerebrotendinous xanthomatosis. Neurology. 48: 258-60. PMID 9008528 DOI: 10.1212/Wnl.48.1.258 |
0.461 |
|
| 1996 |
Isozumi K, DeLong R, Kaplan J, Deng HX, Iqbal Z, Hung WY, Wilhelmsen KC, Hentati A, Pericak-Vance MA, Siddique T. Linkage of scapuloperoneal spinal muscular atrophy to chromosome 12q24.1-q24.31. Human Molecular Genetics. 5: 1377-82. PMID 8872481 DOI: 10.1093/Hmg/5.9.1377 |
0.372 |
|
| 1996 |
Siddique T, Nijhawan D, Hentati A. Molecular genetic basis of familial ALS. Neurology. 47: S27-34; discussion S. PMID 8858048 DOI: 10.1212/Wnl.47.4_Suppl_2.27S |
0.544 |
|
| 1996 |
Fink JK, Heiman-Patterson T, Bird T, Cambi F, Dubé MP, Figlewicz DA, Fink JK, Haines JL, Heiman-Patterson T, Hentati A, Pericak-Vance MA, Raskind W, Rouleau GA, Siddique T. Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group. Neurology. 46: 1507-14. PMID 8649538 DOI: 10.1212/Wnl.46.6.1507 |
0.432 |
|
| 1996 |
Hentati A, Deng HX, Hung WY, Nayer M, Ahmed MS, He X, Tim R, Stumpf DA, Siddique T, Ahmed. Human alpha-tocopherol transfer protein: gene structure and mutations in familial vitamin E deficiency. Annals of Neurology. 39: 295-300. PMID 8602747 DOI: 10.1002/Ana.410390305 |
0.553 |
|
| 1995 |
Deng HX, Tainer JA, Mitsumoto H, Ohnishi A, He X, Hung WY, Zhao Y, Juneja T, Hentati A, Siddique T. Two novel SOD1 mutations in patients with familial amyotrophic lateral sclerosis. Human Molecular Genetics. 4: 1113-6. PMID 7655471 DOI: 10.1093/Hmg/4.6.1113 |
0.469 |
|
| 1994 |
Gurney ME, Pu H, Chiu AY, Dal Canto MC, Polchow CY, Alexander DD, Caliendo J, Hentati A, Kwon YW, Deng HX. Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation. Science (New York, N.Y.). 264: 1772-5. PMID 8209258 DOI: 10.1126/Science.8209258 |
0.401 |
|
| 1994 |
Hentati A, Pericak-Vance MA, Hung WY, Belal S, Laing N, Boustany RM, Hentati F, Ben Hamida M, Siddique T. Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity. Human Molecular Genetics. 3: 1263-7. PMID 7987300 DOI: 10.1093/Hmg/3.8.1263 |
0.461 |
|
| 1994 |
Hentati A, Bejaoui K, Pericak-Vance MA, Hentati F, Speer MC, Hung WY, Figlewicz DA, Haines J, Rimmler J, Ben Hamida C. Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35. Nature Genetics. 7: 425-8. PMID 7920663 DOI: 10.1038/Ng0794-425 |
0.434 |
|
| 1994 |
Hentati A, Pericak-Vance MA, Lennon F, Wasserman B, Hentati F, Juneja T, Angrist MH, Hung WY, Boustany RM, Bohlega S. Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers. Human Molecular Genetics. 3: 1867-71. PMID 7849714 DOI: 10.1093/Hmg/3.10.1867 |
0.426 |
|
| 1993 |
Deng HX, Hentati A, Tainer JA, Iqbal Z, Cayabyab A, Hung WY, Getzoff ED, Hu P, Herzfeldt B, Roos RP, Warner C, Deng G, Soriano E, Smyth C, Parge HE, et al. Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase Science. 261: 1047-1051. PMID 8351519 DOI: 10.1126/Science.8351519 |
0.403 |
|
| 1992 |
Hentati A, Lamy C, Melki J, Zuber M, Munnich A, Recondo Jd. Clinical and genetic heterogeneity of Charcot-Marie-Tooth disease. Genomics. 12: 155-157. PMID 1733853 DOI: 10.1016/0888-7543(92)90419-S |
0.45 |
|
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