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Vincent M. Aita, Ph.D. - Publications

Affiliations: 
2000 Columbia University, New York, NY 
Area:
Genetics, Molecular Biology, Oncology
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18 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, 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
2003 Kljuic A, Bazzi H, Sundberg JP, Martinez-Mir A, O'Shaughnessy R, Mahoney MG, Levy M, Montagutelli X, Ahmad W, Aita VM, Gordon D, Uitto J, Whiting D, Ott J, Fischer S, et al. Desmoglein 4 in hair follicle differentiation and epidermal adhesion: evidence from inherited hypotrichosis and acquired pemphigus vulgaris. Cell. 113: 249-60. PMID 12705872 DOI: 10.1016/S0092-8674(03)00273-3  0.536
2002 Zlotogorski A, Panteleyev AA, Aita VM, Christiano AM. Clinical and molecular diagnostic criteria of congenital atrichia with papular lesions Journal of Investigative Dermatology. 118: 887-890. PMID 11982770 DOI: 10.1046/J.1523-1747.2001.01767.X  0.382
2002 Zlotogorski A, Panteleyev AA, Aita VM, Christiano AM. Clinical and molecular diagnostic criteria of congenital atrichia with papular lesions. The Journal of Investigative Dermatology. 117: 1662-5. PMID 11886538 DOI: 10.1046/J.0022-202X.2001.01618.X  0.382
2002 Ahmad W, Ratterree MS, Panteleyev AA, Aita VM, Sundberg JP, Christiano AM. Atrichia with papular lesions resulting from mutations in the rhesus macaque (Macaca mulatta) hairless gene. Laboratory Animals. 36: 61-7. PMID 11831740 DOI: 10.1258/0023677021911777  0.457
2001 Cserhalmi-Friedman PB, Frank JA, Ahmad W, Panteleyev AA, Aita VM, Christiano AM. Structural analysis reflects the evolutionary relationship between the human desmocollin gene family members. Experimental Dermatology. 10: 95-9. PMID 11260247 DOI: 10.1034/J.1600-0625.2001.010002095.X  0.448
2001 Frank J, Cserhalmi-Friedman PB, Ahmad W, Panteleyev AA, Aita VM, Christiano AM. Characterization of the desmosomal cadherin gene family: genomic organization of two desmoglein genes on human chromosome 18q12. Experimental Dermatology. 10: 90-4. PMID 11260246 DOI: 10.1034/J.1600-0625.2001.010002090.X  0.516
2001 Frank J, Aita VM, Ahmad W, Lam H, Wolff C, Christiano AM. Identification of a founder mutation in the protoporphyrinogen oxidase gene in variegate porphyria patients from chile. Human Heredity. 51: 160-8. PMID 11173967 DOI: 10.1159/000053337  0.467
2001 Aita VM, Christiano AM. The genetics of alopecia areata Dermatologic Therapy. 14: 329-339. DOI: 10.1046/J.1529-8019.2001.01041.X  0.374
2000 Aita VM, Ahmad W, Panteleyev AA, Kozlowska U, Kozlowska A, Gilliam TC, Jablonska S, Christiano AM. A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesions. Experimental Dermatology. 9: 157-62. PMID 10772391 DOI: 10.1034/J.1600-0625.2000.009002157.X  0.58
1999 Aita VM, Christiano AM, Gilliam TC. Mapping complex traits in diseases of the hair and skin. Experimental Dermatology. 8: 439-52. PMID 10597133 DOI: 10.1111/J.1600-0625.1999.Tb00302.X  0.545
1999 Aita VM, Liang XH, Murty VV, Pincus DL, Yu W, Cayanis E, Kalachikov S, Gilliam TC, Levine B. Cloning and genomic organization of beclin 1, a candidate tumor suppressor gene on chromosome 17q21. Genomics. 59: 59-65. PMID 10395800 DOI: 10.1006/Geno.1999.5851  0.561
1999 Frank J, Pignata C, Panteleyev AA, Prowse DM, Baden H, Weiner L, Gaetaniello L, Ahmad W, Pozzi N, Cserhalmi-Friedman PB, Aita VM, Uyttendaele H, Gordon D, Ott J, Brissette JL, et al. Exposing the human nude phenotype [4] Nature. 398: 473-474. PMID 10206641 DOI: 10.1038/18997  0.391
1999 Aita VM, Liu J, Knowles JA, Terwilliger JD, Baltazar R, Grunn A, Loth JE, Kanyas K, Lerer B, Endicott J, Wang Z, Penchaszadeh G, Gilliam TC, Baron M. A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus. American Journal of Human Genetics. 64: 210-7. PMID 9915960 DOI: 10.1086/302185  0.558
1998 Frank J, Wang X, Lam HM, Aita VM, Jugert FK, Goerz G, Merk HF, Poh-Fitzpatrick MB, Christiano AM. C73R is a hotspot mutation in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria Annals of Human Genetics. 62: 225-230. PMID 9803266 DOI: 10.1046/j.1469-1809.1998.6230225.x  0.383
1998 Ahmad W, Brancolini V, Ul Haque MF, Lam H, Ul Haque S, Haider M, Maimon A, Aita VM, Owen J, Brown D, Zegarelli DJ, Ahmad M, Ott J, Christiano AM. A locus for autosomal recessive hypodontia with associated dental anomalies maps to chromosome 16q12.1 [2] American Journal of Human Genetics. 62: 987-991. PMID 9529357 DOI: 10.1086/301799  0.379
1998 Ahmad W, Ul Haque MF, Brancolini V, Tsou HC, Ul Haque S, Lam H, Aita VM, Owen J, DeBlaquiere M, Frank J, Cserhalmi-Friedman PB, Leask A, McGrath JA, Peacocke M, Ahmad M, et al. Alopecia universalis associated with a mutation in the human hairless gene Science. 279: 720-724. PMID 9445480 DOI: 10.1126/Science.279.5351.720  0.498
1998 Lam H, Frank J, Wang X, Aita VM, Jugert FK, Kalka K, Goerz G, Merk HF, Christiano AM, Poh-Fitzpatrick MB. Congenital erythropoietic porphyria: C73R is a hotspot mutation in the uroporphyrinogen III synthase gene Journal of Dermatological Science. 16: S143. DOI: 10.1016/S0923-1811(98)83856-5  0.368
1998 Ahmad W, Brancolini V, ul Haque M, Lam H, ul Haque S, Haider M, Maimon A, Aita V, Ahmad M, Ott J, Christiano A. A locus for autosomal recessive hypodontia maps to chromosome 16q12.1 Journal of Dermatological Science. 16: S107. DOI: 10.1016/S0923-1811(98)83636-0  0.353
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