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Novel and recurrent non-truncating mutations of the MITF basic domain: genotypic and phenotypic variations in Waardenburg and Tietz syndromes.
Léger S, Balguerie X, Goldenberg A, Drouin-Garraud V, Cabot A, Amstutz-Montadert I, Young P, Joly P, Bodereau V, Holder-Espinasse M, Jamieson RV, Krause A, Chen H, Baumann C, Nunes L, Dollfus H, Goossens M, Pingault V. Léger S, et al. Among authors: cabot a. Eur J Hum Genet. 2012 May;20(5):584-7. doi: 10.1038/ejhg.2011.234. Epub 2012 Jan 18. Eur J Hum Genet. 2012. PMID: 22258527 Free PMC article.
A retGC-1 mutation in autosomal dominant cone-rod dystrophy.
Perrault I, Rozet JM, Gerber S, Kelsell RE, Souied E, Cabot A, Hunt DM, Munnich A, Kaplan J. Perrault I, et al. Among authors: cabot a. Am J Hum Genet. 1998 Aug;63(2):651-4. doi: 10.1086/301985. Am J Hum Genet. 1998. PMID: 9683616 Free PMC article. No abstract available.
A Real-World Prospective Multiple Sclerosis Pregnancy Registry in the United States: PREG-MS.
Houtchens MK, Manieri MC, Mahlanza TD, Pol-Patil J, Klawiter EC, Solomon AJ, Lathi E, Katz J, Ionete C, Morales IB, Severson C, Zurawski J, Stankiewicz JM, Cabot A, Sadovnick AD. Houtchens MK, et al. Among authors: cabot a. Neurol Clin Pract. 2025 Apr;15(2):e200425. doi: 10.1212/CPJ.0000000000200425. Epub 2025 Jan 10. Neurol Clin Pract. 2025. PMID: 39810912
Realizing high power factor and thermoelectric performance in band engineered AgSbTe2.
Zhang Y, Xing C, Wang D, Genç A, Lee SH, Chang C, Li Z, Zheng L, Lim KH, Zhu H, Smriti RB, Liu Y, Cheng S, Hong M, Fan X, Mao Z, Zhao LD, Cabot A, Zhu T, Poudel B. Zhang Y, et al. Among authors: cabot a. Nat Commun. 2025 Jan 2;16(1):22. doi: 10.1038/s41467-024-55280-0. Nat Commun. 2025. PMID: 39746968 Free PMC article.
171 results