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Page 1
Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder.
Nemirovsky SI, Córdoba M, Zaiat JJ, Completa SP, Vega PA, González-Morón D, Medina NM, Fabbro M, Romero S, Brun B, Revale S, Ogara MF, Pecci A, Marti M, Vazquez M, Turjanski A, Kauffman MA. Nemirovsky SI, et al. Among authors: zaiat jj. PLoS One. 2015 Feb 3;10(2):e0116358. doi: 10.1371/journal.pone.0116358. eCollection 2015. PLoS One. 2015. PMID: 25646853 Free PMC article.
Human Y chromosome sequences from Q Haplogroup reveal a South American settlement pre-18,000 years ago and a profound genomic impact during the Younger Dryas.
Paz Sepúlveda PB, Mayordomo AC, Sala C, Sosa EJ, Zaiat JJ, Cuello M, Schwab M, Rodríguez Golpe D, Aquilano E, Santos MR, Dipierri JE, Alfaro Gómez EL, Bravi CM, Muzzio M, Bailliet G. Paz Sepúlveda PB, et al. Among authors: zaiat jj. PLoS One. 2022 Aug 17;17(8):e0271971. doi: 10.1371/journal.pone.0271971. eCollection 2022. PLoS One. 2022. PMID: 35976870 Free PMC article.
Germline hypomorphic CARD11 mutations in severe atopic disease.
Ma CA, Stinson JR, Zhang Y, Abbott JK, Weinreich MA, Hauk PJ, Reynolds PR, Lyons JJ, Nelson CG, Ruffo E, Dorjbal B, Glauzy S, Yamakawa N, Arjunaraja S, Voss K, Stoddard J, Niemela J, Zhang Y, Rosenzweig SD, McElwee JJ, DiMaggio T, Matthews HF, Jones N, Stone KD, Palma A, Oleastro M, Prieto E, Bernasconi AR, Dubra G, Danielian S, Zaiat J, Marti MA, Kim B, Cooper MA, Romberg N, Meffre E, Gelfand EW, Snow AL, Milner JD. Ma CA, et al. Among authors: zaiat j. Nat Genet. 2017 Aug;49(8):1192-1201. doi: 10.1038/ng.3898. Epub 2017 Jun 19. Nat Genet. 2017. PMID: 28628108 Free PMC article.
Cost-Effective Method to Perform SARS-CoV-2 Variant Surveillance: Detection of Alpha, Gamma, Lambda, Delta, Epsilon, and Zeta in Argentina.
Torres C, Mojsiejczuk L, Acuña D, Alexay S, Amadio A, Aulicino P, Debat H, Fay F, Fernández F, Giri AA, Goya S, König G, Lucero H, Nabaes Jodar M, Pianciola L, Sfalcin JA, Acevedo RM, Bengoa Luoni S, Bolatti EM, Brusés B, Cacciabue M, Casal PE, Cerri A, Chouhy D, Dus Santos MJ, Eberhardt MF, Fernandez A, Fernández PDC, Fernández Do Porto D, Formichelli L, Gismondi MI, Irazoqui M, Campos ML, Lusso S, Marquez N, Muñoz M, Mussin J, Natale M, Oria G, Pisano MB, Posner V, Puebla A, Re V, Sosa E, Villanova GV, Zaiat J, Zunino S, Acevedo ME, Acosta J, Alvarez Lopez C, Álvarez ML, Angeleri P, Angelletti A, Arca M, Ayala NA, Barbas G, Bertone A, Bonnet A, Bourlot I, Cabassi V, Castello A, Castro G, Cavatorta AL, Ceriani C, Cimmino C, Cipelli J, Colmeiro M, Cordero A, Cristina C, Di Bella S, Dolcini G, Ercole R, Espasandin Y, Espul C, Falaschi A, Fernandez Moll F, Foussal MD, Gatelli A, Goñi S, Jofré ME, Jaramillo J, Labarta N, Lacaze MA, Larreche R, Leiva V, Levin G, Luczak E, Mandile M, Marino G, Massone C, Mazzeo M, Medina C, Monaco B, Montoto L, Mugna V, Musto A, Nadalich V, Nieto MV, Ojeda G, Piedrabuena AC, Pintos C, Pozzati M, Rahhal M, Rechimont C, Remes Lenicov F, Rompato G, Seery … See abstract for full author list ➔ Torres C, et al. Front Med (Lausanne). 2021 Dec 10;8:755463. doi: 10.3389/fmed.2021.755463. eCollection 2021. Front Med (Lausanne). 2021. PMID: 34957143 Free PMC article.
Corrigendum: Germline hypomorphic CARD11 mutations in severe atopic disease.
Ma CA, Stinson JR, Zhang Y, Abbott JK, Weinreich MA, Hauk PJ, Reynolds PR, Lyons JJ, Nelson CG, Ruffo E, Dorjbal B, Glauzy S, Yamakawa N, Arjunaraja S, Voss K, Stoddard J, Niemela J, Zhang Y, Rosenzweig SD, McElwee JJ, DiMaggio T, Matthews HF, Jones N, Stone KD, Palma A, Oleastro M, Prieto E, Bernasconi AR, Dubra G, Danielian S, Zaiat J, Marti MA, Kim B, Cooper MA, Romberg ND, Meffre E, Gelfand EW, Snow AL, Milner JD. Ma CA, et al. Among authors: zaiat j. Nat Genet. 2017 Oct 27;49(11):1661. doi: 10.1038/ng1117-1661b. Nat Genet. 2017. PMID: 29074947