Works by Cosentino, Viviana

Results: 20
    1

    Identification of copy‐number variants in patients with overgrowth disorders.

    Published in:
    Clinical Genetics, 2024, v. 106, n. 5, p. 614, doi. 10.1111/cge.14596
    By:
    • Parra, Alejandro;
    • Tenorio‐Castano, Jair;
    • Nevado, Julián;
    • Cazalla, Mario;
    • Miranda‐Alcaraz, Lucía;
    • Gallego‐Zazo, Natalia;
    • Silván, Cristina;
    • Arias, Pedro;
    • Pozo‐Román, Jesús;
    • Ballesta‐Martínez, María Juliana;
    • Guillén‐Navarro, Encarna;
    • Arroyo, Ignacio;
    • Lotersztein, Vanesa;
    • Cosentino, Viviana;
    • González‐Meneses, Antonio;
    • Galán, Enrique;
    • Rosell, Jordi;
    • Ramos, Feliciano;
    • Plasencia, Antonio;
    • Rosa, Alberto L.
    Publication type:
    Article
    2

    A graph theory approach to analyze birth defect associations.

    Published in:
    PLoS ONE, 2020, v. 15, n. 5, p. 1, doi. 10.1371/journal.pone.0233529
    By:
    • Elias, Dario;
    • Campaña, Hebe;
    • Poletta, Fernando;
    • Heisecke, Silvina;
    • Gili, Juan;
    • Ratowiecki, Julia;
    • Gimenez, Lucas;
    • Pawluk, Mariela;
    • Santos, Maria Rita;
    • Cosentino, Viviana;
    • Uranga, Rocio;
    • Rittler, Monica;
    • Lopez Camelo, Jorge
    Publication type:
    Article
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    Genetic Analysis Algorithm for the Study of Patients with Multiple Congenital Anomalies and Isolated Congenital Heart Disease †.

    Published in:
    Genes, 2022, v. 13, n. 7, p. 1172, doi. 10.3390/genes13071172
    By:
    • Delea, Marisol;
    • Massara, Lucia S.;
    • Espeche, Lucia D.;
    • Bidondo, María Paz;
    • Barbero, Pablo;
    • Oliveri, Jaen;
    • Brun, Paloma;
    • Fabro, Mónica;
    • Galain, Micaela;
    • Fernández, Cecilia S.;
    • Taboas, Melisa;
    • Bruque, Carlos D.;
    • Kolomenski, Jorge E.;
    • Izquierdo, Agustín;
    • Berenstein, Ariel;
    • Cosentino, Viviana;
    • Martinoli, Celeste;
    • Vilas, Mariana;
    • Rittler, Mónica;
    • Mendez, Rodrigo
    Publication type:
    Article
    5

    Genetic Imbalances in Argentinean Patients with Congenital Conotruncal Heart Defects.

    Published in:
    Genes, 2018, v. 9, n. 9, p. 454, doi. 10.3390/genes9090454
    By:
    • Delea, Marisol;
    • Espeche, Lucía D.;
    • Bidondo, María Paz;
    • Perez, Myriam;
    • Buzzalino, Noemí D.;
    • Liascovich, Rosa;
    • Groisman, Boris;
    • Rozental, Sandra;
    • Barbero, Pablo;
    • Dain, Liliana;
    • Bruque, Carlos D.;
    • Furforo, Lilian;
    • Rittler, Mónica;
    • Massara, Lucía S.;
    • Oliveri, Jaen;
    • Brun, Paloma;
    • Cosentino, Viviana R.;
    • Martinoli, Celeste;
    • Tolaba, Norma;
    • Picon, Claudina
    Publication type:
    Article
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    New SHH and Known SIX3 Variants in a Series of Latin American Patients with Holoprosencephaly.

    Published in:
    Molecular Syndromology, 2021, v. 12, n. 4, p. 219, doi. 10.1159/000515044
    By:
    • de Castro, Viviane Freitas;
    • Mattos, Daniel;
    • de Carvalho, Flavia Martinez;
    • Cavalcanti, Denise Pontes;
    • Duenas-Roque, Milagros M.;
    • Llerena Jr, Juan;
    • Cosentino, Viviana Raquel;
    • Honjo, Rachel Sayuri;
    • Leite, Julio Cesar Loguercio;
    • Sanseverino, Maria Teresa;
    • de Souza, Márcia Pereira Alves;
    • Bernardi, Pricila;
    • Bolognese, Ana Maria;
    • Santana da Silva, Luiz Carlos;
    • Barbero, Pablo;
    • Correia, Patricia Santana;
    • Bueno, Larissa Souza Mario;
    • Savastano, Clarice Pagani;
    • Orioli, Iêda Maria
    Publication type:
    Article
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    Diseases during pregnancy in a large unselected South American sample.

    Published in:
    Brazilian Journal of Epidemiology / Revista Brasileira de Epidemiologia, 2022, v. 25, p. 1, doi. 10.1590/1980-549720220043
    By:
    • Rita Santos, María;
    • Campaña, Hebe;
    • Heisecke, Silvina;
    • Ratowiecki, Julia;
    • Elías, Darío;
    • Giménez, Lucas;
    • Adrián Poletta, Fernando;
    • Gili, Juan;
    • Uranga, Rocío;
    • Cosentino, Viviana;
    • Krupitzki, Hugo;
    • Rittler, Mónica;
    • López Camelo, Jorge
    Publication type:
    Article
    12

    Description of the methodology used in an ongoing pediatric care interventional study of children born with cleft lip and palate in South America [NCT00097149].

    Published in:
    BMC Pediatrics, 2006, v. 6, p. 9, doi. 10.1186/1471-2431-6-9
    By:
    • Wehby, George L.;
    • Castilla, Eduardo E.;
    • Goco, Norman;
    • Rittler, Monica;
    • Cosentino, Viviana;
    • Javois, Lorette;
    • McCarthy, Ann Marie;
    • Bobashev, Georgiy;
    • Litavecz, Stephen;
    • Mariona, Alejandra;
    • Dutra, Graca;
    • López-Camelo, Jorge S.;
    • Orioli, Iêda M.;
    • Murray, Jeffrey C.
    Publication type:
    Article
    13

    Genome-Wide Analysis of DNA Methylation in Human Amnion.

    Published in:
    Scientific World Journal, 2013, p. 1, doi. 10.1155/2013/678156
    By:
    • Kim, Jinsil;
    • Pitlick, Mitchell M.;
    • Christine, Paul J.;
    • Schaefer, Amanda R.;
    • Saleme, Cesar;
    • Comas, Belén;
    • Cosentino, Viviana;
    • Gadow, Enrique;
    • Murray, Jeffrey C.
    Publication type:
    Article
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    Sequence variants in oxytocin pathway genes and preterm birth: a candidate gene association study.

    Published in:
    BMC Medical Genetics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2350-14-77
    By:
    • Kim, Jinsil;
    • Stirling, Kara J.;
    • Cooper, Margaret E.;
    • Ascoli, Mario;
    • Momany, Allison M.;
    • McDonald, Erin L.;
    • Ryckman, Kelli K.;
    • Rhea, Lindsey;
    • Schaa, Kendra L.;
    • Cosentino, Viviana;
    • Gadow, Enrique;
    • Saleme, Cesar;
    • Shi, Min;
    • Hallman, Mikko;
    • Plunkett, Jevon;
    • Kari A.;
    • Muglia, Louis J.;
    • Feenstra, Bjarke;
    • Geller, Frank;
    • Boyd, Heather A.
    Publication type:
    Article
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