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Carnevale, Alessandra
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1

P659: A comprehensive genotyping study in Mexican patients ..:

Torres, Leda ; Reyes, Pedro ; Teresa, Benilde García-de...
Genetics in Medicine Open.  2 (2024)  - p. 101564 , 2024
Link: https://doi.org/10.1016/..
 
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Selection scan in Native Americans of Mexico identifies FAD..:

Romero-Hidalgo, Sandra ; Sagaceta-Mejía, Janine ; Villalobos-Comparán, Marisela...
Heliyon.  10 (2024)  15 - p. e35477 , 2024
Link: https://doi.org/10.1016/..
 
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3

KCNQ1 p.D446E Variant as a Risk Allele for Arrhythmogenic P..:

González-Garrido, Antonia ; López-Ramírez, Omar ; Cerda-Mireles, Abel...
International Journal of Molecular Sciences.  25 (2024)  2 - p. 953 , 2024
Link: https://doi.org/10.3390/..
 
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4

Frequent copy number variants in a cohort of Mexican-Mestiz..:

Sánchez, Silvia ; Juárez, Ulises ; Domínguez, Julieta...
Molecular Cytogenetics.  16 (2023)  1 - p. , 2023
Link: https://doi.org/10.1186/..
 
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Leukocyte Nuclear Morphology Alterations in Dilated Cardiom..:

González-Garrido, Antonia ; Rosas-Madrigal, Sandra ; Rojo-Domínguez, Arturo...
International Journal of Molecular Sciences.  23 (2022)  21 - p. 13626 , 2022
Link: https://doi.org/10.3390/..
 
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Fanconi Anemia Patients from an Indigenous Community in Mex..:

Reyes, Pedro ; García-de Teresa, Benilde ; Juárez, Ulises...
International Journal of Molecular Sciences.  23 (2022)  4 - p. 2334 , 2022
Link: https://doi.org/10.3390/..
 
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7

Clinical Spectrum of SCN5A Channelopathy in Children with P..:

Villarreal-Molina, Teresa ; García-Ordóñez, Gabriela Paola ; Reyes-Quintero, Álvaro E....
Genes.  13 (2021)  1 - p. 16 , 2021
Link: https://doi.org/10.3390/..
 
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8

Compound Heterozygous KCNQ1 Mutations Causing Recessive Rom..:

González-Garrido, Antonia ; Domínguez-Pérez, Mayra ; Jacobo-Albavera, Leonor...
Frontiers in Cardiovascular Medicine.  8 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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9

Interaction of HLA Class II rs9272219 and TMPO rs17028450 (..:

Rosas-Madrigal, Sandra ; Villarreal-Molina, María Teresa ; Flores-Rivera, José...
Frontiers in Genetics.  12 (2021)  - p. , 2021
Link: https://doi.org/10.3389/..
 
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10

Genomic study of dilated cardiomyopathy in a group of Mexic..:

Carnevale, Alessandra ; Rosas‐Madrigal, Sandra ; Rosendo‐Gutiérrez, Rigoberto...
Molecular Genetics & Genomic Medicine.  8 (2020)  11 - p. , 2020
Link: https://doi.org/10.1002/..
 
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FANCC Dutch founder mutation in a Mennonite family from Tam..:

García‐de Teresa, Benilde ; Frias, Sara ; Molina, Bertha...
Molecular Genetics & Genomic Medicine.  7 (2019)  6 - p. , 2019
Link: https://doi.org/10.1002/..
 
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12

Low diagnostic accuracy of fragile X tremor/ataxia syndrome..:

Dávila‐Ortiz de Montellano, David José ; Jara‐Prado, Aurelio ; Rodríguez‐Violante, Mayela...
Movement Disorders.  34 (2019)  4 - p. 582-583 , 2019
Link: https://doi.org/10.1002/..
 
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13

Prevalence and ancestral origin of the c.1987delC GAA gene ..:

Grijalva-Pérez, Adriana ; Esmer, Carmen ; Romero-Hidalgo, Sandra...
Meta Gene.  15 (2018)  - p. 60-64 , 2018
Link: https://doi.org/10.1016/..
 
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14

Prevalence of metabolic syndrome among elderly Mexicans:

Ortiz-Rodríguez, María Araceli ; Yáñez-Velasco, Lucía ; Carnevale, Alessandra...
Archives of Gerontology and Geriatrics.  73 (2017)  - p. 288-293 , 2017
Link: https://doi.org/10.1016/..
 
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15

Demographic history and biologically relevant genetic varia..:

Romero-Hidalgo, Sandra ; Ochoa-Leyva, Adrián ; Garcíarrubio, Alejandro...
Nature Communications.  8 (2017)  1 - p. , 2017
Link: https://doi.org/10.1038/..
 
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