| 1 | Frequent copy number variants in a cohort of Mexican-Mestizo individuals | Coautor: Carnevale, Alessandra, Sanchez, Silvia, Juarez, Ulises, Dominguez, Julieta, et al. | 2023 | MOLECULAR CYTOGENETICS | WoS-id: 000912415900001
Scopus-id: 2-s2.0-85146115748
| 4 | 5 |
| 2 | Clinical spectrum of scn5a channelopathy in children with primary electrical disease and structurally normal hearts | Coautor: Carnevale A., Villarreal-Molina T., García-Ordóñez G.P., Reyes-Quintero Á.E., et al. | 2022 | GENES | WoS-id: 000760301400001
Scopus-id: 2-s2.0-85121676186
| 6 | 10 |
| 3 | Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG | Coautor: Carnevale A., Reyes P., García-De Teresa B., Juárez U., et al. | 2022 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | WoS-id: 000971202400001
Scopus-id: 2-s2.0-85124879348
| 7 | 7 |
| 4 | Compound Heterozygous KCNQ1 Mutations Causing Recessive Romano?Ward Syndrome: Functional Characterization by Mutant Co-expression | Coautor: Carnevale A., González-Garrido A., Domínguez-Pérez M., Jacobo-Albavera L., et al. | 2021 | Frontiers in Cardiovascular Medicine | WoS-id: 000625958000001
Scopus-id: 2-s2.0-85128350750
| 6 | 6 |
| 5 | Interaction of HLA Class II rs9272219 and TMPO rs17028450 (Arg690Cys) Variants Affects Neuromyelitis Optica Spectrum Disorder Susceptibility in an Admixed Mexican Population | Coautor: CARNEVALE, ALESSANDRA, Rosas-Madrigal, Sandra, Villarreal-Molina, Maria Teresa, Flores-Rivera, Jose, et al. | 2021 | Frontiers in Genetics | WoS-id: 000679378100001
Scopus-id: 2-s2.0-85111615112
| 2 | 2 |
| 6 | Genomic study of dilated cardiomyopathy in a group of Mexican patients using site-directed next generation sequencing | 1ᵉʳ autor: Carnevale A., Rosas-Madrigal S., Rosendo-Gutiérrez R., López-Mora E., et al. | 2020 | Molecular Genetics & Genomic Medicine | WoS-id: 000572158900001
Scopus-id: 2-s2.0-85091362158
| 11 | 13 |
| 7 | Genes frecuentemente asociados con muerte súbita en miocardiopatía hipertrófica primaria | Coautor: Carnevale A., Herrera-Rodríguez D.L., Totomoch-Serra A., Rosas-Madrigal S., et al. | 2020 | ARCHIVOS DE CARDIOLOGIA DE MEXICO | Scopus-id: 2-s2.0-85078690609
| 0 | 9 |
| 8 | Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes | Coautor: Carnevale, Alessandra, Barrientos-Rios, Rehotbevely, Frias, Sara, Velazquez-Aragon, Jose A., et al. | 2019 | GYNECOLOGICAL ENDOCRINOLOGY | WoS-id: 000461972100001
Scopus-id: 2-s2.0-85063099458
| 4 | 5 |
| 9 | Low diagnostic accuracy of fragile X tremor/ataxia syndrome diagnostic criteria in late onset ataxia | Coautor: Carnevale, Alessandra, Dávila-Ortiz de Montellano D.J., Jara-Prado, Aurelio, Rodriguez-Violante, Mayela, et al. | 2019 | MOVEMENT DISORDERS | WoS-id: 000465047800020
Scopus-id: 2-s2.0-85061282410
| 0 | 0 |
| 10 | FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México | Coautor: Carnevale A., García-de Teresa B., Frias S., Molina B., et al. | 2019 | Molecular Genetics & Genomic Medicine | WoS-id: 000476745400049
Scopus-id: 2-s2.0-85067281483
| 7 | 7 |
| 11 | Prevalence and ancestral origin of the c.1987delC GAA gene mutation causing Pompe disease in Central Mexico | Coautor: Carnevale, Alessandra, Grijalva-Perez, Adriana, Esmer, Carmen, Romero-Hidalgo, Sandra, et al. | 2018 | Meta Gene | WoS-id: 000419720600011
Scopus-id: 2-s2.0-85034577995
| 1 | 3 |
| 12 | In Search of Candidate Genes Genotype Phenotype Correlation: Role of Klotho Polymorphisms and Vitamin D Receptor in Bone Mineral Density in Mexican Children and Adolescents with Turner Syndrome | Coautor: Carnevale, Alessandra, Leon, Adareli, Rios, Rehotbevely, Vazquez, Sara, et al. | 2018 | HORMONE RESEARCH IN PAEDIATRICS | WoS-id: 000453593700002
| 0 | 0 |
| 13 | Interaction between FTO rs9939609 and the Native American-origin ABCA1 rs9282541 affects BMI in the admixed Mexican population | Coautor: Carnevale, Alessandra, Villalobos-Comparan, Marisela, Antuna-Puente, Barbara, Teresa Villarreal-Molina, Maria, et al. | 2017 | BMC MEDICAL GENETICS | WoS-id: 000400584000001
Scopus-id: 2-s2.0-85018742486
| 13 | 13 |
| 14 | Prevalence of metabolic syndrome among elderly Mexicans | Coautor: Carnevale, Alessandra, Araceli Ortiz-Rodriguez, Maria, Yanez-Velasco, Lucia, Romero-Hidalgo, Sandra, et al. | 2017 | ARCHIVES OF GERONTOLOGY AND GERIATRICS | WoS-id: 000413123600040
Scopus-id: 2-s2.0-85029037931
| 27 | 31 |
| 15 | Demographic history and biologically relevant genetic variation of Native Mexicans inferred from whole-genome sequencing | Coautor: Carnevale, Alessandra, Romero-Hidalgo, Sandra, Ochoa-Leyva, Adrian, Garciarrubio, Alejandro, et al. | 2017 | NATURE COMMUNICATIONS | WoS-id: 000413168700001
Scopus-id: 2-s2.0-85031929633
| 40 | 40 |
| 16 | In Mexican Mestizos the HCP5 rs2395029 SNP may be a genetic marker for screening abacavir hypersensitivity | 2ᵒ autor y autor de correspondencia: Carnevale A., Sanchez-Giron F. | 2012 | Pharmacogenomics | WoS-id: 000301886500003
Scopus-id: 2-s2.0-84856699417
| 3 | 4 |
| 17 | Persistent genomic instability in peripheral blood lymphocytes from hodgkin lymphoma survivors | Coautor: Carnevale A., Salas C., Niembro A., Lozano V., et al. | 2012 | ENVIRONMENTAL AND MOLECULAR MUTAGENESIS | WoS-id: 000302612800003
Scopus-id: 2-s2.0-84859614012
| 16 | 17 |
| 18 | Molecular screening of the CFTR gene in Mexican patients with congenital absence of the vas deferens | Coautor: Carnevale A., Saldaña-Alvarez Y., Jiménez-Morales S., Echevarría-Sánchez M., et al. | 2012 | GENETIC TESTING AND MOLECULAR BIOMARKERS | WoS-id: 000303109400012
Scopus-id: 2-s2.0-84860146377
| 4 | 5 |
| 19 | Multiple copies of RUNX1: description of 14 new patients, follow-up, and a review of the literature | Coautor: Carnevale A., Pérez-Vera P., Montero-Ruíz O., Frías S., et al. | 2008 | CANCER GENET CYTOGEN | WoS-id: 000252841800006
Scopus-id: 2-s2.0-38349060647
| 11 | 12 |
| 20 | Physician-assisted death. Opinions of a sample of Mexican physicians | Coautor: Carnevale, A, Lisker, R, del Rio, AA, Villa, AR | 2008 | Archives Of Medical Research | WoS-id: 000254844800013
Scopus-id: 2-s2.0-41149116004
| 12 | 14 |
| 21 | Trisomy of the short arm of chromosome 5 due to a de novo inversion and duplication (5)(p15.3 p13.3) | Coautor: Carnevale A., Cervera M., Sánchez S., Molina B., et al. | 2005 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000230949400017
Scopus-id: 2-s2.0-23044512676
| 22 | 26 |
| 22 | Detection of ETV6 and RUNX1 gene rearrangements using fluorescence in situ hybridization in Mexican patients with acute lymphoblastic leukemia: Experience at a single institution | Coautor: Carnevale A., Pérez-Vera P., Montero-Ruiz O., Frías S., et al. | 2005 | CANCER GENET CYTOGEN | WoS-id: 000233292800008
Scopus-id: 2-s2.0-26444585899
| 11 | 11 |
| 23 | DEB Test for Fanconi Anemia Detection in Patients with Atypical Phenotypes | Coautor: Carnevale A., Esmer C., Sánchez S., Ramos S., et al. | 2004 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000187282500005
Scopus-id: 2-s2.0-0942276983
| 40 | 43 |
| 24 | Carrier detection and prenatal molecular diagnosis in a duchenne muscular dystrophy family without any affected relative available | Coautor: Carnevale A., Alcántara M.A., García-Cavazos R., Hernández-U E., et al. | 2001 | ANN GENET-PARIS | WoS-id: 000172053300008
Scopus-id: 2-s2.0-0034755465
| 9 | 15 |
| 25 | Enfermedad de orina de jarabe de arce: heterogeneidad genética, diagnóstico de heterocigotos y un nuevo enfoque terapéutico. | Coautor: Carnevale A., Velázquez A., Montiel F., Sahw K.N., et al. | 1981 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1981ME80100005
Scopus-id: 2-s2.0-0019595042
| 1 | 1 |
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