Get started
Author

Andrea Avendaño

Observed names: A AVENDANO, A Avendaño, A. Avendaño, Andrea AVENDAÑO, Andrea Avendano
ORCID: 0000-0001-6238-7237
Observed ORCID: 0000-0001-6238-7237
OpenAlex ID: A5043679014
Main genetic entities associated with supernumerary teeth
2018 · Francisco Cammarata-Scalisi, Andrea Avendaño, et al. · Archivos Argentinos de Pediatria · 62
PDF
5-α-Reductase type 2 deficiency: is there a genotype-phenotype correlation? A review
2018 · Andrea Avendaño, Irene Paradisi, et al. · HORMONES · 57
PDF
An updated examination of the perception of barriers for pharmacogenomics implementation and the usefulness of drug/gene pairs in Latin America and the Caribbean
2023 · Aimeé Salas-Hernández, Macarena Galleguillos, et al. · Frontiers in Pharmacology · 35
PDF
Beckwith-Wiedemann syndrome. Clinical and etiopathogenic aspects of a model genomic imprinting entity
2018 · Francisco Cammarata-Scalisi, Andrea Avendaño, et al. · Archivos Argentinos de Pediatria · 17
PDF
Novel clinical features associated with Clouston syndrome
2019 · Francisco Cammarata-Scalisi, Martina Rinelli, et al. · International Journal of Dermatology · 15
PDF
Hallazgos clínicos y genéticos de dos casos con síndrome de Apert
2019 · Francisco Cammarata-Scalisi, Elanur Yilmaz, et al. · Boletín Médico del Hospital Infantil de México · 8
PDF
Clinical and genetic findings of two cases with Apert syndrome
2019 · Francisco Cammarata-Scalisi, Elanur Yilmaz, et al. · Boletín Médico Del Hospital Infantil de México (English Edition) · 7
PDF
Hallazgos clínicos, bioquímicos y moleculares de la acidemia propiónica. Reporte de un caso
2019 · Francisco Cammarata-Scalisi, Chiu Yen-Hui, et al. · Archivos Argentinos de Pediatria · 7
PDF
A Venezuelan Case of Schmid-Type Metaphyseal Chondrodysplasia with a Novel Mutation in COL10A1
2019 · Francisco Cammarata-Scalisi, Uta Matysiak, et al. · Molecular Syndromology · 7
PDF
5α‐Reductase type 2 deficiency in families from an isolated Andean population in Venezuela
2019 · Andrea Avendaño, Mercedes González‐Coira, et al. · Annals of Human Genetics · 6
Síndrome de Wolf-Hirschhorn. Descripción de cinco casos caracterizados por microarrays de polimorfismos de nucleótido único
2019 · Francisco Cammarata-Scalisi, Raquel Blanco Lago, et al. · Archivos Argentinos de Pediatria · 5
PDF
Cleidocranial dysplasia. A molecular and clinical review.
2018 · Andrea Avendaño, Francisco Cammarata-Scalisi, et al. · International Dental Research · 5
PDF
Estudio clínico y molecular en una familia con displasia cleidocraneal
2017 · Michele Callea, Fabiana Fattori, et al. · Archivos Argentinos de Pediatria · 5
PDF
Trisomía 18 en mosaico. Serie de casos.
2017 · Francisco Cammarata-Scalisi, María A Lacruz-Rengel, et al. · Archivos Argentinos de Pediatria · 5
PDF
Hallazgos clínicos y epidemiológicos en la neurofibromatosis tipo 1 y el complejo esclerosis tuberosa en una serie de pacientes pediátricos
2018 · Francisco Cammarata-Scalisi, Frances Stock, et al. · Boletín Médico del Hospital Infantil de México · 4
PDF
Early severe pachyonychia congenita subtype PC ‐K6a with a novel mutation in the KRT 6A gene
2016 · F. Cammarata‐Scalisi, K. Natsuga, et al. · Journal of the European Academy of Dermatology and Venereology · 4
[Clinical and molecular study of the Noonan syndrome].
2012 · Francisco Cammarata-Scalisi, Giovanni Neri, et al. · PubMed · 3
Next generation sequencing panel target genes: possible diagnostic tool for ectodermal dysplasia related diseases
2023 · Michele CALLEA, Emanuele BELLACCHIO, et al. · Italian Journal of Dermatology and Venereology · 2
[Clinical and molecular study in a family with multiple osteochondromatosis].
2018 · F Cammarata-Scalisi, F Stock, et al. · PubMed · 2
Embriopatía por isotretinoína. Una entidad que puede evitarse
2018 · Francisco Cammarata-Scalisi, Dairelis Nieves, et al. · Archivos Argentinos de Pediatria · 2
PDF
Two novel mutations in the TSC 2 gene causing severe phenotype in nervous system and skin in a patient with tuberous sclerosis complex
2017 · F. Cammarata‐Scalisi, C. Vidales Moreno, et al. · Journal of the European Academy of Dermatology and Venereology · 2
[Age of menarche and genetic blood markers].
1990 · C Valenzuela, A Avendaño, et al. · PubMed · 2
[Arachnodactyly and arthrogryposis. Report of a case in an infant with association of both diseases].
1963 · A AVENDANO, E FANTA · PubMed · 2
CYP2C9 Pharmacogenetic Variants and Adverse Drug Reactions to Antiseizure Medications: An Exploratory Analysis in the Venezuelan Andes
2026 · Sol Betzabeth Rondón-Simancas, Gustavo Paredes, et al. · International Journal of Molecular Sciences · 1
[Psychological resistance to use insulin in type 2 diabetes mellitus patients from Venezuela].
2014 · Juan Pablo González Rivas, Mariela Paoli, et al. · PubMed · 1
Works count: 30
Citation count: 266
H-index: 7
I10-index: 5
Year
Topic
Type