Bianca Ethel Gutiérrez-Amavizca

Universidad Autónoma de Ciudad Juárez — Mexico

Medicine · Health Sciences

6h-index132citations16works0.02yr avg
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Research Topics

Lysosomal Storage Disorders Research(5), Circadian rhythm and melatonin(3), Sleep and related disorders(2), Carbohydrate Chemistry and Synthesis(2), Trypanosoma species research and implications(2)

Publications16 total

Association of P10L Polymorphism in Melanopsin Gene with Chronic Insomnia in Mexicans
International Journal of Environmental Research and Public Health·2021· 4 citedOpen Access
Nerve Transfer from the Long Head Triceps Nerve to Posterior Interosseous Nerve for Restoration of Wrist, Finger, and Thumb
Plastic & Reconstructive Surgery Global Open·2019Open Access
Genetic contribution in primary sleep disorders
PubMed·2019
Two familial intrachromosomal insertions with maternal dup(6)(p22.3p25.3) or dup(2)(q24.2q32.1) in recombinant offspring
Clinical Dysmorphology·2017· 34 cited
Mutational analysis of the GLA gene in Mexican families with Fabry disease
Journal of Genetics·2017· 4 cited
Research Article Analysis of melanopsin gene expression in the rabbit retina at different ages.
Genetics and Molecular Research·2017· 2 citedOpen Access
Association of the FTO gene SNP rs17817449 with body fat distribution in Mexican women
Genetics and Molecular Research·2014· 18 citedOpen Access
The 14 bp Del/Ins HLA-G Polymorphism Is Related with High Blood Pressure in Acute Coronary Syndrome and Type 2 Diabetes Mellitus
BioMed Research International·2014· 20 citedOpen Access
Pedigree analysis of Mexican families with Fabry disease as a powerful tool for identification of heterozygous females
Genetics and Molecular Research·2014· 8 cited
Contralateral Spinal Accessory Nerve Transfer: A New Technique in Panavulsive Brachial Plexus Palsy
Indian Journal of Surgery·2013· 3 citedOpen Access
Neuhauser syndrome: a rare association of megalocornea and mental retardation. Review of the literature and further phenotype delineation.
PubMed·2013· 6 cited
Ophthalmic manifestations in Mexican patients with Fabry disease
Archivos de la Sociedad Española de Oftalmología (English Edition)·2012· 2 cited
[Current genetic issues and phenotypic variants in Kallmann syndrome].
PubMed·2012· 5 cited
A novel mutation in CDMP1 causes brachydactyly type C with “angel-shaped phalanx”. A genotype–phenotype correlation in the mutational spectrum
European Journal of Medical Genetics·2012· 18 cited
Manifestaciones oftalmológicas en pacientes mexicanos con enfermedad de Fabry
Archivos de la Sociedad Española de Oftalmología·2012· 6 cited
aspectos de actualidad en enfermedad de Fabry
2012· 2 cited

Frequent Co-authors

Luis E. Figuera(9), R. Orozco-Castellanos(4), Patricio Barros‐Núñez(3), Yeminia Valle(3), Jorge Ramón Padilla‐Gutiérrez(3), Jaime Paul Gutiérrez-Amavizca(3), P. Alberto(3), Aniel Jessica Leticia Brambila‐Tapia(2), Clara Ibet Juárez-Vázquez(2), Jesús Jaime Zermeño-Rivera(2), K.J. Beltrán-Becerra(2), Blanca Estela Ríos‐González(2), D.A. Silva-Noriega(2), Ernesto Prado Montes de(2), Marisela Aguirre-Ramírez(2), M.G. Domínguez(1), Horacio Rivera(1), Adriana Aguilar‐Lemarroy(1), Luis Felipe Jave‐Suárez(1), Azubel Ramírez-Velazco(1)