Muestra la distribución de la producción WoS, Scopus y SciELO del autor.
Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.
Departamento Gestión de Conocimiento, Monitoreo y Prospección
Consultas o comentarios: productividad@anid.cl
Consultas o comentarios: productividad@anid.cl
| Firmas del autor | |
| Nombre | TRANGULAO-ESPINOSA, ALEJANDRA IRENE |
| Género | Mujer |
| Área Principal WOS | Neurosciences; Clinical Neurology; Biology; |
| Afiliación Principal | Universidad De Chile |
Publicaciones en Chile
Citas Totales
Afiliaciones Chilenas
Periodo registrado: 2008 - 2024
| WOS | #Pub |
|---|---|
| Neurosciences | 5 |
| Clinical Neurology | 5 |
| Biology | 1 |
| Multidisciplinary Sciences | 1 |
| Genetics & Heredity | 1 |
| Scopus | #Pub |
|---|---|
| Pediatrics, Perinatology And Child Health | 4 |
| Neurology (Clinical) | 4 |
| Genetics (Clinical) | 4 |
| Neurology | 4 |
| SciELO | #Pub |
|---|
| Año | Firma | Institución (Incites asoc.) | H Index | Average Percentile | Impact Citation | Impact Relative World | Impact Journal Normalized Citation | Impact Category Normalized Citation | Percentage Cited | Percentage Top 1 | Percentage Top 10 | Percentage Journal Q1 | Percentage Journal Q2 | Percentage Journal Q3 | Percentage Journal Q4 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 2019 | Trangulao, A. | Universidad de Chile | 0.0 | 100.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 66.7 | 33.3 | 0.0 |
| 2019 | Trangulao, Alejandra | Universidad de Chile | 1.0 | 27.1 | 9.0 | 1.0 | 1.7 | 1.1 | 100.0 | 0.0 | 0.0 | 0.0 | 100.0 | 0.0 | 0.0 |
| Palabra Clave | #Pub |
|---|---|
| myositis | 1 |
| identification | 1 |
| lgmd | 1 |
| limb-girdle muscle weakness | 1 |
| magnetic-resonance spectroscopy | 1 |
| membranes | 1 |
| miyoshi myopathy | 1 |
| motor function measure | 1 |
| mrc score | 1 |
| muscle mri | 1 |
| muscular-dystrophies | 1 |
| high-throughput sequencing | 1 |
| nemaline myopathy | 1 |
| next-generation sequencing | 1 |
| patient | 1 |
| phenotype | 1 |
| phenotypes | 1 |
| polymyositis | 1 |
| population | 1 |
| recurrent mutations | 1 |
| skeletal-muscle | 1 |
| tpm3 | 1 |
| dermatomyositis | 1 |
| activation | 1 |
| alpha-tropomyosin gene | 1 |
| cap disease | 1 |
| cftd | 1 |
| chile | 1 |
| common | 1 |
| congenital myopathy | 1 |
| contribute | 1 |
| damage | 1 |
| defects | 1 |
| 2b | 1 |
| diagnosis | 1 |
| dysf | 1 |
| dysf mutations | 1 |
| dysferlinopathy | 1 |
| electromyography | 1 |
| features | 1 |
| gene | 1 |
| girdle muscular-dystrophy | 1 |
| guidelines | 1 |
| hereditary myopathies | 1 |
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