Muestra la distribución de la producción WoS, Scopus y SciELO del autor.
Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.
| Firmas del autor | |
| Nombre | CARES, CAROLINA |
| Género | Mujer |
| Área Principal WOS | Pediatrics; Immunology; Biochemistry & Molecular Biology; |
| Afiliación Principal | Universidad De Chile |
Publicaciones en Chile
Citas Totales
Afiliaciones Chilenas
| WOS | #Pub |
|---|---|
| Pediatrics | 1 |
| Immunology | 1 |
| Biochemistry & Molecular Biology | 1 |
| Genetics & Heredity | 1 |
| Hematology | 1 |
| Oncology | 1 |
| Scopus | #Pub |
|---|---|
| Pediatrics, Perinatology And Child Health | 1 |
| Genetics | 1 |
| Genetics (Clinical) | 1 |
| Hematology | 1 |
| Immunology And Allergy | 1 |
| SciELO | #Pub |
|---|---|
| Health Sciences | 1 |
| 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 | Cares, C. | Universidad de Chile | 0.0 | 100.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 0.0 | 100.0 | 0.0 |
| Título | Año | Citas | Tipo | Revista | Indexada |
|---|---|---|---|---|---|
| Congenital Anomalies Of Poor Prognosis. Genetics Consensus Committee | 2016 | 1 | artículo de investigación | Revista Chilena De Pediatría | WoS SciELO Scopus |
| Heterogeneity Of Immune Abnormalities In Children With Nijmegen Breakage Syndrome: Experience In A Single Center | 2013 | 0 | resumen de reunión | Journal Of Clinical Immunology | WoS Scopus |
| Incidence And Clinical Significance Of Flt3 And Nucleophosmin Mutation In Childhood Acute Myeloid Leukemia In Chile | 2023 | 0 | artículo de investigación | Hematology, Transfusion And Cell Therapy | WoS Scopus |
| Decoding Complex Inherited Phenotypes In Rare Disorders: The Decipherd Initiative For Rare Undiagnosed Diseases In Chile | 2024 | 5 | artículo de investigación | European Journal Of Human Genetics | WoS Scopus |