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 | RICE, DEBBIE |
| Género | Mujer |
| Área Principal WOS | Genetics & Heredity; |
| Afiliación Principal | Universidad De Chile |
Publicaciones en Chile
Citas Totales
Afiliaciones Chilenas
| Autor | Género | # Pub |
|---|---|---|
| DONALDSON, ALAN | Hombre | 1 |
| DUNCAN, ALEXIS | Hombre | 1 |
| RENIERI, ALESSANDRA | Mujer | 1 |
| SAGGAR, ANAND | Hombre | 1 |
| FAUNDES, VICTOR | Hombre | 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 | Rice, Debbie | 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 | 0.0 | 0.0 |
| Título | Año | Citas | Tipo | Revista | Indexada |
|---|---|---|---|---|---|
| Heterozygous Variants In <I>Kmt2 E</I> Cause A Spectrum Of Neurodevelopmental Disorders And Epilepsy | 2019 | 37 | artículo de investigación | American Journal Of Human Genetics | WoS Scopus |
| Palabra Clave | #Pub |
|---|---|
| actb | 1 |
| autism | 1 |
| de-novo mutations | 1 |
| defects | 1 |
| epidemiology | 1 |
| epilepsy | 1 |
| epileptic encephalopathy | 1 |
| global developmental delay | 1 |
| h3k4 methylation | 1 |
| intellectual disability | 1 |
| kdm5c | 1 |
| kmt2e | 1 |
| neurodevelopmental disorder | 1 |
| prediction | 1 |
| protein | 1 |