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 | RENIERI, ALESSANDRA |
| Género | Mujer |
| Área Principal WOS | Genetics & Heredity; |
| Afiliación Principal | Università Degli Studi Di Siena |
| ORCID
|
0000-0002-0846-9220 |
Publicaciones en Chile
Citas Totales
Afiliaciones Chilenas
| Autor | Género | # Pub |
|---|---|---|
| DONALDSON, ALAN | Hombre | 1 |
| DUNCAN, ALEXIS | Hombre | 1 |
| RICE, DEBBIE | Mujer | 1 |
| FAUNDEZ-APABLAZA, VICTOR MANUEL | Hombre | 1 |
| SAGGAR, ANAND | Hombre | 1 |
| Institución | # Pub |
|---|---|
| Università Degli Studi Di Siena | 5 |
| Univ Siena | 4 |
| Azienda Ospedaliera Universitaria Senese | 4 |
| Azienda Osped Univ Senese | 2 |
| Azienda Univ Hosp | 1 |
| Scripps Research Institute | 1 |
| Broad Institute | 1 |
| Eberhard Karls Universität Tübingen | 1 |
| University Hospital Of Wales | 1 |
| Università Degli Studi Di Genova | 1 |
| Massachusetts Institute Of Technology | 1 |
| Universidad De Chile | 1 |
| Univ Tuspacing | 1 |
| St Vincents Childrens Hosp | 1 |
| Rady Childrens Hosp San Diego | 1 |
| Massachusetts Inst Technol & Harvard | 1 |
| Scripps Res Inst | 1 |
| Christian Albrechts Univ Kiel | 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 | Renieri, Alessandra | 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 | 50 | 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 |