Concepedia
Statistics
Publications
41
Citations
3.5K
H-Index
27
Active since
2000
Affiliations
University of Siena(Current)
Azienda Ospedaliera Universitaria Senese
Istituto Giannina Gaslini
Istituti di Ricovero e Cura a Carattere Scientifico
Bambino Gesù Children's Hospital
Ilaria Longo is an author at University of Siena specializing in genetics, genetic disorders, and molecular genetics.
Publications per year
2000–2025
FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome
Francesca Ariani, Dalila Rondinella, Rosangela Artuso et al. · The American Journal of Human Genetics · 2008 · 434 citations · Full text
Life Sciences, Genetics, Molecular Genetics +7
CDKL5 belongs to the same molecular pathway of MeCP2 and it is responsible for the early-onset seizure variant of Rett syndrome
Francesca Mari, Sara Azimonti, Ilaria Bertani et al. · Human Molecular Genetics · 2005 · 318 citations · Full text
Life Sciences, Genetics, Neuroscience +17
MYH9-Related Disease
Marco Seri, Alessandro Pecci, Filomena Di Bari et al. · Medicine · 2003 · 313 citations · Full text
Life Sciences, Genetics, Molecular Genetics +9
COL4A3/COL4A4 mutations: From familial hematuria to autosomal-dominant or recessive Alport syndrome
Ilaria Longo, Paola Porcedda, Francesca Mari et al. · Kidney International · 2002 · 232 citations · Full text
Life Sciences, Genetics, Molecular Genetics +13
A Mutation in the Rett Syndrome Gene, MECP2, Causes X-Linked Mental Retardation and Progressive Spasticity in Males
Ilaria Meloni, Mirella Bruttini, Ilaria Longo et al. · The American Journal of Human Genetics · 2000 · 231 citations · Full text
Life Sciences, Genetics, Molecular Genetics +16
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