Paolo Grazioli

About Paolo Grazioli

Paolo Grazioli, With an exceptional h-index of 7 and a recent h-index of 7 (since 2020), a distinguished researcher at Università degli Studi di Milano, specializes in the field of Biotechnology, Molecular Biology, Genetics.

His recent articles reflect a diverse array of research interests and contributions to the field:

Autism-linked NLGN3 is a key regulator of gonadotropin-releasing hormone deficiency

Combined omic analyses reveal autism-linked NLGN3 gene as a key developmental regulator of GnRH neuron biology and disease.

KMT2A: Umbrella Gene for Multiple Diseases

A combined omic analysis revealed autism-linked NLGN3 as a new candidate gene associated to GnRH neuron development and disease

Epigenetic disorders: Lessons from the animals–animal models in chromatinopathies

Combined omic analyses reveal novel loss-of-function NLGN3 variants in GnRH deficiency and autism

Chromatin imbalance as the vertex between fetal valproate syndrome and chromatinopathies

Insights into the Role of the Microbiota and of Short-Chain Fatty Acids in Rubinstein–Taybi Syndrome

Paolo Grazioli Information

University

Position

PhD Student

Citations(all)

197

Citations(since 2020)

193

Cited By

48

hIndex(all)

7

hIndex(since 2020)

7

i10Index(all)

6

i10Index(since 2020)

6

Email

University Profile Page

Google Scholar

Paolo Grazioli Skills & Research Interests

Biotechnology

Molecular Biology

Genetics

Top articles of Paolo Grazioli

Autism-linked NLGN3 is a key regulator of gonadotropin-releasing hormone deficiency

Disease Models & Mechanisms

2023/3/1

Paolo Grazioli
Paolo Grazioli

H-Index: 5

Combined omic analyses reveal autism-linked NLGN3 gene as a key developmental regulator of GnRH neuron biology and disease.

Disease Models & Mechanisms

2023/2/22

Paolo Grazioli
Paolo Grazioli

H-Index: 5

KMT2A: Umbrella Gene for Multiple Diseases

2022/3/15

Paolo Grazioli
Paolo Grazioli

H-Index: 5

Elisa Borghi
Elisa Borghi

H-Index: 5

A combined omic analysis revealed autism-linked NLGN3 as a new candidate gene associated to GnRH neuron development and disease

2022

Paolo Grazioli
Paolo Grazioli

H-Index: 5

Epigenetic disorders: Lessons from the animals–animal models in chromatinopathies

2022/9/26

Paolo Grazioli
Paolo Grazioli

H-Index: 5

Combined omic analyses reveal novel loss-of-function NLGN3 variants in GnRH deficiency and autism

medRxiv

2022/5/25

Paolo Grazioli
Paolo Grazioli

H-Index: 5

Chromatin imbalance as the vertex between fetal valproate syndrome and chromatinopathies

2021/4/20

Paolo Grazioli
Paolo Grazioli

H-Index: 5

Insights into the Role of the Microbiota and of Short-Chain Fatty Acids in Rubinstein–Taybi Syndrome

International Journal of Molecular Sciences

2021/3/31

IN VITRO AND IN VIVO MODELLING OF CORNELIA DE LANGE SYNDROME CAUSATIVE MUTATIONS: WNT ACTIVATION AS A POSSIBLE THERAPEUTIC APPROACH

2021/3/26

Lithium as a possible therapeutic strategy for Cornelia de Lange syndrome

Cell Death Discovery

2021/2/17

Paolo Grazioli
Paolo Grazioli

H-Index: 5

Thomas Vaccari
Thomas Vaccari

H-Index: 18

Neural tube defects: embryonic origin, cell survival equilibrium impact, and clinical features

2021/1/1

Paolo Grazioli
Paolo Grazioli

H-Index: 5

Lithium ameliorates Cornelia de Lange syndrome associated phenotypes in experimental models

bioRxiv

2020/7/15

Paolo Grazioli
Paolo Grazioli

H-Index: 5

Thomas Vaccari
Thomas Vaccari

H-Index: 18

Exogenous and endogenous HDAC inhibitor effects in Rubinstein-Taybi syndrome models

BioRxiv

2020/4/1

Dynamic acetylation profile during mammalian neurulation

Birth Defects Research

2020/1/15

Paolo Grazioli
Paolo Grazioli

H-Index: 5

Chromatinopathies: A focus on Cornelia de Lange syndrome

2020/1

Paolo Grazioli
Paolo Grazioli

H-Index: 5

See List of Professors in Paolo Grazioli University(Università degli Studi di Milano)