Giovanni Neri

7PUBLICATIONS
24CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Medical anthropologyStylistics and textual analysis
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Publications (7)

|May 20, 2024
Simpson-Golabi-Behmel syndrome.

Alessandro Vaisfeld, Giovanni Neri

|Feb 08, 2024
Personal journeys to and in human genetics and dysmorphology.

Charles E Schwartz, Arthur S Aylsworth, Judith Allanson

|Mar 06, 2021
DNA Methylation, Mechanisms of <i>FMR1</i> Inactivation and Therapeutic Perspectives for Fragile X Syndrome.

Veronica Nobile, Cecilia Pucci, Pietro Chiurazzi

|Nov 18, 2020
Chromosome 14 deletions, rings, and epilepsy genes: A riddle wrapped in a mystery inside an enigma.

Alessandro Vaisfeld, Serena Spartano, Giuseppe Gobbi

|Apr 27, 2018
X-linked intellectual disability update 2017.

Giovanni Neri, Charles E Schwartz, Herbert A Lubs

|Nov 15, 2017
"Minimal" holoprosencephaly in a 14q deletion syndrome patient.

Elvio Della Giustina, Alessandro Iodice, Carlotta Spagnoli

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Frequent Collaborators

2 joint publications

Alessandro Vaisfeld

1 joint publications

Elvio Della Giustina

1 joint publications

Roger E Stevenson

1 joint publications

Serena Spartano