Bruno Marino

发表

Social cognition and real-life functioning in patient samples with 22q11.2 deletion syndrome with or without psychosis, compared to a large sample of patients with schizophrenia only and healthy controls.

L. Carlone, P. Bucci, G. Giordano, 2023, Journal of neuropsychology.

The Relationship between Motor Symptoms, Signs, and Parkinsonism with Facial Emotion Recognition Deficits in Individuals with 22q11.2 Deletion Syndrome at High Genetic Risk for Psychosis

C. Di Bonaventura, G. Kotzalidis, M. Fanella, 2023, Acta Neurologica Scandinavica.

Recognition of facial emotion expressions and perceptual processes in 22q11.2 deletion syndrome

C. Di Bonaventura, G. Kotzalidis, M. Fanella, 2022, Early intervention in psychiatry.

The 22q11.2 deletion syndrome.

E. Zackai, N. Philip, B. Emanuel, 2001, Advances in pediatrics.

22q11.2 deletion syndrome

P. Scambler, J. Vermeesch, K. Sullivan, 2015, Nature Reviews Disease Primers.

Biased T‐cell receptor repertoires in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)

B. Marino, G. Novelli, F. Amati, 2003, Clinical and experimental immunology.

22q11.2 deletion syndrome

P. Scambler, J. Vermeesch, K. Sullivan, 2015, Nature Reviews Disease Primers.

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS and sporadic congenital heart disease

C. Marshall, D. Heine-Suñer, D. Zheng, 2022, bioRxiv.

Chromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 1 22q11.2DS and sporadic congenital heart disease 2

M. Owen, C. Marshall, Zhengdong D. Zhang, 2022 .