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Simon Schnabl

Barbara de Sousa Oliveira

Romina Gisonno

Matteo Barel

Sarah Gorkiewicz

Francesca Barbieri

Viktor Voronin

Franco Lombino

Gaia Novarino

Lena Schwarz

Domenico Marano

Farnaz Freeman

Vittoria Mariano

Magdalena Ladrón de Guevara

Lisa Knaus

Ismael Lamas Toranzo

Dora-Clara Tarlungeanu

Ilaria Parenti

Denise Haslinger

Bernadette Basilico

Elena Deliu

Jasmin Morandell

Mike Liu

Chiaradia, Ilaria

Federica Danti

Margit Szigeti

Roberto Sacco

Edina Novak

Gintare Sendzikaite

Dobler, Zoe

Ottavia Palazzo

Jessica Kirchner

Emanuela Morelli

Alberto Coll Manzano

Christoph Dotter

Hagar Moussa



60 Publications

2019 | Journal Article | IST-REx-ID: 7414
L. Knaus, D.-C. Tarlungeanu, and G. Novarino, “S.16.03 A homozygous missense mutation in SLC7A5 leads to autism spectrum disorder and microcephaly,” European Neuropsychopharmacology, vol. 29, no. Supplement 6. Elsevier, p. S11, 2019.
View | DOI | WoS
 
2018 | Journal Article | IST-REx-ID: 456
G. Novarino, “Zika-associated microcephaly: Reduce the stress and race for the treatment,” Science Translational Medicine, vol. 10, no. 423. American Association for the Advancement of Science, 2018.
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2018 | Journal Article | IST-REx-ID: 5888 | OA
D.-C. Tarlungeanu and G. Novarino, “Genomics in neurodevelopmental disorders: an avenue to personalized medicine,” Experimental & Molecular Medicine, vol. 50, no. 8. Springer Nature, 2018.
[Published Version] View | Files available | DOI | WoS | PubMed | Europe PMC
 
2018 | Journal Article | IST-REx-ID: 546
R. Sacco, E. Cacci, and G. Novarino, “Neural stem cells in neuropsychiatric disorders,” Current Opinion in Neurobiology, vol. 48, no. 2. Elsevier, pp. 131–138, 2018.
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2018 | Journal Article | IST-REx-ID: 691 | OA
I. Marin Valencia et al., “A homozygous founder mutation in TRAPPC6B associates with a neurodevelopmental disorder characterised by microcephaly epilepsy and autistic features,” Journal of Medical Genetics, vol. 55, no. 1. BMJ Publishing Group, pp. 48–54, 2018.
[Submitted Version] View | DOI | Download Submitted Version (ext.) | WoS | PubMed | Europe PMC
 

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