Josianne Nunes Carriço

3PUBLICATIONS
4CO-AUTHORS
Genetics not elsewhere classifiedDevelopmental genetics (incl. sex determination)Neurology and neuromuscular diseases
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Publications (3)

|Nov 27, 2024
Kallmann Syndrome: Functional Analysis of a CHD7 Missense Variant Shows Aberrant RNA Splicing.

Josianne Nunes Carriço, Catarina Inês Gonçalves, José Maria Aragüés

|Sep 09, 2022
Disorder of Sex Development Due to 17-Beta-Hydroxysteroid Dehydrogenase Type 3 Deficiency: A Case Report and Review of 70 Different HSD17B3 Mutations Reported in 239 Patients.

Catarina I Gonçalves, Josianne Carriço, Margarida Bastos

|Jun 17, 2021
Sensitive period for rescuing parvalbumin interneurons connectivity and social behavior deficits caused by TSC1 loss.

Clara A Amegandjin, Mayukh Choudhury, Vidya Jadhav

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Frequent Collaborators

2 joint publications

Manuel Carlos Lemos

1 joint publications

Armen Saghatelyan

1 joint publications

Graziella Di Cristo

1 joint publications

Catarina Inês Gonçalves