Maria Ines Perez-Millan

5PUBLICATIONS

20CO-AUTHORS

Gene mappingBiomedical instrumentationInfant and child healthDevelopmental genetics (incl. sex determination)Solid tumours

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Publications (5)

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|Jun 22, 2026

Compound Heterozygous Variants in the Phospholipase Gene PNPLA6 Cause Hypopituitarism and Vision Loss.

|Apr 26, 2026

Generation of a prop1 knock-in zebrafish enables single-cell transcriptomics of early pituitary development.

|Mar 06, 2025

Role of PROP1 in Postnatal Pituitary Gland Maturation.

Amanda Helen Winningham, Eve Camper Rhoads, Michelle Lynn Brinkmeier

|May 08, 2024

Exome Sequencing Has a High Diagnostic Rate in Sporadic Congenital Hypopituitarism and Reveals Novel Candidate Genes.

Julian Martinez-Mayer, Sebastian Vishnopolska, Catalina Perticarari

|Dec 15, 2023

Pituitary stem cells: past, present and future perspectives.

María Inés Pérez Millán, Leonard Y M Cheung, Florencia Mercogliano

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Frequent Collaborators

3 joint publications

Michelle Lynn Brinkmeier

3 joint publications

Sally Ann Camper

2 joint publications

Maria Andrea Camilletti

2 joint publications

Sebastian Vishnopolska

1 joint publications

Leonard Y M Cheung

1 joint publications

Florencia Mercogliano

1 joint publications

Gonzalo T Chirino Felker

1 joint publications

Lucia N Moro

1 joint publications

Santiago Miriuka

1 joint publications

Amanda Helen Winningham

Frequent Collaborators

3 joint publications

Michelle Lynn Brinkmeier

3 joint publications

Sally Ann Camper

2 joint publications

Maria Andrea Camilletti

2 joint publications

Sebastian Vishnopolska