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María-Isabel Tejada

4PUBLICATIONS

4CO-AUTHORS

Medical mycologyGene expression (incl. microarray and other genome-wide approaches)NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)

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Publications (4)

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|Feb 12, 2020

Molecular characterization of Spanish patients with MECP2 duplication syndrome.

Ainhoa Pascual-Alonso, Laura Blasco, Silvia Vidal

|Jan 04, 2020

Non-syndromic X linked intellectual disability: Current knowledge in light of the recent advances in molecular and functional studies.

María Isabel Tejada, Nekane Ibarluzea

|Nov 22, 2018

A novel nonsense homozygous variant in the NLGN1 gene found in a pair of monozygotic twin brothers with intellectual disability and autism.

María-Isabel Tejada, Xabier Elcoroaristizabal, Nekane Ibarluzea

|Mar 04, 2016

The MECP2 variant c.925C>T (p.Arg309Trp) causes intellectual disability in both males and females without classic features of Rett syndrome.

B Schönewolf-Greulich, M-I Tejada, K Stephens

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Frequent Collaborators

1 joint publications

Antonio F Martínez-Monseny

1 joint publications

Eduardo Tizzano

1 joint publications

Soledad Alcántara

1 joint publications

Judith Armstrong

Frequent Collaborators

1 joint publications

Antonio F Martínez-Monseny

1 joint publications

Eduardo Tizzano

1 joint publications

Soledad Alcántara

1 joint publications

Judith Armstrong

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