Daniel L Polla

4PUBLICATIONS
7CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Carbon sequestration scienceDevelopmental genetics (incl. sex determination)Neurogenetics
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Publications (4)

|Jan 27, 2025
Beyond genomics: using RNA-seq from dried blood spots to unlock the clinical relevance of splicing variation in a diagnostic setting.

Aida M Bertoli-Avella, Mandy Radefeldt, Ruslan Al-Ali

|Sep 12, 2019
Correction: Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population.

Daniel L Polla, Elisa Rahikkala, Michaela K Bode

|Aug 16, 2019
A de novo variant in the X-linked gene CNKSR2 is associated with seizures and mild intellectual disability in a female patient.

Daniel L Polla, Harriet R Saunders, Bert B A de Vries

|Mar 28, 2019
Phenotypic spectrum associated with a CRADD founder variant underlying frontotemporal predominant pachygyria in the Finnish population.

Daniel L Polla, Elisa Rahikkala, Michaela K Bode

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Frequent Collaborators

1 joint publications

Aida M Bertoli-Avella

1 joint publications

Ruslan Al-Ali

1 joint publications

Luba M Pardo

1 joint publications

Anika Leubauer