Giedre Grigelioniene

7PUBLICATIONS
91CO-AUTHORS
NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Medical genetics (excl. cancer genetics)
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Publications (7)

|Sep 25, 2026
Deep Phenotyping in ReNU Syndrome Identifies a Recognizable Age-Dependent Clinical Trajectory.

|Jan 16, 2026
International guideline on genetic testing of children with short stature.

Andrew Dauber, Alexander A L Jorge, Ola Nilsson

|Jun 11, 2025
Genome sequencing in a cohort of 32 fetuses with genetic skeletal disorders.

Hillevi Lindelöf, Anna Hammarsjö, Ulrika Voss

|Dec 02, 2024
Unclassifiable short-rib thoracic dysplasia diagnosed using targeted gene panel sequencing.

Erika Nakajima, Yuko Yokohama, Saori Sugiyama

|Mar 10, 2023
Al-Gazali Skeletal Dysplasia Constitutes the Lethal End of ADAMTSL2-Related Disorders.

Dominyka Batkovskyte, Fiona McKenzie, Fulya Taylan

|Apr 20, 2021
High diagnostic yield in skeletal ciliopathies using massively parallel genome sequencing, structural variant screening and RNA analyses.

Anna Hammarsjö, Maria Pettersson, David Chitayat

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Frequent Collaborators

4 joint publications

Ann Nordgren

4 joint publications

Anna Lindstrand

3 joint publications

Fulya Taylan

2 joint publications

Kristina Lagerstedt-Robinson