Giedre Grigelioniene

6PUBLICATIONS
87CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Cardiovascular medicine and haematology not elsewhere classifiedMedical genetics (excl. cancer genetics)
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Publications (6)

|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

|Oct 21, 2024
Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon.

Angelica Maria Delgado-Vega, Helene Cederroth, Fulya Taylan

|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

3 joint publications

Fulya Taylan

3 joint publications

Ann Nordgren

3 joint publications

Anna Lindstrand

2 joint publications

Kristina Lagerstedt-Robinson