Eva-Lena Stattin

Publication Activity (10 Years)

Years Active: 2015-2022
Publications (10 Years): 4

Top Topics

Intellectual Disability

Top Venues

Clinical genetics

Molecular genetics & genomic medicine

International journal of legal medicine

This page only lists publications with an associated author ORCID identifier.

Publications

Eva-Lena Stattin, Emil Hagström, Niklas Dahl, Anneli Strömsöe, Angelica Maria Delgado-Vega, Joakim Klar, Bodil Svennblad, Mats Börjesson, Aase Wisten
Cohort profile: the Swedish study of SUDden cardiac Death in the Young (SUDDY) 2000-2010: a complete nationwide cohort of SCDs. BMJ open 12 (5) (2022)
Ann-Charlotte Thuresson, Brittany Croft, Yasmin D Hailer, Gunnar Liminga, Carl-Göran Arvidsson, Vincent R Harley, Eva-Lena Stattin
A novel heterozygous variant in FGF9 associated with previously unreported features of multiple synostosis syndrome 3. Clinical genetics 99 (2) (2021)
Sofia Frisk, Fulya Taylan, Izabela Blaszczyk, Inger Nennesmo, Göran Annerén, Bettina Herm, Eva-Lena Stattin, Vasilios Zachariadis, Anna Lindstrand, Bianca Tesi, Tobias Laurell, Ann Nordgren
Early activating somatic PIK3CA mutations promote ectopic muscle development and upper limb overgrowth. Clinical genetics 96 (2) (2019)
Pantelis Clewemar, Nils P Hailer, Yasmin Hailer, Joakim Klar, Andreas Kindmark, Östen Ljunggren, Eva-Lena Stattin
Expanding the phenotypic spectrum of osteogenesis imperfecta type V including heterotopic ossification of muscle origins and attachments. Molecular genetics & genomic medicine 7 (7) (2019)
Eva-Lena Stattin, Ida Maria Westin, Kristina Cederquist, Jenni Jonasson, Björn-Anders Jonsson, Stellan Mörner, Anna Norberg, Peter Krantz, Aase Wisten
Genetic screening in sudden cardiac death in the young can save future lives. International journal of legal medicine 130 (1) (2015)