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Author/Creator Pedersen, Inge S.

1. Clinical, splicing, and functional analysis to classify BRCA2 exon 3 variants: Application of a points‐based ACMG/AMP approach. Issue 12 (23rd October 2022)

Authors:
Thomassen, Mads; Mesman, Romy L. S.; Hansen, Thomas V. O.; Menendez, Mireia; Rossing, Maria; Esteban‐Sánchez, Ada; Tudini, Emma; Törngren, Therese; Parsons, Michael T.; Pedersen, Inge S.; Teo, Soo H.; Kruse, Torben A.; Møller, Pål; Borg, Åke; Jensen, Uffe B.; Christensen, Lise L.; Singer, Christi...
Journal:
Human mutation
Issue:
Volume 43:Issue 12(2022)
Page Start:
1921
Record Type:
Journal Article
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2. Patients' choices and opinions on chorionic villous sampling and non‐invasive alternatives for prenatal testing following preimplantation genetic testing for hereditary disorders: A cross‐sectional questionnaire study. (17th January 2022)

Authors:
Toft, Christian L. F.; Diemer, Tue; Ingerslev, Hans J.; Pedersen, Inge S.; Adrian, Stine W.; Kesmodel, Ulrik S.
Journal:
Prenatal diagnosis
Issue:
Volume 42:Number 2(2022)
Page Start:
212
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status. Issue 5 (1st March 2020)

Authors:
Feng, Helian; Gusev, Alexander; Pasaniuc, Bogdan; Wu, Lang; Long, Jirong; Abu‐full, Zomoroda; Aittomäki, Kristiina; Andrulis, Irene L.; Anton‐Culver, Hoda; Antoniou, Antonis C.; Arason, Adalgeir; Arndt, Volker; Aronson, Kristan J.; Arun, Banu K.; Asseryanis, Ella; Auer, Paul L.; Azzollini, Jacopo...
Journal:
Genetic epidemiology
Issue:
Volume 44:Issue 5(2020)
Page Start:
442
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗