A core MYC gene expression signature is prominent in basal-like breast cancer but only partially overlaps the core serum response.

by Sanjay Chandriani, Eirik Frengen, Victoria H Cowling, Sarah A Pendergrass, Charles M Perou, Michael L Whitfield, Michael D Cole
Published 2009-08-01

Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan

by Christeen Ramane J. Pedurupillay, Erlend Christoffer Sommer Landsend, Magnus Dehli Vigeland, Muhammad Ansar, Eirik Frengen, Doriana Misceo, Petter Strømme
Published 2016-07-01

Global gene expression analysis reveals a link between NDRG1 and vesicle transport.

by Hanne A Askautrud, Elisabet Gjernes, Gjermund Gunnes, Marit Sletten, Douglas T Ross, Anne Lise Børresen-Dale, Nina Iversen, Michael A Tranulis, Eirik Frengen
Published 2014-01-01

Novel PIGT Variant in Two Brothers: Expansion of the Multiple Congenital Anomalies-Hypotonia Seizures Syndrome 3 Phenotype

by Nadia Skauli, Sean Wallace, Samuel C. C. Chiang, Tuva Barøy, Asbjørn Holmgren, Asbjørg Stray-Pedersen, Yenan T. Bryceson, Petter Strømme, Eirik Frengen, Doriana Misceo
Published 2016-11-01

Sudden death in epilepsy and ectopic neurohypophysis in Joubert syndrome 23 diagnosed using SNVs/indels and structural variants pipelines on WGS data: a case report

by Dulika Sumathipala, Petter Strømme, Christian Gilissen, Ingunn Holm Einarsen, Hilde J. Bjørndalen, Andrés Server, Jordi Corominas, Bjørnar Hassel, Madeleine Fannemel, Doriana Misceo, Eirik Frengen
Published 2020-05-01

Spastic paraplegia type 7 is associated with multiple mitochondrial DNA deletions.

by Iselin Marie Wedding, Jeanette Koht, Gia Tuong Tran, Doriana Misceo, Kaja Kristine Selmer, Asbjørn Holmgren, Eirik Frengen, Laurence Bindoff, Chantal M E Tallaksen, Charalampos Tzoulis
Published 2014-01-01