Trine Bjørg Hammer

A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy

Ingo Helbig, Tania López-Hernández, Oded Shor et al. · The American Journal of Human Genetics · 2019 · 129 citations · Full text

Epileptic Encephalopathy, Signal Transduction, Developmental Biology +10

SLC35A2‐CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals

Bobby G. Ng, Paulina Sosicka, Satish Agadi et al. · Human Mutation · 2019 · 62 citations · Full text

Immunology, Glycobiology, Molecular Biology +25

NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns

Hannah Stamberger, Trine Bjørg Hammer, Elena Gardella et al. · Genetics in Medicine · 2020 · 54 citations · Full text

Nexmif Encephalopathy, Mendelian Disorder, Fragile X Spectrum +8

The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood

Jan Henje Döring, Afshin Saffari, Thomas Bast et al. · Biomedicines · 2020 · 39 citations · Full text

Stability of prepulse inhibition and habituation of the startle reflex in schizophrenia: a 6-year follow-up study of initially antipsychotic-naive, first-episode schizophrenia patients

Trine Bjørg Hammer, Bob Oranje, Birgitte Fagerlund et al. · The International Journal of Neuropsychopharmacology · 2011 · 37 citations · Full text

Psychopathology, Healthy Subjects, Psychotropic Medication +16