Nella Junna

De Novo Mutations in the Motor Domain of KIF1A Cause Cognitive Impairment, Spastic Paraparesis, Axonal Neuropathy, and Cerebellar Atrophy

Jae-Ran Lee, Myriam Srour, Doyoun Kim et al. · Human Mutation · 2014 · 151 citations

Neurological Disorder, Genetics, Spastic Paraparesis +20

How Communicating Polygenic and Clinical Risk for Atherosclerotic Cardiovascular Disease Impacts Health Behavior: an Observational Follow-up Study

Elisabeth Widén, Nella Junna, Sanni Ruotsalainen et al. · Circulation Genomic and Precision Medicine · 2022 · 137 citations · Full text

Distinct and shared genetic architectures of gestational diabetes mellitus and type 2 diabetes

Amanda Elliott, Raymond K. Walters, Matti Pirinen et al. · Nature Genetics · 2024 · 72 citations · Full text

The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia?

Jaakko T. Leinonen, Lia Crotti, Aurora Djupsjöbacka et al. · International Journal of Cardiology · 2017 · 52 citations · Full text

Cardiac Muscle, Cardiomyopathy, Heart Failure +12

Truncated HSPB1 causes axonal neuropathy and impairs tolerance to unfolded protein stress

Emil Ylikallio, Svetlana Konovalova, Yogesh Dhungana et al. · BBA Clinical · 2015 · 29 citations · Full text