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Annika Winbo
Contact
E-mail
annika.winbo@umu.se
Phone
Works at
Affiliation
Affiliated as research fellow at
Department of Clinical Sciences
Section: Pediatrics
Location
Umeå universitet, Klinisk vetenskap, 901 85 Umeå
Publications
Publications
2023
Effects of cohort, genotype, variant, and maternal β-blocker treatment on foetal heart rate predictors of inherited long QT syndrome
Europace
, Oxford University Press 2023, Vol. 25, (11)
Kaizer, Alexander M.; Winbo, Annika; Clur, Sally-Ann B; et al.
2023
Cardiac response to water activities in children with Long QT syndrome type 1
PLOS ONE
, Public Library of Science (PLoS) 2023, Vol. 18, (12)
Lundström, Anna; Wiklund, Urban; Winbo, Annika; et al.
2022
To Modify or Not to Modify: Allele-Specific Effects of 3’UTR-KCNQ1 Single Nucleotide Polymorphisms on Clinical Phenotype in a Long QT 1 Founder Population Segregating a Dominant-Negative Mutation
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
, American Heart Association 2022, Vol. 11, (18)
Winbo, Annika; Diamant, Ulla-Britt; Persson, Johan; et al.
2021
LQTS founder population in Northern Sweden – the natural history of a potentially fatal inherited cardiac disorder
Biodemography and Social Biology
, Routledge 2021, Vol. 66, (3-4) : 191-207
Diamant, Ulla-Britt; Winbo, Annika; Marcus, Karlsson; et al.
2021
Functional hyperactivity in long OT syndrome type 1 pluripotent stem cell-derived sympathetic neurons
American Journal of Physiology. Heart and Circulatory Physiology
, American Physiological Society 2021, Vol. 321, (1) : H217-H227
Winbo, Annika; Ramanan, Suganeya; Eugster, Emily; et al.
2018
Fetal heart rate and arrhythmia profile predicts long QT syndrome (LQTS) genotype: Results of an 8-center international study
American Journal of Obstetrics and Gynecology
, MOSBY-ELSEVIER 2018, Vol. 218, (1) : S93-S93
Cuneo, Bettina; Clur, Sally Ann; Swan, Heikki; et al.
2018
Fetal heart rate reflects mutation burden and clinical outcome in twin probands with
KCNQ1
mutations
HeartRhythm case reports
, Vol. 4, (6) : 237-240
Winbo, Annika; Rydberg, Annika
2017
Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis
BMC Medical Genetics
, Vol. 18
Winbo, Annika; Stattin, Eva-Lena; Westin, Ida Maria; et al.
2016
Convergence of models of human ventricular myocyte electrophysiology after global optimization to recapitulate clinical long QT phenotypes
Journal of Molecular and Cellular Cardiology
, Vol. 100 : 25-34
Mann, Stefan A.; Imtiaz, Mohammad; Winbo, Annika; et al.
2015
Third Trimester Fetal Heart Rate Predicts Phenotype and Mutation Burden in the Type 1 Long QT Syndrome
Circulation: Arrhythmia and Electrophysiology
, Vol. 8, (4) : 806-814
Winbo, Annika; Fosdal, Inger; Lindh, Maria; et al.
2015
Vestibular dysfunction is a clinical feature of the Jervell and Lange-Nielsen Syndrome
Scandinavian Cardiovascular Journal
, Vol. 49, (1) : 7-13
Winbo, Annika; Rydberg, Annika
2014
Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1 families
BMC Cardiovascular Disorders
, BioMed Central 2014, Vol. 14 : 22-
Winbo, Annika; Stattin, Eva-Lena; Nordin, Charlotte; et al.
2013
Vectorcardiographic recordings of the Q-T interval in a pediatric long Q-T syndrome population
Pediatric Cardiology
, Vol. 34, (2) : 245-249
Diamant, Ulla-Britt; Jensen, Steen M; Winbo, Annika; et al.
2013
Electrophysiological phenotype in the LQTS mutations Y111C and R518X in the KCNQ1 gene
Journal of applied physiology
, American Physiological Society 2013, Vol. 115, (10) : 1423-1432
Diamant, Ulla-Britt; Vahedi, Farzad; Winbo, Annika; et al.
2013
Iron-deficiency anaemia, gastric hyperplasia, and elevated gastrin levels due to potassium channel dysfunction in the Jervell and Lange-Nielsen Syndrome
Cardiology in the Young
, Cambridge University Press 2013, Vol. 23, (3) : 325-334
Winbo, Annika; Sandström, Olof; Palmqvist, Richard; et al.
2012
Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing
BMC Cardiovascular Disorders
, BioMed Central 2012, Vol. 12 : 95-
Stattin, Eva-Lena; Boström, Ida Maria; Winbo, Annika; et al.
2012
Long QT syndrome in Sweden: founder effects and associated cardiac phenotypes
Umeå University medical dissertations
, 1515
Winbo, Annika
2012
Prevalence, mutation spectrum, and cardiac phenotype of the Jervell and Lange-Nielsen syndrome in Sweden
Europace
, Vol. 14, (12) : 1799-1806
Winbo, Annika; Stattin, Eva-Lena; Diamant, Ulla-Britt; et al.
2011
Origin of the Swedish long QT syndrome Y111C/KCNQ1 founder mutation
Heart Rhythm
, Elsevier 2011, Vol. 8, (4) : 541-547
Winbo, Annika; Diamant, Ulla-Britt; Rydberg, Annika; et al.
2010
Two automatic QT algorithms compared with manual measurement in identification of long QT syndrome
Journal of Electrocardiology
, Vol. 43, (1) : 25-30
Diamant, Ulla-Britt; Winbo, Annika; Stattin, Eva-Lena; et al.
2009
Low incidence of sudden cardiac death in a Swedish Y111C type 1 long-QT syndrome population
Circulation: Cardiovascular Genetics
, Philadelphia, PA: Lippincott Williams & Wilkins 2009, Vol. 2, (6) : 558-564
Winbo, Annika; Diamant, Ulla-Britt; Stattin, Eva-Lena; et al.
The Swedish long QT syndrome R518X/
KCNQ1
founder population- origin and clinical phenotype: phenotypic variability partly explained by gender-specific effects of sequence variants in the
NOS1AP
gene
Winbo, Annika; Stattin, Eva-Lena; Norberg, Anna; et al.
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