Annika Winbo

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Anknuten som forskare till Institutionen för klinisk vetenskap Enhet: Pediatrik

Umeå universitet, Klinisk vetenskap, 901 85 Umeå

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.

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.

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

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.

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.

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.

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

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.

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.

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.

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.

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.

Long QT syndrome in Sweden: founder effects and associated cardiac phenotypes

Umeå University medical dissertations, 1515

Winbo, Annika

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.

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.

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.

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.

Visa publikationer i DiVA

Forskargrupper

Gruppmedlem

Centrum för kardiovaskulär genetik