Craig T January
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Explore the profile of Craig T January including associated specialties, affiliations and a list of published articles.
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81
Citations
7855
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Recent Articles
1.
Zhou W, Ye D, Tester D, Bains S, Giudicessi J, Haglund-Turnquist C, et al.
Circ Genom Precis Med
. 2023 Apr;
16(2):e003726.
PMID: 37071726
Background: Long-QT syndrome (LQTS) is characterized by QT prolongation and increased risk for syncope, seizures, and sudden cardiac death. The majority of LQTS stems from pathogenic mutations in , ,...
2.
Anderson C, Munawar S, Reilly L, Kamp T, January C, Delisle B, et al.
Front Cardiovasc Med
. 2022 Jul;
9:900431.
PMID: 35859585
Over the last two decades, an exponentially expanding number of genetic variants have been identified associated with inherited cardiac conditions. These tremendous gains also present challenges in deciphering the clinical...
3.
Kekenes-Huskey P, Burgess D, Sun B, Bartos D, Rozmus E, Anderson C, et al.
Int J Mol Sci
. 2022 Jul;
23(13).
PMID: 35806392
The electrocardiogram (ECG) empowered clinician scientists to measure the electrical activity of the heart noninvasively to identify arrhythmias and heart disease. Shortly after the standardization of the 12-lead ECG for...
4.
Feng L, Zhang J, Lee C, Kim G, Liu F, Petersen A, et al.
Circ Arrhythm Electrophysiol
. 2021 Mar;
14(4):e009343.
PMID: 33729832
[Figure: see text].
5.
Ono M, Burgess D, Schroder E, Elayi C, Anderson C, January C, et al.
Biomolecules
. 2020 Aug;
10(8).
PMID: 32759882
Significant advances in our understanding of the molecular mechanisms that cause congenital long QT syndrome (LQTS) have been made. A wide variety of experimental approaches, including heterologous expression of mutant...
6.
Ng K, Titus E, Lieve K, Roston T, Mazzanti A, Deiter F, et al.
Circulation
. 2020 Jul;
142(10):932-947.
PMID: 32693635
Background: Genetic variants in calsequestrin-2 () cause an autosomal recessive form of catecholaminergic polymorphic ventricular tachycardia (CPVT), although isolated reports have identified arrhythmic phenotypes among heterozygotes. Improved insight into the...
7.
Anderson C, Routes T, Eckhardt L, Delisle B, January C, Kamp T
Genet Med
. 2020 Jun;
22(10):1642-1652.
PMID: 32475984
Purpose: DNA sequencing technology has unmasked a vast number of uncharacterized single-nucleotide variants in disease-associated genes, and efficient methods are needed to determine pathogenicity and enable clinical care. Methods: We...
8.
Kamp T, Hamdan M, January C
J Am Heart Assoc
. 2020 May;
9(12):e016887.
PMID: 32463308
No abstract available.
9.
Qile M, Ji Y, Golden T, Houtman M, Romunde F, Fransen D, et al.
Mol Pharmacol
. 2020 Apr;
97(6):355-364.
PMID: 32241959
Voltage-gated potassium 11.1 (K11.1) channels play a critical role in repolarization of cardiomyocytes during the cardiac action potential (AP). Drug-mediated K11.1 blockade results in AP prolongation, which poses an increased...
10.
January C, Samuel Wann L, Calkins H, Chen L, Cigarroa J, Cleveland Jr J, et al.
Heart Rhythm
. 2019 Feb;
16(8):e66-e93.
PMID: 30703530
No abstract available.