Identification of a gene responsible for familial Wolff-Parkinson-White syndrome.

By M. Gollob, Martin S. Green, A. Tang, Tanya N. Gollob, Akihiko Karibe, Al-Sayegh Hassan, Ferhaan Ahmad, Ryan Lozado, G. Shah, L. Fananapazir and 6 more. New England Journal of Medicine, 2001

668 citations recorded by the source corpus.

Subfields: Cardiology and Cardiovascular Medicine, Molecular Biology

View Paper: https://www.semanticscholar.org/paper/532a5d87d5c4d1086ea4aee1506434dadfcf647a

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Cardiology and Cardiovascular Medicine

1. B. Maron
2. Mark S. Link
3. B. K. Pedersen
4. B. Saltin
5. M. Maron

In Molecular Biology

1. David Carling
2. D. Hardie
3. G. Steinberg

Citations in the corpus

• The AMP-activated protein kinase cascade--a unifying system for energy control. (2004, background): “Shortly after the discovery of the g3 mutation, several studies reported the identification of mutations in the g2 gene from individuals with familial cardiac hypertrophy [35‐3 8] .I n most of the patients identified, there were also marked abnormalities in electrical conductance, such as ventricula”
• Recommendations for interpretation of 12-lead electrocardiogram in the athlete. (2009, background): “Pathogenetic mutations are located in the gene encoding for the regulatory g2-subunit (PRKAG2) of the AMP-activated protein kinase.(91) Familial WPW syndrome is inherited as an autosomal dominant tract with variable clinical expressivity.”
• Hypertrophic Cardiomyopathy: Distribution of Disease Genes, Spectrum of Mutations, and Implications for a Molecular Diagnosis Strategy (2003, neutral): “9 (19) 5 (5) 2 (4, 40) 1 (5, 20) 2 (9, 40)”