L. Lam

发表

Truncations of titin causing dilated cardiomyopathy.

L. Mestroni, J. Seidman, D. Pennell, 2012, The New England journal of medicine.

Nonfamilial Hypertrophic Cardiomyopathy: Prevalence, Natural History, and Clinical Implications.

T. Driscoll, J. Atherton, L. Yeates, 2017, Circulation. Cardiovascular genetics.

Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing

Parth N. Patel, J. Seidman, D. Fatkin, 2017, Proceedings of the National Academy of Sciences.

Titin truncating mutations: A rare cause of dilated cardiomyopathy in the young

Craig C. Benson, W. Chung, J. Seidman, 2016 .

Proteome map of the normal murine ventricular myocardium

J. Arthur, C. Semsarian, L. Lam, 2007, Proteomics.

Differential protein expression profiling of myocardial tissue in a mouse model of hypertrophic cardiomyopathy.

J. Arthur, C. Semsarian, L. Lam, 2010, Journal of molecular and cellular cardiology.

Molecular insights from a novel cardiac troponin I mouse model of familial hypertrophic cardiomyopathy.

D. Allen, C. Semsarian, C. Bailey, 2006, Journal of molecular and cellular cardiology.

Cardiac troponin I mutations in Australian families with hypertrophic cardiomyopathy: clinical, genetic and functional consequences.

R. Weintraub, C. Semsarian, J. Ingles, 2005, Journal of molecular and cellular cardiology.

Nonfamilial Hypertrophic Cardiomyopathy

T. Driscoll, J. Atherton, L. Yeates, 2017 .

Nonfamilial Hypertrophic CardiomyopathyCLINICAL PERSPECTIVE

T. Driscoll, J. Atherton, L. Yeates, 2017 .

Contribution of Noncanonical Splice Variants to TTN Truncating Variant Cardiomyopathy

Parth N. Patel, J. Seidman, S. Cook, 2021, Circulation. Genomic and precision medicine.

A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy

Jacob T. Munro, Angharad M Roberts, J. Seidman, 2018, Genetics in Medicine.

Multiple Gene Variants in Hypertrophic Cardiomyopathy in the Era of Next-Generation Sequencing

C. Semsarian, J. Ingles, C. Burns, 2017, Circulation. Cardiovascular genetics.

Severe Heart Failure and Early Mortality in a Double-Mutation Mouse Model of Familial Hypertrophic Cardiomyopathy

J. Seidman, C. Seidman, M. Bogoyevitch, 2008, Circulation.

A Prospective Study of Sudden Cardiac Death among Children and Young Adults.

J. Skinner, R. Weintraub, J. Atherton, 2016, The New England journal of medicine.

Thyrotoxic Periodic Paralysis

L. Lam, L. Tingle, Rajasree J Nair, 2006, Proceedings.

A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia.

E. Haan, C. Semsarian, J. Ingles, 2016, Heart rhythm.

Abnormal cardiac response to exercise in a murine model of familial hypertrophic cardiomyopathy.

C. Semsarian, L. Lam, T. Tsoutsman, 2007, International journal of cardiology.

Application of proteomics in cardiovascular medicine.

C. Semsarian, L. Lam, J. Lind, 2006, International journal of cardiology.

Exome‐based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsy

I. Scheffer, S. Berkovic, S. Petrovski, 2016, Annals of neurology.

Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant

R. N. Planken, D. Fatkin, M. P. van den Berg, 2021, medRxiv.

GENES, CALCIUM AND MODIFYING FACTORS IN HYPERTROPHIC CARDIOMYOPATHY

Christopher Semsarian, C. Semsarian, L. Lam, 2006, Clinical and experimental pharmacology & physiology.

A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy

Jacob T. Munro, J. Seidman, S. Cook, 2018, Genetics in Medicine.

NON-FAMILIAL HYPERTROPHIC CARDIOMYOPATHY: PREVALENCE, NATURAL HISTORY AND CLINICAL IMPLICATIONS

T. Driscoll, J. Atherton, L. Yeates, 2017 .

Exome sequencing identifies a novel mutation in the MYH6 gene in a family with early-onset sinus node dysfunction, ventricular arrhythmias, and cardiac arrest

C. Semsarian, J. Ingles, R. Bagnall, 2015, HeartRhythm case reports.

Truncations of titin causing dilated cardiomyopathy.

L. Mestroni, J. Seidman, D. Pennell, 2012, The New England journal of medicine.

Identification of pathogenic gene mutations in LMNA and MYBPC3 that alter RNA splicing

Parth N. Patel, J. Seidman, D. Fatkin, 2017, Proceedings of the National Academy of Sciences.