D. Herman

发表

Burden of rare sarcomere gene variants in the Framingham and Jackson Heart Study cohorts.

S. Gabriel, D. Altshuler, J. Hirschhorn, 2012, American journal of human genetics.

Truncations of titin causing dilated cardiomyopathy.

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

Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease

Tan Ru San, S. Gabriel, F. Cunningham, 2015, Science Translational Medicine.

Marked Up-Regulation of ACE2 in Hearts of Patients With Obstructive Hypertrophic Cardiomyopathy: Implications for SARS-CoV-2–Mediated COVID-19

J. Seidman, P. Noseworthy, A. Oberg, 2020, Mayo Clinic Proceedings.

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

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

Does B-type Natriuretic Peptide or Its Gene Polymorphism Predict Patient Outcome after Coronary Artery Bypass Graft Surgery?

Lichtner, Christoph, S. Aranki, 2009 .

Natriuretic Peptide System Gene Variants Are Associated with Ventricular Dysfunction after Coronary Artery Bypass Grafting

J. Seidman, S. Aranki, T. Meitinger, 2009, Anesthesiology.

Filter-based hybridization capture of subgenomes enables resequencing and copy-number detection

J. Seidman, H. Rehm, R. Kucherlapati, 2009, Nature Methods.

5'RNA-Seq identifies Fhl1 as a genetic modifier in cardiomyopathy.

J. Seidman, M. Bulyk, P. D. De Jager, 2014, The Journal of clinical investigation.

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.

Dissection of Chromosome 18 Blood Pressure and Salt-Sensitivity Quantitative Trait Loci in the Spontaneously Hypertensive Rat

Nathan R. Qi, J. Seidman, T. Kurtz, 2009, Hypertension.

Heterozygosity for a loss-of-function mutation in GALNT2 improves plasma triglyceride clearance in man.

A. Zwinderman, J. Seidman, L. Tabak, 2011, Cell metabolism.

Variation in the 4q25 Chromosomal Locus Predicts Atrial Fibrillation After Coronary Artery Bypass Graft Surgery

J. Seidman, P. Ellinor, S. Aranki, 2009, Circulation. Cardiovascular genetics.

Genome-Wide Assessment for Genetic Variants Associated with Ventricular Dysfunction after Primary Coronary Artery Bypass Graft Surgery

Dan M. Roden, Christine E. Seidman, Kuang-Yu Liu, 2011, PloS one.

Construction of normalized RNA-seq libraries for next-generation sequencing using the crab duplex-specific nuclease.

J. Seidman, J. Gorham, Danos C. Christodoulou, 2011, Current protocols in molecular biology.

as a genetic modifier in cardiomyopathy

M. Bulyk, A. Aboukhalil, C. Seidman, 2014 .

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

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

Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease

Tan Ru San, Angharad M Roberts, S. Gabriel, 2015, Science Translational Medicine.

Truncations of titin causing dilated cardiomyopathy.

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

Quantification of gene transcripts with deep sequencing analysis of gene expression (DSAGE) using 1 to 2 µg total RNA.

H. Wakimoto, S. DePalma, Danos C. Christodoulou, 2011, Current protocols in molecular biology.