D. McKean

发表

Single-Cell Resolution of Temporal Gene Expression during Heart Development.

J. Seidman, B. Bruneau, W. Pu, 2016, Developmental cell.

Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis

Brent S. Pedersen, Naftali Kaminski, James D. Crapo, 2013, Nature Genetics.

ViroFind: A novel target-enrichment deep-sequencing platform reveals a complex JC virus population in the brain of PML patients

J. Seidman, C. Seidman, D. McKean, 2018, PloS one.

A common genetic variant within SCN10A modulates cardiac SCN5A expression.

J. Seidman, M. Nóbrega, C. Seidman, 2014, The Journal of clinical investigation.

GWAS of Cerebrospinal Fluid Tau Levels Identifies Risk Variants for Alzheimer’s Disease

Matthew H. Bailey, J. Haines, M. Pericak-Vance, 2013, Neuron.

Defects in GPI biosynthesis perturb Cripto signaling during forebrain development in two new mouse models of holoprosencephaly

D. McKean, L. Niswander, 2012, Biology Open.

D. McKean, R. Nemenoff, P. Jones, 2004, Circulation research.

FAK induces expression of Prx1 to promote tenascin-C–dependent fibroblast migration

D. McKean, D. Ilić, M. Weiser-Evans, 2003, The Journal of cell biology.

EM-mosaic detects mosaic point mutations that contribute to congenital heart disease

K. B. Manheimer, W. Chung, J. Seidman, 2020, Genome Medicine.

Cardiomyocyte Proliferative Capacity Is Restricted in Mice With Lmna Mutation

J. Seidman, C. Seidman, H. Wakimoto, 2021, Frontiers in Cardiovascular Medicine.

Using Next-generation RNA Sequencing to Examine Ischemic Changes Induced by Cold Blood Cardioplegia on the Human Left Ventricular Myocardium Transcriptome

J. Seidman, S. Aranki, M. Heydarpour, 2015, Anesthesiology.

Early post-zygotic mutations contribute to congenital heart disease

K. B. Manheimer, W. Chung, J. Seidman, 2019, bioRxiv.

The iron exporter ferroportin 1 is essential for development of the mouse embryo, forebrain patterning and neural tube closure

D. McKean, I. Zohn, L. Niswander, 2010, Development.

Erratum: Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis (Nature Genetics (2013) 45 (613-620))

Brent S. Pedersen, E. Regan, D. Lynch, 2013 .

Fetal oxygen tension promotes tenascin‐C–dependent lung branching morphogenesis

D. McKean, P. Jones, S. Gebb, 2005, Developmental dynamics : an official publication of the American Association of Anatomists.

Rare genetic variation at transcription factor binding sites modulates local DNA methylation profiles

W. Chung, J. Seidman, A. Sharp, 2020, PLoS genetics.

Tenascin-C is induced by mutated BMP type II receptors in familial forms of pulmonary arterial hypertension.

D. McKean, N. Morrell, J. Loyd, 2006, American journal of physiology. Lung cellular and molecular physiology.

Neither cardiac mitochondrial DNA variation or copy number contribute to congenital heart disease risk

J. Seidman, Yufeng Shen, D. Bernstein, 2022, The American Journal of Human Genetics.

Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia

Brent S. Pedersen, Ivana V. Yang, Pamela H. Russell, 2016, BMC Genetics.

in familial forms of pulmonary arterial hypertension

D. McKean, N. Morrell, J. Loyd, 2006 .

The MUC5B Promoter Polymorphism Is Associated With A Less Severe Pathological Form Of Familial Interstitial Pneumonia (FIP)

D. Schwartz, D. McKean, K. Brown, 2012, ATS 2012.

ORE identifies extreme expression effects enriched for rare variants

F. Richter, G. E. Hoffman, K. B. Manheimer, 2019, Bioinform..

De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies

Stephan J Sanders, M. Daly, W. Chung, 2015, Science.

Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia

Brent S. Pedersen, Pamela H. Russell, E. Regan, 2016, BMC Genetics.

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.

ROCK Controls Matrix Synthesis in Vascular Smooth Muscle Cells: Coupling Vasoconstriction to Vascular Remodeling

Hiroaki Shimokawa, Peter Lloyd Jones, Anne Plant, 2006, Circulation research.

Loss of RNA expression and allele-specific expression associated with congenital heart disease

Yufeng Shen, Andrew J Sharp, Nihir Patel, 2016, Nature Communications.

De novo mutations in Congenital Heart Disease with Neurodevelopmental and Other Birth Defects

Stephan J Sanders, M. Daly, W. Chung, 2016 .

as a genetic modifier in cardiomyopathy

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

Contribution of Previously Unrecognized RNA Splice-Altering Variants to Congenital Heart Disease

Parth N. Patel, J. Seidman, Yufeng Shen, 2023, Circulation. Genomic and precision medicine.