D. Kinnamon

发表

Whole Exome Sequencing Identifies Candidate Genes Associated with Hereditary Predisposition to Uveal Melanoma.

T. Walsh, M. King, N. Hayward, 2019, Ophthalmology.

Valid Monte Carlo Permutation Tests for Genetic Case‐Control Studies With Missing Genotypes

E. Martin, D. Kinnamon, 2014, Genetic epidemiology.

Statistical methods to address the challenges posed by rare variants and missing genotypes in case-control resequencing studies

D. Kinnamon, 2013 .

Antenatal Hydronephrosis as a Predictor of Postnatal Outcome: A Meta-analysis

Richard S. Lee, Hiep T Nguyen, D. Kinnamon, 2006, Pediatrics.

Toward Genetics-Driven Early Intervention in Dilated Cardiomyopathy: Design and Implementation of the DCM Precision Medicine Study

D. Nickerson, C. Bustamante, E. Ashley, 2017, Circulation. Cardiovascular genetics.

Variant Interpretation for Dilated Cardiomyopathy

D. Nickerson, H. Rehm, M. Dorschner, 2020, Circulation. Genomic and precision medicine.

SOS1 Gain-of-Function Variants in Dilated Cardiomyopathy

D. Nickerson, M. Bamshad, R. Hershberger, 2020, Circulation. Genomic and precision medicine.

TTR variants in patients with dilated cardiomyopathy: An investigation of the DCM Precision Medicine Study.

G. Ewald, M. Wheeler, L. Hindorff, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy.

G. Ewald, M. Wheeler, S. Gottlieb, 2022, JAMA.

Smaller mandibular size in infants with a history of an apparent life-threatening event.

M. Curley, D. Kinnamon, N. Ferraro, 2006, The Journal of pediatrics.

An improved estimator for the hydration of fat-free mass from in vivo measurements subject to additive technical errors

S. Lipsitz, D. Ludwig, S. Lipshultz, 2010, Physiological measurement.

Moyamoya following cranial irradiation for primary brain tumors in children

S. Pomeroy, M. Proctor, R. Robertson, 2007, Neurology.

The central role of family-based approaches in understanding the genetic architecture of left ventricular noncompaction.

D. Kinnamon, 2022, International journal of cardiology.

The effect of a structured exercise program on nutrition and fitness outcomes in human immunodeficiency virus-infected children.

T. Miller, D. Kinnamon, G. Somarriba, 2010, AIDS research and human retroviruses.

Communal Coping as a Strategy to Enhance Family Engagement in Dilated Cardiomyopathy

S. Hovick, W. Burke, D. Kinnamon, 2022, Circulation. Genomic and precision medicine.

The Complex and Diverse Genetic Architecture of Dilated Cardiomyopathy.

D. Kinnamon, Jason Cowan, E. Jordan, 2021, Circulation research.

Cerebellar Hemorrhage in the Preterm Infant: Ultrasonographic Findings and Risk Factors

J. Volpe, C. Limperopoulos, H. Bassan, 2005, Pediatrics.

Changes in macronutrient intake among HIV-infected children between 1995 and 2004.

T. Miller, S. Gorbach, D. Kinnamon, 2008, The American journal of clinical nutrition.

Reconsidering Association Testing Methods Using Single-Variant Test Statistics as Alternatives to Pooling Tests for Sequence Data with Rare Variants

Eden R. Martin, Ray E. Hershberger, E. Martin, 2012, PloS one.

Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease

Eden R Martin, Arpit Mehta, Stephan Züchner, 2013, Neurology.

Prospective phase 1/2 study of rituximab in childhood and adolescent chronic immune thrombocytopenic purpura.

M. Loh, E. Neufeld, J. Bussel, 2006, Blood.

Expanded Newborn Screening for Biochemical Disorders: The Effect of a False-Positive Result

S. Waisbren, D. Kinnamon, Susan E Waisbren, 2006, Pediatrics.

Knowledge of Genome Sequencing and Trust in Medical Researchers Among Patients of Different Racial and Ethnic Groups With Idiopathic Dilated Cardiomyopathy.

S. Gottlieb, D. Judge, E. Kransdorf, 2022, JAMA cardiology.

Understanding BRCA Mutation Carriers’ Preferences for Communication of Genetic Modifiers of Breast Cancer Risk

A. Toland, S. Hovick, R. Pyatt, 2019, Journal of health communication.

SeqEM: an adaptive genotype-calling approach for next-generation sequencing studies

Michael A. Schmidt, Stephan Züchner, Eden R. Martin, 2010, Bioinform..

Multigenic Disease and Bilineal Inheritance in Dilated Cardiomyopathy Is Illustrated in Nonsegregating LMNA Pedigrees

D. Nickerson, R. Hershberger, D. Kinnamon, 2018, Circulation. Genomic and precision medicine.

chronic immune thrombocytopenic purpura Prospective phase I/II study of rituximab in childhood and adolescent

M. Loh, E. Neufeld, J. Bussel, 2013 .

Bladder growth and development after complete primary repair of bladder exstrophy in the newborn with comparison to staged approach.

S. Khoshbin, A. Atala, S. Bauer, 2005, The Journal of urology.

Associations between neurohormonal and inflammatory activation and heart failure in children.

Steven E Lipshultz, S. Lipshultz, D. Kinnamon, 2008, American heart journal.

Attitudes of Dilated Cardiomyopathy Patients and Investigators Toward Genomic Study Enrollment, Consent Process, and Return of Genetic Results

R. Hershberger, D. Kinnamon, H. Ni, 2020, Clinical and translational science.

Effectiveness of the Family Heart Talk Communication Tool in Improving Family Member Screening for Dilated Cardiomyopathy: Results of a Randomized Trial

G. Ewald, M. Wheeler, S. Gottlieb, 2023, Circulation.

Screening for Dilated Cardiomyopathy in At-Risk First-Degree Relatives.

G. Ewald, M. Wheeler, S. Gottlieb, 2023, Journal of the American College of Cardiology.

Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry.

G. Ewald, M. Wheeler, H. Rehm, 2023, JAMA.

Differences in Cardiac Mechanics among Genetically At-Risk First-Degree Relatives: The DCM Precision Medicine Study

D. Kinnamon, H. Ni, L. Beussink-Nelson, 2023, medRxiv.

Risk Factors Cerebellar Hemorrhage in the Preterm Infant: Ultrasonographic Findings and

J. Volpe, H. Bassan, D. Disalvo, 2013 .

THE EFFECTS OF PRIVATIZATION ON INDUSTRY WAGES : A STUDY OF FOUR CASES IN MEXICO

D. Kinnamon, 2002 .

Common Susceptibility Variants Examined for Association with Dilated Cardiomyopathy

Eden R Martin, Sawsan Khuri, Kara Hamilton, 2010, Annals of human genetics.