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Recipient Genotype Is a Predictor of Allograft Cytokine Expression and Outcomes After Pediatric Cardiac Transplantation

Journal of the American College of Cardiology, 2009-05, Vol.53 (20), p.1909-1917

2009

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KCNJ11 Mutation in One Family is Associated with Adult-Onset Rather than Neonatal-Onset Diabetes Mellitus

AACE clinical case reports, 2018-09, Vol.4 (5), p.e411-e414

2018

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Novel loci interacting epistatically with bone morphogenetic protein receptor 2 cause familial pulmonary arterial hypertension

The Journal of heart and lung transplantation, 2010-02, Vol.29 (2), p.174-180

2010

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Are KCNK3 Mutations Found in Vasoreactive Patients With Idiopathic Pulmonary Arterial Hypertension?

Chest, 2013, Vol.144 (4), p.878A-878A

2013

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Implementation of Genetics to Personalize Medicine

Gender medicine, 2007-09, Vol.4 (3), p.248-265

Chung, Wendy K., MD, PhD

2007

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Seasonality of respiratory syncytial virus infection in Texas

Ikonne, Ann Ada

2011

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Evaluation of the association between cryptosporidiosis outbreaks and two interactive water fountain parks: Epidemiologic analysis and implications for public health

Brummitt, Sharon Ichiko

2009

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Genetics

Fetal and Neonatal Secrets, 2014, p.266-289

Third Edition, 2014

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Endocrinology and Metabolism

Fetal and Neonatal Secrets, 2014, p.155-180

Third Edition, 2014

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ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2021-08, Vol.23 (8), p.1381-1390

2021

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ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2022-07, Vol.24 (7), p.1407-1414

2022

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Performance of the Abbott SARS-CoV-2 IgG serological assay in South African 2 patients

PloS one, 2022-02, Vol.17 (2), p.e0262442

2022

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Pediatric Cardiomyopathies

Circulation research, 2017-09, Vol.121 (7), p.855-873

2017

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Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association

Circulation (New York, N.Y.), 2018-11, Vol.138 (21), p.e653-e711

2018

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Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2021-08, Vol.23 (8), p.1391-1398

2021

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Precision Medicine in Diabetes: A Consensus Report From the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD)

Diabetes care, 2020-07, Vol.43 (7), p.1617-1635

2020

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Fusobacterium nucleatum Potentiates Intestinal Tumorigenesis and Modulates the Tumor-Immune Microenvironment

Cell host & microbe, 2013-08, Vol.14 (2), p.207-215

2013

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ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Genetics in medicine, 2023-08, Vol.25 (8), p.100866-100866, Article 100866

2023

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Observational study of spinal muscular atrophy type I and implications for clinical trials

Neurology, 2014-08, Vol.83 (9), p.810-817

2014

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Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing

Genetics in medicine, 2016-08, Vol.18 (8), p.823-832

2016

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Unsupervised phenotyping of Severe Asthma Research Program participants using expanded lung data

Journal of allergy and clinical immunology, 2014-05, Vol.133 (5), p.1280-1288

2014

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Diagnosis and management of glycogen storage disease type I: a practice guideline of the American College of Medical Genetics and Genomics

Genetics in medicine, 2014-11, Vol.16 (11), p.e1-e1

2014

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A Recurrent PDGFRB Mutation Causes Familial Infantile Myofibromatosis

American journal of human genetics, 2013-06, Vol.92 (6), p.996-1000

2013

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Recipient Genotype Is a Predictor of Allograft Cytokine Expression and Outcomes After Pediatric Cardiac Transplantation

KCNJ11 Mutation in One Family is Associated with Adult-Onset Rather than Neonatal-Onset Diabetes Mellitus

Novel loci interacting epistatically with bone morphogenetic protein receptor 2 cause familial pulmonary arterial hypertension

Are KCNK3 Mutations Found in Vasoreactive Patients With Idiopathic Pulmonary Arterial Hypertension?

Implementation of Genetics to Personalize Medicine

Seasonality of respiratory syncytial virus infection in Texas

Evaluation of the association between cryptosporidiosis outbreaks and two interactive water fountain parks: Epidemiologic analysis and implications for public health

Genetics

Endocrinology and Metabolism

ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Performance of the Abbott SARS-CoV-2 IgG serological assay in South African 2 patients

Pediatric Cardiomyopathies

Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association

De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders

Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

Precision Medicine in Diabetes: A Consensus Report From the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD)

Fusobacterium nucleatum Potentiates Intestinal Tumorigenesis and Modulates the Tumor-Immune Microenvironment

ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)

Observational study of spinal muscular atrophy type I and implications for clinical trials

Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing

Unsupervised phenotyping of Severe Asthma Research Program participants using expanded lung data

Diagnosis and management of glycogen storage disease type I: a practice guideline of the American College of Medical Genetics and Genomics

PD-L1 Testing for Lung Cancer in 2019: Perspective From the IASLC Pathology Committee

A Recurrent PDGFRB Mutation Causes Familial Infantile Myofibromatosis

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