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High-throughput sequencing analysis of a “hit and run” cell and animal model of KSHV tumorigenesis

PLoS pathogens, 2020-06, Vol.16 (6), p.e1008589-e1008589

2020

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Polymorphisms in the Drug Transporter Gene ABCB1 Predict Antidepressant Treatment Response in Depression

Neuron (Cambridge, Mass.), 2008-01, Vol.57 (2), p.203-209

2008

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Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways

Human molecular genetics, 2012-08, Vol.21 (15), p.3513-3523

2012

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PDGFRA defines the mesenchymal stem cell Kaposi's sarcoma progenitors by enabling KSHV oncogenesis in an angiogenic environment

PLoS pathogens, 2019-12, Vol.15 (12), p.e1008221-e1008221

2019

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Understanding the Impact of Omega-3 Rich Diet on the Gut Microbiota

Case Reports in Medicine, 2016-01, Vol.2016 (2016), p.180-185

2016

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Polymorphisms of the Glucocorticoid Receptor Gene and Major Depression

Biological psychiatry (1969), 2006-04, Vol.59 (8), p.681-688

2006

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A Case-Control Study Evaluating Risk Factors and Outcomes of Hospitalized Children With ESBL-UTI

Clinical pediatrics, 2022-11, Vol.61 (11), p.759-767

2022

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Three-year experience with immediate extubation in pediatric patients after congenital cardiac surgery

Journal of cardiothoracic surgery, 2020-01, Vol.15 (1), p.1-1, Article 1

2020

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A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism

Molecular autism, 2011-01, Vol.2 (1), p.1-1, Article 1

2011

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A Non-Coding RNA Network Involved in KSHV Tumorigenesis

Frontiers in oncology, 2021-06, Vol.11, p.687629

2021

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Report of two cases of Schaaf‐Yang syndrome: Same genotype and different phenotype

Clinical case reports, 2023-08, Vol.11 (8), p.e7753-n/a

2023

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Correlation Between ROTEM FIBTEM Maximum Clot Firmness and Fibrinogen Levels in Pediatric Cardiac Surgery Patients

Clinical and applied thrombosis/hemostasis, 2019-01, Vol.25, p.1076029618816382-1076029618816382

2019

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Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk

PloS one, 2011-10, Vol.6 (10), p.e26049-e26049

2011

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Multi-center implementation of rapid whole genome sequencing provides additional evidence of its utility in the pediatric inpatient setting

Frontiers in pediatrics, 2024-02, Vol.12, p.1349519-1349519

2024

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Genetic abnormalities/syndromes significantly impact perioperative outcomes of conotruncal heart defects

Annals of pediatric cardiology, 2020-01, Vol.13 (1), p.38-45

2020

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Interval changes in ROTEM values during cardiopulmonary bypass in pediatric cardiac surgery patients

Journal of cardiothoracic surgery, 2019-07, Vol.14 (1), p.139-139, Article 139

2019

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Combined effects of exonic polymorphisms in CRHR1 and AVPR1B genes in a case/control study for panic disorder

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2008-10, Vol.147B (7), p.1196-1204

2008

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Health Care Access Barriers Bring Children to Emergency Rooms More Frequently: A Representative Survey

Population health management, 2019-06, Vol.22 (3), p.262-271

2019

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Results and challenges of Cytochrome P450 2D6 (CYP2D6) testing in an ethnically diverse South Florida population

Molecular genetics & genomic medicine, 2019-09, Vol.7 (9), p.e922-n/a

2019

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Pediatric pharmacogenomics: challenges and opportunities: on behalf of the Sanford Children’s Genomic Medicine Consortium

The pharmacogenomics journal, 2021-02, Vol.21 (1), p.8-19

2021

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Cost-effectiveness of exome and genome sequencing for children with rare and undiagnosed conditions

Genetics in medicine, 2022-06, Vol.24 (6), p.1349-1361

2022

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Viral expression associated with gastrointestinal adenocarcinomas in TCGA high-throughput sequencing data

Human genomics, 2013-11, Vol.7 (1), p.23-23, Article 23

2013

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Real-world economic evaluation of prospective rapid whole-genome sequencing compared to a matched retrospective cohort of critically ill pediatric patients in the United States

The pharmacogenomics journal, 2022-07, Vol.22 (4), p.223-229

2022

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Clinical utility and accessibility of functional precision medicine for relapsed/refractory pediatric and adult cancers

Journal of clinical oncology, 2024-06, Vol.42 (16_suppl), p.1551-1551

2024

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High-throughput sequencing analysis of a “hit and run” cell and animal model of KSHV tumorigenesis

Polymorphisms in the Drug Transporter Gene ABCB1 Predict Antidepressant Treatment Response in Depression

Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways

PDGFRA defines the mesenchymal stem cell Kaposi's sarcoma progenitors by enabling KSHV oncogenesis in an angiogenic environment

Understanding the Impact of Omega-3 Rich Diet on the Gut Microbiota

Polymorphisms of the Glucocorticoid Receptor Gene and Major Depression

A Case-Control Study Evaluating Risk Factors and Outcomes of Hospitalized Children With ESBL-UTI

Three-year experience with immediate extubation in pediatric patients after congenital cardiac surgery

A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism

A Non-Coding RNA Network Involved in KSHV Tumorigenesis

Report of two cases of Schaaf‐Yang syndrome: Same genotype and different phenotype

Correlation Between ROTEM FIBTEM Maximum Clot Firmness and Fibrinogen Levels in Pediatric Cardiac Surgery Patients

Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk

Multi-center implementation of rapid whole genome sequencing provides additional evidence of its utility in the pediatric inpatient setting

Genetic abnormalities/syndromes significantly impact perioperative outcomes of conotruncal heart defects

Interval changes in ROTEM values during cardiopulmonary bypass in pediatric cardiac surgery patients

Combined effects of exonic polymorphisms in CRHR1 and AVPR1B genes in a case/control study for panic disorder

Health Care Access Barriers Bring Children to Emergency Rooms More Frequently: A Representative Survey

O38: The impact of whole genome sequencing in a diverse global population of genetic disease patients

Results and challenges of Cytochrome P450 2D6 (CYP2D6) testing in an ethnically diverse South Florida population

Pediatric pharmacogenomics: challenges and opportunities: on behalf of the Sanford Children’s Genomic Medicine Consortium

Cost-effectiveness of exome and genome sequencing for children with rare and undiagnosed conditions

Viral expression associated with gastrointestinal adenocarcinomas in TCGA high-throughput sequencing data

Real-world economic evaluation of prospective rapid whole-genome sequencing compared to a matched retrospective cohort of critically ill pediatric patients in the United States

Clinical utility and accessibility of functional precision medicine for relapsed/refractory pediatric and adult cancers

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