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Photonic Crystal Glucose-Sensing Material for Noninvasive Monitoring of Glucose in Tear Fluid

Clinical chemistry (Baltimore, Md.), 2004-12, Vol.50 (12), p.2353-2360

2004

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Predicting scoliosis progression from skeletal maturity: a simplified classification during adolescence

Journal of bone and joint surgery. American volume, 2008-03, Vol.90 (3), p.540-553

2008

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Connexin 47 Mutations Increase Risk for Secondary Lymphedema Following Breast Cancer Treatment

Clinical cancer research, 2012-04, Vol.18 (8), p.2382-2390

2012

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Metabolic features of treatment-refractory major depressive disorder with suicidal ideation

Translational psychiatry, 2023-12, Vol.13 (1), p.393-393, Article 393

2023

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The transcriptome of the Didelphis virginiana opossum kidney OK proximal tubule cell line

American journal of physiology. Renal physiology, 2017-09, Vol.313 (3), p.F585-F595

2017

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A General Photonic Crystal Sensing Motif: Creatinine in Bodily Fluids

Journal of the American Chemical Society, 2004-03, Vol.126 (9), p.2971-2977

2004

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Photonic Crystal Carbohydrate Sensors: Low Ionic Strength Sugar Sensing

Journal of the American Chemical Society, 2003-03, Vol.125 (11), p.3322-3329

2003

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High Ionic Strength Glucose-Sensing Photonic Crystal

Analytical chemistry (Washington), 2003-05, Vol.75 (10), p.2316-2323

2003

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Tear Glucose Analysis for the Noninvasive Detection and Monitoring of Diabetes Mellitus

The ocular surface, 2007-10, Vol.5 (4), p.280-293

2007

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Mass Spectral Determination of Fasting Tear Glucose Concentrations in Nondiabetic Volunteers

Clinical chemistry (Baltimore, Md.), 2007-07, Vol.53 (7), p.1370-1372

2007

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Correlates of the peak height velocity in girls with idiopathic scoliosis

Spine (Philadelphia, Pa. 1976), 2006-09, Vol.31 (20), p.2289-2295

2006

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HGF and MET mutations in primary and secondary lymphedema

Lymphatic research and biology, 2008-06, Vol.6 (2), p.65-68

2008

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Metabolomic disorders: confirmed presence of potentially treatable abnormalities in patients with treatment refractory depression and suicidal behavior

Psychological medicine, 2023-10, Vol.53 (13), p.6046-6054

2023

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Neurometabolic Disorders: Potentially Treatable Abnormalities in Patients With Treatment-Refractory Depression and Suicidal Behavior

The American journal of psychiatry, 2017-01, Vol.174 (1), p.42-50

2017

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Rare variants and biological pathways identified in treatment‐refractory depression

Journal of neuroscience research, 2020-07, Vol.98 (7), p.1322-1334

2020

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GJC2 Missense Mutations Cause Human Lymphedema

American journal of human genetics, 2010-06, Vol.86 (6), p.943-948

2010

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Selective hypermethylation is evident in small intestine samples from infants with necrotizing enterocolitis

Clinical epigenetics, 2022-12, Vol.14 (1), p.49-49, Article 49

2022

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Problem-solving, Adherence to Lifestyle Goals, and Weight Loss Among Individuals Participating in a Weight Loss Study

International journal of behavioral medicine, 2021-06, Vol.28 (3), p.328-336

2021

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Genetic association and differential expression of PITX2 with acute appendicitis

Human genetics, 2019-01, Vol.138 (1), p.37-47

2019

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Maturity Assessment and Curve Progression in Girls with Idiopathic Scoliosis

Journal of bone and joint surgery. American volume, 2007-01, Vol.89 (1), p.64-73

2007

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Lymphatic endothelial reprogramming of vascular endothelial cells by the Prox-1 homeobox transcription factor

The EMBO journal, 2002-09, Vol.21 (17), p.4593-4599

2002

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Chromosome 15q13.3 microduplications are associated with treatment refractory major depressive disorder

Genes, brain and behavior, 2020-06, Vol.19 (5), p.e12628-n/a

2020

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Neonatal necrotizing enterocolitis-associated DNA methylation signatures in the colon are evident in stool samples of affected individuals

Epigenomics, 2021-06, Vol.13 (11), p.829-844

2021

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Evaluation of disease burden and response to treatment in adults with type 1 Gaucher disease using a validated disease severity scoring system (DS3)

Orphanet journal of rare diseases, 2015-05, Vol.10 (1), p.64-64, Article 64

2015

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A Model for Gene Therapy of Human Hereditary Lymphedema

Proceedings of the National Academy of Sciences - PNAS, 2001-10, Vol.98 (22), p.12677-12682

2001

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Photonic Crystal Glucose-Sensing Material for Noninvasive Monitoring of Glucose in Tear Fluid

Predicting scoliosis progression from skeletal maturity: a simplified classification during adolescence

Connexin 47 Mutations Increase Risk for Secondary Lymphedema Following Breast Cancer Treatment

Metabolic features of treatment-refractory major depressive disorder with suicidal ideation

The transcriptome of the Didelphis virginiana opossum kidney OK proximal tubule cell line

A General Photonic Crystal Sensing Motif: Creatinine in Bodily Fluids

Photonic Crystal Carbohydrate Sensors: Low Ionic Strength Sugar Sensing

High Ionic Strength Glucose-Sensing Photonic Crystal

Tear Glucose Analysis for the Noninvasive Detection and Monitoring of Diabetes Mellitus

Mass Spectral Determination of Fasting Tear Glucose Concentrations in Nondiabetic Volunteers

Correlates of the peak height velocity in girls with idiopathic scoliosis

HGF and MET mutations in primary and secondary lymphedema

Metabolomic disorders: confirmed presence of potentially treatable abnormalities in patients with treatment refractory depression and suicidal behavior

Neurometabolic Disorders: Potentially Treatable Abnormalities in Patients With Treatment-Refractory Depression and Suicidal Behavior

Rare variants and biological pathways identified in treatment‐refractory depression

GJC2 Missense Mutations Cause Human Lymphedema

Selective hypermethylation is evident in small intestine samples from infants with necrotizing enterocolitis

Problem-solving, Adherence to Lifestyle Goals, and Weight Loss Among Individuals Participating in a Weight Loss Study

Genetic association and differential expression of PITX2 with acute appendicitis

Maturity Assessment and Curve Progression in Girls with Idiopathic Scoliosis

Lymphatic endothelial reprogramming of vascular endothelial cells by the Prox-1 homeobox transcription factor

Chromosome 15q13.3 microduplications are associated with treatment refractory major depressive disorder

Neonatal necrotizing enterocolitis-associated DNA methylation signatures in the colon are evident in stool samples of affected individuals

Evaluation of disease burden and response to treatment in adults with type 1 Gaucher disease using a validated disease severity scoring system (DS3)

A Model for Gene Therapy of Human Hereditary Lymphedema

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