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Commentary on A Differential Diagnosis of Thrombotic Microangiopathy in a 7-Year-Old Girl

Clinical chemistry (Baltimore, Md.), 2024-02, Vol.70 (2), p.373-373

Moyer, Ann M

2024

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Personalized Reproductive Hormone Monitoring in Sweat

Clinical chemistry (Baltimore, Md.), 2024-10, Vol.70 (10), p.1299-1300

Maynard, Robert D

2024

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The Pen

Clinical chemistry (Baltimore, Md.), 2021-06, Vol.67 (6), p.917

Annesley, Thomas M

2021

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Detection of DNA Contamination in Prenatal Samples from Whole Exome Sequencing Data

Clinical chemistry (Baltimore, Md.), 2024-08, Vol.70 (8), p.1056-1063

2024

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The Inclusion of Race in Prenatal Screening Algorithms

Clinical chemistry (Baltimore, Md.), 2024-07, Vol.70 (7), p.891-893

2024

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Commentary on A Differential Diagnosis of Thrombotic Microangiopathy in a 7-Year-Old Girl

Clinical chemistry (Baltimore, Md.), 2024-02, Vol.70 (2), p.372-372

2024

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A Differential Diagnosis of Thrombotic Microangiopathy in a 7-Year-Old Girl

Clinical chemistry (Baltimore, Md.), 2024-02, Vol.70 (2), p.368-371

2024

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Circulating Tumor DNA as a Biomarker for Monitoring Patients with Solid Cancers: Comparison with Standard Protein Biomarkers

Clinical chemistry (Baltimore, Md.), 2022-11, Vol.68 (11), p.1381-1390

2022

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Commentary on Multiple Copy Number Variants Detected by Noninvasive Prenatal Screening

Clinical chemistry (Baltimore, Md.), 2022-05, Vol.68 (5), p.633-633

Almontashiri, Naif A M

2022

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Evaluating the Clinical Utility of a Long-Read Sequencing-Based Approach in Prenatal Diagnosis of Thalassemia

Clinical chemistry (Baltimore, Md.), 2023-03, Vol.69 (3), p.239-250

2023

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εγ-Thalassemia, a New Hemoglobinopathy Category

Clinical chemistry (Baltimore, Md.), 2023-07, Vol.69 (7), p.711-717

2023

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Cancer genome scanning in plasma: detection of tumor-associated copy number aberrations, single-nucleotide variants, and tumoral heterogeneity by massively parallel sequencing

Clinical chemistry (Baltimore, Md.), 2013-01, Vol.59 (1), p.211-224

2013

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Thyroid function in pregnancy: what is normal?

Clinical chemistry (Baltimore, Md.), 2015-05, Vol.61 (5), p.704-713

2015

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High-resolution profiling of fetal DNA clearance from maternal plasma by massively parallel sequencing

Clinical chemistry (Baltimore, Md.), 2013-08, Vol.59 (8), p.1228-1237

2013

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Spatial and Temporal Relationship between Epithelial–Mesenchymal Transition (EMT) and Stem Cells in Cancer

Clinical chemistry (Baltimore, Md.), 2024-01, Vol.70 (1), p.190-205

2024

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High-Sensitivity Cardiac Troponin and the Management of Congenital Heart Disease in Newborns and Infants

Clinical chemistry (Baltimore, Md.), 2024-03, Vol.70 (3), p.486-496

2024

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Third-Generation Single-Molecule Sequencing for Preimplantation Genetic Testing of Aneuploidy and Segmental Imbalances

Clinical chemistry (Baltimore, Md.), 2023-08, Vol.69 (8), p.881-889

2023

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Tumor microRNA expression profiling identifies circulating microRNAs for early breast cancer detection

Clinical chemistry (Baltimore, Md.), 2015-08, Vol.61 (8), p.1098-1106

2015

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Comparison of Single Molecule, Real-Time Sequencing and Nanopore Sequencing for Analysis of the Size, End-Motif, and Tissue-of-Origin of Long Cell-Free DNA in Plasma

Clinical chemistry (Baltimore, Md.), 2023-02, Vol.69 (2), p.168-179

2023

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Use of Type 5 Single Nucleotide Polymorphisms Allows Noninvasive Prenatal Diagnosis for Consanguineous Families

Clinical chemistry (Baltimore, Md.), 2024-05, Vol.70 (5), p.687-689

Sistermans, Erik A

2024

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Androgen Excess and Deficiency: Analytical and Diagnostic Approaches

Clinical chemistry (Baltimore, Md.), 2023-12, Vol.69 (12), p.1361-1373

2023

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Variability in Fetal Fraction Estimation: Comparing Fetal Fractions Reported by Noninvasive Prenatal Testing Providers Globally

Clinical chemistry (Baltimore, Md.), 2023-02, Vol.69 (2), p.160-167

2023

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Mining the Gap: Deriving Pregnancy Reference Intervals for Hematology Parameters Using Clinical Datasets

Clinical chemistry (Baltimore, Md.), 2023-12, Vol.69 (12), p.1374-1384

2023

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Exploration of a Novel Noninvasive Prenatal Testing Approach for Monogenic Disorders Based on Fetal Nucleated Red Blood Cells

Clinical chemistry (Baltimore, Md.), 2023-12, Vol.69 (12), p.1396-1408

2023

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Zeitschrift / SerieJnci : Journal Of The National Cancer Institute

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Commentary on A Differential Diagnosis of Thrombotic Microangiopathy in a 7-Year-Old Girl

Personalized Reproductive Hormone Monitoring in Sweat

The Pen

Detection of DNA Contamination in Prenatal Samples from Whole Exome Sequencing Data

The Inclusion of Race in Prenatal Screening Algorithms

Commentary on A Differential Diagnosis of Thrombotic Microangiopathy in a 7-Year-Old Girl

A Differential Diagnosis of Thrombotic Microangiopathy in a 7-Year-Old Girl

Circulating Tumor DNA as a Biomarker for Monitoring Patients with Solid Cancers: Comparison with Standard Protein Biomarkers

Commentary on Multiple Copy Number Variants Detected by Noninvasive Prenatal Screening

Evaluating the Clinical Utility of a Long-Read Sequencing-Based Approach in Prenatal Diagnosis of Thalassemia

εγ-Thalassemia, a New Hemoglobinopathy Category

Cancer genome scanning in plasma: detection of tumor-associated copy number aberrations, single-nucleotide variants, and tumoral heterogeneity by massively parallel sequencing

Thyroid function in pregnancy: what is normal?

High-resolution profiling of fetal DNA clearance from maternal plasma by massively parallel sequencing

Spatial and Temporal Relationship between Epithelial–Mesenchymal Transition (EMT) and Stem Cells in Cancer

High-Sensitivity Cardiac Troponin and the Management of Congenital Heart Disease in Newborns and Infants

Third-Generation Single-Molecule Sequencing for Preimplantation Genetic Testing of Aneuploidy and Segmental Imbalances

Tumor microRNA expression profiling identifies circulating microRNAs for early breast cancer detection

Comparison of Single Molecule, Real-Time Sequencing and Nanopore Sequencing for Analysis of the Size, End-Motif, and Tissue-of-Origin of Long Cell-Free DNA in Plasma

Use of Type 5 Single Nucleotide Polymorphisms Allows Noninvasive Prenatal Diagnosis for Consanguineous Families

Androgen Excess and Deficiency: Analytical and Diagnostic Approaches

Variability in Fetal Fraction Estimation: Comparing Fetal Fractions Reported by Noninvasive Prenatal Testing Providers Globally

Mining the Gap: Deriving Pregnancy Reference Intervals for Hematology Parameters Using Clinical Datasets

Exploration of a Novel Noninvasive Prenatal Testing Approach for Monogenic Disorders Based on Fetal Nucleated Red Blood Cells

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