| # | Title | Journal | Year | Citations |
|---|
| 1 | Validation of Metagenomic Next-Generation Sequencing Tests for Universal Pathogen Detection | Archives of Pathology and Laboratory Medicine | 2017 | 404 |
| 2 | Update on the Epidemiology of Pulmonary Nontuberculous Mycobacterial Infections | Seminars in Respiratory and Critical Care Medicine | 2013 | 179 |
| 3 | Evidence of increased angiogenesis in patients with acute myeloid leukemia | Blood | 2000 | 141 |
| 4 | Familial occurrence of schwannomas and malignant rhabdoid tumour associated with a duplication in SMARCB1 | Journal of Medical Genetics | 2008 | 90 |
| 5 | Evaluation of the Prodesse Hexaplex Multiplex PCR Assay for Direct Detection of Seven Respiratory Viruses in Clinical Specimens | American Journal of Clinical Pathology | 2001 | 78 |
| 6 | Thrombocytopenia: an update | International Journal of Laboratory Hematology | 2014 | 73 |
| 7 | Clinical utility of next‐generation sequencing in the diagnosis of hereditary haemolytic anaemias | British Journal of Haematology | 2016 | 71 |
| 8 | Causes of hemolysis in neonates with extreme hyperbilirubinemia | Journal of Perinatology | 2014 | 67 |
| 9 | Detection of Gene Rearrangements in Targeted Clinical Next-Generation Sequencing | Journal of Molecular Diagnostics | 2014 | 65 |
| 10 | Limited Utility of Culture for Mycoplasma pneumoniae and Chlamydophila pneumoniae for Diagnosis of Respiratory Tract Infections | Journal of Clinical Microbiology | 2010 | 58 |
| 11 | Measurement of Hba1C in patients with chronic renal failure | Clinica Chimica Acta | 2013 | 54 |
| 12 | Polycythemia vera‐associated acquired von Willebrand syndrome despite near‐normal platelet count | American Journal of Hematology | 2010 | 46 |
| 13 | Laboratory testing of CYP2D6 alleles in relation to tamoxifen therapy | Genetics in Medicine | 2012 | 39 |
| 14 | Clinical performance of endobronchial ultrasound‐guided transbronchial needle aspiration for assessing programmed death ligand‐1 expression in nonsmall cell lung cancer | Diagnostic Cytopathology | 2018 | 38 |
| 15 | Anaplerotic therapy in propionic acidemia | Molecular Genetics and Metabolism | 2017 | 28 |
| 16 | What’s New in the AFIP Fascicle on Salivary Gland Tumors: A Few Highlights from the 4th Series Atlas | Head and Neck Pathology | 2009 | 26 |
| 17 | Variations in Both α-Spectrin <b><i>(SPTA1)</i></b> and β-Spectrin (<b><i>SPTB</i></b>) in a Neonate with Prolonged Jaundice in a Family where Nine Individuals Had Hereditary Elliptocytosis | Neonatology | 2014 | 24 |
| 18 | Performance characteristics of a recombinant enzymatic cycling assay for quantification of total homocysteine in serum or plasma | Clinica Chimica Acta | 2004 | 23 |
| 19 | Bacterial contamination rate of platelet components by primary culture: a systematic review and meta‐analysis | Transfusion | 2020 | 23 |
| 20 | Characterization of childhood precursor T‐lymphoblastic lymphoma by immunophenotyping and fluorescent in situ hybridization: A report from the Children's Oncology Group | Pediatric Blood and Cancer | 2008 | 22 |
| 21 | AACC Practical Recommendations for Implementing and Interpreting SARS-CoV-2 Emergency Use Authorization and Laboratory-Developed Test Serologic Testing in Clinical Laboratories | Clinical Chemistry | 2021 | 20 |
| 22 | Analysis of vitamin D status at two academic medical centers and a national reference laboratory: result patterns vary by age, gender, season, and patient location | BMC Endocrine Disorders | 2013 | 19 |
| 23 | Novel α-Spectrin Mutation in <b><i>Trans</i></b> with α-Spectrin<sup>LEPRA</sup> Causing Severe Neonatal Jaundice from Hereditary Spherocytosis | Neonatology | 2014 | 17 |
| 24 | Acute Kernicterus in a Neonate With O/B Blood Group Incompatibility and a Mutation in SLC4A1 | Pediatrics | 2013 | 15 |
| 25 | An Assessment of the State of Current Practice in Coagulation Laboratories | American Journal of Clinical Pathology | 2016 | 15 |
| 26 | The 2013 symposium on pathology data integration and clinical decision support and the current state of field | Journal of Pathology Informatics | 2014 | 14 |
| 27 | Molecular genetics of childhood, adolescent and young adult non‐Hodgkin lymphoma | British Journal of Haematology | 2016 | 14 |
| 28 | Comparison of Sample Preservation Methods for Clinical Trace Element Analysis by Inductively Coupled Plasma Mass Spectrometry | American Journal of Clinical Pathology | 2005 | 14 |
| 29 | Current challenges in personalizing warfarin therapy | Expert Review of Clinical Pharmacology | 2011 | 13 |
| 30 | NF1 exon 22 analysis of individuals with the clinical diagnosis of neurofibromatosis type 1 | American Journal of Medical Genetics, Part A | 2010 | 11 |
| 31 | Laboratory formularies | Clinica Chimica Acta | 2014 | 11 |
| 32 | Uncommon non‐Hodgkin lymphomas of childhood: pathological diagnosis, clinical features and treatment approaches | British Journal of Haematology | 2015 | 11 |
| 33 | Protein S testing in patients with protein S deficiency, factor V Leiden, and rivaroxaban by North American Specialized Coagulation Laboratories | Thrombosis and Haemostasis | 2016 | 11 |
| 34 | Interpretation and Utility of Drug of Abuse Screening Immunoassays: Insights From Laboratory Drug Testing Proficiency Surveys | Archives of Pathology and Laboratory Medicine | 2020 | 11 |
| 35 | POWERPIINC (PreOperative Window of Endocrine TheRapy Provides Information to Increase Compliance) trial: Changes in tumor proliferation index and quality of life with 7 days of preoperative tamoxifen | Breast | 2017 | 10 |
| 36 | Laboratory Workup of Lymphoma in Adults | American Journal of Clinical Pathology | 2021 | 9 |
| 37 | ID Learning Unit—Diagnostics Update: Current Laboratory Methods for Rapid Pathogen Identification in Patients With Bloodstream Infections | Open Forum Infectious Diseases | 2015 | 8 |
| 38 | D-Dimer Varies Widely Across Instrument Platforms and is Not a Reliable Indicator of Periprosthetic Joint Infections | Arthroplasty Today | 2020 | 8 |
| 39 | Pediatric B-Cell Lymphoma With Lymphoblastic Morphology, TdT Expression,MYCRearrangement, and Features Overlapping With Burkitt Lymphoma | Pediatric Blood and Cancer | 2016 | 7 |
| 40 | Testing for dabigatran and rivaroxaban by clinical laboratories | American Journal of Hematology | 2016 | 7 |
| 41 | Response to Biesecker and Harrison | Genetics in Medicine | 2018 | 7 |
| 42 | Comparative Effectiveness of Immune Checkpoint Inhibitors in Patients with Platinum Refractory Advanced Urothelial Carcinoma | Journal of Urology | 2021 | 7 |
| 43 | Quality of factor XI activity testing in North American Specialized Coagulation Laboratories | International Journal of Laboratory Hematology | 2015 | 5 |
| 44 | BCAP31 Mutation Causing a Syndrome of Congenital Dystonia, Facial Dysorphism and Central Hypomyelination Discovered Using Exome Sequencing | Movement Disorders Clinical Practice | 2016 | 5 |
| 45 | The significance of L1CAM expression in clear cell carcinoma of the endometrium | Histopathology | 2018 | 5 |
| 46 | Spinal fluid IgG antibodies from patients with demyelinating diseases bind multiple sclerosis-associated bacteria | Journal of Molecular Medicine | 2021 | 5 |
| 47 | A novel pathogenic variant in DYNC1H1 causes various upper and lower motor neuron anomalies | European Journal of Medical Genetics | 2020 | 4 |
| 48 | Characterization of Reference Materials for Spinal Muscular Atrophy Genetic Testing | Journal of Molecular Diagnostics | 2021 | 4 |
| 49 | FNA diagnosis of a metastatic papillary thyroid carcinoma arising from a previously unknown follicular variant of papillary thyroid microcarcinoma | Diagnostic Cytopathology | 2014 | 3 |
| 50 | An unusual and challenging case of HIV-associated primary CNS Lymphoma with Hodgkin-like morphology and HIV encephalitis | Diagnostic Pathology | 2015 | 3 |
