Works by Jennings, Lawrence J.
Results: 32
Infantile Fibrosarcoma—A Clinical and Histologic Mimicker of Vascular Malformations: Case Report and Review of the Literature.
- Published in:
- 2013
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- Publication type:
- Case Study
Congenital central hypoventilation syndrome: Severe disease caused by co‐occurrence of two PHOX2B variants inherited separately from asymptomatic family members.
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- American Journal of Medical Genetics. Part A, 2019, v. 179, n. 3, p. 503, doi. 10.1002/ajmg.a.61047
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- Publication type:
- Article
Early mixed T-cell chimerism is predictive of pediatric AML or MDS relapse after hematopoietic stem cell transplant.
- Published in:
- 2017
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- Publication type:
- journal article
BRAF Exon 15 Mutations in the Evaluation of Well-Differentiated Epithelial Nephroblastic Neoplasms in Children.
- Published in:
- Archives of Pathology & Laboratory Medicine, 2024, v. 148, n. 10, p. e362, doi. 10.5858/arpa.2022-0528-OA
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- Publication type:
- Article
Pathology of Melanotic Schwannoma.
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- Archives of Pathology & Laboratory Medicine, 2018, v. 142, n. 12, p. 1517, doi. 10.5858/arpa.2017-0162-RA
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- Article
Comparative Performance of Breast Cancer Human Epidermal Growth Factor Receptor 2 Fluorescence In Situ Hybridization and Brightfield In Situ Hybridization on College of American Pathologists Proficiency Tests.
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- Archives of Pathology & Laboratory Medicine, 2018, v. 142, n. 10, p. 1254, doi. 10.5858/arpa.2017-0457-CP
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- Article
Worldwide Frequency of Commonly Detected EGFR Mutations.
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- Archives of Pathology & Laboratory Medicine, 2018, v. 142, n. 2, p. 163, doi. 10.5858/arpa.2016-0579-CP
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- Article
A Window Into Clinical Next-Generation Sequencing-Based Oncology Testing Practices.
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- Archives of Pathology & Laboratory Medicine, 2017, v. 141, n. 12, p. 1679, doi. 10.5858/arpa.2016-0542-CP
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- Publication type:
- Article
Reporting Results of Molecular Tests.
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- Archives of Pathology & Laboratory Medicine, 2017, v. 141, n. 5, p. 658, doi. 10.5858/arpa.2016-0280-CP
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- Publication type:
- Article
Summary of Microsatellite Instability Test Results From Laboratories Participating in Proficiency Surveys: Proficiency Survey Results From 2005 to 2012.
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- Archives of Pathology & Laboratory Medicine, 2014, v. 138, n. 3, p. 363, doi. 10.5858/arpa.2013-0159-CP
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- Publication type:
- Article
A Prospective, Multi-Institutional Diagnostic Trial to Determine Pathologist Accuracy in Estimation of Percentage of Malignant Cells.
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- Archives of Pathology & Laboratory Medicine, 2013, v. 137, n. 11, p. 1545, doi. 10.5858/arpa.2012-0561-CP
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- Publication type:
- Article
Design and Analytic Validation of BCR-ABL1 Quantitative Reverse Transcription Polymerase Chain Reaction Assay for Monitoring Minimal Residual Disease.
- Published in:
- 2012
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- Publication type:
- Journal Article
Design and Analytic Validation of BCR-ABL1 Quantitative Reverse Transcription Polymerase Chain Reaction Assay for Monitoring Minimal Residual Disease.
- Published in:
- Archives of Pathology & Laboratory Medicine, 2012, v. 136, n. 1, p. 33, doi. 10.5858/arpa.2011-0136-OA
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- Publication type:
- Article
Agminated presentation of fusion‐driven melanocytic neoplasms.
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- Journal of Cutaneous Pathology, 2023, v. 50, n. 10, p. 913, doi. 10.1111/cup.14482
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- Publication type:
- Article
Mammary Analogue Secretory Carcinoma of the Parotid Gland in a Pediatric Patient.
- Published in:
- 2012
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- Publication type:
- Case Study
Accurate identification of primary site in tumors of unknown origin (TUO) using DNA methylation.
- Published in:
- NPJ Precision Oncology, 2025, v. 9, n. 1, p. 1, doi. 10.1038/s41698-025-00805-z
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- Article
Malignant Ectomesenchymoma: Series Analysis of a Histologically and Genetically Heterogeneous Tumor.
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- International Journal of Surgical Pathology, 2018, v. 26, n. 3, p. 200, doi. 10.1177/1066896917734915
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- Publication type:
- Article
The classification of pediatric and young adult renal cell carcinomas registered on the children's oncology group (COG) protocol AREN03B2 after focused genetic testing.
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- Cancer (0008543X), 2018, v. 124, n. 16, p. 3381, doi. 10.1002/cncr.31578
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- Publication type:
- Article
The classification of pediatric and young adult renal cell carcinomas registered on the children's oncology group (COG) protocol AREN03B2 after focused genetic testing.
- Published in:
- 2018
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- Publication type:
- journal article
Gain of 1q is associated with inferior event-free and overall survival in patients with favorable histology Wilms tumor: A report from the Children's Oncology Group.
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- Cancer (0008543X), 2013, v. 119, n. 21, p. 3887, doi. 10.1002/cncr.28239
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- Publication type:
- Article
Variant allelic frequency of driver mutations predicts success of genomic DNA methylation classification in central nervous system tumors.
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- Acta Neuropathologica, 2023, v. 145, n. 3, p. 365, doi. 10.1007/s00401-023-02542-8
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- Publication type:
- Article
Normalization of NPM1 mutant transcript to the wild‐type transcript.
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- EJHaem, 2022, v. 3, n. 4, p. 1343, doi. 10.1002/jha2.579
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- Publication type:
- Article
The Essentials of Molecular Testing in CNS Tumors: What to Order and How to Integrate Results.
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- Current Neurology & Neuroscience Reports, 2020, v. 20, n. 7, p. 1, doi. 10.1007/s11910-020-01041-7
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- Publication type:
- Article
Maternal vs Fetal Origin of Placental Intervillous Thrombi.
- Published in:
- 2022
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- Publication type:
- journal article
Liver Pathology and SARS-CoV-2 Detection in Formalin-Fixed Tissue of Patients With COVID-19.
- Published in:
- 2021
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- Publication type:
- journal article
Expanding the spectrum of ALK-rearranged renal cell carcinomas in children: Identification of a novel HOOK1- ALK fusion transcript.
- Published in:
- Genes, Chromosomes & Cancer, 2016, v. 55, n. 10, p. 814, doi. 10.1002/gcc.22382
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- Publication type:
- Article
ALK-Rearranged Renal Cell Carcinomas in Children.
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- Genes, Chromosomes & Cancer, 2016, v. 55, n. 5, p. 442, doi. 10.1002/gcc.22346
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- Publication type:
- Article
Kikuchi-Fujimoto disease presenting in a patient with SARS-CoV-2: a case report.
- Published in:
- 2021
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- Publication type:
- journal article
Variable human phenotype associated with novel deletions of the PHOX2B gene.
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- Pediatric Pulmonology, 2012, v. 47, n. 2, p. 153, doi. 10.1002/ppul.21527
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- Publication type:
- Article
A 13-Year-Old Adolescent Girl With an Abdominal Mass 2 Months After Radiation for Hodgkin Lymphoma.
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- Archives of Pathology & Laboratory Medicine, 2005, v. 129, n. 4, p. e105, doi. 10.5858/2005-129-e105-pqcaya
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- Publication type:
- Article
Lineage switch from acute myeloid leukemia to B‐lymphoblastic lymphoma with an acquired PIK3R1 loss‐of‐function mutation.
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- American Journal of Hematology, 2023, v. 98, n. 1, p. E1, doi. 10.1002/ajh.26770
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- Publication type:
- Article
Germline mosaicism of PHOX2B mutation accounts for familial recurrence of congenital central hypoventilation syndrome (CCHS).
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 9, p. 2297, doi. 10.1002/ajmg.a.35499
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- Publication type:
- Article