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Author Details

Lawrence J Jennings
Northwestern University Feinberg School of Medicine
1998
89
27
PMIDPaper TitleJournal TitlePublished Year
36288429Lineage switch from acute myeloid leukemia to B-lymphoblastic lymphoma with an acquired PIK3R1 loss-of-function mutation.Am J Hematol2023
37532182ROS1 Alterations as a Potential Driver of Gliomas in Infant, Pediatric, and Adult Patients.Mod Pathol2023
37254476Relapse of large B-cell lymphoma with IRF4 rearrangement associated with SLAM-associated protein deficiency.Pediatr Blood Cancer2023
36867463Borderline With Bad Behavior: An Unusual Low-grade Serous Carcinoma With Dedifferentiation From a Serous Borderline Tumor.Int J Gynecol Pathol2023
36502925Clinical and histopathologic characterization of SETD2-mutated colorectal cancer.Hum Pathol2023
36700952Variant allelic frequency of driver mutations predicts success of genomic DNA methylation classification in central nervous system tumors.Acta Neuropathol2023
34546332Maternal vs Fetal Origin of Placental Intervillous Thrombi.Am J Clin Pathol2022
35803414The effect of human immunodeficiency virus and human papillomavirus strain diversity on the progression of anal squamous intraepithelial lesions.Hum Pathol2022
35605901Validation of Whole Genome Methylation Profiling Classifier for Central Nervous System Tumors.J Mol Diagn2022
36467801Normalization of <i>NPM1</i> mutant transcript to the wild-type transcript.EJHaem2022
36215147Non-leukemic presentation of acute promyelocytic leukemia as a testicular mass with associated non-canonical <i>FLT3</i> mutation.Leuk Lymphoma2022
36087739Many faces of SF3B1-mutated myeloid neoplasms: concurrent mutational profiles contribute to the diverse clinical and morphologic features.Hum Pathol2022
36113759Validation Study of a Direct Real-Time PCR Protocol for Detection of Monkeypox Virus.J Mol Diagn2022
35128400Markedly prolonged disease course, with breakthrough seizures, in a glioma with an isolated IDH1 mutation.Neurooncol Adv2022
34865083Next-Generation Sequencing of a Glioblastoma with True Epithelial Differentiation.J Neuropathol Exp Neurol2022
34668265Comparison of myeloid neoplasms with nonclassic 3q26.2/MECOM versus classic inv(3)/t(3;3) rearrangements reveals diverse clinicopathologic features, genetic profiles, and molecular mechanisms of MECOM activation.Genes Chromosomes Cancer2022
33087830Therapy-related B-cell acute lymphoblastic leukemia in adults has unique genetic profile with frequent loss of TP53 and inferior outcome.Leukemia2021
33769390Morphologic and Immunophenotypic Differences in Juvenile Myelomonocytic Leukemias With CBL and Other Canonical RAS-pathway Gene Mutations: A Single Institutional Experience.J Pediatr Hematol Oncol2021
33905777Comprehensive evaluation of bronchoalveolar lavage from patients with severe COVID-19 and correlation with clinical outcomes.Hum Pathol2021
33914058Liver Pathology and SARS-CoV-2 Detection in Formalin-Fixed Tissue of Patients With COVID-19.Am J Clin Pathol2021
34250480Disappearance of MMR-deficient subclones after controlled IL-12 and PD-1 inhibition in a glioma patient.Neurooncol Adv2021
33958749Paired-like homeobox gene (PHOX2B) nonpolyalanine repeat expansion mutations (NPARMs): genotype-phenotype correlation in congenital central hypoventilation syndrome (CCHS).Genet Med2021
34344305Kikuchi-Fujimoto disease presenting in a patient with SARS-CoV-2: a case report.BMC Infect Dis2021
34261406Mast cell sarcoma transdifferentiated from clonally-related T-lymphoblastic leukemia upon acquisition of <i>TP53</i> mutation and genetic complexity.Leuk Lymphoma2021
34171600Solitary fibrous tumor of thoracic cavity, extra-thoracic sites and central nervous system: Clinicopathologic features and association with local recurrence and metastasis.Pathol Res Pract2021
31343482Inv(11)(q21q23); KMT2A-MAML2, a Recurrent Genetic Abnormality in T-Cell Therapy-related Acute Lymphoblastic Leukemia.J Pediatr Hematol Oncol2020
32088209Unique morphologic and genetic characteristics of acute myeloid leukemia with chromothripsis: a clinicopathologic study from a single institution.Hum Pathol2020
33186810A clade of SARS-CoV-2 viruses associated with lower viral loads in patient upper airways.EBioMedicine2020
32445025The Essentials of Molecular Testing in CNS Tumors: What to Order and How to Integrate Results.Curr Neurol Neurosci Rep2020
32511558A Unique Clade of SARS-CoV-2 Viruses is Associated with Lower Viral Loads in Patient Upper Airways.medRxiv2020
30672101Congenital central hypoventilation syndrome: Severe disease caused by co-occurrence of two PHOX2B variants inherited separately from asymptomatic family members.Am J Med Genet A2019
31585812Ewing sarcoma with myxoid stroma: Case report of an unusual histological variant.Pathol Res Pract2019
31125631An integrative approach reveals genetic complexity and epigenetic perturbation in acute promyelocytic leukemia: a single institution experience.Hum Pathol2019
30739805Sinonasal glomangiopericytoma: A clinicopathologic study.Pathol Res Pract2019
28927822CD4 T cell-restricted IL-2 signaling defect in a patient with a novel IFNGR1 deficiency.J Allergy Clin Immunol2018
29905933The classification of pediatric and young adult renal cell carcinomas registered on the children's oncology group (COG) protocol AREN03B2 after focused genetic testing.Cancer2018
29372846Pathology of Melanotic Schwannoma.Arch Pathol Lab Med2018
29733681Comparative 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.Arch Pathol Lab Med2018
29106293Worldwide Frequency of Commonly Detected EGFR Mutations.Arch Pathol Lab Med2018
28994342Malignant Ectomesenchymoma: Series Analysis of a Histologically and Genetically Heterogeneous Tumor.Int J Surg Pathol2018
27769870BRAF exon 15 mutations in pediatric renal stromal tumors: prevalence in metanephric stromal tumors.Hum Pathol2017
28410084Clinical and Electroencephalographic Characteristics of Infantile-Onset Epilepsies Caused by Genetic Mutations.J Pediatr2017
28447902Reporting Results of Molecular Tests: A Retrospective Examination of BRAF Mutation Reporting.Arch Pathol Lab Med2017
28266766Early mixed T-cell chimerism is predictive of pediatric AML or MDS relapse after hematopoietic stem cell transplant.Pediatr Blood Cancer2017
28341590Guidelines for Validation of Next-Generation Sequencing-Based Oncology Panels: A Joint Consensus Recommendation of the Association for Molecular Pathology and College of American Pathologists.J Mol Diagn2017
29028368A Window Into Clinical Next-Generation Sequencing-Based Oncology Testing Practices.Arch Pathol Lab Med2017
28756976Oncocytic papillary cystadenoma with prominent mucinous differentiation of parotid gland: A case report.Pathol Res Pract2017
26773439ALK-rearranged renal cell carcinomas in children.Genes Chromosomes Cancer2016
26523541Expanding the Spectrum of Renal Tumors in Children: Primary Renal Myoepithelial Carcinomas With a Novel EWSR1-KLF15 Fusion.Am J Surg Pathol2016
27763904Primary Cutaneous Mammary Analog Secretory Carcinoma With ETV6-NTRK3 Translocation.Am J Dermatopathol2016
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Collaborators

Elizabeth J Perlman
Ann & Robert H. Lurie Children's Hospital of Chicago
Co-authored papers 12
Min Yu
Ann & Robert H. Lurie Children's Hospital of Chicago
Co-authored papers 12
Craig Horbinski
Co-authored papers 7
Debra E Weese-Mayer
Northwestern University Feinberg School of Medicine
Co-authored papers 7
Daniel J Brat
Co-authored papers 5
Suzanne Kamel-Reid
Toronto General Hospital, University Health Network, University of Toronto
Co-authored papers 3
Charles G Mullighan
St Jude Children's Research Hospital
Co-authored papers 2
Elizabeth A Mullen
Co-authored papers 2
Nitin R Wadhwani
Feinberg School of Medicine, Northwestern University
Co-authored papers 2
Joel T Moncur
Walter Reed National Military Medical Center
Co-authored papers 2
Malcolm A Smith
National Cancer Institute
Co-authored papers 2
Daniela S Gerhard
National Cancer Institute
Co-authored papers 2
Firas H Wehbe
Feinberg School of Medicine, Northwestern University
Co-authored papers 2
Judd F Hultquist
Northwestern University Feinberg School of Medicine
Co-authored papers 2
Julie M Gastier-Foster
Baylor College of Medicine
Co-authored papers 2
Jaime M Guidry Auvil
National Cancer Institute
Co-authored papers 2
David L Rimm
Yale University School of Medicine
Co-authored papers 2
Gang Zhang
Sichuan Provincial Maternal and Child Health Hospital
Co-authored papers 2
Qing-Rong Chen
Center for Biomedical Informatics and Information Technology
Co-authored papers 1
Timothy J Triche
Center for Epigenetics, Van Andel Research Institute
Co-authored papers 1
Christopher L Corless
Oregon Health & Science University
Co-authored papers 1
Alex J Rai
Co-authored papers 1
Mark J Routbort
University of Texas MD Anderson Cancer Center
Co-authored papers 1
Yussanne Ma
Co-authored papers 1
Srishti Nangia
New York-Presbyterian Hospital
Co-authored papers 1
Amanda L Strickland
Northwestern University Feinberg School of Medicine
Co-authored papers 1
Richard G Wunderink
Northwestern University Feinberg School of Medicine
Co-authored papers 1
M Wainwright
Seattle Children's Hospital, University of Washington
Co-authored papers 1
Marco A Marra
University of British Columbia
Co-authored papers 1
Rashmi Kanagal-Shamanna
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Release 1.2