L. Jennings

发表

M. Gulley, V. V. Van Deerlin, Vivianna M Van Deerlin, 2009, Archives of pathology & laboratory medicine.

Detection and quantification of BCR-ABL1 fusion transcripts by droplet digital PCR.

Min Yu, L. Jennings, David George, 2014, The Journal of molecular diagnostics : JMD.

Clinical and Electroencephalographic Characteristics of Infantile‐Onset Epilepsies Caused by Genetic Mutations

J. Millichap, S. Koh, D. Nordli, 2017, The Journal of pediatrics.

Expanding the spectrum of ALK‐rearranged renal cell carcinomas in children: Identification of a novel HOOK1‐ALK fusion transcript

E. Perlman, L. Jennings, David George, 2016, Genes, chromosomes & cancer.

Ewing sarcoma with myxoid stroma: Case report of an unusual histological variant.

L. Jennings, F. Obeidin, B. Alexiev, 2019, Pathology, research and practice.

Characterization of 108 Genomic DNA Reference Materials for 11 Human Leukocyte Antigen Loci: A GeT-RM Collaborative Project.

D. Monos, M. Bettinotti, L. Kalman, 2018, The Journal of molecular diagnostics : JMD.

Summary of microsatellite instability test results from laboratories participating in proficiency surveys: proficiency survey results from 2005 to 2012.

K. Halling, J. Nowak, J. Bridge, 2014, Archives of pathology & laboratory medicine.

Reporting Results of Molecular Tests: A Retrospective Examination of BRAF Mutation Reporting.

A. N. Bartley, M. Gulley, N. Lindeman, 2017, Archives of Pathology & Laboratory Medicine.

A Retrospective Examination of BRAF Mutation Reporting

A. N. Bartley, M. Gulley, N. Lindeman, 2017 .

Molecular Analysis in Pediatric Renal Tumors

L. Jennings, 2012 .

WT1 mutation and 11P15 loss of heterozygosity predict relapse in very low-risk wilms tumors treated with surgery alone: a children's oncology group study.

James R. Anderson, D. Green, J. Dome, 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

BRAF exon 15 mutations in pediatric renal stromal tumors: prevalence in metanephric stromal tumors.

S. Gadd, E. Perlman, Min Yu, 2017, Human pathology.

A Window Into Clinical Next-Generation Sequencing-Based Oncology Testing Practices.

Annette S. Kim, J. Merker, A. Rai, 2017, Archives of pathology & laboratory medicine.

Genetic Testing Requires NGS and Sanger Methodologies

D. Kirschmann, L. Jennings, 2016, Pediatric neurology briefs.

Many faces of SF3B1-mutated myeloid neoplasms: concurrent mutational profiles contribute to the diverse clinical and morphologic features.

A. Behdad, Xinyan Lu, L. Jennings, 2022, Human pathology.

Mediators of receptor tyrosine kinase activation in infantile fibrosarcoma: a Children's Oncology Group study

Chiang-Ching Huang, T. Triche, C. Tognon, 2012, The Journal of pathology.

ALK‐rearranged renal cell carcinomas in children

J. Fletcher, A. Perez-Atayde, E. Perlman, 2016, Genes, chromosomes & cancer.

Normalization of NPM1 mutant transcript to the wild‐type transcript

L. Jennings, 2022, EJHaem.

Inv(11)(q21q23); KMT2A-MAML2, a Recurrent Genetic Abnormality in T-Cell Therapy-related Acute Lymphoblastic Leukemia.

K. Yap, L. Jennings, J. Weinstein, 2020, Journal of pediatric hematology/oncology.

Disappearance of MMR-deficient subclones after controlled IL-12 and PD-1 inhibition in a glioma patient

D. Brat, M. Tate, C. Horbinski, 2021, Neuro-oncology advances.

Developmental alterations of the respiratory human retrotrapezoid nucleus in sudden unexplained fetal and infant death

D. Weese-Mayer, A. Lavezzi, Melissa F. Corna, 2012, Autonomic Neuroscience.

Validation of Whole Genome Methylation Profiling Classifier for Central Nervous System Tumors.

D. Brat, C. Horbinski, L. Santana-Santos, 2022, The Journal of molecular diagnostics : JMD.

Primary Cutaneous Mammary Analog Secretory Carcinoma With ETV6-NTRK3 Translocation

J. Guitart, L. Jennings, S. Amin, 2016, The American Journal of dermatopathology.

The classification of pediatric and young adult renal cell carcinomas registered on the children's oncology group (COG) protocol AREN03B2 after focused genetic testing

D. Kirschmann, J. Dome, E. Perlman, 2018, Cancer.

Signaling impairments in maternal T cells engrafted in an infant with a novel IL-2 receptor γ mutation.

R. Fuleihan, W. Tse, A. Khanolkar, 2015, The Journal of allergy and clinical immunology.

Guidelines for Validation of Next-Generation Sequencing-Based Oncology Panels: A Joint Consensus Recommendation of the Association for Molecular Pathology and College of American Pathologists.

Marina N Nikiforova, John Pfeifer, Karl V Voelkerding, 2017, The Journal of molecular diagnostics : JMD.

Pathologic Quiz Case A 13-Year-Old Adolescent Girl With an Abdominal Mass 2 Months After Radiation for Hodgkin Lymphoma

L. Jennings, V. Alagiozian-Angelova, 2009 .

Mammary Analogue Secretory Carcinoma of the Parotid Gland in a Pediatric Patient

K. Jatana, L. Jennings, H. Melín‐Aldana, 2012, Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery.

Detection and quantification of chimerism by droplet digital PCR

Min Yu, L. Jennings, David George, 2013, Chimerism.

Oncocytic papillary cystadenoma with prominent mucinous differentiation of parotid gland: A case report.

L. Jennings, S. Samant, B. Alexiev, 2017, Pathology, research and practice.

J. Altman, M. Kocherginsky, Xinyan Lu, 2020, Leukemia.

The Essentials of Molecular Testing in CNS Tumors: What to Order and How to Integrate Results

D. Brat, C. Horbinski, L. Jennings, 2020, Current Neurology and Neuroscience Reports.

TCF21 hypermethylation in genetically quiescent clear cell sarcoma of the kidney

D. Gerhard, J. Khan, J. Gastier-Foster, 2015, Oncotarget.

An 18-year-old man with abdominal pain, weight loss, and liver cyst.

L. Jennings, E. Weisenberg, V. Alagiozian-Angelova, 2005, Archives of pathology & laboratory medicine.

Lineage switch from acute myeloid leukemia to B‐lymphoblastic lymphoma with an acquired PIK3R1 loss‐of‐function mutation

K. Yap, L. Jennings, M. Aldulescu, 2022, American journal of hematology.

Validation of Multiplex Ligation-Dependent Probe Amplification for Confirmation of Array Comparative Genomic Hybridization

Frederick A. Smith, Lawrence J. Jennings, Min Yu, 2011, Diagnostic molecular pathology : the American journal of surgical pathology, part B.

Association of Chromosome 1q Gain With Inferior Survival in Favorable-Histology Wilms Tumor: A Report From the Children's Oncology Group.

James R. Anderson, J. Dome, P. Grundy, 2016, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Solitary fibrous tumor of thoracic cavity, extra-thoracic sites and central nervous system: Clinicopathologic features and association with local recurrence and metastasis.

D. Brat, S. Pollack, L. Jennings, 2021, Pathology, research and practice.

A prospective, multi-institutional diagnostic trial to determine pathologist accuracy in estimation of percentage of malignant cells.

David L Rimm, Meera Hameed, Patricia Vasalos, 2013, Archives of pathology & laboratory medicine.

Pathology of Melanotic Schwannoma.

L. Jennings, P. Chou, B. Alexiev, 2018, Archives of pathology & laboratory medicine.

Malignant Ectomesenchymoma: Series Analysis of a Histologically and Genetically Heterogeneous Tumor

N. Arva, L. Jennings, P. Chou, 2018, International journal of surgical pathology.

Variation in pre-PCR processing of FFPE samples leads to discrepancies in BRAF and EGFR mutation detection: a diagnostic RING trial

Marilyn M. Li, Joshua L. Deignan, R. Butler, 2014, Journal of Clinical Pathology.

Borderline With Bad Behavior: An Unusual Low-grade Serous Carcinoma With Dedifferentiation From a Serous Borderline Tumor.

Jian-jun Wei, E. Tanner, K. Maniar, 2023, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

Design and analytic validation of BCR-ABL1 quantitative reverse transcription polymerase chain reaction assay for monitoring minimal residual disease.

Suzanne Kamel-Reid, Lawrence J Jennings, S. Kamel‐Reid, 2012, Archives of pathology & laboratory medicine.

A clade of SARS-CoV-2 viruses associated with lower viral loads in patient upper airways

R. Lorenzo-Redondo, M. Ison, J. Hultquist, 2020, EBioMedicine.

A Unique Clade of SARS-CoV-2 Viruses is Associated with Lower Viral Loads in Patient Upper Airways

R. Lorenzo-Redondo, M. Ison, J. Hultquist, 2020, medRxiv.

CD4 T cell-restricted IL-2 signaling defect in a patient with a novel IFNGR1 deficiency.

R. Fuleihan, D. Kirschmann, A. Khanolkar, 2018, The Journal of allergy and clinical immunology.

Kikuchi-Fujimoto disease presenting in a patient with SARS-CoV-2: a case report

A. Matsuoka, L. Jennings, M. Angarone, 2021, BMC Infectious Diseases.

MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours

Richard A. Moore, Daoud M. Meerzaman, D. Wheeler, 2015, Nature Communications.

TERT Promoter Mutational Analysis as an Ancillary Diagnostic Tool for Diagnostically Challenging Melanocytic Neoplasms

L. Jennings, P. Gerami, Shantel Olivares, 2023, The American Journal of dermatopathology.

Clinically relevant subsets identified by gene expression patterns support a revised ontogenic model of Wilms tumor: a Children's Oncology Group Study.

Chiang-Ching Huang, D. Green, S. Gadd, 2012, Neoplasia.

Methylation Profiling Improves the Care of Pediatric Brain Tumor Patients

M. DeCuypere, C. Horbinski, K. Yap, 2022 .

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

James R. Anderson, J. Dome, P. Grundy, 2013, Cancer.

Expanding the Spectrum of Renal Tumors in Children: Primary Renal Myoepithelial Carcinomas With a Novel EWSR1-KLF15 Fusion

E. Perlman, J. Geller, L. Jennings, 2016, The American journal of surgical pathology.

Sinonasal glomangiopericytoma: A clinicopathologic study.

L. Jennings, F. Obeidin, B. Alexiev, 2019, Pathology, research and practice.

Worldwide Frequency of Commonly Detected EGFR Mutations.

D. Rimm, N. Lindeman, R. Graham, 2017, Archives of pathology & laboratory medicine.

Early mixed T‐cell chimerism is predictive of pediatric AML or MDS relapse after hematopoietic stem cell transplant

W. Tse, I. Helenowski, L. Jennings, 2017, Pediatric blood & cancer.

Liver Pathology and SARS-CoV-2 Detection in Formalin-Fixed Tissue of Patients With COVID-19

R. Nayar, J. Lomasney, A. Yeldandi, 2021, American journal of clinical pathology.

Neisseria Species Identification Assay for the Confirmation of Neisseria gonorrhoeae-Positive Results of the COBAS Amplicor PCR

K. Mangold, K. Kaul, L. Jennings, 2007, Journal of Clinical Microbiology.

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.

Rhona J. Souers, K. Tsuchiya, J. Bridge, 2018, Archives of pathology & laboratory medicine.

Neisseria Species Identification Assay for the Confirmation of Neisseria gonorrhoeae-Positive Results of the COBAS Amplicor PCR

K. Mangold, K. Kaul, L. Jennings, 2007, Journal of Clinical Microbiology.

Validation Study of a Direct Real-Time PCR Protocol for Detection of Monkeypox Virus

L. Jennings, E. Vormittag-Nocito, Michaela Chang, 2022, The Journal of Molecular Diagnostics.

Variable human phenotype associated with novel deletions of the PHOX2B gene

E. Berry-Kravis, Min Yu, D. Weese-Mayer, 2012, Pediatric pulmonology.

Morphologic and Immunophenotypic Differences in Juvenile Myelomonocytic Leukemias With CBL and Other Canonical RAS-pathway Gene Mutations: A Single Institutional Experience

L. Jennings, Shanxiang Zhang, R. Bhat, 2021, Journal of pediatric hematology/oncology.

Comprehensive evaluation of bronchoalveolar lavage from patients with severe COVID-19 and correlation with clinical outcomes

J. Chmiel, R. Wunderink, P. Ji, 2021, Human Pathology.

Comparison of PHOX2B Testing Methods in the Diagnosis of Congenital Central Hypoventilation Syndrome and Mosaic Carriers

E. Berry-Kravis, Min Yu, D. Weese-Mayer, 2010, Diagnostic molecular pathology : the American journal of surgical pathology, part B.

Paired-Like Homeobox Gene 2B (PHOX2B) and Congenital Central Hypoventilation Syndrome (CCHS): Genotype/Phenotype Correlation in Cohort of 347 Cases.

E. Berry-Kravis, Min Yu, D. Weese-Mayer, 2009, ATS 2009.

Congenital central hypoventilation syndrome: Severe disease caused by co‐occurrence of two PHOX2B variants inherited separately from asymptomatic family members

E. Berry-Kravis, Y. Sivan, Min Yu, 2019, American journal of medical genetics. Part A.

Methods-based proficiency testing in molecular genetic pathology.

Carolyn Sue Richards, Karl V Voelkerding, Nazneen Aziz, 2014, The Journal of molecular diagnostics : JMD.

Maternal vs Fetal Origin of Placental Intervillous Thrombi

J. Goldstein, E. Miller, L. Jennings, 2021, American journal of clinical pathology.

Germline mosaicism of PHOX2B mutation accounts for familial recurrence of congenital central hypoventilation syndrome (CCHS)

E. Berry-Kravis, Min Yu, D. Weese-Mayer, 2012, American journal of medical genetics. Part A.

Pilot Study of the Association of the DDAH2 −449G Polymorphism with Asymmetric Dimethylarginine and Hemodynamic Shock in Pediatric Sepsis

M. Wainwright, Min Yu, L. Jennings, 2012, PloS one.

Unique morphologic and genetic characteristics of acute myeloid leukemia with chromothripsis: a clinicopathologic study from a single institution.

J. Altman, Xinyan Lu, L. Jennings, 2020, Human pathology.

Variant allelic frequency of driver mutations predicts success of genomic DNA methylation classification in central nervous system tumors

M. Snuderl, C. Horbinski, L. Santana-Santos, 2023, Acta Neuropathologica.

Comparison 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

O. Frankfurt, J. Altman, M. Kocherginsky, 2021, Genes, chromosomes & cancer.

Paired-like homeobox gene (PHOX2B) nonpolyalanine repeat expansion mutations (NPARMs): genotype–phenotype correlation in congenital central hypoventilation syndrome (CCHS)

E. Berry-Kravis, K. Yap, V. Speare, 2021, Genetics in Medicine.

Clinical and histopathologic characterization of SETD2-mutated colorectal cancer.

Feng Yue, J. Liao, Guang-Yu Yang, 2022, Human pathology.

Markedly prolonged disease course, with breakthrough seizures, in a glioma with an isolated IDH1 mutation

C. Horbinski, L. Jennings, J. Templer, 2022, Neuro-oncology advances.

ROS1 alterations as a potential driver of gliomas in infant, pediatric, and adult patients.

D. Brat, C. Ida, C. Horbinski, 2023, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.