Faculty

Institution

Unit

Venue

Lina Shao

University of Michigan

Affiliations

Michigan Medical School

Pathology

NoneLina Shao is currently serving as a Michigan Medical School faculty at University of Michigan.

Honors

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Experiences

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Education

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Lina Shao

University of Michigan

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genetics oncology cancer genetics genomics pathology medical genetics cancer research molecular diagnostics hematology cancer biology cancer genomics tumor biology medicine neurology oncogenes lymphoid neoplasia leukemia cytogenetics histopathology genome biology clinical pathology gliomas surgical pathology myeloid neoplasia neoplastic disorders cancer care brain tumor research cancer imaging genetic disorders hematological malignancies mixed-phenotype acute leukemia technical laboratory standards myelodysplastic syndrome pediatric brain tumors neuropathology sarcoma surgical oncology mammalian biology medicinal research genome analysis genitourinary cancers human pathology medical diagnostics molecular pathology cancer treatment copy-neutral loss clinicopathologic study cytogenomic studies vascular biology cardiovascular research respiratory medicine cardiovascular surgery variant interpretation biomedical research angiology structural heart disease valve disease clinical medicine biomarker discovery cancer risk human polymorphisms disease gene identification multilevel fusion experimental neuropathology x-ray fluorescence clinical therapeutics germ cells systematic morphologic analysis mitf translocations renal cell carcinomas tfeb fish assays copy-number abnormalities joint consensus recommendation differentiation defect bicuspid aortic valves chromosomal microarray analysis

Notable Scholarly Works

Notable Federal Grants

Collaborators

Genetic Profile, Treatment Response, and Outcomes of Bcr:: Abl1-Positive Mixed-Phenotype Acute Leukemia: A Study From the Bcr:: Abl1 Pathology Group. Modern Pathology (2026)

hematological malignanciesmedicineleukemiahematologycancer researchgeneticsmolecular diagnosticsoncologymixed-phenotype acute leukemiaoncogenespathologyhuman genetics

Hi-C for Genome-Wide Detection of Enhancer-Hijacking Rearrangements in Routine Lymphoid Cancer Biopsies. Cell Genomics (2026)

genome biologygenome editinggeneticscancer genomicsmolecular diagnostics

Optical Genome Mapping Reveals a Recurrent Translocation, T(14;16), in T/Myeloid Mixed Phenotype Acute Leukemia: Report of Two Cases. Molecular Cytogenetics (2026)

leukemiamyeloid neoplasiageneticsmolecular diagnosticsmolecular geneticsmixed-phenotype acute leukemiahuman genetics

P567: Evaluating Dosage Sensitivity Predictors for Clinical Copy Number Variant Classification*. Genetics in Medicine Open (2026)

medicinepharmacogenomicsgeneticsmolecular diagnosticsgenetic epidemiologyhuman genetics

P684: Resolving Genetic Architecture of Complex Supernumerary Marker Chromosomes With Complementary Cytogenomic Methodologies. Genetics in Medicine Open (2026)

genomicsgenome biologygeneticsmolecular geneticsmedical genetics

33. Assessing the Efficacy of Additional Cell Analysis in Detecting Low-Level Constitutional Mosaic Karyotypes. Cancer Genetics (2025)

cancer geneticsgeneticsgenetic analysismolecular diagnosticsoncologytumor heterogeneity

817 Clinical Utility of an Erg Fluorescent in Situ Hybridization (Fish) Assay: Practical Use and Lessons From an 8-Year Tertiary Institution Experience. Laboratory Investigation (2025)

laboratory investigationlaboratory medicineclinical laboratoryfluorescencemedical diagnosticspathology

9: Near Haploidization is Recurrent in Central Nervous System Tumors, Not Exclusive to Giant Cell Glioblastomas. Genetics in Medicine Open (2025)

neurologycarcinogenesisgliomasneurogeneticsbrain tumor researchependymamolecular neurodegenerationneuro-oncologyoncogenestumor heterogeneitypathologytumor biology

A Novel Glcci1:: Braf Fusion With Independent Myc and Mycn Amplifications in Pediatric Pancreatic Acinar Cell Carcinoma. Pediatric and Developmental Pathology (2025)

carcinogenesiscancer geneticspancreatic cancermolecular cancermalignant diseasemolecular diagnosticsmolecular biologyoncogenic agentoncogenescancer biologypathologytumor biologycell biology

Clinical Erg Break-Apart Fluorescence in Situ Hybridization Assay: Practical Utility and Lessons From an 8-Year Tertiary Institution Experience. American Journal of Clinical Pathology (2025)

laboratory medicineimmunocytochemical techniquesclinical laboratorycancer researchhistopathologymolecular diagnosticsfluorescencepathology

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Lina Shao

University of Michigan

Affiliations

Michigan Medical School

Pathology

NoneLina Shao is currently serving as a Michigan Medical School faculty at University of Michigan.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Lina Shao

University of Michigan

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Genetic Profile, Treatment Response, and Outcomes of Bcr:: Abl1-Positive Mixed-Phenotype Acute Leukemia: A Study From the Bcr:: Abl1 Pathology Group. Modern Pathology (2026)

hematological malignanciesmedicineleukemiahematologycancer researchgeneticsmolecular diagnosticsoncologymixed-phenotype acute leukemiaoncogenespathologyhuman genetics

Hi-C for Genome-Wide Detection of Enhancer-Hijacking Rearrangements in Routine Lymphoid Cancer Biopsies. Cell Genomics (2026)

genome biologygenome editinggeneticscancer genomicsmolecular diagnostics

Optical Genome Mapping Reveals a Recurrent Translocation, T(14;16), in T/Myeloid Mixed Phenotype Acute Leukemia: Report of Two Cases. Molecular Cytogenetics (2026)

leukemiamyeloid neoplasiageneticsmolecular diagnosticsmolecular geneticsmixed-phenotype acute leukemiahuman genetics

P567: Evaluating Dosage Sensitivity Predictors for Clinical Copy Number Variant Classification*. Genetics in Medicine Open (2026)

medicinepharmacogenomicsgeneticsmolecular diagnosticsgenetic epidemiologyhuman genetics

P684: Resolving Genetic Architecture of Complex Supernumerary Marker Chromosomes With Complementary Cytogenomic Methodologies. Genetics in Medicine Open (2026)

genomicsgenome biologygeneticsmolecular geneticsmedical genetics

33. Assessing the Efficacy of Additional Cell Analysis in Detecting Low-Level Constitutional Mosaic Karyotypes. Cancer Genetics (2025)

cancer geneticsgeneticsgenetic analysismolecular diagnosticsoncologytumor heterogeneity

817 Clinical Utility of an Erg Fluorescent in Situ Hybridization (Fish) Assay: Practical Use and Lessons From an 8-Year Tertiary Institution Experience. Laboratory Investigation (2025)

laboratory investigationlaboratory medicineclinical laboratoryfluorescencemedical diagnosticspathology

9: Near Haploidization is Recurrent in Central Nervous System Tumors, Not Exclusive to Giant Cell Glioblastomas. Genetics in Medicine Open (2025)

neurologycarcinogenesisgliomasneurogeneticsbrain tumor researchependymamolecular neurodegenerationneuro-oncologyoncogenestumor heterogeneitypathologytumor biology

A Novel Glcci1:: Braf Fusion With Independent Myc and Mycn Amplifications in Pediatric Pancreatic Acinar Cell Carcinoma. Pediatric and Developmental Pathology (2025)

carcinogenesiscancer geneticspancreatic cancermolecular cancermalignant diseasemolecular diagnosticsmolecular biologyoncogenic agentoncogenescancer biologypathologytumor biologycell biology

Clinical Erg Break-Apart Fluorescence in Situ Hybridization Assay: Practical Utility and Lessons From an 8-Year Tertiary Institution Experience. American Journal of Clinical Pathology (2025)

laboratory medicineimmunocytochemical techniquesclinical laboratorycancer researchhistopathologymolecular diagnosticsfluorescencepathology

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urology

prostate cancer

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Johns Hopkins University

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fanconi anemia

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