Faculty

Institution

Unit

Venue

Scott Smith

Associate Professor

Upstate Medical University

Affiliations

Norton College of Medicine

Department Of Anesthesiology

Department Of Pathology, Anatomical Pathology

Department Of Anesthesiology

Norton College Of Medicine

Upstate Medical University

Scott Smith is currently serving as an Anesthesiology Associate Professor at Upstate Medical University.

Honors

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Experiences

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Education

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Scott Smith

Upstate Medical University

Associate Professor

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genetics pathology cancer research genetic disorders molecular diagnostics histopathology hematology oncology medical genetics cytogenetics neurogenetics cancer genetics molecular pathology neuro-oncology brain tumor research leukemia infectious diseases urology protein science mammalian biology tumoral pathology mendelian disorder multiple myeloma osteoporosis regenerative medicine clinical research clinical investigation clinical chemistry bone research laboratory medicine stem cell research liver physiology redox biology biomedical informatics surgical oncology nucleic acids clinical physiology tumor heterogeneity tumor innervation mitochondrial function cellular neurobiology molecular neurobiology gene regulation gene function viral diagnostics cell culture tissue culture somatic variant mutation-based testing hematological malignancies chromosomal rearrangements rna biology transcription regulation pediatric hematology myeloid neoplasia immunomodulation endocrine research disease gene identification developmental anomalies cohort studies genitourinary cancers bone mineral balance genetic profiling who classification paediatric cns tumours high-risk cytogenetics cholesterol biosynthesis genes genomic targets rt-qpcr diagnostic assays single institution methods database 15-year database clinical validation somatic mutation detection rare translocation molecular review

Notable Scholarly Works

Notable Federal Grants

Collaborators

Clinical Manifestations of Chromosome 19P13.11 Duplication. Journal of Medical Genetics (2026)

molecular diagnosticsgeneticsmolecular geneticshistopathologyanatomical pathologycytogeneticssurgical pathologyneurogeneticsgenetic disorderschromosome 19p13.11human geneticsmendelian disorderpathology

56. Clonal 6P Loss of Heterozygosity in Hematolymphoid Neoplasms as the Sole Finding at Diagnosis. Cancer Genetics (2025)

hematologymolecular diagnosticsgeneticssole findinghistopathologyanatomical pathologylaboratory hematologyhematolymphoid neoplasmsclonal 6pmolecular pathologypathology

An Incidental Finding of Gain of a Diminished Chromosome 12 Centromere in an Individual With Lymphocytosis: A Case Report and Clinical Implications in Cytogenetic Testing. Diagnostics (2025)

hematologycytogenetic testingcell divisionchromosome biologyleukemiacytogeneticscase reportdiminished chromosome 12pathology

Germline and Somatic Changes Associated With the Development of Inherited and De Novo Pediatric Acute Myeloid Leukemia. Genes (2025)

developmental biologyhematologygeneticssomatic changes associatedleukemiapediatric hematologyhuman geneticscarcinogenesismyeloid neoplasia

Neurodevelopmental Delay, Musculoskeletal Disorders and Dysmorphia Associated With a Novel Pathogenic Interstitial Deletion of Chromosome 10Q21.1Q21.3. Journal of Medical Genetics (2025)

Dibyendu DuttaJennifer BlackEmily A MontoyaThomas Andrew BurrowJoseph ShiehBobbi McGivernMichelle RaymondChristina B SheedyScott C. SmithRia Garg

musculoskeletal disordersgeneticsneurodevelopmental delaymedical genetics

P469: Complex Mosaicism for Up to Three Marker Chromosomes Causing Partial Trisomy for Portions of 1P and 10P-10Q: A Case. Genetics in Medicine Open (2025)

genetic recombinationgeneticsmolecular geneticschromosome biologyhereditycytogeneticscomplex mosaicismmarker chromosomesgenetic disordersgenome biologyhuman geneticspartial trisomypathology

Proximal Deletions of 14Q32.2 Result in Severe Neurodevelopmental Outcomes, Congenital Anomalies, and Dysmorphic Features. American Journal of Medical Genetics Part A (2025)

geneticsneuropathologysevere neurodevelopmental outcomesdevelopmental neurobiologyhuman geneticsdisease gene identificationdevelopmental anomaliesdysmorphic featuresneuroscienceproximal deletionsneurogeneticsneurodevelopmental disordersgenetic disorderschild neurologyneurologymendelian disorder

14. Ethnic and Molecular Disparities in Prostate Adenocarcinoma Incidence: Data From 19 Cohort Studies. Cancer Genetics (2024)

Amy BradyLisa C. SmithScott C. Smith

urologygeneticscancer researchgenetic epidemiologymolecular cancercohort studiesmolecular disparitiesgenitourinary cancerscancer disparitiesethnicityprostate cancerdisparitiesprostate adenocarcinoma incidenceepidemiology of cancercancer geneticsepidemiology

P468: 22q11ds With Maternal Mosaic Nonoverlapping Isodicentric 22Q11 Duplication. Genetics in Medicine Open (2024)

Zachary SpahrJennifer BlackScott SmithRobert Lebel

geneticsmedicinegenomic medicinematernal mosaicmedical geneticsgenetic disordersgenetic variation

Integrated Genetic Profiling of Archival Pediatric High-Grade Glial Tumors and Reassessment With 2021 Who Classification of Paediatric Cns Tumours. Cancer Genetics (2023)

tumor heterogeneitymolecular diagnosticsgeneticscancer researchoncologyhistopathologyneuro-oncologytumoral pathologygenetic profilingwho classificationneurogeneticspaediatric cns tumoursbrain tumor researchtumor innervationgliomaspathology

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Scott Smith

Associate Professor

Upstate Medical University

Affiliations

Norton College of Medicine

Department Of Anesthesiology

Department Of Pathology, Anatomical Pathology

Department Of Anesthesiology

Norton College Of Medicine

Upstate Medical University

Scott Smith is currently serving as an Anesthesiology Associate Professor at Upstate Medical University.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Scott Smith

Upstate Medical University

Associate Professor

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Clinical Manifestations of Chromosome 19P13.11 Duplication. Journal of Medical Genetics (2026)

56. Clonal 6P Loss of Heterozygosity in Hematolymphoid Neoplasms as the Sole Finding at Diagnosis. Cancer Genetics (2025)

hematologymolecular diagnosticsgeneticssole findinghistopathologyanatomical pathologylaboratory hematologyhematolymphoid neoplasmsclonal 6pmolecular pathologypathology

An Incidental Finding of Gain of a Diminished Chromosome 12 Centromere in an Individual With Lymphocytosis: A Case Report and Clinical Implications in Cytogenetic Testing. Diagnostics (2025)

hematologycytogenetic testingcell divisionchromosome biologyleukemiacytogeneticscase reportdiminished chromosome 12pathology

Germline and Somatic Changes Associated With the Development of Inherited and De Novo Pediatric Acute Myeloid Leukemia. Genes (2025)

developmental biologyhematologygeneticssomatic changes associatedleukemiapediatric hematologyhuman geneticscarcinogenesismyeloid neoplasia

Neurodevelopmental Delay, Musculoskeletal Disorders and Dysmorphia Associated With a Novel Pathogenic Interstitial Deletion of Chromosome 10Q21.1Q21.3. Journal of Medical Genetics (2025)

Dibyendu DuttaJennifer BlackEmily A MontoyaThomas Andrew BurrowJoseph ShiehBobbi McGivernMichelle RaymondChristina B SheedyScott C. SmithRia Garg

musculoskeletal disordersgeneticsneurodevelopmental delaymedical genetics

P469: Complex Mosaicism for Up to Three Marker Chromosomes Causing Partial Trisomy for Portions of 1P and 10P-10Q: A Case. Genetics in Medicine Open (2025)

genetic recombinationgeneticsmolecular geneticschromosome biologyhereditycytogeneticscomplex mosaicismmarker chromosomesgenetic disordersgenome biologyhuman geneticspartial trisomypathology

Proximal Deletions of 14Q32.2 Result in Severe Neurodevelopmental Outcomes, Congenital Anomalies, and Dysmorphic Features. American Journal of Medical Genetics Part A (2025)

14. Ethnic and Molecular Disparities in Prostate Adenocarcinoma Incidence: Data From 19 Cohort Studies. Cancer Genetics (2024)

Amy BradyLisa C. SmithScott C. Smith

P468: 22q11ds With Maternal Mosaic Nonoverlapping Isodicentric 22Q11 Duplication. Genetics in Medicine Open (2024)

Zachary SpahrJennifer BlackScott SmithRobert Lebel

geneticsmedicinegenomic medicinematernal mosaicmedical geneticsgenetic disordersgenetic variation

Integrated Genetic Profiling of Archival Pediatric High-Grade Glial Tumors and Reassessment With 2021 Who Classification of Paediatric Cns Tumours. Cancer Genetics (2023)

1
2
3
10 / page