Faculty

Institution

Unit

Venue

Louise C. Strong

The University of Texas MD Anderson Cancer Center

Affiliations

Department Of Breast Surgical Oncology

Division Of Cancer Medicine

Department Of Thoracic-Head And Neck Medical Oncology

Division Of Cancer Medicine

The University of Texas MD Anderson Cancer Center

NoneLouise C. Strong is currently serving as a Breast Surgical Oncology faculty at The University of Texas Md Anderson Cancer Center.

Honors

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Experiences

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Education

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Louise C. Strong

The University of Texas MD Anderson Cancer Center

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genetics oncology cancer research cancer genetics pathology human genetics tumor biology medical genetics oncogenes genomics carcinogenesis molecular biology cancer genomics cancer risk cancer biology li-fraumeni syndrome radiation oncology molecular genetics genome biology genetic disorders molecular cancer genetic epidemiology cytogenetics molecular diagnostics cancer care cancer discovery disease gene identification cancer cells heredity malignant disease histopathology chromosome biology childhood cancer medicinal research cancer letter leukemia nucleic acids hematological malignancies molecular pathology colorectal cancer forensic genetics molecular cell biology radiation therapy cancer treatment cancer prevention mendelian disorder cancer imaging radiation biology genetic predisposition tumor suppressors variant interpretation genetic testing mutagenesis linkage analysis somatic variant genome analysis human polymorphisms clinical radiation oncology long-term survivors genetic susceptibility adolescent cancer wilms tumor familial wilms genomic medicine lymphoid neoplasia cancer growth pediatric surgery childhood sarcoma segregation analysis joint effects familial predisposition genomic instability parental origin genetic heterogeneity secondary germline findings familial syndrome

Notable Scholarly Works

Notable Federal Grants

Collaborators

Ccr Translation for This Article From Telomere Content and Risk of Second Malignant Neoplasm in Survivors of Childhood Cancer: A Report From the Childhood Cancer Survivor Study. (2023)

Maria M. GramatgesQi LiuYutaka YasuiM. Fatih OkcuJoseph P. NegliaLouise C. StrongGregory T. ArmstrongLeslie L. RobisonSmita Bhatia

pediatricschildhood cancertelomere contentccr translationradiologysecond malignant neoplasmoncologygenetics

Data From Common Familial Colorectal Cancer Linked to Chromosome 7Q31: A Genome-Wide Analysis. (2023)

Deborah W. NeklasonRichard A. KerberDavid B. NilsonHoda Anton-CulverAnn G. SchwartzConstance A. GriffinJan T. LoweryJoellen M. SchildkrautJames P. EvansGail E. TomlinsonLouise C. StrongAlexander R. MillerJill E. StopferDianne M. FinkelsteinPrakash M. NadkarniCarol H. KastenGeraldine P. MineauRandall W. Burt

cytogeneticscolorectal cancergenome-wide analysisgenomicscancer geneticsdata sciencemedical geneticsgenetics

Data From Estimating I Tp53 /I Mutation Carrier Probability in Families With LI–Fraumeni Syndrome Using Lfspro. (2023)

biostatisticsgenetic disordersmendelian disordermutagenesis (molecular biology technique)disease gene identificationmolecular geneticsmolecular diagnosticshereditymutation carrier probabilityhuman geneticsgenetic epidemiologystatistical geneticsgenetics

Data From Penetrance Estimates Over Time to First and Second Primary Cancer Diagnosis in Families With LI-Fraumeni Syndrome: A Single Institution Perspective. (2023)

pathologypenetrance estimatesdiagnosisli-fraumeni syndromesingle institution perspectiveanatomical pathologyfamily medicine

Supplementary Figure 1 From Common Familial Colorectal Cancer Linked to Chromosome 7Q31: A Genome-Wide Analysis. (2023)

cytogeneticscolorectal cancergenome-wide analysisgenomicscancer geneticsgenetics

Supplementary Figure 2 From Telomere Content and Risk of Second Malignant Neoplasm in Survivors of Childhood Cancer: A Report From the Childhood Cancer Survivor Study. (2023)

Maria M. GramatgesQi LiuYutaka YasuiM. Fatih OkcuJoseph P. NegliaLouise C. StrongGregory T. ArmstrongLeslie L. RobisonSmita Bhatia

childhood cancercancer risktelomere contentsecond malignant neoplasm

Supplementary Figures From Recommended Guidelines for Validation, Quality Control, and Reporting of Tp53 Variants in Clinical Practice. (2023)

Bernard LeroyMandy L. BallingerFanny Baran-MarszakGareth L. BondAntony BraithwaiteNicole ConcinLawrence A. DonehowerWafik S. El-DeiryPierre FenauxGianluca GaidanoAnita LangerødEva Hellstrom-LindbergRichard IggoJacqueline Lehmann-ChePhuong L. MaiDavid MalkinUte M. MollJeffrey N. MyersKim E. NicholsSarka PospisilovaPatricia Ashton-ProllaDavide RossiSharon A. SavageLouise C. StrongPatricia N. ToninRobert ZeillingerThorsten ZenzJoseph F. FraumeniPeter E.M. TaschnerPierre HainautThierry Soussi

allelic variantvariant interpretationclinical practicemedicinegeneticsclinical researchsupplementary figuresgenetic variation

Abstract Ps8-04: Clinical and Pathological Characteristics and Screening Outcome for Secondary Cancers in Breast Cancer Patients With LI-Fraumeni Syndrome Attending the MD Anderson LI-Fraumeni Education and Early Detection Program Clinic. Cancer Research (2021)

breast oncologyabstract ps8-04pathologyradiation oncologycancer screeningdiagnosissurgical pathologybreast cancer patientscancer researchcancer riskcancer detectionsecondary cancerscancer careoncologybreast cancer

A Pedigree-Based Prediction Model Identifies Carriers of Deleterious De Novo Mutations in Families With LI-Fraumeni Syndrome. Genome Research (2020)

Fan GaoXuedong PanElissa B. Dodd-EatonCarlos Vera RecioMatthew D. MontierthJasmina BojadzievaPhuong L. MaiKristin ZelleyValen E. JohnsonDanielle BraunKim E. NicholsJudy E. GarberSharon A. SavageLouise C. StrongWenyi Wang

gene expressiongenome analysistumor biologygenomicsgenome biologypopulation genomicsdisease gene identificationmolecular geneticspedigree-based prediction modelcancer geneticsli-fraumeni syndromemolecular biologypopulation geneticsmedical geneticsgenetics

Clinically Relevant Changes in Family History of Cancer Over Time. UNC Libraries (2020)

pathologyfamily historycarcinogenesiscancer researchcancer discoverycancer riskepidemiology of cancercancer managementfamily medicinecancer geneticscancer careoncology

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Louise C. Strong

The University of Texas MD Anderson Cancer Center

Affiliations

Department Of Breast Surgical Oncology

Division Of Cancer Medicine

Department Of Thoracic-Head And Neck Medical Oncology

Division Of Cancer Medicine

The University of Texas MD Anderson Cancer Center

NoneLouise C. Strong is currently serving as a Breast Surgical Oncology faculty at The University of Texas Md Anderson Cancer Center.

Honors

Create free account to unlock more features

Experiences

Create free account to unlock more features

Education

Create free account to unlock more features

Louise C. Strong

The University of Texas MD Anderson Cancer Center

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

Ccr Translation for This Article From Telomere Content and Risk of Second Malignant Neoplasm in Survivors of Childhood Cancer: A Report From the Childhood Cancer Survivor Study. (2023)

Maria M. GramatgesQi LiuYutaka YasuiM. Fatih OkcuJoseph P. NegliaLouise C. StrongGregory T. ArmstrongLeslie L. RobisonSmita Bhatia

pediatricschildhood cancertelomere contentccr translationradiologysecond malignant neoplasmoncologygenetics

Data From Common Familial Colorectal Cancer Linked to Chromosome 7Q31: A Genome-Wide Analysis. (2023)

cytogeneticscolorectal cancergenome-wide analysisgenomicscancer geneticsdata sciencemedical geneticsgenetics

Data From Estimating I Tp53 /I Mutation Carrier Probability in Families With LI–Fraumeni Syndrome Using Lfspro. (2023)

Data From Penetrance Estimates Over Time to First and Second Primary Cancer Diagnosis in Families With LI-Fraumeni Syndrome: A Single Institution Perspective. (2023)

pathologypenetrance estimatesdiagnosisli-fraumeni syndromesingle institution perspectiveanatomical pathologyfamily medicine

Supplementary Figure 1 From Common Familial Colorectal Cancer Linked to Chromosome 7Q31: A Genome-Wide Analysis. (2023)

cytogeneticscolorectal cancergenome-wide analysisgenomicscancer geneticsgenetics

Supplementary Figure 2 From Telomere Content and Risk of Second Malignant Neoplasm in Survivors of Childhood Cancer: A Report From the Childhood Cancer Survivor Study. (2023)

Maria M. GramatgesQi LiuYutaka YasuiM. Fatih OkcuJoseph P. NegliaLouise C. StrongGregory T. ArmstrongLeslie L. RobisonSmita Bhatia

childhood cancercancer risktelomere contentsecond malignant neoplasm

Supplementary Figures From Recommended Guidelines for Validation, Quality Control, and Reporting of Tp53 Variants in Clinical Practice. (2023)

allelic variantvariant interpretationclinical practicemedicinegeneticsclinical researchsupplementary figuresgenetic variation

A Pedigree-Based Prediction Model Identifies Carriers of Deleterious De Novo Mutations in Families With LI-Fraumeni Syndrome. Genome Research (2020)

Clinically Relevant Changes in Family History of Cancer Over Time. UNC Libraries (2020)

pathologyfamily historycarcinogenesiscancer researchcancer discoverycancer riskepidemiology of cancercancer managementfamily medicinecancer geneticscancer careoncology

1
2
3
4
5
21
10 / page