Faculty

Institution

Unit

Venue

Joann Bodurtha

Professor of Genetic Medicine

Johns Hopkins University

Affiliations

School of Medicine

Genetic Medicine

Joann Bodurtha is currently serving as a Genetic Medicine Professor of Genetic Medicine at Johns Hopkins University.

Honors

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Experiences

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Education

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Joann Bodurtha

Johns Hopkins University

Professor of Genetic Medicine

You can click a keyword to filter the displayed items

genetics pediatrics medical genetics human genetics medicine health sciences genomics oncology child development genetic counseling population genetics genetic disorders breast cancer women's health molecular genetics cancer care neonatology family history child health genomic medicine genetic testing family health history genetic services respiratory medicine genome biology higher education cancer genetics cancer risk cancer treatment end-of-life care dna banking hereditary cancer palliative medicine gynecologic oncology obstetrics and gynaecology developmental genetics clinical genetics coffin-siris syndrome medical college women's studies child neurology counseling psychology heredity career development genetic predisposition obstetrics clinical medicine genetic analysis parental care cerebrovascular disease pediatric hematology health disparities health care disparities academic medicine congenital anomalies systematic review dysmorphic features medical students natural history human genetics education protein science reproductive medicine science advance thoracic oncology jama oncology mutagenesis gene evolution genotype-phenotype association disease gene identification medical diagnostics protein chemistry protein function investigative studies men's studies general internal medicine cowden syndrome

Notable Scholarly Works

Notable Federal Grants

Collaborators

P473: Minding the Gaps: Integrating Family History, Genomic Medicine, and Public Health in Pipeline Training and Community Engagement Since 2017. Genetics in Medicine Open (2026)

genomic medicinefamily medicineforensic geneticscommunity-engaged researchpublic health

P273: A Decade of Rapid Exome Sequencing at a Tertiary Care Center. Genetics in Medicine Open (2025)

gynecologymolecular diagnosticsproteome researchmolecular geneticsgynecologic cancersbioinformaticsfunctional genomicsoncogenesmolecular biologycancer discoverypathologygenome biologyhuman geneticsclinical proteomicsmolecular medicinegynecologic oncologyomics

Pathogenic Xpo1 Variants Cause a Dominant Neurodevelopmental Disorder. Genetics in Medicine (2025)

geneticsdevelopmental neurobiologyneurogeneticsneurodevelopmental disordersgenetic disordersmolecular neurodegenerationchild neurologypathogenic xpo1 variants

The 2023 Medical Genetics Workforce in the United States. Genetics in Medicine (2025)

geneticsgenomic medicinegenetic epidemiologyhereditymedical genetics workforcehuman geneticshealth sciencesgenetic counseling

Community-Driven Partnerships With Community-Engaged Research Teams Bring Resources and Reliable Information to Baltimore Residents. Journal of Clinical and Translational Science (2024)

Emily KumpfVeena ThamilselvanEthan WangPatricia BargerJanice GentryChevelle BashDonald YoungSamuel ByiringiroJoann BodurthaAntoinette BrownMinli GuoAudrey CarterLatrice PricePercy SmithCyd LacanientaCheryl HimmelfarbAlbert W Wu

community engagementcommunity-driven partnershipspublic healthcenr teamsreliable information

Craniofacial Cases: Congenital Hearing Loss. Elsevier eBooks (2024)

Daniah AlbokhariJessica OgawaJoann Bodurtha

developmental biologycraniofacial caseshearing losscongenital hearing losscraniofacial disorders

Craniofacial Cases: Hearing Loss and Night Blindness in a Teenager. Elsevier eBooks (2024)

Jessica OgawaDaniah AlbokhariJoann Bodurtha

night blindnesscraniofacial casesgeneticshearing lossneuroscienceophthalmology

Craniofacial Cases: Hearing Loss and Renal Agenesis. Elsevier eBooks (2024)

Daniah AlbokhariJessica OgawaJoann Bodurtha

craniofacial caseshearing losscraniofacial researchneuroscienceophthalmologyrenal agenesisneurology

Newborn Screening Cases: Abnormal Newborn Hearing Screening. Elsevier eBooks (2024)

Jessica OgawaDaniah AlbokhariJoann Bodurtha

neonatologypediatrics

P499: Us Genetics Professional Workforce in 2023. Genetics in Medicine Open (2024)

Megan LyonDeborah MaieseRhonda WestMarci SontagVivian PanCinthya Zepeda MendozaJoann Bodurtha

professional workforcegeneticsworkforce development

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Joann Bodurtha

Professor of Genetic Medicine

Johns Hopkins University

Affiliations

School of Medicine

Genetic Medicine

Joann Bodurtha is currently serving as a Genetic Medicine Professor of Genetic Medicine at Johns Hopkins 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

Joann Bodurtha

Johns Hopkins University

Professor of Genetic Medicine

You can click a keyword to filter the displayed items

Notable Scholarly Works

Notable Federal Grants

Collaborators

P473: Minding the Gaps: Integrating Family History, Genomic Medicine, and Public Health in Pipeline Training and Community Engagement Since 2017. Genetics in Medicine Open (2026)

genomic medicinefamily medicineforensic geneticscommunity-engaged researchpublic health

P273: A Decade of Rapid Exome Sequencing at a Tertiary Care Center. Genetics in Medicine Open (2025)

Pathogenic Xpo1 Variants Cause a Dominant Neurodevelopmental Disorder. Genetics in Medicine (2025)

geneticsdevelopmental neurobiologyneurogeneticsneurodevelopmental disordersgenetic disordersmolecular neurodegenerationchild neurologypathogenic xpo1 variants

The 2023 Medical Genetics Workforce in the United States. Genetics in Medicine (2025)

geneticsgenomic medicinegenetic epidemiologyhereditymedical genetics workforcehuman geneticshealth sciencesgenetic counseling

Community-Driven Partnerships With Community-Engaged Research Teams Bring Resources and Reliable Information to Baltimore Residents. Journal of Clinical and Translational Science (2024)

community engagementcommunity-driven partnershipspublic healthcenr teamsreliable information

Craniofacial Cases: Congenital Hearing Loss. Elsevier eBooks (2024)

Daniah AlbokhariJessica OgawaJoann Bodurtha

developmental biologycraniofacial caseshearing losscongenital hearing losscraniofacial disorders

Craniofacial Cases: Hearing Loss and Night Blindness in a Teenager. Elsevier eBooks (2024)

Jessica OgawaDaniah AlbokhariJoann Bodurtha

night blindnesscraniofacial casesgeneticshearing lossneuroscienceophthalmology

Craniofacial Cases: Hearing Loss and Renal Agenesis. Elsevier eBooks (2024)

Daniah AlbokhariJessica OgawaJoann Bodurtha

craniofacial caseshearing losscraniofacial researchneuroscienceophthalmologyrenal agenesisneurology

Newborn Screening Cases: Abnormal Newborn Hearing Screening. Elsevier eBooks (2024)

Jessica OgawaDaniah AlbokhariJoann Bodurtha

neonatologypediatrics

P499: Us Genetics Professional Workforce in 2023. Genetics in Medicine Open (2024)

Megan LyonDeborah MaieseRhonda WestMarci SontagVivian PanCinthya Zepeda MendozaJoann Bodurtha

professional workforcegeneticsworkforce development

1
2
3
4
5
21
10 / page