Professor of Pediatrics, Professor of Oncology, Johns Hopkins University School of Medicine

Pediatrics

Joann N. Bodurtha, MD practices Pediatrics. He graduated from Yale University School of Medicine. Yale University School of Medicine is a top medical college. Yale University School of Medicine is ranked 7/57 in Research/PrimaryCare. He received 1 awards: "Regional Top Doctor". Joann N. Bodurtha is a published physician. He has 101 publications published. The most current publication ""What's this going to cost, Doctor?"."

Publications

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• Family Ties: The Role of Family Context in Family Health History Communication About Cancer.
• What Women Think: Cancer Causal Attributions in a Diverse Sample of Women.
• The KinFact Intervention - A Randomized Controlled Trial to Increase Family Communication About Cancer History.
• AMEN in Challenging Conversations: Bridging the Gaps Between Faith, Hope, and Medicine.
• Horizontal integration of OMIM across the medical school preclinical curriculum for early reinforcement of clinical genetics principles.
• Youth with special health care needs: transition to adult health care services.
• Myoclonus-dystonia and Silver-Russell syndrome resulting from maternal uniparental disomy of chromosome 7.
• Talking (or Not) About Family Health History in Families of Latino Young Adults.
• Patient-reported hereditary breast and ovarian cancer in a primary care practice.
• Deletion 12p12 Involving SOX5 in Two Children With Developmental Delay and Dysmorphic Features.
• Intraventricular twin fetuses in fetu.
• The Impact of Co-Occurring Birth Defects on the Timing of Newborn Hearing Screening and Diagnosis.
• Comparing Screening and Preventive Health Behaviors in Two Study Populations: Daughters of Mothers with Breast Cancer and Women Responding to the Behavioral Risk Facto...
• Physicians' current practices and opportunities for DNA banking of dying patients with cancer.
• Genetic screening and DNA banking at the end of life #206.
• Genetic risk, perceived risk, and cancer worry in daughters of breast cancer patients.
• Evolution of an integrated public health surveillance system.
• Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations.
• Exploring hereditary cancer among dying cancer patients--a cross-sectional study of hereditary risk and perceived awareness of DNA testing and banking.
• A genetic perspective on infant mortality.
• GJA1 mutations, variants, and connexin 43 dysfunction as it relates to the oculodentodigital dysplasia phenotype.
• Duration of an intervention's impact on perceived breast cancer risk.
• Genetics assessment at the end of life: suggestions for implementation in clinic and future research.
• The effect of a school-based educational intervention on gender differences in reported family cancer history.
• Recruiting diverse patients to a breast cancer risk communication trial--waiting rooms can improve access.
• Underinsurance and key health outcomes for children with special health care needs.
• Spiritual coping, family history, and perceived risk for breast cancer--can we make sense of it?
• Defining underinsurance among children with special health care needs: a Virginia sample.
• II. Recent innovations in human genetics education: The curricularization of McKusick.
• Waardenburg syndrome type 3 (Klein-Waardenburg syndrome) segregating with a heterozygous deletion in the paired box domain of PAX3: a simple variant or a true syndrome?
• "What's this going to cost, Doctor?".
• Teaching efficacy of a medical education module on genetic testing for cancer.
• The effect of fetomaternal bleeding on the risk of adverse pregnancy outcome in patients with elevated second-trimester maternal serum alpha-fetoprotein levels.
• Brief clinical and laboratory observations.
• Ethical considerations in oncology: balancing the interests of patients, oncologists, and society.
• Pediatric care after snakebite: comfort from shared experience.
• Café au lait spots: the pediatrician's perspective.
• Report of another family with Simpson-Golabi-Behmel syndrome and a review of the literature.
• Development of the Virginia Congenital Anomalies Reporting and Education System (VaCARES): two pilot projects.
• Genetic and environmental contributions to cholesterol and its subfractions in 11-year-old twins. The Medical College of Virginia Twin Study.
• Univariate genetic analysis of blood pressure in children (the Medical College of Virginia Twin Study).
• Congenital central hypoventilation syndrome and Hirschsprung''s disease in half sibs.
• Human genetics education videoshare: Round One.
• Genetic analysis of anthropometric measures in 11-year-old twins: the Medical College of Virginia Twin Study.
• Lipoprotein and oxygen transport alterations in passive smoking preadolescent children. The MCV Twin Study.
• Seminoma in pubertal patient with androgen insensitivity syndrome.
• Affect of late-onset prenatal care on antenatal diagnosis.
• Case report: partial trisomy 20q (20q13.13----qter).
• High-density lipoprotein-cholesterol subfractions in adolescent twins.
• Updating McKusick: an educational exercise for medical students.
• In encephaloceles, autopsy holds key to genetic counseling: case reports.
• Distinctive gastrointestinal anomaly associated with Coffin-Siris syndrome.
• Arthritis, bleeding disorder and a chromosome marker--a family study.
• Aortic stiffness: a new Doppler echocardiographic measure predictive of systolic blood pressure in children.
• Goldenhar complex in discordant monozygotic twins: a case report and review of the literature.
• Nail size in normal infants. Establishing standards for healthy term infants.
• Report of the Task Force on Teaching Human Genetics in North American Medical Schools.
• Seroepidemiology of cytomegalovirus and herpes simplex virus in twins and their families.
• Femoral duplication: a case report.
• Human genetics teaching.
• Prenatal detection of non-cardiac rhabdomyosarcoma.
• Atelosteogenesis type III: a distinct skeletal dysplasia with features overlapping atelosteogenesis and oto-palato-digital syndrome type II.
• Evidence for a major gene in familial anencephaly.
• Ascertainment of families with hereditary deafness for linkage studies. Waardenburg and Usher syndromes.
• Monozygotic twins discordant for Ullrich-Turner syndrome.
• Innovations in human genetics education. Medical student elective in clinical genetics.
• Partial trisomy 19p: case report and natural history.
• Prospects, realities, and safety concerns of gene therapy.
• Prenatal genetic counseling: what is fragile X?
• DNA testing: diagnostic role in single gene conditions.
• Three methods of fetal sampling in prenatal diagnosis.
• Prenatal testing in the nineties.
• Progressive bilateral nasal alar collapse: a dominantly inherited trait.
• A doctor in purgatory. Etching with watercolor (1802) by George M. Woodward (1760-1809), London.
• The risk of neural tube defects to first cousins of affected individuals.
• Magdalen Hospital engraved by George Quinton, 1797, after a painting by T. S. Duché.
• Rhabdomyosarcoma complicating multiple neurofibromatosis.
• Coffin-Siris syndrome: review and presentation of new cases from a questionnaire study.
• A 17-month-old with extreme prenatal-onset growth delay. Microcephalic osteodysplastic primordial dwarfism type II.
• Fluorescence in situ hybridization detectable mosaicism for Angelman syndrome with biparental methylation.
• Validation of a multiplex methylation-sensitive PCR assay for the diagnosis of Prader-Willi and Angelman's syndromes.
• Counseling dilemmas in EEC syndrome.
• Overlap of dyskeratosis congenita with the Hoyeraal-Hreidarsson syndrome.
• Ophthalmo-acromelic syndrome: report and review.
• Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1.
• Further family with possible autosomal recessive inheritance of Adams-Oliver syndrome.
• PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome.
• Assessment of the newborn with dysmorphic features.
• Models for the longitudinal genetic analysis of same-age twins: application to HDL cholesterol.
• 46XY/47XYY mosaicism and fragile X.
• Acute myocarditis. Rapid diagnosis by PCR in children.
• Analysis of variability of clinical manifestations in Waardenburg syndrome.
• The density and distribution of intramembrane particles in erythrocytes from persons with muscular dystrophies.
• The bacteriologically battered baby: another case of Munchausen by proxy.
• Using premedical students in a community hospital summer volunteer program.
• Whole genomewide linkage screen for neural tube defects reveals regions of interest on chromosomes 7 and 10.
• Gail model risk assessment and risk perceptions.
• Increased risk of birth defects among children from multiple births.
• The link between providers and patients: how laboratories can ensure quality results with genetic testing.
• Autosomal dominant myocardial disease diagnosed by fetal presentation of proband with an aneurysm of the muscular interventricular septum.

Schools

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• Yale University School Of Medicine

• Chldns Hospital Of Philadelphia

• Med College Va

Doctors Specialties

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• Clinical Genetics
• Pediatrics

Accepted Insurances

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Awards

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• Regional Top Doctor

Education

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• Children's Hospital of Philadelphia
• Yale University School of Medicine

Hospital

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• Johns Hopkins Bayview Medical Center
• Johns Hopkins Hospital

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