Associate Professor, Pathology-Brigham and Women's Hospital, Harvard Medical School
Medical Genetics
Dr. Frederick R. Bieber, PHD
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Frederick Bieber is an expert in the field of Medical Genetics. Frederick R. Bieber, PHD is a published doctor. He has 56 papers published. The most current publication "Twins, placentas, and genetics: acardiac twinning in a dichorionic, diamniotic, monozygotic twin gestation."
Publications
- Reporting of diagnostic cytogenetic results.
- Turning base hits into earned runs: improving the effectiveness of forensic DNA data bank programs.
- Human genetics. Finding criminals through DNA of their relatives.
- Epidemiology. DNA identifications after the 9/11 World Trade Center attack.
- Forensic applications of laser capture microdissection: use in DNA-based parentage testing and platform validation.
- Forensic aspects of mass disasters: strategic considerations for DNA-based human identification.
- Guilt by association: should the law be able to use one person''s DNA to carry out surveillance on their family? Not without a public debate.
- Interpretation of complex forensic DNA mixtures.
- Manual methods for PCR-based forensic DNA analysis.
- RFLP analysis of forensic DNA samples with single-locus VNTR genetic markers.
- Isolation of DNA from forensic evidence.
- Collecting and handling samples for parentage and forensics DNA-based genetic testing.
- Overview of human identity testing and forensic genetics.
- Fluorescence in situ hybridization (FISH) for rapid detection of aneuploidy: experience in 911 prenatal cases.
- Detection of mosaicism in amniotic fluid cultures: a CYTO2000 collaborative study.
- Twins, placentas, and genetics: acardiac twinning in a dichorionic, diamniotic, monozygotic twin gestation.
- Mapping and characterization of a novel cochlear gene in human and in mouse: a positional candidate gene for a deafness disorder, DFNA9.
- An ancient conserved gene expressed in the human inner ear: identification, expression analysis, and chromosomal mapping of human and mouse antiquitin (ATQ1).
- Epidemiology of osteochondrodysplasias: changing trends due to advances in prenatal diagnosis.
- Massive chronic intervillositis associated with recurrent abortions.
- GNAZ in human fetal cochlea: expression, localization, and potential role in inner ear function.
- Fetoplacental histology as a predictor of karyotype: a controlled study of spontaneous first trimester abortions.
- Expression of the Kallmann syndrome gene in human fetal brain and in the manipulated chick embryo.
- Isolation of novel and known genes from a human fetal cochlear cDNA library using subtractive hybridization and differential screening.
- X-linked phenotype of absent radius and anogenital anomalies.
- Prenatal sonography in trisomy 9.
- Etiologic complexities of diaphragmatic defects: right diaphragmatic hernia, pulmonary hypoplasia/agenesis, and hydrocephalus in sibs.
- Complexities of limb anomalies: the lower extremity in the "prune belly" phenotype.
- Homologous ribosomal protein genes on the human X and Y chromosomes: escape from X inactivation and possible implications for Turner syndrome.
- Duchenne and Becker muscular dystrophies: genetics, prenatal diagnosis, and future prospects.
- Diagnosis and management of infantile marfan syndrome.
- Dystrophin analysis in duchenne muscular dystrophy: use in fetal diagnosis and in genetic counseling.
- The biology of tetraploid hydatidiform moles: histopathology, cytogenetics, and flow cytometry.
- Doppler demonstration of reversed umbilical blood flow in an acardiac twin.
- Incidence of spontaneous abortion among normal women and insulin-dependent diabetic women whose pregnancies were identified within 21 days of conception.
- Lack of relation of increased malformation rates in infants of diabetic mothers to glycemic control during organogenesis.
- Questionable role of amniocentesis in the etiology of amniotic band formation. A case report.
- Stimulation of human hematopoietic colony formation by recombinant gibbon multi-colony-stimulating factor or interleukin 3.
- Transposition of the external genitalia associated with caudal regression.
- Normal cellular counterparts of B cell chronic lymphocytic leukemia.
- Transient cysts of the fetal choroid plexus: morphology and histogenesis.
- Cutaneous and visceral hemangiomata in the Klippel-Trenaunay-Weber syndrome: antenatal sonographic detection.
- Heterotopic cervical salivary gland tissue in a family with probable branchio-otorenal syndrome.
- Pathologic findings in fetal GM1 gangliosidosis.
- Sonographic findings in otocephaly (synotia).
- Ocular findings in a new heritable syndrome of brain, eye, and urogenital abnormalities.
- Amniotic band sequence associated with ectopia cordis in one twin.
- The fetal face: ultrasound examination.
- Achondrogenesis type I: ultrasound diagnosis in utero.
- Sonographic and radiologic findings in campomelic dysplasia.
- Genetic studies of an acardiac monster: evidence of polar body twinning in man.
- Comments on "a Turner-like phenotype in the aborted fetus".
- Neural tube defects in two offspring of an affected female.
- Prenatal detection of a familial nuchal bleb simulating encephalocele.
- Ethical problems of screening for neural-tube defects.
Doctors Specialties
- Clinical Cytogenetics
- Clinical Molecular Genetics
- Medical Genetics
Accepted Insurances
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