Professor and Chair
Obstetrics & Gynecology
Dr. William A. Hogge, MD
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William A. Hogge works in the field of Obstetrics & Gynecology. He researched medicine at University of Virginia School of Medicine. William Hogge has written publications. He has 74 publications published with PubMed. The lastest publication is: 'The use of interphase FISH for prenatal diagnosis of Pallister-Killian syndrome.'
Publications
- Cell-free nucleic acids as non-invasive biomarkers of gynecological disorders, fetal aneuploidy and constitutional maternal chromosomal mosaicism.
- [78-OR]: A systems biology approach reveals evidence for defective endometrial maturation in women destined to develop preeclampsia (PE).
- Bioinformatics Approach Reveals Evidence for Impaired Endometrial Maturation Before and During Early Pregnancy in Women Who Developed Preeclampsia.
- High resolution non-invasive detection of a fetal microdeletion using the GCREM algorithm.
- Mannose binding lectin genotypes are not associated with increased risk of unexplained recurrent pregnancy loss.
- Association study of schizophrenia and the dopamine D3 receptor gene locus in two independent samples.
- Preconception genetic counseling.
- Molecular cytogenetics: an essential component of modern prenatal diagnosis.
- Increased echogenicity in the fetal abdomen: use of DNA analysis to establish a diagnosis of cystic fibrosis.
- Prenatal diagnosis of cytomegalovirus (CMV) infection: a preliminary report.
- Intraamniotic 15(s)-15-methyl prostaglandin F2 alpha and termination of middle and late second-trimester pregnancy for genetic indications: a contemporary approach.
- Antenatal diagnosis of fetal pelvic kidneys.
- Gorlin syndrome (naevoid basal cell carcinoma syndrome): prenatal detection in a fetus with macrocephaly and ventriculomegaly.
- Desbuquois syndrome: clinical, radiographic, and morphologic characterization.
- Osteogenesis imperfecta and campomelic dysplasia: difficulties in prenatal diagnosis.
- Early prenatal diagnosis of an infratentorial arachnoid cyst: association with an unbalanced translocation.
- Determination of normal human fetal immunoglobulin M levels.
- Prenatal diagnosis of fragile (X) syndrome.
- Chorion villi sampling (CVS) for prenatal diagnosis of genetic disorders: first results and future research.
- Recent developments in the prenatal diagnosis of genetic diseases and birth defects.
- Prenatal diagnosis by chorionic villus sampling: lessons of the first 600 cases.
- The lethal multiple pterygium syndromes: is prenatal detection possible?
- Chorionic villus sampling: experience of the first 1000 cases.
- Septic shock with renal failure after chorionic villus sampling.
- Chorionic villus sampling.
- Analysis of chromosomally normal spontaneous abortions after chorionic villus sampling.
- Fetal evaluation by percutaneous blood sampling.
- Cystic sacrococcygeal teratoma: ultrasound diagnosis and perinatal management.
- Ontogeny of fetal liver glucose-6-phosphatase activity.
- Bilateral renal agenesis and Mullerian anomalies in a 47,XXX fetus.
- The role of ultrasonography and amniocentesis in the evaluation of pregnancies at risk for neural tube defects.
- Alpha fetoprotein and acetylcholinesterase levels in twins discordant for neural tube defects: dependence on type of fetal membranes.
- OEIS complex (cloacal exstrophy): prenatal diagnosis in the second trimester.
- Transcervical chorionic villus sampling and amniocentesis: a comparison of reliability, culture findings, and fetal outcome.
- Neonatal progeroid syndrome: more than one disease?
- Diagnosis and management of prenatally detected myelomeningocele: a preliminary report.
- Early diagnosis of spina bifida: the value of cranial ultrasound markers.
- Multicystic dysplastic kidney: natural history of prenatally detected cases.
- Prenatal diagnosis of eventration of the diaphragm.
- Chorionic villus sampling: the University of Maryland experience.
- Congenital nephrosis: detection of index cases through maternal serum alpha-fetoprotein screening.
- Three cases of tetrasomy 9p.
- First-trimester trisomy screening: nuchal translucency measurement training and quality assurance to correct and unify technique.
- A novel X chromosome-linked genetic cause of recurrent spontaneous abortion.
- Maternal serum screening for fetal trisomy 18: benefits of patient-specific risk protocol.
- Pathological case of the month: Desbuquois syndrome.
- X chromosome defects as an etiology of recurrent spontaneous abortion.
- Second-trimester levels of maternal serum human chorionic gonadotropin and inhibin a as predictors of preeclampsia in the third trimester of pregnancy.
- Cord blood banking and stem cell transplantation: implications for the practicing Ob/Gyn.
- Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion.
- Insights into the pathogenesis and natural history of fetuses with multicystic dysplastic kidney disease.
- Sex Chromosome Genetics '99. The X chromosome and recurrent spontaneous abortion: the significance of transmanifesting carriers.
- The use of interphase FISH for prenatal diagnosis of Pallister-Killian syndrome.
- Choroid plexus cysts and trisomy 18: risk modification based on maternal age and multiple-marker screening.
- 45,X/46,XY mosaicism: the role of ultrasound in prenatal diagnosis and counselling.
- Infant with severe penicillamine embryopathy born to a woman with Wilson disease.
- Obstetrics and gynecology: chorionic villus sampling.
- Noninvasive prenatal diagnosis of a fetal microdeletion syndrome.
- Structural and regulatory characterization of the placental epigenome at its maternal interface.
- A novel approach toward the challenge of accurately quantifying fetal DNA in maternal plasma.
- Gene expression in first trimester preeclampsia placenta.
- Statistical considerations for digital approaches to non-invasive fetal genotyping.
- Comprehensive analysis of HLA-G: implications for recurrent spontaneous abortion.
- Statistical model for whole genome sequencing and its application to minimally invasive diagnosis of fetal genetic disease.
- Altered global gene expression in first trimester placentas of women destined to develop preeclampsia.
- Recurrent spontaneous abortion and skewed X-inactivation: is there an association?
- Variable outcomes in mosaic trisomy 16: five case reports and literature analysis.
- Elevated first-trimester nuchal translucency increases the risk of congenital heart defects.
- Association of extreme first-trimester free human chorionic gonadotropin-beta, pregnancy-associated plasma protein A, and nuchal translucency with intraUterine growth ...
- Sequential pathways of testing after first-trimester screening for trisomy 21.
- Association of undetectable unconjugated estriol on multiple marker screening with steroid sulfatase deficiency.
- First-trimester screening for trisomies 21 and 18.
- The clinical use of karyotyping spontaneous abortions.
Schools
University of Virginia Main Campus
University Va School Med
Conditions Treated
- Gestational Diabetes
- Ovarian Cancer
- Pregestational Diabetes Mellitus
- Uterine Cancer
Doctors Specialties
- Clinical Genetics
- Obstetrics
- Gynecology
Accepted Insurances
Education
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University of Virginia -
University of Virginia School of Medicine
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