Physician
Medical Genetics
Dr. Walter E. Nance, MD
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Walter Nance practices Medical Genetics. He graduated from Harvard Medical School. Harvard Medical School is a one of the best medicals schools. Harvard Medical School has a rank of 1 in research and a 12 in primary care He has 6 awards "University Award for Excellence in Teaching Service and Research", "Sigma Xi", "Boyleston Society Award, First Prize", "Graduated Optime Merens", "Phi Beta Kappa" and "Freshman Chemistry Prize". Walter E. Nance is a published doctor as well. He has 100 publications published. The latest was: Waardenburg syndrome and gastric stasis in adults.
Publications
- The Clinical and Audiologic Features of Hearing Loss Due to Mitochondrial Mutations.
- Etiology of unilateral hearing loss in a national hereditary deafness repository.
- Vestibular dysfunction in DFNB1 deafness.
- Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental p...
- A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apart.
- Familial unilateral deafness and delayed endolymphatic hydrops.
- Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness? Penetrance of GJB2 deafness.
- Education in the genetics of hearing loss: a survey of early hearing detection and intervention programs.
- Newborn hearing screening--a silent revolution.
- Audiological features of GJB2 (connexin 26) deafness.
- Superficial siderosis: a potentially important cause of genetic as well as non-genetic deafness.
- Relevance of connexin deafness (DFNB1) to human evolution.
- Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study.
- Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands.
- Chudley-McCullough syndrome: expanded phenotype and review of the literature.
- The genetics of deafness.
- Human reproductive cloning.
- Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autoso...
- beta-Arrestins modulate Adenovirus-vector-induced innate immune responses: differential regulation by beta-arrestin-1 and beta-arrestin-2.
- Longitudinal assessment of adaptive and maladaptive behaviors in fragile X males: growth, development, and profiles.
- Age-related language characteristics of children and adolescents with fragile X syndrome.
- A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variation.
- Ascertainment of families with hereditary deafness for linkage studies. Waardenburg and Usher syndromes.
- Aortic stiffness: a new Doppler echocardiographic measure predictive of systolic blood pressure in children.
- Factor VIII and factor IX in a twin population. Evidence for a major effect of ABO locus on factor VIII level.
- Neurologic aspects of typical and atypical Down''s syndrome.
- Waardenburg syndrome and gastric stasis in adults.
- Mosaic "tetrasomy" 8p: case report and review of the literature.
- Major-locus contributions to variability of the craniofacial feature dystopia canthorum in Waardenburg syndrome.
- Common fragile site expression in lymphocytes from an individual mosaic for trisomy 8.
- Univariate genetic analysis of oxygen transport regulation in children: the Medical College of Virginia Twin Study.
- Genetic epidemiological studies of early-onset deafness in the U.S. school-age population.
- 1992 American Society of Human Genetics presidential address: back to the future.
- Combined pedigree and twin family study to determine the sources of variation in serum biotinidase activity: the usefulness of multiple study designs.
- Self-reported periodontal disease in a Virginia twin population.
- Maternal environment defines blood pressure and its response to troleandomycin in spontaneously hypertensive rats.
- Analysis of variability of clinical manifestations in Waardenburg syndrome.
- A genetic study of anodontia in X-linked hypohidrotic ectodermal dysplasia.
- Population genetic studies of retinitis pigmentosa.
- The contribution of assays for lymphocyte capping and creatine kinase to detection of the Becker-type dystrophy trait.
- Twinning rates in Virginia: secular trends and the effects of maternal age and parity.
- Spondylocostal dysostosis associated with anal and urogenital anomalies in a Mennonite sibship.
- The genetic analysis of profound prelingual deafness.
- Determinants of ridge counts in MZ twin kinships.
- A genetic analysis of taste threshold for phenylthiocarbamide.
- Quinacrine mustard and nucleolar organizer region heteromorphisms in twins.
- Relevance of the marriages of twins to the causal analysis of nonrandom mating.
- Blood pressure in Norwegian twins.
- A study of dietary intake in adult monozygotic twins.
- The MZ half-sib design: an approach for the examination of the etiology of congenital malformations.
- A model for the analysis of mate selection in the marriages of twins: application to data on stature.
- Genetic studies of an acardiac monster: evidence of polar body twinning in man.
- Data from kinships of monozygotic twins indicate maternal effects on verbal intelligence.
- Distribution of common eye diseases in the families of Norwegian twins.
- Discordant expression of fetal hydantoin syndrome in heteropaternal dizygotic twins.
- Malformations unique to the twinning process.
- Nonsyndromic deafness.
- Myofascial pain dysfunction (MPD) syndrome in twins.
- Apparent influence of marker genotypes on variation in serum cholesterol in monozygotic twins.
- Genetic analysis of continuous qualitative and multivariate traits in the families of twins.
- Clinical heterogeneity in 80 home-reared children with cri du chat syndrome.
- The analysis of spontaneous abortion using a new half-sib model for qualitative traits.
- Antenatally detected Klinefelter''s syndrome in twins.
- Are reference limits for serum creatine kinase valid in detection of the carrier state for Duchenne muscular dystrophy?
- Genetic studies of ocular albinism in a large Virginia kindred.
- Sampling from a skewed population distribution as exemplified by estimation of the creatine kinase upper reference limit.
- A causal analysis of birth weight in the offspring of monozygotic twins.
- Analysis of the covariance structure of digital ridge counts in the offspring of monozygotic twins.
- Orientation of loci within the human major histocompatibility complex by chromosomal in situ hybridization.
- Predicting zygosity in Norwegian twin pairs born 1915-1960.
- Adaptation to maximal effort: genetics vs. environment. A case history.
- Parental determinants of birth weight.
- Pulmonary arteriovenous malformations related to Rendu-Osler-Weber syndrome.
- The relevance of twin studies to cardiovascular research.
- Autoimmunity in congenital rubella syndrome.
- Genetics of the low density lipoprotein receptor: II. Genetic control of variation in cell membrane low density lipoprotein receptor activity in cultured fibroblasts.
- Stain intensity of human nucleolus organizer region reflects incorporation of uridine into mature ribosomal RNA.
- Persistent tachycardia, paroxymal hypertension, and seizures: association with hyperglycinuria, dominantly inherited microphthalmia, and cataracts.
- Pycnodysostosis, with a familial chromosome anomaly.
- Human blood pressure and the ABO blood group system: an apparent association.
- Further evidence for close linkage of the Hb-beta and Hb-delta loci in man.
- A "new" form of hereditary cerebral sclerosis. An autosomal recessive neurologic disease with distinctive electron electron microscopic findings.
- The larynx in the cri du chat (cat cry) syndrome.
- Haptoglobin and catalase loci in man: possible genetic linkage.
- Symmelia in one of monozygotic twins.
- The principles and practice of genetic counseling.
- Diagnosis of mongolism with a dermatoglyphic nomogram.
- A recessively inherited chondrodystrophy.
- Amish albinism: a distinctive autosomal recessive phenotype.
- C autosomal trisomy with mosaicism: a new syndrome?
- Genetic linkage analysis of human hemoglobin variants.
- E ring chromosome with persistent left superior vena cava and hypertrophic subaortic stenosis.
- Recent developments in genetics: control genes and the genetic code.
- Clinical variation in Usher''s syndrome.
- Genetic linkage studies in a Negro kindred with Norrie''s disease.
- Evidence for autosomal recessive inheritance of the syndrome of renal tubular acidosis with deafness.
- X-linked mixed deafness with congenital fixation of the stapedial footplate and perilymphatic gusher.
- Classification of albinism in man.
- Genetic and biochemical evidence for two forms of oculocutaneous albinism in man.
Schools
Harvard Medical School
Vanderbilt Med School
University Wisconsin
Doctors Specialties
- Clinical Genetics
- Medical Genetics
Accepted Insurances
Awards
- University Award for Excellence in Teaching Service and Research
- Sigma Xi
- Boyleston Society Award, First Prize
- Graduated Optime Merens
- Phi Beta Kappa
- Freshman Chemistry Prize
Education
-
Vanderbilt University -
Harvard Medical School
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