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Walter Nance

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DNA Mutational Analysis

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Joshua C Yelverton; Kathleen Arnos; Walter E Nance; Arti Pandya; Xia-Juan Xia; Kelley M Dodson
The clinical and audiologic features of hearing loss due to mitochondrial mutations.
Kelley M Dodson; Alexandros Georgolios; Walter E Nance; Bich Nguyen; Virginia W Norris; Kathleen S Arnos; Noelle Barr; Derek Chapman; Aristides Sismanis; Arti Pandya
Etiology of unilateral hearing loss in a national hereditary deafness repository.
Kelley M Dodson; S Blanton; Katherine O Welch; Virginia W Norris; Regina L Nuzzo; Jacob A Wegelin; Ruth S Marin; Walter E Nance; Arti Pandya; Kathleen S Arnos
Vestibular dysfunction in DFNB1 deafness.

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All Publications

2013: Joshua C Yelverton; Kathleen Arnos; Walter E Nance; Arti Pandya; Xia-Juan Xia; Kelley M Dodson
The clinical and audiologic features of hearing loss due to mitochondrial mutations.
Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery 2013;148(6):1017-22.
2012: Kelley M Dodson; Alexandros Georgolios; Walter E Nance; Bich Nguyen; Virginia W Norris; Kathleen S Arnos; Noelle Barr; Derek Chapman; Aristides Sismanis; Arti Pandya
Etiology of unilateral hearing loss in a national hereditary deafness repository.
American journal of otolaryngology 2012;33(5):590-4.
2011: Kelley M Dodson; S Blanton; Katherine O Welch; Virginia W Norris; Regina L Nuzzo; Jacob A Wegelin; Ruth S Marin; Walter E Nance; Arti Pandya; Kathleen S Arnos
Vestibular dysfunction in DFNB1 deafness.
American journal of medical genetics. Part A 2011;155A(5):993-1000.
2010: Mustafa Tekin; Xia Juan Xia; Radnaabazar Erdenetungalag; Filiz Basak Cengiz; Thomas W White; Janchiv Radnaabazar; Begzsuren Dangaasuren; Hakki Tastan; Walter E Nance; Arti Pandya
GJB2 mutations in Mongolia: complex alleles, low frequency, and reduced fitness of the deaf.
Annals of human genetics 2010;74(2):155-64.
2010: S Blanton; Walter E Nance; Virginia W Norris; Katherine O Welch; Amber Burt; Arti Pandya; Kathleen S Arnos
Fitness among individuals with early childhood deafness: Studies in alumni families from Gallaudet University.
Annals of human genetics 2010;74(1):27-33.
2009: Byung Yoon Choi; Anne C Madeo; K A King; Christopher K Zalewski; Shannon P Pryor; J A Muskett; Walter E Nance; John A Butman; Carmen C Brewer; Andrew J Griffith
Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypes.
Journal of medical genetics 2009;46(12):856-61.
2009: Byung Yoon Choi; Andrew K Stewart; Anne C Madeo; Shannon P Pryor; Suzanne Lenhard; Rick Kittles; David J Eisenman; H Jeffrey Kim; John K Niparko; James Thomsen; Kathleen S Arnos; Walter E Nance; Kelly A King; Christopher K Zalewski; Carmen C Brewer; Thomas Shawker; James C Reynolds; John A Butman; Lawrence P Karniski; Seth L Alper; Andrew J Griffith
Hypo-functional SLC26A4 variants associated with nonsyndromic hearing loss and enlargement of the vestibular aqueduct: genotype-phenotype correlation or coincidental polymorphisms?
Human mutation 2009;30(4):599-608.
2008: Kathleen S Arnos; Katherine O Welch; Mustafa Tekin; Virginia W Norris; S Blanton; Arti Pandya; Walter E Nance
A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apart.
American journal of human genetics 2008;83(2):200-7.
2008: V Labay; G Garrido; Anne C Madeo; Walter E Nance; Thomas B Friedman; P L Friedman; Ignacio del Castillo; Andrew J Griffith
Haplogroup analysis supports a pathogenic role for the 7510T>C mutation of mitochondrial tRNA(Ser(UCN)) in sensorineural hearing loss.
Clinical genetics 2008;73(1):50-4.
2007: Kelley M Dodson; Tamio Kamei; Aristides Sismanis; Walter E Nance
Familial unilateral deafness and delayed endolymphatic hydrops.
American journal of medical genetics. Part A 2007;143A(14):1661-5.
2006: Virginia W Norris; Kathleen S Arnos; Wendy D Hanks; Xia Xia; Walter E Nance; Arti Pandya
Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness? Penetrance of GJB2 deafness.
Ear and hearing 2006;27(6):732-41.
2006: Sarah K Burton; S Blanton; Brandt Culpepper; Karl R White; Arti Pandya; Walter E Nance; Kathleen S Arnos
Education in the genetics of hearing loss: a survey of early hearing detection and intervention programs.
Genetics in medicine : official journal of the American College of Medical Genetics 2006;8(8):510-7.
2006: Walter E Nance; B Gail Lim; Kelley M Dodson
Importance of congenital cytomegalovirus infections as a cause for pre-lingual hearing loss.
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology 2006;35(2):221-5.
2006: Denise Yan; X Ke; S Blanton; Xiao Mei Ouyang; Arti Pandya; Li Lin Du; Walter E Nance; Xue Zhong Liu
A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12.
Journal of medical genetics 2006;43(2):170-4.
2005: Francisco del Castillo; Montserrat Rodríguez-Ballesteros; Araceli Alvarez; Tim Hutchin; Emanuela Leonardi; Camila Andréa de Oliveira; Hela Azaiez; Zippora Brownstein; M R Avenarius; Sandrine Marlin; A Pandya; Hashem Shahin; Kirby R Siemering; Dominique Weil; W Wuyts; Luis A Aguirre; Yolanda Martín; Miguel A Moreno-Pelayo; Manuela Villamar; Karen B Avraham; Hans-Henrik M Dahl; Moien Kanaan; Walter E Nance; Christine Petit; R J H Smith; Guy Van Camp; Edi Sartorato; Alessandra Murgia; Felipe Moreno; Ignacio del Castillo
A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impairment.
Journal of medical genetics 2005;42(7):588-94.
2005: Xue Zhong Liu; Arti Pandya; Simon I Angeli; Fred F Telischi; Kathleen S Arnos; Walter E Nance; Thomas J Balkany
Audiological features of GJB2 (connexin 26) deafness.
Ear and hearing 2005;26(3):361-9.
2005: Xiao Mei Ouyang; Denise Yan; Li Lin Du; J Fielding Hejtmancik; Samuel G Jacobson; Walter E Nance; An Ren Li; Simon I Angeli; Muriel Kaiser; Valerie Newton; Steve D M Brown; Thomas J Balkany; Xue Zhong Liu
Characterization of Usher syndrome type I gene mutations in an Usher syndrome patient population.
Human genetics 2005;116(4):292-9.
2005: Shannon P Pryor; Anne C Madeo; J C Reynolds; Nicholas Sarlis; Kathleen S Arnos; Walter E Nance; Yandan Yang; Christopher K Zalewski; Carmen C Brewer; John A Butman; Andrew J Griffith
SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entities.
Journal of medical genetics 2005;42(2):159-65.
2004: Kelley M Dodson; Aristides Sismanis; Walter E Nance
Superficial siderosis: a potentially important cause of genetic as well as non-genetic deafness.
American journal of medical genetics. Part A 2004;130A(1):22-5.
2004: Walter E Nance; Michael J Kearsey
Relevance of connexin deafness (DFNB1) to human evolution.
American journal of human genetics 2004;74(6):1081-7.
2003: Ignacio del Castillo; Miguel A Moreno-Pelayo; Francisco del Castillo; Zippora Brownstein; Sandrine Marlin; Quint Adina; David J Cockburn; Arti Pandya; Kirby R Siemering; G Parker Chamberlin; Ester Ballana; Wim Wuyts; Andréa T Maciel-Guerra; Araceli Alvarez; Manuela Villamar; Mordechai Shohat; Dvorah Abeliovich; Hans-Henrik M Dahl; Xavier Estivill; Paolo Gasparini; Tim Hutchin; Walter E Nance; Edi Sartorato; Richard J H Smith; Guy Van Camp; Karen B Avraham; Christine Petit; Felipe Moreno
Prevalence and evolutionary origins of the del(GJB6-D13S1830) mutation in the DFNB1 locus in hearing-impaired subjects: a multicenter study.
American journal of human genetics 2003;73(6):1452-8.
2003: Denise Yan; Hong-Joon Park; Xiao Mei Ouyang; Arti Pandya; Katsumi Doi; Raadnabazar Erdenetungalag; Li Lin Du; Naoki Matsushiro; Walter E Nance; Andrew J Griffith; Xue Zhong Liu
Evidence of a founder effect for the 235delC mutation of GJB2 (connexin 26) in east Asians.
Human genetics 2003;114(1):44-50.
2003: Arti Pandya; Kathleen S Arnos; Xia Juan Xia; Katherine O Welch; S Blanton; Thomas B Friedman; Guillermina Garcia Sanchez; Xiu Z Liu MD; Robert J Morell; Walter E Nance
Frequency and distribution of GJB2 (connexin 26) and GJB6 (connexin 30) mutations in a large North American repository of deaf probands.
Genetics in medicine : official journal of the American College of Medical Genetics 2003;5(4):295-303.
2003: Xue Zhong Liu; Xiao Mei Ouyang; Xia Juan Xia; Jing Zheng; Arti Pandya; Fang Li; Li Lin Du; Katherine O Welch; Christine Petit; Richard J H Smith; Bradley T Webb; Denise Yan; Kathleen S Arnos; David Corey; Peter Dallos; Walter E Nance; Zheng Yi Chen
Prestin, a cochlear motor protein, is defective in non-syndromic hearing loss.
Human molecular genetics 2003;12(10):1155-62.
2003: Katherine O Welch; Mustafa Tekin; Walter E Nance; S Blanton; Kathleen S Arnos; Arti Pandya
Chudley-McCullough syndrome: expanded phenotype and review of the literature.
American journal of medical genetics. Part A 2003;119A(1):71-6.
2003: H-J Park; S Shaukat; Xue Zhong Liu; S H Hahn; Sadaf Naz; M Ghosh; H-N Kim; S-K Moon; S Abe; K Tukamoto; S Riazuddin; M Kabra; Raadnabazar Erdenetungalag; J Radnaabazar; S Khan; Arti Pandya; S-I Usami; Walter E Nance; Edward R Wilcox; Sheikh Amer Riazuddin; Andrew J Griffith
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafness.
Journal of medical genetics 2003;40(4):242-8.
2003: Xiao Mei Ouyang; J Fielding Hejtmancik; S G Jacobson; Xia Juan Xia; A Li; Li Lin Du; V Newton; M Kaiser; Thomas J Balkany; Walter E Nance; Xue Zhong Liu
USH1C: a rare cause of USH1 in a non-Acadian population and a founder effect of the Acadian allele.
Clinical genetics 2003;63(2):150-3.
2003: Walter E Nance
The genetics of deafness.
Mental retardation and developmental disabilities research reviews 2003;9(2):109-19.
2002: Xue Zhong Liu; Xia Juan Xia; Xiao Mei Ke; Xiao Mei Ouyang; Li Lin Du; Yu He Liu; Simon I Angeli; Fred F Telischi; Walter E Nance; Thomas J Balkany; Li Rong Xu
The prevalence of connexin 26 ( GJB2) mutations in the Chinese population.
Human genetics 2002;111(4-5):394-7.
2002: S Blanton; C Y Liang; M W Cai; Arti Pandya; Li Lin Du; BL Landa; S Mummalanni; K S Li; Zheng Yi Chen; X N Qin; Y F Liu; Thomas J Balkany; Walter E Nance; Xue Zhong Liu
A novel locus for autosomal dominant non-syndromic deafness (DFNA41) maps to chromosome 12q24-qter.
Journal of medical genetics 2002;39(8):567-70.
2002: Xiao Mei Ouyang; Xia Juan Xia; Elisabeth Verpy; Li Lin Du; Arti Pandya; Christine Petit; Thomas J Balkany; Walter E Nance; Xue Zhong Liu
Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness.
Human genetics 2002;111(1):26-30.
2002: S J Stern; Kathleen S Arnos; L Murrelle; Katherine O Welch; Walter E Nance; Arti Pandya
Attitudes of deaf and hard of hearing subjects towards genetic testing and prenatal diagnosis of hearing loss.
Journal of medical genetics 2002;39(6):449-53.
2002: Ingrid Zwaenepoel; Mirna Mustapha; Michel Leibovici; Elisabeth Verpy; Richard J Goodyear; Xue Zhong Liu; Sylvie Nouaille; Walter E Nance; Moien Kanaan; Karen B Avraham; Fredj Tekaia; Jacques Loiselet; Mark Lathrop; Guy Richardson; Christine Petit
Otoancorin, an inner ear protein restricted to the interface between the apical surface of sensory epithelia and their overlying acellular gels, is defective in autosomal recessive deafness DFNB22.
Proceedings of the National Academy of Sciences of the United States of America 2002;99(9):6240-5.
2001: Xue Zhong Liu; Xia Juan Xia; J Adams; Zheng Yi Chen; Katherine O Welch; Mustafa Tekin; Xiao Mei Ouyang; A Kristiansen; Arti Pandya; Thomas J Balkany; Kathleen S Arnos; Walter E Nance
Mutations in GJA1 (connexin 43) are associated with non-syndromic autosomal recessive deafness.
Human molecular genetics 2001;10(25):2945-51.
2001: Mustafa Tekin; Joann Bodurtha; Walter E Nance; Arti Pandya
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?
Clinical genetics 2001;60(4):301-4.
2001: Xue Zhong Liu; S Blanton; Maria Bitner-Glindzicz; Arti Pandya; BL Landa; B MacArdle; Kaukat Rajput; S Bellman; Bradley T Webb; X Ping; Richard J H Smith; Walter E Nance
Haplotype analysis of the USH1D locus and genotype-phenotype correlations.
Clinical genetics 2001;60(1):58-62.
2001: Tamar Ben-Yosef; Marie Wattenhofer; S Riazuddin; Z M Ahmed; Hamish Scott; Jun Kudoh; Kazunori Shibuya; Stylianos E Antonarakis; Batsheva Bonne-Tamir; Uppala Radhakrishna; Sadaf Naz; Zubair M Ahmed; Sheikh Amer Riazuddin; Arti Pandya; Walter E Nance; Edward R Wilcox; Thomas B Friedman; Robert J Morell
Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness.
Journal of medical genetics 2001;38(6):396-400.
2001: Mustafa Tekin; N Akar; Sükrü Cin; S Blanton; Xia Juan Xia; Xue Zhong Liu; Walter E Nance; Arti Pandya
Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians.
Human genetics 2001;108(5):385-9.
2001: Xue Zhong Liu; Li Rong Xu; Y Hu; Walter E Nance; Aristides Sismanis; S L Zhang; Y Xu
Epidemiological studies on hearing impairment with reference to genetic factors in Sichuan, China.
The Annals of otology, rhinology, and laryngology 2001;110(4):356-63.
2001: Mustafa Tekin; Kathleen S Arnos; Xia Juan Xia; M K Oelrich; Xue Zhong Liu; Walter E Nance; Arti Pandya
W44C mutation in the connexin 26 gene associated with dominant non-syndromic deafness.
Clinical genetics 2001;59(4):269-73.
2001: Julie M Bork; Linda M Peters; S Riazuddin; Steven L Bernstein; Z M Ahmed; Seth L Ness; R Polomeno; Arabandi Ramesh; M Schloss; C R Srisailpathy; S Wayne; S Bellman; D Desmukh; Zubair M Ahmed; Shaheen N Khan; V M Kaloustian; XC Li; Anil K Lalwani; Sheikh Amer Riazuddin; Maria Bitner-Glindzicz; Walter E Nance; Xue Zhong Liu; G Wistow; Richard J H Smith; Andrew J Griffith; Edward R Wilcox; Thomas B Friedman; Robert J Morell
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.
American journal of human genetics 2001;68(1):26-37.
2000: Walter E Nance; Xue Zhong Liu; Arti Pandya
Relation between choice of partner and high frequency of connexin-26 deafness.
Lancet 2000;356(9228):500-1.
2000: S Blanton; Arti Pandya; BL Landa; R Javaheri; X Xia; Walter E Nance; RJ Pomponio; KJ Norrgard; KL Swango; Mübeccel Demirkol; H Gülden; Turgay Coskun; Aysegul Tokatli; Imran Ozalp; Barry Wolf
Fine mapping of the human biotinidase gene and haplotype analysis of five common mutations.
Human heredity 2000;50(2):102-11.
2000: Jeffrey S Nye; E A Hayes; M Amendola; D Vaughn; J Charrow; David G McLone; Marcy C Speer; Walter E Nance; A Pandya
Myelocystocele-cloacal exstrophy in a pedigree with a mitochondrial 12S rRNA mutation, aminoglycoside-induced deafness, pigmentary disturbances, and spinal anomalies.
Teratology 2000;61(3):165-71.
2000: Xue Zhong Liu; Xia Juan Xia; Li Rong Xu; Arti Pandya; C Y Liang; S Blanton; Steve D M Brown; Karen P Steel; Walter E Nance
Mutations in connexin31 underlie recessive as well as dominant non-syndromic hearing loss.
Human molecular genetics 2000;9(1):63-7.
1999: Arti Pandya; Xia Juan Xia; Raadnabazar Erdenetungalag; M Amendola; BL Landa; J Radnaabazar; B Dangaasuren; G Van Tuyle; Walter E Nance
Heterogenous point mutations in the mitochondrial tRNA Ser(UCN) precursor coexisting with the A1555G mutation in deaf students from Mongolia.
American journal of human genetics 1999;65(6):1803-6.
1999: Xue Zhong Liu; CI Hope; C Y Liang; J M Zou; Li Rong Xu; T Cole; Robert F Mueller; SE Bundey; Walter E Nance; Karen P Steel; Steve D M Brown
A mutation (2314delG) in the Usher syndrome type IIA gene: high prevalence and phenotypic variation.
American journal of human genetics 1999;64(4):1221-5.
1998: Walter E Nance; Joann Bodurtha; Lindon J Eaves; J Hewitt; Hermine Maes; J Segrest; J Meyer; Michael C Neale; RM Schieken
Models for the longitudinal genetic analysis of same-age twins: application to HDL cholesterol.
Twin research : the official journal of the International Society for Twin Studies 1998;1(1):3-8.
1998: Anita L DeStefano; L A Cupples; Kathleen S Arnos; JH Asher; Clinton T Baldwin; S Blanton; ML Carey; E O da Silva; Thomas B Friedman; J Greenberg; A K Lalwani; Aubrey Milunsky; Walter E Nance; Arti Pandya; Rajkumar Ramesar; A P Read; M Tassabejhi; Edward R Wilcox; Lindsay A Farrer
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations.
Human genetics 1998;102(5):499-506.
1998: RJ Pomponio; Jeanne Hymes; Arti Pandya; BL Landa; Pamela Melone; R Javaheri; R Mardach; S W Morton; GA Meyers; T Reynolds; G Buck; Walter E Nance; Barry Wolf
Prenatal diagnosis of heterozygosity for biotinidase deficiency by enzymatic and molecular analyses.
Prenatal diagnosis 1998;18(2):117-22.
1997: Arti Pandya; X Xia; J Radnaabazar; J Batsuuri; B Dangaansuren; N Fischel-Ghodsian; Walter E Nance
Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity.
Journal of medical genetics 1997;34(2):169-72.
1997: Arti Pandya; Xia Juan Xia; S Blanton; BL Landa; T Markello; Walter E Nance
Implications of molecular diagnostic testing in families with hereditary pancreatitis.
Genetic testing 1997;1(3):207-11.
1996: Arti Pandya; S Blanton; BL Landa; R Javaheri; E Melvin; Walter E Nance; T Markello
Linkage studies in a large kindred with hereditary pancreatitis confirms mapping of the gene to a 16-cM region on 7q.
Genomics 1996;38(2):227-30.
1996: Arti Pandya; Xia Juan Xia; B L Landa; K S Arnos; J Israel; J Lloyd; A L James; S R Diehl; S Blanton; Walter E Nance
Phenotypic variation in Waardenburg syndrome: mutational heterogeneity, modifier genes or polygenic background?
Human molecular genetics 1996;5(4):497-502.
1996: J E Reynolds; Mary L Marazita; J M Meyer; C A Stevens; Lindon J Eaves; K S Arnos; L M Ploughman; C MacLean; Walter E Nance; S R Diehl
Major-locus contributions to variability of the craniofacial feature dystopia canthorum in Waardenburg syndrome.
American journal of human genetics 1996;58(2):384-92.
1995: J Winters; T Markello; Walter E Nance; Colleen Jackson-Cook
Mosaic "tetrasomy" 8p: case report and review of the literature.
Clinical genetics 1995;48(4):195-8.
1995: J E Reynolds; J M Meyer; BL Landa; C A Stevens; K S Arnos; J Israel; Mary L Marazita; J Bodurtha; Walter E Nance; S R Diehl
Analysis of variability of clinical manifestations in Waardenburg syndrome.
American journal of medical genetics 1995;57(4):540-7.
1993: Linda A Corey; Walter E Nance; P Hofstede; Harvey A Schenkein
Self-reported periodontal disease in a Virginia twin population.
Journal of periodontology 1993;64(12):1205-8.
1993: K A Weissbecker; Barry Wolf; Lindon J Eaves; M L Marazita; Walter E Nance
Combined pedigree and twin family study to determine the sources of variation in serum biotinidase activity: the usefulness of multiple study designs.
American journal of medical genetics 1993;47(2):231-40.
1993: Walter E Nance
1992 American Society of Human Genetics presidential address: back to the future.
American journal of human genetics 1993;53(1):6-15.
1993: Mary L Marazita; L M Ploughman; B Rawlings; E Remington; K S Arnos; Walter E Nance
Genetic epidemiological studies of early-onset deafness in the U.S. school-age population.
American journal of medical genetics 1993;46(5):486-91.
1993: William B Moskowitz; M Mosteller; J K Hewitt; Lindon J Eaves; Walter E Nance; RM Schieken
Univariate genetic analysis of oxygen transport regulation in children: the Medical College of Virginia Twin Study.
Pediatric research 1993;33(6):645-8.
1993: M J Austin; Michael C Neale; Linda A Corey; Walter E Nance; RM Schieken; J A Brown
Common fragile site expression in lymphocytes from an individual mosaic for trisomy 8.
American journal of medical genetics 1993;45(5):570-1.
1992: RM Schieken; M Mosteller; Monica M Goble; William B Moskowitz; J K Hewitt; Lindon J Eaves; Walter E Nance
Multivariate genetic analysis of blood pressure and body size. The Medical College of Virginia Twin Study.
Circulation 1992;86(6):1780-8.
1992: Linda A Corey; K Berg; M H Solaas; Walter E Nance
The epidemiology of pregnancy complications and outcome in a Norwegian twin population.
Obstetrics and gynecology 1992;80(6):989-94.
1992: Mary L Marazita; J N Bodurtha; Linda A Corey; A Rogers; C E Barbosa; L Funkhouser; A Linyear; Walter E Nance
Development of the Virginia Congenital Anomalies Reporting and Education System (VaCARES): two pilot projects.
Southern medical journal 1992;85(6):608-15.
1992: M J Austin; J M Collins; Linda A Corey; Walter E Nance; Michael C Neale; RM Schieken; J A Brown
Aphidicolin-inducible common fragile-site expression: results from a population survey of twins.
American journal of human genetics 1992;50(1):76-83.
1991: Linda A Corey; K Berg; John M Pellock; M H Solaas; Walter E Nance; Robert J Delorenzo
The occurrence of epilepsy and febrile seizures in Virginian and Norwegian twins.
Neurology 1991;41(9):1433-6.
1991: Henri Verhaaren; RM Schieken; M Mosteller; J K Hewitt; Lindon J Eaves; Walter E Nance
Bivariate genetic analysis of left ventricular mass and weight in pubertal twins (the Medical College of Virginia twin study).
The American journal of cardiology 1991;68(6):661-8.
1991: J N Bodurtha; C W Chen; M Mosteller; Walter E Nance; RM Schieken; J Segrest
Genetic and environmental contributions to cholesterol and its subfractions in 11-year-old twins. The Medical College of Virginia Twin Study.
Arteriosclerosis and thrombosis : a journal of vascular biology / American Heart Association 1991;11(4):844-50.
1991: K A Weissbecker; Walter E Nance; Lindon J Eaves; C Piussan; Barry Wolf
Statistical approaches for the detection of heterozygotes for biotinidase deficiency.
American journal of medical genetics 1991;39(4):385-90.
1991: C Stevens; K Arnos; J Bodurtha; L Wright; B Rawlings; Mary L Marazita; Walter E Nance; S Diehl
Ascertainment of families with hereditary deafness for linkage studies. Waardenburg and Usher syndromes.
Annals of the New York Academy of Sciences 1991;630():293-4.
1990: J N Bodurtha; M Mosteller; J K Hewitt; Walter E Nance; Lindon J Eaves; William B Moskowitz; S Katz; RM Schieken
Genetic analysis of anthropometric measures in 11-year-old twins: the Medical College of Virginia Twin Study.
Pediatric research 1990;28(1):1-4.
1990: Lisa Shaffer; Mary L Marazita; J Bodurtha; A Newlin; Walter E Nance
Evidence for a major gene in familial anencephaly.
American journal of medical genetics 1990;36(1):97-101.
1990: Walter E Nance
Do twin Lyons have larger spots?
American journal of human genetics 1990;46(4):646-8.
1989: RM Schieken; Lindon J Eaves; J K Hewitt; M Mosteller; J N Bodurtha; William B Moskowitz; Walter E Nance
Univariate genetic analysis of blood pressure in children (the Medical College of Virginia Twin Study).
The American journal of cardiology 1989;64(19):1333-7.
1989: Mary L Marazita; Walter E Nance; K S Arnos
Further comments on the genetics of prelingual deafness.
American journal of human genetics 1989;45(4):637-8.
1989: K A Weissbecker; H D Gruemer; G S Heard; W Greg Miller; Walter E Nance; Barry Wolf
An automated procedure for measuring biotinidase activity in serum.
Clinical chemistry 1989;35(5):831-3.
1988: RM Schieken; William B Moskowitz; J Bodurtha; M Mosteller; L Eaves; Walter E Nance
Aortic stiffness: a new Doppler echocardiographic measure predictive of systolic blood pressure in children.
Journal of the American College of Cardiology 1988;11(6):1297-300.
1987: D J Boles; J Bodurtha; Walter E Nance
Goldenhar complex in discordant monozygotic twins: a case report and review of the literature.
American journal of medical genetics 1987;28(1):103-9.
1986: J N Bodurtha; J I Townsend; V K Proud; Walter E Nance
Updating McKusick: an educational exercise for medical students.
American journal of medical genetics 1986;24(3):505-11.
1986: G S Heard; Barry Wolf; L G Jefferson; K A Weissbecker; Walter E Nance; J R McVoy; A Napolitano; P L Mitchell; F W Lambert; A S Linyear
Neonatal screening for biotinidase deficiency: results of a 1-year pilot study.
The Journal of pediatrics 1986;108(1):40-6.
1985: H D Gruemer; W Greg Miller; V M Chinchilli; R T Leshner; Peter A Blasco; C R Hassler; Walter E Nance
Prediction of carrier status in Duchenne dystrophy by creatine kinase measurement.
American journal of clinical pathology 1985;84(5):655-8.
1985: Barry Wolf; G S Heard; L G Jefferson; V K Proud; Walter E Nance; K A Weissbecker
Clinical findings in four children with biotinidase deficiency detected through a statewide neonatal screening program.
The New England journal of medicine 1985;313(1):16-9.
1985: A C Heath; K Berg; L J Eaves; M H Solaas; J Sundet; Walter E Nance; Linda A Corey; Per Magnus
No decline in assortative mating for educational level.
Behavior genetics 1985;15(4):349-69.
1984: H D Gruemer; W Greg Miller; V M Chinchilli; R T Leshner; C R Hassler; Peter A Blasco; Walter E Nance; B M Goldsmith
Are reference limits for serum creatine kinase valid in detection of the carrier state for Duchenne muscular dystrophy?
Clinical chemistry 1984;30(5):724-30.
1984: W Greg Miller; V M Chinchilli; H D Gruemer; Walter E Nance
Sampling from a skewed population distribution as exemplified by estimation of the creatine kinase upper reference limit.
Clinical chemistry 1984;30(1):18-23.
1981: M Mosteller; J I Townsend; L A Corey; Walter E Nance
Twinning rates in Virginia: secular trends and the effects of maternal age and parity.
Progress in clinical and biological research 1981;69A():57-69.
1980: B M Goldsmith; H D Gruemer; R J Hawley; N A Pickard; H L Verrill; Walter E Nance; G Miller; R G Crawford
The contribution of assays for lymphocyte capping and creatine kinase to detection of the Becker-type dystrophy trait.
Clinical chemistry 1980;26(6):754-9.