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Celia Kaye

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Cynthia F Hinton; Timothy Geleske; Ruth S Gubernick; Jill Healy; Alex R Kemper; Puryear Michele; Daniel R Neuspiel; Robert A Saul; Barry H Thompson; Celia I Kaye
Improving newborn screening follow-up in pediatric practices: quality improvement innovation network.
Celia I Kaye
Genetic service delivery: infrastructure, assessment and information.
Celia I Kaye; Robert Feinstein
University of Colorado Denver School of Medicine.

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All Publications

2012: Cynthia F Hinton; Timothy Geleske; Ruth S Gubernick; Jill Healy; Alex R Kemper; Puryear Michele; Daniel R Neuspiel; Robert A Saul; Barry H Thompson; Celia I Kaye
Improving newborn screening follow-up in pediatric practices: quality improvement innovation network.
Pediatrics 2012;130(3):e669-75.
2012: Celia I Kaye
Genetic service delivery: infrastructure, assessment and information.
Public health genomics 2012;15(3-4):164-71.
2010: Celia I Kaye; Robert Feinstein
University of Colorado Denver School of Medicine.
Academic medicine : journal of the Association of American Medical Colleges 2010;85(9 Suppl):S114-9.
2010: Jeffrey R Botkin; Steven M Teutsch; Celia I Kaye; Maxine Hayes; James E Haddow; Linda A Bradley; Kathleen Szegda; W David Dotson
Outcomes of interest in evidence-based evaluations of genetic tests.
Genetics in medicine : official journal of the American College of Medical Genetics 2010;12(4):228-35.
2007: Celia I Kaye; Judith Livingston; Mark A Canfield; Marie Y Mann; Puryear Michele; Bradford L Therrell
Assuring clinical genetic services for newborns identified through U.S. newborn screening programs.
Genetics in medicine : official journal of the American College of Medical Genetics 2007;9(8):518-27.
2006: Celia I Kaye; Frank Accurso; Stephen H LaFranchi; Peter A Lane; Hope Northrup; Sonya Pang; G Bradley Schaefer
Introduction to the newborn screening fact sheets.
Pediatrics 2006;118(3):1304-12.
2006: Celia I Kaye; Frank Accurso; Stephen H LaFranchi; Peter A Lane; Northrup Hope; Pang Sonya; Schaefer G Bradley; Lloyd-Puryear Michele A
Newborn screening fact sheets.
Pediatrics 2006;118(3):e934-63.
2006: Susan R Rose; Rosalind S Brown; Thomas Foley; Paul B Kaplowitz; Celia I Kaye; Sumana Sundararajan; Surendra K Varma
Update of newborn screening and therapy for congenital hypothyroidism.
Pediatrics 2006;117(6):2290-303.
2005: Tod B Sloan; Celia I Kaye; William R Allen; Brian E Magness; STEVEN WARTMAN
Implementing a simpler approach to mission-based planning in a medical school.
Academic medicine : journal of the Association of American Medical Colleges 2005;80(11):994-1004.
2005: Jannine Cody; Margaret Semrud-Clikeman; L Jean Hardies; Jack Lancaster; Patricia D Ghidoni; Rebecca L Schaub; Nora M Thompson; Lynda Wells; John Cornell; Tanzy M Love; Peter Fox; Robin J Leach; Celia I Kaye; Daniel Hale
Growth hormone benefits children with 18q deletions.
American journal of medical genetics. Part A 2005;137(1):9-15.
2002: Mark A Canfield; James L Anderson; D Kim Waller; Susan E Palmer; Celia I Kaye
Folic acid awareness and use among women with a history of a neural tube defect pregnancy--Texas, 2000-2001.
MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports / Centers for Disease Control 2002;51(RR-13):16-9.
2002: María Luisa Urdaneta; Judith Livingston; Maricela Aguilar; Sandy Suther; Vicky Enciso; Celia I Kaye
Perceptions of Mexican American clients receiving genetic services in South Texas.
Community genetics 2002;5(4):239-48.
2001: Celia I Kaye; R Laxova; J E Livingston; Puryear Michele; M Mann; Edward RB McCabe; Bradford L Therrell
Integrating genetic services into public health--guidance for state and territorial programs from the National Newborn Screening and Genetics Resource Center (NNSGRC).
Community genetics 2001;4(3):175-96.
1999: Jannine Cody; Patricia D Ghidoni; BR DuPont; Daniel Hale; S G Hilsenbeck; Robert F Stratton; D S Hoffman; S Muller; Rebecca L Schaub; Robin J Leach; Celia I Kaye
Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q.
American journal of medical genetics 1999;85(5):455-62.
1997: Jannine Cody; Daniel Hale; Z Brkanac; Celia I Kaye; Robin J Leach
Growth hormone insufficiency associated with haploinsufficiency at 18q23.
American journal of medical genetics 1997;71(4):420-5.
1997: CT Gay; L Jean Hardies; R A Rauch; Jack Lancaster; Rosemarie Plaetke; BR DuPont; Jannine Cody; John Cornell; R C Herndon; Patricia D Ghidoni; J M Schiff; Celia I Kaye; Robin J Leach; Peter Fox
Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome: evidence for myelin basic protein haploinsufficiency.
American journal of medical genetics 1997;74(4):422-31.
1997: Jannine Cody; J F Pierce; Z Brkanac; Rosemarie Plaetke; Patricia D Ghidoni; Celia I Kaye; Robin J Leach
Preferential loss of the paternal alleles in the 18q- syndrome.
American journal of medical genetics 1997;69(3):280-6.
1997: Patricia D Ghidoni; Daniel Hale; Jannine Cody; CT Gay; Nora M Thompson; E B McClure; M M Danney; Robin J Leach; Celia I Kaye
Growth hormone deficiency associated in the 18q deletion syndrome.
American journal of medical genetics 1997;69(1):7-12.
1996: Christi A Walter; Lisa Shaffer; Celia I Kaye; R W Huff; Patricia D Ghidoni; Christopher McCaskill; M B McFarland; Charleen M Moore
Short-limb dwarfism and hypertrophic cardiomyopathy in a patient with paternal isodisomy 14: 45,XY,idic(14)(p11).
American journal of medical genetics 1996;65(4):259-65.
1992: P J Gillar; Celia I Kaye; S G Ryan; Charleen M Moore
Proximal 7q interstitial deletion in a severely mentally retarded and mildly abnormal infant.
American journal of medical genetics 1992;44(2):138-41.
1992: Celia I Kaye; A O Martin; B R Rollnick; K Nagatoshi; J Israel; M Hermanoff; B Tropea; Joan T Richtsmeier; N E Morton
Oculoauriculovertebral anomaly: segregation analysis.
American journal of medical genetics 1992;43(6):913-7.
1989: Celia I Kaye; B R Rollnick; W W Hauck; A O Martin; Joan T Richtsmeier; K Nagatoshi
Microtia and associated anomalies: statistical analysis.
American journal of medical genetics 1989;34(4):574-8.
1989: M M Cohen; B R Rollnick; Celia I Kaye
Oculoauriculovertebral spectrum: an updated critique.
The Cleft palate journal 1989;26(4):276-86.
1987: B R Rollnick; Celia I Kaye
Branchio-oto-renal syndrome: reduced penetrance and variable expressivity in four generations of a large kindred.
American journal of medical genetics 1987;27(1):233.
1987: B R Rollnick; Celia I Kaye; K Nagatoshi; W Hauck; A O Martin
Oculoauriculovertebral dysplasia and variants: phenotypic characteristics of 294 patients.
American journal of medical genetics 1987;26(2):361-75.
1987: B R Rollnick; Celia I Kaye
A response: a further X-linked isolated nonsyndromic cleft palate family with a nonexpressing obligate affected male.
American journal of medical genetics 1987;26(1):241.
1986: B R Rollnick; Celia I Kaye
Mendelian inheritance of isolated nonsyndromic cleft palate.
American journal of medical genetics 1986;24(3):465-73.
1985: Celia I Kaye; B R Rollnick
Samuel Pruzansky and the Center for Craniofacial Anomalies.
Journal of craniofacial genetics and developmental biology. Supplement 1985;1():25-30.
1985: B R Rollnick; Celia I Kaye
Hemifacial microsomia and the branchio-oto-renal syndrome.
Journal of craniofacial genetics and developmental biology. Supplement 1985;1():287-95.
1983: B R Rollnick; Celia I Kaye
Hemifacial microsomia and variants: pedigree data.
American journal of medical genetics 1983;15(2):233-53.