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Items: 1 to 50 of 62

1.

Improving newborn screening follow-up in pediatric practices: quality improvement innovation network.

Hinton CF, Neuspiel DR, Gubernick RS, Geleske T, Healy J, Kemper AR, Lloyd-Puryear MA, Saul RA, Thompson BH, Kaye CI.

Pediatrics. 2012 Sep;130(3):e669-75. doi: 10.1542/peds.2011-2920. Epub 2012 Aug 6.

PMID:
22869832
2.

Genetic service delivery: infrastructure, assessment and information.

Kaye CI.

Public Health Genomics. 2012;15(3-4):164-71. doi: 10.1159/000335552. Epub 2012 Apr 4.

PMID:
22488459
3.

Tracking clinical genetic services for newborns identified through newborn dried bloodspot screening in the United States-lessons learned.

Livingston J, Therrell BL Jr, Mann MY, Anderson CS, Christensen K, Gorski JL, Grange DK, Peck D, Roberston M, Rogers S, Taylor M, Kaye CI.

J Community Genet. 2011 Dec;2(4):191-200. doi: 10.1007/s12687-011-0055-z. Epub 2011 Jul 6.

4.

University of Colorado Denver School of Medicine.

Kaye CI, Feinstein R.

Acad Med. 2010 Sep;85(9 Suppl):S114-9. doi: 10.1097/ACM.0b013e3181e86c02. No abstract available.

PMID:
20736527
5.

Outcomes of interest in evidence-based evaluations of genetic tests.

Botkin JR, Teutsch SM, Kaye CI, Hayes M, Haddow JE, Bradley LA, Szegda K, Dotson WD; EGAPP Working Group.

Genet Med. 2010 Apr;12(4):228-35. doi: 10.1097/GIM.0b013e3181cdde04.

PMID:
20118789
6.

Assuring clinical genetic services for newborns identified through U.S. newborn screening programs.

Kaye CI, Livingston J, Canfield MA, Mann MY, Lloyd-Puryear MA, Therrell BL Jr.

Genet Med. 2007 Aug;9(8):518-27.

PMID:
17700390
7.

Introduction to the newborn screening fact sheets.

Kaye CI; Committee on Genetics, Accurso F, La Franchi S, Lane PA, Northrup H, Pang S, Schaefer GB.

Pediatrics. 2006 Sep;118(3):1304-12. Review.

PMID:
16960984
8.

Newborn screening fact sheets.

Kaye CI; Committee on Genetics, Accurso F, La Franchi S, Lane PA, Hope N, Sonya P, G Bradley S, Michele A LP.

Pediatrics. 2006 Sep;118(3):e934-63.

PMID:
16950973
9.

Update of newborn screening and therapy for congenital hypothyroidism.

American Academy of Pediatrics, Rose SR; Section on Endocrinology and Committee on Genetics, American Thyroid Association, Brown RS; Public Health Committee, Lawson Wilkins Pediatric Endocrine Society, Foley T, Kaplowitz PB, Kaye CI, Sundararajan S, Varma SK.

Pediatrics. 2006 Jun;117(6):2290-303. Review.

PMID:
16740880
10.

Implementing a simpler approach to mission-based planning in a medical school.

Sloan TB, Kaye CI, Allen WR, Magness BE, Wartman SA.

Acad Med. 2005 Nov;80(11):994-1004.

PMID:
16249297
11.

Growth hormone benefits children with 18q deletions.

Cody JD, Semrud-Clikeman M, Hardies LJ, Lancaster J, Ghidoni PD, Schaub RL, Thompson NM, Wells L, Cornell JE, Love TM, Fox PT, Leach RJ, Kaye CI, Hale DE.

Am J Med Genet A. 2005 Aug 15;137(1):9-15.

PMID:
16007630
12.

Integrating genetic services into public health--guidance for state and territorial programs from the National Newborn Screening and Genetics Resource Center (NNSGRC).

Kaye CI, Laxova R, Livingston JE, Lloyd-Puryear MA, Mann M, McCabe ER, Therrell BL; Genetics Advisory Committee, National Newborn Screening and Geneitcs Resource Center.

Community Genet. 2001;4(3):175-96. No abstract available.

PMID:
14960911
13.

Perceptions of Mexican American clients receiving genetic services in South Texas.

Urdaneta ML, Livingston J, Aguilar M, Suther S, Enciso V, Kaye CI.

Community Genet. 2002;5(4):239-48.

PMID:
14960878
14.

Folic acid awareness and use among women with a history of a neural tube defect pregnancy--Texas, 2000-2001.

Canfield MA, Anderson JL, Waller DK, Palmer SE, Kaye CI.

MMWR Recomm Rep. 2002 Sep 13;51(RR-13):16-9.

15.

Measuring contributions to the research mission of medical schools.

Holmes EW, Burks TF, Dzau V, Hindery MA, Jones RF, Kaye CI, Korn D, Limbird LE, Marchase RB, Perlmutter R, Sanfilippo F, Strom BL.

Acad Med. 2000 Mar;75(3):303-13.

PMID:
10724325
16.

Congenital anomalies and anthropometry of 42 individuals with deletions of chromosome 18q.

Cody JD, Ghidoni PD, DuPont BR, Hale DE, Hilsenbeck SG, Stratton RF, Hoffman DS, Muller S, Schaub RL, Leach RJ, Kaye CI.

Am J Med Genet. 1999 Aug 27;85(5):455-62.

PMID:
10405442
17.

Genetics education for primary care providers in community health settings.

Kolb SE, Aguilar MC, Dinenberg M, Kaye CI.

J Community Health. 1999 Feb;24(1):45-59.

PMID:
10036647
18.

Growth hormone insufficiency associated with haploinsufficiency at 18q23.

Cody JD, Hale DE, Brkanac Z, Kaye CI, Leach RJ.

Am J Med Genet. 1997 Sep 5;71(4):420-5.

PMID:
9286448
19.

Magnetic resonance imaging demonstrates incomplete myelination in 18q- syndrome: evidence for myelin basic protein haploinsufficiency.

Gay CT, Hardies LJ, Rauch RA, Lancaster JL, Plaetke R, DuPont BR, Cody JD, Cornell JE, Herndon RC, Ghidoni PD, Schiff JM, Kaye CI, Leach RJ, Fox PT.

Am J Med Genet. 1997 Jul 25;74(4):422-31.

PMID:
9259379
20.

Preferential loss of the paternal alleles in the 18q- syndrome.

Cody JD, Pierce JF, Brkanac Z, Plaetke R, Ghidoni PD, Kaye CI, Leach RJ.

Am J Med Genet. 1997 Mar 31;69(3):280-6.

PMID:
9096757
21.

Growth hormone deficiency associated in the 18q deletion syndrome.

Ghidoni PD, Hale DE, Cody JD, Gay CT, Thompson NM, McClure EB, Danney MM, Leach RJ, Kaye CI.

Am J Med Genet. 1997 Mar 3;69(1):7-12.

PMID:
9066876
22.

Short-limb dwarfism and hypertrophic cardiomyopathy in a patient with paternal isodisomy 14: 45,XY,idic(14)(p11).

Walter CA, Shaffer LG, Kaye CI, Huff RW, Ghidoni PD, McCaskill C, McFarland MB, Moore CM.

Am J Med Genet. 1996 Nov 11;65(4):259-65.

PMID:
8923931
23.

Membranous nephropathy in two human leukocyte antigen-identical brothers.

Elshihabi I, Kaye CI, Brzowski A.

J Pediatr. 1993 Dec;123(6):940-2.

PMID:
8229527
24.

Proximal 7q interstitial deletion in a severely mentally retarded and mildly abnormal infant.

Gillar PJ, Kaye CI, Ryan SG, Moore CM.

Am J Med Genet. 1992 Sep 15;44(2):138-41.

PMID:
1456281
25.

Oculoauriculovertebral anomaly: segregation analysis.

Kaye CI, Martin AO, Rollnick BR, Nagatoshi K, Israel J, Hermanoff M, Tropea B, Richtsmeier JT, Morton NE.

Am J Med Genet. 1992 Aug 1;43(6):913-7.

PMID:
1415339
26.

Trisomy 8p: unusual origin detected by fluorescence in situ hybridization.

Moore CM, Barnum K, Kaye CI, Kagan-Hallett KS, Liang JC.

Hum Genet. 1992 May;89(3):307-10.

PMID:
1601422
27.

Rumination risk of aspiration of gastric contents in the Prader-Willi syndrome.

Sloan TB, Kaye CI.

Anesth Analg. 1991 Oct;73(4):492-5. Review. No abstract available.

PMID:
1897775
28.

Progressive early dermatologic changes in Hutchinson-Gilford progeria syndrome.

Gillar PJ, Kaye CI, McCourt JW.

Pediatr Dermatol. 1991 Sep;8(3):199-206.

PMID:
1745628
29.

Geneticists and sex selection.

Kaye CI, La Puma J.

Hastings Cent Rep. 1990 Jul-Aug;20(4):40-1. No abstract available.

PMID:
2211088
30.

Microtia and associated anomalies: statistical analysis.

Kaye CI, Rollnick BR, Hauck WW, Martin AO, Richtsmeier JT, Nagatoshi K.

Am J Med Genet. 1989 Dec;34(4):574-8.

PMID:
2624271
31.

Oculoauriculovertebral spectrum: an updated critique.

Cohen MM Jr, Rollnick BR, Kaye CI.

Cleft Palate J. 1989 Oct;26(4):276-86. Review.

PMID:
2680167
32.

Autosomal recessive transmission of neuroectodermal syndrome.

Zunich J, Esterly NB, Kaye CI.

Arch Dermatol. 1988 Aug;124(8):1188-9. No abstract available.

PMID:
3041916
33.

Branchio-oto-renal syndrome: reduced penetrance and variable expressivity in four generations of a large kindred.

Rollnick BR, Kaye CI.

Am J Med Genet. 1987 May;27(1):233. No abstract available.

PMID:
3605200
34.

Oculoauriculovertebral dysplasia and variants: phenotypic characteristics of 294 patients.

Rollnick BR, Kaye CI, Nagatoshi K, Hauck W, Martin AO.

Am J Med Genet. 1987 Feb;26(2):361-75.

PMID:
3812588
35.

A response: a further X-linked isolated nonsyndromic cleft palate family with a nonexpressing obligate affected male.

Rollnick BR, Kaye CI.

Am J Med Genet. 1987 Jan;26(1):241. No abstract available.

PMID:
3812574
36.

Mendelian inheritance of isolated nonsyndromic cleft palate.

Rollnick BR, Kaye CI.

Am J Med Genet. 1986 Jul;24(3):465-73.

PMID:
3728565
37.

Congenital migratory ichthyosiform dermatosis with neurologic and ophthalmologic abnormalities.

Zunich J, Esterly NB, Holbrook KA, Kaye CI.

Arch Dermatol. 1985 Sep;121(9):1149-56.

PMID:
4037840
38.

Samuel Pruzansky and the Center for Craniofacial Anomalies.

Kaye CI, Rollnick BR.

J Craniofac Genet Dev Biol Suppl. 1985;1:25-30.

PMID:
3902947
39.

Hemifacial microsomia and the branchio-oto-renal syndrome.

Rollnick BR, Kaye CI.

J Craniofac Genet Dev Biol Suppl. 1985;1:287-95.

PMID:
3877103
40.

Evaluation of chromosomal damage in males exposed to agent orange and their families.

Kaye CI, Rao S, Simpson SJ, Rosenthal FS, Cohen MM.

J Craniofac Genet Dev Biol Suppl. 1985;1:259-65.

PMID:
3877099
41.

Additional case report of new neuroectodermal syndrome.

Zunich J, Kaye CI.

Am J Med Genet. 1984 Mar;17(3):707-10. No abstract available.

PMID:
6711621
42.

Hemifacial microsomia and variants: pedigree data.

Rollnick BR, Kaye CI.

Am J Med Genet. 1983 Jun;15(2):233-53.

PMID:
6881197
43.

New syndrome of congenital ichthyosis with neurologic abnormalities.

Zunich J, Kaye CI.

Am J Med Genet. 1983 Jun;15(2):331-3, 335. No abstract available.

PMID:
6192719
44.

Characterization of a human colonic adenocarcinoma cell line, LS123.

Rutzky LP, Giovanella BC, Tom BH, Kaye CI, Noguchi PD, Kahan BD.

In Vitro. 1983 Feb;19(2):99-107.

PMID:
6826200
45.

Neonatal bromism secondary to maternal exposure in a photographic laboratory.

Mangurten HH, Kaye CI.

J Pediatr. 1982 Apr;100(4):596-8. No abstract available.

PMID:
7062210
46.

Classification, etiology, and genetic aspects of craniofacial anomalies.

Kaye CI.

Otolaryngol Clin North Am. 1981 Nov;14(4):827-64.

PMID:
7335360
47.

Hemifacial microsomia in a patient with Klinefelter syndrome.

Poonawalla HH, Kaye CI, Rosenthal IM, Pruzansky S.

Cleft Palate J. 1980 Jul;17(3):194-6.

PMID:
6930993
48.

Longitudinal karyotype and genetic signature analysis of cultured human colon adenocarcinoma cell lines LS180 and LS174T.

Rutzky LP, Kaye CI, Siciliano MJ, Chao M, Kahan BD.

Cancer Res. 1980 May;40(5):1443-8.

49.

Ganglioneuroblastoma and fetal hydantoin-alcohol syndromes.

Seeler RA, Israel JN, Royal JE, Kaye CI, Rao S, Abulaban M.

Pediatrics. 1979 Apr;63(4):524-7.

PMID:
440860
50.

Malformations of the auricle: isolated and in syndromes. IV. Cumulative pedigree data.

Kaye CI, Rollnick BR, Pruzansky S.

Birth Defects Orig Artic Ser. 1979;15(5C):163-9. No abstract available.

PMID:
526600

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