Health Services Research & Administration

Research Output

2004

An analysis of the agreement between financial data between the Medicare Cost Report and the audited hospital financial statement.

Chen, L. W., Stoner, J., Makhanu, C., Minikus, K. & Mueller, K. J., May 2004, In : Rural policy brief / RUPRI Rural Health Panel. 9, 4 (PB2004-4), p. 1-8 8 p.

Research output: Contribution to journalArticle

4 Scopus citations

Predictive Model to Determine Need for Nursing Workforce

Cramer, M. E., Chen, L. W., Mueller, K. J., Shambaugh-Miller, M. & Agrawal, S., Aug 2004, In : Policy, Politics, & Nursing Practice. 5, 3, p. 174-190 17 p.

Research output: Contribution to journalArticle

10 Scopus citations

Teaching the Basics of Clinical Pharmaceutical Care: Innovative Pharmacy Workshops at the University of Wisconsin and the University of Nebraska

Keller, D. R., O'Dell, D. V., Skochelak, S. E., Cochran, G. L., Shull, S. J. & Gjerde, C. L., Jan 2004, In : Family Medicine. 36, SUPPL., p. S89-S92

Research output: Contribution to journalArticle

6 Scopus citations

The Economies of Scale for Nursing Home Care

Chen, L. W. & Shea, D. G., Mar 2004, In : Medical Care Research and Review. 61, 1, p. 38-63 26 p.

Research output: Contribution to journalArticle

9 Scopus citations

Translating research into practice: Voluntary reporting of medication errors in critical access hospitals

Jones, K. J., Cochran, G., Hicks, R. W. & Mueller, K. J., Sep 2004, In : Journal of Rural Health. 20, 4, p. 335-343 9 p.

Research output: Contribution to journalArticle

21 Scopus citations
2003

Comprehensive Evaluation of a Community Coalition: A Case Study of Environmental Tobacco Smoke Reduction

Cramer, M. E., Mueller, K. J. & Harrop, D., Nov 2003, In : Public Health Nursing. 20, 6, p. 464-477 14 p.

Research output: Contribution to journalArticle

12 Scopus citations

Evaluation Informs Coalition Programming for Environmental Tobacco Smoke Reduction

Cramer, M. E., Mueller, K. J. & Harrop, D., Dec 2003, In : Journal of Community Health Nursing. 20, 4, p. 245-258 14 p.

Research output: Contribution to journalArticle

7 Scopus citations

In frame fibrillin-1 gene deletion in autosomal dominant Weill-Marchesani syndrome

Faivre, L., Gorlin, R. J., Wirtz, M. K., Godfrey, M., Dagoneau, N., Samples, J. R., Le Merrer, M., Collod-Beroud, G., Boileau, C., Munnich, A. & Cormier-Daire, V., Jan 1 2003, In : Journal of medical genetics. 40, 1, p. 34-36 3 p.

Research output: Contribution to journalArticle

Open Access
183 Scopus citations
2002

Does prospective payment really contain nursing home costs?

Chen, L. W. & Shea, D. G., Apr 2002, In : Health Services Research. 37, 2, p. 251-271 21 p.

Research output: Contribution to journalReview article

15 Scopus citations

Factors Influencing Organized Political Participation in Nursing

Cramer, M. E., May 2002, In : Policy, Politics, & Nursing Practice. 3, 2, p. 97-107 11 p.

Research output: Contribution to journalArticle

30 Scopus citations

Interorganizational networks: Using a theoretical model to predict effectiveness of rural health care delivery networks

Schumaker, A. M., Dec 2002, In : Journal of Health and Human Services Administration. 25, 3, p. 371-406 36 p.

Research output: Contribution to journalReview article

11 Scopus citations

Pan-cadherin as a high level phenotypic biomarker for prostate cancer

Wehbi, N. K., Dugger, A. L., Bonner, R. B., Pitha, J. V., Hurst, R. E. & Hemstreet, G. P., 2002, In : Journal of Urology. 167, 5, p. 2215-2221 7 p.

Research output: Contribution to journalArticle

15 Scopus citations

Spontaneous spinal cerebrospinal fluid leaks and minor skeletal features of Marfan syndrome: A microfibrillopathy

Schrijver, I., Schievink, W. I., Godfrey, M., Meyer, F. B. & Francke, U., 2002, In : Journal of neurosurgery. 96, 3, p. 483-489 7 p.

Research output: Contribution to journalArticle

80 Scopus citations
2001

Classic, atypically severe and neonatal Marfan syndrome: Twelve mutations and genotype-phenotype correlations in FBN1 exons 24-40

Tiecke, F., Katzke, S., Booms, P., Robinson, P. N., Neumann, L., Godfrey, M., Mathews, K. R., Scheuner, M., Hinkel, G. K., Brenner, R. E., Hövels-Gürich, H. H., Hagemeier, C., Fuchs, J., Skovby, F. & Rosenberg, T., 2001, In : European Journal of Human Genetics. 9, 1, p. 13-21 9 p.

Research output: Contribution to journalArticle

Open Access
110 Scopus citations
2000

Partial cloning and sequencing of chick fibrillin-1 cDNA

Zhou, G., Price, C. E., Rosenquist, T. H., Gadson, P. F. & Godfrey, M., Jan 2000, In : In Vitro Cellular and Developmental Biology - Animal. 36, 1, p. 19-25 7 p.

Research output: Contribution to journalArticle

1 Scopus citations

The molecular genetics of Marfan syndrome and related microfibrillopathies

Robinson, P. N. & Godfrey, M., 2000, In : Journal of medical genetics. 37, 1, p. 9-25 17 p.

Research output: Contribution to journalReview article

Open Access
222 Scopus citations

Two novel fibrillin-2 mutations in congenital contractural arachnodactyly

Belleh, S., Zhou, G., Wang, M., Der Kaloustian, V. M., Pagon, R. A. & Godfrey, M., May 1 2000, In : American journal of medical genetics. 92, 1, p. 7-12 6 p.

Research output: Contribution to journalArticle

26 Scopus citations
1999

Novel exon skipping mutation in the fibrillin-1 gene: Two 'hot spots' for the neonatal Marfan syndrome

Booms, P., Cisler, J., Mathews, K. R., Godfrey, M., Tiecke, F., Kaufmann, U. C., Vetter, U., Hagemeier, C. & Robinson, P. N., 1999, In : Clinical Genetics. 55, 2, p. 110-117 8 p.

Research output: Contribution to journalArticle

77 Scopus citations

Thrombocytopenia-associated costs in an adult intensive care unit population

Rebuck, J. A., Yee, G. C., Peddicord, T. E., Nelson, C., Cochran, G. L. & Olsen, K. M., 1999, In : Critical care medicine. 27, 12 SUPPL., p. A47

Research output: Contribution to journalArticle

3 Scopus citations
1998

Heritable connective tissue disorders in cervical artery dissections: A prospective study

Schievink, W. I., Wijdicks, E. F. M., Michels, V. V., Vockley, J. & Godfrey, M., Apr 1998, In : Neurology. 50, 4, p. 1166-1169 4 p.

Research output: Contribution to journalArticle

84 Scopus citations
1 Scopus citations

Prenatal diagnosis in congenital contractural arachnodactyly

Belleh, S., Spooner, L., Allanson, J. & Godfrey, M., 1998, In : Genetic Testing. 1, 4, p. 293-296 4 p.

Research output: Contribution to journalArticle

3 Scopus citations

Use of Health Services by Chinese Elderly in Beijing

Foreman, S. E., Yu, L. C., Barley, D. & Chen, L. W., Aug 1998, In : Medical Care. 36, 8, p. 1265-1282 18 p.

Research output: Contribution to journalArticle

12 Scopus citations
1997

Marfan Database (second edition): Software and database for the analysis of mutations in the human FBN1 gene

Collod-Béroud, G., Béroud, C., Adès, L., Black, C., Boxer, M., Brock, D. J., Godfrey, M., Hayward, C., Karttunen, L., Milewicz, D., Peltonen, L., Richards, R. I., Wang, M., Junien, C. & Boileau, C., Jan 1 1997, In : Nucleic acids research. 25, 1, p. 147-150 4 p.

Research output: Contribution to journalArticle

25 Scopus citations

P1148A in fibrillin-1 is not a mutation anymore

Wang, M., Mathews, K. R., Imaizumi, K., Beiraghi, S., Blumberg, B., Scheuner, M., Graham, J. M. & Godfrey, M., Jan 1 1997, In : Nature Genetics. 15, 1, p. 12 1 p.

Research output: Contribution to journalLetter

16 Scopus citations

Three novel fibrillin mutations in exons 25 and 27: Classic versus neonatal Marfan syndrome

Wang, M., Wang, J. Y., Cisler, J., Imaizumi, K., Burton, B. K., Jones, M. C., Lamberti, J. J. & Godfrey, M., 1997, In : Human mutation. 9, 4, p. 359-362 4 p.

Research output: Contribution to journalArticle

20 Scopus citations
1996

An accurate method for comparing transcript levels of two alleles or highly homologous genes: Application to fibrillin transcripts in Marfan patients' fibroblasts

Karttunen, L., Lönnqvist, L., Godfrey, M., Peltonen, L. & Syvänen, A. C., 1996, In : Genome Research. 6, 5, p. 392-403 12 p.

Research output: Contribution to journalArticle

Open Access
16 Scopus citations

Delivery of a hammerhead ribozyme specifically down-regulates the production of fibrillin-1 by cultured dermal fibroblasts

Kilpatrick, M. W., Phylactou, L. A., Godfrey, M., Wu, C. H., Wu, G. Y. & Tsipouras, P., Dec 1996, In : Human Molecular Genetics. 5, 12, p. 1939-1944 6 p.

Research output: Contribution to journalArticle

Open Access
27 Scopus citations

Double mutant fibrillin-1 (FBN1) allele in a patient with neonatal Marfan syndrome

Wang, M., Kishnani, P., Decker-Phillips, M., Kahler, S. G., Chen, Y. T. & Godfrey, M., 1996, In : Journal of medical genetics. 33, 9, p. 760-763 4 p.

Research output: Contribution to journalArticle

Open Access
22 Scopus citations
64 Scopus citations

Variable expression of congenital contractural arachnodactyly due to maternal mosaicism of a fibrillin-2 mutation

Clericuzio, C. L., Wang, M. & Godfrey, M., 1996, In : Journal of Investigative Medicine. 44, 1, p. 131A

Research output: Contribution to journalArticle

Weill-Marchesani syndrome - Possible linkage of the autosomal dominant form to 15q21.1

Wirtz, M. K., Samples, J. R., Kramer, P. L., Rust, K., Yount, J., Acott, T. S., Koler, R. D., Cisler, J., Jahed, A., Gorlin, R. J. & Godfrey, M., Oct 2 1996, In : American journal of medical genetics. 65, 1, p. 68-75 8 p.

Research output: Contribution to journalArticle

37 Scopus citations
1995

Abnormal morphology of fibrillin microfibrils in fibroblast cultures from patients with neonatal Marfan syndrome

Godfrey, M., Raghunath, M., Cisler, J., Bevins, C. L., DePaepe, A., Di Rocco, M., Gregoritch, J., Imaizumi, K., Kaplan, P., Kuroki, Y., Silberbach, M., Superti-Furga, A., Van Thienen, M. N., Vetter, U. & Steinmann, B., 1995, In : American Journal of Pathology. 146, 6, p. 1414-1421 8 p.

Research output: Contribution to journalArticle

30 Scopus citations

Fibrillin immunofluorescence in pseudoxanthoma elasticum

Godfrey, M., Cisler, J., Geerts, M. L., Christiano, A., Uitto, J., Bie, S. D. & DePaepe, A., Apr 1995, In : Journal of the American Academy of Dermatology. 32, 4, p. 589-594 6 p.

Research output: Contribution to journalArticle

4 Scopus citations

Prenatal and presymptomatic diagnosis of the marfan syndrome using fluorescence pcr and an automated sequencer

Wang, M., Mata, J., Price, C. E., Iversen, P. L. & Godfrey, M., Jun 1995, In : Prenatal Diagnosis. 15, 6, p. 499-507 9 p.

Research output: Contribution to journalArticle

7 Scopus citations

Quantitation of fibrillin immunofluorescence in fibroblast cultures in the Marfan syndrome

Schaefer, G. B. & Godfrey, M., Mar 1995, In : Clinical Genetics. 47, 3, p. 144-149 6 p.

Research output: Contribution to journalArticle

8 Scopus citations

Recurrent mis-splicing of fibrillin exon 32 in two patients with neonatal marfan syndrome

Wang, M., Price, C. E., Han, J., Cisler, J., Imaizumi, K., Van Thienen, M. N., Depaepe, A. & Godfrey, M., Apr 1995, In : Human Molecular Genetics. 4, 4, p. 607-613 7 p.

Research output: Contribution to journalArticle

32 Scopus citations
1994

From fluorescence to the gene: The skin in the Marfan syndrome

Godfrey, M., 1994, In : Journal of Investigative Dermatology. 103, 5 SUPPL., p. S58-S62

Research output: Contribution to journalArticle

Open Access
7 Scopus citations

The need for health care reform in Nebraska.

Palm, D. & Frederick, S., Mar 1994, In : The Nebraska medical journal. 79, 3, p. 54-61 8 p.

Research output: Contribution to journalArticle

1 Scopus citations
1993

Decreased extracellular deposition of fibrillin and decorin in neonatal Marfan syndrome fibroblasts

Raghunath, M., Superti-Furga, A., Godfrey, M. & Steinmann, B., Jan 1993, In : Human genetics. 90, 5, p. 511-515 5 p.

Research output: Contribution to journalArticle

44 Scopus citations

Elastin and fibrillin mrna and protein levels in the ontogeny of normal human aorta

Godfrey, M., Nejezchleb, P. A., Schaefer, G. B., Minion, D. J., Wang, Y. & Baxter, B. T., 1993, In : Connective Tissue Research. 29, 1, p. 61-69 9 p.

Research output: Contribution to journalArticle

24 Scopus citations
11 Scopus citations

Prenatal diagnosis and a donor splice site mutation in fibrillin in a family with Marfan syndrome

Godfrey, M., Vandemark, N., Wang, M., Velinov, M., Wargowski, D., Tsipouras, P., Han, J., Becker, J., Robertson, W., Droste, S. & Rao, V. H., 1993, In : American Journal of Human Genetics. 53, 2, p. 472-480 9 p.

Research output: Contribution to journalArticle

57 Scopus citations
1992

Genetic linkage of the marfan syndrome, ectopia lentis, and congenital contractural arachnodactyly to the fibrillin genes on chromosomes 15 and 5

Peter A. Famdon,Birmingham Maternity Hospital, Birmingham, United Kingdom; Maureen Boxer, Ninewells Medical School, Dundee, United Kingdom; David J.H. Brock, Caroline Hayward. and Marion Keston, University of Edinburgh, Edinburgh, United Kingdom; Dianna M. Milewicz, University of Texas, Houston; Peter H. Byers, University of Washington, Seattle; Andrea Superti-Furga, University of Zurich, Zurich, Switzerland; Rajkumar S. Ramesar, University of Cape Town Medical School, Cape Town, South Africa; Margaret Anne Davee and David D. Weaver. Indiana University. Indianapolis; Stephen Wainer. University of Witwatersrand, Johannesburg, South Africa; and Randi Kramer-Fox, Cornell Medical Center~ New York., Apr 2 1992, In : New England Journal of Medicine. 326, 14, p. 905-909 5 p.

Research output: Contribution to journalArticle

222 Scopus citations

Repeated helical epitopes of defined amino acid sequence in human type III collagen identified by monoclonal antibodies

Hisae, H., Keene, D. R., Sakai, L. Y., Wirtz, M. K., Bächinger, H. P., Godfrey, M. & Hollister, D. W., Jun 1992, In : Molecular Immunology. 29, 6, p. 759-770 12 p.

Research output: Contribution to journalArticle

11 Scopus citations
1991

Characterization of a COL1A1 splicing defect in a case of Ehlers-Danlos syndrome type VII: Further evidence of molecular homogeneity

D'Alessio, M., Ramirez, F., Blumberg, B. D., Wirtz, M. K., Rao, V. H., Godfrey, M. D. & Hollister, D. W., 1991, In : American Journal of Human Genetics. 49, 2, p. 400-406 7 p.

Research output: Contribution to journalArticle

30 Scopus citations

G/A polymorphism in an intron of the fibrillin gene FBNI

Hewett, D. R., Lynch, J. R., Godfrey, M. & Sykes, B. C., Dec 25 1991, In : Nucleic acids research. 19, 24, p. 6975 1 p.

Research output: Contribution to journalArticle

4 Scopus citations

Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes

Lee, B., Godfrey, M., Vitale, E., Hori, H., Mattei, M. G., Sarfarazi, M., Tsipouras, P., Ramirez, F. & Hollister, D. W., 1991, In : Nature. 352, 6333, p. 330-334 5 p.

Research output: Contribution to journalArticle

526 Scopus citations
1990

Cosegregation of elastin-associated microfibrillar abnormalities with the Marfan phenotype in families

Godfrey, M., Menashe, V., Weleber, R. G., Koler, R. D., Bigley, R. H., Lovrien, E., Zonana, J. & Hollister, D. W., 1990, In : American Journal of Human Genetics. 46, 4, p. 652-660 9 p.

Research output: Contribution to journalArticle

61 Scopus citations

Immunohistologic Abnormalities of the Microfibrillar-Fiber System in the Marfan Syndrome

Hollister, D. W., Godfrey, M., Sakai, L. Y. & Pyeritz, R. E., Jul 19 1990, In : New England Journal of Medicine. 323, 3, p. 152-159 8 p.

Research output: Contribution to journalArticle

272 Scopus citations