Medical & Molecular Genetics

Publications

1993

Reluctance to undergo predictive testing: The case of Huntington Disease

Quaid, K. A. & Morris, M., Jan 20 1993, In : American journal of medical genetics. 45, 1, p. 41-45 5 p.

Research output: Contribution to journalArticle

146 Scopus citations

Tissue specific and developmental expression of rat long-and medium-chain acyl-CoA dehydrogenases

Hainline, B. E., Kahlenbeck, D. J., Grant, J. & Strauss, A. W., Dec 14 1993, In : BBA - Gene Structure and Expression. 1216, 3, p. 460-468 9 p.

Research output: Contribution to journalArticle

34 Scopus citations
1992

Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15

Young, K., Foroud, T., Williams, P., Jackson, C. E., Beckmann, J. S., Cohen, D., Conneally, P. M., Tischfield, J. & Hodes, M. E., Aug 1992, In : Genomics. 13, 4, p. 1370-1371 2 p.

Research output: Contribution to journalArticle

38 Scopus citations

Linkage of the Indiana kindred of gerstmann-sträussler-scheinker disease to the prion protein gene

Dlouhy, S. R., Hsiao, K., Farlow, M. R., Foroud, T., Conneally, P. M., Johnson, P., Prusiner, S. B., Hodes, M. E. & Ghetti, B., Apr 1992, In : Nature genetics. 1, 1, p. 64-67 4 p.

Research output: Contribution to journalArticle

176 Scopus citations

Mutant prion proteins in gerstmann-sträussler-scheinker disease with neurofibrillary tangles

Hsiao, K., Dlouhy, S. R., Farlow, M. R., Cass, C., Da Costa, M., Conneally, P. M., Hodes, M. E., Ghetti, B. & Prusiner, S. B., Apr 1992, In : Nature genetics. 1, 1, p. 68-71 4 p.

Research output: Contribution to journalArticle

204 Scopus citations

New variant in exon 3 of the proteolipid protein (PLP) gene in a family with Pelizaeus-Merzbacher disease

Pratt, V. M., Trofatter, J. A., Larsen, M. B., Hodes, M. E. & Dlouhy, S. R., Jun 15 1992, In : American journal of medical genetics. 43, 3, p. 642-646 5 p.

Research output: Contribution to journalArticle

20 Scopus citations

Presymptomatic testing for huntington diseases: Recommendations for counseling

Quaid, K. A., Dec 1 1992, In : Journal of Genetic Counseling. 1, 4, p. 277-302 26 p.

Research output: Contribution to journalArticle

35 Scopus citations

Retroviral-Mediated Gene Transfer of Bone Marrow Cells during Autologous Bone Marrow Transplantation for Acute Leukemia. University of Indiana

Cornetta, K., Tricot, G., Broun, E. R., Hromas, R., Srour, E., Hoffman, R., Anderson, W. F., Moen, R. C. & Morgan, R. A., Jun 1 1992, In : Human gene therapy. 3, 3, p. 305-318 14 p.

Research output: Contribution to journalArticle

17 Scopus citations

SAFETY ASPECTS OF GENE THERAPY

Cornetta, K., Apr 1992, In : British journal of haematology. 80, 4, p. 421-426 6 p.

Research output: Contribution to journalArticle

35 Scopus citations
1991

Ahall polymorphism in human X-linked proteolipid protein gene (PLP)

Trofatter, J. A., Pratt, V. M., Dlouhy, S. R. & Hodes, M. E., Nov 11 1991, In : Nucleic acids research. 19, 21, 1 p.

Research output: Contribution to journalArticle

19 Scopus citations

A new mutation in the proteolipid protein (PLP) gene in a German family with Pelizaeus-Merzbacher disease

Pratt, V. M., Trofatter, J. A., Schinzel, A., Dlouhy, S. R., Conneally, P. M. & Hodes, M. E., Feb 11 1991, In : American journal of medical genetics. 38, 1, p. 136-139 4 p.

Research output: Contribution to journalArticle

34 Scopus citations

No retroviremia or pathology in long-term follow-up of monkeys exposed to a murine amphotropic retrovirus

Cornetta, K., Morgan, R. A., Gillio, A., Sturm, S., Baltrucki, L., O'Reilly, R. & Anderson, W. F., 1991, In : Human gene therapy. 2, 3, p. 215-219 5 p.

Research output: Contribution to journalArticle

67 Scopus citations

Predictive testing for HD: maximizing patient autonomy.

Quaid, K. A., Dec 1 1991, In : The Journal of clinical ethics. 2, 4, p. 238-240 3 p.

Research output: Contribution to journalArticle

7 Scopus citations

Safety issues related to retroviral-mediated gene transfer in humans

Cornetta, K., Morgan, R. A. & Anderson, W. F., 1991, In : Human gene therapy. 2, 1, p. 5-14 10 p.

Research output: Contribution to journalReview article

187 Scopus citations

Salivary androgen-binding protein variation in Mus and other rodents

Karn, R. C. & Dlouhy, S. R., Nov 1991, In : Journal of Heredity. 82, 6, p. 453-458 6 p.

Research output: Contribution to journalArticle

27 Scopus citations

Unique cerebellar phenotype combining granule and Purkinje cell loss: Morphological evidence for weaver*pcd double mutant mice

Ghetti, B., Triarhou, L. C., Alyea, C. J., Dlouhy, S. R. & Karn, R. C., Jan 1 1991, In : Journal of Neurocytology. 20, 1, p. 27-38 12 p.

Research output: Contribution to journalArticle

6 Scopus citations
1990

Amphotropic Murine Leukemia Retrovirus Is Not an Acute Pathogen for Primates

Cornetta, K., Moen, R. C., Morgan, R. A., McLachlin, J. R., Sturm, S., Selegue, J., Anderson, W. F., Culver, K., Blaese, R. M., London, W., Cornetta, K. & Moen, R. C., Apr 1 1990, In : Human gene therapy. 1, 1, p. 15-30 16 p.

Research output: Contribution to journalArticle

143 Scopus citations

Applications of the Polymerase Chain Reaction in Retroviral-Mediated Gene Transfer and the Analysis of Gene-Marked Human TIL Cells

Morgan, R. A., Cornetta, K. & Anderson, W. F., Jul 1 1990, In : Human gene therapy. 1, 2, p. 135-149 15 p.

Research output: Contribution to journalArticle

93 Scopus citations

Fetal brain disruption sequence

Moore, C. A., Weaver, D. D. & Bull, M. J., Mar 1990, In : The Journal of pediatrics. 116, 3, p. 383-386 4 p.

Research output: Contribution to journalArticle

30 Scopus citations

Gene transfer into humans — immunotherapy of patients with advanced melanoma, using tumor-infiltrating lymphocytes modified by retroviral gene transduction

Rosenberg, S. A., Aebersold, P., Cornetta, K., Kasid, A., Morgan, R. A., Moen, R., Karson, E. M., Lotze, M. T., Yang, J. C., Topalian, S. L., Merino, M. J., Culver, K., Miller, A. D., Blaese, R. M. & Anderson, W. F., Aug 30 1990, In : New England Journal of Medicine. 323, 9, p. 570-578 9 p.

Research output: Contribution to journalArticle

959 Scopus citations

Informed consent for a prescription drug: Impact of disclosed information on patient understanding and medical outcomes

Quaid, K. A., Faden, R. R., Vining, E. P. & Freeman, J. M., Jun 1990, In : Patient Education and Counseling. 15, 3, p. 249-259 11 p.

Research output: Contribution to journalArticle

29 Scopus citations

In Vivo Expression and Survival of Gene-Modified T Lymphocytes in Rhesus Monkeys

Culver, K. W., Morgan, R. A., Osborne, W. R. A., Lee, R. T., Lenschow, D., Able, C., Cornetta, K., Anderson, W. F. & Blaese, R. M., Dec 1 1990, In : Human gene therapy. 1, 4, p. 399-410 12 p.

Research output: Contribution to journalArticle

43 Scopus citations

Mouse transgenes in human cells detect specific base substitutions

Schaff, D. A., Jarrett, R. A., Dlouhy, S. R., Ponniah, S., Stockelman, M., Stambrook, P. J. & Tischfield, J. A., Jan 1 1990, In : Proceedings of the National Academy of Sciences of the United States of America. 87, 21, p. 8675-8679 5 p.

Research output: Contribution to journalArticle

Open Access
4 Scopus citations

Prenatal testing for Huntington disease

Corson, V., Quaid, K., Kasch, L. & Kazazian, H. H., Dec 1 1990, In : Birth Defects: Original Article Series. 26, 3, p. 226-230 5 p.

Research output: Contribution to journalArticle

2 Scopus citations

Retroviral-Mediated Gene Transfer

McLachlin, J. R., Cornetta, K., Eglitis, M. A. & Anderson, W. F., Jan 1 1990, In : Progress in nucleic acid research and molecular biology. 38, C, p. 91-135 45 p.

Research output: Contribution to journalArticle

60 Scopus citations

The Moebius syndrome: Aetiology, incidence of mental retardation, and genetics

Lipson, T., Webster, W. & Weaver, D. D., Jan 1 1990, In : Journal of Medical Genetics. 27, 8, p. 533-535 3 p.

Research output: Contribution to journalLetter

9 Scopus citations

Unilateral duplication of the cerebellar hemisphere and internal, middle, and external ear: A clinical case study

Jackson, J. M., Sadove, A. M., Weaver, D. D., Edwards, M. K. & Bull, M. J., Sep 1990, In : Plastic and reconstructive surgery. 86, 3, p. 550-553 4 p.

Research output: Contribution to journalArticle

6 Scopus citations
1989

Denaturing Gradient Gel Analysis of Single‐Base Substitutions at a Mouse Adenine Phosphoribosyltransferase Splice Acceptor Site

Dlouhy, S. R., Schaff, D. A., Trofatter, J. A., Liu, HS. S., Stambrook, P. J. & Tischfield, J. A., 1989, In : Molecular Carcinogenesis. 2, 4, p. 217-225 9 p.

Research output: Contribution to journalArticle

4 Scopus citations

Familial distal arthrogryposis with craniofacial abnormalities: A new subtype of type II?

Moore, C. A. & Weaver, D. D., Jan 1 1989, In : American journal of medical genetics. 33, 2, p. 231-237 7 p.

Research output: Contribution to journalArticle

13 Scopus citations

Gene Transfer into Primates and Prospects for Gene Therapy in Humans

Cornetta, K., Wieder, R. & Anderson, W. F., Jan 1 1989, In : Progress in nucleic acid research and molecular biology. 36, C, p. 311-322 12 p.

Research output: Contribution to journalArticle

19 Scopus citations

Gerstmann-straussler-scheinker disease. I. extending the clinical spectrum

Farlow, M. R., Yee, R. D., Dlouhy, S. R., Conneally, P. M., Azzarelli, B. & Ghetti, B., Nov 1989, In : Neurology. 39, 11, p. 1446-1452 7 p.

Research output: Contribution to journalArticle

79 Scopus citations

Gerstmann-sträussler-scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family

Ghetti, B., Tagliavini, F., Masters, C. L., Beyreuther, K., Ciaccone, G., Verga, L., Farlow, M. R., Conneally, P. M., Dlouhy, S. R., Azzarelli, B. & Bugiani, O., Nov 1989, In : Neurology. 39, 11, p. 1453-1461 9 p.

Research output: Contribution to journalArticle

155 Scopus citations

Holoprosencephaly, ear abnormalities, congenital heart defect, and microphallus in a patient with 11q- mosaicism

Helmuth, R. A., Weaver, D. D. & Wills, E. R., Jan 1 1989, In : American journal of medical genetics. 32, 2, p. 178-181 4 p.

Research output: Contribution to journalArticle

15 Scopus citations

Knowledge, attitude, and the decision to be tested for Huntington's disease

Quaid, K. A., Brandt, J., Faden, R. R. & Folstein, S. E., Dec 12 1989, In : Clinical Genetics. 36, 6, p. 431-438 8 p.

Research output: Contribution to journalArticle

31 Scopus citations

Larsen syndrome and craniosynostosis: Idaho syndrome?

Escobar, L. F., Bixler, D., Weaver, D. D., Bull, M. J. & Bader, P., Dec 1 1989, In : Dysmorphology and Clinical Genetics. 3, 2, p. 24-27 4 p.

Research output: Contribution to journalArticle

1 Scopus citations

Pelizaeus-Merzbacher disease: Tight linkage to proteolipid protein gene exon variant

Trofatter, J. A., Dlouhy, S. R., DeMyer, W., Conneally, P. M. & Hodes, M. E., Dec 22 1989, In : Proceedings of the National Academy of Sciences of the United States of America. 86, 23, p. 9427-9430 4 p.

Research output: Contribution to journalArticle

91 Scopus citations

Presymptomatic Diagnosis of Delayed-Onset Disease With Linked DNA Markers: The Experience in Huntington’s Disease

Brandt, J., Quaid, K. A., Folstein, S. E., Garber, P., Maestri, N. E., Abbott, M. H., Slavney, P. R., Franz, M. L., Kasch, L. & Kazazian, H. H., Jun 2 1989, In : JAMA: The Journal of the American Medical Association. 261, 21, p. 3108-3114 7 p.

Research output: Contribution to journalArticle

93 Scopus citations

Presymptomatic DNA testing for Huntington's disease

Brandt, J., Quaid, K. A. & Folstein, S. E., Jan 1 1989, In : Journal of Neuropsychiatry and Clinical Neurosciences. 1, 2, p. 195-197 3 p.

Research output: Contribution to journalArticle

7 Scopus citations
1988

An unusual craniofacial condition: Holoprosencephaly, ocular hyperterolism, and anterior encephalocele associated with tissue bands

Moore, C. A., Weaver, D. D. & DeMyer, W. E., Jan 1 1988, In : Dysmorphology and Clinical Genetics. 2, 3, p. 68-71 4 p.

Research output: Contribution to journalArticle

2 Scopus citations

A survey of prenatally diagnosed disorders

Weaver, D. D., Jan 1 1988, In : Clinical Obstetrics and Gynecology. 31, 2, p. 253-269 17 p.

Research output: Contribution to journalArticle

6 Scopus citations

Autosomal Recessive Transmission of Neuroectodermal Syndrome

Zunich, J., Esterly, N. B. & Kaye, C. I., Aug 1988, In : Archives of Dermatology. 124, 8, p. 1188-1189 2 p.

Research output: Contribution to journalLetter

9 Scopus citations

Fetal craniofacial morphometrics: In utero evaluation at 16 weeks’ gestation

Escobar, L. F., Bixler, D., Padilla, L. M. & Weaver, D. D., Oct 1988, In : Obstetrics and gynecology. 72, 4, p. 674-679 6 p.

Research output: Contribution to journalArticle

14 Scopus citations

Localization of the gene for X-linked nephrogenic diabetes insipidus to Xq28

Kambouris, M., Dlouhy, S. R., Trofatter, J. A., Conneally, P. M. & Hodes, M. E., Jan 1 1988, In : American Journal of Medical Genetics. 29, 1, p. 239-246 8 p.

Research output: Contribution to journalArticle

37 Scopus citations

Mouse placental 57-kDa calcium-binding protein: II. Localization of mRNA in mouse and human placentae by in situ cDNA hybridization

Tuan, R. S., Lamb, B. T. & Jesinkey, C. B., 1988, In : Differentiation. 37, 3, p. 198-204 7 p.

Research output: Contribution to journalArticle

14 Scopus citations

Neural tube defects and omphalocele in trisomy 18

Moore, C. A., Harmon, J. P., Padilla, LM. M., Castro, V. B. & Weaver, D. D., Aug 1988, In : Clinical Genetics. 34, 2, p. 98-103 6 p.

Research output: Contribution to journalArticle

23 Scopus citations
1987

A counseling guide to the Martin-Bell syndrome.

Weaver, D. D. & Sherman, S. L., Jan 1987, In : American journal of medical genetics. 26, 1, p. 39-44 6 p.

Research output: Contribution to journalArticle

4 Scopus citations

Brief clinical report: A syndrome of microcephaly, eye anomalies, short stature, and mental deficiency

Bouwes Bavinck, J. N., Weaver, D. D., Ellis, F. D. & Ward, R. E., Jan 1 1987, In : American Journal of Medical Genetics. 26, 4, p. 825-831 7 p.

Research output: Contribution to journalArticle

10 Scopus citations

Localization of the gene for a syndrome of X-linked skeletal dysplasia and mental retardation to Xq27-qter

Dlouhy, S. R., Christian, J. C., Haines, J. L., Conneally, P. M. & Hodes, M. E., Feb 1 1987, In : Human genetics. 75, 2, p. 136-139 4 p.

Research output: Contribution to journalArticle

16 Scopus citations

Prenatal screening and pregnant women's attitudes toward the abortion of defective fetuses

Faden, R. R., Chwalow, A. J., Quaid, K., Chase, G. A., Lopes, C., Leonard, C. O. & Holtzman, N. A., Jan 1 1987, In : American journal of public health. 77, 3, p. 288-290 3 p.

Research output: Contribution to journalArticle

Open Access
38 Scopus citations

Presymptomatic testing for Huntington chorea: Guidelines for moral and social accountability

Smurl, J. F. & Weaver, D. D., Feb 1 1987, In : American journal of medical genetics. 26, 2, p. 247-257 11 p.

Research output: Contribution to journalArticle

18 Scopus citations