Tatiana Foroud

  • 82108 Citations
  • 114 h-Index
1976 …2020

Research output per year

If you made any changes in Pure these will be visible here soon.

Publications

1997

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17

Murrell, J. R., Koller, D., Foroud, T., Goedert, M., Spillantini, M. G., Edenberg, H. J., Farlow, M. R. & Ghetti, B., Nov 1997, In : American Journal of Human Genetics. 61, 5, p. 1131-1138 8 p.

Research output: Contribution to journalArticle

64 Scopus citations

Genomewide search for genes influencing percent body fat in Pima Indians: Suggestive linkage at chromosome 11q21-q22

Norman, R. A., Thompson, D. B., Foroud, T., Garvey, W. T., Bennett, P. H., Bogardus, C., Ravussin, E., Allan, C., Baier, L., Bowden, D., Hanson, R., Knowler, W., Kobes, S., Pettitt, D. & Prochazka, M., Jan 1997, In : American Journal of Human Genetics. 60, 1, p. 166-173 8 p.

Research output: Contribution to journalArticle

130 Scopus citations

Genomic survey of bipolar illness in the NIMH genetics initiative pedigrees: A preliminary report

Nurnberger, J. I., DePaulo, J. R., Gershon, E. S., Reich, T., Blehar, M. C., Edenberg, H. J., Foroud, T., Miller, M., Bowman, E., Mayeda, A., Rau, N. L., Smiley, C., Conneally, P. M., McMahon, F., Meyers, D., Simpson, S., McInnis, M., Stine, O. C., Detera-Wadleigh, S., Goldin, L. & 9 others, Guroff, J., Maxwell, E., Kazuba, D., Gejman, P. V., Badner, J., Sanders, A., Rice, J., Bierut, L. & Goate, A., 1997, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 74, 3, p. 227-237 11 p.

Research output: Contribution to journalArticle

115 Scopus citations

Initial genome scan of the nimh genetics initiative bipolar pedigrees: Chromosomes 1, 6, 8, 10, and 12

Rice, J. P., Goate, A., Williams, J. T., Bierut, L., Dorr, D., Wu, W., Shears, S., Gopalakrishnan, G., Edenberg, H. J., Foroud, T., Nurnberger, J., Gershon, E. S., Detera-Wadleigh, S. D., Goldin, L. R., Guroff, J. J., McMahon, F. J., Simpson, S., MacKinnon, D., McInnis, M., Stine, O. C. & 3 others, DePaulo, J. R., Blehar, M. C. & Reich, T., 1997, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 74, 3, p. 247-253 7 p.

Research output: Contribution to journalArticle

109 Scopus citations

Initial genome scan of the NIMH genetics initiative bipolar pedigrees: Chromosomes 4, 7, 9, 18, 19, 20, and 21q

Detera-Wadleigh, S. D., Badner, J. A., Yoshikawa, T., Sanders, A. R., Goldin, L. R., Turner, G., Rolling, D. Y., Moses, T., Guroff, J. J., Kazuba, D., Maxwell, M. E., Edenberg, H. J., Foroud, T., Lahiri, D., Nurnberger, J. I., Stine, O. C., McMahon, F., Meyers, D. A., MacKinnon, D., Simpson, S. & 7 others, McInnis, M., DePaulo, J. R., Rice, J., Goate, A., Reich, T., Blehar, M. C. & Gershon, E. S., 1997, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 74, 3, p. 254-262 9 p.

Research output: Contribution to journalArticle

115 Scopus citations

Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: Chromosomes 2, 11, 13, 14, and x

Stine, O. C., McMahon, F. J., Chen, L. S., Xu, J., Meyers, D. A., MacKinnon, D. F., Simpson, S., McInnis, M. G., Rice, J. P., Goate, A., Reich, T., Edenberg, H. J., Foroud, T., Nurnberger, J. I., Detera-Wadleigh, S. D., Goldin, L. R., Guroff, J., Gershon, E. S., Blehar, M. C. & DePaulo, J. R., Jun 26 1997, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 74, 3, p. 263-269 7 p.

Research output: Contribution to journalArticle

93 Scopus citations

Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: Chromosomes 3, 5, 15, 16, 17, and 22

Edenberg, H. J., Foroud, T., Conneally, P. M., Sorbel, J. J., Carr, K., Crose, C., Willig, C., Zhao, J., Miller, M., Bowman, E., Mayeda, A., Rau, N. L., Smiley, C., Rice, J. P., Goate, A., Reich, T., Stine, O. C., McMahon, F., DePaulo, J. R., Meyers, D. & 5 others, Detera-Wadleigh, S. D., Goldin, L. R., Gershon, E. S., Blehar, M. C. & Nurnberger, J. I., Jun 26 1997, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 74, 3, p. 238-246 9 p.

Research output: Contribution to journalArticle

144 Scopus citations

Introduction to genetic linkage analysis

Foroud, T., Jan 1 1997, In : Cancer Investigation. 15, 6, p. 548-552 5 p.

Research output: Contribution to journalReview article

1 Scopus citations

Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32

Nichols, W. C., Koller, D. L., Slovis, B., Foroud, T., Terry, V. H., Arnold, N. D., Siemieniak, D. R., Wheeler, L., Phillips, J. A., Newman, J. H., Conneally, P. M., Ginsburg, D. & Loyd, J. E., Mar 1 1997, In : Nature genetics. 15, 3, p. 277-280 4 p.

Research output: Contribution to journalArticle

221 Scopus citations

Spheroid body myopathy revisited

Goebel, H. H., D'Agostino, A. N., Wilson, J., Cole, G., Foroud, T., Koller, D., Farlow, M., Azzarelli, B. & Muller, J., 1997, In : Muscle and Nerve. 20, 9, p. 1127-1136 10 p.

Research output: Contribution to journalArticle

22 Scopus citations
1996

Motor changes in presymptomatic Huntington disease gene carriers

Siemers, E., Foroud, T., Bill, D. J., Sorbel, J., Norton, J. A., Hodes, M. E., Niebler, G., Conneally, P. M. & Christian, J. C., Jun 1996, In : Archives of Neurology. 53, 6, p. 487-492 6 p.

Research output: Contribution to journalArticle

60 Scopus citations
1995

Cognitive scores in carriers of huntington's disease gene compared to noncarriers

Foroud, T., Siemers, E., Kleindorfer, D., Bill, D. J., Hodes, M. E., Norton, J. A., Conneally, P. M. & Christian, J. C., May 1995, In : Annals of neurology. 37, 5, p. 657-664 8 p.

Research output: Contribution to journalArticle

112 Scopus citations

Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertension

Loyd, J. E., Butler, M. C., Foroud, T. M., Conneally, P. M., Phillips, J. A. & Newman, J. H., Jul 1995, In : American journal of respiratory and critical care medicine. 152, 1, p. 93-97 5 p.

Research output: Contribution to journalArticle

189 Scopus citations
1994

Possible localization of a major gene for cleft lip and palate to 4q

Beiraghi, S., Foroud, T., Diouhy, S., Bixler, D., Conneally, P. M., Delozier‐Blanchet, D. & Hodes, M. E., Sep 1994, In : Clinical Genetics. 46, 3, p. 255-256 2 p.

Research output: Contribution to journalArticle

52 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
1991

Gene mapping using linkage analysis.

Sanal, O., Foroud, T. & Gatti, R. A., Jan 1 1991, In : The Turkish journal of pediatrics. 33, 1, p. 1-12 12 p.

Research output: Contribution to journalArticle

Localization of an ataxia-telangiectasia locus to a 3-cM interval on chromosome 11q23: Linkage analysis of III families by an international consortium

Foroud, T., Wei, S., Ziv, Y., Sobel, E., Lange, E., Chao, A., Goradia, T., Huo, Y., Tolun, A., Chessa, L., Charmley, P., Sanal, O., Salman, N., Julier, C., Concannon, P., McConville, C., Taylor, A. M. R., Shiloh, Y., Lange, K. & Gatti, R. A., Dec 1 1991, In : American Journal of Human Genetics. 49, 6, p. 1263-1279 17 p.

Research output: Contribution to journalArticle

42 Scopus citations

The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22-q23

Ziv, Y., Rotman, G., Frydman, M., Dagan, J., Cohen, T., Foroud, T., Gatti, R. A. & Shiloh, Y., Feb 1991, In : Genomics. 9, 2, p. 373-375 3 p.

Research output: Contribution to journalArticle

43 Scopus citations
1990

A primary linkage map of the human chromosome 11q22-23 region

Charmley, P., Foroud, T., Wei, S., Concannon, P., Weeks, D. E., Lange, K. & Gatti, R. A., Feb 1990, In : Genomics. 6, 2, p. 316-323 8 p.

Research output: Contribution to journalArticle

24 Scopus citations

Further mapping of an ataxia-telangiectasia locus to the chromosome 11q23 region

Sanal, O., Wei, S., Foroud, T., Malhotra, U., Concannon, P., Charmley, P., Salser, W., Lange, K. & Gatti, R. A., Nov 21 1990, In : American Journal of Human Genetics. 47, 5, p. 860-866 7 p.

Research output: Contribution to journalArticle

29 Scopus citations
1988

Localization of an ataxia-telangiectasia gene to chromosome 11q22-23

Gatti, R. A., Berkel, I., Boder, E., Braedt, G., Charmley, P., Concannon, P., Ersoy, F., Foroud, T., Jaspers, N. G. J., Lange, K., Lathrop, G. M., Leppert, M., Nakamura, Y., O'Connell, P., Paterson, M., Salser, W., Sanal, O., Silver, J., Sparkes, R. S., Susi, E. & 4 others, Weeks, D. E., Wei, S., White, R. & Yoder, F., 1988, In : Nature. 336, 6199, p. 577-580 4 p.

Research output: Contribution to journalArticle

524 Scopus citations