Tatiana Foroud

  • 54092 Citations
  • 108 h-Index
1976 …2020

Research output per year

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

Publications

Filter
Article
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., Jan 1 1988, In : Nature. 336, 6199, p. 577-580 4 p.

Research output: Contribution to journalArticle

523 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
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
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
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
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

111 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
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
1997

Association of the angiotensinogen gene to serum angiotensinogen in blacks and whites

Bloem, L. J., Foroud, T. M., Ambrosius, W. T., Hanna, M. P., Tewksbury, D. A. & Pratt, J. H., May 1997, In : Hypertension. 29, 5, p. 1078-1082 5 p.

Research output: Contribution to journalArticle

73 Scopus citations

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 1 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., Jun 26 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., Jun 26 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., Jun 26 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

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., Sep 2 1997, In : Muscle and Nerve. 20, 9, p. 1127-1136 10 p.

Research output: Contribution to journalArticle

22 Scopus citations
1998

A family-based analysis of the association of the dopamine D2 receptor (DRD2) with alcoholism

Edenberg, H. J., Foroud, T., Koller, D. L., Goate, A., Rice, J., Van Eerdewegh, P., Reich, T., Cloninger, C. R., Nurnberger, J. I., Kowalczuk, M., Wu, B., Li, T. K., Conneally, P. M., Tischfield, J. A., Wu, W., Shears, S., Crowe, R., Hesselbrock, V., Schuckit, M., Porjesz, B. & 1 others, Begleiter, H., Jan 1 1998, In : Alcoholism: Clinical and Experimental Research. 22, 2, p. 505-512 8 p.

Research output: Contribution to journalArticle

98 Scopus citations

A family-based analysis of whether the functional promoter alleles of the serotonin transporter gene HTT affect the risk for alcohol dependence

Edenberg, H. J., Reynolds, J., Koller, D. L., Begleiter, H., Bucholz, K. K., Conneally, P. M., Crowe, R., Goate, A., Hesselbrock, V., Li, T. K., Nurnberger, J. I., Porjesz, B., Reich, T., Rice, J. P., Schuckit, M., Tischfield, J. A. & Foroud, T., Aug 1998, In : Alcoholism: Clinical and Experimental Research. 22, 5, p. 1080-1085 6 p.

Research output: Contribution to journalArticle

84 Scopus citations

Amplitude of visual P3 event-related potential as a phenotypic marker for a predisposition to alcoholism: Preliminary results from the COGA project

Porjesz, B., Begleiter, H., Reich, T., Van Eerdewegh, P., Edenberg, H. J., Foroud, T., Goate, A., Litke, A., Chorlian, D. B., Stimus, A., Rice, J., Blangero, J., Almasy, L., Sorbell, J., Bauer, L. O., Kuperman, S., O'Connor, S. J. & Rohrbaugh, J., Sep 1 1998, In : Alcoholism: Clinical and Experimental Research. 22, 6, p. 1317-1323 7 p.

Research output: Contribution to journalArticle

105 Scopus citations

An autosomal genomic scan for loci linked to prediabetic phenotypes in pima indians

Pratley, R. E., Thompson, D. B., Prochazka, M., Baier, L., Mott, D., Ravussin, E., Sakul, H., Ehm, M. G., Burns, D. K., Foroud, T., Garvey, W. T., Hanson, R. L., Knowler, W. C., Bennett, P. H. & Bogardus, C., Apr 15 1998, In : Journal of Clinical Investigation. 101, 8, p. 1757-1764 8 p.

Research output: Contribution to journalArticle

Open Access
205 Scopus citations

An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians

Hanson, R. L., Ehm, M. G., Pettitt, D. J., Prochazka, M., Thompson, D. B., Timberlake, D., Foroud, T., Kobes, S., Baier, L., Burns, D. K., Almasy, L., Blangero, J., Garvey, W. T., Bennett, P. H. & Knowler, W. C., Jan 1 1998, In : American Journal of Human Genetics. 63, 4, p. 1130-1138 9 p.

Research output: Contribution to journalArticle

421 Scopus citations

Anxiety proneness linked to epistatic loci in genome scan of human personality traits

Cloninger, C. R., Van Eerdewegh, P., Goate, A., Edenberg, H. J., Blangero, J., Hesselbrock, V., Reich, T., Nurnberger, J., Schuckit, M., Porjesz, B., Crowe, R., Rice, J. P., Foroud, T., Przybeck, T. R., Almasy, L., Bucholz, K., Wu, W., Shears, S., Carr, K., Crose, C. & 6 others, Willig, C., Zhao, J., Tischfield, J. A., Li, T. K., Conneally, P. M. & Begleiter, H., Jul 10 1998, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 81, 4, p. 313-317 5 p.

Research output: Contribution to journalArticle

133 Scopus citations

A quantitative trait locus for alcohol consumption in selectively bred rat lines

Carr, L. G., Foroud, T., Bice, P., Gobbett, T., Ivashina, J., Edenberg, H., Lumeng, L. & Li, T. K., Jan 1 1998, In : Alcoholism: Clinical and Experimental Research. 22, 4, p. 884-887 4 p.

Research output: Contribution to journalArticle

172 Scopus citations

Autosomal genomic scan for loci linked to obesity and energy metabolism in Pima Indians

Norman, R. A., Tataranni, P. A., Pratley, R., Thompson, D. B., Hanson, R. L., Prochazka, M., Baier, L., Ehm, M. G., Sakul, H., Foroud, T., Garvey, W. T., Burns, D., Knowler, W. C., Bennett, P. H., Bogardus, C. & Ravussin, E., Mar 1998, In : American Journal of Human Genetics. 62, 3, p. 659-668 10 p.

Research output: Contribution to journalArticle

171 Scopus citations

Chromosome 6 workshop

Nurnberger, J. I. & Foroud, T., Jan 1 1998, In : Psychiatric genetics. 8, 2, p. 79-83 5 p.

Research output: Contribution to journalArticle

6 Scopus citations

Evidence for a susceptibility locus for bipolar disorder on chromosome 11p11.5

McInnis, M. G., MacKinnon, D. F., McMahon, F. J., Foroud, T., Edenberg, H. J., Goate, A., Detera-Wadleigh, S., Stine, O. C., Rice, J., Blehar, M., Reich, T., Gershon, E., Nurnberger, J. I., Simpson, S. G. & DePaulo, J. R., Nov 6 1998, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 81, 6, 1 p.

Research output: Contribution to journalArticle

3 Scopus citations

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

Loyd, J. E., Butler, M. G., Foroud, T. M., Conneally, P. M., Phillips, I. A. & Newman, I. H., Dec 1 1998, In : Pneumologie. 52, 4, 1 p.

Research output: Contribution to journalArticle

Genomewide scan of affected relative pairs using the NIMH Genetics Initiative Bipolar affective Disorder pedigrees

Foroud, T., Castellucio, P. F., Koller, D. L., Edenberg, H. J., Goate, A., Detera-Wadleigh, S., Stine, O. C., McMahon, F. J., McInnis, M. G., Rice, J., Blehar, M., Goldin, L. R., Badner, J., Guroff, J., Reich, T., DePaulo, J. R., Gershon, E. & Nurnberger, J. I., Nov 6 1998, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 81, 6, 1 p.

Research output: Contribution to journalArticle

13 Scopus citations

Genome-wide search for genes affecting the risk for alcohol dependence

Reich, T., Edenberg, H. J., Goate, A., Williams, J. T., Rice, J. P., Van Eerdewegh, P., Foroud, T., Hesselbrock, V., Schuckit, M. A., Bucholz, K., Porjesz, B., Li, T. K., Conneally, P. M., Nurnberger, J. I., Tischfield, J. A., Crowe, R. R., Cloninger, C. R., Wu, W., Shears, S., Carr, K. & 3 others, Crose, C., Willig, C. & Begleiter, H., May 8 1998, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 81, 3, p. 207-215 9 p.

Research output: Contribution to journalArticle

608 Scopus citations

Genomic screen for QTLs underlying alcohol consumption in the P and NP rat lines

Bice, P., Foroud, T., Bo, R., Castelluccio, P., Lumeng, L., Li, T. K. & Carr, L. G., Dec 1 1998, In : Mammalian Genome. 9, 12, p. 949-955 7 p.

Research output: Contribution to journalArticle

83 Scopus citations

Heterogeneity in hereditary pancreatitis

Dasouki, M. J., Cogan, J., Summar, M. L., Neblitt, W., Foroud, T., Koller, D. & Phillips, J. A., Apr 28 1998, In : American journal of medical genetics. 77, 1, p. 47-53 7 p.

Research output: Contribution to journalArticle

38 Scopus citations

Linkage of an alcoholism-related severity phenotype to chromosome 16

Foroud, T., Bucholz, K. K., Edenberg, H. J., Goate, A., Neuman, R. J., Porjesz, B., Koller, D. L., Rice, J., Reich, T., Bierut, L. J., Cloninger, C. R., Nurnberger, J. I., Li, T. K., Conneally, P. M., Tischfield, J. A., Crowe, R., Hesselbrock, V., Schuckit, M. & Begleiter, H., Dec 1 1998, In : Alcoholism: Clinical and Experimental Research. 22, 9, p. 2035-2042 8 p.

Research output: Contribution to journalArticle

59 Scopus citations

Linkage of an alcoholism-related severity phenotype to chromosome 16

Foroud, T., Bucholz, K. K., Edenberg, H. J., Goate, A., Neuman, R. J., Porjesz, B., Koller, D. L., Rice, J., Reich, T., Bierut, L. J., Cloninger, C. R., Nurnberger, J. I., Li, T. K., Conneally, P. M., Tischfield, J. A., Crowe, R., Hesselbrock, V., Schuckit, M. & Begleiter, H., Nov 6 1998, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 81, 6, 1 p.

Research output: Contribution to journalArticle

1 Scopus citations

Linkage of a QTL contributing to normal variation in bone mineral density to chromosome 11q12-13

Koller, D. L., Rodriguez, L. A., Christian, J. C., Slemenda, C. W., Econs, M. J., Hui, S. L., Morin, P., Conneally, P. M., Joslyn, G., Curran, M. E., Peacock, M., Johnston, C. C. & Foroud, T., Dec 1998, In : Journal of Bone and Mineral Research. 13, 12, p. 1903-1908 6 p.

Research output: Contribution to journalArticle

120 Scopus citations

Quantitative trait loci analysis of human event-related brain potentials: P3 voltage

Begleiter, H., Porjesz, B., Reich, T., Edenberg, H. J., Goate, A., Blangero, J., Almasy, L., Foroud, T., Van Eerdewegh, P., Polich, J., Rohrbaugh, J., Kuperman, S., Bauer, L. O., O'Connor, S. J., Chorlian, D. B., Li, T. K., Conneally, P. M., Hesselbrock, V., Rice, J. P., Schuckit, M. A. & 4 others, Cloninger, R., Nurnberger, J., Crowe, R. & Bloom, F. E., Apr 1 1998, In : Electroencephalography and Clinical Neurophysiology - Evoked Potentials. 108, 3, p. 244-250 7 p.

Research output: Contribution to journalArticle

137 Scopus citations

Replicating genetic linkage in the collaborative study on the genetics of alcoholism (COGA)

Reich, T., Goate, A., Edenberg, H., Rice, J., Foroud, T., Hesselbrock, V., Schuckit, M., Porjesz, B., Nurnberger, J., Crowe, R. & Begleiter, H., Nov 6 1998, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 81, 6, p. 478-479 2 p.

Research output: Contribution to journalArticle

3 Scopus citations

Twelfth Annual Symposia on Etiology, Pathogenesis, and Treatment of Parkinson's Disease and Etiology, Pathogenesis, and Treatment of Huntington's Disease, Queen Elizabeth Hotel, Montreal, Canada, 18 October 1998

Kieburtz, K., Frey, K., Albin, R., Marek, K., Bates, G., Aylward, E., Guttman, M., Rouleau, G., Baehr, M., Pahwa, R., Lyons, K. E., Wilkinson, S. B., Kieltyka, J., Koller, W. C., Bertoni, J. M., Strickland, D., Eberly, C., Seeland, M., Brewer, M., Stacy, M. & 57 others, Ellgring, H., Pfeiffer, B., Ulm, G., Factor, S. A., Seibyl, J., Innis, R., Marek, K., Frey, K. A., Bohnen, N. I., Elmer, L. W., Koeppe, R. A., Kilbourn, M. R., Lyons, K. E., Troster, A. I., DeCarti, C., Paulson, G. W., Sax, D. S., Kornetsky, C., Siemers, E. R., Hubble, J., Tuite, P., Comella, C., Kompoliti, K., Oakes, D., Wojcieszek, J., Foroud, T., Conneally, P. M., Takanashi, M., Abe, K., Yanagihara, T., Weiner, W. J., Minagar, A., Shulman, L. M., Zakzanis, K. K., Kaplan, E., Leach, L., Freedman, M., Zesiewicz, T. A., Cardoza, F., Malik, A., Willing, A., Sanchez-Ramos, J., Hauser, R. A., Cha, J. H. J., Frey, A. S., Menon, A. S., Chung, W. M., Alsdorf, S. A., Mangiarini, L., Davies, S. W., Penney, J. B., Bates, G. P., Young, A. B., Moskowitz, C. B., Quinn, L., Francis, K. & Schwartz, R., Sep 30 1998, In : Movement Disorders. 13, 5, p. 858-863 6 p.

Research output: Contribution to journalArticle

1999

Chromosome 6 workshop report

Nurnberger, J. I. & Foroud, T., Jun 18 1999, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 88, 3, p. 233-238 6 p.

Research output: Contribution to journalArticle

34 Scopus citations

Differences in duration of Huntington's disease based on age at onset

Foroud, T., Gray, J., Ivashina, J. & Conneally, P. M., Jan 1999, In : Journal of Neurology Neurosurgery and Psychiatry. 66, 1, p. 52-56 5 p.

Research output: Contribution to journalArticle

Open Access
139 Scopus citations

Genome screen for platelet monoamine oxidase (MAO) activity

Saccone, N. L., Rice, J. P., Rochberg, N., Goate, A., Reich, T., Shears, S., Wu, W., Nurnberger, J. I., Foroud, T., Edenberg, H. J. & Li, T. K., Oct 15 1999, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 88, 5, p. 517-521 5 p.

Research output: Contribution to journalArticle

12 Scopus citations

Joint multipoint linkage analysis of multivariate qualitative and quantitative trait. II. Alcoholism and event-related potentials

Williams, J. T., Begleiter, H., Porjesz, B., Edenberg, H. J., Foroud, T., Reich, T., Goate, A., Van Eerdewegh, P., Almasy, L. & Blangero, J., Jan 1 1999, In : American Journal of Human Genetics. 65, 4, p. 1148-1160 13 p.

Research output: Contribution to journalArticle

157 Scopus citations

Linkage of type II and type III cystinuria to 19q13.1: Codominant inheritance of two cystinuric alleles at 19q13.1 produces an extreme stone- forming phenotype

Stoller, M. L., Bruce, J. E., Bruce, C. A., Foroud, T., Kirkwood, S. C. & Stambrook, P. J., Sep 10 1999, In : American journal of medical genetics. 86, 2, p. 134-139 6 p.

Research output: Contribution to journalArticle

14 Scopus citations

Locus heterogeneity of autosomal dominant osteopetrosis (ADO)

White, K. E., Koller, D. L., Takacs, I., Buckwalter, K. A., Foroud, T. & Econs, M. J., Jan 1 1999, In : Journal of Clinical Endocrinology and Metabolism. 84, 3, p. 1047-1051 5 p.

Research output: Contribution to journalArticle

15 Scopus citations

Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers

Kirkwood, S. C., Siemers, E., Stout, J. C., Hodes, M. E., Conneally, P. M., Christian, J. C. & Foroud, T., May 1 1999, In : Archives of Neurology. 56, 5, p. 563-568 6 p.

Research output: Contribution to journalArticle

90 Scopus citations