Tatiana Foroud

  • 42200 Citations
  • 101 h-Index
1976 …2021
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Publications 1988 2019

1998
1 Citation (Scopus)

Linkage of an alcoholism-related severity phenotype to chromosome 16

Foroud, T., Bucholz, K. K., Edenberg, H., Goate, A., Neuman, R. J., Porjesz, B., Koller, D. L., Rice, J., Reich, T., Bierut, L. J., Cloninger, C. R., Nurnberger, J., 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, Part B: Neuropsychiatric Genetics. 81, 6, p. 479 1 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 16
Alcoholism
Phenotype
Lod Score
Alcoholics
59 Citations (Scopus)

Linkage of an alcoholism-related severity phenotype to chromosome 16

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

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 16
Chromosomes
Alcoholism
Genes
Alcohols
120 Citations (Scopus)

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., Hui, S., 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 : the official journal of the American Society for Bone and Mineral Research. 13, 12, p. 1903-1908 6 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 13
Bone Density
Osteoporosis
Genes
Population
137 Citations (Scopus)

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

Begleiter, H., Porjesz, B., Reich, T., Edenberg, H., Goate, A., Blangero, J., Almasy, L., Foroud, T., Van Eerdewegh, P., Polich, J., Rohrbaugh, J., Kuperman, S., Bauer, L. O., O'Connor, S., 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 1998, In : Electroencephalography and Clinical Neurophysiology/ Evoked Potentials. 108, 3, p. 244-250 7 p.

Research output: Contribution to journalArticle

P300 Event-Related Potentials
Quantitative Trait Loci
Evoked Potentials
Brain
Genetic Loci
3 Citations (Scopus)

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, Part B: Neuropsychiatric Genetics. 81, 6, p. 478-479 2 p.

Research output: Contribution to journalArticle

Genetic Linkage
Alcoholism
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 4
Phenotype

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., 1998, In : Movement Disorders. 13, 5, p. 858-863 6 p.

Research output: Contribution to journalArticle

1997
73 Citations (Scopus)

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

Bloem, L. J., Foroud, T., 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

Angiotensinogen
Haplotypes
Serum
Genes
Blood Pressure
64 Citations (Scopus)

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., Farlow, M. & Ghetti, B., Nov 1997, In : American Journal of Human Genetics. 61, 5, p. 1131-1138 8 p.

Research output: Contribution to journalArticle

Frontotemporal Dementia
Chromosomes, Human, Pair 17
Oligodendroglia
Memory Disorders
Pedigree
129 Citations (Scopus)

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

Potassium Iodide
Adipose Tissue
Obesity
Chromosomes
Genetic Markers
115 Citations (Scopus)

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, Part B: Neuropsychiatric Genetics. 74, 3, p. 227-237 11 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Pedigree
Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 1
Surveys and Questionnaires
109 Citations (Scopus)

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., 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, Part B: Neuropsychiatric Genetics. 74, 3, p. 247-253 7 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 1
Pedigree
Lod Score
Genome
114 Citations (Scopus)

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., Foroud, T., Lahiri, D., Nurnberger, J., 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, Part B: Neuropsychiatric Genetics. 74, 3, p. 254-262 9 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 7
Pedigree
Alleles
93 Citations (Scopus)

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., Foroud, T., Nurnberger, J., Detera-Wadleigh, S. D., Goldin, L. R., Guroff, J., Gershon, E. S., Blehar, M. C. & DePaulo, J. R., 1997, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 74, 3, p. 263-269 7 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 2
Pedigree
Bipolar Disorder
143 Citations (Scopus)

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

Edenberg, H., 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., 1997, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 74, 3, p. 238-246 9 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 3
Pedigree
Alleles
1 Citation (Scopus)

Introduction to genetic linkage analysis

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

Research output: Contribution to journalArticle

Genetic Linkage
Neurofibromatoses
Chromosome Mapping
Huntington Disease
Cystic Fibrosis
218 Citations (Scopus)

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 1997, In : Nature Genetics. 15, 3, p. 277-280 4 p.

Research output: Contribution to journalArticle

Lod Score
Chromosomes
Pulmonary Artery
Genes
Chromosomes, Human, Pair 2
22 Citations (Scopus)

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

Muscles
Crystallins
Desmin
Ubiquitin
Spheroid body myopathy
1996
60 Citations (Scopus)

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

Asymptomatic Diseases
Huntington Disease
Genes
Alleles
Trinucleotide Repeats
1995
110 Citations (Scopus)

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

Huntington Disease
Genes
Alleles
Trinucleotide Repeats
Chromosomes, Human, Pair 4
188 Citations (Scopus)

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

Loyd, J. E., Butler, M. G., Foroud, T., Conneally, P. M., Phillips, J. A. & Newman, J. H., 1995, In : American Journal of Respiratory and Critical Care Medicine. 152, 1, p. 93-97 5 p.

Research output: Contribution to journalArticle

Genetic Anticipation
Parturition
Genes
Trinucleotide Repeats
Fragile X Syndrome
1994
51 Citations (Scopus)

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., 1994, In : Clinical Genetics. 46, 3, p. 255-256 2 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 4
Cleft Lip
Cleft Palate
Polymerase Chain Reaction
Genes
1992
38 Citations (Scopus)

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., 1992, In : Genomics. 13, 4, p. 1370-1371 2 p.

Research output: Contribution to journalArticle

176 Citations (Scopus)

Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene

Dlouhy, S., Hsiao, K., Farlow, M., 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

Prion Diseases
Codon
Valine
Genes
Lod Score
1991

Gene mapping using linkage analysis.

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

Research output: Contribution to journalArticle

Chromosome Mapping
Lod Score
Genes
Chromosomes
Genetic Loci
42 Citations (Scopus)

Localization of an ataxia-telangiectasia locus to a 3-cM interval on chromosome 11q23: Linkage analysis of 111 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 1991, In : American Journal of Human Genetics. 49, 6, p. 1263-1279 17 p.

Research output: Contribution to journalArticle

Ataxia Telangiectasia
Chromosomes
Lod Score
Monte Carlo Method
Neural Cell Adhesion Molecules
43 Citations (Scopus)

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., 1991, In : Genomics. 9, 2, p. 373-375 3 p.

Research output: Contribution to journalArticle

Ataxia Telangiectasia
Genes
Chromosomes, Human, Pair 11
Restriction Fragment Length Polymorphisms
Chromosomes
1990
24 Citations (Scopus)

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., 1990, In : Genomics. 6, 2, p. 316-323 8 p.

Research output: Contribution to journalArticle

Human Chromosomes
Ataxia Telangiectasia
DNA Fingerprinting
Hybrid Cells
Linkage Disequilibrium
28 Citations (Scopus)

Further mapping of an ataxia-telangiectasia locus to the chromosome IIq23 region

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

Research output: Contribution to journalArticle

Chromosomes, Human, 1-3
Ataxia Telangiectasia
Genetic Markers
Chromosomes
Genes
1988
510 Citations (Scopus)

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

Ataxia Telangiectasia
Chromosomes
Genes
Heterozygote
Lymphocytes