Tatiana Foroud

  • 40289 Citations
  • 101 h-Index
1976 …2021
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Publications 1988 2019

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1988
506 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
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
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
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

175 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
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
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
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
1997
72 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
114 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
94 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
1998
97 Citations (Scopus)

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

Edenberg, H., Foroud, T., Koller, D. L., Goate, A., Rice, J., Van Eerdewegh, P., Reich, T., Cloninger, C. R., Nurnberger, J., 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., 1998, In : Alcoholism: Clinical and Experimental Research. 22, 2, p. 505-512 8 p.

Research output: Contribution to journalArticle

Dopamine D2 Receptors
Alcoholism
Alcohols
Gene Frequency
Population
82 Citations (Scopus)

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

Edenberg, H., Reynolds, J., Koller, D. L., Begleiter, H., Bucholz, K. K., Conneally, P. M., Crowe, R., Goate, A., Hesselbrock, V., Li, T. K., Nurnberger, J., 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

Serotonin Plasma Membrane Transport Proteins
Alcoholism
Genes
Alleles
Alcohols
103 Citations (Scopus)

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., 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. & Rohrbaugh, J., Sep 1998, In : Alcoholism: Clinical and Experimental Research. 22, 6, p. 1317-1323 7 p.

Research output: Contribution to journalArticle

P300 Event-Related Potentials
Alcoholism
Psychiatry
Alcohols
Sex Distribution
201 Citations (Scopus)

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

Potassium Iodide
Type 2 Diabetes Mellitus
Insulin
Phenotype
Fasting
419 Citations (Scopus)

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., 1998, In : American Journal of Human Genetics. 63, 4, p. 1130-1138 9 p.

Research output: Contribution to journalArticle

Potassium Iodide
Type 2 Diabetes Mellitus
Body Mass Index
Chromosomes
Genetic Loci
131 Citations (Scopus)

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

Cloninger, C. R., Van Eerdewegh, P., Goate, A., Edenberg, H., 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, Part B: Neuropsychiatric Genetics. 81, 4, p. 313-317 5 p.

Research output: Contribution to journalArticle

Human Genome
Personality
Anxiety
Chromosomes
Twin Studies
171 Citations (Scopus)

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., 1998, In : Alcoholism: Clinical and Experimental Research. 22, 4, p. 884-887 4 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Alcohol Drinking
Rats
Alcohols
Chromosomes, Human, Pair 4
171 Citations (Scopus)

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

Potassium Iodide
Energy Metabolism
Obesity
Adipose Tissue
Siblings
6 Citations (Scopus)

Chromosome 6 workshop

Nurnberger, J. & Foroud, T., 1998, In : Psychiatric Genetics. 8, 2, p. 79-83 5 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 6
Psychiatry
Education
3 Citations (Scopus)

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., Goate, A., Detera-Wadleigh, S., Stine, O. C., Rice, J., Blehar, M., Reich, T., Gershon, E., Nurnberger, J., Simpson, S. G. & DePaulo, J. R., Nov 6 1998, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 81, 6, p. 463 1 p.

Research output: Contribution to journalArticle

Pedigree
Bipolar Disorder
Chromosomes
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 2

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, I. A. & Newman, I. H., 1998, In : Pneumologie. 52, 4, p. 238 1 p.

Research output: Contribution to journalArticle

Genetic Anticipation
Parturition
Familial Primary Pulmonary Hypertension
14 Citations (Scopus)

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., 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., Nov 6 1998, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 81, 6, p. 462 1 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 6
Pedigree
Mood Disorders
Bipolar Disorder
604 Citations (Scopus)

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

Reich, T., Edenberg, H., 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., 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, Part B: Neuropsychiatric Genetics. 81, 3, p. 207-215 9 p.

Research output: Contribution to journalArticle

Alcoholism
Genome
Genes
Chromosomes, Human, Pair 4
Twin Studies
83 Citations (Scopus)

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., 1998, In : Mammalian Genome. 9, 12, p. 949-955 7 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Alcohol Drinking
Chromosomes, Human, Pair 4
Lod Score
Inbreeding
38 Citations (Scopus)

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

Trypsinogen
Mutation
Chronic Pancreatitis
Radiation Hybrid Mapping
Genes
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
135 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

1999
34 Citations (Scopus)

Chromosome 6 workshop report

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

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 6
Psychiatry
Schizophrenia
Education
Bipolar Disorder
130 Citations (Scopus)

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

Huntington Disease
Age of Onset
Research
45 Citations (Scopus)

Genetics of alcoholism: A review of recent studies in human and animal models

Foroud, T. & Li, T. K., Sep 1999, In : American Journal on Addictions. 8, 4, p. 261-278 18 p.

Research output: Contribution to journalArticle

Alcoholism
Animal Models
Alcohols
Genes
Genetic Loci
12 Citations (Scopus)

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., Foroud, T., Edenberg, H. & Li, T. K., Oct 15 1999, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 88, 5, p. 517-521 5 p.

Research output: Contribution to journalArticle

Monoamine Oxidase
Alcoholism
Blood Platelets
Genome
Lod Score
155 Citations (Scopus)

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., Foroud, T., Reich, T., Goate, A., Van Eerdewegh, P., Almasy, L. & Blangero, J., 1999, In : American Journal of Human Genetics. 65, 4, p. 1148-1160 13 p.

Research output: Contribution to journalArticle

Evoked Potentials
Alcoholism
Multivariate Analysis
Joints
P300 Event-Related Potentials
14 Citations (Scopus)

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

Cystinuria
Alleles
Lod Score
Phenotype
Chromosomes