Tatiana Foroud

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

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2003
8 Citations (Scopus)

Visual function in Hungtington's disease patients and presymptomatic gene carriers

O'Donnell, B., Wilt, M. A., Hake, A., Stout, J. C., Kirkwood, S. C. & Foroud, T., Sep 1 2003, In : Movement Disorders. 18, 9, p. 1027-1034 8 p.

Research output: Contribution to journalArticle

Asymptomatic Diseases
Huntington Disease
Contrast Sensitivity
Genes
Motion Perception
99 Citations (Scopus)

α-Synuclein maps to a quantitative trait locus for alcohol preference and is differentially expressed in alcohol-preferring and -nonpreferring rats

Liang, T., Spence, J., Liu, L., Strother, W. N., Chang, H. W., Ellison, J. A., Lumeng, L., Li, T. K., Foroud, T. & Carr, L. G., Apr 15 2003, In : Proceedings of the National Academy of Sciences of the United States of America. 100, 8, p. 4690-4695 6 p.

Research output: Contribution to journalArticle

Synucleins
Quantitative Trait Loci
Alcohols
3' Untranslated Regions
Hippocampus
2002
32 Citations (Scopus)

Apparent replication of suggestive linkage on chromosome 16 in the NIMH genetics initiative bipolar pedigrees

Dick, D. M., Foroud, T., Edenberg, H., Miller, M., Bowman, E., Leela Rau, N., Raymond Depaulo, J., McInnis, M., Gershon, E., McMahon, F., Rice, J. P., Bierut, L. J., Reich, T. & Nurnberger, J., May 8 2002, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 114, 4, p. 407-412 6 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 16
Pedigree
Chromosomes, Human, Pair 5
Bipolar Disorder
64 Citations (Scopus)

Defining alcohol-related phenotypes in humans: The collaborative study on the genetics of alcoholism

Bierut, L. J., Saccone, N. L., Rice, J. P., Goate, A., Foroud, T., Edenberg, H., Almasy, L., Conneally, P. M., Crowe, R., Hesselbrock, V., Li, T. K., Nurnberger, J., Porjesz, B., Schuckit, M. A., Tischfield, J., Begleiter, H. & Reich, T., 2002, In : Alcohol Research and Health. 26, 3, p. 208-213 6 p.

Research output: Contribution to journalArticle

Alcoholism
Alcohols
Phenotype
Alcoholics
Chromosomes
6 Citations (Scopus)
Hypercalciuria
Metabolic Diseases
Calcium
Mutation
12 Citations (Scopus)

Evaluation of psychological symptoms among presymptomatic HD gene carriers as measured by selected MMPI scales

Close Kirkwood, S., Siemers, E., Viken, R. J., Hodes, M. E., Conneally, P. M., Christian, J. C. & Foroud, T., Nov 2002, In : Journal of Psychiatric Research. 36, 6, p. 377-382 6 p.

Research output: Contribution to journalArticle

Asymptomatic Diseases
MMPI
Symptom Assessment
Huntington Disease
Psychology
17 Citations (Scopus)

Genetic strategies to detect genes involved in alcoholism and alcohol-related traits

Dick, D. M. & Foroud, T., 2002, In : Alcohol Research and Health. 26, 3, p. 172-180 9 p.

Research output: Contribution to journalArticle

Alcoholism
Alcohols
Genes
Pharmacogenetics
Genetic Counseling
142 Citations (Scopus)

Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations

Pankratz, N., Nichols, W. C., Uniacke, S. K., Halter, C., Rudolph, A., Shults, C., Conneally, P. M., Foroud, T., Golbe, L., Koller, W., Marder, K., Marshall, F., Oakes, D., Shinaman, A., Siemers, E., Carter, J., Camicioli, R., Andrews, P., Wojcieszek, J., Belden, J. & 79 others, Frenandez, M., Hubble, J., Reider, C., Rajput, A., Rajput, A., Shirley, T., Panisset, M., Hall, J., Mendis, T., Grimes, D. A., Gray, P., Ramos, C. S., Roque, S., Reich, S., Dunlop, B., Hauser, R., Sanchez-Ramos, J., Zesiewicz, T., Delgado, H., Pfeiffer, R., Pfeiffer, B., Friedman, J., Fernandez, H., Lannon, M., Fontaine, D., Seeberger, L., O'Brien, C., Judd, D., Pahwa, R., Thomas, S., Elmer, L., Davis, K., Jennings, D., Marek, K., Mendick, S., Truong, D., Pathak, M., Tran, A., Rodnitzyk, R., Dobson, J., Kurlan, R., Berry, D., Tuite, P., Schacher, R., Aminoff, M., DiMinno, M., Marder, K., Harris, J., Lewitt, P., DeAngelis, M., Koller, W., Weiner, W., Lyons, K., Martin, W., Wieler, M., Jankovic, J., Hunter, C., Bertoni, J., Peterson, C., Factor, S., Evans, S., Walker, F., Hunt, V., Un, J. K., Uy, S., Stacy, M., Williamson, K., Simon, D., Scollins, L., Brindauer, K., Petit, J., Manyam, B., Simpson, P., Nieves, A., So, J., Velickovic, M., Phipps, S., Gordon, M. F. & Hamann, J., 2002, In : American Journal of Human Genetics. 71, 1, p. 124-135 12 p.

Research output: Contribution to journalArticle

Parkinson Disease
Genome
Mutation
Genes
Chromosomes, Human, Pair 5
48 Citations (Scopus)

Influence of ADH1B polymorphism on alcohol use and its subjective effects in a Jewish population

Carr, L. G., Foroud, T., Stewart, T., Castelluccio, P., Edenberg, H. & Li, T. K., Oct 1 2002, In : American Journal of Medical Genetics. 112, 2, p. 138-143 6 p.

Research output: Contribution to journalArticle

Alcohol Drinking
Alcohols
Population
Alleles
Alcohol Dehydrogenase
30 Citations (Scopus)

Is there a genetic relationship between alcoholism and depression?

Nurnberger, J., Foroud, T., Flury, L., Meyer, E. T. & Wiegand, R., 2002, In : Alcohol Research and Health. 26, 3, p. 233-240 8 p.

Research output: Contribution to journalArticle

Alcoholism
Depression
Phenotype
Chromosomes, Human, Pair 1
Genes
227 Citations (Scopus)

Linkage disequilibrium between the beta frequency of the human EEG and a GABAA receptor gene locus

Porjesz, B., Almasy, L., Edenberg, H., Wang, K., Chorlian, D. B., Foroud, T., Goate, A., Rice, J. P., O'Connor, S., Rohrbaugh, J., Kuperman, S., Bauer, L. O., Crowe, R. R., Schuckit, M. A., Hesselbrock, V., Conneally, P. M., Tischfield, J. A., Li, T. K., Reich, T. & Begleiter, H., Mar 19 2002, In : Proceedings of the National Academy of Sciences of the United States of America. 99, 6, p. 3729-3733 5 p.

Research output: Contribution to journalArticle

Aminobutyrates
Linkage Disequilibrium
Automatic Data Processing
Electroencephalography
Brain
6 Citations (Scopus)

Linkage for platelet monoamine oxidase (MAO) activity: Results from a replication sample

Saccone, N. L., Rice, J. P., Rochberg, N., Williams, J. T., Goate, A., Reich, T., Edenberg, H., Foroud, T., Nurnberger, J., Bierut, L. J., Crowe, R. & Li, T. K., 2002, In : Alcoholism: Clinical and Experimental Research. 26, 5, p. 603-609 7 p.

Research output: Contribution to journalArticle

Monoamine Oxidase
Chromosomes
Platelets
Lod Score
Blood Platelets
48 Citations (Scopus)

Linkage stratification and mutation analysis at the parkin locus identifies mutation positive Parkinson's disease families [1]

Nichols, W. C., Pankratz, N., Uniacke, S. K., Pauciulo, M. W., Halter, C., Rudolph, A., Conneally, P. M., Foroud, T., Carter, J., Camicioli, R., Wojcieszek, J., Fernandez, M., Hubble, J., Rajput, A., Panisset, M., Mendis, T., Grimes, D. A., Serrano Ramos, C., Reich, S., Hauser, R. & 53 others, Sanchez-Ramos, J., Zesiewicz, T., Pfeiffer, R., Friedman, J., Fernandez, H., Shults, C., Seeberger, L., O'Brien, C., Pahwa, R., Elmer, L., Jennings, D., Marek, K., Truong, D., Pathak, M., Rodnitzyk, R., Kurlan, R., Tuite, P., Aminoff, M., Marder, K., Lewitt, P., Koller, W., Martin, W., Jankovic, J., Bertoni, J., Factor, S., Walker, F., Jung Kang, U., Stacy, M., Simon, D., Blindauer, K., Manyam, B., Nieves, A., Velickovic, M., Gordon, M. F., Leehey, M., Gordon, P., Rao, J., Dalvi, A., Racette, B., Sethi, K., Sudarsky, L., Saunders Pullman, R., Simuni, T., Dewey, R., Hermanowicz, N., Feigin, A., Calabresse, V., Sutton, J., Ajax, T., Podakalny, G. D., Suchowersky, O., Uitti, R. & Shulman, L., 2002, In : Journal of Medical Genetics. 39, 7, p. 489-492 4 p.

Research output: Contribution to journalArticle

49 Citations (Scopus)

Longitudinal personality changes among presymptomatic Huntington disease gene carriers

Kirkwood, S. C., Siemers, E., Viken, R., Hodes, M. E., Conneally, P. M., Christian, J. C. & Foroud, T., Sep 2002, In : Neuropsychiatry, Neuropsychology and Behavioral Neurology. 15, 3, p. 192-197 6 p.

Research output: Contribution to journalArticle

Asymptomatic Diseases
MMPI
Huntington Disease
Personality
Hostility
20 Citations (Scopus)

Mapping of QTL influencing saccharin consumption in the selectively bred alcohol-preferring and -nonpreferring rat lines

Foroud, T., Bice, P., Castelluccio, P., Bo, R., Ritchotte, A., Stewart, R., Lumeng, L., Li, T. K. & Carr, L., 2002, In : Behavior Genetics. 32, 1, p. 57-67 11 p.

Research output: Contribution to journalArticle

saccharin
Saccharin
Quantitative Trait Loci
alcohol
quantitative trait loci
44 Citations (Scopus)

Recent drinking history: Association with family history of alcoholism and the acute response to alcohol during a 60 mg% clamp

Ramchandani, V. A., Flury, L., Morzorati, S., Kareken, D., Blekher, T., Foroud, T., Li, T. K. & O'Connor, S., Nov 2002, In : Journal of Studies on Alcohol. 63, 6, p. 734-744 11 p.

Research output: Contribution to journalArticle

Clamping devices
genealogy
alcoholism
Alcoholism
Drinking
29 Citations (Scopus)

Saccadic eye movements are associated with a family history of alcoholism at baseline and after exposure to alcohol

Blekher, T., Ramchandani, V. A., Flury, L., Foroud, T., Kareken, D., Yee, R. D., Li, T. K. & O'Connor, S., Oct 2002, In : Alcoholism: Clinical and Experimental Research. 26, 10, p. 1568-1573 6 p.

Research output: Contribution to journalArticle

Eye movements
Saccades
Alcoholism
Alcohols
Placebos
23 Citations (Scopus)
Proton Pumps
Chromosomes, Human, Pair 13
Osteoclasts
Chromosomes
Bone Density
72 Citations (Scopus)

Suggestive linkage on chromosome 1 for a quantitative alcohol-related phenotype

Dick, D. M., Nurnberger, J., Edenberg, H., Goate, A., Crowe, R., Rice, J., Bucholz, K. K., Kramer, J., Schuckit, M. A., Smith, T. L., Porjesz, B., Begleiter, H., Hesselbrock, V. & Foroud, T., Oct 2002, In : Alcoholism: Clinical and Experimental Research. 26, 10, p. 1453-1460 8 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 1
Chromosomes
Alcoholism
Alcohols
Phenotype
9 Citations (Scopus)

The effect of shared genetic and environmental factors on periodontal disease parameters in untreated adult siblings in Guatemala

Dowsett, S. A., Archila, L., Foroud, T., Koller, D., Eckert, G. J. & Kowolik, M., Oct 1 2002, In : Journal of Periodontology. 73, 10, p. 1160-1168 9 p.

Research output: Contribution to journalArticle

Guatemala
Periodontal Diseases
Spouses
Siblings
Periodontal Index
2001
151 Citations (Scopus)

A genome-wide search for genes that relate to a low level of response to alcohol

Schuckit, M. A., Edenberg, H., Kalmijn, J., Flury, L., Smith, T. L., Reich, T., Bierut, L., Goate, A. & Foroud, T., 2001, In : Alcoholism: Clinical and Experimental Research. 25, 3, p. 323-329 7 p.

Research output: Contribution to journalArticle

Alcoholism
Genes
Alcohols
Genome
Lod Score
69 Citations (Scopus)

Alcohol dehydrogenase-2*2 allele is associated with decreased prevalence of fetal alcohol syndrome in the mixed-ancestry population of the Western Cape Province, South Africa

Viljoen, D. L., Carr, L. G., Foroud, T., Brooke, L., Ramsay, M. & Li, T. K., 2001, In : Alcoholism: Clinical and Experimental Research. 25, 12, p. 1719-1722 4 p.

Research output: Contribution to journalArticle

Fetal Alcohol Spectrum Disorders
Alcohol Dehydrogenase
South Africa
Alleles
Alcohols

Alcoholism and mania: Is there a genetic relationship?

Nurnberger, J., Meyer, E. T., Flury, L., Hu, K. & Foroud, T., Oct 8 2001, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 105, 7, p. 567 1 p.

Research output: Contribution to journalArticle

Bipolar Disorder
Alcoholism
Chromosomes, Human, Pair 1
National Institute of Mental Health (U.S.)
Viverridae

A quantitative estimate of genetic vulnerability for a multifactorial condition

Nurnberger, J., Foroud, T., Hu, K., Castellucio, P., Edenberg, H. & Meyer, E. T., Oct 8 2001, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 105, 7, p. 565 1 p.

Research output: Contribution to journalArticle

Pedigree
Internal-External Control
Alleles
Education
Datasets
163 Citations (Scopus)

Evidence for a locus on chromosome 1 that influences vulnerability to alcoholism and affective disorder

Nurnberger, J. I., Foroud, T., Flury, L., Su, J., Meyer, E. T., Hu, K., Crowe, R., Edenberg, H., Goate, A., Bierut, L., Reich, T., Schuckit, M. & Reich, W., May 2001, In : American Journal of Psychiatry. 158, 5, p. 718-724 7 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 1
Mood Disorders
Alcoholism
Depression
Lod Score
65 Citations (Scopus)

Functional relevance of human ADH polymorphism

Eriksson, C. J. P., Fukunaga, T., Sarkola, T., Chen, W. J., Chen, C. C., Ju, J. M., Cheng, A. T. A., Yamamoto, H., Kohlenberg-Müller, K., Kimura, M., Murayama, M., Matsushita, S., Kashima, H., Higuchi, S., Carr, L., Viljoen, D., Brooke, L., Stewart, T., Foroud, T., Su, J. & 2 others, Li, T. K. & Whitfield, J. B., 2001, In : Alcoholism: Clinical and Experimental Research. 25, 5 SUPPL.

Research output: Contribution to journalArticle

Polymorphism
Genotype
Alcohols
Tolnaftate
Alcoholics
101 Citations (Scopus)

Genome screen for quantitative trait loci underlying normal variation in femoral structure

Koller, D. L., Liu, G., Econs, M., Hui, S., Morin, P. A., Joslyn, G., Rodriguez, L. A., Michael Conneally, P., Christian, J. C., Conrad Johnston, C., Foroud, T. & Peacock, M., 2001, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 16, 6, p. 985-991 7 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Thigh
Odds Ratio
Genome
Femur Head
1203 Citations (Scopus)

Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura

Levy, G. G., Nichols, W. C., Lian, E. C., Foroud, T., McClintick, J., McGee, B. M., Yang, A. Y., Siemieniak, D. R., Stark, K. R., Gruppo, R., Sarode, R., Shurin, S. B., Chandrasekaran, V., Stabler, S. P., Sabio, H., Bouhassira, E. E., Upshaw, J. D., Ginsburg, D. & Tsai, H. M., Oct 4 2001, In : Nature. 413, 6855, p. 488-494 7 p.

Research output: Contribution to journalArticle

Thrombotic Thrombocytopenic Purpura
Mutation
Genes
von Willebrand Factor
Proteolysis
1 Citation (Scopus)

Parametric linkage analysis and disequilibrium methods to identify loci for complex disease

McClintick, J., Koller, D. L., Pankratz, N., Kirkwood, S. C., Naughton, B. & Foroud, T., 2001, In : Genetic Epidemiology. 21, SUPPL. 1

Research output: Contribution to journalArticle

Linkage Disequilibrium
Haplotypes
Phenotype
Base Pairing
Alleles
151 Citations (Scopus)

Progression of symptoms in the early and middle stages of Huntington disease

Kirkwood, S. C., Su, J. L., Conneally, P. M. & Foroud, T., 2001, In : Archives of Neurology. 58, 2, p. 273-278 6 p.

Research output: Contribution to journalArticle

Huntington Disease
Disease Progression
Dyskinesias
Paranoid Disorders
Behavioral Symptoms

Replication of suggestive linkage on chromosomes 5 and 16 in the NIMH genetics initiative bipolar pedigrees

Dick, D. M., Nurnberger, J., Edenberg, H., McInnis, M. G., Reich, T., Gershon, E. S. & Foroud, T., Oct 8 2001, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 105, 7, p. 592 1 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 3
Pedigree
10 Citations (Scopus)

Stoppage: An issue for segregation analysis

Slager, S. L., Foroud, T., Haghighi, F., Spence, M. A. & Hodge, S. E., 2001, In : Genetic Epidemiology. 20, 3, p. 328-339 12 p.

Research output: Contribution to journalArticle

Parents
Viverridae
Autistic Disorder
Nuclear Family
Early Diagnosis
1 Citation (Scopus)

Use of variable marker density, principal components, and neural networks in the dissection of disease etiology.

Pankratz, N., Kirkwood, S. C., Flury, L., Koller, D. L. & Foroud, T., 2001, In : Genetic Epidemiology. 21 Suppl 1

Research output: Contribution to journalArticle

Quantitative Trait Loci
Dissection
Phenotype
Principal Component Analysis
Genome
63 Citations (Scopus)
Inbred Strains Rats
Genetic Models
Femur Neck
Bone and Bones
Alleles
2000
175 Citations (Scopus)

A genome screen of maximum number of drinks as an alcoholism phenotype

Saccone, N. L., Kwon, J. M., Corbett, J., Goate, A., Rochberg, N., Edenberg, H., Foroud, T., Li, T. K., Begleiter, H., Reich, T. & Rice, J. P., Oct 9 2000, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 96, 5, p. 632-637 6 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 4
Alcoholism
Genome
Phenotype
Twin Studies
206 Citations (Scopus)

Alcoholism susceptibility loci: Confirmation studies in a replicate sample and further mapping

Foroud, T., Edenberg, H., Goate, A., Rice, J., Flury, L., Koller, D. L., Bierut, L. J., Conneally, P. M., Nurnberger, J., Bucholz, K. K., Li, T. K., Hesselbrock, V., Crowe, R., Schuckit, M., Porjesz, B., Begleiter, H. & Reich, T., Jul 2000, In : Alcoholism: Clinical and Experimental Research. 24, 7, p. 933-945 13 p.

Research output: Contribution to journalArticle

Chromosomes
Alcoholism
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 1

Allele frequency heterogeneity in the collaborative study on the genetics of alcoholism (COGA)

Saccone, N. L., Rice, J. P., Goate, A., Conneally, P. M., Edenberg, H., Foroud, T., Nurnberger, J. & Reich, T., Aug 7 2000, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 96, 4, p. 563 1 p.

Research output: Contribution to journalArticle

Gene Frequency
Alcoholism
Genome
Alcoholics
African Americans
Pedigree
Alleles
Multifactorial Inheritance
National Institute of Mental Health (U.S.)
Genetic Counseling
5 Citations (Scopus)

Common and specific factors in the familial transmission of substance dependence

Bierut, L., Rice, J., Goate, A., Foroud, T., Edenberg, H., Crowe, R., Hesselbrock, V., Li, T. K., Nurnberger, J., Porjesz, B., Schuckit, M., Begleiter, H. & Reich, T., Aug 7 2000, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 96, 4, p. 459 1 p.

Research output: Contribution to journalArticle

Alcoholism
Substance-Related Disorders
Marijuana Abuse
Smoking
Cocaine-Related Disorders
62 Citations (Scopus)

Confirmation of subtle motor changes among presymptomatic carriers of the huntington disease gene

Kirhwood, S. C., Siemers, E., Bond, C., Comically, P. M., Christian, J. C. & Foroud, T., Jul 2000, In : Archives of Neurology. 57, 7, p. 1040-1044 5 p.

Research output: Contribution to journalArticle

Huntington Disease
Reaction Time
Genes
Chorea
Neurologic Examination
Endocrinology
Insulin-Like Growth Factor I
Metabolism
Minerals
Bone
96 Citations (Scopus)

Family-based study of the association of the dopamine D2 receptor gene (DRD2) with habitual smoking

Bierut, L. J., Rice, J. P., Edenberg, H., Goate, A., Foroud, T., Cloninger, C. R., Begleiter, H., Conneally, P. M., Crowe, R. R., Hesselbrock, V., Li, T. K., Nurnberger, J., Porjesz, B., Schuckit, M. A. & Reich, T., 2000, In : American Journal of Medical Genetics. 90, 4, p. 299-302 4 p.

Research output: Contribution to journalArticle

Dopamine D2 Receptors
Smoking
Genes
Alcoholism
Alleles

Further analyses of the NIMH bipolar dataset: Follow up on suggestive linkage results on 1p and 10p

Corbett, J., Rice, J., Saccone, N., Goate, A., Reich, T., Foroud, T., Nurnberger, J., Edenberg, H., DePaulo, J. R. & Gershon, E., Aug 7 2000, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 96, 4, p. 469 1 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 1
Mood Disorders
Bipolar Disorder
Datasets
42 Citations (Scopus)

Genetics of bipolar affective disorder.

Nurnberger, J. & Foroud, T., Apr 2000, In : Current Psychiatry Reports. 2, 2, p. 147-157 11 p.

Research output: Contribution to journalArticle

Mood Disorders
Bipolar Disorder
Genes
Schizophrenia
Catechol O-Methyltransferase
183 Citations (Scopus)

Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis

Koller, D. L., Econs, M., Morin, P. A., Christian, J. C., Hui, S., Parry, P., Curran, M. E., Rodriguez, L. A., Conneally, P. M., Joslyn, G., Peacock, M., Johnston, C. C. & Foroud, T., 2000, In : Journal of Clinical Endocrinology and Metabolism. 85, 9, p. 3116-3120 5 p.

Research output: Contribution to journalArticle

Bone Density
Osteoporosis
Minerals
Bone
Genes
1027 Citations (Scopus)

Heterozygous germline mutations in BMPR2, encoding a TGF-β receptor, cause familial primary pulmonary hypertension

Lane, K. B., Machado, R. D., Pauciulo, M. W., Thomson, J. R., Phillips, J. A., Loyd, J. E., Nichols, W. C., Trembath, R. C., Aldred, M., Brannon, C. A., Conneally, P. M., Foroud, T., Fretwell, N., Gaddipati, R., Koller, D., Loyd, E. J., Morgan, N., Newman, J. H., Prince, M. A., Güell, C. V. & 1 others, Wheeler, L., Sep 2000, In : Nature Genetics. 26, 1, p. 81-84 4 p.

Research output: Contribution to journalArticle

Germ-Line Mutation
Type II Bone Morphogenetic Protein Receptors
Penetrance
Protein-Serine-Threonine Kinases
Pulmonary Artery
39 Citations (Scopus)

Identification of quantitative trait loci influencing alcohol consumption in the high alcohol drinking and low alcohol drinking rat lines

Foroud, T., Bice, P., Castelluccio, P., Bo, R., Miller, L., Ritchotte, A., Lumeng, L., Li, T. K. & Carr, L. G., 2000, In : Behavior Genetics. 30, 2, p. 131-140 10 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
drinking
Alcohol Drinking
alcohol
quantitative trait loci
31 Citations (Scopus)

Sib pair linkage and association studies between bone mineral density and the interleukin-6 gene locus

Takacs, I., Koller, D. L., Peacock, M., Christian, J. C., Evans, W. E., Hui, S., Conneally, P. M., Johnston, C. C., Foroud, T. & Econs, M., Jul 2000, In : Bone. 27, 1, p. 169-173 5 p.

Research output: Contribution to journalArticle

Bone Density
Interleukin-6
Osteoporosis
Genes
Alleles
106 Citations (Scopus)

Subtle changes among presymptomatic carriers of the Huntington's disease gene

Kirkwood, S. C., Siemers, E., Hodes, M. E., Conneally, P. M., Christian, J. C. & Foroud, T., 2000, In : Journal of Neurology, Neurosurgery and Psychiatry. 69, 6, p. 773-779 7 p.

Research output: Contribution to journalArticle

Huntington Disease
Genes
Reaction Time
Intelligence
Stretch Reflex
61 Citations (Scopus)

Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees

Foroud, T., Castelluccio, P. F., Koller, D. L., Edenberg, H., Miller, M., Bowman, E., Rau, N. L., Smiley, C., Rice, J. P., Goate, A., Armstrong, C., Bierut, L. J., Reich, T., Detera-Wadleigh, S. D., Goldin, L. R., Badner, J. A., Guroff, J. J., Gershon, E. S., McMahon, F. J., Simpson, S. & 6 others, MacKinnon, D., McInnis, M., Stine, O. C., DePaulo, J. R., Blehar, M. C. & Nurnberger, J., Feb 7 2000, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 96, 1, p. 18-23 6 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Lod Score
Pedigree
Depressive Disorder
Mood Disorders