Tatiana Foroud

  • 82108 Citations
  • 114 h-Index
1976 …2020

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2006

Development of congenic rat strains for alcohol consumption derived from the alcohol-preferring and nonpreferring rats

Carr, L. G., Habegger, K., Spence, J. P., Liu, L., Lumeng, L. & Foroud, T., Mar 1 2006, In : Behavior Genetics. 36, 2, p. 285-290 6 p.

Research output: Contribution to journalArticle

13 Scopus citations

Endophenotypes successfully lead to gene identification: Results from the collaborative study on the genetics of alcoholism

Dick, D. M., Jones, K., Saccone, N., Hinrichs, A., Wang, J. C., Goate, A., Bierut, L., Almasy, L., Schuckit, M., Hesselbrock, V., Tischfield, J., Foroud, T., Edenberg, H., Porjesz, B. & Begleiter, H., Jan 1 2006, In : Behavior Genetics. 36, 1, p. 112-126 15 p.

Research output: Contribution to journalArticle

86 Scopus citations

Functional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependence

Hinrichs, A. L., Wang, J. C., Bufe, B., Kwon, J. M., Budde, J., Allen, R., Bertelsen, S., Evans, W., Dick, D., Rice, J., Foroud, T., Nurnberger, J., Tischfield, J. A., Kuperman, S., Crowe, R., Hesselbrock, V., Schuckit, M., Almasy, L., Porjesz, B., Edenberg, H. J. & 4 others, Begleiter, H., Meyerhof, W., Bierut, L. J. & Goate, A. M., Jan 2006, In : American Journal of Human Genetics. 78, 1, p. 103-111 9 p.

Research output: Contribution to journalArticle

104 Scopus citations

Genetic association between endothelial nitric oxide synthase and Alzheimer disease

Akomolafe, A., Lunetta, K. L., Erlich, P. M., Cupples, L. A., Baldwin, C. T., Huyck, M., Green, R. C., Farrer, L. A., Auerbach, S., Griffith, P., Ofili, E., Browndyke, J., Schmechel, D., Welsh-Bohmer, K., Chui, H., DeCarli, C., Duara, R., Foroud, T., Farlow, M., Friedland, R. & 9 others, Go, R., Kurz, A., Obisesan, T., Petrovitch, H., White, L., Relkin, N., Sabbagh, M., Sadovnick, D. & Tsolaki, M., Jul 1 2006, In : Clinical Genetics. 70, 1, p. 49-56 8 p.

Research output: Contribution to journalArticle

23 Scopus citations

Heritability of changes in bone size and bone mass with age in premenopausal white sisters

Hui, S. L., Koller, D. L., Foroud, T. M., Econs, M. J., Johnston, C. C. & Peacock, M., Jul 1 2006, In : Journal of Bone and Mineral Research. 21, 7, p. 1121-1125 5 p.

Research output: Contribution to journalArticle

22 Scopus citations

Human ALOX12, but not ALOX15, is associated with BMD in white men and women

Ichikawa, S., Koller, D. L., Johnson, M. L., Lai, D., Xuei, X., Edenberg, H. J., Klein, R. F., Orwoll, E. S., Hui, S. L., Foroud, T. M., Peacock, M. & Econs, M. J., Apr 1 2006, In : Journal of Bone and Mineral Research. 21, 4, p. 556-564 9 p.

Research output: Contribution to journalArticle

62 Scopus citations

Identification of a quantitative trait locus on rat chromosome 4 that is strongly linked to femoral neck structure and strength

Alam, I., Sun, Q., Liu, L., Koller, D. L., Fishburn, T., Carr, L. G., Econs, M. J., Foroud, T. & Turner, C. H., Jul 1 2006, In : Bone. 39, 1, p. 93-99 7 p.

Research output: Contribution to journalArticle

23 Scopus citations

Identification of QTLs influencing alcohol preference in the High Alcohol Preferring (HAP) and Low Alcohol Preferring (LAP) mouse lines

Bice, P. J., Foroud, T., Carr, L. G., Zhang, L., Liu, L., Grahame, N. J., Lumeng, L., Li, T. K. & Belknap, J. K., Mar 1 2006, In : Behavior Genetics. 36, 2, p. 248-260 13 p.

Research output: Contribution to journalArticle

28 Scopus citations

Marital status, alcohol dependence, and GABRA2: Evidence for gene-environment correlation and interaction

Dick, D. M., Agrawal, A., Schuckit, M. A., Bierut, L., Hinrichs, A., Fox, L., Mullaney, J., Cloninger, C. R., Hesselbrock, V., Nurnberger, J. I., Almasy, L., Foroud, T., Porjesz, B., Edenberg, H. & Begleiter, H., Mar 2006, In : Journal of Studies on Alcohol. 67, 2, p. 185-194 10 p.

Research output: Contribution to journalArticle

91 Scopus citations

Mutations in DJ-1 are rare in familial Parkinson disease

Pankratz, N., Pauciulo, M. W., Elsaesser, V. E., Marek, D. K., Halter, C. A., Wojcieszek, J., Rudolph, A., Shults, C. W., Foroud, T. & Nichols, W. C., Nov 20 2006, In : Neuroscience Letters. 408, 3, p. 209-213 5 p.

Research output: Contribution to journalArticle

35 Scopus citations

Mutations in LRRK2 other than G2019S are rare in a north-American based sample of familial Parkinson's didease

Pankratz, N., Pauciulo, M. W., Elsaesser, V. E., Marek, D. K., Halter, C. A., Rudolph, A., Shults, C. W., Foroud, T., Nichols, W. C., Shults, C., Marshall, F., Oakes, D., Shinaman, A., Marder, K., Conneally, P. M., Lyons, K., Siemers, E., Factor, S., Higgins, D., Evans, S. & 79 others, Shill, H., Stacy, M., Danielson, J., Marlor, L., Williamson, K., Jankovic, J., Hunter, C., Simon, D., Ryan, P., Scollins, L., Saunders-Pullman, R., Boyar, K., Costan-Toth, C., Ohmann, E., Sudarsky, L., Joubert, C., Friedman, J., Chou, K., Fernandez, H., Lannon, M., Galvez-Jimenez, N., Podichetty, A., Lewitt, P., DeAngelis, M., O'Brien, C., Seeberger, L., Dingmann, C., Judd, D., Fraser, J., Harris, J., Bertoni, J., Peterson, C., Chouinard, S., Panisset, M., Hall, J., Poiffaut, H., Calabrese, V., Roberge, P., Wojcieszek, J., Belden, J., Halter, C., Jennings, D., Marek, K., Mendick, S., Reich, S., Dunlop, B., Jog, M., Horn, C., Rao, J., Cook, M., Uitti, R., Turk, M., Ajax, T., Mannetter, J., Sethi, K., Carpenter, J., Ligon, K., Narayan, S., Woodward, L., Blindauer, K., Petit, J., Elmer, L., Aiken, E., Davis, K., Schell, C., Wilson, S., Velickovic, M., Koller, W., Phipps, S., Feigin, A., Gordon, M., Hamann, J., Licari, E., Marotta-Kollarus, M., Shannon, B., Winnick, R., Simuni, T., Kaczmarek, A. & Williams, K., Dec 1 2006, In : Movement Disorders. 21, 12, p. 2257-2260 4 p.

Research output: Contribution to journalArticle

23 Scopus citations

Polymorphisms in the bone morphogenetic protein 2 (BMP2) gene do not affect bone mineral density in white men or women

Ichikawa, S., Johnson, M. L., Koller, D. L., Lai, D., Xuei, X., Edenberg, H. J., Hui, S. L., Foroud, T. M., Peacock, M. & Econs, M. J., Apr 1 2006, In : Osteoporosis International. 17, 4, p. 587-592 6 p.

Research output: Contribution to journalArticle

13 Scopus citations

Polymorphisms in the PON gene cluster are associated with Alzheimer disease

Erlich, P. M., Lunetta, K. L., Cupples, L. A., Huyck, M., Green, R. C., Baldwin, C. T., Farrer, L. A., Auerbach, S., Akomolafe, A., Griffith, P., Ofili, E., Browndyke, J., Schmechel, D., Welsh-Bohmer, K., Chui, H., DeCarli, C., Duara, R., Foroud, T., Farlow, M., Friedland, R. & 9 others, Go, R., Kurz, A., Obisesan, T., Petrovitch, H., White, L., Relkin, N., Sabbagh, M., Sadovnick, D. & Tsolaki, M., Jan 1 2006, In : Human molecular genetics. 15, 1, p. 77-85 9 p.

Research output: Contribution to journalArticle

70 Scopus citations
121 Scopus citations

Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia

Pankratz, N., Byder, L., Halter, C., Rudolph, A., Shults, C. W., Conneally, P. M., Foroud, T., Nichols, W. C., Lyons, K., Marder, K., Marshall, F., Oakes, D., Rudolph, A., Shinaman, A., Siemers, E., Wojcieszek, J., Belden, J., Carter, J., Camicioli, R., Andrews, P. & 79 others, Panisset, M., Hall, J., Hubble, J., Fernandez, M., Reider, C., Rajput, A., Rajput, A., Shirley, T., Mendis, T., Grimes, D. A., Gray, P., Ramos, C. S., Roque, S., Pfeiffer, R., Pfeiffer, B., Elmer, L., Davis, K., Friedman, J., Fernandez, H., Lannon, M., Reich, S., Dunlop, B., Seeberger, L., O'Brien, C., Judd, D., Hauser, R., Zesiewicz, T., Delgado, H., Fontaine, D., Jennings, D., Marek, K., Mendick, S., Aminoff, M., DiMinno, M., Lewitt, P., De Angelis, M., Pahwa, R., Thomas, S., Truong, D., Pathak, M., Tran, A., Rodnitzky, R., Dobson, J., Koller, W., Weiner, W., Lyons, K., Kurlan, R., Berry, D., Bertoni, J., Peterson, C., Martin, W., Wieler, M., Tuite, P., Schacherer, R., Harris, J., Jankovic, J., Hunter, C., Lang, A., Kleimer-Fisman, G., Nieves, A., So, J., Factor, S., Evans, S., Manyam, B., Wulbrecht, B., Walker, F., Hunt, V., Gordon, M. F., Hamman, J., Kang, U. J., Young, J., Blindauer, K., Petit, J., Rao, J., Cook, M., Stacy, M., Williamson, K., Pullman, R. S. & Boyar, K., Jan 1 2006, In : Movement Disorders. 21, 1, p. 45-49 5 p.

Research output: Contribution to journalArticle

65 Scopus citations

Root resorption associated with orthodontic force in inbred mice: Genetic contributions

Al-Qawasmi, R. A., Hartsfield, J. K., Everett, E. T., Weaver, M. R., Foroud, T. M., Faust, D. M. & Roberts, W. E., Feb 1 2006, In : European Journal of Orthodontics. 28, 1, p. 13-19 7 p.

Research output: Contribution to journalArticle

40 Scopus citations

Saccades in presymptomatic and early stages of Huntington disease

Blekher, T., Johnson, S. A., Marshall, J., White, K., Hui, S., Weaver, M., Gray, J., Yee, R., Stout, J. C., Beristain, X., Wojcieszek, J. & Foroud, T., Aug 1 2006, In : Neurology. 67, 3, p. 394-399 6 p.

Research output: Contribution to journalArticle

94 Scopus citations

The role of GABRA2 in risk for conduct disorder and alcohol and drug dependence across developmental stages

Dick, D. M., Bierut, L., Hinrichs, A., Fox, L., Bucholz, K. K., Kramer, J., Kuperman, S., Hesselbrock, V., Schuckit, M., Almasy, L., Tischfield, J., Porjesz, B., Begleiter, H., Nurnberger, J., Xuei, X., Edenberg, H. J. & Foroud, T., Jul 1 2006, In : Behavior Genetics. 36, 4, p. 577-590 14 p.

Research output: Contribution to journalArticle

172 Scopus citations
2005

A mutation in myotilin causes spheroid body myopathy

Foroud, T., Pankratz, N., Batchman, A. P., Pauciulo, M. W., Vidal, R., Miravalle, L., Goebel, H. H., Cushman, L. J., Azzarelli, B., Horak, H., Farlow, M. & Nichols, W. C., Dec 1 2005, In : Neurology. 65, 12, p. 1936-1940 5 p.

Research output: Contribution to journalArticle

62 Scopus citations

Analysis of variation in expression of autosomal dominant osteopetrosis type 2: Searching for modifier genes

Chu, K., Koller, D. L., Snyder, R., Fishburn, T., Lai, D., Waguespack, S. G., Foroud, T. & Econs, M. J., Nov 1 2005, In : Bone. 37, 5, p. 655-661 7 p.

Research output: Contribution to journalArticle

28 Scopus citations

A sex-adjusted and age-adjusted genome screen for nested alcohol dependence diagnoses

Corbett, J., Saccone, N. L., Foroud, T., Goate, A., Edenberg, H., Nurnberger, J., Porjesz, B., Begleiter, H., Reich, T. & Rice, J. P., Mar 1 2005, In : Psychiatric genetics. 15, 1, p. 25-30 6 p.

Research output: Contribution to journalArticle

19 Scopus citations

A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors

Duan, Q. L., Nikpoor, B., Dubé, M. P., Molinaro, G., Meijer, I. A., Dion, P., Rochefort, D., Saint-Onge, J., Flury, L., Brown, N. J., Gainer, J. V., Rouleau, J. L., Agostoni, A., Cugno, M., Simon, P., Clavel, P., Potier, J., Wehbe, B., Benarbia, S., Marc-Aurèle, J. & 4 others, Chanard, J., Foroud, T., Adam, A. & Rouleau, G. A., Oct 2005, In : American Journal of Human Genetics. 77, 4, p. 617-626 10 p.

Research output: Contribution to journalArticle

100 Scopus citations

Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q

McQueen, M. B., Devlin, B., Faraone, S. V., Nimgaonkar, V. L., Sklar, P., Smoller, J. W., Jamra, R. A., Albus, M., Bacanu, S. A., Baron, M., Barrett, T. B., Berrettini, W., Blacker, D., Byerley, W., Cichon, S., Coryell, W., Craddock, N., Daly, M. J., DePaulo, J. R., Edenberg, H. J. & 33 others, Foroud, T., Gill, M., Gilliam, T. C., Hamshere, M., Jones, I., Jones, L., Juo, S. H., Kelsoe, J. R., Lambert, D., Lange, C., Lerer, B., Liu, J., Maier, W., MacKinnon, J. D., McInnis, M. G., McMahon, F. J., Murphy, D. L., Nöthen, M. M., Nurnberger, J. I., Pato, C. N., Pato, M. T., Potash, J. B., Propping, P., Pulver, A. E., Rice, J. P., Rietschel, M., Scheftner, W., Schumacher, J., Segurado, R., Van Steen, K., Xie, W., Zandi, P. P. & Laird, N. M., Oct 2005, In : American Journal of Human Genetics. 77, 4, p. 582-595 14 p.

Research output: Contribution to journalArticle

164 Scopus citations

Contribution of the LRP5 gene to normal variation in peak BMD in women

Koller, D. L., Ichikawa, S., Johnson, M. L., Lai, D., Xuei, X., Edenberg, H. J., Conneally, P. M., Hui, S. L., Johnston, C. C., Peacock, M., Foroud, T. & Econs, M. J., Dec 9 2005, In : Journal of Bone and Mineral Research. 20, 1, p. 75-80 6 p.

Research output: Contribution to journalArticle

80 Scopus citations

Expression profiling and QTL analysis: A powerful complementary strategy in drug abuse research

Spence, J. P., Liang, T., Foroud, T., Lo, D. & Carr, L. G., Mar 1 2005, In : Addiction Biology. 10, 1, p. 47-51 5 p.

Research output: Contribution to journalArticle

15 Scopus citations

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

Nichols, W. C., Pankratz, N., Hernandez, D., Paisán-Ruíz, C., Jain, S., Halter, C. A., Michaels, V. E., Reed, T., Rudolph, A., Shults, C. W., Singleton, A. & Foroud, T., Jan 29 2005, In : Lancet. 365, 9457, p. 410-412 3 p.

Research output: Contribution to journalArticle

362 Scopus citations

Genome screen for bone mineral density phenotypes in Fisher 344 and Lewis rat strains

Koller, D. L., Alam, I., Sun, Q., Liu, L., Fishburn, T., Carr, L. G., Econs, M. J., Foroud, T. & Turner, C. H., Aug 1 2005, In : Mammalian Genome. 16, 8, p. 578-586 9 p.

Research output: Contribution to journalArticle

24 Scopus citations

No association of the GABAA receptor genes on chromosome 5 with alcoholism in the collaborative study on the genetics of alcoholism sample

Dick, D. M., Edenberg, H. J., Xuei, X., Goate, A., Hesselbrock, V., Schuckit, M., Crowe, R. & Foroud, T., Jan 5 2005, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 132 B, 1, p. 24-28 5 p.

Research output: Contribution to journalArticle

29 Scopus citations

Polymorphisms in the estrogen receptor β (ESR2) gene are associated with bone mineral density in Caucasian men and women

Ichikawa, S., Koller, D. L., Peacock, M., Johnson, M. L., Lai, D., Hui, S. L., Johnston, C. C., Foroud, T. M. & Econs, M. J., Nov 1 2005, In : Journal of Clinical Endocrinology and Metabolism. 90, 11, p. 5921-5927 7 p.

Research output: Contribution to journalArticle

43 Scopus citations

Relationship of age of first drink to child behavioral problems and family psychopathology

Kuperman, S., Chan, G., Kramer, J. R., Bierut, L., Bucholz, K. K., Fox, L., Hesselbrock, V., Numberger, J. I., Reich, T., Reich, W., Schuckit, M. A., Edenberg, H., Connealfy, P. M., Foroud, T., Crowe, R., Porjesz, B., Begleiter, H., Rice, J., Goate, A., Taylor, R. & 2 others, Tischfield, J. & Almasy, L., Oct 1 2005, In : Alcoholism: Clinical and Experimental Research. 29, 10, p. 1869-1876 8 p.

Research output: Contribution to journalArticle

59 Scopus citations

Sex-specific and non-sex-specific quantitative trait loci contribute to normal variation in bone mineral density in men

Peacock, M., Koller, D. L., Fishburn, T., Krishnan, S., Lai, D., Hui, S., Johnston, C. C., Foroud, T. & Econs, M. J., May 2005, In : Journal of Clinical Endocrinology and Metabolism. 90, 5, p. 3060-3066 7 p.

Research output: Contribution to journalArticle

60 Scopus citations

Sex-specific quantitative trait loci contribute to normal variation in bone structure at the proximal femur in men

Peacock, M., Koller, D. L., Lai, D., Hui, S., Foroud, T. & Econs, M. J., Oct 2005, In : Bone. 37, 4, p. 467-473 7 p.

Research output: Contribution to journalArticle

32 Scopus citations

Standard linkage and association methods identify the mechanism of four susceptibility genes for a simulated complex disease

Pankratz, N., Edenberg, E. & Foroud, T., Dec 30 2005, In : BMC genetics. 6, SUPPL.1, S142.

Research output: Contribution to journalArticle

1 Scopus citations

The Familial Intracranial Aneurysm (FIA) study protocol

Broderick, J. P., Sauerbeck, L. R., Foroud, T., Huston, J., Pankratz, N., Meissner, I. & Brown, R. D., Apr 26 2005, In : BMC Medical Genetics. 6, 17.

Research output: Contribution to journalArticle

49 Scopus citations

The North American Multiple System Atrophy Study Group

Gilman, S., May, S. J., Shults, C. W., Tanner, C. M., Kukull, W., Lee, V. M. Y., Masliah, E., Low, P., Sandroni, P., Trojanowski, J. Q., Ozelius, L. & Foroud, T., Dec 1 2005, In : Journal of Neural Transmission. 112, 12, p. 1687-1694 8 p.

Research output: Contribution to journalArticle

57 Scopus citations

Whole-genome scan for linkage to bone strength and structure in inbred Fischer 344 and Lewis rats

Alam, I., Sun, Q., Liu, L., Koller, D. L., Fishburn, T., Carr, L. G., Econs, M. J., Foroud, T. & Turner, C. H., Sep 1 2005, In : Journal of Bone and Mineral Research. 20, 9, p. 1589-1596 8 p.

Research output: Contribution to journalArticle

28 Scopus citations
2004

A genome-wide screen for genes influencing conduct disorder

Dick, D. M., Li, T. K., Edenberg, H. J., Hesselbrock, V., Kramer, J., Kuperman, S., Porjesz, B., Bucholz, K., Goate, A., Nurnberger, J. & Foroud, T., Feb 17 2004, In : Molecular Psychiatry. 9, 1, p. 81-86 6 p.

Research output: Contribution to journalArticle

73 Scopus citations

A Genomic Scan for Habitual Smoking in Families of Alcoholics: Common and Specific Genetic Factors in Substance Dependence

Bierut, L. J., Rice, J. P., Goate, A., Hinrichs, A. L., Saccone, N. L., Foroud, T., Edenberg, H. J., Cloninger, C. R., Begleiter, H., Conneally, P. M., Crowe, R. R., Hesselbrock, V., Li, T. K., Nurnberger, J. I., Porjesz, B., Schuckit, M. A. & Reich, T., Jan 1 2004, In : American Journal of Medical Genetics. 124 A, 1, p. 19-27 9 p.

Research output: Contribution to journalArticle

100 Scopus citations

Association of GABRG3 with Alcohol Dependence

Dick, D. M., Edenberg, H. J., Xuei, X., Goate, A., Kuperman, S., Schuckit, M., Crowe, R., Smith, T. L., Porjesz, B., Begleiter, H. & Foroud, T., Jan 2004, In : Alcoholism: Clinical and Experimental Research. 28, 1, p. 4-9 6 p.

Research output: Contribution to journalArticle

114 Scopus citations

Confirmation of Linkage to Chromosome 1q for Peak Vertebral Bone Mineral Density in Premenopausal White Women

Econs, M. J., Koller, D. L., Hui, S. L., Fishburn, T., Conneally, P. M., Johnston, C. C., Peacock, M. & Foroud, T. M., Feb 2004, In : American Journal of Human Genetics. 74, 2, p. 223-228 6 p.

Research output: Contribution to journalArticle

47 Scopus citations

Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease

Nichols, W. C., Uniacke, S. K., Pankratz, N., Reed, T., Simon, D. K., Halter, C., Rudolph, A., Shults, C. W., Conneally, P. M., Foroud, T., Wojcieszek, J., Belden, J., Carter, J., Camicioli, R., Andrews, P., Panisset, M., Hall, J., Hubble, J., Fernandez, M., Reider, C. & 79 others, Rajput, A., Rajput, A., Shirley, T., Mendis, T., Grimes, D. A., Gray, P., Ramos, C. S., Roque, S., Pfeiffer, R., Pfeiffer, B., Elmer, L., Davis, K., Friedman, J., Fernandez, H., Lannon, M., Reich, S., Dunlop, B., Seeberger, L., O'Brien, C., Judd, D., Hauser, R., Zesiewicz, T., Delgado, H., Shults, C., Fontaine, D., Jennings, D., Marek, K., Mendick, S., Aminoff, M., DiMinno, M., Lewitt, P., DeAngelis, M., Pahwa, R., Thomas, S., Truong, D., Pathak, M., Tran, A., Rodnitzky, R., Dobson, J., Koller, W., Weiner, W., Lyons, K., Kurlan, R., Berry, D., Bertoni, J., Peterson, C., Martin, W., Tuite, P., Schacherer, R., Marder, K., Harris, J., Jankovic, J., Hunter, C., Lang, A., Kleimer-Fisman, G., Nieves, A., So, J., Factor, S., Evans, S., Manyam, B., Wulbrecht, B., Walker, F., Hunt, V., Gordon, M. F., Hamman, J., Kang, U. J., Young, J., Blindauer, K., Petit, J., Rao, J., Cook, M., Stacy, M., Williamson, K., Pullman, R. S., Boyar, K., Leehey, M., Derian, T., Gordon, P. & Werner, J., Jun 1 2004, In : Movement Disorders. 19, 6, p. 649-655 7 p.

Research output: Contribution to journalArticle

32 Scopus citations

False positive rates in association studies as a function of degree of stratification

Koller, D. L., Peacock, M., Lai, D., Foroud, T. & Econs, M. J., Aug 1 2004, In : Journal of Bone and Mineral Research. 19, 8, p. 1291-1295 5 p.

Research output: Contribution to journalArticle

17 Scopus citations

Genes influencing Parkinson disease onset: Replication of PARK3 and identification of novel loci

Pankratz, N., Uniacke, S. K., Halter, C. A., Rudolph, A., Shults, C. W., Conneally, P. M., Foroud, T. & Nichols, W. C., May 11 2004, In : Neurology. 62, 9, p. 1616-1618 3 p.

Research output: Contribution to journalArticle

33 Scopus citations

Genetics of Parkinson Disease

Pankratz, N. & Foroud, T., Apr 1 2004, In : NeuroRx. 1, 2, p. 235-242 8 p.

Research output: Contribution to journalArticle

36 Scopus citations

Genome-Wide Scan for a Healthy Aging Phenotype Provides Support for a Locus Near D4S1564 Promoting Healthy Aging

Reed, T., Dick, D. M., Uniacke, S. K., Foroud, T. & Nichols, W. C., Mar 1 2004, In : Journals of Gerontology - Series A Biological Sciences and Medical Sciences. 59, 3, p. 227-232 6 p.

Research output: Contribution to journalArticle

37 Scopus citations

Glutathione S-transferase 8-8 expression is lower in alcohol-preferring than in alcohol-nonpreferring rats

Liang, T., Habegger, K., Spence, J. P., Foroud, T., Ellison, J. A., Lumeng, L., Li, T. K. & Carr, L. G., Nov 2004, In : Alcoholism: Clinical and Experimental Research. 28, 11, p. 1622-1628 7 p.

Research output: Contribution to journalArticle

20 Scopus citations

Linkage and linkage disequilibrium of evoked EEG oscillations with CHRM2 receptor gene polymorphisms: Implications for human brain dynamics and cognition

Jones, K. A., Porjesz, B., Almasy, L., Bierut, L., Goate, A., Wang, J. C., Dick, D. M., Hinrichs, A., Kwon, J., Rice, J. P., Rohrbaugh, J., Stock, H., Wu, W., Bauer, L. O., Chorlian, D. B., Crowe, R. R., Edenberg, H. J., Foroud, T., Hesselbrock, V., Kuperman, S. & 7 others, Nurnberger, J., O'Connor, S. J., Schuckit, M. A., Stimus, A. T., Tischfield, J. A., Reich, T. & Begleiter, H., Jul 1 2004, In : International Journal of Psychophysiology. 53, 2, p. 75-90 16 p.

Research output: Contribution to journalArticle

110 Scopus citations

Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees

Schulze, T. G., Buervenich, S., Badner, J. A., Steele, C. J. M., Detera-Wadleigh, S. D., Dick, D., Foroud, T., Cox, N. J., MacKinnon, D. F., Potash, J. B., Berrettini, W. H., Byerley, W., Coryell, W., DePaulo, J. R., Gershon, E. S., Kelsoe, J. R., McInnis, M. G., Murphy, D. L., Reich, T., Scheftner, W. & 2 others, Nurnberger, J. I. & McMahon, F. J., Jul 1 2004, In : Biological psychiatry. 56, 1, p. 18-23 6 p.

Research output: Contribution to journalArticle

57 Scopus citations

Oculomotor control in asymptomatic and recently diagnosed individuals with the genetic marker for Huntington's disease

Blekher, T. M., Yee, R. D., Kirkwood, S. C., Hake, A. M., Stout, J. C., Weaver, M. R. & Foroud, T. M., Oct 1 2004, In : Vision Research. 44, 23, p. 2729-2736 8 p.

Research output: Contribution to journalArticle

62 Scopus citations

Peak bone mineral density at the hip is linked to chromosomes 14q and 15q

Peacock, M., Koller, D. L., Hui, S., Johnston, C. C., Foroud, T. & Econs, M. J., Jun 2004, In : Osteoporosis International. 15, 6, p. 489-496 8 p.

Research output: Contribution to journalArticle

51 Scopus citations