Tatiana Foroud

  • 43539 Citations
  • 102 h-Index
1976 …2021

Research output per year

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2008

Screening for brain aneurysm in the Familial Intracranial Aneurysm study: Frequency and predictors of lesion detection

Brown, R. D., Huston, J., Hornung, R., Foroud, T., Kallmes, D. F., Kleindorfer, D., Meissner, I., Woo, D., Sauerbeck, L. & Broderick, J., Jun 1 2008, In : Journal of neurosurgery. 108, 6, p. 1132-1138 7 p.

Research output: Contribution to journalArticle

55 Scopus citations

Sex-specific genetic loci for femoral neck bone mass and strength identified in inbred COP and DA rats

Alam, I., Sun, Q., Liu, L., Koller, D. L., Carr, L. G., Econs, M. J., Foroud, T. & Turner, C. H., Jun 1 2008, In : Journal of Bone and Mineral Research. 23, 6, p. 850-859 10 p.

Research output: Contribution to journalArticle

9 Scopus citations

Ten-year rate of longitudinal change in neurocognitive and motor function in prediagnosis Huntington disease

Solomon, A. C., Stout, J. C., Weaver, M., Queller, S., Tomusk, A., Whitlock, K. B., Hui, S. L., Marshall, J., Jackson, J. G., Siemens, E. R., Beristain, X., Wojcieszek, J. & Foroud, T., Oct 15 2008, In : Movement Disorders. 23, 13, p. 1830-1836 7 p.

Research output: Contribution to journalArticle

44 Scopus citations

The tachykinin receptor 3 is associated with alcohol and cocaine dependence

Foroud, T., Wetherill, L. F., Kramer, J., Tischfield, J. A., Nurnberger, J. I., Schuckit, M. A., Xuei, X. & Edenberg, H. J., Jun 1 2008, In : Alcoholism: Clinical and Experimental Research. 32, 6, p. 1023-1030 8 p.

Research output: Contribution to journalArticle

33 Scopus citations

Variants in nicotinic receptors and risk for nicotine dependence

Bierut, L. J., Stitzel, J. A., Wang, J. C., Hinrichs, A. L., Grucza, R. A., Xuei, X., Saccone, N. L., Saccone, S. F., Bertelsen, S., Fox, L., Horton, W. J., Breslau, N., Budde, J., Cloninger, C. R., Dick, D. M., Foroud, T., Hatsukami, D., Hesselbrock, V., Johnson, E. O., Kramer, J. & 13 others, Kuperman, S., Madden, P. A. F., Mayo, K., Nurnberger, J., Pomerleau, O., Porjesz, B., Reyes, O., Schuckit, M., Swan, G., Tischfield, J. A., Edenberg, H. J., Rice, J. P. & Goate, A. M., Sep 1 2008, In : American Journal of Psychiatry. 165, 9, p. 1163-1171 9 p.

Research output: Contribution to journalArticle

437 Scopus citations

Visual perception in prediagnostic and early stage Huntington's disease

O'Donnell, B. F., Blekhert, T. M., Weaver, M., White, K. M., Marshall, J., Beristain, X., Stout, J. C., Gray, J., Wojcieszek, J. M. & Foroud, T. M., May 2008, In : Journal of the International Neuropsychological Society. 14, 3, p. 446-453 8 p.

Research output: Contribution to journalArticle

15 Scopus citations
2007

Are cognitive changes progressive in prediagnostic HD?

Stout, J. C., Weaver, M., Solomon, A. C., Queller, S., Hui, S., Johnson, S. A., Gray, J., Beristain, X., Wojcieszek, J. & Foroud, T., Dec 1 2007, In : Cognitive and Behavioral Neurology. 20, 4, p. 212-218 7 p.

Research output: Contribution to journalArticle

20 Scopus citations

Association of alcohol craving with α-synuclein (SNCA)

Foroud, T., Wetherill, L. F., Liang, T., Dick, D. M., Hesselbrock, V., Kramer, J., Nurnberger, J., Schuckit, M., Carr, L., Porjesz, B., Xuei, X. & Edenberg, H. J., Apr 1 2007, In : Alcoholism: Clinical and Experimental Research. 31, 4, p. 537-545 9 p.

Research output: Contribution to journalArticle

67 Scopus citations

G2019S mutation in the leucine-rich repeat kinase 2 gene is not associated with multiple system atrophy

Ozelius, L. J., Foroud, T., May, S., Senthil, G., Sandroni, P., Low, P. A., Reich, S., Colcher, A., Stern, M. B., Ondo, W. G., Jankovic, J., Huang, N., Tanner, C. M., Novak, P., Gilman, S., Marshall, F. J., Wooten, G. F., Chelimsky, T. C., Shults, C. W., Masliah, E. & 5 others, Kukull, W., Lee, V., Trojanowski, J., Shoulson, I. & Ozelius, L., Mar 15 2007, In : Movement Disorders. 22, 4, p. 546-549 4 p.

Research output: Contribution to journalArticle

20 Scopus citations

Lack of association of alcohol dependence and habitual smoking with catechol-O-methyltransferase

Foroud, T., Wetherill, L. F., Dick, D. M., Hesselbrock, V., Nurnberger, J. I., Kramer, J., Tischfield, J., Schuckit, M., Bierut, L. J., Xuei, X. & Edenberg, H. J., Nov 1 2007, In : Alcoholism: Clinical and Experimental Research. 31, 11, p. 1773-1779 7 p.

Research output: Contribution to journalArticle

29 Scopus citations

LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8

Nichols, W. C., Elsaesser, V. E., Pankratz, N., Pauciulo, M. W., Marek, D. K., Halter, C. A., Rudolph, A., Shults, C. W. & Foroud, T., Oct 2007, In : Neurology. 69, 18, p. 1737-1744 8 p.

Research output: Contribution to journalArticle

44 Scopus citations

Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone mass

Ioannidis, J. P. A., Ng, M. Y., Sham, P. C., Zintzaras, E., Lewis, C. M., Deng, H. W., Econs, M. J., Karasik, D., Devoto, M., Kammerer, C. M., Spector, T., Andrew, T., Cupples, L. A., Duncan, E. L., Foroud, T., Kiel, D. P., Koller, D., Langdahl, B., Mitchell, B. D., Peacock, M. & 8 others, Recker, R., Shen, H., Sol-Church, K., Spotila, L. D., Uitterlinden, A. G., Wilson, S. G., Kung, A. W. C. & Ralston, S. H., Feb 1 2007, In : Journal of Bone and Mineral Research. 22, 2, p. 173-183 11 p.

Research output: Contribution to journalArticle

130 Scopus citations

Potential outcome measures and trial design issues for multiple system atrophy

May, S., Gilman, S., Sowell, B. B., Thomas, R. G., Stern, M. B., Colcher, A., Tanner, C. M., Huang, N., Novak, P., Reich, S. G., Jankovic, J., Ondo, W. G., Low, P. A., Sandroni, P., Lipp, A., Marshall, F. J., Wooten, F., Shults, C. W., Masliah, E., Thomas, R. & 8 others, Tanner, C., Kukull, W., Lee, V., Trojanowski, J., Low, P., Shoulson, I., Ozelius, L. & Foroud, T., Dec 1 2007, In : Movement Disorders. 22, 16, p. 2371-2377 7 p.

Research output: Contribution to journalArticle

52 Scopus citations

R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation

Nichols, W. C., Marek, D. K., Pauciulo, M. W., Pankratz, N., Halter, C. A., Rudolph, A., Shults, C. W., Wojcieszek, J., Foroud, T., Shults, C., Marshall, F., Oakes, D., Rudolph, A., Shinaman, A., Marder, K., Conneally, P. M., Foroud, T., Halter, C., Lyons, K., Siemers, E. & 198 others, Factor, S., Higgins, D., Evans, S., 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., Marder, K., 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., Panisset, M., Hall, 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., Wolff, M., Fernandez, M., Hubble, J., Kostyk, S., Campbell, A., Reider, C., Camicioli, R., Carter, J., Andrews, P., Morehouse, S., Stone, C., Mendis, T., Grimes, D., Gray, P., Haas, K., Sutton, J., Hutchinson, B., Young, J., Rajput, A., Rajput, A., Klassen, L., Shirley, T., Manyam, B., Simpson, P., Whetteckey, J., Wulbrecht, B., Truong, D., Pathak, M., Luong, N., Tra, T., Tran, A., Vo, J., Lang, A., Kleiner-Fisman, G., Nieves, A., So, J., Podskalny, G., Giffin, L., Atchison, P., Allen, C., Martin, W., Wieler, M., Suchowersky, O., Klimek, M., Hermanowicz, N., Niswonger, S., Shults, C., Fontaine, D., Aminoff, M., Christine, C., Diminno, M., Hevezi, J., Dalvi, A., Kang, U., Richman, J., Uy, S., Young, J., Dalvi, A., Sahay, A., Schwieterman, D., Leehey, M., Culver, S., Derian, T., Demarcaida, T., Belber, S., Rodnitzky, R., Dobson, J., Pahwa, R., Lyons, K., Gales, T., Thomas, S., Shulman, L., Weiner, W., Dustin, K., Singer, C., Koller, W., Lyons, K., Weiner, W., Zelaya, L., Tuite, P., Hagen, V., Rolandelli, S., Schacherer, R., Gordon, P., Werner, J., Serrano, C., Roque, S., Kurlan, R., Berry, D., Gardiner, I., Hauser, R., Sanchez-Ramos, J., Zesiewicz, T., Delgado, H., Price, K., Rodriguez, P., Pfeiffer, R., Davis, L., Pfeiffer, B., Dewey, R., Hayward, B., Meacham, M., Walker, F., Hunt, V., Racette, B., Good, L., Rundle, M., Watts, A., Wang, A., Ross, T., Bennett, S., Kamp, D. & Julian-Baros, E., Jan 15 2007, In : Movement Disorders. 22, 2, p. 254-256 3 p.

Research output: Contribution to journalArticle

7 Scopus citations

Specific psychiatric manifestations among preclinical huntington disease mutation carriers

Marshall, J., White, K., Weaver, M., Flury Wetherill, L., Hui, S., Stout, J. C., Johnson, S. A., Beristain, X., Gray, J., Wojcieszek, J. & Foroud, T., Jan 1 2007, In : Archives of Neurology. 64, 1, p. 116-121 6 p.

Research output: Contribution to journalArticle

53 Scopus citations

The opioid system in alcohol and drug dependence: Family-based association study

Xuei, X., Flury-Wetherill, L., Bierut, L., Dick, D., Nurnberger, J., Foroud, T. & Edenberg, H. J., Oct 5 2007, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 144, 7, p. 877-884 8 p.

Research output: Contribution to journalArticle

61 Scopus citations

Unique facial features distinguish fetal alcohol syndrome patients and controls in diverse ethnic populations

Moore, E. S., Ward, R. E., Wetherill, L. F., Rogers, J. L., Autti-Rämö, I., Fagerlund, Å., Jacobson, S. W., Robinson, L. K., Hoyme, H. E., Mattson, S. N., Foroud, T., Riley, E., Autti-Rämö, I., Fagerlund, Å., Korkman, M., Jacobson, S. W., Robinson, L. K. & Mattson, S. N., Oct 1 2007, In : Alcoholism: Clinical and Experimental Research. 31, 10, p. 1707-1713 7 p.

Research output: Contribution to journalArticle

58 Scopus citations
2006

A cholinergic receptor gene (CHRM2) affects event-related oscillations

Jones, K. A., Porjesz, B., Almasy, L., Bierut, L., Dick, D., Goate, A., Hinrichs, A., Rice, J. P., Wang, J. C., Bauer, L. O., Crowe, R., Foroud, T., Hesselbrock, V., Kuperman, S., Nurnberger, J., O'Connor, S. J., Rohrbaugh, J., Schuckit, M. A., Tischfield, J., Edenberg, H. J. & 1 others, Begleiter, H., Sep 1 2006, In : Behavior Genetics. 36, 5, p. 627-639 13 p.

Research output: Contribution to journalArticle

55 Scopus citations

Association between GABRA1 and drinking behaviors in the Collaborative Study on the Genetics of Alcoholism sample

Dick, D. M., Plunkett, J., Wetherill, L. F., Xuei, X., Goate, A., Hesselbrock, V., Schuckit, M., Crowe, R., Edenberg, H. J. & Foroud, T., Jul 1 2006, In : Alcoholism: Clinical and Experimental Research. 30, 7, p. 1101-1110 10 p.

Research output: Contribution to journalArticle

78 Scopus citations

Association of alcohol dehydrogenase genes with alcohol dependence: A comprehensive analysis

Edenberg, H. J., Xuei, X., Chen, H. J., Tian, H., Wetherill, L. F., Dick, D. M., Almasy, L., Bierut, L., Bucholz, K. K., Goate, A., Hesselbrock, V., Kuperman, S., Nurnberger, J., Porjesz, B., Rice, J., Schuckit, M., Tischfield, J., Begleiter, H. & Foroud, T., May 1 2006, In : Human molecular genetics. 15, 9, p. 1539-1549 11 p.

Research output: Contribution to journalArticle

184 Scopus citations

Association of GABRA2 with drug dependence in the collaborative study of the genetics of alcoholism sample

Agrawal, A., Edenberg, H. J., Foroud, T., Bierut, L. J., Dunne, G., Hinrichs, A. L., Nurnberger, J. I., Crowe, R., Kuperman, S., Schuckit, M. A., Begleiter, H., Porjesz, B. & Dick, D. M., Sep 1 2006, In : Behavior Genetics. 36, 5, p. 640-650 11 p.

Research output: Contribution to journalArticle

124 Scopus citations

Association of the κ-opioid system with alcohol dependence

Xuei, X., Dick, D., Flury-Wetherill, L., Tian, H. J., Agrawal, A., Bierut, L., Goate, A., Bucholz, K., Schuckit, M., Nurnberger, J., Tischfield, J., Kuperman, S., Porjesz, B., Begleiter, H., Foroud, T. & Edenberg, H. J., Nov 27 2006, In : Molecular Psychiatry. 11, 11, p. 1016-1024 9 p.

Research output: Contribution to journalArticle

133 Scopus citations

Chromosome 5 and Parkinson disease

Foroud, T., Pankratz, N. & Martinez, M., Oct 1 2006, In : European Journal of Human Genetics. 14, 10, p. 1106-1110 5 p.

Research output: Contribution to journalArticle

4 Scopus citations

Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations

Ishihara, L., Warren, L., Gibson, R., Amouri, R., Lesage, S., Dürr, A., Tazir, M., Wszolek, Z. K., Uitti, R. J., Nichols, W. C., Griffith, A., Hattori, N., Leppert, D., Watts, R., Zabetian, C. P., Foroud, T. M., Farrer, M. J., Brice, A., Middleton, L. & Hentati, F., Sep 19 2006, In : Archives of Neurology. 63, 9, p. 1250-1254 5 p.

Research output: Contribution to journalArticle

72 Scopus citations

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

83 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

102 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

61 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

33 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

38 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

93 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

97 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

359 Scopus citations