Tatiana Foroud

  • 42200 Citations
  • 101 h-Index
1976 …2021
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Publications 1988 2020

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2012
13 Citations (Scopus)

Relation Over Time Between Facial Measurements and Cognitive Outcomes in Fetal Alcohol-Exposed Children

Foroud, T., Wetherill, L., Vinci-Booher, S., Moore, E. S., Ward, R. E., Hoyme, H. E., Robinson, L. K., Rogers, J., Meintjes, E. M., Molteno, C. D., Jacobson, J. L. & Jacobson, S. W., Sep 2012, In : Alcoholism: Clinical and Experimental Research. 36, 9, p. 1634-1646 13 p.

Research output: Contribution to journalArticle

Fetal Alcohol Spectrum Disorders
Alcohols
Ear
Central Nervous System
Logistic Models
17 Citations (Scopus)

Subjective Perceptions Associated with the Ascending and Descending Slopes of Breath Alcohol Exposure Vary with Recent Drinking History

Wetherill, L., Morzorati, S., Foroud, T., Windisch, K., Darlington, T., Zimmerman, U. S., Plawecki, M. H. & O'Connor, S., Jun 2012, In : Alcoholism: Clinical and Experimental Research. 36, 6, p. 1050-1057 8 p.

Research output: Contribution to journalArticle

Drinking
Alcohols
Alcoholism
Young Adult
Emotions
18 Citations (Scopus)

Variants located upstream of CHRNB4 on chromosome 15q25.1 are associated with age at onset of daily smoking and habitual smoking

Kapoor, M., Wang, J. C., Bertelsen, S., Bucholz, K., Budde, J. P., Hinrichs, A., Agrawal, A., Brooks, A., Chorlian, D., Dick, D., Hesselbrock, V., Foroud, T., Kramer, J., Kuperman, S., Manz, N., Nurnberger, J., Porjesz, B., Rice, J., Tischfield, J., Xuei, X. & 4 others, Schuckit, M., Edenberg, H., Bierut, L. J. & Goate, A. M., Mar 16 2012, In : PLoS One. 7, 3, e33513.

Research output: Contribution to journalArticle

alcohol abuse
Chromosomes
young adults
Age of Onset
Genes
2011
9 Citations (Scopus)

Abnormal Error-Related Antisaccade Activation in Premanifest and Early Manifest Huntington Disease

Rupp, J., Dzemidzic, M., Blekher, T., Bragulat, V., West, J., Jackson, J., Hui, S., Wojcieszek, J., Saykin, A., Kareken, D. & Foroud, T., May 2011, In : Neuropsychology. 25, 3, p. 306-318 13 p.

Research output: Contribution to journalArticle

Huntington Disease
Saccades
Gyrus Cinguli
Motor Cortex
Eye Movements
1 Citation (Scopus)

Assessing the genetic risk for alcohol use disorders

Foroud, T. & Phillips, T. J., 2011, In : Alcohol Research and Health. 34, 3, p. 266-273 8 p.

Research output: Contribution to journalArticle

Alcoholism
Alcohols
Genes
Genome
Animal Disease Models

Common genetic determinants of vitamin D insufficiency: A genome-wide association study

Wang, T. J., Zhang, F., Richards, J. B., Kestenbaum, B., Van Meurs, J. B., Berry, D., Kiel, D. P., Streeten, E. A., Ohlsson, C., Koller, D. L., Peltonen, L., Cooper, J. D., O'Reilly, P. F., Houston, D. K., Glazer, N. L., Vandenput, L., Peacock, M., Shi, J., Rivadeneira, F., McCarthy, M. I. & 56 others, Anneli, P., De Boer, I. H., Mangino, M., Kato, B., Smyth, D. J., Booth, S. L., Jacques, P. F., Burke, G. L., Goodarzi, M., Cheung, C. L., Wolf, M., Rice, K., Goltzman, D., Hidiroglou, N., Ladouceur, M., Wareham, N. J., Hocking, L. J., Hart, D., Arden, N. K., Cooper, C., Malik, S., Fraser, W. D., Hartikainen, A. L., Zhai, G., MacDonald, H. M., Forouhi, N. G., Loos, R. J. F., Reid, D. M., Hakim, A., Dennison, E., Liu, Y., Power, C., Stevens, H. E., Jaana, L., Vasan, R. S., Soranzo, N., Bojunga, J., Psaty, B. M., Lorentzon, M., Foroud, T., Harris, T. B., Hofman, A., Jansson, J. O., Cauley, J. A., Uitterlinden, A. G., Gibson, Q., Järvelin, M. R., Karasik, D., Siscovick, D. S., Econs, M., Kritchevsky, S. B., Florez, J. C., Todd, J. A., Dupuis, J., Hyppönen, E. & Spector, T. D., Feb 2011, In : Obstetrical and Gynecological Survey. 66, 2, p. 91-93 3 p.

Research output: Contribution to journalArticle

1102 Citations (Scopus)

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

Naj, A. C., Jun, G., Beecham, G. W., Wang, L. S., Vardarajan, B. N., Buros, J., Gallins, P. J., Buxbaum, J. D., Jarvik, G. P., Crane, P. K., Larson, E. B., Bird, T. D., Boeve, B. F., Graff-Radford, N. R., De Jager, P. L., Evans, D., Schneider, J. A., Carrasquillo, M. M., Ertekin-Taner, N., Younkin, S. G. & 135 others, Cruchaga, C., Kauwe, J. S. K., Nowotny, P., Kramer, P., Hardy, J., Huentelman, M. J., Myers, A. J., Barmada, M. M., Demirci, F. Y., Baldwin, C. T., Green, R. C., Rogaeva, E., George-Hyslop, P. S., Arnold, S. E., Barber, R., Beach, T., Bigio, E. H., Bowen, J. D., Boxer, A., Burke, J. R., Cairns, N. J., Carlson, C. S., Carney, R. M., Carroll, S. L., Chui, H. C., Clark, D. G., Corneveaux, J., Cotman, C. W., Cummings, J. L., Decarli, C., Dekosky, S. T., Diaz-Arrastia, R., Dick, M., Dickson, D. W., Ellis, W. G., Faber, K. M., Fallon, K. B., Farlow, M., Ferris, S., Frosch, M. P., Galasko, D. R., Ganguli, M., Gearing, M., Geschwind, D. H., Ghetti, B., Gilbert, J. R., Gilman, S., Giordani, B., Glass, J. D., Growdon, J. H., Hamilton, R. L., Harrell, L. E., Head, E., Honig, L. S., Hulette, C. M., Hyman, B. T., Jicha, G. A., Jin, L. W., Johnson, N., Karlawish, J., Karydas, A., Kaye, J. A., Kim, R., Koo, E. H., Kowall, N. W., Lah, J. J., Levey, A. I., Lieberman, A. P., Lopez, O. L., MacK, W. J., Marson, D. C., Martiniuk, F., Mash, D. C., Masliah, E., McCormick, W. C., McCurry, S. M., McDavid, A. N., McKee, A. C., Mesulam, M., Miller, B. L., Miller, C. A., Miller, J. W., Parisi, J. E., Perl, D. P., Peskind, E., Petersen, R. C., Poon, W. W., Quinn, J. F., Rajbhandary, R. A., Raskind, M., Reisberg, B., Ringman, J. M., Roberson, E. D., Rosenberg, R. N., Sano, M., Schneider, L. S., Seeley, W., Shelanski, M. L., Slifer, M. A., Smith, C. D., Sonnen, J. A., Spina, S., Stern, R. A., Tanzi, R. E., Trojanowski, J. Q., Troncoso, J. C., Van Deerlin, V. M., Vinters, H. V., Vonsattel, J. P., Weintraub, S., Welsh-Bohmer, K. A., Williamson, J., Woltjer, R. L., Cantwell, L. B., Dombroski, B. A., Beekly, D., Lunetta, K. L., Martin, E. R., Kamboh, M. I., Saykin, A., Reiman, E. M., Bennett, D. A., Morris, J. C., Montine, T. J., Goate, A. M., Blacker, D., Tsuang, D. W., Hakonarson, H., Kukull, W. A., Foroud, T., Haines, J. L., Mayeux, R., Pericak-Vance, M. A., Farrer, L. A. & Schellenberg, G. D., May 2011, In : Nature Genetics. 43, 5, p. 436-443 8 p.

Research output: Contribution to journalArticle

Alzheimer Disease
Meta-Analysis
Genome-Wide Association Study
Disease Susceptibility
Genome
7 Citations (Scopus)

Copy number variation accuracy in genome-wide association studies

Lin, P., Hartz, S. M., Wang, J. C., Krueger, R. F., Foroud, T., Edenberg, H., Nurnberger, J., Brooks, A. I., Tischfield, J. A., Almasy, L., Webb, B. T., Hesselbrock, V. M., Porjesz, B., Goate, A. M., Bierut, L. J. & Rice, J. P., Jul 2011, In : Human Heredity. 71, 3, p. 141-147 7 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Research Personnel
Chromosome Duplication
Reproducibility of Results
Software
39 Citations (Scopus)

Copy number variation in familial parkinson disease

Pankratz, N., Dumitriu, A., Hetrick, K. N., Sun, M., Latourelle, J. C., Wilk, J. B., Halter, C., Doheny, K. F., Gusella, J. F., Nichols, W. C., Myers, R. H., Foroud, T. & DeStefano, A. L., 2011, In : PLoS One. 6, 8, e20988.

Research output: Contribution to journalArticle

Parkinson disease
Parkinson Disease
Genes
loci
DNA
9 Citations (Scopus)

Fine mapping quantitative trait loci that influence alcohol preference behavior in the high and low alcohol preferring (HAP and LAP) mice

Bice, P. J., Lai, D., Zhang, L. & Foroud, T., Jul 2011, In : Behavior Genetics. 41, 4, p. 565-570 6 p.

Research output: Contribution to journalArticle

preference behavior
Quantitative Trait Loci
alcohol
chromosome
quantitative trait loci
5 Citations (Scopus)

Genetic association of bipolar disorder with the β3 nicotinic receptor subunit gene

Hartz, S. M., Lin, P., Edenberg, H., Xuei, X., Rochberg, N., Saccone, S., Berrettini, W., Nelson, E., Nurnberger, J., Bierut, L. J., Rice, J. P., Miller, M. J., Bowman, E. S., Rau, N. L., Moe, P. R., Samavedy, N., El-Mallakh, R., Manji, H., Glitz, D. A., Meyer, E. T. & 42 others, Smiley, C., Foroud, T., Flury, L., Dick, D. M., Reich, T., Goate, A., McInnis, M., DePaulo, J. R., MacKinnon, D. F., Mondimore, F. M., Potash, J. B., Zandi, P. P., Avramopoulos, D., Payne, J., Byerley, W., Vinogradov, S., Coryell, W., Crowe, R., Gershon, E., Badner, J., McMahon, F., Liu, C., Sanders, A., Caserta, M., Dinwiddie, S., Nguyen, T., Harakal, D., Kelsoe, J., McKinney, R., Scheftner, W., Kravitz, H. M., Marta, D., Vaughn-Brown, A., Bederow, L., McMahon, F. J., Kassem, L., Detera-Wadleigh, S., Austin, L., Murphy, D. L., Lawson, W. B., Nwulia, E. & Hipolito, M., Apr 2011, In : Psychiatric Genetics. 21, 2, p. 77-84 8 p.

Research output: Contribution to journalArticle

Nicotinic Receptors
Tobacco Use Disorder
Bipolar Disorder
Genes
Single Nucleotide Polymorphism
4 Citations (Scopus)

Genetics and genomics of late-onset Alzheimer's disease and its endophenotypes

Reitz, C., Rogaeva, E., Foroud, T. & Farrer, L. A., 2011, In : International Journal of Alzheimer's Disease. 284728.

Research output: Contribution to journalArticle

181 Citations (Scopus)

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

Schumann, G., Coin, L. J., Lourdusamy, A., Charoen, P., Berger, K. H., Stacey, D., Desrivières, S., Aliev, F. A., Khan, A. A., Amin, N., Aulchenko, Y. S., Bakalkin, G., Bakker, S. J., Balkau, B., Beulens, J. W., Bilbao, A., De Boer, R. A., Beury, D., Bots, M. L., Breetvelt, E. J. & 96 others, Cauchi, S., Cavalcanti-Proença, C., Chambers, J. C., Clarke, T. K., Dahmen, N., De Geus, E. J., Dick, D., Ducci, F., Easton, A., Edenberg, H., Esk, T., Fernández-Medarde, A., Foroud, T., Freimer, N. B., Girault, J. A., Grobbee, D. E., Guarrera, S., Gudbjartsson, D. F., Hartikainen, A. L., Heath, A. C., Hesselbrock, V., Hofman, A., Hottenga, J. J., Isohanni, M. K., Kaprio, J., Khaw, K. T., Kuehnel, B., Laitinen, J., Lobbens, S., Luan, J., Mangino, M., Maroteaux, M., Matullo, G., McCarthy, M. I., Mueller, C., Navis, G., Numans, M. E., Núñez, A., Nyholt, D. R., Onland-Moret, C. N., Oostra, B. A., O'Reilly, P. F., Palkovits, M., Penninx, B. W., Polidoro, S., Pouta, A., Prokopenko, I., Ricceri, F., Santos, E., Smit, J. H., Soranzo, N., Song, K., Sovio, U., Stumvoll, M., Surakk, I., Thorgeirsson, T. E., Thorsteinsdottir, U., Troakes, C., Tyrfingsson, T., Tönjes, A., Uiterwaal, C. S., Uitterlinden, A. G., Van Der Harst, P., Van Der Schouw, Y. T., Staehlin, O., Vogelzangs, N., Vollenweider, P., Waeber, G., Wareham, N. J., Waterworth, D. M., Whitfield, J. B., Wichmann, E. H., Willemsen, G., Witteman, J. C., Yuan, X., Zhai, G., Zhao, J. H., Zhang, W., Martin, N. G., Metspalu, A., Doering, A., Scott, J., Spector, T. D., Loos, R. J., Boomsma, D. I., Mooser, V., Peltonen, L., Stefansson, K., Van Duijn, C. M., Vineis, P., Sommer, W. H., Kooner, J. S., Spanagel, R., Heberlein, U. A., Jarvelin, M. R. & Elliott, P., Apr 26 2011, In : Proceedings of the National Academy of Sciences of the United States of America. 108, 17, p. 7119-7124 6 p.

Research output: Contribution to journalArticle

Genetic Association Studies
Autistic Disorder
Alcohol Drinking
Genome
Genes
2 Citations (Scopus)

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (Proceedings of the National Academy Sciences of the United States of America (2011) 108, 17, (7119-7124))

Schumann, G., Coin, L. J., Lourdusamy, A., Charoen, P., Berger, K. H., Stacey, D., Desrivières, S., Aliev, F. A., Khan, A. A., Amin, N., Aulchenko, Y. S., Bakalkin, G., Bakker, S. J., Balkau, B., Beulens, J. W., Bilbao, A., De Boer, R. A., Beury, D., Bots, M. L., Breetvelt, E. J. & 96 others, Cauchi, S., Cavalcanti-Proença, C., Chambers, J. C., Clarke, T. K., Dahmen, N., De Geus, E. J., Dick, D., Ducci, F., Easton, A., Edenberg, H., Esk, T., Fernández-Medarde, A., Foroud, T., Freimer, N. B., Girault, J. A., Grobbee, D. E., Guarrera, S., Gudbjartsson, D. F., Hartikainen, A. L., Heath, A. C., Hesselbrock, V., Hofman, A., Hottenga, J. J., Isohanni, M. K., Kaprio, J., Khaw, K. T., Kuehnel, B., Laitinen, J., Lobbens, S., Luan, J., Mangino, M., Maroteaux, M., Matullo, G., McCarthy, M. I., Mueller, C., Navis, G., Numans, M. E., Núñez, A., Nyholt, D. R., Onland-Moret, C. N., Oostra, B. A., O'Reilly, P. F., Palkovits, M., Penninx, B. W., Polidoro, S., Pouta, A., Prokopenko, I., Ricceri, F., Santos, E., Smit, J. H., Soranzo, N., Song, K., Sovio, U., Stumvoll, M., Surakk, I., Thorgeirsson, T. E., Thorsteinsdottir, U., Troakes, C., Tyrfingsson, T., Tönjes, A., Uiterwaal, C. S., Uitterlinden, A. G., Van Der Harst, P., Van Der Schouw, Y. T., Staehlin, O., Vogelzangs, N., Vollenweider, P., Waeber, G., Wareham, N. J., Waterworth, D. M., Whitfield, J. B., Wichmann, E. H., Willemsen, G., Witteman, J. C., Yuan, X., Zhai, G., Zhao, J. H., Zhang, W., Martin, N. G., Metspalu, A., Doering, A., Scott, J., Spector, T. D., Loos, R. J., Boomsma, D. I., Mooser, V., Peltonen, L., Stefansson, K., Van Duijn, C. M., Vineis, P., Sommer, W. H., Kooner, J. S., Spanagel, R., Heberlein, U. A., Jarvelin, M. R. & Elliott, P., May 31 2011, In : Proceedings of the National Academy of Sciences of the United States of America. 108, 22, p. 9316 1 p.

Research output: Contribution to journalArticle

45 Citations (Scopus)

Genome-Wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes

Smith, E. N., Koller, D. L., Panganiban, C., Szelinger, S., Zhang, P., Badner, J. A., Barrett, T. B., Berrettini, W. H., Bloss, C. S., Byerley, W., Coryell, W., Edenberg, H., Foroud, T., Gershon, E. S., Greenwood, T. A., Guo, Y., Hipolito, M., Keating, B. J., Lawson, W. B., Liu, C. & 18 others, Mahon, P. B., McInnis, M. G., McMahon, F. J., McKinney, R., Murray, S. S., Nievergelt, C. M., Nurnberger, J., Nwulia, E. A., Potash, J. B., Rice, J., Schulze, T. G., Scheftner, W. A., Shilling, P. D., Zandi, P. P., Zöllner, S., Craig, D. W., Schork, N. J. & Kelsoe, J. R., Jun 2011, In : PLoS Genetics. 7, 6, e1002134.

Research output: Contribution to journalArticle

Bipolar Disorder
exons
genome
Genome-Wide Association Study
Genome
148 Citations (Scopus)

Genome-wide association of familial late-onset alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE

Wijsman, E. M., Pankratz, N. D., Choi, Y., Rothstein, J. H., Faber, K. M., Cheng, R., Lee, J. H., Bird, T. D., Bennett, D. A., Diaz-Arrastia, R., Goate, A. M., Farlow, M., Ghetti, B., Sweet, R. A., Foroud, T. & Mayeux, R., Feb 2011, In : PLoS Genetics. 7, 2, e1001308.

Research output: Contribution to journalArticle

Alzheimer disease
Social Adjustment
Alzheimer Disease
genome
Genome
135 Citations (Scopus)

Genome-wide association study of CSF biomarkers Aβ1-42, t-tau, and p-tau181p in the ADNI cohort

Kim, S., Swaminathan, S., Shen, L., Risacher, S. L., Nho, K., Foroud, T., Shaw, L. M., Trojanowski, J. Q., Potkin, S. G., Huentelman, M. J., Craig, D. W., Dechairo, B. M., Aisen, P. S., Petersen, R. C., Weiner, M. W. & Saykin, A., Jan 4 2011, In : Neurology. 76, 1, p. 69-79 11 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Single Nucleotide Polymorphism
Biomarkers
Genes
Alzheimer Disease
58 Citations (Scopus)

Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence

Zlojutro, M., Manz, N., Rangaswamy, M., Xuei, X., Flury-Wetherill, L., Koller, D., Bierut, L. J., Goate, A., Hesselbrock, V., Kuperman, S., Nurnberger, J., Rice, J. P., Schuckit, M. A., Foroud, T., Edenberg, H., Porjesz, B. & Almasy, L., Jan 2011, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 156, 1, p. 44-58 15 p.

Research output: Contribution to journalArticle

Serotonin Receptors
Genome-Wide Association Study
Alcoholism
Brain
Genes
5 Citations (Scopus)

Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease

Latourelle, J. C., Hendricks, A. E., Pankratz, N., Wilk, J. B., Halter, C., Nichols, W. C., Gusella, J. F., Destefano, A. L., Myers, R. H. & Foroud, T., Sep 2011, In : Movement Disorders. 26, 11, p. 2039-2044 6 p.

Research output: Contribution to journalArticle

Leucine
Parkinson Disease
Phosphotransferases
Age of Onset
Single Nucleotide Polymorphism
38 Citations (Scopus)

Genomic copy number analysis in Alzheimer's disease and mild cognitive impairment: An ADNI study

Saykin, A., Swaminathan, S., Kim, S., Shen, L., Risacher, S. L., Foroud, T., Pankratz, N., Potkin, S. G., Huentelman, M. J., Craig, D. W. & Weiner, M. W., 2011, In : International Journal of Alzheimer's Disease. 729478.

Research output: Contribution to journalArticle

Alzheimer Disease
Overlapping Genes
Genetic Association Studies
Neuroimaging
Quality Control
40 Citations (Scopus)

Heritability of different forms of memory in the late onset alzheimer's disease family study

Wilson, R. S., Barral, S., Lee, J. H., Leurgans, S. E., Foroud, T., Sweet, R. A., Graff-Radford, N., Bird, T. D., Mayeux, R. & Bennett, D. A., 2011, In : Journal of Alzheimer's Disease. 23, 2, p. 249-255 7 p.

Research output: Contribution to journalArticle

Alzheimer Disease
Episodic Memory
Short-Term Memory
Semantics
Endophenotypes
12 Citations (Scopus)

Heterogeneous stock rat: A unique animal model for mapping genes influencing bone fragility

Alam, I., Koller, D. L., Sun, Q., Roeder, R. K., Cañete, T., Blázquez, G., López-Aumatell, R., Martínez-Membrives, E., Vicens-Costa, E., Mont, C., Díaz, S., Tobeña, A., Fernández-Teruel, A., Whitley, A., Strid, P., Diez, M., Johannesson, M., Flint, J., Econs, M., Turner, C. H. & 1 others, Foroud, T., May 1 2011, In : Bone. 48, 5, p. 1169-1177 9 p.

Research output: Contribution to journalArticle

Chromosome Mapping
Animal Models
Bone and Bones
Phenotype
Inbred Strains Rats

Interactive feature visualization and detection for 3D face classification

McLaughlin, J., Fang, S., Jacobson, S. W., Hoyme, H. E., Robinson, L. & Foroud, T., Apr 2011, In : International Journal of Cognitive Informatics and Natural Intelligence. 5, 2, p. 1-16 16 p.

Research output: Contribution to journalArticle

Visualization
Alcohols
Lighting
Decision making
Geometry
834 Citations (Scopus)

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

Sklar, P., Ripke, S., Scott, L. J., Andreassen, O. A., Cichon, S., Craddock, N., Edenberg, H., Nurnberger, J., Rietschel, M., Blackwood, D., Corvin, A., Flickinger, M., Guan, W., Mattingsdal, M., McQuillin, A., Kwan, P., Wienker, T. F., Daly, M., Dudbridge, F., Holmans, P. A. & 152 others, Lin, D., Burmeister, M., Greenwood, T. A., Hamshere, M. L., Muglia, P., Smith, E. N., Zandi, P. P., Nievergelt, C. M., McKinney, R., Shilling, P. D., Schork, N. J., Bloss, C. S., Foroud, T., Koller, D. L., Gershon, E. S., Liu, C., Badner, J. A., Scheftner, W. A., Lawson, W. B., Nwulia, E. A., Hipolito, M., Coryell, W., Rice, J., Byerley, W., McMahon, F. J., Schulze, T. G., Berrettini, W., Lohoff, F. W., Potash, J. B., Mahon, P. B., McInnis, M. G., Zöllner, S., Zhang, P., Craig, D. W., Szelinger, S., Barrett, T. B., Breuer, R., Meier, S., Strohmaier, J., Witt, S. H., Tozzi, F., Farmer, A., McGuffin, P., Strauss, J., Xu, W., Kennedy, J. L., Vincent, J. B., Matthews, K., Day, R., Ferreira, M. A., O'Dushlaine, C., Perlis, R., Raychaudhuri, S., Ruderfer, D., Lee, P. H., Smoller, J. W., Li, J., Absher, D., Bunney, W. E., Barchas, J. D., Schatzberg, A. F., Jones, E. G., Meng, F., Thompson, R. C., Watson, S. J., Myers, R. M., Akil, H., Boehnke, M., Chambert, K., Moran, J., Scolnick, E., Djurovic, S., Melle, I., Morken, G., Gill, M., Morris, D., Quinn, E., Mühleisen, T. W., Degenhardt, F. A., Mattheisen, M., Schumacher, J., Maier, W., Steffens, M., Propping, P., Nöthen, M. M., Anjorin, A., Bass, N., Gurling, H., Kandaswamy, R., Lawrence, J., McGhee, K., McIntosh, A., McLean, A. W., Muir, W. J., Pickard, B. S., Breen, G., St. Clair, D., Caesar, S., Gordon-Smith, K., Jones, L., Fraser, C., Green, E. K., Grozeva, D., Jones, I. R., Kirov, G., Moskvina, V., Nikolov, I., O'Donovan, M. C., Owen, M. J., Collier, D. A., Elkin, A., Williamson, R., Young, A. H., Nicol Ferrier, I., Stefansson, K., Stefansson, H., Porgeirsson, P., Steinberg, S., Gustafsson, Ó., Bergen, S. E., Nimgaonkar, V., Hultman, C., Landén, M., Lichtenstein, P., Sullivan, P., Schalling, M., Osby, U., Backlund, L., Frisén, L., Langstrom, N., Jamain, S., Leboyer, M., Etain, B., Bellivier, F., Petursson, H., Sigurdsson, E., Müller-Mysok, B., Lucae, S., Schwarz, M., Fullerton, J. M., Schofield, P. R., Martin, N., Montgomery, G. W., Lathrop, M., Óskarsson, H., Bauer, M., Wright, A., Mitchell, P. B., Hautzinger, M., Reif, A., Kelsoe, J. R. & Purcell, S. M., Oct 2011, In : Nature Genetics. 43, 10, p. 977-985 9 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Bipolar Disorder
Single Nucleotide Polymorphism
Calcium Channels
Sample Size
176 Citations (Scopus)

Translation initiator EIF4G1 mutations in familial parkinson disease

Chartier-Harlin, M. C., Dachsel, J. C., Vilariño-Güell, C., Lincoln, S. J., Leprêtre, F., Hulihan, M. M., Kachergus, J., Milnerwood, A. J., Tapia, L., Song, M. S., Le Rhun, E., Mutez, E., Larvor, L., Duflot, A., Vanbesien-Mailliot, C., Kreisler, A., Ross, O. A., Nishioka, K., Soto-Ortolaza, A. I., Cobb, S. A. & 30 others, Melrose, H. L., Behrouz, B., Keeling, B. H., Bacon, J. A., Hentati, E., Williams, L., Yanagiya, A., Sonenberg, N., Lockhart, P. J., Zubair, A. C., Uitti, R. J., Aasly, J. O., Krygowska-Wajs, A., Opala, G., Wszolek, Z. K., Frigerio, R., Maraganore, D. M., Gosal, D., Lynch, T., Hutchinson, M., Bentivoglio, A. R., Valente, E. M., Nichols, W. C., Pankratz, N., Foroud, T., Gibson, R. A., Hentati, F., Dickson, D. W., Destée, A. & Farrer, M. J., Sep 9 2011, In : American Journal of Human Genetics. 89, 3, p. 398-406 9 p.

Research output: Contribution to journalArticle

Parkinsonian Disorders
Parkinson Disease
Mutation
Eukaryotic Initiation Factor-4G
Lewy Body Disease
4 Citations (Scopus)

Understanding the effects of prenatal alcohol exposure using threedimensional facial imaging

Wetherill, L. & Foroud, T., 2011, In : Alcohol Research and Health. 34, 1, p. 38-41 4 p.

Research output: Contribution to journalArticle

Prenatal Exposure Delayed Effects
Fetal Alcohol Spectrum Disorders
Three-Dimensional Imaging
Alcohol Drinking
Alcohols
81 Citations (Scopus)

Voxelwise gene-wide association study (vGeneWAS): Multivariate gene-based association testing in 731 elderly subjects

Hibar, D. P., Stein, J. L., Kohannim, O., Jahanshad, N., Saykin, A., Shen, L., Kim, S., Pankratz, N., Foroud, T., Huentelman, M. J., Potkin, S. G., Jack, C. R., Weiner, M. W., Toga, A. W. & Thompson, P. M., Jun 15 2011, In : NeuroImage. 56, 4, p. 1875-1891 17 p.

Research output: Contribution to journalArticle

Genes
Brain
Single Nucleotide Polymorphism
Genome
Neuroimaging
2010
172 Citations (Scopus)

A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly

Ho, A. J., Stein, J. L., Hua, X., Lee, S., Hibar, D. P., Leow, A. D., Dinov, I. D., Toga, A. W., Saykin, A., Shen, L., Foroud, T., Pankratz, N., Huentelman, M. J., Craig, D. W., Gerber, J. D., Allen, A. N., Corneveaux, J. J., Stephan, D. A., DeCarli, C. S., DeChairo, B. M. & 8 others, Potkin, S. G., Jack, C. R., Weiner, M. W., Raji, C. A., Lopez, O. L., Becker, J. T., Carmichael, O. T. & Thompson, P. M., May 4 2010, In : Proceedings of the National Academy of Sciences of the United States of America. 107, 18, p. 8404-8409 6 p.

Research output: Contribution to journalArticle

Obesity
Fats
Alleles
Brain
Genes
337 Citations (Scopus)

A genome-wide association study of alcohol dependence

Bierut, L. J., Agrawal, A., Bucholz, K. K., Doheny, K. F., Laurie, C., Pugh, E., Fisher, S., Fox, L., Howells, W., Bertelsen, S., Hinrichs, A. L., Almasy, L., Breslau, N., Culverhouse, R. C., Dick, D. M., Edenberg, H., Foroud, T., Grucza, R. A., Hatsukami, D., Hesselbrock, V. & 19 others, Johnson, E. O., Kramer, J., Krueger, R. F., Kuperman, S., Lynskey, M., Mann, K., Neuman, R. J., Nöthen, M. M., Nurnberger, J., Porjesz, B., Ridinger, M., Saccone, N. L., Saccone, S. F., Schuckit, M. A., Tischfield, J. A., Wang, J. C., Rietschel, M., Goate, A. M. & Rice, J. P., Mar 16 2010, In : Proceedings of the National Academy of Sciences of the United States of America. 107, 11, p. 5082-5087 6 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Alcoholism
Single Nucleotide Polymorphism
Drinking
Alcohols
199 Citations (Scopus)

Alzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans

Saykin, A., Shen, L., Foroud, T., Potkin, S. G., Swaminathan, S., Kim, S., Risacher, S. L., Nho, K., Huentelman, M. J., Craig, D. W., Thompson, P. M., Stein, J. L., Moore, J. H., Farrer, L. A., Green, R. C., Bertram, L., Jack, C. R. & Weiner, M. W., May 2010, In : Alzheimer's and Dementia. 6, 3, p. 265-273 9 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Neuroimaging
Alzheimer Disease
Biomarkers
Phenotype
48 Citations (Scopus)

A polymorphism in GABRA2 is associated with the medial frontal response to alcohol cues in an fMRI study

Kareken, D., Liang, T., Wetherill, L., Dzemidzic, M., Bragulat, V., Cox, C., Talavage, T., O'Connor, S. & Foroud, T., Dec 2010, In : Alcoholism: Clinical and Experimental Research. 34, 12, p. 2169-2178 10 p.

Research output: Contribution to journalArticle

Polymorphism
Cues
Odor control
Alcohols
Magnetic Resonance Imaging
14 Citations (Scopus)

A principal components analysis of the abbreviated desires for alcohol questionnaire (DAQ)

Kramer, J. R., Chan, G., Hesselbrock, V. M., Kuperman, S., Bucholz, K. K., Edenberg, H., Schuckit, M. A., Nurnberger, J., Foroud, T., Dick, D. M., Bierut, L. J. & Porjesz, B., Jan 2010, In : Journal of Studies on Alcohol and Drugs. 71, 1, p. 150-155 6 p.

Research output: Contribution to journalArticle

Principal Component Analysis
Principal component analysis
alcohol
Alcohols
questionnaire
16 Citations (Scopus)
Alzheimer Disease
Magnetic Resonance Imaging
Cognitive Dysfunction
Early Diagnosis
Brain
15 Citations (Scopus)

Clinical implications of gene discovery in Parkinson's disease and parkinsonism

Wider, C., Foroud, T. & Wszolek, Z. K., 2010, In : Movement Disorders. 25, SUPPL. 1

Research output: Contribution to journalArticle

Genetic Association Studies
Parkinsonian Disorders
Parkinson Disease
Genes
Mutation
56 Citations (Scopus)

Collaborative initiative on fetal alcohol spectrum disorders: Methodology of clinical projects

Mattson, S. N., Foroud, T., Sowell, E. R., Jones, K. L., Coles, C. D., Fagerlund, Å., Autti-Rämö, I., May, P. A., Adnams, C. M., Konovalova, V., Wetherill, L., Arenson, A. D., Barnett, W. K. & Riley, E. P., Nov 2010, In : Alcohol. 44, 7-8, p. 635-641 7 p.

Research output: Contribution to journalArticle

Fetal Alcohol Spectrum Disorders
alcohol
Alcohols
Imaging techniques
Three-Dimensional Imaging
978 Citations (Scopus)

Common genetic determinants of vitamin D insufficiency: A genome-wide association study

Wang, T. J., Zhang, F., Richards, J. B., Kestenbaum, B., Van Meurs, J. B., Berry, D., Kiel, D. P., Streeten, E. A., Ohlsson, C., Koller, D. L., Peltonen, L., Cooper, J. D., O'Reilly, P. F., Houston, D. K., Glazer, N. L., Vandenput, L., Peacock, M., Shi, J., Rivadeneira, F., McCarthy, M. I. & 56 others, Anneli, P., De Boer, I. H., Mangino, M., Kato, B., Smyth, D. J., Booth, S. L., Jacques, P. F., Burke, G. L., Goodarzi, M., Cheung, C. L., Wolf, M., Rice, K., Goltzman, D., Hidiroglou, N., Ladouceur, M., Wareham, N. J., Hocking, L. J., Hart, D., Arden, N. K., Cooper, C., Malik, S., Fraser, W. D., Hartikainen, A. L., Zhai, G., Macdonald, H. M., Forouhi, N. G., Loos, R. J. F., Reid, D. M., Hakim, A., Dennison, E., Liu, Y., Power, C., Stevens, H. E., Jaana, L., Vasan, R. S., Soranzo, N., Bojunga, J., Psaty, B. M., Lorentzon, M., Foroud, T., Harris, T. B., Hofman, A., Jansson, J. O., Cauley, J. A., Uitterlinden, A. G., Gibson, Q., Järvelin, M. R., Karasik, D., Siscovick, D. S., Econs, M., Kritchevsky, S. B., Florez, J. C., Todd, J. A., Dupuis, J., Hyppönen, E. & Spector, T. D., 2010, In : The Lancet. 376, 9736, p. 180-188 9 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Vitamin D
Genome
Genotype
Luminescent Measurements
24 Citations (Scopus)

Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts

Dick, D. M., Meyers, J., Aliev, F., Nurnberger, J., Kramer, J., Kuperman, S., Porjesz, B., Tischfield, J., Edenberg, H., Foroud, T., Schuckit, M., Goate, A., Hesselbrock, V. & Bierut, L., Sep 2010, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153, 6, p. 1179-1188 10 p.

Research output: Contribution to journalArticle

Conduct Disorder
Chromosomes, Human, Pair 2
Suicide
Alcoholism
Phenotype
16 Citations (Scopus)

Fine mapping and expression of candidate genes within the chromosome 10 QTL region of the high and low alcohol-drinking rats

Bice, P. J., Liang, T., Zhang, L., Graves, T. J., Carr, L. G., Lai, D., Kimpel, M. W. & Foroud, T., Sep 2010, In : Alcohol. 44, 6, p. 477-485 9 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 10
Quantitative Trait Loci
Chromosomes
Alcohol Drinking
Rats
37 Citations (Scopus)

GABRR1 and GABRR2, encoding the GABA-A receptor subunits ρ1 and ρ2, are associated with alcohol dependence

Xuei, X., Flury-Wetherill, L., Dick, D., Goate, A., Tischfield, J., Nurnberger, J., Schuckit, M., Kramer, J., Kuperman, S., Hesselbrock, V., Porjesz, B., Foroud, T. & Edenberg, H., Mar 2010, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153, 2, p. 418-427 10 p.

Research output: Contribution to journalArticle

GABA-A Receptors
Alcoholism
Single Nucleotide Polymorphism
Haplotypes
Genes
8 Citations (Scopus)

Genes influencing spinal bone mineral density in inbred F344, LEW, COP, and DA rats

Alam, I., Sun, Q., Koller, D. L., Liu, L., Liu, Y., Edenberg, H., Foroud, T. & Turner, C. H., Mar 2010, In : Functional and Integrative Genomics. 10, 1, p. 63-72 10 p.

Research output: Contribution to journalArticle

Bone Density
Genes
Quantitative Trait Loci
Polymerase Chain Reaction
Inbred F344 Rats
26 Citations (Scopus)

Genetic research: who is at risk for alcoholism

Foroud, T., Edenberg, H. & Crabbe, J. C., 2010, In : Alcohol Research and Health. 33, 1-2, p. 64-75 12 p.

Research output: Contribution to journalArticle

Genetic Research
Alcoholism
National Institute on Alcohol Abuse and Alcoholism (U.S.)
Genes
Alcohols
106 Citations (Scopus)

Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease

Stein, J. L., Hua, X., Morra, J. H., Lee, S., Hibar, D. P., Ho, A. J., Leow, A. D., Toga, A. W., Sul, J. H., Kang, H. M., Eskin, E., Saykin, A., Shen, L., Foroud, T., Pankratz, N., Huentelman, M. J., Craig, D. W., Gerber, J. D., Allen, A. N., Corneveaux, J. J. & 7 others, Stephan, D. A., Webster, J., DeChairo, B. M., Potkin, S. G., Jack, C. R., Weiner, M. W. & Thompson, P. M., Jun 2010, In : NeuroImage. 51, 2, p. 542-554 13 p.

Research output: Contribution to journalArticle

Temporal Lobe
Single Nucleotide Polymorphism
Alzheimer Disease
Genome
Genes
224 Citations (Scopus)

Genome-wide association study of alcohol dependence implicates a region on chromosome 11

Edenberg, H., Koller, D. L., Xuei, X., Wetherill, L., McClintick, J., Almasy, L., Bierut, L. J., Bucholz, K. K., Goate, A., Aliev, F., Dick, D., Hesselbrock, V., Hinrichs, A., Kramer, J., Kuperman, S., Nurnberger, J., Rice, J. P., Schuckit, M. A., Taylor, R., Todd Webb, B. & 3 others, Tischfield, J. A., Porjesz, B. & Foroud, T., May 2010, In : Alcoholism: Clinical and Experimental Research. 34, 5, p. 840-852 13 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 11
Genome-Wide Association Study
Chromosomes
Alcoholism
Single Nucleotide Polymorphism
58 Citations (Scopus)

Genome-wide association study of bone mineral density in premenopausal European-American Women and replication in African-American women

Koller, D. L., Ichikawa, S., Lai, D., Padgett, L. R., Doheny, K. F., Pugh, E., Paschall, J., Hui, S., Edenberg, H., Xuei, X., Peacock, M., Econs, M. & Foroud, T., Apr 2010, In : Journal of Clinical Endocrinology and Metabolism. 95, 4, p. 1802-1809 8 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
African Americans
Bone Density
Minerals
Bone
11 Citations (Scopus)

Implementation of a shared data repository and common data dictionary for fetal alcohol spectrum disorders research

Arenson, A. D., Bakhireva, L. N., Chambers, C. D., Deximo, C. A., Foroud, T., Jacobson, J. L., Jacobson, S. W., Jones, K. L., Mattson, S. N., May, P. A., Moore, E. S., Ogle, K., Riley, E. P., Robinson, L. K., Rogers, J., Streissguth, A. P., Tavares, M. C., Urbanski, J., Yezerets, Y., Surya, R. & 2 others, Stewart, C. A. & Barnett, W. K., Nov 2010, In : Alcohol. 44, 7-8, p. 643-647 5 p.

Research output: Contribution to journalArticle

Fetal Alcohol Spectrum Disorders
dictionary
alcohol
Alcohols
Research Personnel
21 Citations (Scopus)

Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease

Simon, D. K., Pankratz, N., Kissell, D. K., Pauciulo, M. W., Halter, C. A., Rudolph, A., Pfeiffer, R. F., Nichols, W. C. & Foroud, T., Apr 1 2010, In : BMC Medical Genetics. 11, 1, 53.

Research output: Contribution to journalArticle

Mitochondrial DNA
Parkinson Disease
Mutation
Age of Onset
Maternal Inheritance
280 Citations (Scopus)

Meta-analysis confirms CR1, CLU, and PICALM as Alzheimer disease risk loci and reveals interactions with APOE genotypes

Jun, G., Naj, A. C., Beecham, G. W., Wang, L. S., Buros, J., Gallins, P. J., Buxbaum, J. D., Ertekin-Taner, N., Fallin, M. D., Friedland, R., Inzelberg, R., Kramer, P., Rogaeva, E., St George-Hyslop, P., Cantwell, L. B., Dombroski, B. A., Saykin, A., Reiman, E. M., Bennett, D. A., Morris, J. C. & 16 others, Lunetta, K. L., Martin, E. R., Montine, T. J., Goate, A. M., Blacker, D., Tsuang, D. W., Beekly, D., Cupples, L. A., Hakonarson, H., Kukull, W., Foroud, T., Haines, J., Mayeux, R., Farrer, L. A., Pericak-Vance, M. A. & Schellenberg, G. D., Dec 2010, In : Archives of Neurology. 67, 12, p. 1473-1484 12 p.

Research output: Contribution to journalArticle

Apolipoproteins E
Meta-Analysis
Alzheimer Disease
Genotype
Single Nucleotide Polymorphism
68 Citations (Scopus)

Predicting sensation seeking from dopamine genes: A candidate-system approach

Derringer, J., Krueger, R. F., Dick, D. M., Saccone, S., Grucza, R. A., Agrawal, A., Lin, P., Almasy, L., Edenberg, H., Foroud, T., Nurnberger, J., Hesselbrock, V. M., Kramer, J. R., Kuperman, S., Porjesz, B., Schuckit, M. A. & Bierut, L. J., Sep 2010, In : Psychological Science. 21, 9, p. 1282-1290 9 p.

Research output: Contribution to journalArticle

Dopamine
Single Nucleotide Polymorphism
Genes
Observational Studies
Personality
67 Citations (Scopus)

Prenatal alcohol exposure alters the patterns of facial asymmetry

Klingenberg, C. P., Wetherill, L., Rogers, J., Moore, E., Ward, R., Autti-Rämö, I., Fagerlund, Å., Jacobson, S. W., Robinson, L. K., Hoyme, H. E., Mattson, S. N., Li, T. K., Riley, E. P. & Foroud, T., Nov 2010, In : Alcohol. 44, 7-8, p. 649-657 9 p.

Research output: Contribution to journalArticle

Facial Asymmetry
Fetal Alcohol Spectrum Disorders
asymmetry
alcohol
Alcohols
34 Citations (Scopus)

Progression in prediagnostic Huntington disease

Rupp, J., Blekher, T., Jackson, J., Beristain, X., Marshall, J., Hui, S., Wojcieszek, J. & Foroud, T., Apr 2010, In : Journal of Neurology, Neurosurgery and Psychiatry. 81, 4, p. 379-384 6 p.

Research output: Contribution to journalArticle

Huntington Disease
Age of Onset
chorionic alpha(2)-microglobulin