Tatiana Foroud

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

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2011
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

44 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
128 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
56 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
35 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
812 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
175 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
3 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
80 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
160 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
323 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
187 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
47 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
958 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
15 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
35 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
7 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
25 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
105 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
221 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
273 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
66 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
60 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
33 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
17 Citations (Scopus)
Genome-Wide Association Study
Bone Density
Single Nucleotide Polymorphism
Femur Neck
Spine
50 Citations (Scopus)

Single-nucleotide polymorphisms in corticotropin releasing hormone receptor 1 gene (CRHR1) are associated with quantitative trait of event-related potential and alcohol dependence

Chen, A. C. H., Manz, N., Tang, Y., Rangaswamy, M., Almasy, L., Kuperman, S., Nurnberger, J., O'Connor, S., Edenberg, H., Schuckit, M. A., Tischfield, J., Foroud, T., Bierut, L. J., Rohrbaugh, J., Rice, J. P., Goate, A., Hesselbrock, V. & Porjesz, B., 2010, In : Alcoholism: Clinical and Experimental Research. 34, 6, p. 988-996 9 p.

Research output: Contribution to journalArticle

Corticotropin-Releasing Hormone Receptors
Polymorphism
Evoked Potentials
Alcoholism
Single Nucleotide Polymorphism
25 Citations (Scopus)

Telephone assessment of cognitive function in the late-onset Alzheimer's disease family study

Wilson, R. S., Leurgans, S. E., Foroud, T., Sweet, R. A., Graff-Radford, N., Mayeux, R. & Bennett, D. A., Jul 2010, In : Archives of Neurology. 67, 7, p. 855-861 7 p.

Research output: Contribution to journalArticle

Telephone
Cognition
Alzheimer Disease
Episodic Memory
Short-Term Memory
37 Citations (Scopus)

The relationship between smoking and replicated sequence variants on chromosomes 8 and 9 with familial intracranial aneurysm

Deka, R., Koller, D. L., Lai, D., Indugula, S. R., Sun, G., Woo, D., Sauerbeck, L., Moomaw, C. J., Hornung, R., Connolly, E. S., Anderson, C., Rouleau, G., Meissner, I., Bailey-Wilson, J. E., Huston, J., Brown, R. D., Kleindorfer, D. O., Flaherty, M. L., Langefeld, C. D., Foroud, T. & 1 others, Broderick, J. P., Jun 2010, In : Stroke. 41, 6, p. 1132-1137 6 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 9
Intracranial Aneurysm
Smoking
Single Nucleotide Polymorphism
312 Citations (Scopus)

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

Elks, C. E., Perry, J. R. B., Sulem, P., Chasman, D. I., Franceschini, N., He, C., Lunetta, K. L., Visser, J. A., Byrne, E. M., Cousminer, D. L., Gudbjartsson, D. F., Esko, T., Feenstra, B., Hottenga, J. J., Koller, D. L., Kutalik, Z., Lin, P., Mangino, M., Marongiu, M., McArdle, P. F. & 154 others, Smith, A. V., Stolk, L., Van Wingerden, S. H., Zhao, J. H., Albrecht, E., Corre, T., Ingelsson, E., Hayward, C., Magnusson, P. K. E., Smith, E. N., Ulivi, S., Warrington, N. M., Zgaga, L., Alavere, H., Amin, N., Aspelund, T., Bandinelli, S., Barroso, I., Berenson, G. S., Bergmann, S., Blackburn, H., Boerwinkle, E., Buring, J. E., Busonero, F., Campbell, H., Chanock, S. J., Chen, W., Cornelis, M. C., Couper, D., Coviello, A. D., D'Adamo, P., De Faire, U., De Geus, E. J. C., Deloukas, P., Döring, A., Smith, G. D., Easton, D. F., Eiriksdottir, G., Emilsson, V., Eriksson, J., Ferrucci, L., Folsom, A. R., Foroud, T., Garcia, M., Gasparini, P., Geller, F., Gieger, C., Gudnason, V., Hall, P., Hankinson, S. E., Ferreli, L., Heath, A. C., Hernandez, D. G., Hofman, A., Hu, F. B., Illig, T., Järvelin, M. R., Johnson, A. D., Karasik, D., Khaw, K. T., Kiel, D. P., Kilpelänen, T. O., Kolcic, I., Kraft, P., Launer, L. J., Laven, J. S. E., Li, S., Liu, J., Levy, D., Martin, N. G., McArdle, W. L., Melbye, M., Mooser, V., Murray, J. C., Murray, S. S., Nalls, M. A., Navarro, P., Nelis, M., Ness, A. R., Northstone, K., Oostra, B. A., Peacock, M., Palmer, L. J., Palotie, A., Paré, G., Parker, A. N., Pedersen, N. L., Peltonen, L., Pennell, C. E., Pharoah, P., Polasek, O., Plump, A. S., Pouta, A., Porcu, E., Rafnar, T., Rice, J. P., Ring, S. M., Rivadeneira, F., Rudan, I., Sala, C., Salomaa, V., Sanna, S., Schlessinger, D., Schork, N. J., Scuteri, A., Segrè, A. V., Shuldiner, A. R., Soranzo, N., Sovio, U., Srinivasan, S. R., Strachan, D. P., Tammesoo, M. L., Tikkanen, E., Toniolo, D., Tsui, K., Tryggvadottir, L., Tyrer, J., Uda, M., Van Dam, R. M., Van Meurs, J. B. J., Vollenweider, P., Waeber, G., Wareham, N. J., Waterworth, D. M., Weedon, M. N., Wichmann, H. E., Willemsen, G., Wilson, J. F., Wright, A. F., Young, L., Zhai, G., Zhuang, W. V., Bierut, L. J., Boomsma, D. I., Boyd, H. A., Crisponi, L., Demerath, E. W., Van Duijn, C. M., Econs, M., Harris, T. B., Hunter, D. J., Loos, R. J. F., Metspalu, A., Montgomery, G. W., Ridker, P. M., Spector, T. D., Streeten, E. A., Stefansson, K., Thorsteinsdottir, U., Uitterlinden, A. G., Widen, E., Murabito, J. M., Ong, K. K. & Murray, A., Dec 1 2010, In : Nature Genetics. 42, 12, p. 1077-1085 9 p.

Research output: Contribution to journalArticle

Menarche
Genome-Wide Association Study
Meta-Analysis
Genes
Biological Phenomena
165 Citations (Scopus)

Voxelwise genome-wide association study (vGWAS)

Stein, J. L., Hua, X., Lee, S., Ho, A. J., Leow, A. 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., DeChairo, B. M., Potkin, S. G., Weiner, M. W. & Thompson, P. M., Nov 2010, In : NeuroImage. 53, 3, p. 1160-1174 15 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Brain
Neuroimaging
Alzheimer Disease
Genome
212 Citations (Scopus)

Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort

Shen, L., Kim, S., Risacher, S. L., Nho, K., Swaminathan, S., West, J. D., Foroud, T., Pankratz, N., Moore, J. H., Sloan, C. D., Huentelman, M. J., Craig, D. W., DeChairo, B. M., Potkin, S. G., Jack, C. R., Weiner, M. W. & Saykin, A., Nov 2010, In : NeuroImage. 53, 3, p. 1051-1063 13 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Genome-Wide Association Study
Neuroimaging
Single Nucleotide Polymorphism
Cohort Studies
2009
9 Citations (Scopus)

Age at intracranial aneurysm rupture among generations: Familial Intracranial Aneurysm Study

Woo, D., Hornung, R., Sauerbeck, L., Brown, R., Meissner, I., Huston, J., Foroud, T. & Broderick, J., Jul 24 2009, In : Neurology. 72, 8, p. 695-698 4 p.

Research output: Contribution to journalArticle

Intracranial Aneurysm
Rupture
Ruptured Aneurysm
Molecular Epidemiology
Proportional Hazards Models
12 Citations (Scopus)

Allelic-based gene-gene interaction associated with quantitative traits

Jung, J., Sun, B., Kwon, D., Koller, D. L. & Foroud, T., 2009, In : Genetic Epidemiology. 33, 4, p. 332-343 12 p.

Research output: Contribution to journalArticle

Genes
Single Nucleotide Polymorphism
Blood Pressure
Calcium-Sensing Receptors
Chloride Channels
32 Citations (Scopus)

Alpha-synuclein and familial Parkinson's disease

Pankratz, N., Nichols, W. C., Elsaesser, V. E., Pauciulo, M. W., Marek, D. K., Halter, C. A., Wojcieszek, J., Rudolph, A., Pfeiffer, R. F. & Foroud, T., Jun 15 2009, In : Movement Disorders. 24, 8, p. 1125-1131 7 p.

Research output: Contribution to journalArticle

alpha-Synuclein
Parkinson Disease
Haplotypes
Age of Onset
Genetic Promoter Regions
13 Citations (Scopus)

Association of adenylate cyclase 10 (ADCY10) polymorphisms and bone mineral density in healthy adults

Ichikawa, S., Koller, D. L., Curry, L. R., Lai, D., Xuei, X., Edenberg, H., Hui, S., Peacock, M., Foroud, T. & Econs, M., Feb 2009, In : Calcified Tissue International. 84, 2, p. 97-102 6 p.

Research output: Contribution to journalArticle

Adenylyl Cyclases
Bone Density
Single Nucleotide Polymorphism
Pelvic Bones
Femur Neck
47 Citations (Scopus)

Association of single nucleotide polymorphisms in a glutamate receptor gene (GRM8) with theta power of event-related oscillations and alcohol dependence

Chen, A. C. H., Tang, Y., Rangaswamy, M., Wang, J. C., Almasy, L., Foroud, T., Edenberg, H., Hesselbrock, V., Nurnberger, J., Kuperman, S., O'Connor, S., Schuckit, M. A., Bauer, L. O., Tischfield, J., Rice, J. P., Bierut, L., Goate, A. & Porjesz, B., Apr 5 2009, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 150, 3, p. 359-368 10 p.

Research output: Contribution to journalArticle

Glutamate Receptors
Alcoholism
Single Nucleotide Polymorphism
Genes
Delta Rhythm
29 Citations (Scopus)

Association of the calcium-sensing receptor gene with blood pressure and urinary calcium in african-americans

Jung, J., Foroud, T., Eckert, G. J., Flury-Wetherill, L., Edenberg, H., Xuei, X., Zaidi, S. A. & Pratt, J. H., Mar 2009, In : Journal of Clinical Endocrinology and Metabolism. 94, 3, p. 1042-1048 7 p.

Research output: Contribution to journalArticle

Calcium-Sensing Receptors
Blood pressure
African Americans
Genes
Blood Pressure