Tatiana Foroud

  • 41759 Citations
  • 101 h-Index
1976 …2021
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Publications 1988 2019

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Detecting significant genotype–phenotype association rules in bipolar disorder: market research meets complex genetics

Breuer, R., Mattheisen, M., Frank, J., Krumm, B., Treutlein, J., Kassem, L., Strohmaier, J., Herms, S., Mühleisen, T. W., Degenhardt, F., Cichon, S., Nöthen, M. M., Karypis, G., Kelsoe, J., Greenwood, T., Nievergelt, C., Shilling, P., Shekhtman, T., Edenberg, H., Craig, D. & 32 others, Szelinger, S., Nurnberger, J., Gershon, E., Alliey-Rodriguez, N., Zandi, P., Goes, F., Schork, N., Smith, E., Koller, D., Zhang, P., Badner, J., Berrettini, W., Bloss, C., Byerley, W., Coryell, W., Foroud, T., Guo, Y., Hipolito, M., Keating, B., Lawson, W., Liu, C., Mahon, P., McInnis, M., Murray, S., Nwulia, E., Potash, J., Rice, J., Scheftner, W., Zöllner, S., McMahon, F. J., Rietschel, M. & Schulze, T. G., Dec 1 2018, In : International Journal of Bipolar Disorders. 6, 1, 24.

Research output: Contribution to journalArticle

Marketing
Bipolar Disorder
Genome-Wide Association Study
Genetic Research
Data Mining
29 Citations (Scopus)

Detection of dental fluorosis-associated quantitative trait loci on mouse chromosomes 2 and 11

Everett, E. T., Yan, D., Weaver, M., Liu, L., Foroud, T. & Martinez Mier, E., Dec 2008, In : Cells Tissues Organs. 189, 1-4, p. 212-218 7 p.

Research output: Contribution to journalArticle

Dental Fluorosis
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 2
Quantitative Trait Loci
Dental Enamel
13 Citations (Scopus)

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 2006, In : Behavior Genetics. 36, 2, p. 285-290 6 p.

Research output: Contribution to journalArticle

Alcohol Drinking
alcohol
alcohols
Alcohols
Quantitative Trait Loci
136 Citations (Scopus)

Differences in duration of Huntington's disease based on age at onset

Foroud, T., Gray, J., Ivashina, J. & Conneally, P. M., Jan 1999, In : Journal of Neurology, Neurosurgery and Psychiatry. 66, 1, p. 52-56 5 p.

Research output: Contribution to journalArticle

Huntington Disease
Age of Onset
Research
6 Citations (Scopus)

Differentially expressed genes strongly correlated with femur strength in rats

Alam, I., Sun, Q., Koller, D. L., Liu, L., Liu, Y., Edenberg, H., Li, J., Foroud, T. & Turner, C. H., Oct 2009, In : Genomics. 94, 4, p. 257-262 6 p.

Research output: Contribution to journalArticle

Femur
Quantitative Trait Loci
Genes
Hepatocyte Nuclear Factor 4
NF-kappa B
26 Citations (Scopus)

Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking

Stephens, S. H., Hartz, S. M., Hoft, N. R., Saccone, N. L., Corley, R. C., Hewitt, J. K., Hopfer, C. J., Breslau, N., Coon, H., Chen, X., Ducci, F., Dueker, N., Franceschini, N., Frank, J., Han, Y., Hansel, N. N., Jiang, C., Korhonen, T., Lind, P. A., Liu, J. & 106 others, Lyytikäinen, L. P., Michel, M., Shaffer, J. R., Short, S. E., Sun, J., Teumer, A., Thompson, J. R., Vogelzangs, N., Vink, J. M., Wenzlaff, A., Wheeler, W., Yang, B. Z., Aggen, S. H., Balmforth, A. J., Baumeister, S. E., Beaty, T. H., Benjamin, D. J., Bergen, A. W., Broms, U., Cesarini, D., Chatterjee, N., Chen, J., Cheng, Y. C., Cichon, S., Couper, D., Cucca, F., Dick, D., Foroud, T., Furberg, H., Giegling, I., Gillespie, N. A., Gu, F., Hall, A. S., Hällfors, J., Han, S., Hartmann, A. M., Heikkilä, K., Hickie, I. B., Hottenga, J. J., Jousilahti, P., Kaakinen, M., Kähönen, M., Koellinger, P. D., Kittner, S., Konte, B., Landi, M. T., Laatikainen, T., Leppert, M., Levy, S. M., Mathias, R. A., Mcneil, D. W., Medland, S. E., Montgomery, G. W., Murray, T., Nauck, M., North, K. E., Paré, P. D., Pergadia, M., Ruczinski, I., Salomaa, V., Viikari, J., Willemsen, G., Barnes, K. C., Boerwinkle, E., Boomsma, D. I., Caporaso, N., Edenberg, H., Francks, C., Gelernter, J., Grabe, H. J., Hops, H., Jarvelin, M. R., Johannesson, M., Kendler, K. S., Lehtimäki, T., Magnusson, P. K. E., Marazita, M. L., Marchini, J., Mitchell, B. D., Nöthen, M. M., Penninx, B. W., Raitakari, O., Rietschel, M., Rujescu, D., Samani, N. J., Schwartz, A. G., Shete, S., Spitz, M., Swan, G. E., Völzke, H., Veijola, J., Wei, Q., Amos, C., Cannon, D. S., Grucza, R., Hatsukami, D., Heath, A., Johnson, E. O., Kaprio, J., Madden, P., Martin, N. G., Stevens, V. L., Weiss, R. B., Kraft, P., Bierut, L. J. & Ehringer, M. A., Dec 2013, In : Genetic Epidemiology. 37, 8, p. 846-859 14 p.

Research output: Contribution to journalArticle

Multigene Family
Smoking
Tobacco Use Disorder
Phenotype
Tobacco
27 Citations (Scopus)

DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study

Trinh, J., Gustavsson, E. K., Vilariño-Güell, C., Bortnick, S., Latourelle, J., McKenzie, M. B., Tu, C. S., Nosova, E., Khinda, J., Milnerwood, A., Lesage, S., Brice, A., Tazir, M., Aasly, J. O., Parkkinen, L., Haytural, H., Foroud, T., Myers, R. H., Sassi, S. B., Hentati, E. & 5 others, Nabli, F., Farhat, E., Amouri, R., Hentati, F. & Farrer, M. J., Nov 1 2016, In : The Lancet Neurology. 15, 12, p. 1248-1256 9 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Parkinsonian Disorders
Age of Onset
Leucine
Phosphotransferases
25 Citations (Scopus)

DSM-5 cannabis use disorder: A phenotypic and genomic perspective

Agrawal, A., Lynskey, M. T., Bucholz, K. K., Kapoor, M., Almasy, L., Dick, D. M., Edenberg, H., Foroud, T., Goate, A., Hancock, D. B., Hartz, S., Johnson, E. O., Hesselbrock, V., Kramer, J. R., Kuperman, S., Nurnberger, J., Schuckit, M. & Bierut, L. J., Jan 1 2014, In : Drug and Alcohol Dependence. 134, 1, p. 362-369 8 p.

Research output: Contribution to journalArticle

Cannabis
Polymorphism
Single Nucleotide Polymorphism
Genes
Nucleotides
217 Citations (Scopus)

Early role of vascular dysregulation on late-onset Alzheimer's disease based on multifactorial data-driven analysis

The Alzheimer's Disease Neuroimaging Initiative, Jun 21 2016, In : Nature Communications. 7, 11934.

Research output: Contribution to journalArticle

Blood Vessels
Alzheimer Disease
Biomarkers
biomarkers
Disease Progression
6 Citations (Scopus)
Hypercalciuria
Metabolic Diseases
Calcium
Mutation
83 Citations (Scopus)

Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: A genome-wide association study

Alzheimer Disease Genetics Consortium, Nov 1 2014, In : JAMA Neurology. 71, 11, p. 1394-1404 11 p.

Research output: Contribution to journalArticle

Genetic Loci
Genome-Wide Association Study
Age of Onset
Alzheimer Disease
Genetic Databases

Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder

Budde, M., Friedrichs, S., Alliey-Rodriguez, N., Ament, S., Badner, J. A., Berrettini, W. H., Bloss, C. S., Byerley, W., Cichon, S., Comes, A. L., Coryell, W., Craig, D. W., Degenhardt, F., Edenberg, H., Foroud, T., Forstner, A. J., Frank, J., Gershon, E. S., Goes, F. S., Greenwood, T. A. & 40 others, Guo, Y., Hipolito, M., Hood, L., Keating, B. J., Koller, D. L., Lawson, W. B., Liu, C., Mahon, P. B., McInnis, M. G., McMahon, F. J., Meier, S. M., Mühleisen, T. W., Murray, S. S., Nievergelt, C. M., Nurnberger, J., Nwulia, E. A., Potash, J. B., Quarless, D., Rice, J., Roach, J. C., Scheftner, W. A., Schork, N. J., Shekhtman, T., Shilling, P. D., Smith, E. N., Streit, F., Strohmaier, J., Szelinger, S., Treutlein, J., Witt, S. H., Zandi, P. P., Zhang, P., Zöllner, S., Bickeböller, H., Falkai, P. G., Kelsoe, J. R., Nöthen, M. M., Rietschel, M., Schulze, T. G. & Malzahn, D., Jan 1 2019, In : European Neuropsychopharmacology. 29, 1, p. 156-170 15 p.

Research output: Contribution to journalArticle

Open Access
Bipolar Disorder
Single Nucleotide Polymorphism
Haplotypes
Genes
Chromosomes, Human, Pair 15
82 Citations (Scopus)

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 2006, In : Behavior Genetics. 36, 1, p. 112-126 15 p.

Research output: Contribution to journalArticle

Endophenotypes
alcohol abuse
Alcoholism
phenotype
genet
99 Citations (Scopus)

Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants

Gamazon, E. R., Badner, J. A., Cheng, L., Zhang, C., Zhang, D., Cox, N. J., Gershon, E. S., Kelsoe, J. R., Greenwood, T. A., Nievergelt, C. M., Chen, C., McKinney, R., Shilling, P. D., Schork, N. J., Smith, E. N., Bloss, C. S., Nurnberger, J., Edenberg, H., Foroud, T., Koller, D. L. & 20 others, Scheftner, W. A., Coryell, W., Rice, J., Lawson, W. B., Nwulia, E. A., Hipolito, M., Byerley, W., McMahon, F. J., Schulze, T. G., Berrettini, W. H., Potash, J. B., Zandi, P. P., Mahon, P. B., McInnis, M. G., Zöllner, S., Zhang, P., Craig, D. W., Szelinger, S., Barrett, T. B. & Liu, C., Mar 2013, In : Molecular Psychiatry. 18, 3, p. 340-346 7 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Regulator Genes
Bipolar Disorder
Methylation
Single Nucleotide Polymorphism
5 Citations (Scopus)

Epistasis between QTLs for bone density variation in Copenhagen x dark agouti F2 rats

Koller, D. L., Liu, L., Alam, I., Sun, Q., Econs, M., Foroud, T. & Turner, C. H., Mar 2009, In : Mammalian Genome. 20, 3, p. 180-186 7 p.

Research output: Contribution to journalArticle

Bone Density
Quantitative Trait Loci
Genome
Femur
Chromosomes, Human, Pair 15
9 Citations (Scopus)
Genome
Osteoporotic Fractures
Quantitative Trait Loci
Chromosomes, Human, Pair 20
Chromosomes, Human, Pair 15
Endocrinology
Insulin-Like Growth Factor I
Bone Density
Genes
5 Citations (Scopus)

Ethanol treatment of lymphoblastoid cell lines from alcoholics and non-alcoholics causes many subtle changes in gene expression

McClintick, J., Brooks, A. I., Deng, L., Liang, L., Wang, J. C., Kapoor, M., Xuei, X., Foroud, T., Tischfield, J. A. & Edenberg, H., Sep 1 2014, In : Alcohol. 48, 6, p. 603-610 8 p.

Research output: Contribution to journalArticle

Alcoholics
alcoholism
Gene expression
Ethanol
Cells
2 Citations (Scopus)

Evaluation of gene-based family-based methods to detect novel genes associated with familial late onset Alzheimer disease

NIA-LOAD family study group & NCRAD, Apr 4 2018, In : Frontiers in Neuroscience. 12, APR, 209.

Research output: Contribution to journalArticle

Genes
Software
Phenotype
Genome-Wide Association Study
Alzheimer disease type 2
1 Citation (Scopus)

Evaluation of laboratory tests for cirrhosis and for alcohol use, in the context of alcoholic cirrhosis

Whitfield, J. B., Masson, S., Liangpunsakul, S., Hyman, J., Mueller, S., Aithal, G., Eyer, F., Gleeson, D., Thompson, A., Stickel, F., Soyka, M., Daly, A. K., Cordell, H. J., Liang, T., Foroud, T., Lumeng, L., Pirmohamed, M., Nalpas, B., Bence, C., Jacquet, J. M. & 12 others, Louvet, A., Moirand, R., Nahon, P., Naveau, S., Perney, P., Podevin, P., Haber, P. S., Seitz, H. K., Day, C. P., Mathurin, P., Morgan, T. M. & Seth, D., Feb 1 2018, In : Alcohol. 66, p. 1-7 7 p.

Research output: Contribution to journalArticle

Alcoholic Liver Cirrhosis
alcoholism
Fibrosis
alcohol
Alcohols
13 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

Parkinson Disease
Introns
Genes
DNA Restriction Enzymes
Age of Onset
164 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

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

Evidence for a role of the rare p.A152T variant in mapt in increasing the risk for FTD-spectrum and Alzheimer's diseases

Coppola, G., Chinnathambi, S., Lee, J. J., Dombroski, B. A., Baker, M. C., Soto-ortolaza, A. I., Lee, S. E., Klein, E., Huang, A. Y., Sears, R., Lane, J. R., Karydas, A. M., Kenet, R. O., Biernat, J., Wang, L. S., Cotman, C. W., Decarli, C. S., Levey, A. I., Ringman, J. M., Mendez, M. F. & 210 others, Chui, H. C., Le ber, I., Brice, A., Lupton, M. K., Preza, E., Lovestone, S., Powell, J., Graff-radford, N., Petersen, R. C., Boeve, B. F., Lippa, C. F., Bigio, E. H., Mackenzie, I., Finger, E., Kertesz, A., Caselli, R. J., Gearing, M., Juncos, J. L., Ghetti, B., Spina, S., Bordelon, Y. M., Tourtellotte, W. W., Frosch, M. P., Vonsattel, J. P. G., Zarow, C., Beach, T. G., Albin, R. L., Lieberman, A. P., Lee, V. M., Trojanowski, J. Q., Van deerlin, V. M., Bird, T. D., Galasko, D. R., Masliah, E., White, C. L., Troncoso, J. C., Hannequin, D., Boxer, A. L., Geschwind, M. D., Kumar, S., Mandelkow, E. M., Wszolek, Z. K., Uitti, R. J., Dickson, D. W., Haines, J. L., Mayeux, R., Pericak-vance, M. A., Farrer, L. A., Apostolova, L. G., Arnold, S. E., Baldwin, C. T., Barber, R., Barmada, M. M., Beach, T., Beecham, G. W., Beekly, D., Bennett, D. A., Bigio, E. H., Bird, T. D., Blacker, D., Boeve, B. F., Bowen, J. D., Boxer, A., Burke, J. R., Buros, J., Buxbaum, J. D., Cairns, N. J., Cantwell, L. B., Cao, C., Carlson, C. S., Carney, R. M., Carrasquillo, M. M., Carroll, S. L., Chui, H. C., Clark, D. G., Corneveaux, J., Cotman, C. W., Crane, P. K., Cruchaga, C., Cummings, J. L., De Jager, P. L., DeCarli, C., DeKosky, S. T., Demirci, F. Y., Diaz-Arrastia, R., Dick, M., Dickson, D. W., Dombroski, B. A., Duara, R., Ellis, W. G., Ertekin-Taner, N. N., Evans, D., Faber, K. M., Fallon, K. B., Farlow, M., Ferris, S., Foroud, T., Frosch, M. P., Galasko, D. R., Gallins, P. J., Ganguli, M., Gearing, M., Geschwind, D. H., Ghetti, B., Gilbert, J. R., Gilman, S., Giordani, B., Glass, J. D., Goate, A. M., Graff-Radford, N. R., Green, R. C., Growdon, J. H., Hakonarson, H., Hamilton, R. L., Hardy, J., Harrell, L. E., Head, E., Honig, L. S., Huentelman, M. J., Hulette, C. M., Hyman, B. T., Jarvik, G. P., Jicha, G. A., Jin, L. W., Johnson, N., Jun, G., Kamboh, M. I., Karlawish, J., Karydas, A., Kauwe, J. S. K., Kaye, J. A., Kim, R., Koo, E. H., Kowall, N. W., Kramer, P., Kukull, W. A., Lah, J. J., Larson, E. B., Levey, A. I., Lieberman, A. P., Lopez, O. L., Lunetta, K. L., Mack, W. J., Marson, D. C., Martin, E. R., 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., Montine, T. J., Morris, J. C., Myers, A. J., Naj, A. C., Nowotny, P., Parisi, J. E., Perl, D. P., Peskind, E., Petersen, R. C., Poon, W. W., Potter, H., Quinn, J. F., Raj, A., Rajbhandary, R. A., Raskind, M., Reiman, E. M., Reisberg, B., Reitz, C., Ringman, J. M., Roberson, E. D., Rogaeva, E., Rosenberg, R. N., Sano, M., Saykin, A., Schneider, J. A., Schneider, L. S., Seeley, W., Shelanski, M. L., Slifer, M. A., Smith, C. D., Sonnen, J. A., Spina, S., George-Hyslop, P. S., Stern, R. A., Tanzi, R. E., Trojanowski, J. Q., Troncoso, J. C., Tsuang, D. W., Van Deerlin, V. M., Vardarajan, B. N., Vinters, H. V., Vonsattel, J. P., Wang, L. S., Weintraub, S., Welsh-Bohmer, K. A., Williamson, J., Woltjer, R. L., Younkin, S. G., Ross, O. A., Rademakers, R., Schellenberg, G. D., Miller, B. L., Mandelkow, E. & Geschwind, D. H., 2012, In : Human Molecular Genetics. 21, 15, p. 3500-3512 13 p., dds161.

Research output: Contribution to journalArticle

Progressive Supranuclear Palsy
Frontotemporal Dementia
Microtubule-Associated Proteins
Microtubules
tau Proteins
41 Citations (Scopus)

Evidence for association between polymorphisms in the cannabinoid receptor 1 (CNR1) gene and cannabis dependence

Agrawal, A., Wetherill, L., Dick, D. M., Xuei, X., Hinrichs, A., Hesselbrock, V., Kramer, J., Nurnberger, J., Schuckit, M., Bierut, L. J., Edenberg, H. & Foroud, T., Jul 5 2009, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 150, 5, p. 736-740 5 p.

Research output: Contribution to journalArticle

Marijuana Abuse
Cannabinoid Receptors
Single Nucleotide Polymorphism
Genes
Chromosomes, Human, Pair 15
3 Citations (Scopus)

Evidence for a susceptibility locus for bipolar disorder on chromosome 11p11.5

McInnis, M. G., MacKinnon, D. F., McMahon, F. J., Foroud, T., Edenberg, H., Goate, A., Detera-Wadleigh, S., Stine, O. C., Rice, J., Blehar, M., Reich, T., Gershon, E., Nurnberger, J., Simpson, S. G. & DePaulo, J. R., Nov 6 1998, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 81, 6, p. 463 1 p.

Research output: Contribution to journalArticle

Pedigree
Bipolar Disorder
Chromosomes
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 2
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
24 Citations (Scopus)

Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

Price Foundation Collaborative Group, Children’s Hospital of Philadelphia/Price Foundation, GCAN, WTCCC3, GIANT & EGG, Feb 1 2017, In : Molecular Psychiatry. 22, 2, p. 192-201 10 p.

Research output: Contribution to journalArticle

Genetic Loci
Anorexia Nervosa
Body Mass Index
Genome-Wide Association Study
Meta-Analysis
43 Citations (Scopus)

Evidence of association between brain-derived neurotrophic factor gene and bipolar disorder

Liu, L., Foroud, T., Xuei, X., Berrettini, W., Byerley, W., Coryell, W., El-Mallakh, R., Gershon, E. S., Kelsoe, J. R., Lawson, W. B., MacKinnon, D. F., McInnis, M., McMahon, F. J., Murphy, D. L., Rice, J., Scheftner, W., Zandi, P. R., Lohoff, F. W., Niculescu, A., Meyer, E. T. & 2 others, Edenberg, H. & Nurnberger, J., Dec 2008, In : Psychiatric Genetics. 18, 6, p. 267-274 8 p.

Research output: Contribution to journalArticle

Brain-Derived Neurotrophic Factor
Bipolar Disorder
Single Nucleotide Polymorphism
Genes
Mood Disorders
6 Citations (Scopus)

Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use

CHD Exome+ Consortium & Consortium for Genetics of Smoking Behaviour, Jun 1 2019, In : Biological Psychiatry. 85, 11, p. 946-955 10 p.

Research output: Contribution to journalArticle

Exome
Meta-Analysis
Smoking
Alcohols
Phenotype
4 Citations (Scopus)

Exome Sequencing Identifies Candidate Genetic Modifiers of Syndromic and Familial Thoracic Aortic Aneurysm Severity

Landis, B., Schubert, J. A., Lai, D., Jegga, A. G., Shikany, A. R., Foroud, T., Ware, S. & Hinton, R. B., May 26 2017, (Accepted/In press) In : Journal of Cardiovascular Translational Research. p. 1-10 10 p.

Research output: Contribution to journalArticle

Exome
Thoracic Aortic Aneurysm
Genes
Phenotype
Inborn Genetic Diseases
15 Citations (Scopus)

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 2005, In : Addiction Biology. 10, 1, p. 47-51 5 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Substance-Related Disorders
Alcohols
Gene Expression
Alcohol Drinking
6 Citations (Scopus)

Facial Curvature Detects and Explicates Ethnic Differences in Effects of Prenatal Alcohol Exposure

the CIFASD, Aug 1 2017, In : Alcoholism: Clinical and Experimental Research. 41, 8, p. 1471-1483 13 p.

Research output: Contribution to journalArticle

Fetal Alcohol Spectrum Disorders
Alcohols
Lip
Hypertelorism
Ethnic Groups
55 Citations (Scopus)

Facial dysmorphism across the fetal alcohol spectrum

Suttie, M., Foroud, T., Wetherill, L., Jacobson, J. L., Molteno, C. D., Meintjes, E. M., Hoyme, H. E., Khaole, N., Robinson, L. K., Riley, E. P., Jacobson, S. W. & Hammond, P., Mar 2013, In : Pediatrics. 131, 3

Research output: Contribution to journalArticle

Alcohols
Fetal Alcohol Spectrum Disorders
Alcohol
Eyelids
Lip
17 Citations (Scopus)
Femur Neck
Alleles
Gene Frequency
Population
Genetic Markers
12 Citations (Scopus)

Familial intracranial aneurysms: Is anatomic vulnerability heritable?

Mackey, J., Brown, R. D., Moomaw, C. J., Hornung, R., Sauerbeck, L., Woo, D., Foroud, T., Gandhi, D., Kleindorfer, D., Flaherty, M. L., Meissner, I., Anderson, C., Rouleau, G., Connolly, E. S., Deka, R., Koller, D. L., Abruzzo, T., Huston, J. & Broderick, J. P., Jan 2013, In : Stroke. 44, 1, p. 38-42 5 p.

Research output: Contribution to journalArticle

Intracranial Aneurysm
Odds Ratio
Middle Cerebral Artery
Internal Carotid Artery
Rupture
64 Citations (Scopus)

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17

Murrell, J. R., Koller, D., Foroud, T., Goedert, M., Spillantini, M. G., Edenberg, H., Farlow, M. & Ghetti, B., Nov 1997, In : American Journal of Human Genetics. 61, 5, p. 1131-1138 8 p.

Research output: Contribution to journalArticle

Frontotemporal Dementia
Chromosomes, Human, Pair 17
Oligodendroglia
Memory Disorders
Pedigree
16 Citations (Scopus)

Family-Based Association Analysis of Alcohol Dependence Criteria and Severity

Wetherill, L., Kapoor, M., Agrawal, A., Bucholz, K., Koller, D., Bertelsen, S. E., Le, N., Wang, J. C., Almasy, L., Hesselbrock, V., Kramer, J., Nurnberger, J., Schuckit, M., Tischfield, J. A., Xuei, X., Porjesz, B., Edenberg, H., Goate, A. M. & Foroud, T., Feb 2014, In : Alcoholism: Clinical and Experimental Research. 38, 2, p. 354-366 13 p.

Research output: Contribution to journalArticle

Alcoholism
Alcohols
Diagnostic and Statistical Manual of Mental Disorders
Genes
Single Nucleotide Polymorphism
121 Citations (Scopus)

Family-based association of FKBP5 in bipolar disorder

Willour, V. L., Chen, H., Toolan, J., Belmonte, P., Cutler, D. J., Goes, F. S., Zandi, P. P., Lee, R. S., MacKinnon, D. F., Mondimore, F. M., Schweizer, B., DePaulo, J. R., Gershon, E. S., McMahon, F. J., Potash, J. B., McMahon, F., Steele, J., Pearl, J., Kassem, L., Lopez, V. & 64 others, Potash, J., MacKinnon, D., Miller, E., Toolan, J., Zandi, P., Schulze, T., Nwulia, E., Simpson, S., Nurnberger, J., Miller, M., Bowman, E., Reich, T., Goate, A., Rice, J., DePaulo, J. R., Stine, C., Gershon, E., Kazuba, D., Maxwell, E., 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., Smiley, C., Foroud, T., Flury, L., Dick, D. M., Edenberg, H., Bierut, L., McInnis, M., MacKinnon, D. F., Mondimore, F. M., Potash, J. B., Zandi, P. P., Avramopoulos, D., Payne, J., Berrettini, W., Byerley, W., Vawter, M., Coryell, W., Crowe, R., Badner, J., 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., Detera-Wadleigh, S., Austin, L. & Murphy, D. L., Mar 2009, In : Molecular Psychiatry. 14, 3, p. 261-268 8 p.

Research output: Contribution to journalArticle

Bipolar Disorder
Single Nucleotide Polymorphism
Genetic Models
Glucocorticoid Receptors
Antidepressive Agents
34 Citations (Scopus)

Family-based association of YWHAH in psychotic bipolar disorder

Grover, D., Verma, R., Goes, F. S., Belmonte Mahon, P. L., Gershon, E. S., McMahon, F. J., Potash, J. B., McMahon, F. J., Steele, J., Pearl, J., Kassem, L., Lopez, V., Schulze, T., Potash, J., MacKinnon, D., Miller, E., Toolan, J., Zandi, P., Simpson, S., Nurnberger, J. & 64 others, Miller, M., Bowman, E., Reich, T., Goate, A., Rice, J., DePaulo, J. R., Simpson, S., Stine, C., Gershon, E., Kazuba, D., Maxwell, E., Nurnberger, J., 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., Smiley, C., Foroud, T., Flury, L., Dick, D. M., Edenberg, H., Rice, J., Reich, T., Goate, A., Bierut, L., McInnis, M., DePaulo, J. R., MacKinnon, D. F., Mondimore, F. M., Potash, J. B., Zandi, P. P., Avramopoulos, D., Payne, J., Berrettini, W., Byerley, W., Vawter, M., 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., Kassem, L., Detera-Wadleigh, S., Austin, L. & Murphy, D. L., Oct 5 2009, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 150, 7, p. 977-983 7 p.

Research output: Contribution to journalArticle

Bipolar Disorder
Psychotic Disorders
Schizophrenia
Single Nucleotide Polymorphism
Chromosome Disorders
40 Citations (Scopus)

Family-based genome-wide association study of frontal theta oscillations identifies potassium channel gene KCNJ6

Kang, S. J., Rangaswamy, M., Manz, N., Wang, J. C., Wetherill, L., Hinrichs, T., Almasy, L., Brooks, A., Chorlian, D. B., Dick, D., Hesselbrock, V., Kramer, J., Kuperman, S., Nurnberger, J., Rice, J., Schuckit, M., Tischfield, J., Bierut, L. J., Edenberg, H., Goate, A. & 2 others, Foroud, T. & Porjesz, B., Aug 2012, In : Genes, Brain and Behavior. 11, 6, p. 712-719 8 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Potassium Channels
Single Nucleotide Polymorphism
Alcoholism
Genes
96 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Dopamine D2 Receptors
Smoking
Genes
Alcoholism
Alleles
12 Citations (Scopus)

FASTKD2 is associated with memory and hippocampal structure in older adults

Ramanan, V. K., Nho, K., Shen, L., Risacher, S. L., Kim, S., McDonald, B., Farlow, M., Foroud, T., Gao, S., Soininen, H., Kłoszewska, I., Mecocci, P., Tsolaki, M., Vellas, B., Lovestone, S., Aisen, P. S., Petersen, R. C., Jack, C. R., Shaw, L. M., Trojanowski, J. Q. & 7 others, Weiner, M. W., Green, R. C., Toga, A. W., De Jager, P. L., Yu, L., Bennett, D. A. & Saykin, A., Oct 29 2015, In : Molecular Psychiatry. 20, 10, p. 1197-1204 8 p.

Research output: Contribution to journalArticle

Protein-Serine-Threonine Kinases
Memory Disorders
Neuroprotective Agents
Sirolimus
Genomics
1 Citation (Scopus)

Feasibility and safety of lumbar puncture in the Parkinson's disease research participants: Parkinson's Progression Marker Initiative (PPMI)

The Parkinson's Progression Markers InitiativeSteering Committee, Study Cores, Site Investigators, Coordinators & Industry and Scientific Advisory Board, Jan 1 2019, In : Parkinsonism and Related Disorders.

Research output: Contribution to journalArticle

Spinal Puncture
Parkinson Disease
Safety
Research
Needles
3 Citations (Scopus)

Feasibility and Safety of Multicenter Tissue and Biofluid Sampling for α-Synuclein in Parkinson's Disease: The Systemic Synuclein Sampling Study (S4)

Systemic sSynuclein Sampling study, Jan 1 2018, In : Journal of Parkinson's Disease. 8, 4, p. 517-527 11 p.

Research output: Contribution to journalArticle

Synucleins
Sampling Studies
Parkinson Disease
Safety
Submandibular Gland
99 Citations (Scopus)

Ferritin levels in the cerebrospinal fluid predict Alzheimer's disease outcomes and are regulated by APOE

Alzheimer's Disease Neuroimaging Initiative, May 19 2015, In : Nature Communications. 6, 6760.

Research output: Contribution to journalArticle

cerebrospinal fluid
Cerebrospinal fluid
Ferritins
Cerebrospinal Fluid
Alzheimer Disease

Fibroblast Growth Factor 23 Genotype and Cardiovascular Disease in Patients Undergoing Hemodialysis

Schwantes-An, T. H., Liu, S., Stedman, M., Decker, B., Wetherill, L., Edenberg, H., Vatta, M., Foroud, T., Chertow, G. M. & Moe, S., Jan 1 2019, (Accepted/In press) In : American Journal of Nephrology. p. 125-132 8 p.

Research output: Contribution to journalArticle

Renal Dialysis
Cardiovascular Diseases
Genotype
Heart Failure
Mortality
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
3 Citations (Scopus)

Fine mapping of bone structure and strength QTLs in heterogeneous stock rat

Alam, I., Koller, D. L., Cañete, T., Blázquez, G., Mont-Cardona, C., López-Aumatell, R., Martínez-Membrives, E., Díaz-Morán, S., Tobeña, A., Fernández-Teruel, A., Stridh, P., Diez, M., Olsson, T., Johannesson, M., Baud, A., Econs, M. & Foroud, T., Dec 1 2015, In : Bone. 81, p. 417-426 10 p., 10840.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Femur Neck
Phenotype
Bone and Bones
Haplotypes
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