Tatiana Foroud

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

2010
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

Interactive feature visualization and detection for 3D face classification

McLaughlin, J., Fang, S., Huang, J., Jacobson, S., Hoyme, H. E., Robinson, L. & Foroud, T., 2010, Proceedings of the 9th IEEE International Conference on Cognitive Informatics, ICCI 2010. p. 160-167 8 p. 5599748

Research output: Chapter in Book/Report/Conference proceedingConference contribution

Visualization
Alcohols
Lighting
Decision making
Geometry
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
17 Citations (Scopus)
Genome-Wide Association Study
Bone Density
Single Nucleotide Polymorphism
Femur Neck
Spine
51 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
38 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
316 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
170 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
218 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
49 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
20 Citations (Scopus)

Bone mineral density variation in men is influenced by sex-specific and non sex-specific quantitative trait loci

Peacock, M., Koller, D. L., Lai, D., Hui, S., Foroud, T. & Econs, M., Sep 2009, In : Bone. 45, 3, p. 443-448 6 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Bone Density
Hip
Siblings
Spine
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
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
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
122 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
35 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
24 Citations (Scopus)

From QTL to candidate gene: A genetic approach to alcoholism research

Spence, J. P., Liang, T., Liu, L., Johnson, P., Foroud, T., Carr, L. G. & Shekhar, A., Jun 2009, In : Current Drug Abuse Reviews. 2, 2, p. 127-134 8 p.

Research output: Contribution to journalArticle

Alcoholism
Research
Alcohol Drinking
Genes
Alcohol-Related Disorders
24 Citations (Scopus)

Genome screen in familial intracranial aneurysm.

Foroud, T., Sauerbeck, L., Brown, R., Anderson, C., Woo, D., Kleindorfer, D., Flaherty, M. L., Deka, R., Hornung, R., Meissner, I., Bailey-Wilson, J. E., Langefeld, C., Rouleau, G., Connolly, E. S., Lai, D., Koller, D. L., Huston, J. & Broderick, J. P., 2009, In : BMC Medical Genetics. 10, p. 3 1 p.

Research output: Contribution to journalArticle

Intracranial Aneurysm
Genome
Chromosomes
Smoking
Diagnostic Imaging
12 Citations (Scopus)

Genome screen to detect linkage to common susceptibility genes for intracranial and aortic aneurysms

Worrall, B. B., Foroud, T., Brown, R. D., Connolly, E. S., Hornung, R. W., Huston, J., Kleindorfer, D., Koller, D. L., Lai, D., Moomaw, C. J., Sauerbeck, L., Woo, D. & Broderick, J. P., Jan 1 2009, In : Stroke. 40, 1, p. 71-76 6 p.

Research output: Contribution to journalArticle

Aortic Aneurysm
Intracranial Aneurysm
Genome
Thoracic Aortic Aneurysm
Genes
60 Citations (Scopus)

Genomewide association study for onset age in Parkinson disease

Latourelle, J. C., Pankratz, N., Dumitriu, A., Wilk, J. B., Goldwurm, S., Pezzoli, G., Mariani, C. B., DeStefano, A. L., Halter, C., Gusella, J. F., Nichols, W. C., Myers, R. H. & Foroud, T., Sep 22 2009, In : BMC Medical Genetics. 10, p. 98 1 p., 1471.

Research output: Contribution to journalArticle

Age of Onset
Parkinson Disease
Single Nucleotide Polymorphism
Genes
Meta-Analysis
298 Citations (Scopus)

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

Pankratz, N., Wilk, J. B., Latourelle, J. C., DeStefano, A. L., Halter, C., Pugh, E. W., Doheny, K. F., Gusella, J. F., Nichols, W. C., Foroud, T. & Myers, R. H., 2009, In : Human Genetics. 124, 6, p. 593-605 13 p.

Research output: Contribution to journalArticle

Parkinson Disease
Genes
Disease Susceptibility
Chromosomes, Human, Pair 4
Single Nucleotide Polymorphism
238 Citations (Scopus)

Genome-wide association study of bipolar disorder in European American and African American individuals

Smith, E. N., Bloss, C. S., Badner, J. A., Barrett, T., Belmonte, P. L., Berrettini, W., Byerley, W., Coryell, W., Craig, D., Edenberg, H., Eskin, E., Foroud, T., Gershon, E., Greenwood, T. A., Hipolito, M., Koller, D. L., Lawson, W. B., Liu, C., Lohoff, F., McInnis, M. G. & 17 others, McMahon, F. J., Mirel, D. B., Murray, S. S., Nievergelt, C., Nurnberger, J., Nwulia, E. A., Paschall, J., Potash, J. B., Rice, J., Schulze, T. G., Scheftner, W., Panganiban, C., Zaitlen, N., Zandi, P. P., Zöllner, S., Schork, N. J. & Kelsoe, J. R., Aug 2009, In : Molecular Psychiatry. 14, 8, p. 755-763 9 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Bipolar Disorder
African Americans
Single Nucleotide Polymorphism
Intergenic DNA
15 Citations (Scopus)

Genomewide SNP screen to detect quantitative trait loci for alcohol preference in the high alcohol preferring and low alcohol preferring mice

Bice, P., Valdar, W., Zhang, L., Liu, L., Lai, D., Grahame, N., Flint, J., Li, T. K., Lumeng, L. & Foroud, T., Mar 2009, In : Alcoholism: Clinical and Experimental Research. 33, 3, p. 531-537 7 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Single Nucleotide Polymorphism
Genes
Alcohols
Chromosomes
89 Citations (Scopus)

Greater rupture risk for familial as compared to sporadic unruptured intracranial aneurysms

Broderick, J. P., Brown, R. D., Sauerbeck, L., Hornung, R., Huston, J., Woo, D., Anderson, C., Rouleau, G., Kleindorfer, D., Flaherty, M. L., Meissner, I., Foroud, T., Moomaw, E. C. J. & Connolly, E. S., Jun 1 2009, In : Stroke. 40, 6, p. 1952-1957 6 p.

Research output: Contribution to journalArticle

Intracranial Aneurysm
Rupture
Angiography
Cerebral Angiography
Ruptured Aneurysm
43 Citations (Scopus)

Multiple step pattern as a biomarker in Parkinson disease

Blekher, T., Weaver, M., Rupp, J., Nichols, W. C., Hui, S., Gray, J., Yee, R. D., Wojcieszek, J. & Foroud, T., Aug 2009, In : Parkinsonism and Related Disorders. 15, 7, p. 506-510 5 p.

Research output: Contribution to journalArticle

Parkinson Disease
Biomarkers
Saccades
Siblings
Aptitude
120 Citations (Scopus)

Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset

Nichols, W. C., Pankratz, N., Marek, D. K., Pauciulo, M. W., Elsaesser, V. E., Halter, C. A., Rudolph, A., Wojcieszek, J., Pfeiffer, R. F. & Foroud, T., Jan 27 2009, In : Neurology. 72, 4, p. 310-316 7 p.

Research output: Contribution to journalArticle

Glucosylceramidase
Disease Susceptibility
Age of Onset
Parkinson Disease
Mutation
52 Citations (Scopus)

Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations

Pankratz, N., Kissell, D. K., Pauciulo, M. W., Halter, C. A., Rudolph, A., Pfeiffer, R. F., Marder, K. S., Foroud, T. & Nichols, W. C., Jul 2009, In : Neurology. 73, 4, p. 279-286 8 p.

Research output: Contribution to journalArticle

Parkinson Disease
Virulence
Mutation
Haploinsufficiency
Age of Onset