Tatiana Foroud

  • 42505 Citations
  • 101 h-Index
1976 …2021
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Publications 1988 2020

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2010
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
26 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
171 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
219 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
36 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
300 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
239 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
121 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
9 Citations (Scopus)

Premenstrual mood symptoms: Study of familiality and personality correlates in mood disorder pedigrees

NIMH Genetics Initiative Bipolar Disorder Consortium, Feb 1 2009, In : Archives of Women's Mental Health. 12, 1, p. 27-34 8 p.

Research output: Contribution to journalArticle

Pedigree
Mood Disorders
Personality
Bipolar Disorder
Major Depressive Disorder
113 Citations (Scopus)

Singleton deletions throughout the genome increase risk of bipolar disorder

Zhang, D., Cheng, L., Qian, Y., Alliey-Rodriguez, N., Kelsoe, J. R., Greenwood, T., Nievergelt, C., Barrett, T. B., McKinney, R., Schork, N., Smith, E. N., Bloss, C., Nurnberger, J., Edenberg, H., Foroud, T., Sheftner, W., Lawson, W. B., Nwulia, E. A., Hipolito, M., Coryell, W. & 16 others, Rice, J., Byerley, W., McMahon, F., Schulze, T. G., Berrettini, W., Potash, J. B., Belmonte, P. L., Zandi, P. P., McInnis, M. G., Zöllner, S., Craig, D., Szelinger, S., Koller, D., Christian, S. L., Liu, C. & Gershon, E. S., Apr 2009, In : Molecular Psychiatry. 14, 4, p. 376-380 5 p.

Research output: Contribution to journalArticle

Bipolar Disorder
Genome
Single Nucleotide Polymorphism
Genomic Structural Variation
Age of Onset
20 Citations (Scopus)

Test-retest reliability of saccadic measures in subjects at risk for Huntington disease

Blekher, T., Weaver, M. R., Cai, X., Hui, S., Marshall, J., Jackson, J. G., Wojcieszek, J., Yee, R. D. & Foroud, T., Dec 2009, In : Investigative Ophthalmology and Visual Science. 50, 12, p. 5707-5711 5 p.

Research output: Contribution to journalArticle

Saccades
Huntington Disease
Reproducibility of Results
Biomarkers
Eye Movements
33 Citations (Scopus)

Variation in GIGYF2 is not associated with Parkinson disease

Nichols, W. C., Kissell, D. K., Pankratz, N., Pauciulo, M. W., Elsaesser, V. E., Clark, K. A., Halter, C. A., Rudolph, A., Wojcieszek, J., Pfeiffer, R. F. & Foroud, T., Jun 2 2009, In : Neurology. 72, 22, p. 1886-1892 7 p.

Research output: Contribution to journalArticle

Parkinson Disease
Chromosomes
Mutation
Genes
13 Citations (Scopus)

Visual scanning and cognitive performance in prediagnostic and early-stage Huntington's disease

Blekher, T., Weaver, M. R., Marshall, J., Hui, S., Jackson, J. G., Stout, J. C., Beristain, X., Wojcieszek, J., Yee, R. D. & Foroud, T., Mar 15 2009, In : Movement Disorders. 24, 4, p. 533-540 8 p.

Research output: Contribution to journalArticle

Huntington Disease
Eye Movements
Genes
2008
69 Citations (Scopus)

Analyses of the national institute on aging late-onset Alzheimer's disease family study: Implication of additional loci

Lee, J. H., Cheng, R., Graff-Radford, N., Foroud, T. & Mayeux, R., Nov 2008, In : Archives of Neurology. 65, 11, p. 1518-1526 9 p.

Research output: Contribution to journalArticle

National Institute on Aging (U.S.)
Alzheimer Disease
Genetic Loci
Onset
Alzheimer's Disease
4 Citations (Scopus)

A novel non-parametric regression reveals linkage on chromosome 4 for the number of externalizing symptoms in sib-pairs

Ghosh, S., Bierut, L. J., Porjesz, B., Edenberg, H., Dick, D., Goate, A., Hesselbrock, V., Nurnberger, J., Foroud, T., Kramer, J., Rice, J. & Begleiter, H., Oct 5 2008, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 147, 7, p. 1301-1305 5 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 4
Alcoholism
Chromosomes, Human, Pair 15
Chromosomes, Human, Pair 1
Multigene Family
55 Citations (Scopus)

A regulatory variation in OPRK1, the gene encoding the κ-opioid receptor, is associated with alcohol dependence

Edenberg, H., Wang, J., Tian, H., Pochareddy, S., Xuei, X., Wetherill, L., Goate, A., Hinrichs, T., Kuperman, S., Nurnberger, J., Schuckit, M., Tischfield, J. A. & Foroud, T., Jun 15 2008, In : Human Molecular Genetics. 17, 12, p. 1783-1789 7 p.

Research output: Contribution to journalArticle

Opioid Receptors
Alcoholism
Genes
Transcription Initiation Site
DNA Sequence Analysis
35 Citations (Scopus)

Association analysis of genes encoding the nociceptin receptor (OPRL1) and its endogenous ligand (PNOC) with alcohol or illicit drug dependence

Xuei, X., Flury-Wetherill, L., Almasy, L., Bierut, L., Tischfield, J., Schuckit, M., Nurnberger, J., Foroud, T. & Edenberg, H., Mar 2008, In : Addiction Biology. 13, 1, p. 80-87 8 p.

Research output: Contribution to journalArticle

Street Drugs
Substance-Related Disorders
Single Nucleotide Polymorphism
Alcohols
Ligands
71 Citations (Scopus)

Association of NFKB1, which encodes a subunit of the transcription factor NF-κB, with alcohol dependence

Edenberg, H., Xuei, X., Wetherill, L. F., Bierut, L., Bucholz, K., Dick, D. M., Hesselbrock, V., Kuperman, S., Porjesz, B., Schuckit, M. A., Tischfield, J. A., Almasy, L. A., Nurnberger, J. & Foroud, T., Apr 1 2008, In : Human Molecular Genetics. 17, 7, p. 963-970 8 p.

Research output: Contribution to journalArticle

Alcoholism
Transcription Factors
Single Nucleotide Polymorphism
Genes
Alcoholics
10 Citations (Scopus)

Association studies of ALOX5 and bone mineral density in healthy adults

Foroud, T., Ichikawa, S., Koller, D., Lai, D., Curry, L., Xuei, X., Edenberg, H., Hui, S., Peacock, M. & Econs, M., May 2008, In : Osteoporosis International. 19, 5, p. 637-643 7 p.

Research output: Contribution to journalArticle

Bone Density
Single Nucleotide Polymorphism
Siblings
Arachidonate 5-Lipoxygenase
Femur Neck
36 Citations (Scopus)

A Systematic Single Nucleotide Polymorphism Screen to Fine-Map Alcohol Dependence Genes on Chromosome 7 Identifies Association With a Novel Susceptibility Gene ACN9

Dick, D. M., Aliev, F., Wang, J. C., Saccone, S., Hinrichs, A., Bertelsen, S., Budde, J., Saccone, N., Foroud, T., Nurnberger, J., Xuei, X., Conneally, P. M., Schuckit, M., Almasy, L., Crowe, R., Kuperman, S., Kramer, J., Tischfield, J. A., Hesselbrock, V., Edenberg, H. & 4 others, Porjesz, B., Rice, J. P., Bierut, L. & Goate, A., Jun 1 2008, In : Biological Psychiatry. 63, 11, p. 1047-1053 7 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 7
Alcoholism
Single Nucleotide Polymorphism
Genes
HapMap Project
27 Citations (Scopus)

Automated diagnosis of fetal alcohol syndrome using 3D facial image analysis

Fang, S., McLaughlin, J., Fang, J., Huang, J., Autti-Rämö, I., Fagerlund, Å., Jacobson, S. W., Robinson, L. K., Hoyme, H. E., Mattson, S. N., Riley, E., Zhou, F., Ward, R., Moore, E. S. & Foroud, T., Aug 2008, In : Orthodontics and Craniofacial Research. 11, 3, p. 162-171 10 p.

Research output: Contribution to journalArticle

Fetal Alcohol Spectrum Disorders
Lasers
Alcohols
Computer Graphics
Finland
5 Citations (Scopus)

CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white men

Chu, K., Koller, D. L., Ichikawa, S., Snyder, R., Curry, L., Lai, D., Austin, A., Xuei, X., Edenberg, H., Hui, S., Foroud, T., Peacock, M. & Econs, M., Dec 2008, In : Bone. 43, 6, p. 995-998 4 p.

Research output: Contribution to journalArticle

Chloride Channels
Bone Density
Genes
Femur Neck
Osteopetrosis
26 Citations (Scopus)

Clinical correlates of depressive symptoms in familial Parkinson's disease

Pankratz, N., Marder, K. S., Halter, C. A., Rudolph, A., Shults, C. W., Nichols, W. C. & Foroud, T., Nov 15 2008, In : Movement Disorders. 23, 15, p. 2216-2223 8 p.

Research output: Contribution to journalArticle

Parkinson Disease
Depression
Geriatrics
Activities of Daily Living
Logistic Models
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
9 Citations (Scopus)
Genome
Osteoporotic Fractures
Quantitative Trait Loci
Chromosomes, Human, Pair 20
Chromosomes, Human, Pair 15
44 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
10 Citations (Scopus)

Genetic loci affecting bone structure and strength in inbred COP and DA rats

Sun, Q., Alam, I., Liu, L., Koller, D. L., Carr, L. G., Econs, M., Foroud, T. & Turner, C. H., Mar 2008, In : Bone. 42, 3, p. 547-553 7 p.

Research output: Contribution to journalArticle

Genetic Loci
Lumbar Vertebrae
Femur
Bone and Bones
Genome