Tatiana Foroud

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

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2008
30 Citations (Scopus)

The tachykinin receptor 3 is associated with alcohol and cocaine dependence

Foroud, T., Wetherill, L. F., Kramer, J., Tischfield, J. A., Nurnberger, J., Schuckit, M. A., Xuei, X. & Edenberg, H., Jun 2008, In : Alcoholism: Clinical and Experimental Research. 32, 6, p. 1023-1030 8 p.

Research output: Contribution to journalArticle

Tachykinin Receptors
Cocaine-Related Disorders
Cocaine
Alcoholism
Alcohols
410 Citations (Scopus)

Variants in nicotinic receptors and risk for nicotine dependence

Bierut, L. J., Stitzel, J. A., Wang, J. C., Hinrichs, A. L., Grucza, R. A., Xuei, X., Saccone, N. L., Saccone, S. F., Bertelsen, S., Fox, L., Horton, W. J., Breslau, N., Budde, J., Cloninger, C. R., Dick, D. M., Foroud, T., Hatsukami, D., Hesselbrock, V., Johnson, E. O., Kramer, J. & 13 others, Kuperman, S., Madden, P. A. F., Mayo, K., Nurnberger, J., Pomerleau, O., Porjesz, B., Reyes, O., Schuckit, M., Swan, G., Tischfield, J. A., Edenberg, H., Rice, J. P. & Goate, A. M., Sep 2008, In : American Journal of Psychiatry. 165, 9, p. 1163-1171 9 p.

Research output: Contribution to journalArticle

Tobacco Use Disorder
Nicotinic Receptors
Smoking
Population
Amino Acids
12 Citations (Scopus)

Visual perception in prediagnostic and early stage Huntington's disease

O'Donnell, B., Blekhert, T. M., Weaver, M., White, K. M., Marshall, J., Beristain, X., Stout, J. C., Gray, J., Wojcieszek, J. & Foroud, T., May 2008, In : Journal of the International Neuropsychological Society. 14, 3, p. 446-453 8 p.

Research output: Contribution to journalArticle

Visual Perception
Huntington Disease
Contrast Sensitivity
Genes
Visual Pathways
2007
20 Citations (Scopus)

Are cognitive changes progressive in prediagnostic HD?

Stout, J. C., Weaver, M., Solomon, A. C., Queller, S., Hui, S., Johnson, S. A., Gray, J., Beristain, X., Wojcieszek, J. & Foroud, T., Dec 2007, In : Cognitive and Behavioral Neurology. 20, 4, p. 212-218 7 p.

Research output: Contribution to journalArticle

Huntington Disease
Disease Progression
Executive Function
Genetic Testing
63 Citations (Scopus)

Association of alcohol craving with α-synuclein (SNCA)

Foroud, T., Wetherill, L. F., Liang, T., Dick, D. M., Hesselbrock, V., Kramer, J., Nurnberger, J., Schuckit, M., Carr, L., Porjesz, B., Xuei, X. & Edenberg, H., Apr 2007, In : Alcoholism: Clinical and Experimental Research. 31, 4, p. 537-545 9 p.

Research output: Contribution to journalArticle

Synucleins
Alcohols
Alcoholism
Single Nucleotide Polymorphism
Haplotypes
18 Citations (Scopus)

G2019S mutation in the leucine-rich repeat kinase 2 gene is not associated with multiple system atrophy

Ozelius, L. J., Foroud, T., May, S., Senthil, G., Sandroni, P., Low, P. A., Reich, S., Colcher, A., Stern, M. B., Ondo, W. G., Jankovic, J., Huang, N., Tanner, C. M., Novak, P., Gilman, S., Marshall, F. J., Wooten, G. F., Chelimsky, T. C., Shults, C. W., Masliah, E. & 5 others, Kukull, W., Lee, V., Trojanowski, J., Shoulson, I. & Ozelius, L., Mar 15 2007, In : Movement Disorders. 22, 4, p. 546-549 4 p.

Research output: Contribution to journalArticle

Multiple System Atrophy
Leucine
Parkinsonian Disorders
Phosphotransferases
Mutation
61 Citations (Scopus)

Genetics of Parkinson disease

Pankratz, N. & Foroud, T., Dec 2007, In : Genetics in Medicine. 9, 12, p. 801-811 11 p.

Research output: Contribution to journalArticle

Inborn Genetic Diseases
Parkinson Disease
Genes
Mutation
Molecular Diagnostic Techniques
29 Citations (Scopus)

Lack of association of alcohol dependence and habitual smoking with catechol-O-methyltransferase

Foroud, T., Wetherill, L. F., Dick, D. M., Hesselbrock, V., Nurnberger, J., Kramer, J., Tischfield, J., Schuckit, M., Bierut, L. J., Xuei, X. & Edenberg, H., Nov 2007, In : Alcoholism: Clinical and Experimental Research. 31, 11, p. 1773-1779 7 p.

Research output: Contribution to journalArticle

Catechol O-Methyltransferase
Alcoholism
Smoking
Alcohols
Polymorphism
43 Citations (Scopus)

LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8

Nichols, W. C., Elsaesser, V. E., Pankratz, N., Pauciulo, M. W., Marek, D. K., Halter, C. A., Rudolph, A., Shults, C. W. & Foroud, T., Oct 2007, In : Neurology. 69, 18, p. 1737-1744 8 p.

Research output: Contribution to journalArticle

Leucine
Parkinson Disease
Phosphotransferases
Mutation
Genes
129 Citations (Scopus)

Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone mass

Ioannidis, J. P. A., Ng, M. Y., Sham, P. C., Zintzaras, E., Lewis, C. M., Deng, H. W., Econs, M., Karasik, D., Devoto, M., Kammerer, C. M., Spector, T., Andrew, T., Cupples, L. A., Duncan, E. L., Foroud, T., Kiel, D. P., Koller, D., Langdahl, B., Mitchell, B. D., Peacock, M. & 8 others, Recker, R., Shen, H., Sol-Church, K., Spotila, L. D., Uitterlinden, A. G., Wilson, S. G., Kung, A. W. C. & Ralston, S. H., Feb 2007, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 22, 2, p. 173-183 11 p.

Research output: Contribution to journalArticle

Meta-Analysis
Genome
Spine
Bone and Bones
Chromosomes
52 Citations (Scopus)

Potential outcome measures and trial design issues for multiple system atrophy

May, S., Gilman, S., Sowell, B. B., Thomas, R. G., Stern, M. B., Colcher, A., Tanner, C. M., Huang, N., Novak, P., Reich, S. G., Jankovic, J., Ondo, W. G., Low, P. A., Sandroni, P., Lipp, A., Marshall, F. J., Wooten, F., Shults, C. W., Masliah, E., Thomas, R. & 8 others, Tanner, C., Kukull, W., Lee, V., Trojanowski, J., Low, P., Shoulson, I., Ozelius, L. & Foroud, T., Dec 2007, In : Movement Disorders. 22, 16, p. 2371-2377 7 p.

Research output: Contribution to journalArticle

Multiple System Atrophy
Outcome Assessment (Health Care)
Health Surveys
Sample Size
Cerebellar Ataxia
7 Citations (Scopus)

R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation

Nichols, W. C., Marek, D. K., Pauciulo, M. W., Pankratz, N., Halter, C. A., Rudolph, A., Shults, C. W., Wojcieszek, J., Foroud, T., Shults, C., Marshall, F., Oakes, D., Rudolph, A., Shinaman, A., Marder, K., Conneally, P. M., Foroud, T., Halter, C., Lyons, K., Siemers, E. & 199 others, Factor, S., Higgins, D., Evans, S., Shill, H., Stacy, M., Danielson, J., Marlor, L., Williamson, K., Jankovic, J., Hunter, C., Simon, D., Ryan, P., Scollins, L., Saunders-Pullman, R., Boyar, K., Costan-Toth, C., Ohmann, E., Sudarsky, L., Joubert, C., Friedman, J., Chou, K., Fernandez, H., Lannon, M., Galvez-Jimenez, N., Podichetty, A., Lewitt, P., DeAngelis, M., O'Brien, C., Seeberger, L., Dingmann, C., Judd, D., Marder, K., Fraser, J., Harris, J., Bertoni, J., Peterson, C., Chouinard, S., Panisset, M., Hall, J., Poiffaut, H., Calabrese, V., Roberge, P., Wojcieszek, J., Belden, J., Halter, C., Jennings, D., Marek, K., Mendick, S., Reich, S., Dunlop, B., Jog, M., Horn, C., Rao, J., Cook, M., Uitti, R., Turk, M., Ajax, T., Mannetter, J., Panisset, M., Hall, J., Sethi, K., Carpenter, J., Ligon, K., Narayan, S., Woodward, L., Blindauer, K., Petit, J., Elmer, L., Aiken, E., Davis, K., Schell, C., Wilson, S., Velickovic, M., Koller, W., Phipps, S., Feigin, A., Gordon, M., Hamann, J., Licari, E., Marotta-Kollarus, M., Shannon, B., Winnick, R., Simuni, T., Kaczmarek, A., Williams, K., Wolff, M., Fernandez, M., Hubble, J., Kostyk, S., Campbell, A., Reider, C., Camicioli, R., Carter, J., Andrews, P., Morehouse, S., Stone, C., Mendis, T., Grimes, D., Gray, P., Haas, K., Sutton, J., Hutchinson, B., Young, J., Rajput, A., Rajput, A., Klassen, L., Shirley, T., Manyam, B., Simpson, P., Whetteckey, J., Wulbrecht, B., Truong, D., Pathak, M., Luong, N., Tra, T., Tran, A., Vo, J., Lang, A., Kleiner-Fisman, G., Nieves, A., So, J., Podskalny, G., Giffin, L., Atchison, P., Allen, C., Martin, W., Wieler, M., Suchowersky, O., Klimek, M., Hermanowicz, N., Niswonger, S., Shults, C., Fontaine, D., Aminoff, M., Christine, C., Diminno, M., Hevezi, J., Dalvi, A., Kang, U., Richman, J., Uy, S., Young, J., Dalvi, A., Sahay, A., Schwieterman, D., Leehey, M., Culver, S., Derian, T., Demarcaida, T., Belber, S., Rodnitzky, R., Dobson, J., Pahwa, R., Lyons, K., Gales, T., Thomas, S., Shulman, L., Weiner, W., Dustin, K., Singer, C., Koller, W., Lyons, K., Weiner, W., Zelaya, L., Tuite, P., Hagen, V., Rolandelli, S., Schacherer, R., Gordon, P., Werner, J., Serrano, C., Roque, S., Kurlan, R., Berry, D., Gardiner, I., Hauser, R., Sanchez-Ramos, J., Zesiewicz, T., Delgado, H., Price, K., Rodriguez, P., Pfeiffer, R., Davis, L., Pfeiffer, B., Dewey, R., Hayward, B., Meacham, M., Walker, F., Hunt, V., Racette, B., Good, L., Rundle, M., Oakes, D., Watts, A., Wang, A., Ross, T., Bennett, S., Kamp, D. & Julian-Baros, E., Jan 15 2007, In : Movement Disorders. 22, 2, p. 254-257 4 p.

Research output: Contribution to journalArticle

Parkinson Disease
Mutation
Guanine Nucleotides
Adenine
Glutamine
51 Citations (Scopus)

Specific psychiatric manifestations among preclinical huntington disease mutation carriers

Marshall, J., White, K., Weaver, M., Flury Wetherill, L., Hui, S., Stout, J. C., Johnson, S. A., Beristain, X., Gray, J., Wojcieszek, J. & Foroud, T., Jan 2007, In : Archives of Neurology. 64, 1, p. 116-121 6 p.

Research output: Contribution to journalArticle

Huntington Disease
Psychiatry
Mutation
Checklist
Depression
57 Citations (Scopus)

The opioid system in alcohol and drug dependence: Family-based association study

Xuei, X., Flury-Wetherill, L., Bierut, L., Dick, D., Nurnberger, J., Foroud, T. & Edenberg, H., Oct 5 2007, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 144, 7, p. 877-884 8 p.

Research output: Contribution to journalArticle

Pro-Opiomelanocortin
Opioid Analgesics
Alcoholism
Substance-Related Disorders
Single Nucleotide Polymorphism
55 Citations (Scopus)

Unique facial features distinguish fetal alcohol syndrome patients and controls in diverse ethnic populations

Moore, E. S., Ward, R. E., Wetherill, L. F., Rogers, J. L., Autti-Rämö, I., Fagerlund, Å., Jacobson, S. W., Robinson, L. K., Hoyme, H. E., Mattson, S. N., Foroud, T., Riley, E., Autti-Rämö, I., Fagerlund, Å., Korkman, M., Jacobson, S. W., Robinson, L. K. & Mattson, S. N., Oct 2007, In : Alcoholism: Clinical and Experimental Research. 31, 10, p. 1707-1713 7 p.

Research output: Contribution to journalArticle

Fetal Alcohol Spectrum Disorders
Alcohols
Population
Anthropometry
Orbits
2006
53 Citations (Scopus)

A cholinergic receptor gene (CHRM2) affects event-related oscillations

Jones, K. A., Porjesz, B., Almasy, L., Bierut, L., Dick, D., Goate, A., Hinrichs, A., Rice, J. P., Wang, J. C., Bauer, L. O., Crowe, R., Foroud, T., Hesselbrock, V., Kuperman, S., Nurnberger, J., O'Connor, S., Rohrbaugh, J., Schuckit, M. A., Tischfield, J., Edenberg, H. & 1 others, Begleiter, H., Sep 2006, In : Behavior Genetics. 36, 5, p. 627-639 13 p.

Research output: Contribution to journalArticle

cholinergic receptors
cholinergic agents
Cholinergic Receptors
cognition
Cholinergic Agents
77 Citations (Scopus)

Association between GABRA1 and drinking behaviors in the Collaborative Study on the Genetics of Alcoholism sample

Dick, D. M., Plunkett, J., Wetherill, L. F., Xuei, X., Goate, A., Hesselbrock, V., Schuckit, M., Crowe, R., Edenberg, H. & Foroud, T., Jul 2006, In : Alcoholism: Clinical and Experimental Research. 30, 7, p. 1101-1110 10 p.

Research output: Contribution to journalArticle

Drinking Behavior
Alcoholism
Alcohols
Alcoholic Intoxication
Diagnostic and Statistical Manual of Mental Disorders
181 Citations (Scopus)

Association of alcohol dehydrogenase genes with alcohol dependence: A comprehensive analysis

Edenberg, H., Xuei, X., Chen, H. J., Tian, H., Wetherill, L. F., Dick, D. M., Almasy, L., Bierut, L., Bucholz, K. K., Goate, A., Hesselbrock, V., Kuperman, S., Nurnberger, J., Porjesz, B., Rice, J., Schuckit, M., Tischfield, J., Begleiter, H. & Foroud, T., May 2006, In : Human Molecular Genetics. 15, 9, p. 1539-1549 11 p.

Research output: Contribution to journalArticle

Alcohol Dehydrogenase
Alcoholism
Single Nucleotide Polymorphism
Genes
Haplotypes
123 Citations (Scopus)

Association of GABRA2 with drug dependence in the collaborative study of the genetics of alcoholism sample

Agrawal, A., Edenberg, H., Foroud, T., Bierut, L. J., Dunne, G., Hinrichs, A. L., Nurnberger, J., Crowe, R., Kuperman, S., Schuckit, M. A., Begleiter, H., Porjesz, B. & Dick, D. M., Sep 2006, In : Behavior Genetics. 36, 5, p. 640-650 11 p.

Research output: Contribution to journalArticle

drug abuse
Street Drugs
alcohol abuse
Alcoholism
Substance-Related Disorders
130 Citations (Scopus)

Association of the κ-opioid system with alcohol dependence

Xuei, X., Dick, D., Flury-Wetherill, L., Tian, H. J., Agrawal, A., Bierut, L., Goate, A., Bucholz, K., Schuckit, M., Nurnberger, J., Tischfield, J., Kuperman, S., Porjesz, B., Begleiter, H., Foroud, T. & Edenberg, H., Nov 27 2006, In : Molecular Psychiatry. 11, 11, p. 1016-1024 9 p.

Research output: Contribution to journalArticle

Opioid Receptors
Opioid Analgesics
Alcoholism
Ligands
Single Nucleotide Polymorphism
3 Citations (Scopus)

Chromosome 5 and Parkinson disease

Foroud, T., Pankratz, N. & Martinez, M., Oct 2006, In : European Journal of Human Genetics. 14, 10, p. 1106-1110 5 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 5
Parkinson Disease
Age of Onset
Chromosomes
Disease Susceptibility
69 Citations (Scopus)

Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations

Ishihara, L., Warren, L., Gibson, R., Amouri, R., Lesage, S., Dürr, A., Tazir, M., Wszolek, Z. K., Uitti, R. J., Nichols, W. C., Griffith, A., Hattori, N., Leppert, D., Watts, R., Zabetian, C. P., Foroud, T., Farrer, M. J., Brice, A., Middleton, L. & Hentati, F., 2006, In : Archives of Neurology. 63, 9, p. 1250-1254 5 p.

Research output: Contribution to journalArticle

Leucine
Parkinson Disease
Phosphotransferases
Mutation
Gene Dosage
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
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
98 Citations (Scopus)

Functional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependence

Hinrichs, A. L., Wang, J. C., Bufe, B., Kwon, J. M., Budde, J., Allen, R., Bertelsen, S., Evans, W., Dick, D., Rice, J., Foroud, T., Nurnberger, J., Tischfield, J. A., Kuperman, S., Crowe, R., Hesselbrock, V., Schuckit, M., Almasy, L., Porjesz, B., Edenberg, H. & 4 others, Begleiter, H., Meyerhof, W., Bierut, L. J. & Goate, A. M., Jan 2006, In : American Journal of Human Genetics. 78, 1, p. 103-111 9 p.

Research output: Contribution to journalArticle

Alcoholism
Alleles
Gene Frequency
African Americans
Single Nucleotide Polymorphism
22 Citations (Scopus)

Genetic association between endothelial nitric oxide synthase and Alzheimer disease

Akomolafe, A., Lunetta, K. L., Erlich, P. M., Cupples, L. A., Baldwin, C. T., Huyck, M., Green, R. C., Farrer, L. A., Auerbach, S., Griffith, P., Ofili, E., Browndyke, J., Schmechel, D., Welsh-Bohmer, K., Chui, H., DeCarli, C., Duara, R., Foroud, T., Farlow, M., Friedland, R. & 9 others, Go, R., Kurz, A., Obisesan, T., Petrovitch, H., White, L., Relkin, N., Sabbagh, M., Sadovnick, D. & Tsolaki, M., Jul 2006, In : Clinical Genetics. 70, 1, p. 49-56 8 p.

Research output: Contribution to journalArticle

Nitric Oxide Synthase Type III
Alzheimer Disease
African Americans
Single Nucleotide Polymorphism
Meta-Analysis
22 Citations (Scopus)
Femur Neck
Siblings
Bone and Bones
Weights and Measures
Body Weight
60 Citations (Scopus)

Human ALOX12, but not ALOX15, is associated with BMD in white men and women

Ichikawa, S., Koller, D. L., Johnson, M. L., Lai, D., Xuei, X., Edenberg, H., Klein, R. F., Orwoll, E. S., Hui, S., Foroud, T., Peacock, M. & Econs, M., Apr 2006, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 21, 4, p. 556-564 9 p.

Research output: Contribution to journalArticle

Spine
Genes
Single Nucleotide Polymorphism
Haplotypes
Osteoporosis
23 Citations (Scopus)

Identification of a quantitative trait locus on rat chromosome 4 that is strongly linked to femoral neck structure and strength

Alam, I., Sun, Q., Liu, L., Koller, D. L., Fishburn, T., Carr, L. G., Econs, M., Foroud, T. & Turner, C. H., Jul 2006, In : Bone. 39, 1, p. 93-99 7 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 4
Quantitative Trait Loci
Femur Neck
Bone Density
Phenotype
28 Citations (Scopus)

Identification of QTLs influencing alcohol preference in the High Alcohol Preferring (HAP) and Low Alcohol Preferring (LAP) mouse lines

Bice, P. J., Foroud, T., Carr, L. G., Zhang, L., Liu, L., Grahame, N. J., Lumeng, L., Li, T. K. & Belknap, J. K., Mar 2006, In : Behavior Genetics. 36, 2, p. 248-260 13 p.

Research output: Contribution to journalArticle

alcohol
quantitative trait loci
alcohols
Alcohols
Chromosomes, Human, Pair 9
91 Citations (Scopus)

Marital status, alcohol dependence, and GABRA2: Evidence for gene-environment correlation and interaction

Dick, D. M., Agrawal, A., Schuckit, M. A., Bierut, L., Hinrichs, A., Fox, L., Mullaney, J., Cloninger, C. R., Hesselbrock, V., Nurnberger, J., Almasy, L., Foroud, T., Porjesz, B., Edenberg, H. & Begleiter, H., Mar 2006, In : Journal of Studies on Alcohol. 67, 2, p. 185-194 10 p.

Research output: Contribution to journalArticle

Gene-Environment Interaction
Marital Status
marital status
Alcoholism
Genes
30 Citations (Scopus)

Mutations in DJ-1 are rare in familial Parkinson disease

Pankratz, N., Pauciulo, M. W., Elsaesser, V. E., Marek, D. K., Halter, C. A., Wojcieszek, J., Rudolph, A., Shults, C. W., Foroud, T. & Nichols, W. C., Nov 20 2006, In : Neuroscience Letters. 408, 3, p. 209-213 5 p.

Research output: Contribution to journalArticle

Parkinson Disease
Exons
Mutation
Multiplex Polymerase Chain Reaction
Homozygote
22 Citations (Scopus)

Mutations in LRRK2 other than G2019S are rare in a north-American based sample of familial Parkinson's didease

Pankratz, N., Pauciulo, M. W., Elsaesser, V. E., Marek, D. K., Halter, C. A., Rudolph, A., Shults, C. W., Foroud, T., Nichols, W. C., Shults, C., Marshall, F., Oakes, D., Shinaman, A., Marder, K., Conneally, P. M., Lyons, K., Siemers, E., Factor, S., Higgins, D., Evans, S. & 79 others, Shill, H., Stacy, M., Danielson, J., Marlor, L., Williamson, K., Jankovic, J., Hunter, C., Simon, D., Ryan, P., Scollins, L., Saunders-Pullman, R., Boyar, K., Costan-Toth, C., Ohmann, E., Sudarsky, L., Joubert, C., Friedman, J., Chou, K., Fernandez, H., Lannon, M., Galvez-Jimenez, N., Podichetty, A., Lewitt, P., DeAngelis, M., O'Brien, C., Seeberger, L., Dingmann, C., Judd, D., Fraser, J., Harris, J., Bertoni, J., Peterson, C., Chouinard, S., Panisset, M., Hall, J., Poiffaut, H., Calabrese, V., Roberge, P., Wojcieszek, J., Belden, J., Halter, C., Jennings, D., Marek, K., Mendick, S., Reich, S., Dunlop, B., Jog, M., Horn, C., Rao, J., Cook, M., Uitti, R., Turk, M., Ajax, T., Mannetter, J., Sethi, K., Carpenter, J., Ligon, K., Narayan, S., Woodward, L., Blindauer, K., Petit, J., Elmer, L., Aiken, E., Davis, K., Schell, C., Wilson, S., Velickovic, M., Koller, W., Phipps, S., Feigin, A., Gordon, M., Hamann, J., Licari, E., Marotta-Kollarus, M., Shannon, B., Winnick, R., Simuni, T., Kaczmarek, A. & Williams, K., Dec 2006, In : Movement Disorders. 21, 12, p. 2257-2260 4 p.

Research output: Contribution to journalArticle

Mutation
Parkinson Disease
Pedigree
14 Citations (Scopus)

Polymorphisms in the bone morphogenetic protein 2 (BMP2) gene do not affect bone mineral density in white men or women

Ichikawa, S., Johnson, M. L., Koller, D. L., Lai, D., Xuei, X., Edenberg, H., Hui, S., Foroud, T., Peacock, M. & Econs, M., Apr 2006, In : Osteoporosis International. 17, 4, p. 587-592 6 p.

Research output: Contribution to journalArticle

Bone Morphogenetic Protein 2
Bone Density
Genes
Haplotypes
Single Nucleotide Polymorphism
68 Citations (Scopus)

Polymorphisms in the PON gene cluster are associated with Alzheimer disease

Erlich, P. M., Lunetta, K. L., Cupples, L. A., Huyck, M., Green, R. C., Baldwin, C. T., Farrer, L. A., Auerbach, S., Akomolafe, A., Griffith, P., Ofili, E., Browndyke, J., Schmechel, D., Welsh-Bohmer, K., Chui, H., DeCarli, C., Duara, R., Foroud, T., Farlow, M., Friedland, R. & 9 others, Go, R., Kurz, A., Obisesan, T., Petrovitch, H., White, L., Relkin, N., Sabbagh, M., Sadovnick, D. & Tsolaki, M., Jan 1 2006, In : Human Molecular Genetics. 15, 1, p. 77-85 9 p.

Research output: Contribution to journalArticle

Multigene Family
Single Nucleotide Polymorphism
Alzheimer Disease
African Americans
Aryldialkylphosphatase
119 Citations (Scopus)
Alcoholism
Single Nucleotide Polymorphism
Genome
Alcohols
Gene Frequency
62 Citations (Scopus)

Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia

Pankratz, N., Byder, L., Halter, C., Rudolph, A., Shults, C. W., Conneally, P. M., Foroud, T., Nichols, W. C., Lyons, K., Marder, K., Marshall, F., Oakes, D., Rudolph, A., Shinaman, A., Siemers, E., Wojcieszek, J., Belden, J., Carter, J., Camicioli, R., Andrews, P. & 79 others, Panisset, M., Hall, J., Hubble, J., Fernandez, M., Reider, C., 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., Fontaine, D., Jennings, D., Marek, K., Mendick, S., Aminoff, M., DiMinno, M., Lewitt, P., De Angelis, 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., Wieler, M., Tuite, P., Schacherer, R., 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., Jan 2006, In : Movement Disorders. 21, 1, p. 45-49 5 p.

Research output: Contribution to journalArticle

Parkinson Disease
Dementia
Alleles
Age of Onset
Alzheimer Disease
38 Citations (Scopus)

Root resorption associated with orthodontic force in inbred mice: Genetic contributions

Al-Qawasmi, R. A., Hartsfield, J. K., Everett, E. T., Weaver, M. R., Foroud, T., Faust, D. M. & Roberts, W. E., Feb 2006, In : European Journal of Orthodontics. 28, 1, p. 13-19 7 p.

Research output: Contribution to journalArticle

Root Resorption
Orthodontics
Inbred Strains Mice
Orthodontic Appliances
Tooth
88 Citations (Scopus)

Saccades in presymptomatic and early stages of Huntington disease

Blekher, T., Johnson, S. A., Marshall, J., White, K., Hui, S., Weaver, M., Gray, J., Yee, R., Stout, J. C., Beristain, X., Wojcieszek, J. & Foroud, T., Aug 2006, In : Neurology. 67, 3, p. 394-399 6 p.

Research output: Contribution to journalArticle

Saccades
Huntington Disease
Eye Movements
Biomarkers
Eye Abnormalities
154 Citations (Scopus)

The genetics of alcoholism: Identifying specific genes through family studies

Edenberg, H. & Foroud, T., Sep 2006, In : Addiction Biology. 11, 3-4, p. 386-396 11 p.

Research output: Contribution to journalArticle

Alcoholism
Genes
Phenotype
Single Nucleotide Polymorphism
Research Personnel
164 Citations (Scopus)

The role of GABRA2 in risk for conduct disorder and alcohol and drug dependence across developmental stages

Dick, D. M., Bierut, L., Hinrichs, A., Fox, L., Bucholz, K. K., Kramer, J., Kuperman, S., Hesselbrock, V., Schuckit, M., Almasy, L., Tischfield, J., Porjesz, B., Begleiter, H., Nurnberger, J., Xuei, X., Edenberg, H. & Foroud, T., Jul 2006, In : Behavior Genetics. 36, 4, p. 577-590 14 p.

Research output: Contribution to journalArticle

drug abuse
Conduct Disorder
alcohol abuse
developmental stage
Alcoholism
2005
61 Citations (Scopus)

A mutation in myotilin causes spheroid body myopathy

Foroud, T., Pankratz, N., Batchman, A. P., Pauciulo, M. W., Vidal, R., Miravalle, L., Goebel, H. H., Cushman, L. J., Azzarelli, B., Horak, H., Farlow, M. & Nichols, W. C., Dec 2005, In : Neurology. 65, 12, p. 1936-1940 5 p.

Research output: Contribution to journalArticle

Mutation
Genes
Lod Score
Biopsy
Muscles
28 Citations (Scopus)

Analysis of variation in expression of autosomal dominant osteopetrosis type 2: Searching for modifier genes

Chu, K., Koller, D. L., Snyder, R., Fishburn, T., Lai, D., Waguespack, S. G., Foroud, T. & Econs, M., Nov 2005, In : Bone. 37, 5, p. 655-661 7 p.

Research output: Contribution to journalArticle

Modifier Genes
Osteopetrosis
Alleles
Genes
Single Nucleotide Polymorphism
18 Citations (Scopus)

A sex-adjusted and age-adjusted genome screen for nested alcohol dependence diagnoses

Corbett, J., Saccone, N. L., Foroud, T., Goate, A., Edenberg, H., Nurnberger, J., Porjesz, B., Begleiter, H., Reich, T. & Rice, J. P., Mar 2005, In : Psychiatric Genetics. 15, 1, p. 25-30 6 p.

Research output: Contribution to journalArticle

Alcoholism
Genome
Phenotype
Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 4
92 Citations (Scopus)

A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors

Duan, Q. L., Nikpoor, B., Dubé, M. P., Molinaro, G., Meijer, I. A., Dion, P., Rochefort, D., Saint-Onge, J., Flury, L., Brown, N. J., Gainer, J. V., Rouleau, J. L., Agostoni, A., Cugno, M., Simon, P., Clavel, P., Potier, J., Wehbe, B., Benarbia, S., Marc-Aurèle, J. & 4 others, Chanard, J., Foroud, T., Adam, A. & Rouleau, G. A., Oct 2005, In : American Journal of Human Genetics. 77, 4, p. 617-626 10 p.

Research output: Contribution to journalArticle

Angioedema
Angiotensin-Converting Enzyme Inhibitors
Single Nucleotide Polymorphism
Pedigree
Microsatellite Repeats
161 Citations (Scopus)

Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q

McQueen, M. B., Devlin, B., Faraone, S. V., Nimgaonkar, V. L., Sklar, P., Smoller, J. W., Jamra, R. A., Albus, M., Bacanu, S. A., Baron, M., Barrett, T. B., Berrettini, W., Blacker, D., Byerley, W., Cichon, S., Coryell, W., Craddock, N., Daly, M. J., DePaulo, J. R., Edenberg, H. & 33 others, Foroud, T., Gill, M., Gilliam, T. C., Hamshere, M., Jones, I., Jones, L., Juo, S. H., Kelsoe, J. R., Lambert, D., Lange, C., Lerer, B., Liu, J., Maier, W., MacKinnon, J. D., McInnis, M. G., McMahon, F. J., Murphy, D. L., Nöthen, M. M., Nurnberger, J., Pato, C. N., Pato, M. T., Potash, J. B., Propping, P., Pulver, A. E., Rice, J. P., Rietschel, M., Scheftner, W., Schumacher, J., Segurado, R., Van Steen, K., Xie, W., Zandi, P. P. & Laird, N. M., Oct 2005, In : American Journal of Human Genetics. 77, 4, p. 582-595 14 p.

Research output: Contribution to journalArticle

Bipolar Disorder
Chromosomes
Meta-Analysis
Genotype
Genome
80 Citations (Scopus)

Contribution of the LRP5 gene to normal variation in peak BMD in women

Koller, D. L., Ichikawa, S., Johnson, M. L., Lai, D., Xuei, X., Edenberg, H., Conneally, P. M., Hui, S., Johnston, C. C., Peacock, M., Foroud, T. & Econs, M., 2005, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 20, 1, p. 75-80 6 p.

Research output: Contribution to journalArticle

Low Density Lipoprotein Receptor-Related Protein-5
Single Nucleotide Polymorphism
Genes
Spine
Hip
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
347 Citations (Scopus)

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

Nichols, W. C., Pankratz, N., Hernandez, D., Paisán-Ruíz, C., Jain, S., Halter, C. A., Michaels, V. E., Reed, T., Rudolph, A., Shults, C. W., Singleton, A. & Foroud, T., Jan 29 2005, In : The Lancet. 365, 9457, p. 410-412 3 p.

Research output: Contribution to journalArticle

Genetic Testing
Leucine
Parkinson Disease
Phosphotransferases
Mutation
24 Citations (Scopus)

Genome screen for bone mineral density phenotypes in Fisher 344 and Lewis rat strains

Koller, D. L., Alam, I., Sun, Q., Liu, L., Fishburn, T., Carr, L. G., Econs, M., Foroud, T. & Turner, C. H., Aug 2005, In : Mammalian Genome. 16, 8, p. 578-586 9 p.

Research output: Contribution to journalArticle

Bone Density
Genome
Phenotype
Inbred Lew Rats
Spine