Tatiana Foroud

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

2009
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
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

Genetic inheritance and population genetics

Foroud, T. & Koller, D. L., 2008, Molecular Genetic Pathology. Humana Press, p. 393-403 11 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Population Genetics
Genetic Polymorphisms
Blood Group Antigens
Alleles
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
39 Citations (Scopus)

Genome screen to detect linkage to intracranial aneurysm susceptibility genes: The familial intracranial aneurysm (FIA) study

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., Rouleau, G., Connolly, E. S., Lai, D., Koller, D. L., Huston, J. & Broderick, J. P., May 1 2008, In : Stroke. 39, 5, p. 1434-1440 7 p.

Research output: Contribution to journalArticle

Intracranial Aneurysm
Genome
Smoking
Chromosomes, Human, Pair 4
Genes
11 Citations (Scopus)

Genome-wide parametric linkage analyses of 644 bipolar pedigrees suggest susceptibility loci at chromosomes 16 and 20

Ross, J., Berrettini, W., Coryell, W., Gershon, E. S., Badner, J. A., Kelsoe, J. R., McInnis, M. G., McMahon, F. J., Murphy, D. L., Nurnberger, J., Foroud, T., Rice, J. P., Scheftner, W. B., Zandi, P., Edenberg, H. & Byerley, W., Aug 2008, In : Psychiatric Genetics. 18, 4, p. 191-198 8 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 20
Chromosomes, Human, Pair 16
Pedigree
Genome
Bipolar Disorder
10 Citations (Scopus)

Genomic expression analysis of rat chromosome 4 for skeletal traits at femoral neck

Alam, I., Sun, Q., Liu, L., Koller, D. L., Liu, Y., Edenberg, H., Econs, M., Foroud, T. & Turner, C. H., Oct 2008, In : Physiological Genomics. 35, 2, p. 191-196 6 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 4
Femur Neck
Quantitative Trait Loci
Inbred F344 Rats
Hip Fractures
4 Citations (Scopus)

Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white women

Ichikawa, S., Koller, D. L., Curry, L. R., Lai, D., Xuei, X., Pugh, E. W., Tsai, Y. Y., Doheny, K. F., Edenberg, H., Hui, S., Foroud, T., Peacock, M. & Econs, M., Oct 2008, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 23, 10, p. 1680-1688 9 p.

Research output: Contribution to journalArticle

Linkage Disequilibrium
Chromosomes
Single Nucleotide Polymorphism
Genes
Spine
14 Citations (Scopus)

Inheritance of susceptibility to root resorption associated with orthodontic force in mice

Abass, S. K., Hartsfield, J. K., Al-Qawasmi, R. A., Everett, E. T., Foroud, T. & Roberts, W. E., Dec 2008, In : American Journal of Orthodontics and Dentofacial Orthopedics. 134, 6, p. 742-750 9 p.

Research output: Contribution to journalArticle

Root Resorption
Orthodontics
Multifactorial Inheritance
Inheritance Patterns
Genetic Heterogeneity
53 Citations (Scopus)

Linkage scan for quantitative traits identifies new regions of interest for substance dependence in the Collaborative Study on the Genetics of Alcoholism (COGA) sample

Agrawal, A., Hinrichs, A. L., Dunn, G., Bertelsen, S., Dick, D. M., Saccone, S. F., Saccone, N. L., Grucza, R. A., Wang, J. C., Cloninger, C. R., Edenberg, H., Foroud, T., Hesselbrock, V., Kramer, J., Bucholz, K. K., Kuperman, S., Nurnberger, J., Porjesz, B., Schuckit, M. A., Goate, A. M. & 1 others, Bierut, L. J., Jan 11 2008, In : Drug and Alcohol Dependence. 93, 1-2, p. 12-20 9 p.

Research output: Contribution to journalArticle

alcoholism
Alcoholism
Substance-Related Disorders
drug dependence
alcohol
7 Citations (Scopus)

Linkage screen for BMD phenotypes in male and female COP and DA rat strains

Koller, D. L., Liu, L., Alam, I., Sun, Q., Econs, M., Foroud, T. & Turner, C. H., Sep 2008, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 23, 9, p. 1382-1388 7 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Phenotype
Chromosomes, Human, Pair 1
Femur
Inbred Strains Animals
89 Citations (Scopus)

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease

Haugarvoll, K., Rademakers, R., Kachergus, J. M., Nuytemans, K., Ross, O. A., Gibson, J. M., Tan, E. K., Gaig, C., Tolosa, E., Goldwurm, S., Guidi, M., Riboldazzi, G., Brown, L., Walter, U., Benecke, R., Berg, D., Gasser, T., Theuns, J., Pals, P., Cras, P. & 14 others, De Deyn, P. P., Engelborghs, S., Pickut, B., Uitti, R. J., Foroud, T., Nichols, W. C., Hagenah, J., Klein, C., Samii, A., Zabetian, C. P., Bonifati, V., Van Broeckhoven, C., Farrer, M. J. & Wszolek, Z. K., Apr 2008, In : Neurology. 70, 16 PART 2, p. 1456-1460 5 p.

Research output: Contribution to journalArticle

Parkinsonian Disorders
Parkinson Disease
Age of Onset
Leucine
Mutation
58 Citations (Scopus)

Neuropeptide Y receptor genes are associated with alcohol dependence, alcohol withdrawal phenotypes, and cocaine dependence

Wetherill, L., Schuckit, M. A., Hesselbrock, V., Xuei, X., Liang, T., Dick, D. M., Kramer, J., Nurnberger, J., Tischfield, J. A., Porjesz, B., Edenberg, H. & Foroud, T., Dec 2008, In : Alcoholism: Clinical and Experimental Research. 32, 12, p. 2031-2040 10 p.

Research output: Contribution to journalArticle

Neuropeptide Y Receptors
Cocaine-Related Disorders
Cocaine
Alcoholism
Genes

Reply from the Authors

Nichols, W. C., Elsaesser, V. E., Pankratz, N., Pauciulo, M. W., Marek, D. K., Halter, C. A., Rudolph, A. & Foroud, T., Jun 10 2008, In : Neurology. 70, 24, p. 2348-2349 2 p.

Research output: Contribution to journalArticle

Response

Brown, R. D., Huston, J., Hornung, R., Foroud, T., Kallmes, D. F., Kleindorfer, D., Meissner, I., Woo, D., Sauerbeck, L. & Broderick, J., Jun 2008, In : Journal of Neurosurgery. 108, 6, p. 1131 1 p.

Research output: Contribution to journalArticle

54 Citations (Scopus)

Screening for brain aneurysm in the Familial Intracranial Aneurysm study: Frequency and predictors of lesion detection

Brown, R. D., Huston, J., Hornung, R., Foroud, T., Kallmes, D. F., Kleindorfer, D., Meissner, I., Woo, D., Sauerbeck, L. & Broderick, J., Jun 2008, In : Journal of Neurosurgery. 108, 6, p. 1132-1138 7 p.

Research output: Contribution to journalArticle

Intracranial Aneurysm
Aneurysm
Magnetic Resonance Angiography
Smoking
Odds Ratio
9 Citations (Scopus)
Genetic Loci
Quantitative Trait Loci
Femur Neck
Bone and Bones
Chromosomes, Human, Pair 1
44 Citations (Scopus)

Ten-year rate of longitudinal change in neurocognitive and motor function in prediagnosis Huntington disease

Solomon, A. C., Stout, J. C., Weaver, M., Queller, S., Tomusk, A., Whitlock, K. B., Hui, S., Marshall, J., Jackson, J. G., Siemens, E. R., Beristain, X., Wojcieszek, J. & Foroud, T., Oct 15 2008, In : Movement Disorders. 23, 13, p. 1830-1836 7 p.

Research output: Contribution to journalArticle

Huntington Disease
Age of Onset
Longitudinal Studies
32 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
425 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
15 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

A multinational deployment of 3D laser scanning to study craniofacial dysmorphology in fetal alcohol spectrum disorders

Rogers, J., Wernert, E., Moore, E., Ward, R., Wetherill, L. F. & Foroud, T., 2007, Proceedings of SPIE - The International Society for Optical Engineering. Vol. 6491. 64910I

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

anthropometry
Anthropometry
alcohols
Alcohols
disorders
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
65 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
19 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

Implementation of a distributed architecture for managing collection and dissemination of data for fetal alcohol spectrum disorders research

Arenson, A., Bakhireva, L., Chambers, T., Deximo, C., Foroud, T., Jacobson, J., Jacobson, S., Jones, K. L., Mattson, S., May, P., Moore, E., Ogle, K., Riley, E., Robinson, L., Rogers, J., Streissguth, A., Tavares, M., Urbanski, J., Yezerets, H. & Stewart, C. A., 2007, Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). Vol. 4360 LNBI. p. 33-44 12 p.

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

Fetal Alcohol Spectrum Disorders
Distributed Architecture
Alcohol
Disorder
Alcohols
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
44 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
130 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
53 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