Tatiana Foroud

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

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9 Citations (Scopus)

Abnormal Error-Related Antisaccade Activation in Premanifest and Early Manifest Huntington Disease

Rupp, J., Dzemidzic, M., Blekher, T., Bragulat, V., West, J., Jackson, J., Hui, S., Wojcieszek, J., Saykin, A., Kareken, D. & Foroud, T., May 2011, In : Neuropsychology. 25, 3, p. 306-318 13 p.

Research output: Contribution to journalArticle

Huntington Disease
Saccades
Gyrus Cinguli
Motor Cortex
Eye Movements
15 Citations (Scopus)

Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease

Nuytemans, K., Inchausti, V., Beecham, G. W., Wang, L., Dickson, D. W., Trojanowski, J. Q., Lee, V. M. Y., Mash, D. C., Frosch, M. P., Foroud, T., Honig, L. S., Montine, T. J., Dawson, T. M., Martin, E. R., Scott, W. K. & Vance, J. M., 2014, In : Movement Disorders. 29, 6, p. 827-830 4 p.

Research output: Contribution to journalArticle

Parkinson Disease
Autopsy
Haplotypes
Parkinsonian Disorders
Neurodegenerative Diseases
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
160 Citations (Scopus)

A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly

Ho, A. J., Stein, J. L., Hua, X., Lee, S., Hibar, D. P., Leow, A. D., Dinov, I. 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., Stephan, D. A., DeCarli, C. S., DeChairo, B. M. & 8 others, Potkin, S. G., Jack, C. R., Weiner, M. W., Raji, C. A., Lopez, O. L., Becker, J. T., Carmichael, O. T. & Thompson, P. M., May 4 2010, In : Proceedings of the National Academy of Sciences of the United States of America. 107, 18, p. 8404-8409 6 p.

Research output: Contribution to journalArticle

Obesity
Fats
Alleles
Brain
Genes

A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework

Schizophrenia and Bipolar Disorder Working Groups of the Psychiatric Genomics Consortium, Jun 25 2018, In : BMC Genomics. 19, 1, 494.

Research output: Contribution to journalArticle

Genome-Wide Association Study
11 Citations (Scopus)
Drinking
Genotype
Alcohols
Alcoholism
Single Nucleotide Polymorphism
31 Citations (Scopus)

A description of the methods of the Nulliparous Pregnancy Outcomes Study: Monitoring mothers-to-be (nuMoM2b)

Haas, D., Parker, C. B., Wing, D. A., Parry, S., Grobman, W. A., Mercer, B. M., Simhan, H. N., Hoffman, M. K., Silver, R. M., Wadhwa, P., Iams, J. D., Koch, M. A., Caritis, S. N., Wapner, R. J., Esplin, M. S., Elovitz, M. A., Foroud, T., Peaceman, A. M., Saade, G. R., Willinger, M. & 1 others, Reddy, U. M., Apr 1 2015, In : American Journal of Obstetrics and Gynecology. 212, 4, p. 539.e1-539.e24

Research output: Contribution to journalArticle

Pregnancy Outcome
Mothers
Outcome Assessment (Health Care)
Pregnancy
Cohort Studies
116 Citations (Scopus)

ADH1B is associated with alcohol dependence and alcohol consumption in populations of European and African ancestry

Bierut, L. J., Goate, A. M., Breslau, N., Johnson, E. O., Bertelsen, S., Fox, L., Agrawal, A., Bucholz, K. K., Grucza, R., Hesselbrock, V., Kramer, J., Kuperman, S., Nurnberger, J., Porjesz, B., Saccone, N. L., Schuckit, M., Tischfield, J., Wang, J. C., Foroud, T., Rice, J. P. & 1 others, Edenberg, H., Apr 2012, In : Molecular Psychiatry. 17, 4, p. 445-450 6 p.

Research output: Contribution to journalArticle

Alcohol Dehydrogenase
Alcohol Drinking
Alcoholism
Population
Diagnostic and Statistical Manual of Mental Disorders
97 Citations (Scopus)

A family-based analysis of the association of the dopamine D2 receptor (DRD2) with alcoholism

Edenberg, H., Foroud, T., Koller, D. L., Goate, A., Rice, J., Van Eerdewegh, P., Reich, T., Cloninger, C. R., Nurnberger, J., Kowalczuk, M., Wu, B., Li, T. K., Conneally, P. M., Tischfield, J. A., Wu, W., Shears, S., Crowe, R., Hesselbrock, V., Schuckit, M., Porjesz, B. & 1 others, Begleiter, H., 1998, In : Alcoholism: Clinical and Experimental Research. 22, 2, p. 505-512 8 p.

Research output: Contribution to journalArticle

Dopamine D2 Receptors
Alcoholism
Alcohols
Gene Frequency
Population
82 Citations (Scopus)

A family-based analysis of whether the functional promoter alleles of the serotonin transporter gene HTT affect the risk for alcohol dependence

Edenberg, H., Reynolds, J., Koller, D. L., Begleiter, H., Bucholz, K. K., Conneally, P. M., Crowe, R., Goate, A., Hesselbrock, V., Li, T. K., Nurnberger, J., Porjesz, B., Reich, T., Rice, J. P., Schuckit, M., Tischfield, J. A. & Foroud, T., Aug 1998, In : Alcoholism: Clinical and Experimental Research. 22, 5, p. 1080-1085 6 p.

Research output: Contribution to journalArticle

Serotonin Plasma Membrane Transport Proteins
Alcoholism
Genes
Alleles
Alcohols
7 Citations (Scopus)

Affected twins in the familial intracranial aneurysm study

Mackey, J., Brown, R. D., Sauerbeck, L., Hornung, R., Moomaw, C. J., Koller, D. L., Foroud, T., Deka, R., Woo, D., Kleindorfer, D., Flaherty, M. L., Meissner, I., Anderson, C., Rouleau, G., Connolly, E. S., Huston, J. & Broderick, J. P., Mar 6 2015, In : Cerebrovascular Diseases. 39, 2, p. 82-86 5 p.

Research output: Contribution to journalArticle

Intracranial Aneurysm
Dizygotic Twins
Monozygotic Twins
Rupture
Aneurysm
1 Citation (Scopus)

A GABRA2 polymorphism improves a model for prediction of drinking initiation

Kuperman, S., Chan, G., Kramer, J., Wetherill, L., Acion, L., Edenberg, H., Foroud, T., Nurnberger, J., Agrawal, A., Anokhin, A., Brooks, A., Hesselbrock, V., Hesselbrock, M., Schuckit, M., Tischfield, J. & Liu, X., Sep 1 2017, In : Alcohol. 63, p. 1-8 8 p.

Research output: Contribution to journalArticle

Polymorphism
Drinking
Genotype
Self Report
Single Nucleotide Polymorphism
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
175 Citations (Scopus)

A genome screen of maximum number of drinks as an alcoholism phenotype

Saccone, N. L., Kwon, J. M., Corbett, J., Goate, A., Rochberg, N., Edenberg, H., Foroud, T., Li, T. K., Begleiter, H., Reich, T. & Rice, J. P., Oct 9 2000, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 96, 5, p. 632-637 6 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 4
Alcoholism
Genome
Phenotype
Twin Studies
323 Citations (Scopus)

A genome-wide association study of alcohol dependence

Bierut, L. J., Agrawal, A., Bucholz, K. K., Doheny, K. F., Laurie, C., Pugh, E., Fisher, S., Fox, L., Howells, W., Bertelsen, S., Hinrichs, A. L., Almasy, L., Breslau, N., Culverhouse, R. C., Dick, D. M., Edenberg, H., Foroud, T., Grucza, R. A., Hatsukami, D., Hesselbrock, V. & 19 others, Johnson, E. O., Kramer, J., Krueger, R. F., Kuperman, S., Lynskey, M., Mann, K., Neuman, R. J., Nöthen, M. M., Nurnberger, J., Porjesz, B., Ridinger, M., Saccone, N. L., Saccone, S. F., Schuckit, M. A., Tischfield, J. A., Wang, J. C., Rietschel, M., Goate, A. M. & Rice, J. P., Mar 16 2010, In : Proceedings of the National Academy of Sciences of the United States of America. 107, 11, p. 5082-5087 6 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Alcoholism
Single Nucleotide Polymorphism
Drinking
Alcohols
49 Citations (Scopus)

A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53

Wang, J. C., Foroud, T., Hinrichs, A. L., Le, N. X. H., Bertelsen, S., Budde, J. P., Harari, O., Koller, D. L., Wetherill, L., Agrawal, A., Almasy, L., Brooks, A. I., Bucholz, K., Dick, D., Hesselbrock, V., Johnson, E. O., Kang, S., Kapoor, M., Kramer, J., Kuperman, S. & 17 others, Madden, P. A. F., Manz, N., Martin, N. G., McClintick, J., Montgomery, G. W., Nurnberger, J., Rangaswamy, M., Rice, J., Schuckit, M., Tischfield, J. A., Whitfield, J. B., Xuei, X., Porjesz, B., Heath, A. C., Edenberg, H., Bierut, L. J. & Goate, A. M., Nov 2013, In : Molecular Psychiatry. 18, 11, p. 1218-1224 7 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Pedigree
Alcoholism
Diagnostic and Statistical Manual of Mental Disorders
Genes
18 Citations (Scopus)

A genome-wide association study of bipolar disorder with comorbid eating disorder replicates the SOX2-OT region

Bipolar Genome Study (BiGS), Jan 1 2016, In : Journal of Affective Disorders. 189, p. 141-149 9 p., 7712.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Bipolar Disorder
Comorbidity
Genome
Mood Disorders
3 Citations (Scopus)

A genome wide association study of fast beta EEG in families of European ancestry

Meyers, J. L., Zhang, J., Manz, N., Rangaswamy, M., Kamarajan, C., Wetherill, L., Chorlian, D. B., Kang, S. J., Bauer, L., Hesselbrock, V., Kramer, J., Kuperman, S., Nurnberger, J., Tischfield, J., Wang, J. C., Edenberg, H., Goate, A., Foroud, T. & Porjesz, B., Sep 15 2015, (Accepted/In press) In : International Journal of Psychophysiology.

Research output: Contribution to journalArticle

Racemases and Epimerases
Genome-Wide Association Study
Dermatan Sulfate
Electroencephalography
Genes
67 Citations (Scopus)

A genome-wide screen for genes influencing conduct disorder

Dick, D. M., Li, T. K., Edenberg, H., Hesselbrock, V., Kramer, J., Kuperman, S., Porjesz, B., Bucholz, K., Goate, A., Nurnberger, J. & Foroud, T., 2004, In : Molecular Psychiatry. 9, 1, p. 81-86 6 p.

Research output: Contribution to journalArticle

Conduct Disorder
Genome
Genes
Alcoholism
Chromosomes, Human, Pair 2
151 Citations (Scopus)

A genome-wide search for genes that relate to a low level of response to alcohol

Schuckit, M. A., Edenberg, H., Kalmijn, J., Flury, L., Smith, T. L., Reich, T., Bierut, L., Goate, A. & Foroud, T., 2001, In : Alcoholism: Clinical and Experimental Research. 25, 3, p. 323-329 7 p.

Research output: Contribution to journalArticle

Alcoholism
Genes
Alcohols
Genome
Lod Score
101 Citations (Scopus)

A Genomic Scan for Habitual Smoking in Families of Alcoholics: Common and Specific Genetic Factors in Substance Dependence

Bierut, L. J., Rice, J. P., Goate, A., Hinrichs, A. L., Saccone, N. L., Foroud, T., Edenberg, H., Cloninger, C. R., Begleiter, H., Conneally, P. M., Crowe, R. R., Hesselbrock, V., Li, T. K., Nurnberger, J., Porjesz, B., Schuckit, M. A. & Reich, T., Jan 1 2004, In : American Journal of Medical Genetics. 124 A, 1, p. 19-27 9 p.

Research output: Contribution to journalArticle

Alcoholics
Substance-Related Disorders
Alcoholism
Smoking
Chromosomes, Human, Pair 2
24 Citations (Scopus)

Age-specific incidence rates for dementia and alzheimer disease in NIA-LOAD/NCRAD and EFIGA families: National Institute on Aging Genetics Initiative for late-onset Alzheimer disease/National Cell Repository for Alzheimer disease (NIA-LOAD/NCRAD) and Estudio Familiar de Influencia Genetica en Alzheimer (EFIGA)

Vardarajan, B. N., Faber, K. M., Bird, T. D., Bennett, D. A., Rosenberg, R., Boeve, B. F., Graff-Radford, N. R., Goate, A. M., Farlow, M., Sweet, R. A., Lantigua, R., Medrano, M. Z., Ottman, R., Schaid, D. J., Foroud, T. & Mayeux, R., 2014, In : JAMA Neurology. 71, 3, p. 315-323 9 p.

Research output: Contribution to journalArticle

National Institute on Aging (U.S.)
Dementia
Alzheimer Disease
Incidence
Onset
69 Citations (Scopus)

Alcohol dehydrogenase-2*2 allele is associated with decreased prevalence of fetal alcohol syndrome in the mixed-ancestry population of the Western Cape Province, South Africa

Viljoen, D. L., Carr, L. G., Foroud, T., Brooke, L., Ramsay, M. & Li, T. K., 2001, In : Alcoholism: Clinical and Experimental Research. 25, 12, p. 1719-1722 4 p.

Research output: Contribution to journalArticle

Fetal Alcohol Spectrum Disorders
Alcohol Dehydrogenase
South Africa
Alleles
Alcohols

Alcoholism and mania: Is there a genetic relationship?

Nurnberger, J., Meyer, E. T., Flury, L., Hu, K. & Foroud, T., Oct 8 2001, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 105, 7, p. 567 1 p.

Research output: Contribution to journalArticle

Bipolar Disorder
Alcoholism
Chromosomes, Human, Pair 1
National Institute of Mental Health (U.S.)
Viverridae
206 Citations (Scopus)

Alcoholism susceptibility loci: Confirmation studies in a replicate sample and further mapping

Foroud, T., Edenberg, H., Goate, A., Rice, J., Flury, L., Koller, D. L., Bierut, L. J., Conneally, P. M., Nurnberger, J., Bucholz, K. K., Li, T. K., Hesselbrock, V., Crowe, R., Schuckit, M., Porjesz, B., Begleiter, H. & Reich, T., Jul 2000, In : Alcoholism: Clinical and Experimental Research. 24, 7, p. 933-945 13 p.

Research output: Contribution to journalArticle

Chromosomes
Alcoholism
Chromosomes, Human, Pair 2
Chromosomes, Human, Pair 7
Chromosomes, Human, Pair 1
14 Citations (Scopus)

Alcohol-preferring rats show decreased corticotropin-releasing hormone-2 receptor expression and differences in hpa activation compared to alcohol-nonpreferring rats

Yong, W., Spence, J. P., Eskay, R., Fitz, S. D., Damadzic, R., Lai, D., Foroud, T., Carr, L. G., Shekhar, A., Chester, J. A., Heilig, M. & Liang, T., 2014, In : Alcoholism: Clinical and Experimental Research. 38, 5, p. 1275-1283 9 p.

Research output: Contribution to journalArticle

Corticotropin-Releasing Hormone Receptors
Corticotropin-Releasing Hormone
Rats
Chemical activation
Alcohols

Allele frequency heterogeneity in the collaborative study on the genetics of alcoholism (COGA)

Saccone, N. L., Rice, J. P., Goate, A., Conneally, P. M., Edenberg, H., Foroud, T., Nurnberger, J. & Reich, T., Aug 7 2000, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 96, 4, p. 563 1 p.

Research output: Contribution to journalArticle

Gene Frequency
Alcoholism
Genome
Alcoholics
African Americans

Allele-specific expression and high-throughput reporter assay reveal functional genetic variants associated with alcohol use disorders

Rao, X., Thapa, K. S., Chen, A. B., Lin, H., Gao, H., Reiter, J., Hargreaves, K. A., Ipe, J., Lai, D., Xuei, X., Wang, Y., Gu, H., Kapoor, M., Farris, S. P., Tischfield, J., Foroud, T., Goate, A. M., Skaar, T., Mayfield, R. D., Edenberg, H. & 1 others, Liu, Y., Jan 1 2019, (Accepted/In press) In : Molecular Psychiatry.

Research output: Contribution to journalArticle

Alleles
Single Nucleotide Polymorphism
Alcohols
Genome-Wide Association Study
3' Untranslated Regions
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
36 Citations (Scopus)

AluY-mediated germline deletion, duplication and somatic stem cell reversion in UBE2T defines a new subtype of Fanconi anemia

Virts, E. L., Jankowska, A., Mackay, C., Glaas, M. F., Wiek, C., Kelich, S. L., Lottmann, N., Kennedy, F. M., Marchal, C., Lehnert, E., Scharf, R. E., Dufour, C., Lanciotti, M., Farruggia, P., Santoro, A., Savasan, S., Scheckenbach, K., Schipper, J., Wagenmann, M., Lewis, T. & 12 others, Leffak, M., Farlow, J. L., Foroud, T., Honisch, E., Niederacher, D., Chakraborty, S. C., Vance, G., Pruss, D., Timms, K. M., Lanchbury, J. S., Alpi, A. F. & Hanenberg, H., Apr 9 2015, In : Human Molecular Genetics. 24, 18, p. 5093-5108 16 p., ddv227.

Research output: Contribution to journalArticle

Fanconi Anemia
Adult Stem Cells
Exons
Germ-Line Mutation
Mothers
187 Citations (Scopus)

Alzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans

Saykin, A., Shen, L., Foroud, T., Potkin, S. G., Swaminathan, S., Kim, S., Risacher, S. L., Nho, K., Huentelman, M. J., Craig, D. W., Thompson, P. M., Stein, J. L., Moore, J. H., Farrer, L. A., Green, R. C., Bertram, L., Jack, C. R. & Weiner, M. W., May 2010, In : Alzheimer's and Dementia. 6, 3, p. 265-273 9 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Neuroimaging
Alzheimer Disease
Biomarkers
Phenotype
30 Citations (Scopus)

Alzheimer's disease risk polymorphisms regulate gene expression in the ZCWPW1 and the CELF1 loci

Alzheimer's Disease Genetics Consortium (ADGC), Feb 1 2016, In : PLoS One. 11, 2, e0148717.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Alzheimer disease
Polymorphism
Gene expression
Alzheimer Disease
2 Citations (Scopus)
Autopsy
Alzheimer Disease
Cohort Studies
Prospective Studies
Neurofibrillary Tangles
49 Citations (Scopus)

A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks

Kapoor, M., Wang, J. C., Wetherill, L., Le, N., Bertelsen, S., Hinrichs, A. L., Budde, J., Agrawal, A., Bucholz, K., Dick, D., Harari, O., Hesselbrock, V., Kramer, J., Nurnberger, J., Rice, J., Saccone, N., Schuckit, M., Tischfield, J., Porjesz, B., Edenberg, H. & 3 others, Bierut, L., Foroud, T. & Goate, A., Oct 2013, In : Human Genetics. 132, 10, p. 1141-1151 11 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Alcohol Drinking
Meta-Analysis
Alcoholism
Single Nucleotide Polymorphism
103 Citations (Scopus)

Amplitude of visual P3 event-related potential as a phenotypic marker for a predisposition to alcoholism: Preliminary results from the COGA project

Porjesz, B., Begleiter, H., Reich, T., Van Eerdewegh, P., Edenberg, H., Foroud, T., Goate, A., Litke, A., Chorlian, D. B., Stimus, A., Rice, J., Blangero, J., Almasy, L., Sorbell, J., Bauer, L. O., Kuperman, S., O'Connor, S. & Rohrbaugh, J., Sep 1998, In : Alcoholism: Clinical and Experimental Research. 22, 6, p. 1317-1323 7 p.

Research output: Contribution to journalArticle

P300 Event-Related Potentials
Alcoholism
Psychiatry
Alcohols
Sex Distribution
18 Citations (Scopus)

A multiancestral genome-wide exome array study of Alzheimer Disease, frontotemporal dementia, and progressive supranuclear palsy

Chen, J. A., Wang, Q., Davis-Turak, J., Li, Y., Karydas, A. M., Hsu, S. C., Sears, R. L., Chatzopoulou, D., Huang, A. Y., Wojta, K. J., Klein, E., Lee, J., Beekly, D. L., Boxer, A., Faber, K. M., Haase, C. M., Miller, J., Poon, W. W., Rosen, A., Rosen, H. & 15 others, Sapozhnikova, A., Shapira, J., Varpetian, A., Foroud, T., Levenson, R. W., Levey, A. I., Kukull, W. A., Mendez, M. F., Ringman, J., Chui, H., Cotman, C., DeCarli, C., Miller, B. L., Geschwind, D. H. & Coppola, G., Apr 1 2015, In : JAMA Neurology. 72, 4, p. 414-422 9 p.

Research output: Contribution to journalArticle

Exome
Progressive Supranuclear Palsy
Frontotemporal Dementia
Alzheimer Disease
Genome
171 Citations (Scopus)

A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies

Nalls, M. A., Duran, R., Lopez, G., Kurzawa-Akanbi, M., McKeith, I. G., Chinnery, P. F., Morris, C. M., Theuns, J., Crosiers, D., Cras, P., Engelborghs, S., De Deyn, P. P., Van Broeckhoven, C., Mann, D. M. A., Snowden, J., Pickering-Brown, S., Halliwell, N., Davidson, Y., Gibbons, L., Harris, J. & 38 others, Sheerin, U. M., Bras, J., Hardy, J., Clark, L., Marder, K., Honig, L. S., Berg, D., Maetzler, W., Brockmann, K., Gasser, T., Novellino, F., Quattrone, A., Annesi, G., De Marco, E. V., Rogaeva, E., Masellis, M., Black, S. E., Bilbao, J. M., Foroud, T., Ghetti, B., Nichols, W. C., Pankratz, N., Halliday, G., Lesage, S., Klebe, S., Durr, A., Duyckaerts, C., Brice, A., Giasson, B. I., Trojanowski, J. Q., Hurtig, H. I., Tayebi, N., Landazabal, C., Knight, M. A., Keller, M., Singleton, A. B., Wolfsberg, T. G. & Sidransky, E., 2013, In : JAMA Neurology. 70, 6, p. 727-735 9 p.

Research output: Contribution to journalArticle

Glucosylceramidase
Lewy Body Disease
Multicenter Studies
Mutation
Parkinson Disease
3 Citations (Scopus)

A multivariate finite mixture latent trajectory model with application to dementia studies

Lai, D., Xu, H., Koller, D., Foroud, T. & Gao, S., Feb 17 2016, (Accepted/In press) In : Journal of Applied Statistics. p. 1-21 21 p.

Research output: Contribution to journalArticle

Dementia
Finite Mixture
Multiple Tests
Trajectory
Latent Class
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)

Amyloid pathway-based candidate gene analysis of [ 11 C]PiB-PET in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort

Swaminathan, S., Shen, L., Risacher, S. L., Yoder, K., West, J. D., Kim, S., Nho, K., Foroud, T., Inlow, M., Potkin, S. G., Huentelman, M. J., Craig, D. W., Jagust, W. J., Koeppe, R. A., Mathis, C. A., Jack, C. R., Weiner, M. W. & Saykin, A., Mar 2012, In : Brain Imaging and Behavior. 6, 1, p. 1-15 15 p.

Research output: Contribution to journalArticle

Genetic Association Studies
Amyloid
Neuroimaging
Alzheimer Disease
Alleles
21 Citations (Scopus)

An ADH1B variant and peer drinking in progression to adolescent drinking milestones: Evidence of a gene-by-environment interaction

Olfson, E., Edenberg, H., Nurnberger, J., Agrawal, A., Bucholz, K. K., Almasy, L. A., Chorlian, D., Dick, D. M., Hesselbrock, V. M., Kramer, J. R., Kuperman, S., Porjesz, B., Schuckit, M. A., Tischfield, J. A., Wang, J. C., Wetherill, L., Foroud, T., Rice, J., Goate, A. & Bierut, L. J., Oct 1 2014, In : Alcoholism: Clinical and Experimental Research. 38, 10, p. 2541-2549 9 p.

Research output: Contribution to journalArticle

Gene-Environment Interaction
Alcohol Dehydrogenase
Drinking
Genes
Alcohols
19 Citations (Scopus)

Analyses of Quantitative Trait Loci Contributing to Alcohol Preference in HAD1/LAD1 and HAD2/LAD2 Rats

Carr, L. G., Habegger, K., Spence, J., Ritchotte, A., Liu, L., Lumeng, L., Li, T. K. & Foroud, T., Nov 2003, In : Alcoholism: Clinical and Experimental Research. 27, 11, p. 1710-1717 8 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Rats
Alcohols
Animals
Chromosomes
65 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
38 Citations (Scopus)

Analysis of copy number variation in Alzheimer's disease: The NIALOAD/ NCRAD family study

Swaminathan, S., Shen, L., Kim, S., Inlow, M., West, J. D., Faber, K. M., Foroud, T., Mayeux, R. & Saykin, A., 2012, In : Current Alzheimer Research. 9, 7, p. 801-814 14 p.

Research output: Contribution to journalArticle

Alzheimer Disease
Genes
Neuroimaging
DNA Copy Number Variations
Gene Dosage
22 Citations (Scopus)

Analysis of Copy Number Variation in Alzheimer's Disease in a Cohort of Clinically Characterized and Neuropathologically Verified Individuals

Swaminathan, S., Huentelman, M. J., Corneveaux, J. J., Myers, A. J., Faber, K. M., Foroud, T., Mayeux, R., Shen, L., Kim, S., Turk, M., Hardy, J., Reiman, E. M. & Saykin, A., Dec 5 2012, In : PLoS One. 7, 12, e50640.

Research output: Contribution to journalArticle

Alzheimer disease
Alzheimer Disease
Genes
genes
Quality Control
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

Analysis of whole genome-transcriptomic organization in brain to identify genes associated with alcoholism

Kapoor, M., Wang, J. C., Farris, S. P., Liu, Y., McClintick, J., Gupta, I., Meyers, J. L., Bertelsen, S., Chao, M., Nurnberger, J., Tischfield, J., Harari, O., Zeran, L., Hesselbrock, V., Bauer, L., Raj, T., Porjesz, B., Agrawal, A., Foroud, T., Edenberg, H. & 2 others, Mayfield, R. D. & Goate, A., Dec 1 2019, In : Translational psychiatry. 9, 1, 89.

Research output: Contribution to journalArticle

Alcoholism
Genome
Alcohol Drinking
Brain
Genes
201 Citations (Scopus)

An autosomal genomic scan for loci linked to prediabetic phenotypes in pima indians

Pratley, R. E., Thompson, D. B., Prochazka, M., Baier, L., Mott, D., Ravussin, E., Sakul, H., Ehm, M. G., Burns, D. K., Foroud, T., Garvey, W. T., Hanson, R. L., Knowler, W. C., Bennett, P. H. & Bogardus, C., Apr 15 1998, In : Journal of Clinical Investigation. 101, 8, p. 1757-1764 8 p.

Research output: Contribution to journalArticle

Potassium Iodide
Type 2 Diabetes Mellitus
Insulin
Phenotype
Fasting
419 Citations (Scopus)

An autosomal genomic scan for loci linked to type II diabetes mellitus and body-mass index in Pima Indians

Hanson, R. L., Ehm, M. G., Pettitt, D. J., Prochazka, M., Thompson, D. B., Timberlake, D., Foroud, T., Kobes, S., Baier, L., Burns, D. K., Almasy, L., Blangero, J., Garvey, W. T., Bennett, P. H. & Knowler, W. C., 1998, In : American Journal of Human Genetics. 63, 4, p. 1130-1138 9 p.

Research output: Contribution to journalArticle

Potassium Iodide
Type 2 Diabetes Mellitus
Body Mass Index
Chromosomes
Genetic Loci