Tatiana Foroud

  • 41759 Citations
  • 101 h-Index
1976 …2021
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Publications 1988 2019

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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
32 Citations (Scopus)
MicroRNAs
Alzheimer Disease
Neurodegenerative Diseases
Neoplasms
Apoptosis
66 Citations (Scopus)

Functional relevance of human ADH polymorphism

Eriksson, C. J. P., Fukunaga, T., Sarkola, T., Chen, W. J., Chen, C. C., Ju, J. M., Cheng, A. T. A., Yamamoto, H., Kohlenberg-Müller, K., Kimura, M., Murayama, M., Matsushita, S., Kashima, H., Higuchi, S., Carr, L., Viljoen, D., Brooke, L., Stewart, T., Foroud, T., Su, J. & 2 others, Li, T. K. & Whitfield, J. B., 2001, In : Alcoholism: Clinical and Experimental Research. 25, 5 SUPPL.

Research output: Contribution to journalArticle

Polymorphism
Genotype
Alcohols
Tolnaftate
Alcoholics
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
49 Citations (Scopus)

Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease

Hui, K. Y., Fernandez-Hernandez, H., Hu, J., Schaffner, A., Pankratz, N., Hsu, N. Y., Chuang, L. S., Carmi, S., Villaverde, N., Li, X., Rivas, M., Levine, A. P., Bao, X., Labrias, P. R., Haritunians, T., Ruane, D., Gettler, K., Chen, E., Li, D., Schiff, E. R. & 31 others, Pontikos, N., Barzilai, N., Brant, S. R., Bressman, S., Cheifetz, A. S., Clark, L. N., Daly, M. J., Desnick, R. J., Duerr, R. H., Katz, S., Lencz, T., Myers, R. H., Ostrer, H., Ozelius, L., Payami, H., Peter, Y., Rioux, J. D., Segal, A. W., Scott, W. K., Silverberg, M. S., Vance, J. M., Ubarretxena-Belandia, I., Foroud, T., Atzmon, G., Pe'er, I., Ioannou, Y., McGovern, D. P. B., Yue, Z., Schadt, E. E., Cho, J. H. & Peter, I., Jan 10 2018, In : Science Translational Medicine. 10, 423, eaai7795.

Research output: Contribution to journalArticle

Crohn Disease
Parkinson Disease
Genes
Phosphotransferases
Haplotypes

Further analyses of the NIMH bipolar dataset: Follow up on suggestive linkage results on 1p and 10p

Corbett, J., Rice, J., Saccone, N., Goate, A., Reich, T., Foroud, T., Nurnberger, J., Edenberg, H., DePaulo, J. R. & Gershon, E., Aug 7 2000, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 96, 4, p. 469 1 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 1
Mood Disorders
Bipolar Disorder
Datasets
28 Citations (Scopus)

Further mapping of an ataxia-telangiectasia locus to the chromosome IIq23 region

Sanal, O., Wei, S., Foroud, T., Malhotra, U., Concannon, P., Charmley, P., Salser, W., Lange, K. & Gatti, R. A., Nov 1990, In : American Journal of Human Genetics. 47, 5, p. 860-866 7 p.

Research output: Contribution to journalArticle

Chromosomes, Human, 1-3
Ataxia Telangiectasia
Genetic Markers
Chromosomes
Genes
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
36 Citations (Scopus)

GABRR1 and GABRR2, encoding the GABA-A receptor subunits ρ1 and ρ2, are associated with alcohol dependence

Xuei, X., Flury-Wetherill, L., Dick, D., Goate, A., Tischfield, J., Nurnberger, J., Schuckit, M., Kramer, J., Kuperman, S., Hesselbrock, V., Porjesz, B., Foroud, T. & Edenberg, H., Mar 2010, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153, 2, p. 418-427 10 p.

Research output: Contribution to journalArticle

GABA-A Receptors
Alcoholism
Single Nucleotide Polymorphism
Haplotypes
Genes
40 Citations (Scopus)

Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation

Dumitriu, A., Latourelle, J. C., Hadzi, T. C., Pankratz, N., Garza, D., Miller, J. P., Vance, J. M., Foroud, T., Beach, T. G. & Myers, R. H., Jun 2012, In : PLoS Genetics. 8, 6, e1002794.

Research output: Contribution to journalArticle

Parkinson disease
Prefrontal Cortex
Transcriptome
gene expression
Parkinson Disease

Gene mapping using linkage analysis.

Sanal, O., Foroud, T. & Gatti, R. A., Jan 1991, In : Turkish Journal of Pediatrics. 33, 1, p. 1-12 12 p.

Research output: Contribution to journalArticle

Chromosome Mapping
Lod Score
Genes
Chromosomes
Genetic Loci
6 Citations (Scopus)

Genes associated with alcohol outcomes show enrichment of effects with broad externalizing and impulsivity phenotypes in an independent sample

Aliev, F., Wetherill, L., Bierut, L., Bucholz, K. K., Edenberg, H., Foroud, T., Investigators, C. & Xuei, X., Jan 1 2015, In : Journal of Studies on Alcohol and Drugs. 76, 1, p. 38-46 9 p.

Research output: Contribution to journalArticle

Impulsive Behavior
Genes
Polymorphism
alcohol
Alcohols
33 Citations (Scopus)

Genes influencing Parkinson disease onset: Replication of PARK3 and identification of novel loci

Pankratz, N., Uniacke, S. K., Halter, C. A., Rudolph, A., Shults, C. W., Conneally, P. M., Foroud, T. & Nichols, W. C., May 11 2004, In : Neurology. 62, 9, p. 1616-1618 3 p.

Research output: Contribution to journalArticle

Parkinson Disease
Chromosomes
Disease Susceptibility
Genes
Genome
7 Citations (Scopus)

Genes influencing spinal bone mineral density in inbred F344, LEW, COP, and DA rats

Alam, I., Sun, Q., Koller, D. L., Liu, L., Liu, Y., Edenberg, H., Foroud, T. & Turner, C. H., Mar 2010, In : Functional and Integrative Genomics. 10, 1, p. 63-72 10 p.

Research output: Contribution to journalArticle

Bone Density
Genes
Quantitative Trait Loci
Polymerase Chain Reaction
Inbred F344 Rats

Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease

International Genomics of Alzheimer's Project (IGAP), ARUK Consortium & GERAD/PERADES, CHARGE, ADGC, EADI, Jan 1 2018, In : Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring. 10, p. 595-598 4 p.

Research output: Contribution to journalArticle

Cholesterol Ester Transfer Proteins
HDL Cholesterol
Alzheimer Disease
Genes
Single Nucleotide Polymorphism
19 Citations (Scopus)

Genetically predicted body mass index and Alzheimer's disease-related phenotypes in three large samples: Mendelian randomization analyses

Adult Changes in Thought Study Investigators, Religious Orders Study/Memory and Aging Project Investigators & Alzheimer's Disease Genetics Consortium, Dec 1 2015, In : Alzheimer's and Dementia. 11, 12, p. 1439-1451 13 p.

Research output: Contribution to journalArticle

Mendelian Randomization Analysis
Alzheimer Disease
Body Mass Index
Phenotype
Odds Ratio
74 Citations (Scopus)

Genetic analysis of quantitative phenotypes in AD and MCI: Imaging, cognition and biomarkers

Shen, L., Thompson, P. M., Potkin, S. G., Bertram, L., Farrer, L. A., Foroud, T., Green, R. C., Hu, X., Huentelman, M. J., Kim, S., Kauwe, J. S. K., Li, Q., Liu, E., Macciardi, F., Moore, J. H., Munsie, L., Nho, K., Ramanan, V. K., Risacher, S. L., Stone, D. J. & 4 others, Swaminathan, S., Toga, A. W., Weiner, M. W. & Saykin, A., 2014, In : Brain Imaging and Behavior. 8, 2, p. 183-207 25 p.

Research output: Contribution to journalArticle

Cognition
Alzheimer Disease
Neuroimaging
Biomarkers
Phenotype
16 Citations (Scopus)

Genetic and neurophysiological correlates of the age of onset of alcohol use disorders in adolescents and young adults

Chorlian, D. B., Rangaswamy, M., Manz, N., Wang, J. C., Dick, D., Almasy, L., Bauer, L., Bucholz, K., Foroud, T., Hesselbrock, V., Kang, S. J., Kramer, J., Kuperman, S., Nurnberger, J., Rice, J., Schuckit, M., Tischfield, J., Edenberg, H., Goate, A., Bierut, L. & 1 others, Porjesz, B., 2013, In : Behavior Genetics. 43, 5, p. 386-401 16 p.

Research output: Contribution to journalArticle

young adults
Age of Onset
Alcoholism
Young Adult
alcohol

Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertension

Loyd, J. E., Butler, M. G., Foroud, T., Conneally, P. M., Phillips, I. A. & Newman, I. H., 1998, In : Pneumologie. 52, 4, p. 238 1 p.

Research output: Contribution to journalArticle

Genetic Anticipation
Parturition
Familial Primary Pulmonary Hypertension
188 Citations (Scopus)

Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertension

Loyd, J. E., Butler, M. G., Foroud, T., Conneally, P. M., Phillips, J. A. & Newman, J. H., 1995, In : American Journal of Respiratory and Critical Care Medicine. 152, 1, p. 93-97 5 p.

Research output: Contribution to journalArticle

Genetic Anticipation
Parturition
Genes
Trinucleotide Repeats
Fragile X Syndrome
7 Citations (Scopus)

Genetic architecture of age-related cognitive decline in African Americans

Raj, T., Chibnik, L. B., McCabe, C., Wong, A., Replogle, J. M., Yu, L., Gao, S., Unverzagt, F., Stranger, B., Murrell, J., Barnes, L., Hendrie, H., Foroud, T., Krichevsky, A., Bennett, D. A., Hall, K., Evans, D. A. & De Jager, P. L., Jan 1 2016, In : Neurology: Genetics. 3, 1, e125.

Research output: Contribution to journalArticle

African Americans
Alzheimer Disease
Genome-Wide Association Study
Disease Susceptibility
Lipid Metabolism
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
5 Citations (Scopus)

Genetic association of bipolar disorder with the β3 nicotinic receptor subunit gene

Hartz, S. M., Lin, P., Edenberg, H., Xuei, X., Rochberg, N., Saccone, S., Berrettini, W., Nelson, E., Nurnberger, J., Bierut, L. J., Rice, J. P., 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. & 42 others, Smiley, C., Foroud, T., Flury, L., Dick, D. M., Reich, T., Goate, A., McInnis, M., DePaulo, J. R., MacKinnon, D. F., Mondimore, F. M., Potash, J. B., Zandi, P. P., Avramopoulos, D., Payne, J., Byerley, W., Vinogradov, S., 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. J., Kassem, L., Detera-Wadleigh, S., Austin, L., Murphy, D. L., Lawson, W. B., Nwulia, E. & Hipolito, M., Apr 2011, In : Psychiatric Genetics. 21, 2, p. 77-84 8 p.

Research output: Contribution to journalArticle

Nicotinic Receptors
Tobacco Use Disorder
Bipolar Disorder
Genes
Single Nucleotide Polymorphism
63 Citations (Scopus)

Genetic Effects for Femoral Biomechanics, Structure, and Density in C57BL/6J and C3H/HeJ Inbred Mouse Strains

Koller, D. L., Schriefer, J., Sun, Q., Shultz, K. L., Donahue, L. R., Rosen, C. J., Foroud, T., Beamer, W. G. & Turner, C. H., Oct 2003, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 18, 10, p. 1758-1765 8 p.

Research output: Contribution to journalArticle

Inbred Strains Mice
Quantitative Trait Loci
Thigh
Biomechanical Phenomena
Phenotype
33 Citations (Scopus)

Genetic influences on craving for alcohol

Agrawal, A., Wetherill, L., Bucholz, K. K., Kramer, J., Kuperman, S., Lynskey, M. T., Nurnberger, J., Schuckit, M., Tischfield, J. A., Edenberg, H., Foroud, T. & Bierut, L. J., Feb 2013, In : Addictive Behaviors. 38, 2, p. 1501-1508 8 p.

Research output: Contribution to journalArticle

Alcohols
Alcoholism
Genes
Polymorphism
Nucleotides
5 Citations (Scopus)

Genetic influences on plasma homocysteine levels in African Americans and Yoruba Nigerians

Kim, S., Nho, K., Ramanan, V. K., Lai, D., Foroud, T., Lane, K., Murrell, J. R., Gao, S., Hall, K., Unverzagt, F., Baiyewu, O., Ogunniyi, A., Gureje, O., Kling, M. A., Doraiswamy, P. M., Kaddurah-Daouk, R., Hendrie, H. & Saykin, A., Dec 24 2015, In : Journal of Alzheimer's Disease. 49, 4, p. 991-1003 13 p.

Research output: Contribution to journalArticle

Homocysteine
African Americans
GABA Receptors
Dementia
Alzheimer Disease
99 Citations (Scopus)

Genetic influences on schizophrenia and subcortical brain volumes: Large-scale proof of concept

Franke, B., Stein, J. L., Ripke, S., Anttila, V., Hibar, D. P., Van Hulzen, K. J. E., Arias-Vasquez, A., Smoller, J. W., Nichols, T. E., Neale, M. C., McIntosh, A. M., Lee, P., McMahon, F. J., Meyer-Lindenberg, A., Mattheisen, M., Andreassen, O. A., Gruber, O., Sachdev, P. S., Roiz-Santiañez, R., Saykin, A. J. & 14 others, Ehrlich, S., Mather, K. A., Turner, J. A., Schwarz, E., Thalamuthu, A., Yao, Y., Ho, Y. Y. W., Martin, N. G., Wright, M. J., O'Donovan, M. C., Thompson, P. M., Neale, B. M., Medland, S. E. & Foroud, T., Feb 23 2016, In : Nature Neuroscience. 19, 3, p. 420-431 12 p.

Research output: Contribution to journalArticle

Schizophrenia
Brain
Psychiatry
Phenotype
Genetic Markers
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
50 Citations (Scopus)

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Alzheimer Disease Genetics Consortium (ADGC), The European Alzheimer’s Disease Initiative (EADI), Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium (CHARGE), & Genetic and Environmental Risk in AD/Defining Genetic, Polygenic and Environmental Risk for Alzheimer’s Disease Consortium (GERAD/PERADES), Mar 1 2019, In : Nature genetics. 51, 3, p. 414-430 17 p.

Research output: Contribution to journalArticle

Meta-Analysis
Immunity
Alzheimer Disease
Lipids
Serum Amyloid A Protein
24 Citations (Scopus)

Genetic Overlap Between Attention-Deficit/Hyperactivity Disorder and Bipolar Disorder: Evidence From Genome-wide Association Study Meta-analysis

PGC ADHD Working Group & PGC Bipolar Disorder Working Group, Nov 1 2017, In : Biological Psychiatry. 82, 9, p. 634-641 8 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Attention Deficit Disorder with Hyperactivity
Bipolar Disorder
Meta-Analysis
Nucleotides
127 Citations (Scopus)

Genetic predisposition to external apical root resorption

Al-Qawasmi, R. A., Hartsfield, J. K., Everett, E. T., Flury, L., Liu, L., Foroud, T., Macri, J. V. & Roberts, W. E., Mar 2003, In : American Journal of Orthodontics and Dentofacial Orthopedics. 123, 3, p. 242-252 11 p.

Research output: Contribution to journalArticle

Root Resorption
Genetic Predisposition to Disease
Interleukin-1
Incisor
Alleles
91 Citations (Scopus)

Genetic predisposition to external apical root resorption in orthodontic patients: Linkage of chromosome-18 marker

Al-Qawasmi, R. A., Hartsfield, J. K., Everett, E. T., Flury, L., Liu, L., Foroud, T., Macri, J. V. & Roberts, W. E., May 2003, In : Journal of Dental Research. 82, 5, p. 356-360 5 p.

Research output: Contribution to journalArticle

Root Resorption
Chromosomes, Human, Pair 18
Genetic Predisposition to Disease
Orthodontics
Genetic Markers
1105 Citations (Scopus)

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Lee, S. H., Ripke, S., Neale, B. M., Faraone, S. V., Purcell, S. M., Perlis, R. H., Mowry, B. J., Thapar, A., Goddard, M. E., Witte, J. S., Absher, D., Agartz, I., Akil, H., Amin, F., Andreassen, O. A., Anjorin, A., Anney, R., Anttila, V., Arking, D. E., Asherson, P. & 350 others, Azevedo, M. H., Backlund, L., Badner, J. A., Bailey, A. J., Banaschewski, T., Barchas, J. D., Barnes, M. R., Barrett, T. B., Bass, N., Battaglia, A., Bauer, M., Bayés, M., Bellivier, F., Bergen, S. E., Berrettini, W., Betancur, C., Bettecken, T., Biederman, J., Binder, E. B., Black, D. W., Blackwood, D. H. R., Bloss, C. S., Boehnke, M., Boomsma, D. I., Breen, G., Breuer, R., Bruggeman, R., Cormican, P., Buccola, N. G., Buitelaar, J. K., Bunney, W. E., Buxbaum, J. D., Byerley, W. F., Byrne, E. M., Caesar, S., Cahn, W., Cantor, R. M., Casas, M., Chakravarti, A., Chambert, K., Choudhury, K., Cichon, S., Cloninger, C. R., Collier, D. A., Cook, E. H., Coon, H., Cormand, B., Corvin, A., Coryell, W. H., Craig, D. W., Craig, I. W., Crosbie, J., Cuccaro, M. L., Curtis, D., Czamara, D., Datta, S., Dawson, G., Day, R., De Geus, E. J., Degenhardt, F., Djurovic, S., Donohoe, G. J., Doyle, A. E., Duan, J., Dudbridge, F., Duketis, E., Ebstein, R. P., Edenberg, H., Elia, J., Ennis, S., Etain, B., Fanous, A., Farmer, A. E., Ferrier, I. N., Flickinger, M., Fombonne, E., Foroud, T., Frank, J., Franke, B., Fraser, C., Freedman, R., Freimer, N. B., Freitag, C. M., Friedl, M., Frisén, L., Gallagher, L., Gejman, P. V., Georgieva, L., Gershon, E. S., Geschwind, D. H., Giegling, I., Gill, M., Gordon, S. D., Gordon-Smith, K., Green, E. K., Greenwood, T. A., Grice, D. E., Gross, M., Grozeva, D., Guan, W., Gurling, H., De Haan, L., Haines, J. L., Hakonarson, H., Hallmayer, J., Hamilton, S. P., Hamshere, M. L., Hansen, T. F., Hartmann, A. M., Hautzinger, M., Heath, A. C., Henders, A. K., Herms, S., Hickie, I. B., Hipolito, M., Hoefels, S., Holmans, P. A., Holsboer, F., Hoogendijk, W. J., Hottenga, J. J., Hultman, C. M., Hus, V., Ingason, A., Ising, M., Jamain, S., Jones, E. G., Jones, I., Jones, L., Tzeng, J. Y., Kähler, A. K., Kahn, R. S., Kandaswamy, R., Keller, M. C., Kennedy, J. L., Kenny, E., Kent, L., Kim, Y., Kirov, G. K., Klauck, S. M., Klei, L., Knowles, J. A., Kohli, M. A., Koller, D. L., Konte, B., Korszun, A., Krabbendam, L., Krasucki, R., Kuntsi, J., Kwan, P., Landén, M., Långström, N., Lathrop, M., Lawrence, J., Lawson, W. B., Leboyer, M., Ledbetter, D. H., Lee, P. H., Lencz, T., Lesch, K. P., Levinson, D. F., Lewis, C. M., Li, J., Lichtenstein, P., Lieberman, J. A., Lin, D. Y., Linszen, D. H., Liu, C., Lohoff, F. W., Loo, S. K., Lord, C., Lowe, J. K., Lucae, S., Macintyre, D. J., Madden, P. A. F., Maestrini, E., Magnusson, P. K. E., Mahon, P. B., Maier, W., Malhotra, A. K., Mane, S. M., Martin, C. L., Martin, N. G., Mattheisen, M., Matthews, K., Mattingsdal, M., Mccarroll, S. A., Mcghee, K. A., Mcgough, J. J., Mcgrath, P. J., Mcguffin, P., Mcinnis, M. G., Mcintosh, A., Mckinney, R., Mclean, A. W., Mcmahon, F. J., Mcmahon, W. M., Mcquillin, A., Medeiros, H., Medland, S. E., Meier, S., Melle, I., Meng, F., Meyer, J., Middeldorp, C. M., Middleton, L., Milanova, V., Miranda, A., Monaco, A. P., Montgomery, G. W., Moran, J. L., Moreno-De-Luca, D., Morken, G., Morris, D. W., Morrow, E. M., Moskvina, V., Muglia, P., Mühleisen, T. W., Muir, W. J., Müller-Myhsok, B., Murtha, M., Myers, R. M., Myin-Germeys, I., Neale, M. C., Nelson, S. F., Nievergelt, C. M., Nikolov, I., Nimgaonkar, V., Nolen, W. A., Nöthen, M. M., Nurnberger, J., Nwulia, E. A., Nyholt, D. R., O'dushlaine, C., Oades, R. D., Olincy, A., Oliveira, G., Olsen, L., Ophoff, R. A., Osby, U., Owen, M. J., Palotie, A., Parr, J. R., Paterson, A. D., Pato, C. N., Pato, M. T., Penninx, B. W., Pergadia, M. L., Pericak-Vance, M. A., Pickard, B. S., Pimm, J., Piven, J., Posthuma, D., Potash, J. B., Poustka, F., Propping, P., Puri, V., Quested, D. J., Quinn, E. M., Ramos-Quiroga, J. A., Rasmussen, H. B., Raychaudhuri, S., Rehnström, K., Reif, A., Ribasés, M., Rice, J. P., Rietschel, M., Roeder, K., Roeyers, H., Rossin, L., Rothenberger, A., Rouleau, G., Ruderfer, D., Rujescu, D., Sanders, A. R., Sanders, S. J., Santangelo, S. L., Sergeant, J. A., Schachar, R., Schalling, M., Schatzberg, A. F., Scheftner, W. A., Schellenberg, G. D., Scherer, S. W., Schork, N. J., Schulze, T. G., Schumacher, J., Schwarz, M., Scolnick, E., Scott, L. J., Shi, J., Shilling, P. D., Shyn, S. I., Silverman, J. M., Slager, S. L., Smalley, S. L., Smit, J. H., Smith, E. N., Sonuga-Barke, E. J. S., St. Clair, D., State, M., Steffens, M., Steinhausen, H. C., Strauss, J. S., Strohmaier, J., Stroup, T. S., Sutcliffe, J. S., Szatmari, P., Szelinger, S., Thirumalai, S., Thompson, R. C., Todorov, A. A., Tozzi, F., Treutlein, J., Uhr, M., Van Den Oord, E. J. C. G., Van Grootheest, G., Van Os, J., Vicente, A. M., Vieland, V. J., Vincent, J. B., Visscher, P. M., Walsh, C. A., Wassink, T. H., Watson, S. J., Weissman, M. M., Werge, T., Wienker, T. F., Wijsman, E. M., Willemsen, G., Williams, N., Willsey, A. J., Witt, S. H., Xu, W., Young, A. H., Yu, T. W., Zammit, S., Zandi, P. P., Zhang, P., Zitman, F. G., Zöllner, S., Devlin, B., Kelsoe, J. R., Sklar, P., Daly, M. J., O'donovan, M. C., Craddock, N., Sullivan, P. F., Smoller, J. W., Kendler, K. S. & Wray, N. R., Sep 2013, In : Nature Genetics. 45, 9, p. 984-994 11 p.

Research output: Contribution to journalArticle

Major Depressive Disorder
Single Nucleotide Polymorphism
Psychiatry
Schizophrenia
Bipolar Disorder
26 Citations (Scopus)

Genetic research: who is at risk for alcoholism

Foroud, T., Edenberg, H. & Crabbe, J. C., 2010, In : Alcohol Research and Health. 33, 1-2, p. 64-75 12 p.

Research output: Contribution to journalArticle

Genetic Research
Alcoholism
National Institute on Alcohol Abuse and Alcoholism (U.S.)
Genes
Alcohols
12 Citations (Scopus)

Genetic risk for schizophrenia and psychosis in Alzheimer disease

Demichele-Sweet, M. A. A., Weamer, E. A., Klei, L., Vrana, D. T., Hollingshead, D. J., Seltman, H. J., Sims, R., Foroud, T., Hernandez, I., Moreno-Grau, S., Tárraga, L., Boada, M., Ruiz, A., Williams, J., Mayeux, R., Lopez, O. L., Sibille, E. L., Kamboh, M. I., Devlin, B. & Sweet, R. A., Apr 1 2018, In : Molecular Psychiatry. 23, 4, p. 963-972 10 p.

Research output: Contribution to journalArticle

Psychotic Disorders
Schizophrenia
Alzheimer Disease
Single Nucleotide Polymorphism
Delusions
61 Citations (Scopus)

Genetics and alcoholism

Edenberg, H. & Foroud, T., Aug 2013, In : Nature Reviews Gastroenterology and Hepatology. 10, 8, p. 487-494 8 p.

Research output: Contribution to journalArticle

Alcoholism
Genes
Alcohols
Inborn Genetic Diseases
Social Problems
4 Citations (Scopus)

Genetics and genomics of late-onset Alzheimer's disease and its endophenotypes

Reitz, C., Rogaeva, E., Foroud, T. & Farrer, L. A., 2011, In : International Journal of Alzheimer's Disease. 284728.

Research output: Contribution to journalArticle

355 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
45 Citations (Scopus)

Genetics of alcoholism: A review of recent studies in human and animal models

Foroud, T. & Li, T. K., Sep 1999, In : American Journal on Addictions. 8, 4, p. 261-278 18 p.

Research output: Contribution to journalArticle

Alcoholism
Animal Models
Alcohols
Genes
Genetic Loci
21 Citations (Scopus)

Genetics of alcoholism

Edenberg, H. & Foroud, T., 2014, In : Handbook of Clinical Neurology. 125, p. 561-571 11 p.

Research output: Contribution to journalArticle

Alcoholism
Alcohols
Genes
Aldehyde Dehydrogenase
Genetic Linkage
42 Citations (Scopus)

Genetics of bipolar affective disorder.

Nurnberger, J. & Foroud, T., Apr 2000, In : Current Psychiatry Reports. 2, 2, p. 147-157 11 p.

Research output: Contribution to journalArticle

Mood Disorders
Bipolar Disorder
Genes
Schizophrenia
Catechol O-Methyltransferase
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
35 Citations (Scopus)

Genetics of Parkinson Disease

Pankratz, N. & Foroud, T., Apr 2004, In : NeuroRx. 1, 2, p. 235-242 8 p.

Research output: Contribution to journalArticle

Inborn Genetic Diseases
Parkinson Disease
Genes
Mutation
Disease Susceptibility
17 Citations (Scopus)

Genetic strategies to detect genes involved in alcoholism and alcohol-related traits

Dick, D. M. & Foroud, T., 2002, In : Alcohol Research and Health. 26, 3, p. 172-180 9 p.

Research output: Contribution to journalArticle

Alcoholism
Alcohols
Genes
Pharmacogenetics
Genetic Counseling
1436 Citations (Scopus)

Genetic studies of body mass index yield new insights for obesity biology

Collaborators, LifeLines Cohort Study & ADIPOGen Consortium; AGEN-BMI Working Group; CARDIOGRAMplusC4D Consortium; CKDGen Consortium; GLGC; ICBP; MAGIC Investigators; MuTHER Consortium; MIGen Consortium; PAGE Consortium; ReproGen Consortium; GENIE Consortium; International Endogene Consortium, Feb 12 2015, In : Nature. 518, 7538, p. 197-206 10 p.

Research output: Contribution to journalArticle

Body Mass Index
Obesity
Adipogenesis
Genome-Wide Association Study
Adiposity
78 Citations (Scopus)

Genetic studies of quantitative MCI and AD phenotypes in ADNI: Progress, opportunities, and plans

Saykin, A., Shen, L., Yao, X., Kim, S., Nho, K., Risacher, S. L., Ramanan, V. K., Foroud, T., Faber, K. M., Sarwar, N., Munsie, L. M., Hu, X., Soares, H. D., Potkin, S. G., Thompson, P. M., Kauwe, J. S. K., Kaddurah-Daouk, R., Green, R. C., Toga, A. W. & Weiner, M. W., Jul 1 2015, In : Alzheimer's and Dementia. 11, 7, p. 792-814 23 p.

Research output: Contribution to journalArticle

Neuroimaging
Alzheimer Disease
Phenotype
Genome-Wide Association Study
Exome
23 Citations (Scopus)

Genetic variant predicts bevacizumab-induced hypertension in ECOG-5103 and ECOG-2100

Schneider, B., Li, L., Shen, F., Miller, K., Radovich, M., O'Neill, A., Gray, R. J., Lane, D., Flockhart, D. A., Jiang, G., Wang, Z., Lai, D., Koller, D., Pratt, J. H., Dang, C. T., Northfelt, D., Perez, E. A., Shenkier, T., Cobleigh, M., Smith, M. L. & 7 others, Railey, E., Partridge, A., Gralow, J., Sparano, J., Davidson, N. E., Foroud, T. & Sledge, G. W., Sep 9 2014, In : British Journal of Cancer. 111, 6, p. 1241-1248 8 p.

Research output: Contribution to journalArticle

Hypertension
Blood Pressure
Genome-Wide Association Study
Single Nucleotide Polymorphism
Genome
3 Citations (Scopus)

Genetic variants associated with circulating fibroblast growth factor 23

Robinson-Cohen, C., Bartz, T. M., Lai, D., Alp Ikizler, T., Peacock, M., Imel, E., Michos, E. D., Foroud, T., Akesson, K., Taylor, K. D., Malmgren, L., Matsushita, K., Nethander, M., Eriksson, J., Ohlsson, C., Mellström, D., Wolf, M., Ljunggren, O., McGuigan, F., Rotter, J. I. & 7 others, Karlsson, M., Econs, M., Ix, J. H., Lutsey, P. L., Psaty, B. M., De Boer, I. H. & Kestenbaum, B. R., Oct 1 2018, In : Journal of the American Society of Nephrology. 29, 10, p. 2583-2592 10 p.

Research output: Contribution to journalArticle

Single Nucleotide Polymorphism
Vitamin D
Phosphates
Genes
Kidney
5 Citations (Scopus)

Genetic variants associated with susceptibility to psychosis in late-onset Alzheimer's disease families

NIA-LOAD/NCRAD Family Study Group, Nov 1 2015, In : Neurobiology of Aging. 36, 11, p. 3116.e9-3116.e16

Research output: Contribution to journalArticle

Psychotic Disorders
Alzheimer Disease
Hispanic Americans
Brain
Genes
57 Citations (Scopus)

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

Escott-Price, V., Bellenguez, C., Wang, L. S., Choi, S. H., Harold, D., Jones, L., Holmans, P., Gerrish, A., Vedernikov, A., Richards, A., DeStefano, A. L., Lambert, J. C., Ibrahim-Verbaas, C. A., Naj, A. C., Sims, R., Jun, G., Bis, J. C., Beecham, G. W., Grenier-Boley, B., Russo, G. & 167 others, Thornton-Wells, T. A., Denning, N., Smith, A. V., Chouraki, V., Thomas, C., Arfan Ikram, M., Zelenika, D., Vardarajan, B. N., Kamatani, Y., Lin, C. F., Schmidt, H., Kunkle, B., Dunstan, M. L., Vronskaya, M., Johnson, A. D., Ruiz, A., Bihoreau, M. T., Reitz, C., Pasquier, F., Hollingworth, P., Hanon, O., Fitzpatrick, A. L., Buxbaum, J. D., Campion, D., Crane, P. K., Becker, C. B. T., Gudnason, V., Cruchaga, C., Craig, D., Amin, N., Berr, C., Lopez, O. L., De Jager, P. L., Deramecourt, V., Johnston, J. A., Evans, D., Lovestone, S., Letenneur, L., Hernández, I., Rubinsztein, D. C., Eiriksdottir, G., Sleegers, K., Goate, A. M., Fiévet, N., Huentelman, M. J., Gill, M., Brown, K., Kamboh, M. I., Keller, L., Barberger-Gateau, P., McGuinness, B., Larson, E. B., Myers, A. J., Dufouil, C., Todd, S., Wallon, D., Love, S., Rogaeva, E., Gallacher, J., St George-Hyslop, P., Clarimon, J., Lleo, A., Bayer, A., Tsuang, D. W., Yu, L., Tsolaki, M., Bossù, P., Spalletta, G., Proitsi, P., Collinge, J., Sorbi, S., Sanchez Garcia, F., Fox, N. C., Hardy, J., Naranjo, M. C. D., Bosco, P., Clarke, R., Brayne, C., Galimberti, D., Scarpini, E., Bonuccelli, U., Mancuso, M., Siciliano, G., Moebus, S., Mecocci, P., Del Zompo, M., Maier, W., Hampel, H., Pilotto, A., Frank-García, A., Panza, F., Solfrizzi, V., Caffarra, P., Nacmias, B., Perry, W., Mayhaus, M., Lannfelt, L., Hakonarson, H., Pichler, S., Carrasquillo, M. M., Ingelsson, M., Beekly, D., Alvarez, V., Zou, F., Valladares, O., Younkin, S. G., Coto, E., Hamilton-Nelson, K. L., Gu, W., Razquin, C., Pastor, P., Mateo, I., Owen, M. J., Faber, K. M., Jonsson, P. V., Combarros, O., O'Donovan, M. C., Cantwell, L. B., Soininen, H., Blacker, D., Mead, S., Mosley, T. H., Bennett, D. A., Harris, T. B., Fratiglioni, L., Holmes, C., De Bruijn, R. F. A. G., Passmore, P., Montine, T. J., Bettens, K., Rotter, J. I., Brice, A., Morgan, K., Foroud, T., Kukull, W. A., Hannequin, D., Powell, J. F., Nalls, M. A., Ritchie, K., Lunetta, K. L., Kauwe, J. S. K., Boerwinkle, E., Riemenschneider, M., Boada, M., Hiltunen, M., Martin, E. R., Schmidt, R., Rujescu, D., Dartigues, J. F., Mayeux, R., Tzourio, C., Hofman, A., Nöthen, M. M., Graff, C., Psaty, B. M., Haines, J. L., Lathrop, M., Pericak-Vance, M. A., Launer, L. J., Van Broeckhoven, C., Farrer, L. A., Van Duijn, C. M., Ramirez, A., Seshadri, S., Schellenberg, G. D., Amouyel, P. & Williams, J., Jun 12 2014, In : PLoS One. 9, 6, e94661.

Research output: Contribution to journalArticle

Alzheimer disease
Alzheimer Disease
Genes
genes
loci