Tatiana Foroud

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

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9 Citations (Scopus)

Genomes and phenomes of a population of outbred rats and its progenitors

The Rat Genome Sequencing and Mapping Consortium, Jun 10 2014, In : Scientific data. 1, 140011.

Research output: Contribution to journalArticle

Rats
Genome
Genes
Osteoporosis
bone disease
338 Citations (Scopus)

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

Segurado, R., Detera-Wadleigh, S. D., Levinson, D. F., Lewis, C. M., Gill, M., Nurnberger, J., Craddock, N., DePaulo, J. R., Baron, M., Gershon, E. S., Ekholm, J., Cichon, S., Turecki, G., Claes, S., Kelsoe, J. R., Schofield, P. R., Badenhop, R. F., Morissette, J., Coon, H., Blackwood, D. & 58 others, Mclnnes, L. A., Foroud, T., Edenberg, H., Reich, T., Rice, J. P., Goate, A., McInnis, M. G., McMahon, F. J., Badner, J. A., Goldin, L. R., Bennett, P., Willour, V. L., Zandi, P. P., Liu, J., Gilliam, C., Juo, S. H., Berrettini, W. H., Yoshikawa, T., Peltonen, L., Lönnqvist, J., Nöthen, M. M., Schumacher, J., Windemuth, C., Rietschel, M., Propping, P., Maier, W., Alda, M., Grof, P., Rouleau, G. A., Del-Favero, J., Van Broeckhoven, C., Mendlewicz, J., Adolfsson, R., Spence, M. A., Luebbert, H., Adams, L. J., Donald, J. A., Mitchell, P. B., Barden, N., Shink, E., Byerley, W., Muir, W., Visscher, P. M., Macgregor, S., Gurling, H., Kalsi, G., McQuillin, A., Escamilla, M. A., Reus, V. I., Leon, P., Freimer, N. B., Ewald, H., Kruse, T. A., Mors, O., Radhakrishna, U., Blouin, J. L., Antonarakis, S. E. & Akarsu, N., Jul 1 2003, In : American Journal of Human Genetics. 73, 1, p. 49-62 14 p.

Research output: Contribution to journalArticle

Bipolar Disorder
Meta-Analysis
Schizophrenia
Chromosomes
Genome
36 Citations (Scopus)

Genome scan of a second wave of NIMH genetics initiative bipolar pedigrees: Chromosomes 2, 11, 13, 14, and X

Zandi, P. P., Willour, V. L., Huo, Y., Chellis, J., Potash, J. B., MacKinnon, D. F., Simpson, S. G., McMahon, F. J., Gershon, E., Reich, T., Foroud, T., Nurnberger, J., DePaulo, J. R. & McInnis, M. G., May 15 2003, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 119 B, 1, p. 69-76 8 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 2
Pedigree
Bipolar Disorder
25 Citations (Scopus)

Genome scan of the fifty-six bipolar pedigrees from the NIMH genetics initiative replication sample: Chromosomes 4, 7, 9, 18, 19, 20, and 21

Willour, V. L., Zandi, P. P., Huo, Y., Diggs, T. L., Chellis, J. L., MacKinnon, D. F., Simpson, S. G., McMahon, F. J., Potash, J. B., Gershon, E. S., Reich, T., Foroud, T., Nurnberger, J., DePaulo, J. R. & McInnis, M. G., Aug 15 2003, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 121 B, 1, p. 21-27 7 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 7
Pedigree
Genome
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
12 Citations (Scopus)

Genome screen for platelet monoamine oxidase (MAO) activity

Saccone, N. L., Rice, J. P., Rochberg, N., Goate, A., Reich, T., Shears, S., Wu, W., Nurnberger, J., Foroud, T., Edenberg, H. & Li, T. K., Oct 15 1999, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 88, 5, p. 517-521 5 p.

Research output: Contribution to journalArticle

Monoamine Oxidase
Alcoholism
Blood Platelets
Genome
Lod Score
183 Citations (Scopus)

Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis

Koller, D. L., Econs, M., Morin, P. A., Christian, J. C., Hui, S., Parry, P., Curran, M. E., Rodriguez, L. A., Conneally, P. M., Joslyn, G., Peacock, M., Johnston, C. C. & Foroud, T., 2000, In : Journal of Clinical Endocrinology and Metabolism. 85, 9, p. 3116-3120 5 p.

Research output: Contribution to journalArticle

Bone Density
Osteoporosis
Minerals
Bone
Genes
101 Citations (Scopus)

Genome screen for quantitative trait loci underlying normal variation in femoral structure

Koller, D. L., Liu, G., Econs, M., Hui, S., Morin, P. A., Joslyn, G., Rodriguez, L. A., Michael Conneally, P., Christian, J. C., Conrad Johnston, C., Foroud, T. & Peacock, M., 2001, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 16, 6, p. 985-991 7 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Thigh
Odds Ratio
Genome
Femur Head
24 Citations (Scopus)

Genome screen in familial intracranial aneurysm.

Foroud, T., Sauerbeck, L., Brown, R., Anderson, C., Woo, D., Kleindorfer, D., Flaherty, M. L., Deka, R., Hornung, R., Meissner, I., Bailey-Wilson, J. E., Langefeld, C., Rouleau, G., Connolly, E. S., Lai, D., Koller, D. L., Huston, J. & Broderick, J. P., 2009, In : BMC Medical Genetics. 10, p. 3 1 p.

Research output: Contribution to journalArticle

Intracranial Aneurysm
Genome
Chromosomes
Smoking
Diagnostic Imaging
12 Citations (Scopus)

Genome screen to detect linkage to common susceptibility genes for intracranial and aortic aneurysms

Worrall, B. B., Foroud, T., Brown, R. D., Connolly, E. S., Hornung, R. W., Huston, J., Kleindorfer, D., Koller, D. L., Lai, D., Moomaw, C. J., Sauerbeck, L., Woo, D. & Broderick, J. P., Jan 1 2009, In : Stroke. 40, 1, p. 71-76 6 p.

Research output: Contribution to journalArticle

Aortic Aneurysm
Intracranial Aneurysm
Genome
Thoracic Aortic Aneurysm
Genes
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
144 Citations (Scopus)

Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations

Pankratz, N., Nichols, W. C., Uniacke, S. K., Halter, C., Rudolph, A., Shults, C., Conneally, P. M., Foroud, T., Golbe, L., Koller, W., Marder, K., Marshall, F., Oakes, D., Shinaman, A., Siemers, E., Carter, J., Camicioli, R., Andrews, P., Wojcieszek, J., Belden, J. & 79 others, Frenandez, M., Hubble, J., Reider, C., Rajput, A., Rajput, A., Shirley, T., Panisset, M., Hall, J., Mendis, T., Grimes, D. A., Gray, P., Ramos, C. S., Roque, S., Reich, S., Dunlop, B., Hauser, R., Sanchez-Ramos, J., Zesiewicz, T., Delgado, H., Pfeiffer, R., Pfeiffer, B., Friedman, J., Fernandez, H., Lannon, M., Fontaine, D., Seeberger, L., O'Brien, C., Judd, D., Pahwa, R., Thomas, S., Elmer, L., Davis, K., Jennings, D., Marek, K., Mendick, S., Truong, D., Pathak, M., Tran, A., Rodnitzyk, R., Dobson, J., Kurlan, R., Berry, D., Tuite, P., Schacher, R., Aminoff, M., DiMinno, M., Marder, K., Harris, J., Lewitt, P., DeAngelis, M., Koller, W., Weiner, W., Lyons, K., Martin, W., Wieler, M., Jankovic, J., Hunter, C., Bertoni, J., Peterson, C., Factor, S., Evans, S., Walker, F., Hunt, V., Un, J. K., Uy, S., Stacy, M., Williamson, K., Simon, D., Scollins, L., Brindauer, K., Petit, J., Manyam, B., Simpson, P., Nieves, A., So, J., Velickovic, M., Phipps, S., Gordon, M. F. & Hamann, J., 2002, In : American Journal of Human Genetics. 71, 1, p. 124-135 12 p.

Research output: Contribution to journalArticle

Parkinson Disease
Genome
Mutation
Genes
Chromosomes, Human, Pair 5
105 Citations (Scopus)

Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease

Stein, J. L., Hua, X., Morra, J. H., Lee, S., Hibar, D. P., Ho, A. J., Leow, A. D., Toga, A. W., Sul, J. H., Kang, H. M., Eskin, E., Saykin, A., Shen, L., Foroud, T., Pankratz, N., Huentelman, M. J., Craig, D. W., Gerber, J. D., Allen, A. N., Corneveaux, J. J. & 7 others, Stephan, D. A., Webster, J., DeChairo, B. M., Potkin, S. G., Jack, C. R., Weiner, M. W. & Thompson, P. M., Jun 2010, In : NeuroImage. 51, 2, p. 542-554 13 p.

Research output: Contribution to journalArticle

Temporal Lobe
Single Nucleotide Polymorphism
Alzheimer Disease
Genome
Genes
2 Citations (Scopus)

Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population

Zhou, S., Gan-Or, Z., Ambalavanan, A., Lai, D., Xie, P., Bourassa, C. V., Strong, S., Ross, J. P., Dionne-Laporte, A., Spiegelman, D., Dupré, N., Foroud, T., Xiong, L., Dion, P. A. & Rouleau, G. A., Dec 1 2018, In : Scientific Reports. 8, 1, 4356.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Intracranial Aneurysm
Population
Founder Effect
Exome
172 Citations (Scopus)

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

Schumann, G., Coin, L. J., Lourdusamy, A., Charoen, P., Berger, K. H., Stacey, D., Desrivières, S., Aliev, F. A., Khan, A. A., Amin, N., Aulchenko, Y. S., Bakalkin, G., Bakker, S. J., Balkau, B., Beulens, J. W., Bilbao, A., De Boer, R. A., Beury, D., Bots, M. L., Breetvelt, E. J. & 96 others, Cauchi, S., Cavalcanti-Proença, C., Chambers, J. C., Clarke, T. K., Dahmen, N., De Geus, E. J., Dick, D., Ducci, F., Easton, A., Edenberg, H., Esk, T., Fernández-Medarde, A., Foroud, T., Freimer, N. B., Girault, J. A., Grobbee, D. E., Guarrera, S., Gudbjartsson, D. F., Hartikainen, A. L., Heath, A. C., Hesselbrock, V., Hofman, A., Hottenga, J. J., Isohanni, M. K., Kaprio, J., Khaw, K. T., Kuehnel, B., Laitinen, J., Lobbens, S., Luan, J., Mangino, M., Maroteaux, M., Matullo, G., McCarthy, M. I., Mueller, C., Navis, G., Numans, M. E., Núñez, A., Nyholt, D. R., Onland-Moret, C. N., Oostra, B. A., O'Reilly, P. F., Palkovits, M., Penninx, B. W., Polidoro, S., Pouta, A., Prokopenko, I., Ricceri, F., Santos, E., Smit, J. H., Soranzo, N., Song, K., Sovio, U., Stumvoll, M., Surakk, I., Thorgeirsson, T. E., Thorsteinsdottir, U., Troakes, C., Tyrfingsson, T., Tönjes, A., Uiterwaal, C. S., Uitterlinden, A. G., Van Der Harst, P., Van Der Schouw, Y. T., Staehlin, O., Vogelzangs, N., Vollenweider, P., Waeber, G., Wareham, N. J., Waterworth, D. M., Whitfield, J. B., Wichmann, E. H., Willemsen, G., Witteman, J. C., Yuan, X., Zhai, G., Zhao, J. H., Zhang, W., Martin, N. G., Metspalu, A., Doering, A., Scott, J., Spector, T. D., Loos, R. J., Boomsma, D. I., Mooser, V., Peltonen, L., Stefansson, K., Van Duijn, C. M., Vineis, P., Sommer, W. H., Kooner, J. S., Spanagel, R., Heberlein, U. A., Jarvelin, M. R. & Elliott, P., Apr 26 2011, In : Proceedings of the National Academy of Sciences of the United States of America. 108, 17, p. 7119-7124 6 p.

Research output: Contribution to journalArticle

Genetic Association Studies
Autistic Disorder
Alcohol Drinking
Genome
Genes
2 Citations (Scopus)

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (Proceedings of the National Academy Sciences of the United States of America (2011) 108, 17, (7119-7124))

Schumann, G., Coin, L. J., Lourdusamy, A., Charoen, P., Berger, K. H., Stacey, D., Desrivières, S., Aliev, F. A., Khan, A. A., Amin, N., Aulchenko, Y. S., Bakalkin, G., Bakker, S. J., Balkau, B., Beulens, J. W., Bilbao, A., De Boer, R. A., Beury, D., Bots, M. L., Breetvelt, E. J. & 96 others, Cauchi, S., Cavalcanti-Proença, C., Chambers, J. C., Clarke, T. K., Dahmen, N., De Geus, E. J., Dick, D., Ducci, F., Easton, A., Edenberg, H., Esk, T., Fernández-Medarde, A., Foroud, T., Freimer, N. B., Girault, J. A., Grobbee, D. E., Guarrera, S., Gudbjartsson, D. F., Hartikainen, A. L., Heath, A. C., Hesselbrock, V., Hofman, A., Hottenga, J. J., Isohanni, M. K., Kaprio, J., Khaw, K. T., Kuehnel, B., Laitinen, J., Lobbens, S., Luan, J., Mangino, M., Maroteaux, M., Matullo, G., McCarthy, M. I., Mueller, C., Navis, G., Numans, M. E., Núñez, A., Nyholt, D. R., Onland-Moret, C. N., Oostra, B. A., O'Reilly, P. F., Palkovits, M., Penninx, B. W., Polidoro, S., Pouta, A., Prokopenko, I., Ricceri, F., Santos, E., Smit, J. H., Soranzo, N., Song, K., Sovio, U., Stumvoll, M., Surakk, I., Thorgeirsson, T. E., Thorsteinsdottir, U., Troakes, C., Tyrfingsson, T., Tönjes, A., Uiterwaal, C. S., Uitterlinden, A. G., Van Der Harst, P., Van Der Schouw, Y. T., Staehlin, O., Vogelzangs, N., Vollenweider, P., Waeber, G., Wareham, N. J., Waterworth, D. M., Whitfield, J. B., Wichmann, E. H., Willemsen, G., Witteman, J. C., Yuan, X., Zhai, G., Zhao, J. H., Zhang, W., Martin, N. G., Metspalu, A., Doering, A., Scott, J., Spector, T. D., Loos, R. J., Boomsma, D. I., Mooser, V., Peltonen, L., Stefansson, K., Van Duijn, C. M., Vineis, P., Sommer, W. H., Kooner, J. S., Spanagel, R., Heberlein, U. A., Jarvelin, M. R. & Elliott, P., May 31 2011, In : Proceedings of the National Academy of Sciences of the United States of America. 108, 22, p. 9316 1 p.

Research output: Contribution to journalArticle

15 Citations (Scopus)

Genome-wide association data suggest ABCB1 and immune-related gene sets may be involved in adult antisocial behavior

Salvatore, J. E., Edwards, A. C., McClintick, J., Bigdeli, T. B., Adkins, A., Aliev, F., Edenberg, H., Foroud, T., Hesselbrock, V., Kramer, J., Nurnberger, J., Schuckit, M., Tischfield, J. A., Xuei, X. & Dick, D. M., Apr 28 2015, In : Translational Psychiatry. 5, 4, e558.

Research output: Contribution to journalArticle

Genome
Diagnostic and Statistical Manual of Mental Disorders
Genes
Alcoholism
Single Nucleotide Polymorphism
44 Citations (Scopus)

Genome-Wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes

Smith, E. N., Koller, D. L., Panganiban, C., Szelinger, S., Zhang, P., Badner, J. A., Barrett, T. B., Berrettini, W. H., Bloss, C. S., Byerley, W., Coryell, W., Edenberg, H., Foroud, T., Gershon, E. S., Greenwood, T. A., Guo, Y., Hipolito, M., Keating, B. J., Lawson, W. B., Liu, C. & 18 others, Mahon, P. B., McInnis, M. G., McMahon, F. J., McKinney, R., Murray, S. S., Nievergelt, C. M., Nurnberger, J., Nwulia, E. A., Potash, J. B., Rice, J., Schulze, T. G., Scheftner, W. A., Shilling, P. D., Zandi, P. P., Zöllner, S., Craig, D. W., Schork, N. J. & Kelsoe, J. R., Jun 2011, In : PLoS Genetics. 7, 6, e1002134.

Research output: Contribution to journalArticle

Bipolar Disorder
exons
genome
Genome-Wide Association Study
Genome
148 Citations (Scopus)

Genome-wide association of familial late-onset alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE

Wijsman, E. M., Pankratz, N. D., Choi, Y., Rothstein, J. H., Faber, K. M., Cheng, R., Lee, J. H., Bird, T. D., Bennett, D. A., Diaz-Arrastia, R., Goate, A. M., Farlow, M., Ghetti, B., Sweet, R. A., Foroud, T. & Mayeux, R., Feb 2011, In : PLoS Genetics. 7, 2, e1001308.

Research output: Contribution to journalArticle

Alzheimer disease
Social Adjustment
Alzheimer Disease
genome
Genome
51 Citations (Scopus)

Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199

Schneider, B., Li, L., Radovich, M., Shen, F., Miller, K., Flockhart, D. A., Jiang, G., Vance, G., Gardner, L., Vatta, M., Bai, S., Lai, D., Koller, D., Zhao, F., O'Neill, A., Smith, M. L., Railey, E., White, C., Partridge, A., Sparano, J. & 3 others, Davidson, N. E., Foroud, T. & Sledge, G. W., Nov 15 2015, In : Clinical Cancer Research. 21, 22, p. 5082-5091 10 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Peripheral Nervous System Diseases
Single Nucleotide Polymorphism
taxane
Breast Neoplasms
3 Citations (Scopus)

Genome-wide association studies of alcohol dependence, DSM-IV criterion count and individual criteria

Lai, D., Wetherill, L., Bertelsen, S., Carey, C. E., Kamarajan, C., Kapoor, M., Meyers, J. L., Anokhin, A. P., Bennett, D. A., Bucholz, K. K., Chang, K. K., De Jager, P. L., Dick, D. M., Hesselbrock, V., Kramer, J., Kuperman, S., Nurnberger, J., Raj, T., Schuckit, M., Scott, D. M. & 9 others, Taylor, R. E., Tischfield, J., Hariri, A. R., Edenberg, H., Agrawal, A., Bogdan, R., Porjesz, B., Goate, A. M. & Foroud, T., Jul 1 2019, In : Genes, Brain and Behavior. 18, 6, e12579.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Diagnostic and Statistical Manual of Mental Disorders
Alcoholism
Drinking
Meta-Analysis

Genome-wide association studies of the self-rating of effects of ethanol (SRE)

Lai, D., Wetherill, L., Kapoor, M., Johnson, E. C., Schwandt, M., Ramchandani, V. A., Goldman, D., Joslyn, G., Rao, X., Liu, Y., Farris, S., Mayfield, R. D., Dick, D., Hesselbrock, V., Kramer, J., McCutcheon, V. V., Nurnberger, J., Tischfield, J., Goate, A., Edenberg, H. & 4 others, Porjesz, B., Agrawal, A., Foroud, T. & Schuckit, M., Jan 1 2019, In : Addiction Biology. e12800.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Alcoholism
Ethanol
Alcohols
Drinking
14 Citations (Scopus)

Genome-wide association study for anthracycline-induced congestive heart failure

Schneider, B., Shen, F., Gardner, L., Radovich, M., Li, L., Miller, K., Jiang, G., Lai, D., O'Neill, A., Sparano, J. A., Davidson, N. E., Cameron, D., Gradus-Pizlo, I., Mastouri, R., Suter, T. M., Foroud, T. & Sledge, G. W., Jan 1 2017, In : Clinical Cancer Research. 23, 1, p. 43-51 9 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Anthracyclines
Heart Failure
Single Nucleotide Polymorphism
Breast Neoplasms
60 Citations (Scopus)

Genomewide association study for onset age in Parkinson disease

Latourelle, J. C., Pankratz, N., Dumitriu, A., Wilk, J. B., Goldwurm, S., Pezzoli, G., Mariani, C. B., DeStefano, A. L., Halter, C., Gusella, J. F., Nichols, W. C., Myers, R. H. & Foroud, T., Sep 22 2009, In : BMC Medical Genetics. 10, p. 98 1 p., 1471.

Research output: Contribution to journalArticle

Age of Onset
Parkinson Disease
Single Nucleotide Polymorphism
Genes
Meta-Analysis
297 Citations (Scopus)

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

Pankratz, N., Wilk, J. B., Latourelle, J. C., DeStefano, A. L., Halter, C., Pugh, E. W., Doheny, K. F., Gusella, J. F., Nichols, W. C., Foroud, T. & Myers, R. H., 2009, In : Human Genetics. 124, 6, p. 593-605 13 p.

Research output: Contribution to journalArticle

Parkinson Disease
Genes
Disease Susceptibility
Chromosomes, Human, Pair 4
Single Nucleotide Polymorphism
41 Citations (Scopus)

Genome-wide association study identifies 30 loci associated with bipolar disorder

eQTLGen Consortium, BIOS Consortium & the Bipolar Disorder Working Group of the Psychiatric Genomics Consortium, May 1 2019, In : Nature genetics. 51, 5, p. 793-803 11 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Bipolar Disorder
Genome
Neurotransmitter Transport Proteins
Endocannabinoids
6 Citations (Scopus)

Genome-wide association study identifies a novel locus for cannabis dependence

Agrawal, A., Chou, Y. L., Carey, C. E., Baranger, D. A. A., Zhang, B., Sherva, R., Wetherill, L., Kapoor, M., Wang, J. C., Bertelsen, S., Anokhin, A. P., Hesselbrock, V., Kramer, J., Lynskey, M. T., Meyers, J. L., Nurnberger, J., Rice, J. P., Tischfield, J., Bierut, L. J., Degenhardt, L. & 16 others, Farrer, L. A., Gelernter, J., Hariri, A. R., Heath, A. C., Kranzler, H. R., Madden, P. A. F., Martin, N. G., Montgomery, G. W., Porjesz, B., Wang, T., Whitfield, J. B., Edenberg, H., Foroud, T., Goate, A. M., Bogdan, R. & Nelson, E. C., May 1 2018, In : Molecular Psychiatry. 23, 5, p. 1293-1302 10 p.

Research output: Contribution to journalArticle

Marijuana Abuse
Genome-Wide Association Study
Cannabis
Genome
Single Nucleotide Polymorphism
1 Citation (Scopus)

Genome-wide association study identifies loci associated with liability to alcohol and drug dependence that is associated with variability in reward-related ventral striatum activity in African- and European-Americans

Wetherill, L., Lai, D., Johnson, E. C., Anokhin, A., Bauer, L., Bucholz, K. K., Dick, D. M., Hariri, A. R., Hesselbrock, V., Kamarajan, C., Kramer, J., Kuperman, S., Meyers, J. L., Nurnberger, J., Schuckit, M., Scott, D. M., Taylor, R. E., Tischfield, J., Porjesz, B., Goate, A. M. & 4 others, Edenberg, H., Foroud, T., Bogdan, R. & Agrawal, A., Jan 1 2019, In : Genes, Brain and Behavior. e12580.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Reward
African Americans
Alcoholism
Substance-Related Disorders
52 Citations (Scopus)

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

Hou, L., Bergen, S. E., Akula, N., Song, J., Hultman, C. M., Landén, M., Adli, M., Alda, M., Ardau, R., Arias, B., Aubry, J. M., Backlund, L., Badner, J. A., Barrett, T. B., Bauer, M., Baune, B. T., Bellivier, F., Benabarre, A., Bengesser, S., Berrettini, W. H. & 119 others, Bhattacharjee, A. K., Biernacka, J. M., Birner, A., Bloss, C. S., Brichant-Petitjean, C., Bui, E. T., Byerley, W., Cervantes, P., Chillotti, C., Cichon, S., Colom, F., Coryell, W., Craig, D. W., Cruceanu, C., Czerski, P. M., Davis, T., Dayer, A., Degenhardt, F., Del Zompo, M., DePaulo, J. R., Edenberg, H., Étain, B., Falkai, P., Foroud, T., Forstner, A. J., Frisén, L., Frye, M. A., Fullerton, J. M., Gard, S., Garnham, J. S., Gershon, E. S., Goes, F. S., Greenwood, T. A., Grigoroiu-Serbanescu, M., Hauser, J., Heilbronner, U., Heilmann-Heimbach, S., Herms, S., Hipolito, M., Hitturlingappa, S., Hoffmann, P., Hofmann, A., Jamain, S., Jiménez, E., Kahn, J. P., Kassem, L., Kelsoe, J. R., Kittel-Schneider, S., Kliwicki, S., Koller, D. L., König, B., Lackner, N., Laje, G., Lang, M., Lavebratt, C., Lawson, W. B., Leboyer, M., Leckband, S. G., Liu, C., Maaser, A., Mahon, P. B., Maier, W., Maj, M., Manchia, M., Martinsson, L., McCarthy, M. J., McElroy, S. L., McInnis, M. G., McKinney, R., Mitchell, P. B., Mitjans, M., Mondimore, F. M., Monteleone, P., Mühleisen, T. W., Nievergelt, C. M., Nöthen, M. M., Novák, T., Nurnberger, J., Nwulia, E. A., Ösby, U., Pfennig, A., Potash, J. B., Propping, P., Reif, A., Reininghaus, E., Rice, J., Rietschel, M., Rouleau, G. A., Rybakowski, J. K., Schalling, M., Scheftner, W. A., Schofield, P. R., Schork, N. J., Schulze, T. G., Schumacher, J., Schweizer, B. W., Severino, G., Shekhtman, T., Shilling, P. D., Simhandl, C., Slaney, C. M., Smith, E. N., Squassina, A., Stamm, T., Stopkova, P., Streit, F., Strohmaier, J., Szelinger, S., Tighe, S. K., Tortorella, A., Turecki, G., Vieta, E., Volkert, J., Witt, S. H., Wright, A., Zandi, P. P., Zhang, P., Zollner, S. & McMahon, F. J., 2015, In : Human Molecular Genetics. 25, 15, p. 3383-3394 12 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Bipolar Disorder
X Chromosome
Lithium
Odds Ratio
15 Citations (Scopus)

Genomewide Association Study of Alcohol Dependence Identifies Risk Loci Altering Ethanol-Response Behaviors in Model Organisms

Collaborative Study of the Genetics of Alcoholism Consortium & the German Study of the Genetics of Addiction Consortium, May 1 2017, In : Alcoholism: Clinical and Experimental Research. 41, 5, p. 911-928 18 p.

Research output: Contribution to journalArticle

Alcoholism
Ethanol
Genes
Alcohols
Long Noncoding RNA
223 Citations (Scopus)

Genome-wide association study of alcohol dependence implicates a region on chromosome 11

Edenberg, H., Koller, D. L., Xuei, X., Wetherill, L., McClintick, J., Almasy, L., Bierut, L. J., Bucholz, K. K., Goate, A., Aliev, F., Dick, D., Hesselbrock, V., Hinrichs, A., Kramer, J., Kuperman, S., Nurnberger, J., Rice, J. P., Schuckit, M. A., Taylor, R., Todd Webb, B. & 3 others, Tischfield, J. A., Porjesz, B. & Foroud, T., May 2010, In : Alcoholism: Clinical and Experimental Research. 34, 5, p. 840-852 13 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 11
Genome-Wide Association Study
Chromosomes
Alcoholism
Single Nucleotide Polymorphism
236 Citations (Scopus)

Genome-wide association study of bipolar disorder in European American and African American individuals

Smith, E. N., Bloss, C. S., Badner, J. A., Barrett, T., Belmonte, P. L., Berrettini, W., Byerley, W., Coryell, W., Craig, D., Edenberg, H., Eskin, E., Foroud, T., Gershon, E., Greenwood, T. A., Hipolito, M., Koller, D. L., Lawson, W. B., Liu, C., Lohoff, F., McInnis, M. G. & 17 others, McMahon, F. J., Mirel, D. B., Murray, S. S., Nievergelt, C., Nurnberger, J., Nwulia, E. A., Paschall, J., Potash, J. B., Rice, J., Schulze, T. G., Scheftner, W., Panganiban, C., Zaitlen, N., Zandi, P. P., Zöllner, S., Schork, N. J. & Kelsoe, J. R., Aug 2009, In : Molecular Psychiatry. 14, 8, p. 755-763 9 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Bipolar Disorder
African Americans
Single Nucleotide Polymorphism
Intergenic DNA
58 Citations (Scopus)

Genome-wide association study of bone mineral density in premenopausal European-American Women and replication in African-American women

Koller, D. L., Ichikawa, S., Lai, D., Padgett, L. R., Doheny, K. F., Pugh, E., Paschall, J., Hui, S., Edenberg, H., Xuei, X., Peacock, M., Econs, M. & Foroud, T., Apr 2010, In : Journal of Clinical Endocrinology and Metabolism. 95, 4, p. 1802-1809 8 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
African Americans
Bone Density
Minerals
Bone
135 Citations (Scopus)

Genome-wide association study of CSF biomarkers Aβ1-42, t-tau, and p-tau181p in the ADNI cohort

Kim, S., Swaminathan, S., Shen, L., Risacher, S. L., Nho, K., Foroud, T., Shaw, L. M., Trojanowski, J. Q., Potkin, S. G., Huentelman, M. J., Craig, D. W., Dechairo, B. M., Aisen, P. S., Petersen, R. C., Weiner, M. W. & Saykin, A., Jan 4 2011, In : Neurology. 76, 1, p. 69-79 11 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Single Nucleotide Polymorphism
Biomarkers
Genes
Alzheimer Disease
29 Citations (Scopus)

Genome-wide association study of intracranial aneurysm identifies a new association on chromosome 7

Foroud, T., Lai, D., Koller, D., Van't Hof, F., Kurki, M. I., Anderson, C. S., Brown, R. D., Connolly, E. S., Eriksson, J. G., Flaherty, M., Fornage, M., Von Und Zu Fraunberg, M., Gaál, E. I., Laakso, A., Hernesniemi, J., Huston, J., Jääskeläinen, J. E., Kiemeney, L. A., Kivisaari, R., Kleindorfer, D. & 20 others, Ko, N., Lehto, H., Mackey, J., Meissner, I., Moomaw, C. J., Mosley, T. H., Moskala, M., Niemelä, M., Palotie, A., Pera, J., Rinkel, G., Ripke, S., Rouleau, G., Ruigrok, Y., Sauerbeck, L., Słowik, A., Vermeulen, S. H., Woo, D., Worrall, B. B. & Broderick, J., 2014, In : Stroke. 45, 11, p. 3194-3199 6 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 7
Genome-Wide Association Study
Intracranial Aneurysm
Stroke
Meta-Analysis
71 Citations (Scopus)

Genome-wide association study of intracranial aneurysms confirms role of anril and SOX17 in disease risk

Foroud, T., Koller, D. L., Lai, D., Sauerbeck, L., Anderson, C., Ko, N., Deka, R., Mosley, T. H., Fornage, M., Woo, D., Moomaw, C. J., Hornung, R., Huston, J., Meissner, I., Baileywilson, J. E., Langefeld, C., Rouleau, G., Sander Connolly, E., Worrall, B. B., Kleindorfer, D. & 6 others, Flaherty, M. L., Martini, S., Mackey, J., De Los Rios La Rosa, F., Brown, R. D. & Broderick, J. P., Nov 2012, In : Stroke. 43, 11, p. 2846-2852 7 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Intracranial Aneurysm
Single Nucleotide Polymorphism
Chromosomes
Logistic Models
14 Citations (Scopus)

Genome-Wide Association Study of Irritable vs. Elated Mania Suggests Genetic Differences between Clinical Subtypes of Bipolar Disorder

Greenwood, T. A., Kelsoe, J. R., Kelsoe, J. R., Greenwood, T. A., Nievergelt, C. M., McKinney, R., Shilling, P. D., Smith, E. N., Schork, N. J., Bloss, C. S., Nurnberger, J. I., Edenberg, H. J., Foroud, T., Koller, D. L., Gershon, E. S., Liu, C., Badner, J. A., Scheftner, W. A., Lawson, W. B., Nwulia, E. A. & 16 others, Hipolito, M., Coryell, W., Potash, J. B., Rice, J., Byerley, W., McMahon, F. J., Nurnberger, J., Edenberg, H., Foroud, T., Mahon, P. B., McInnis, M. G., Zöllner, S., Zhang, P., Craig, D. W., Szelinger, S. & Barrett, T. B., Jan 17 2013, In : PLoS One. 8, 1, e53804.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Bipolar Disorder
Genes
Chromosomes
Genome
1 Citation (Scopus)

Genome-wide association study of serum iron phenotypes in premenopausal women of European descent

Koller, D. L., Imel, E., Lai, D., Padgett, L. R., Acton, D., Gray, A., Peacock, M., Econs, M. & Foroud, T., Mar 1 2016, In : Blood Cells, Molecules and Diseases. 57, p. 50-53 4 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Iron
Phenotype
Serum
Phosphate Transport Proteins
41 Citations (Scopus)

Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty

The ReproGen Consortium, The Early Growth Genetics (EGG) Consortium, The Early Growth Genetics (EGG) Consortium, The ReproGen Consortium & The GIANT Consortium, Jan 1 2014, In : Human molecular genetics. 23, 16, p. 4452-4464 13 p.

Research output: Contribution to journalArticle

Open Access
Sexual Maturation
Menarche
Genome-Wide Association Study
Puberty
Sexual Development
58 Citations (Scopus)

Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence

Zlojutro, M., Manz, N., Rangaswamy, M., Xuei, X., Flury-Wetherill, L., Koller, D., Bierut, L. J., Goate, A., Hesselbrock, V., Kuperman, S., Nurnberger, J., Rice, J. P., Schuckit, M. A., Foroud, T., Edenberg, H., Porjesz, B. & Almasy, L., Jan 2011, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 156, 1, p. 44-58 15 p.

Research output: Contribution to journalArticle

Serotonin Receptors
Genome-Wide Association Study
Alcoholism
Brain
Genes
173 Citations (Scopus)

Genomewide linkage analyses of bipolar disorder: A new sample of 250 pedigrees from the national institute of mental health genetics initiative

Dick, D. M., Foroud, T., Flury, L., Bowman, E. S., Miller, M. J., Rau, N. L., Moe, P. R., Samavedy, N., El-Mallakh, R., Manji, H., Glitz, D. A., Meyer, E. T., Smiley, C., Hahn, R., Widmark, C., McKinney, R., Sutton, L., Ballas, C., Grice, D., Berrettini, W. & 12 others, Byerley, W., Coryell, W., DePaulo, R., MacKinnon, D. F., Gershon, E. S., Kelsoe, J. R., McMahon, F. J., McInnis, M., Murphy, D. L., Reich, T., Scheftner, W. & Nurnberger, J., Jul 1 2003, In : American Journal of Human Genetics. 73, 1, p. 107-114 8 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Pedigree
Bipolar Disorder
Chromosomes
Chromosomes, Human, Pair 10
10 Citations (Scopus)

Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease

Kunkle, B. W., Jaworski, J., Barral, S., Vardarajan, B., Beecham, G. W., Martin, E. R., Cantwell, L. S., Partch, A., Bird, T. D., Raskind, W. H., Destefano, A. L., Carney, R. M., Cuccaro, M., Vance, J. M., Farrer, L. A., Goate, A. M., Foroud, T., Mayeux, R. P., Schellenberg, G. D., Haines, J. L. & 1 others, Pericak-Vance, M. A., Jan 1 2016, In : Alzheimer's and Dementia. 12, 1, p. 2-10 9 p.

Research output: Contribution to journalArticle

Alzheimer Disease
Genome
Penetrance
Multigene Family
MicroRNAs
111 Citations (Scopus)

Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families

Pankratz, N., Nichols, W. C., Uniacke, S. K., Halter, C., Murrell, J., Rudolph, A., Shults, C. W., Conneally, P. M., Foroud, T., Truong, D., Pathak, M., Tran, A., Rodnitzky, R., Dobson, J., Koller, W., Weiner, W., Lyons, K., Kurlan, R., Berry, D., Bertoni, J. & 71 others, Peterson, C., Martin, W., Wieler, M., Tuite, P., Schacherer, R., Marder, K., 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., Leehey, M., Derian, T., Gordon, P., Werner, J., Racette, B., Good, L., Simon, D., Scollins, L., Schwieterman, D., Dewey, R., Meacham, M., Sutton, J., Hutchinson, B., Jog, M., Horn, C., Sethi, K., Carpenter, J., Atchison, P., Rolli, S., Sudarsky, L., Corwin, C., Velickovic, M., Phipps, S., Simuni, T., Kaczmarek, A., Hermanowicz, N., Niswonger, S., Feigin, A., Shannon, B., Calabrese, V., Roberge, P., Homes, H., Shulman, L., Dustin, K., Ajax, T., Mannetter, J., Podskalny, G. D., Giffin, L., Uitti, R. & Turk, M. F., Oct 15 2003, In : Human Molecular Genetics. 12, 20, p. 2599-2608 10 p.

Research output: Contribution to journalArticle

Parkinson Disease
Genome
Genes
Chromosomes, Human, Pair 2
Siblings
19 Citations (Scopus)

Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms

Badner, J. A., Koller, D., Foroud, T., Edenberg, H., Nurnberger, J., Zandi, P. P., Willour, V. L., McMahon, F. J., Potash, J. B., Hamshere, M., Grozeva, D., Green, E., Kirov, G., Jones, I., Jones, L., Craddock, N., Morris, D., Segurado, R., Gill, M., Sadovnick, D. & 13 others, Remick, R., Keck, P., Kelsoe, J., Ayub, M., MacLean, A., Blackwood, D., Liu, C. Y., Gershon, E. S., McMahon, W., Lyon, G. J., Robinson, R., Ross, J. & Byerley, W., Aug 2012, In : Molecular Psychiatry. 17, 8, p. 818-826 9 p.

Research output: Contribution to journalArticle

Pedigree
Bipolar Disorder
Single Nucleotide Polymorphism
Genome
Depression
5 Citations (Scopus)

Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease

Latourelle, J. C., Hendricks, A. E., Pankratz, N., Wilk, J. B., Halter, C., Nichols, W. C., Gusella, J. F., Destefano, A. L., Myers, R. H. & Foroud, T., Sep 2011, In : Movement Disorders. 26, 11, p. 2039-2044 6 p.

Research output: Contribution to journalArticle

Leucine
Parkinson Disease
Phosphotransferases
Age of Onset
Single Nucleotide Polymorphism
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
44 Citations (Scopus)

Genome-wide pathway analysis of memory impairment in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort implicates gene candidates, canonical pathways, and networks

Ramanan, V. K., Kim, S., Holohan, K., Shen, L., Nho, K., Risacher, S. L., Foroud, T., Mukherjee, S., Crane, P. K., Aisen, P. S., Petersen, R. C., Weiner, M. W. & Saykin, A., 2012, In : Brain Imaging and Behavior. 6, 4, p. 634-648 15 p.

Research output: Contribution to journalArticle

Neuroimaging
Alzheimer Disease
Genome
Genes
Memory Disorders
8 Citations (Scopus)

Genome-wide polygenic scores for age at onset of alcohol dependence and association with alcohol-related measures

Kapoor, M., Chou, Y. L., Edenberg, H., Foroud, T., Martin, N. G., Madden, P. A. F., Wang, J. C., Bertelsen, S., Wetherill, L., Brooks, A., Chan, G., Hesselbrock, V., Kuperman, S., Medland, S. E., Montgomery, G., Tischfield, J., Whitfield, J. B., Bierut, L. J., Heath, A. C., Bucholz, K. K. & 2 others, Goate, A. M. & Agrawal, A., Mar 22 2016, In : Translational Psychiatry. 6, p. e761

Research output: Contribution to journalArticle

Age of Onset
Alcoholism
Alcohols
Genome
Genome-Wide Association Study
67 Citations (Scopus)

Genome-wide scan and conditional analysis in bipolar disorder: Evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees

McInnis, M. G., Dick, D. M., Willour, V. L., Avramopoulos, D., MacKinnon, D. F., Simpson, S. G., Potash, J. B., Edenberg, H., Bowman, E. S., McMahon, F. J., Smiley, C., Chellis, J. L., Huo, Y., Diggs, T., Meyer, E. T., Miller, M., Matteini, A. T., Rau, N. L., DePaulo, J. R., Gershon, E. S. & 8 others, Badner, J. A., Rice, J. P., Goate, A. M., Detera-Wadleigh, S. D., Nurnberger, J., Reich, T., Zandi, P. P. & Foroud, T., Dec 1 2003, In : Biological Psychiatry. 54, 11, p. 1265-1273 9 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Pedigree
Bipolar Disorder
Genome
Genes
35 Citations (Scopus)

Genome-Wide Scan for a Healthy Aging Phenotype Provides Support for a Locus Near D4S1564 Promoting Healthy Aging

Reed, T., Dick, D. M., Uniacke, S. K., Foroud, T. & Nichols, W. C., Mar 2004, In : Journals of Gerontology - Series A Biological Sciences and Medical Sciences. 59, 3, p. 227-232 6 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 4
Genome
Phenotype
Dizygotic Twins
Prostatic Neoplasms