Tatiana Foroud

  • 43539 Citations
  • 102 h-Index
1976 …2021

Research output per year

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From QTL to candidate gene: A genetic approach to alcoholism research

Spence, J. P., Liang, T., Liu, L., Johnson, P. L., Foroud, T., Carr, L. G. & Shekhar, A., Jun 1 2009, In : Current Drug Abuse Reviews. 2, 2, p. 127-134 8 p.

Research output: Contribution to journalArticle

25 Scopus citations

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., Jun 27 2001, In : Alcoholism: Clinical and Experimental Research. 25, 5 SUPPL., p. 157S-163S

Research output: Contribution to journalArticle

66 Scopus citations

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. J. & 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

102 Scopus citations

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

65 Scopus citations

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 - Neuropsychiatric Genetics. 96, 4, 1 p.

Research output: Contribution to journalArticle

Further mapping of an ataxia-telangiectasia locus to the chromosome 11q23 region

Sanal, O., Wei, S., Foroud, T., Malhotra, U., Concannon, P., Charmley, P., Salser, W., Lange, K. & Gatti, R. A., Nov 21 1990, In : American Journal of Human Genetics. 47, 5, p. 860-866 7 p.

Research output: Contribution to journalArticle

28 Scopus citations

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

20 Scopus citations

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. J., Mar 1 2010, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153, 2, p. 418-427 10 p.

Research output: Contribution to journalArticle

37 Scopus citations

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 1 2012, In : PLoS Genetics. 8, 6, e1002794.

Research output: Contribution to journalArticle

41 Scopus citations

Gene mapping using linkage analysis.

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

Research output: Contribution to journalArticle

6 Scopus citations

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

33 Scopus citations

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. J., Foroud, T. & Turner, C. H., Mar 1 2010, In : Functional and Integrative Genomics. 10, 1, p. 63-72 10 p.

Research output: Contribution to journalArticle

8 Scopus citations

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

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

21 Scopus citations

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. M., 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. J., Jun 2014, In : Brain Imaging and Behavior. 8, 2, p. 183-207 25 p.

Research output: Contribution to journalArticle

83 Scopus citations

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. J., Goate, A., Bierut, L. & 1 others, Porjesz, B., Aug 21 2013, In : Behavior Genetics. 43, 5, p. 386-401 16 p.

Research output: Contribution to journalArticle

18 Scopus citations

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

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

Research output: Contribution to journalArticle

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

Loyd, J. E., Butler, M. C., Foroud, T. M., Conneally, P. M., Phillips, J. A. & Newman, J. H., Jul 1995, In : American journal of respiratory and critical care medicine. 152, 1, p. 93-97 5 p.

Research output: Contribution to journalArticle

189 Scopus citations

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

10 Scopus citations

Genetic architecture of subcortical brain structures in 38,851 individuals

Satizabal, C. L., Adams, H. H. H., Hibar, D. P., White, C. C., Knol, M. J., Stein, J. L., Scholz, M., Sargurupremraj, M., Jahanshad, N., Roshchupkin, G. V., Smith, A. V., Bis, J. C., Jian, X., Luciano, M., Hofer, E., Teumer, A., van der Lee, S. J., Yang, J., Yanek, L. R., Lee, T. V. & 269 others, Li, S., Hu, Y., Koh, J. Y., Eicher, J. D., Desrivières, S., Arias-Vasquez, A., Chauhan, G., Athanasiu, L., Rentería, M. E., Kim, S., Hoehn, D., Armstrong, N. J., Chen, Q., Holmes, A. J., den Braber, A., Kloszewska, I., Andersson, M., Espeseth, T., Grimm, O., Abramovic, L., Alhusaini, S., Milaneschi, Y., Papmeyer, M., Axelsson, T., Ehrlich, S., Roiz-Santiañez, R., Kraemer, B., Håberg, A. K., Jones, H. J., Pike, G. B., Stein, D. J., Stevens, A., Bralten, J., Vernooij, M. W., Harris, T. B., Filippi, I., Witte, A. V., Guadalupe, T., Wittfeld, K., Mosley, T. H., Becker, J. T., Doan, N. T., Hagenaars, S. P., Saba, Y., Cuellar-Partida, G., Amin, N., Hilal, S., Nho, K., Mirza-Schreiber, N., Arfanakis, K., Becker, D. M., Ames, D., Goldman, A. L., Lee, P. H., Boomsma, D. I., Lovestone, S., Giddaluru, S., Le Hellard, S., Mattheisen, M., Bohlken, M. M., Kasperaviciute, D., Schmaal, L., Lawrie, S. M., Agartz, I., Walton, E., Tordesillas-Gutierrez, D., Davies, G. E., Shin, J., Ipser, J. C., Vinke, L. N., Hoogman, M., Jia, T., Burkhardt, R., Klein, M., Crivello, F., Janowitz, D., Carmichael, O., Haukvik, U. K., Aribisala, B. S., Schmidt, H., Strike, L. T., Cheng, C. Y., Risacher, S. L., Pütz, B., Fleischman, D. A., Assareh, A. A., Mattay, V. S., Buckner, R. L., Mecocci, P., Dale, A. M., Cichon, S., Boks, M. P., Matarin, M., Penninx, B. W. J. H., Calhoun, V. D., Chakravarty, M. M., Marquand, A. F., Macare, C., Kharabian Masouleh, S., Oosterlaan, J., Amouyel, P., Hegenscheid, K., Rotter, J. I., Schork, A. J., Liewald, D. C. M., de Zubicaray, G. I., Wong, T. Y., Shen, L., Sämann, P. G., Brodaty, H., Roffman, J. L., de Geus, E. J. C., Tsolaki, M., Erk, S., van Eijk, K. R., Cavalleri, G. L., van der Wee, N. J. A., McIntosh, A. M., Gollub, R. L., Bulayeva, K. B., Bernard, M., Richards, J. S., Himali, J. J., Loeffler, M., Rommelse, N., Hoffmann, W., Westlye, L. T., Valdés Hernández, M. C., Hansell, N. K., van Erp, T. G. M., Wolf, C., Kwok, J. B. J., Vellas, B., Heinz, A., Olde Loohuis, L. M., Delanty, N., Ho, B. C., Ching, C. R. K., Shumskaya, E., Singh, B., Hofman, A., van der Meer, D., Homuth, G., Psaty, B. M., Bastin, M. E., Montgomery, G. W., Foroud, T. M., Reppermund, S., Hottenga, J. J., Simmons, A., Meyer-Lindenberg, A., Cahn, W., Whelan, C. D., van Donkelaar, M. M. J., Yang, Q., Hosten, N., Green, R. C., Thalamuthu, A., Mohnke, S., Hulshoff Pol, H. E., Lin, H., Jack, C. R., Schofield, P. R., Mühleisen, T. W., Maillard, P., Potkin, S. G., Wen, W., Fletcher, E., Toga, A. W., Gruber, O., Huentelman, M., Davey Smith, G., Launer, L. J., Nyberg, L., Jönsson, E. G., Crespo-Facorro, B., Koen, N., Greve, D. N., Uitterlinden, A. G., Weinberger, D. R., Steen, V. M., Fedko, I. O., Groenewold, N. A., Niessen, W. J., Toro, R., Tzourio, C., Longstreth, W. T., Ikram, M. K., Smoller, J. W., van Tol, M. J., Sussmann, J. E., Paus, T., Lemaître, H., Schroeter, M. L., Mazoyer, B., Andreassen, O. A., Holsboer, F., Depondt, C., Veltman, D. J., Turner, J. A., Pausova, Z., Schumann, G., van Rooij, D., Djurovic, S., Deary, I. J., McMahon, K. L., Müller-Myhsok, B., Brouwer, R. M., Soininen, H., Pandolfo, M., Wassink, T. H., Cheung, J. W., Wolfers, T., Martinot, J. L., Zwiers, M. P., Nauck, M., Melle, I., Martin, N. G., Kanai, R., Westman, E., Kahn, R. S., Sisodiya, S. M., White, T., Saremi, A., van Bokhoven, H., Brunner, H. G., Völzke, H., Wright, M. J., van ‘t Ent, D., Nöthen, M. M., Ophoff, R. A., Buitelaar, J. K., Fernández, G., Sachdev, P. S., Rietschel, M., van Haren, N. E. M., Fisher, S. E., Beiser, A. S., Francks, C., Saykin, A. J., Mather, K. A., Romanczuk-Seiferth, N., Hartman, C. A., DeStefano, A. L., Heslenfeld, D. J., Weiner, M. W., Walter, H., Hoekstra, P. J., Nyquist, P. A., Franke, B., Bennett, D. A., Grabe, H. J., Johnson, A. D., Chen, C., van Duijn, C. M., Lopez, O. L., Fornage, M., Wardlaw, J. M., Schmidt, R., DeCarli, C., De Jager, P. L., Villringer, A., Debette, S., Gudnason, V., Medland, S. E., Shulman, J. M., Thompson, P. M., Seshadri, S. & Ikram, M. A., Nov 1 2019, In : Nature genetics. 51, 11, p. 1624-1636 13 p.

Research output: Contribution to journalArticle

4 Scopus citations

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 1 2006, In : Clinical Genetics. 70, 1, p. 49-56 8 p.

Research output: Contribution to journalArticle

23 Scopus citations

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

Hartz, S. M., Lin, P., Edenberg, H. J., 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 1 2011, In : Psychiatric genetics. 21, 2, p. 77-84 8 p.

Research output: Contribution to journalArticle

5 Scopus citations

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 1 2003, In : Journal of Bone and Mineral Research. 18, 10, p. 1758-1765 8 p.

Research output: Contribution to journalArticle

63 Scopus citations

Genetic influences on craving for alcohol

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

Research output: Contribution to journalArticle

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

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

Research output: Contribution to journalArticle

5 Scopus citations

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

Psychosis Endophenotypes International Consortium, Feb 23 2016, In : Nature Neuroscience. 19, 3, p. 420-431 12 p.

Research output: Contribution to journalArticle

106 Scopus citations

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. J., Foroud, T. & Turner, C. H., Mar 1 2008, In : Bone. 42, 3, p. 547-553 7 p.

Research output: Contribution to journalArticle

10 Scopus citations

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

117 Scopus citations

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

30 Scopus citations

Genetic predisposition to external apical root resorption

Al-Qawasmi, R. A., Hartsfield, J. K., Everett, E. T., Flury, L., Liu, L., Foroud, T. M., 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

133 Scopus citations

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. M., 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

93 Scopus citations

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. J., 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. 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1172 Scopus citations
26 Scopus citations

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.

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15 Scopus citations

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 : Lancet. 365, 9457, p. 410-412 3 p.

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359 Scopus citations

Genetics of alcoholism

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

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24 Scopus citations

Genetics of Parkinson Disease

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

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36 Scopus citations

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

Dick, D. M. & Foroud, T., Dec 1 2002, In : Alcohol Research and Health. 26, 3, p. 172-180 9 p.

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18 Scopus citations

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

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.

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1580 Scopus citations

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

Schneider, B. P., Li, L., Shen, F., Miller, K. D., 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.

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24 Scopus citations

Genetic variants associated with circulating fibroblast growth factor 23

Robinson-Cohen, C., Bartz, T. M., Lai, D., Alp Ikizler, T., Peacock, M., Imel, E. A., Michos, E. D., Foroud, T. M., 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. J., Ix, J. H., Lutsey, P. L., Psaty, B. M., De Boer, I. H. & Kestenbaum, B. R., Oct 2018, In : Journal of the American Society of Nephrology. 29, 10, p. 2583-2592 10 p.

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5 Scopus citations

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

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6 Scopus citations

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

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61 Scopus citations

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.

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10 Scopus citations

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. I., 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. J., 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.

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340 Scopus citations

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 - Neuropsychiatric Genetics. 119 B, 1, p. 69-76 8 p.

Research output: Contribution to journalArticle

37 Scopus citations

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. I., DePaulo, J. R. & McInnis, M. G., Aug 15 2003, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 121 B, 1, p. 21-27 7 p.

Research output: Contribution to journalArticle

26 Scopus citations

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. J., Foroud, T. & Turner, C. H., Aug 1 2005, In : Mammalian Genome. 16, 8, p. 578-586 9 p.

Research output: Contribution to journalArticle

24 Scopus citations

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. I., Foroud, T., Edenberg, H. J. & Li, T. K., Oct 15 1999, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 88, 5, p. 517-521 5 p.

Research output: Contribution to journalArticle

12 Scopus citations