Tatiana Foroud

  • 82045 Citations
  • 113 h-Index
1976 …2020

Research output per year

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Publications

Article

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

114 Scopus citations

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

Badner, J. A., Koller, D., Foroud, T., Edenberg, H., Nurnberger, J. I., 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

21 Scopus citations

Genome-wide linkage and follow-up association study of postpartum mood symptoms

NIMH Bipolar Disorder Genetics Initiative, the "Molecular Genetics of Schizophrenia II" (MGS-2) collaboration, Bipolar Genetics Studies (BiGS) Collaboration & NIMH Genetics of Recurrent Early-Onset Depression (GenRED) project, Nov 1 2009, In : American Journal of Psychiatry. 166, 11, p. 1229-1237 9 p.

Research output: Contribution to journalArticle

60 Scopus citations

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

5 Scopus citations

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. I., Foroud, T., Rice, J. P., Scheftner, W. B., Zandi, P., Edenberg, H. & Byerley, W., Aug 1 2008, In : Psychiatric genetics. 18, 4, p. 191-198 8 p.

Research output: Contribution to journalArticle

11 Scopus citations

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. M., Mukherjee, S., Crane, P. K., Aisen, P. S., Petersen, R. C., Weiner, M. W. & Saykin, A. J., Aug 6 2012, In : Brain Imaging and Behavior. 6, 4, p. 634-648 15 p.

Research output: Contribution to journalArticle

48 Scopus citations

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

Kapoor, M., Chou, Y. L., Edenberg, H. J., 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., 2016, In : Translational psychiatry. 6, 3, e761.

Research output: Contribution to journalArticle

10 Scopus citations

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. J., 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. I., Reich, T., Zandi, P. P. & Foroud, T. M., Dec 1 2003, In : Biological psychiatry. 54, 11, p. 1265-1273 9 p.

Research output: Contribution to journalArticle

70 Scopus citations

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 1 2004, In : Journals of Gerontology - Series A Biological Sciences and Medical Sciences. 59, 3, p. 227-232 6 p.

Research output: Contribution to journalArticle

37 Scopus citations

Genomewide scan of affected relative pairs using the NIMH Genetics Initiative Bipolar affective Disorder pedigrees

Foroud, T., Castellucio, P. F., Koller, D. L., Edenberg, H. J., Goate, A., Detera-Wadleigh, S., Stine, O. C., McMahon, F. J., McInnis, M. G., Rice, J., Blehar, M., Goldin, L. R., Badner, J., Guroff, J., Reich, T., DePaulo, J. R., Gershon, E. & Nurnberger, J. I., Nov 6 1998, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 81, 6, 1 p.

Research output: Contribution to journalArticle

13 Scopus citations

Genome-wide search for genes affecting the risk for alcohol dependence

Reich, T., Edenberg, H. J., Goate, A., Williams, J. T., Rice, J. P., Van Eerdewegh, P., Foroud, T., Hesselbrock, V., Schuckit, M. A., Bucholz, K., Porjesz, B., Li, T. K., Conneally, P. M., Nurnberger, J. I., Tischfield, J. A., Crowe, R. R., Cloninger, C. R., Wu, W., Shears, S., Carr, K. & 3 others, Crose, C., Willig, C. & Begleiter, H., May 8 1998, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 81, 3, p. 207-215 9 p.

Research output: Contribution to journalArticle

612 Scopus citations

Genomewide search for genes influencing percent body fat in Pima Indians: Suggestive linkage at chromosome 11q21-q22

Norman, R. A., Thompson, D. B., Foroud, T., Garvey, W. T., Bennett, P. H., Bogardus, C., Ravussin, E., Allan, C., Baier, L., Bowden, D., Hanson, R., Knowler, W., Kobes, S., Pettitt, D. & Prochazka, M., Jan 1997, In : American Journal of Human Genetics. 60, 1, p. 166-173 8 p.

Research output: Contribution to journalArticle

130 Scopus citations

Genomewide SNP screen to detect quantitative trait loci for alcohol preference in the high alcohol preferring and low alcohol preferring mice

Bice, P., Valdar, W., Zhang, L., Liu, L., Lai, D., Grahame, N., Flint, J., Li, T. K., Lumeng, L. & Foroud, T., Mar 1 2009, In : Alcoholism: Clinical and Experimental Research. 33, 3, p. 531-537 7 p.

Research output: Contribution to journalArticle

15 Scopus citations

Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families

Kapoor, M., Wang, J. C., Wetherill, L., Le, N., Bertelsen, S., Hinrichs, A. L., Budde, J., Agrawal, A., Almasy, L., Bucholz, K., Dick, D. M., Harari, O., Xiaoling, X., Hesselbrock, V., Kramer, J., Nurnberger, J. I., Rice, J., Schuckit, M., Tischfield, J., Porjesz, B. & 4 others, Edenberg, H. J., Bierut, L., Foroud, T. & Goate, A., Sep 1 2014, In : Drug and Alcohol Dependence. 142, p. 56-62 7 p.

Research output: Contribution to journalArticle

16 Scopus citations

Genome-wide transcriptome analysis identifies novel dysregulated genes implicated in Alzheimer's pathology

Nho, K., Nudelman, K., Allen, M., Hodges, A., Kim, S., Risacher, S. L., Apostolova, L. G., Lin, K., Lunnon, K., Wang, X., Burgess, J. D., Ertekin-Taner, N., Petersen, R. C., Wang, L., Qi, Z., He, A., Neuhaus, I., Patel, V., Foroud, T., Faber, K. M. & 4 others, Lovestone, S., Simmons, A., Weiner, M. W. & Saykin, A. J., 2020, (Accepted/In press) In : Alzheimer's and Dementia.

Research output: Contribution to journalArticle

Genomic copy number analysis in Alzheimer's disease and mild cognitive impairment: An ADNI study

Saykin, A. J., Swaminathan, S., Kim, S., Shen, L., Risacher, S. L., Foroud, T., Pankratz, N., Potkin, S. G., Huentelman, M. J., Craig, D. W. & Weiner, M. W., 2011, In : International Journal of Alzheimer's Disease. 729478.

Research output: Contribution to journalArticle

39 Scopus citations

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

Bipolar Disorder and Schizophrenia Working Group of the Psychiatric Genomics Consortium douglas.ruderfer@vanderbilt.edu, Psychosis Endophenotypes International Consortium & Wellcome Trust Case-Control Consortium, Jun 14 2018, In : Cell. 173, 7, p. 1705-1715.e16

Research output: Contribution to journalArticle

142 Scopus citations

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

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

Research output: Contribution to journalArticle

10 Scopus citations

Genomic screen for QTLs underlying alcohol consumption in the P and NP rat lines

Bice, P., Foroud, T., Bo, R., Castelluccio, P., Lumeng, L., Li, T. K. & Carr, L. G., Dec 1 1998, In : Mammalian Genome. 9, 12, p. 949-955 7 p.

Research output: Contribution to journalArticle

83 Scopus citations

Genomic survey of bipolar illness in the NIMH genetics initiative pedigrees: A preliminary report

Nurnberger, J. I., DePaulo, J. R., Gershon, E. S., Reich, T., Blehar, M. C., Edenberg, H. J., Foroud, T., Miller, M., Bowman, E., Mayeda, A., Rau, N. L., Smiley, C., Conneally, P. M., McMahon, F., Meyers, D., Simpson, S., McInnis, M., Stine, O. C., Detera-Wadleigh, S., Goldin, L. & 9 others, Guroff, J., Maxwell, E., Kazuba, D., Gejman, P. V., Badner, J., Sanders, A., Rice, J., Bierut, L. & Goate, A., 1997, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 74, 3, p. 227-237 11 p.

Research output: Contribution to journalArticle

115 Scopus citations

Genotype patterns at PICALM, CR1, BIN1, CLU, and APOE genes are associated with episodic memory

Barral, S., Bird, T., Goate, A., Farlow, M. R., Diaz-Arrastia, R., Bennett, D. A., Graff-Radford, N., Boeve, B. F., Sweet, R. A., Stern, Y., Wilson, R. S., Foroud, T., Ott, J. & Mayeux, R., May 8 2012, In : Neurology. 78, 19, p. 1464-1471 8 p.

Research output: Contribution to journalArticle

67 Scopus citations

Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk

Alzheimer Disease Genetics Consortium, Mar 1 2016, In : Alzheimer's and Dementia. 12, 3, p. 233-243 11 p.

Research output: Contribution to journalArticle

11 Scopus citations

Glutathione S-transferase 8-8 expression is lower in alcohol-preferring than in alcohol-nonpreferring rats

Liang, T., Habegger, K., Spence, J. P., Foroud, T., Ellison, J. A., Lumeng, L., Li, T. K. & Carr, L. G., Nov 2004, In : Alcoholism: Clinical and Experimental Research. 28, 11, p. 1622-1628 7 p.

Research output: Contribution to journalArticle

20 Scopus citations

Greater rupture risk for familial as compared to sporadic unruptured intracranial aneurysms

Broderick, J. P., Brown, R. D., Sauerbeck, L., Hornung, R., Huston, J., Woo, D., Anderson, C., Rouleau, G., Kleindorfer, D., Flaherty, M. L., Meissner, I., Foroud, T., Moomaw, E. C. J. & Connolly, E. S., Jun 1 2009, In : Stroke. 40, 6, p. 1952-1957 6 p.

Research output: Contribution to journalArticle

94 Scopus citations

GWAS of longitudinal amyloid accumulation on 18F-florbetapir PET in Alzheimer's disease implicates microglial activation gene IL1RAP

Ramanan, V. K., Risacher, S. L., Nho, K., Kim, S., Shen, L., McDonald, B. C., Yoder, K. K., Hutchins, G. D., West, J. D., Tallman, E. F., Gao, S., Foroud, T. M., Farlow, M. R., De Jager, P. L., Bennett, D. A., Aisen, P. S., Petersen, R. C., Jack, C. R., Toga, A. W., Green, R. C. & 3 others, Jagust, W. J., Weiner, M. W. & Saykin, A. J., Oct 1 2015, In : Brain. 138, 10, p. 3076-3088 13 p.

Research output: Contribution to journalArticle

61 Scopus citations

Harnessing peripheral DNA methylation differences in the Alzheimer's Disease Neuroimaging Initiative (ADNI) to reveal novel biomarkers of disease

Vasanthakumar, A., Davis, J. W., Idler, K., Waring, J. F., Asque, E., Riley-Gillis, B., Grosskurth, S., Srivastava, G., Kim, S., Kim, S., Nho, K., Nudelman, K. N. H., Nudelman, K. N. H., Faber, K., Sun, Y., Sun, Y., Foroud, T. M., Estrada, K., Estrada, K., Apostolova, L. G. & 3 others, Li, Q. S., Li, Q. S. & Saykin, A. J., Jun 15 2020, In : Clinical Epigenetics. 12, 1, 84.

Research output: Contribution to journalArticle

Open Access
1 Scopus citations

Heritability of changes in bone size and bone mass with age in premenopausal white sisters

Hui, S. L., Koller, D. L., Foroud, T. M., Econs, M. J., Johnston, C. C. & Peacock, M., Jul 1 2006, In : Journal of Bone and Mineral Research. 21, 7, p. 1121-1125 5 p.

Research output: Contribution to journalArticle

22 Scopus citations

Heritability of different forms of memory in the late onset alzheimer's disease family study

Wilson, R. S., Barral, S., Lee, J. H., Leurgans, S. E., Foroud, T. M., Sweet, R. A., Graff-Radford, N., Bird, T. D., Mayeux, R. & Bennett, D. A., 2011, In : Journal of Alzheimer's Disease. 23, 2, p. 249-255 7 p.

Research output: Contribution to journalArticle

42 Scopus citations

Heterogeneity in hereditary pancreatitis

Dasouki, M. J., Cogan, J., Summar, M. L., Neblitt, W., Foroud, T., Koller, D. & Phillips, J. A., Apr 28 1998, In : American journal of medical genetics. 77, 1, p. 47-53 7 p.

Research output: Contribution to journalArticle

38 Scopus citations

Heterogeneous stock rat: A unique animal model for mapping genes influencing bone fragility

Alam, I., Koller, D. L., Sun, Q., Roeder, R. K., Cañete, T., Blázquez, G., López-Aumatell, R., Martínez-Membrives, E., Vicens-Costa, E., Mont, C., Díaz, S., Tobeña, A., Fernández-Teruel, A., Whitley, A., Strid, P., Diez, M., Johannesson, M., Flint, J., Econs, M. J., Turner, C. H. & 1 others, Foroud, T., May 1 2011, In : Bone. 48, 5, p. 1169-1177 9 p.

Research output: Contribution to journalArticle

13 Scopus citations

Heterozygosity for a mutation in the parkin gene leads to later onset Parkinson disease

Foroud, T., Uniacke, S. K., Liu, L., Pankratz, N., Rudolph, A., Halter, C., Shults, C., Marder, K., Conneally, P. M., Nichols, W. C., Golbe, L., Koller, W., Lyons, K., Marshall, F., Oakes, D., Shinaman, A., Siemers, E., Wojcieszek, J., Belden, J., Carter, J. & 79 others, Camicioli, R., Andrews, P., Fernandez, M., Hubble, J., Reider, C., Rajput, A., Rajput, A., Shirley, T., Panisset, M., Hall, J., Mendis, T., Grimes, D. A., Gray, P., Serrano Ramos, C., Roque, S., Reich, S., Dunlop, B., Hauser, R., Sanchez-Ramos, J., Zesiewicz, T., Delgado, H., Friedman, J., Fernandez, H., Lannon, M., Seeberger, L., O'Brien, C., Judd, D., Elmer, L., Davis, K., Fontaine, D., Pfeiffer, R., Pfeiffer, B., Aminoff, M., DiMinno, M., Truong, D., Pathak, M., Tran, A., Rodnitzky, R., Dobson, J., Pahwa, R., Thomas, S., Jennings, D., Marek, K., Mendick, S., Harris, J., Weiner, W., Kurlan, R., Berry, D., Lewitt, P., DeAngelis, M., Tuite, P., Schacherer, R., Martin, W., Wieler, M., Manyam, B., Simpson, P., Bertoni, J., Peterson, C., Gordon, M. F., Hamann, J., Jankovic, J., Hunter, C., Factor, S., Evans, S., Nieves, A., So, J., Stacy, M., Williamson, K., Walker, F., Hunt, V., Kang, U. J., Uy, S., Bindauer, K., Petit, J., Simon, D., Scollins, L., Pullman, R. S., Boyer, K. & Gordon, P., Mar 11 2003, In : Neurology. 60, 5, p. 796-801 6 p.

Research output: Contribution to journalArticle

178 Scopus citations

Heterozygous germline mutations in BMPR2, encoding a TGF-β receptor, cause familial primary pulmonary hypertension

Lane, K. B., Machado, R. D., Pauciulo, M. W., Thomson, J. R., Phillips, J. A., Loyd, J. E., Nichols, W. C., Trembath, R. C., Aldred, M., Brannon, C. A., Conneally, P. M., Foroud, T., Fretwell, N., Gaddipati, R., Koller, D., Loyd, E. J., Morgan, N., Newman, J. H., Prince, M. A., Güell, C. V. & 1 others, Wheeler, L., Sep 2000, In : Nature genetics. 26, 1, p. 81-84 4 p.

Research output: Contribution to journalArticle

1082 Scopus citations

High-resolution genome screen for bone mineral density in heterogeneous stock rat

Alam, I., Koller, D. L., Cañete, T., Blázquez, G., López-Aumatell, R., Martínez-Membrives, E., Díaz-Morán, S., Tobeña, A., Fernández-Teruel, A., Stridh, P., Diez, M., Olsson, T., Johannesson, M., Baud, A., Econs, M. J. & Foroud, T., Jul 2014, In : Journal of Bone and Mineral Research. 29, 7, p. 1619-1626 8 p.

Research output: Contribution to journalArticle

5 Scopus citations

Human ALOX12, but not ALOX15, is associated with BMD in white men and women

Ichikawa, S., Koller, D. L., Johnson, M. L., Lai, D., Xuei, X., Edenberg, H. J., Klein, R. F., Orwoll, E. S., Hui, S. L., Foroud, T. M., Peacock, M. & Econs, M. J., Apr 1 2006, In : Journal of Bone and Mineral Research. 21, 4, p. 556-564 9 p.

Research output: Contribution to journalArticle

62 Scopus citations

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

Ichikawa, S., Koller, D. L., Curry, L. R., Lai, D., Xuei, X., Pugh, E. W., Tsai, Y. Y., Doheny, K. F., Edenberg, H. J., Hui, S. L., Foroud, T., Peacock, M. & Econs, M. J., Oct 1 2008, In : Journal of Bone and Mineral Research. 23, 10, p. 1680-1688 9 p.

Research output: Contribution to journalArticle

4 Scopus citations

Identification of a quantitative trait locus on rat chromosome 4 that is strongly linked to femoral neck structure and strength

Alam, I., Sun, Q., Liu, L., Koller, D. L., Fishburn, T., Carr, L. G., Econs, M. J., Foroud, T. & Turner, C. H., Jul 1 2006, In : Bone. 39, 1, p. 93-99 7 p.

Research output: Contribution to journalArticle

23 Scopus citations

Identification of common variants associated with human hippocampal and intracranial volumes

Stein, J. L., Medland, S. E., Vasquez, A. A., Hibar, D. P., Senstad, R. E., Winkler, A. M., Toro, R., Appel, K., Bartecek, R., Bergmann, Ø., Bernard, M., Brown, A. A., Cannon, D. M., Chakravarty, M. M., Christoforou, A., Domin, M., Grimm, O., Hollinshead, M., Holmes, A. J., Homuth, G. & 182 others, Hottenga, J. J., Langan, C., Lopez, L. M., Hansell, N. K., Hwang, K. S., Kim, S., Laje, G., Lee, P. H., Liu, X., Loth, E., Lourdusamy, A., Mattingsdal, M., Mohnke, S., Maniega, S. M., Nho, K., Nugent, A. C., O'brien, C., Papmeyer, M., Pütz, B., Ramasamy, A., Rasmussen, J., Rijpkema, M., Risacher, S. L., Roddey, J. C., Rose, E. J., Ryten, M., Shen, L., Sprooten, E., Strengman, E., Teumer, A., Trabzuni, D., Turner, J., Van Eijk, K., Van Erp, T. G. M., Van Tol, M. J., Wittfeld, K., Wolf, C., Woudstra, S., Aleman, A., Alhusaini, S., Almasy, L., Binder, E. B., Brohawn, D. G., Cantor, R. M., Carless, M. A., Corvin, A., Czisch, M., Curran, J. E., Davies, G., De Almeida, M. A. A., Delanty, N., Depondt, C., Duggirala, R., Dyer, T. D., Erk, S., Fagerness, J., Fox, P. T., Freimer, N. B., Gill, M., Göring, H. H. H., Hagler, D. J., Hoehn, D., Holsboer, F., Hoogman, M., Hosten, N., Jahanshad, N., Johnson, M. P., Kasperaviciute, D., Kent, J. W., Kochunov, P., Lancaster, J. L., Lawrie, S. M., Liewald, D. C., Mandl, R., Matarin, M., Mattheisen, M., Meisenzahl, E., Melle, I., Moses, E. K., Mühleisen, T. W., Nauck, M., Nöthen, M. M., Olvera, R. L., Pandolfo, M., Pike, G. B., Puls, R., Reinvang, I., Rentería, M. E., Rietschel, M., Roffman, J. L., Royle, N. A., Rujescu, D., Savitz, J., Schnack, H. G., Schnell, K., Seiferth, N., Smith, C., Steen, V. M., Hernández, M. C. V., Van Den Heuvel, M., Van Der Wee, N. J., Van Haren, N. E. M., Veltman, J. A., Völzke, H., Walker, R., Westlye, L. T., Whelan, C. D., Agartz, I., Boomsma, D. I., Cavalleri, G. L., Dale, A. M., Djurovic, S., Drevets, W. C., Hagoort, P., Hall, J., Heinz, A., Jack, C. R., Foroud, T. M., Le Hellard, S., Macciardi, F., Montgomery, G. W., Poline, J. B., Porteous, D. J., Sisodiya, S. M., Starr, J. M., Sussmann, J., Toga, A. W., Veltman, D. J., Walter, H., Weiner, M. W., Bis, J. C., Ikram, M. A., Smith, A. V., Gudnason, V., Tzourio, C., Vernooij, M. W., Launer, L. J., Decarli, C., Seshadri, S., Andreassen, O. A., Apostolova, L. G., Bastin, M. E., Blangero, J., Brunner, H. G., Buckner, R. L., Cichon, S., Coppola, G., De Zubicaray, G. I., Deary, I. J., Donohoe, G., De Geus, E. J. C., Espeseth, T., Fernéndez, G., Glahn, D. C., Grabe, H. J., Hardy, J., Hulshoff Pol, H. E., Jenkinson, M., Kahn, R. S., Mcdonald, C., Mcintosh, A. M., Mcmahon, F. J., Mcmahon, K. L., Meyer-Lindenberg, A., Morris, D. W., Müller-Myhsok, B., Nichols, T. E., Ophoff, R. A., Paus, T., Pausova, Z., Penninx, B. W., Potkin, S. G., Sämann, P. G., Saykin, A. J., Schumann, G., Smoller, J. W., Wardlaw, J. M., Weale, M. E., Martin, N. G., Franke, B., Wright, M. J. & Thompson, P. M., May 2012, In : Nature genetics. 44, 5, p. 552-561 10 p.

Research output: Contribution to journalArticle

429 Scopus citations

Identification of genes for complex disease using longitudinal phenotypes.

Pankratz, N., Mukhopadhyay, N., Huang, S., Foroud, T. & Kirkwood, S. C., 2003, In : BMC genetics. 4 Suppl 1

Research output: Contribution to journalArticle

Open Access
4 Scopus citations

Identification of pathways for bipolar disorder: A meta-analysis

Psychiatric Genomics Consortium Bipolar Group, Jun 1 2014, In : JAMA psychiatry. 71, 6, p. 657-664 8 p.

Research output: Contribution to journalArticle

124 Scopus citations

Identification of QTLs influencing alcohol preference in the High Alcohol Preferring (HAP) and Low Alcohol Preferring (LAP) mouse lines

Bice, P. J., Foroud, T., Carr, L. G., Zhang, L., Liu, L., Grahame, N. J., Lumeng, L., Li, T. K. & Belknap, J. K., Mar 1 2006, In : Behavior Genetics. 36, 2, p. 248-260 13 p.

Research output: Contribution to journalArticle

28 Scopus citations

Identification of quantitative trait loci influencing alcohol consumption in the high alcohol drinking and low alcohol drinking rat lines

Foroud, T., Bice, P., Castelluccio, P., Bo, R., Miller, L., Ritchotte, A., Lumeng, L., Li, T. K. & Carr, L. G., Jan 1 2000, In : Behavior Genetics. 30, 2, p. 131-140 10 p.

Research output: Contribution to journalArticle

39 Scopus citations

Identification of TMEM230 mutations in familial Parkinson's disease

Deng, H. X., Shi, Y., Yang, Y., Ahmeti, K. B., Miller, N., Huang, C., Cheng, L., Zhai, H., Deng, S., Nuytemans, K., Corbett, N. J., Kim, M. J., Deng, H., Tang, B., Yang, Z., Xu, Y., Chan, P., Huang, B., Gao, X. P., Song, Z. & 14 others, Liu, Z., Fecto, F., Siddique, N., Foroud, T., Jankovic, J., Ghetti, B., Nicholson, D. A., Krainc, D., Melen, O., Vance, J. M., Pericak-Vance, M. A., Ma, Y. C., Rajput, A. H. & Siddique, T., Jul 1 2016, In : Nature genetics. 48, 7, p. 733-739 7 p.

Research output: Contribution to journalArticle

93 Scopus citations

Immunohistochemical method and histopathology judging for the systemic synuclein sampling study (S4)

Beach, T. G., Serrano, G. E., Kremer, T., Canamero, M., Dziadek, S., Sade, H., Derkinderen, P., Corbillé, A. G., Letournel, F., Munoz, D. G., White, C. L., Schneider, J., Crary, J. F., Sue, L. I., Adler, C. H., Glass, M. J., Intorcia, A. J., Walker, J. E., Foroud, T., Coffey, C. S. & 13 others, Ecklund, D., Riss, H., Goßmann, J., König, F., Kopil, C. M., Arnedo, V., Riley, L., Linder, C., Dave, K. D., Jennings, D., Seibyl, J., Mollenhauer, B. & Chahine, L., 2018, In : Journal of Neuropathology and Experimental Neurology. 77, 9, p. 793-802 10 p.

Research output: Contribution to journalArticle

8 Scopus citations

Impact of genetic ancestry on outcomes in ECOG-ACRIN-5103

Schneider, B. P., Shen, F., Jiang, G., O'Neill, A., Radovich, M., Li, L., Gardner, L., Lai, D., Foroud, T., Sparano, J. A., Sledge, G. W. & Miller, K. D., Jan 1 2017, In : JCO Precision Oncology. 2017, 1, p. 1-9 9 p.

Research output: Contribution to journalArticle

4 Scopus citations

Implementation of a shared data repository and common data dictionary for fetal alcohol spectrum disorders research

Arenson, A. D., Bakhireva, L. N., Chambers, C. D., Deximo, C. A., Foroud, T., Jacobson, J. L., Jacobson, S. W., Jones, K. L., Mattson, S. N., May, P. A., Moore, E. S., Ogle, K., Riley, E. P., Robinson, L. K., Rogers, J., Streissguth, A. P., Tavares, M. C., Urbanski, J., Yezerets, Y., Surya, R. & 2 others, Stewart, C. A. & Barnett, W. K., Nov 1 2010, In : Alcohol. 44, 7-8, p. 643-647 5 p.

Research output: Contribution to journalArticle

12 Scopus citations

Improving genetic prediction by leveraging genetic correlations among human diseases and traits

Maier, R. M., Zhu, Z., Lee, S. H., Trzaskowski, M., Ruderfer, D. M., Stahl, E. A., Ripke, S., Wray, N. R., Yang, J., Visscher, P. M., Robinson, M. R., Forstner, A. J., Mcquillin, A., Trubetskoy, V., Wang, W., Wang, Y., Coleman, J. R. I., Gaspar, H. A., De Leeuw, C. A., Whitehead Pavlides, J. M. & 221 others, Olde Loohuis, L. M., Pers, T. H., Lee, P. H., Charney, A. W., Dobbyn, A. L., Huckins, L., Boocock, J., Giambartolomei, C., Roussos, P., Mullins, N., Awasthi, S., Agerbo, E., Als, T. D., Pedersen, C. B., Grove, J., Kupka, R., Regeer, E. J., Anjorin, A., Casas, M., Mahon, P. B., Allardyce, J., Escott-Price, V., Forty, L., Fraser, C., Kogevinas, M., Frank, J., Streit, F., Strohmaier, J., Treutlein, J., Witt, S. H., Kennedy, J. L., Strauss, J. S., Garnham, J., O'donovan, C., Slaney, C., Steinberg, S., Thorgeirsson, T. E., Hautzinger, M., Steffens, M., Perlis, R. H., Sánchez-Mora, C., Hipolito, M., Lawson, W. B., Nwulia, E. A., Levy, S. E., Foroud, T. M., Jamain, S., Young, A. H., Mckay, J. D., Albani, D., Zandi, P., Potash, J. B., Zhang, P., Raymond Depaulo, J., Bergen, S. E., Juréus, A., Karlsson, R., Kandaswamy, R., Mcguffin, P., Rivera, M., Lissowska, J., Cruceanu, C., Lucae, S., Cervantes, P., Budde, M., Gade, K., Heilbronner, U., Pedersen, M. G., Morris, D. W., Weickert, C. S., Weickert, T. W., Macintyre, D. J., Lawrence, J., Elvsåshagen, T., Smeland, O. B., Djurovic, S., Xi, S., Green, E. K., Czerski, P. M., Hauser, J., Xu, W., Vedder, H., Oruc, L., Spijker, A. T., Gordon, S. D., Medland, S. E., Curtis, D., Mühleisen, T. W., Badner, J., Scheftner, W. A., Sigurdsson, E., Schork, N. J., Schatzberg, A. F., Bækvad-Hansen, M., Bybjerg-Grauholm, J., Hansen, C. S., Knowles, J. A., Szelinger, S., Montgomery, G. W., Boks, M., Adolfsson, A. N., Hoffmann, P., Bauer, M., Pfennig, A., Leber, M., Kittel-Schneider, S., Reif, A., Del-Favero, J., Fischer, S. B., Herms, S., Reinbold, C. S., Degenhardt, F., Koller, A. C., Maaser, A., Ori, A., Dale, A. M., Fan, C. C., Greenwood, T. A., Nievergelt, C. M., Shehktman, T., Shilling, P. D., Byerley, W., Bunney, W., Alliey-Rodriguez, N., Clarke, T. K., Liu, C., Coryell, W., Akil, H., Burmeister, M., Flickinger, M., Li, J. Z., Mcinnis, M. G., Meng, F., Thompson, R. C., Watson, S. J., Zollner, S., Guan, W., Green, M. J., Craig, D., Sobell, J. L., Milani, L., Gordon-Smith, K., Knott, S. V., Perry, A., Parra, J. G., Mayoral, F., Rivas, F., Rice, J. P., Barchas, J. D., Børglum, A. D., Mortensen, P. B., Mors, O., Grigoroiu-Serbanescu, M., Bellivier, F., Etain, B., Leboyer, M., Ramos-Quiroga, J. A., Agartz, I., Amin, F., Azevedo, M. H., Bass, N., Black, D. W., Blackwood, D. H. R., Bruggeman, R., Buccola, N. G., Choudhury, K., Cloninger, C. R., Corvin, A., Craddock, N., Daly, M. J., Datta, S., Donohoe, G. J., Duan, J., Dudbridge, F., Fanous, A., Freedman, R., Freimer, N. B., Friedl, M., Gill, M., Gurling, H., De Haan, L., Hamshere, M. L., Hartmann, A. M., Holmans, P. A., Kahn, R. S., Keller, M. C., Kenny, E., Kirov, G. K., Krabbendam, L., Krasucki, R., Lencz, T., Levinson, D. F., Lieberman, J. A., Lin, D. Y., Linszen, D. H., Magnusson, P. K. E., Maier, W., Malhotra, A. K., Mattheisen, M., Mattingsdal, M., Mccarroll, S. A., Medeiros, H., Melle, I., Milanova, V., Myin-Germeys, I., Neale, B. M., Ophoff, R. A., Owen, M. J., Pimm, J., Purcell, S. M., Puri, V., Quested, D. J., Rossin, L., Sanders, A. R., Shi, J., Sklar, P., St Clair, D., Stroup, T. S., Van Os, J., Wiersma, D. & Zammit, S., Dec 1 2018, In : Nature communications. 9, 1, 989.

Research output: Contribution to journalArticle

32 Scopus citations

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

Hartz, S. M., Short, S. E., Saccone, N. L., Culverhouse, R., Chen, L. S., Schwantes-An, T. H., Coon, H., Han, Y., Stephens, S. H., Sun, J., Chen, X., Ducci, F., Dueker, N., Franceschini, N., Frank, J., Geller, F., Guobjartsson, D., Hansel, N. N., Jiang, C., Keskitalo-Vuokko, K. & 132 others, Liu, Z., Lyytikäinen, L. P., Michel, M., Rawal, R., Rosenberger, A., Scheet, P., Shaffer, J. R., Teumer, A., Thompson, J. R., Vink, J. M., Vogelzangs, N., Wenzlaff, A. S., Wheeler, W., Xiao, X., Yang, B. Z., Aggen, S. H., Balmforth, A. J., Baumeister, S. E., Beaty, T., Bennett, S., Bergen, A. W., Boyd, H. A., Broms, U., Campbell, H., Chatterjee, N., Chen, J., Cheng, Y. C., Cichon, S., Couper, D., Cucca, F., Dick, D. M., Foroud, T., Furberg, H., Giegling, I., Gu, F., Hall, A. S., Hällfors, J., Han, S., Hartmann, A. M., Hayward, C., Heikkilä, K., Hewitt, J. K., Hottenga, J. J., Jensen, M. K., Jousilahti, P., Kaakinen, M., Kittner, S. J., Konte, B., Korhonen, T., Landi, M. T., Laatikainen, T., Leppert, M., Levy, S. M., Mathias, R. A., McNeil, D. W., Medland, S. E., Montgomery, G. W., Muley, T., Murray, T., Nauck, M., North, K., Pergadia, M., Polasek, O., Ramos, E. M., Ripatti, S., Risch, A., Ruczinski, I., Rudan, I., Salomaa, V., Schlessinger, D., Styrkársdóttir, U., Terracciano, A., Uda, M., Willemsen, G., Wu, X., Abecasis, G., Barnes, K., Bickeböller, H., Boerwinkle, E., Boomsma, D. I., Caporaso, N., Duan, J., Edenberg, H. J., Francks, C., Gejman, P. V., Gelernter, J., Grabe, H. J., Hops, H., Jarvelin, M. R., Viikari, J., Kähönen, M., Kendler, K. S., Lehtimäki, T., Levinson, D. F., Marazita, M. L., Marchini, J., Melbye, M., Mitchell, B. D., Murray, J. C., Nöthen, M. M., Penninx, B. W., Raitakari, O., Rietschel, M., Rujescu, D., Samani, N. J., Sanders, A. R., Schwartz, A. G., Shete, S., Shi, J., Spitz, M., Stefansson, K., Swan, G. E., Thorgeirsson, T., Völzke, H., Wei, Q., Wichmann, H. E., Amos, C. I., Breslau, N., Cannon, D. S., Ehringer, M., Grucza, R., Hatsukami, D., Heath, A., Johnson, E. O., Kaprio, J., Madden, P., Martin, N. G., Stevens, V. L., Stitzel, J. A., Weiss, R. B., Kraft, P. & Bierut, L. J., Aug 2012, In : Archives of general psychiatry. 69, 8, p. 854-861 8 p.

Research output: Contribution to journalArticle

48 Scopus citations

Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP)

Reitz, C., Tosto, G., Vardarajan, B., Rogaeva, E., Ghani, M., Rogers, R. S., Conrad, C., Haines, J. L., Pericak-Vance, M. A., Fallin, M. D., Foroud, T., Farrer, L. A., Schellenberg, G. D., George-Hyslop, P. S. & Mayeux, R., 2013, In : Translational psychiatry. 3, e256.

Research output: Contribution to journalArticle

39 Scopus citations

Individualized atrophy scores predict dementia onset in familial frontotemporal lobar degeneration

on behalf of the ARTFL/LEFFTDS consortium, Jan 1 2020, In : Alzheimer's and Dementia. 16, 1, p. 37-48 12 p.

Research output: Contribution to journalArticle

Open Access
6 Scopus citations

Inflammatory profile discriminates clinical subtypes in LRRK2-associated Parkinson's disease

Brockmann, K., Schulte, C., Schneiderhan-Marra, N., Apel, A., Pont-Sunyer, C., Vilas, D., Ruiz-Martinez, J., Langkamp, M., Corvol, J. C., Cormier, F., Knorpp, T., Joos, T. O., Bernard, A., Gasser, T., Marras, C., Schüle, B., Aasly, J. O., Foroud, T., Marti-Masso, J. F., Brice, A. & 3 others, Tolosa, E., Berg, D. & Maetzler, W., Feb 1 2017, In : European Journal of Neurology. 24, 2, p. 427-e6

Research output: Contribution to journalArticle

16 Scopus citations