Tatiana Foroud

  • 43024 Citations
  • 102 h-Index
1976 …2021

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Large-scale genomics unveil polygenic architecture of human cortical surface area

Chen, C. H., Peng, Q., Schork, A. J., Lo, M. T., Fan, C. C., Wang, Y., Desikan, R. S., Bettella, F., Hagler, D. J., Westlye, L. T., Kremen, W. S., Jernigan, T. L., Le Hellard, S., Steen, V. M., Espeseth, T., Huentelman, M., Håberg, A. K., Agartz, I., Djurovic, S., Andreassen, O. A. & 86 others, Schork, N., Dale, A. M., McCabe, C., Chang, L., Akshoomoff, N., Newman, E., Ernst, T., Van Zijl, P., Kuperman, J., Murray, S., Bloss, C., Appelbaum, M., Gamst, A., Thompson, W., Bartsch, H., Weiner, M., Aisen, P., Petersen, R., Jack, C. R., Jagust, W., Trojanowki, J. Q., Toga, A. W., Beckett, L., Green, R. C., Saykin, A. J., Morris, J., Shaw, L. M., Khachaturian, Z., Sorensen, G., Carrillo, M., Kuller, L., Raichle, M., Paul, S., Davies, P., Fillit, H., Hefti, F., Holtzman, D., Mesulman, M. M., Potter, W., Snyder, P. J., Schwartz, A., Montine, T., Thomas, R. G., Donohue, M., Walter, S., Gessert, D., Sather, T., Jiminez, G., Harvey, D., Bernstein, M., Fox, N., Thompson, P., Schuff, N., DeCarli, C., Borowski, B., Gunter, J., Senjem, M., Vemuri, P., Jones, D., Kantarci, K., Ward, C., Koeppe, R. A., Foster, N., Reiman, E. M., Chen, K., Mathis, C., Landau, S., Cairns, N. J., Householder, E., Taylor-Reinwald, L., Lee, V. M. Y., Korecka, M., Figurski, M., Crawford, K., Neu, S., Foroud, T. M., Potkin, S., Shen, L., Faber, K., Kim, S., Nho, K., Thal, L., Frank, R., Buckholtz, N., Albert, M. & Hsiao, J., Jul 20 2015, In : Nature communications. 6, 7549.

Research output: Contribution to journalArticle

20 Scopus citations

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

International Parkinson's Disease Genomics Consortium (IPDGC), Parkinson's Study Group (PSG) Parkinson's Research: The Organized GENetics Initiative (PROGENI), 23andMe, GenePD, NeuroGenetics Research Consortium (NGRC), Hussman Institute of Human Genomics (HIHG), The Ashkenazi Jewish Dataset Investigator, Cohorts for Health and Aging Research in Genetic Epidemiology (CHARGE), North American Brain Expression Consortium (NABEC), United Kingdom Brain Expression Consortium (UKBEC), Greek Parkinson's Disease Consortium & Alzheimer Genetic Analysis Group, Jan 1 2014, In : Nature genetics. 46, 9, p. 989-993 5 p.

Research output: Contribution to journalArticle

785 Scopus citations

Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm

Farlow, J. L., Lin, H., Sauerbeck, L., Lai, D., Koller, D. L., Pugh, E., Hetrick, K., Ling, H., Kleinloog, R., Van Der Vlies, P., Deelen, P., Swertz, M. A., Verweij, B. H., Regli, L., Rinkel, G. J. E., Ruigrok, Y. M., Doheny, K., Liu, Y., Foroud, T., Broderick, J. & 59 others, Woo, D., Kissela, B., Kleindorfer, D., Schneider, A., Zuccarello, M., Ringer, A., Deka, R., Brown, R. D., Huston, J., Mesissner, I., Wiebers, D., Qureshi, A. I., Rasmussen, P. A., Connolly, E. S., Sacco, R. L., Malkaff, M., Payner, T. D., Ferguson, G. G., Aldrich, E. F., Rouleau, G., Anderson, C. S., Mee, E. W., Hankey, G. J., Knuckey, N., Reilly, P. L., Laidlaw, J. D., D'Urso, P., Rosenfeld, J. V., Morgan, M. K., Dorsch, N., Besser, M., Batjer, H. H., Richard, M. T., Kassam, A., Steinberg, G. K., Johnston, S. C., Ko, N. U., Giannotta, S. L., Kassell, N. F., Worrall, B. B., Lui, K. C., Dumont, A., Tirschell, D. L., Kaufmann, A. M., Fisher, W. S., Aziz, K. M. A., Day, A. L., Du, R., Ogilvy, C., Lewis, S. B., Murphy, K. P., Radvany, M., Gandhi, D., Lisabeth, L., Pandey, A., Morgenstern, L., Derdeyn, C., Langefeld, C. & Bailey-Wilson, J., Mar 24 2015, In : PLoS ONE. 10, 3, e0121104.

Research output: Contribution to journalArticle

20 Scopus citations

Linkage analyses in Caribbean Hispanic families identify novel loci associated with familial late-onset Alzheimer's disease

Barral, S., Cheng, R., Reitz, C., Vardarajan, B., Lee, J., Kunkle, B., Beecham, G., Cantwell, L. S., Pericak-Vance, M. A., Farrer, L. A., Haines, J. L., Goate, A. M., Foroud, T., Boerwinkle, E., Schellenberg, G. D. & Mayeux, R., Dec 1 2015, In : Alzheimer's and Dementia. 11, 12, p. 1397-1406 10 p.

Research output: Contribution to journalArticle

14 Scopus citations

Linkage and linkage disequilibrium of evoked EEG oscillations with CHRM2 receptor gene polymorphisms: Implications for human brain dynamics and cognition

Jones, K. A., Porjesz, B., Almasy, L., Bierut, L., Goate, A., Wang, J. C., Dick, D. M., Hinrichs, A., Kwon, J., Rice, J. P., Rohrbaugh, J., Stock, H., Wu, W., Bauer, L. O., Chorlian, D. B., Crowe, R. R., Edenberg, H. J., Foroud, T., Hesselbrock, V., Kuperman, S. & 7 others, Nurnberger, J., O'Connor, S. J., Schuckit, M. A., Stimus, A. T., Tischfield, J. A., Reich, T. & Begleiter, H., Jul 1 2004, In : International Journal of Psychophysiology. 53, 2, p. 75-90 16 p.

Research output: Contribution to journalArticle

108 Scopus citations

Linkage disequilibrium between the beta frequency of the human EEG and a GABAA receptor gene locus

Porjesz, B., Almasy, L., Edenberg, H. J., Wang, K., Chorlian, D. B., Foroud, T., Goate, A., Rice, J. P., O'Connor, S. J., Rohrbaugh, J., Kuperman, S., Bauer, L. O., Crowe, R. R., Schuckit, M. A., Hesselbrock, V., Conneally, P. M., Tischfield, J. A., Li, T. K., Reich, T. & Begleiter, H., Mar 19 2002, In : Proceedings of the National Academy of Sciences of the United States of America. 99, 6, p. 3729-3733 5 p.

Research output: Contribution to journalArticle

230 Scopus citations

Linkage for platelet monoamine oxidase (MAO) activity: Results from a replication sample

Saccone, N. L., Rice, J. P., Rochberg, N., Williams, J. T., Goate, A., Reich, T., Edenberg, H. J., Foroud, T., Nurnberger, J. I., Bierut, L. J., Crowe, R. & Li, T. K., Jan 1 2002, In : Alcoholism: Clinical and Experimental Research. 26, 5, p. 603-609 7 p.

Research output: Contribution to journalArticle

6 Scopus citations

Linkage mapping of Beta 2 EEG waves via non-parametric regression

Ghosh, S., Begleiter, H., Porjesz, B., Chorlian, D. B., Edenberg, H. J., Foroud, T., Goate, A. & Reich, T., Apr 1 2003, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 118 B, 1, p. 66-71 6 p.

Research output: Contribution to journalArticle

32 Scopus citations

Linkage of an alcoholism-related severity phenotype to chromosome 16

Foroud, T., Bucholz, K. K., Edenberg, H. J., Goate, A., Neuman, R. J., Porjesz, B., Koller, D. L., Rice, J., Reich, T., Bierut, L. J., Cloninger, C. R., Nurnberger, J. I., Li, T. K., Conneally, P. M., Tischfield, J. A., Crowe, R., Hesselbrock, V., Schuckit, M. & Begleiter, H., Nov 6 1998, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 81, 6, 1 p.

Research output: Contribution to journalArticle

1 Scopus citations

Linkage of an alcoholism-related severity phenotype to chromosome 16

Foroud, T., Bucholz, K. K., Edenberg, H. J., Goate, A., Neuman, R. J., Porjesz, B., Koller, D. L., Rice, J., Reich, T., Bierut, L. J., Cloninger, C. R., Nurnberger, J. I., Li, T. K., Conneally, P. M., Tischfield, J. A., Crowe, R., Hesselbrock, V., Schuckit, M. & Begleiter, H., Dec 1 1998, In : Alcoholism: Clinical and Experimental Research. 22, 9, p. 2035-2042 8 p.

Research output: Contribution to journalArticle

59 Scopus citations

Linkage of a QTL contributing to normal variation in bone mineral density to chromosome 11q12-13

Koller, D. L., Rodriguez, L. A., Christian, J. C., Slemenda, C. W., Econs, M. J., Hui, S. L., Morin, P., Conneally, P. M., Joslyn, G., Curran, M. E., Peacock, M., Johnston, C. C. & Foroud, T., Dec 1998, In : Journal of Bone and Mineral Research. 13, 12, p. 1903-1908 6 p.

Research output: Contribution to journalArticle

120 Scopus citations

Linkage of Structure at the Proximal Femur to Chromosomes 3, 7, 8, and 19

Koller, D. L., White, K. E., Liu, G., Hui, S. L., Conneally, P. M., Johnston, C. C., Econs, M. J., Foroud, T. & Peacock, M., Jun 1 2003, In : Journal of Bone and Mineral Research. 18, 6, p. 1057-1065 9 p.

Research output: Contribution to journalArticle

39 Scopus citations

Linkage of the Indiana kindred of gerstmann-sträussler-scheinker disease to the prion protein gene

Dlouhy, S. R., Hsiao, K., Farlow, M. R., Foroud, T., Conneally, P. M., Johnson, P., Prusiner, S. B., Hodes, M. E. & Ghetti, B., Apr 1992, In : Nature genetics. 1, 1, p. 64-67 4 p.

Research output: Contribution to journalArticle

176 Scopus citations

Linkage of type II and type III cystinuria to 19q13.1: Codominant inheritance of two cystinuric alleles at 19q13.1 produces an extreme stone- forming phenotype

Stoller, M. L., Bruce, J. E., Bruce, C. A., Foroud, T., Kirkwood, S. C. & Stambrook, P. J., Sep 10 1999, In : American journal of medical genetics. 86, 2, p. 134-139 6 p.

Research output: Contribution to journalArticle

14 Scopus citations

Linkage scan for quantitative traits identifies new regions of interest for substance dependence in the Collaborative Study on the Genetics of Alcoholism (COGA) sample

Agrawal, A., Hinrichs, A. L., Dunn, G., Bertelsen, S., Dick, D. M., Saccone, S. F., Saccone, N. L., Grucza, R. A., Wang, J. C., Cloninger, C. R., Edenberg, H. J., Foroud, T., Hesselbrock, V., Kramer, J., Bucholz, K. K., Kuperman, S., Nurnberger, J. I., Porjesz, B., Schuckit, M. A., Goate, A. M. & 1 others, Bierut, L. J., Jan 11 2008, In : Drug and Alcohol Dependence. 93, 1-2, p. 12-20 9 p.

Research output: Contribution to journalArticle

55 Scopus citations

Linkage screen for BMD phenotypes in male and female COP and DA rat strains

Koller, D. L., Liu, L., Alam, I., Sun, Q., Econs, M. J., Foroud, T. & Turner, C. H., Sep 1 2008, In : Journal of Bone and Mineral Research. 23, 9, p. 1382-1388 7 p.

Research output: Contribution to journalArticle

7 Scopus citations

Localization of an ataxia-telangiectasia gene to chromosome 11q22-23

Gatti, R. A., Berkel, I., Boder, E., Braedt, G., Charmley, P., Concannon, P., Ersoy, F., Foroud, T., Jaspers, N. G. J., Lange, K., Lathrop, G. M., Leppert, M., Nakamura, Y., O'Connell, P., Paterson, M., Salser, W., Sanal, O., Silver, J., Sparkes, R. S., Susi, E. & 4 others, Weeks, D. E., Wei, S., White, R. & Yoder, F., Jan 1 1988, In : Nature. 336, 6199, p. 577-580 4 p.

Research output: Contribution to journalArticle

516 Scopus citations

Localization of an ataxia-telangiectasia locus to a 3-cM interval on chromosome 11q23: Linkage analysis of III families by an international consortium

Foroud, T., Wei, S., Ziv, Y., Sobel, E., Lange, E., Chao, A., Goradia, T., Huo, Y., Tolun, A., Chessa, L., Charmley, P., Sanal, O., Salman, N., Julier, C., Concannon, P., McConville, C., Taylor, A. M. R., Shiloh, Y., Lange, K. & Gatti, R. A., Dec 1 1991, In : American Journal of Human Genetics. 49, 6, p. 1263-1279 17 p.

Research output: Contribution to journalArticle

42 Scopus citations

Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32

Nichols, W. C., Koller, D. L., Slovis, B., Foroud, T., Terry, V. H., Arnold, N. D., Siemieniak, D. R., Wheeler, L., Phillips, J. A., Newman, J. H., Conneally, P. M., Ginsburg, D. & Loyd, J. E., Mar 1 1997, In : Nature genetics. 15, 3, p. 277-280 4 p.

Research output: Contribution to journalArticle

220 Scopus citations

Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees

Schulze, T. G., Buervenich, S., Badner, J. A., Steele, C. J. M., Detera-Wadleigh, S. D., Dick, D., Foroud, T., Cox, N. J., MacKinnon, D. F., Potash, J. B., Berrettini, W. H., Byerley, W., Coryell, W., DePaulo, J. R., Gershon, E. S., Kelsoe, J. R., McInnis, M. G., Murphy, D. L., Reich, T., Scheftner, W. & 2 others, Nurnberger, J. I. & McMahon, F. J., Jul 1 2004, In : Biological psychiatry. 56, 1, p. 18-23 6 p.

Research output: Contribution to journalArticle

57 Scopus citations

Locus heterogeneity of autosomal dominant osteopetrosis (ADO)

White, K. E., Koller, D. L., Takacs, I., Buckwalter, K. A., Foroud, T. & Econs, M. J., Jan 1 1999, In : Journal of Clinical Endocrinology and Metabolism. 84, 3, p. 1047-1051 5 p.

Research output: Contribution to journalArticle

15 Scopus citations

Longitudinal Change of Clinical and Biological Measures in Early Parkinson's Disease: Parkinson's Progression Markers Initiative Cohort

the Parkinson's Progression Marker Initiative*, May 2018, In : Movement Disorders. 33, 5, p. 771-782 12 p.

Research output: Contribution to journalArticle

21 Scopus citations

Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers

Kirkwood, S. C., Siemers, E., Stout, J. C., Hodes, M. E., Conneally, P. M., Christian, J. C. & Foroud, T., May 1 1999, In : Archives of Neurology. 56, 5, p. 563-568 6 p.

Research output: Contribution to journalArticle

89 Scopus citations

Longitudinal personality changes among presymptomatic Huntington disease gene carriers

Kirkwood, S. C., Siemers, E., Viken, R., Hodes, M. E., Conneally, P. M., Christian, J. C. & Foroud, T., Sep 1 2002, In : Neuropsychiatry, Neuropsychology and Behavioral Neurology. 15, 3, p. 192-197 6 p.

Research output: Contribution to journalArticle

52 Scopus citations

LRRK2 mutation analysis in Parkinson disease families with evidence of linkage to PARK8

Nichols, W. C., Elsaesser, V. E., Pankratz, N., Pauciulo, M. W., Marek, D. K., Halter, C. A., Rudolph, A., Shults, C. W. & Foroud, T., Oct 2007, In : Neurology. 69, 18, p. 1737-1744 8 p.

Research output: Contribution to journalArticle

44 Scopus citations

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease

Haugarvoll, K., Rademakers, R., Kachergus, J. M., Nuytemans, K., Ross, O. A., Gibson, J. M., Tan, E. K., Gaig, C., Tolosa, E., Goldwurm, S., Guidi, M., Riboldazzi, G., Brown, L., Walter, U., Benecke, R., Berg, D., Gasser, T., Theuns, J., Pals, P., Cras, P. & 14 others, De Deyn, P. P., Engelborghs, S., Pickut, B., Uitti, R. J., Foroud, T., Nichols, W. C., Hagenah, J., Klein, C., Samii, A., Zabetian, C. P., Bonifati, V., Van Broeckhoven, C., Farrer, M. J. & Wszolek, Z. K., Apr 2008, In : Neurology. 70, 16 PART 2, p. 1456-1460 5 p.

Research output: Contribution to journalArticle

89 Scopus citations

Mapping of QTL influencing saccharin consumption in the selectively bred alcohol-preferring and -nonpreferring rat lines

Foroud, T., Bice, P., Castelluccio, P., Bo, R., Ritchotte, A., Stewart, R., Lumeng, L., Li, T. K. & Carr, L., Apr 15 2002, In : Behavior Genetics. 32, 1, p. 57-67 11 p.

Research output: Contribution to journalArticle

20 Scopus citations

Marital status, alcohol dependence, and GABRA2: Evidence for gene-environment correlation and interaction

Dick, D. M., Agrawal, A., Schuckit, M. A., Bierut, L., Hinrichs, A., Fox, L., Mullaney, J., Cloninger, C. R., Hesselbrock, V., Nurnberger, J. I., Almasy, L., Foroud, T., Porjesz, B., Edenberg, H. & Begleiter, H., Mar 2006, In : Journal of Studies on Alcohol. 67, 2, p. 185-194 10 p.

Research output: Contribution to journalArticle

91 Scopus citations

Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease

Simon, D. K., Pankratz, N., Kissell, D. K., Pauciulo, M. W., Halter, C. A., Rudolph, A., Pfeiffer, R. F., Nichols, W. C. & Foroud, T., Apr 1 2010, In : BMC Medical Genetics. 11, 1, 53.

Research output: Contribution to journalArticle

21 Scopus citations

Measurement invariance of DSM-IV alcohol, marijuana and cocaine dependence between community-sampled and clinically overselected studies

Derringer, J., Krueger, R. F., Dick, D. M., Agrawal, A., Bucholz, K. K., Foroud, T., Grucza, R. A., Hesselbrock, M. N., Hesselbrock, V., Kramer, J., Nurnberger, J. I., Schuckit, M., Bierut, L. J., Iacono, W. G. & Mcgue, M., Oct 1 2013, In : Addiction. 108, 10, p. 1767-1776 10 p.

Research output: Contribution to journalArticle

12 Scopus citations

Meta-Analyses of Externalizing Disorders: Genetics or Prenatal Alcohol Exposure?

Wetherill, L., Foroud, T. & Goodlett, C., Jan 1 2017, (Accepted/In press) In : Alcoholism: Clinical and Experimental Research.

Research output: Contribution to journalArticle

Meta-analysis confirms CR1, CLU, and PICALM as Alzheimer disease risk loci and reveals interactions with APOE genotypes

Jun, G., Naj, A. C., Beecham, G. W., Wang, L. S., Buros, J., Gallins, P. J., Buxbaum, J. D., Ertekin-Taner, N., Fallin, M. D., Friedland, R., Inzelberg, R., Kramer, P., Rogaeva, E., St George-Hyslop, P., Cantwell, L. B., Dombroski, B. A., Saykin, A. J., Reiman, E. M., Bennett, D. A., Morris, J. C. & 16 others, Lunetta, K. L., Martin, E. R., Montine, T. J., Goate, A. M., Blacker, D., Tsuang, D. W., Beekly, D., Cupples, L. A., Hakonarson, H., Kukull, W., Foroud, T. M., Haines, J., Mayeux, R., Farrer, L. A., Pericak-Vance, M. A. & Schellenberg, G. D., Dec 2010, In : Archives of Neurology. 67, 12, p. 1473-1484 12 p.

Research output: Contribution to journalArticle

284 Scopus citations

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

Lambert, J. C., Ibrahim-Verbaas, C. A., Harold, D., Naj, A. C., Sims, R., Bellenguez, C., Jun, G., DeStefano, A. L., Bis, J. C., Beecham, G. W., Grenier-Boley, B., Russo, G., Thornton-Wells, T. A., Jones, N., Smith, A. V., Chouraki, V., Thomas, C., Ikram, M. A., Zelenika, D., Vardarajan, B. N. & 162 others, Kamatani, Y., Lin, C. F., Gerrish, A., Schmidt, H., Kunkle, B., Fiévet, N., Amouyel, P., Pasquier, F., Deramecourt, V., De Bruijn, R. F. A. G., Amin, N., Hofman, A., Van Duijn, C. M., Dunstan, M. L., Hollingworth, P., Owen, M. J., O'Donovan, M. C., Jones, L., Holmans, P. A., Moskvina, V., Williams, J., Baldwin, C., Farrer, L. A., Choi, S. H., Lunetta, K. L., Fitzpatrick, A. L., Harris, T. B., Psaty, B. M., Gilbert, J. R., Hamilton-Nelson, K. L., Martin, E. R., Pericak-Vance, M. A., Haines, J. L., Gudnason, V., Jonsson, P. V., Eiriksdottir, G., Bihoreau, M. T., Lathrop, M., Valladares, O., Cantwell, L. B., Wang, L. S., Schellenberg, G. D., Ruiz, A., Boada, M., Reitz, C., Mayeux, R., Ramirez, A., Maier, W., Hanon, O., Kukull, W. A., Buxbaum, J. D., Campion, D., Wallon, D., Hannequin, D., Crane, P. K., Larson, E. B., Becker, T., Cruchaga, C., Goate, A. M., Craig, D., Johnston, J. A., Mc-Guinness, B., Todd, S., Passmore, P., Berr, C., Ritchie, K., Lopez, O. L., De Jager, P. L., Evans, D., Lovestone, S., Proitsi, P., Powell, J. F., Letenneur, L., Barberger-Gateau, P., Dufouil, C., Dartigues, J. F., Morón, F. J., Rubinsztein, D. C., St. George-Hyslop, P., Sleegers, K., Bettens, K., Van Broeckhoven, C., Huentelman, M. J., Gill, M., Brown, K., Morgan, K., Kamboh, M. I., Keller, L., Fratiglioni, L., Green, R., Myers, A. J., Love, S., Rogaeva, E., Gallacher, J., Bayer, A., Clarimon, J., Lleo, A., Tsuang, D. W., Yu, L., Bennett, D. A., Tsolaki, M., Bossù, P., Spalletta, G., Collinge, J., Mead, S., Sorbi, S., Nacmias, B., Sanchez-Garcia, F., Deniz Naranjo, M. C., Fox, N. C., Hardy, J., Bosco, P., Clarke, R., Brayne, C., Galimberti, D., Mancuso, M., Matthews, F., Moebus, S., Mecocci, P., Del Zompo, M., Hampel, H., Pilotto, A., Bullido, M., Panza, F., Caffarra, P., Mayhaus, M., Pichler, S., Gu, W., Riemenschneider, M., Lannfelt, L., Ingelsson, M., Hakonarson, H., Carrasquillo, M. M., Zou, F., Younkin, S. G., Beekly, D., Alvarez, V., Coto, E., Razquin, C., Pastor, P., Mateo, I., Combarros, O., Faber, K. M., Foroud, T. M., Soininen, H., Hiltunen, M., Blacker, D., Mosley, T. H., Graff, C., Holmes, C., Montine, T. J., Rotter, J. I., Brice, A., Nalls, M. A., Kauwe, J. S. K., Boerwinkle, E., Schmidt, R., Rujescu, D., Tzourio, C., Nöthen, M. M., Launer, L. J. & Seshadri, S., Dec 1 2013, In : Nature genetics. 45, 12, p. 1452-1458 7 p.

Research output: Contribution to journalArticle

1614 Scopus citations

Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity

Edwards, A. C., Deak, J. D., Gizer, I. R., Lai, D., Chatzinakos, C., Wilhelmsen, K. P., Lindsay, J., Heron, J., Hickman, M., Webb, B. T., Bacanu, S. A., Foroud, T. M., Kendler, K. S., Dick, D. M. & Schuckit, M. A., Dec 2018, In : Alcoholism: Clinical and Experimental Research. 42, 12, p. 2349-2359 11 p.

Research output: Contribution to journalArticle

5 Scopus citations

Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone mass

Ioannidis, J. P. A., Ng, M. Y., Sham, P. C., Zintzaras, E., Lewis, C. M., Deng, H. W., Econs, M. J., Karasik, D., Devoto, M., Kammerer, C. M., Spector, T., Andrew, T., Cupples, L. A., Duncan, E. L., Foroud, T., Kiel, D. P., Koller, D., Langdahl, B., Mitchell, B. D., Peacock, M. & 8 others, Recker, R., Shen, H., Sol-Church, K., Spotila, L. D., Uitterlinden, A. G., Wilson, S. G., Kung, A. W. C. & Ralston, S. H., Feb 1 2007, In : Journal of Bone and Mineral Research. 22, 2, p. 173-183 11 p.

Research output: Contribution to journalArticle

130 Scopus citations

Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women

Koller, D. L., Zheng, H. F., Karasik, D., Yerges-Armstrong, L., Liu, C. T., McGuigan, F., Kemp, J. P., Giroux, S., Lai, D., Edenberg, H. J., Peacock, M., Czerwinski, S. A., Choh, A. C., McMahon, G., St Pourcain, B., Timpson, N. J., Lawlor, D. A., Evans, D. M., Towne, B., Blangero, J. & 14 others, Carless, M. A., Kammerer, C., Goltzman, D., Kovacs, C. S., Prior, J. C., Spector, T. D., Rousseau, F., Tobias, J. H., Akesson, K., Econs, M. J., Mitchell, B. D., Richards, J. B., Kiel, D. P. & Foroud, T., Mar 1 2013, In : Journal of Bone and Mineral Research. 28, 3, p. 547-558 12 p.

Research output: Contribution to journalArticle

56 Scopus citations

Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2

Pankratz, N., Beecham, G. W., Destefano, A. L., Dawson, T. M., Doheny, K. F., Factor, S. A., Hamza, T. H., Hung, A. Y., Hyman, B. T., Ivinson, A. J., Krainc, D., Latourelle, J. C., Clark, L. N., Marder, K., Martin, E. R., Mayeux, R., Ross, O. A., Scherzer, C. R., Simon, D. K., Tanner, C. & 7 others, Vance, J. M., Wszolek, Z. K., Zabetian, C. P., Myers, R. H., Payami, H., Scott, W. K. & Foroud, T., Mar 1 2012, In : Annals of Neurology. 71, 3, p. 370-384 15 p.

Research output: Contribution to journalArticle

151 Scopus citations

Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci

Understanding Society Scientific Group, EPIC-CVD, GSCAN, Consortium for Genetics of Smoking Behaviour, CHD Exome+ consortium, Jan 1 2019, (Accepted/In press) In : Molecular Psychiatry.

Research output: Contribution to journalArticle

Open Access
3 Scopus citations

Motor changes in presymptomatic Huntington disease gene carriers

Siemers, E., Foroud, T., Bill, D. J., Sorbel, J., Norton, J. A., Hodes, M. E., Niebler, G., Conneally, P. M. & Christian, J. C., Jun 1996, In : Archives of Neurology. 53, 6, p. 487-492 6 p.

Research output: Contribution to journalArticle

60 Scopus citations

Multimodal Hippocampal Subfield Grading For Alzheimer’s Disease Classification

Alzheimer’s Disease Neuroimaging Initiative, Dec 1 2019, In : Scientific reports. 9, 1, 13845.

Research output: Contribution to journalArticle

Open Access

Multiple step pattern as a biomarker in Parkinson disease

Blekher, T., Weaver, M., Rupp, J., Nichols, W. C., Hui, S. L., Gray, J., Yee, R. D., Wojcieszek, J. & Foroud, T., Aug 1 2009, In : Parkinsonism and Related Disorders. 15, 7, p. 506-510 5 p.

Research output: Contribution to journalArticle

43 Scopus citations

Mutations in COQ2 in familial and sporadic multiple-system atrophy the multiple-system atrophy research collaboration

Mitsui, J., Matsukawa, T., Ishiura, H., Fukuda, Y., Ichikawa, Y., Date, H., Ahsan, B., Nakahara, Y., Momose, Y., Takahashi, Y., Iwata, A., Goto, J., Yamamoto, Y., Komata, M., Shirahige, K., Hara, K., Kakita, A., Yamada, M., Takahashi, H., Onodera, O. & 54 others, Nishizawa, M., Takashima, H., Kuwano, R., Watanabe, H., Ito, M., Sobue, G., Soma, H., Yabe, I., Sasaki, H., Aoki, M., Ishikawa, K., Mizusawa, H., Kanai, K., Hattori, T., Kuwabara, S., Arai, K., Koyano, S., Kuroiwa, Y., Hasegawa, K., Yuasa, T., Yasui, K., Nakashima, K., Ito, H., Izumi, Y., Kaji, R., Kato, T., Kusunoki, S., Osaki, Y., Horiuchi, M., Kondo, T., Murayama, S., Hattori, N., Yamamoto, M., Murata, M., Satake, W., Toda, T., Dürr, A., Brice, A., Filla, A., Klockgether, T., Wallner, U., Nicholson, G., Gilman, S., Shults, C. W., Tanner, C. M., Kukull, W. A., Lee, V. M. Y., Masliah, E., Low, P. A., Sandroni, P., Trojanowski, J. Q., Ozelius, L., Foroud, T. & Tsuji, S., Jan 1 2013, In : New England Journal of Medicine. 369, 3, p. 233-244 12 p.

Research output: Contribution to journalArticle

164 Scopus citations

Mutations in DJ-1 are rare in familial Parkinson disease

Pankratz, N., Pauciulo, M. W., Elsaesser, V. E., Marek, D. K., Halter, C. A., Wojcieszek, J., Rudolph, A., Shults, C. W., Foroud, T. & Nichols, W. C., Nov 20 2006, In : Neuroscience Letters. 408, 3, p. 209-213 5 p.

Research output: Contribution to journalArticle

33 Scopus citations

Mutations in GBA are associated with familial Parkinson disease susceptibility and age at onset

Nichols, W. C., Pankratz, N., Marek, D. K., Pauciulo, M. W., Elsaesser, V. E., Halter, C. A., Rudolph, A., Wojcieszek, J., Pfeiffer, R. F. & Foroud, T., Jan 27 2009, In : Neurology. 72, 4, p. 310-316 7 p.

Research output: Contribution to journalArticle

122 Scopus citations

Mutations in LRRK2 other than G2019S are rare in a north-American based sample of familial Parkinson's didease

Pankratz, N., Pauciulo, M. W., Elsaesser, V. E., Marek, D. K., Halter, C. A., Rudolph, A., Shults, C. W., Foroud, T., Nichols, W. C., Shults, C., Marshall, F., Oakes, D., Shinaman, A., Marder, K., Conneally, P. M., Lyons, K., Siemers, E., Factor, S., Higgins, D., Evans, S. & 79 others, Shill, H., Stacy, M., Danielson, J., Marlor, L., Williamson, K., Jankovic, J., Hunter, C., Simon, D., Ryan, P., Scollins, L., Saunders-Pullman, R., Boyar, K., Costan-Toth, C., Ohmann, E., Sudarsky, L., Joubert, C., Friedman, J., Chou, K., Fernandez, H., Lannon, M., Galvez-Jimenez, N., Podichetty, A., Lewitt, P., DeAngelis, M., O'Brien, C., Seeberger, L., Dingmann, C., Judd, D., Fraser, J., Harris, J., Bertoni, J., Peterson, C., Chouinard, S., Panisset, M., Hall, J., Poiffaut, H., Calabrese, V., Roberge, P., Wojcieszek, J., Belden, J., Halter, C., Jennings, D., Marek, K., Mendick, S., Reich, S., Dunlop, B., Jog, M., Horn, C., Rao, J., Cook, M., Uitti, R., Turk, M., Ajax, T., Mannetter, J., Sethi, K., Carpenter, J., Ligon, K., Narayan, S., Woodward, L., Blindauer, K., Petit, J., Elmer, L., Aiken, E., Davis, K., Schell, C., Wilson, S., Velickovic, M., Koller, W., Phipps, S., Feigin, A., Gordon, M., Hamann, J., Licari, E., Marotta-Kollarus, M., Shannon, B., Winnick, R., Simuni, T., Kaczmarek, A. & Williams, K., Dec 1 2006, In : Movement Disorders. 21, 12, p. 2257-2260 4 p.

Research output: Contribution to journalArticle

23 Scopus citations

Neuropeptide Y receptor genes are associated with alcohol dependence, alcohol withdrawal phenotypes, and cocaine dependence

Wetherill, L., Schuckit, M. A., Hesselbrock, V., Xuei, X., Liang, T., Dick, D. M., Kramer, J., Nurnberger, J. I., Tischfield, J. A., Porjesz, B., Edenberg, H. J. & Foroud, T., Dec 1 2008, In : Alcoholism: Clinical and Experimental Research. 32, 12, p. 2031-2040 10 p.

Research output: Contribution to journalArticle

58 Scopus citations

New genetic loci link adipose and insulin biology to body fat distribution

ADIPOGen Consortium; CARDIOGRAMplusC4D Consortium; CKDGen Consortium; GEFOS Consortium; GENIE Consortium; GLGC; ICBP; International Endogene Consortium; LifeLines Cohort Study; MAGIC Investigators; MuTHER Consortium; PAGE Consortium; ReproGen Consortium, Feb 12 2015, In : Nature. 518, 7538, p. 187-196 10 p.

Research output: Contribution to journalArticle

532 Scopus citations

NIPT and Informed Consent: an Assessment of Patient Understanding of a Negative NIPT Result

Piechan, J. L., Hines, K. A., Koller, D. L., Stone, K., Quaid, K., Torres-Martinez, W., Wilson Mathews, D., Foroud, T. & Cook, L., Apr 1 2016, (Accepted/In press) In : Journal of Genetic Counseling. p. 1-11 11 p.

Research output: Contribution to journalArticle

19 Scopus citations

No association of the GABAA receptor genes on chromosome 5 with alcoholism in the collaborative study on the genetics of alcoholism sample

Dick, D. M., Edenberg, H. J., Xuei, X., Goate, A., Hesselbrock, V., Schuckit, M., Crowe, R. & Foroud, T., Jan 5 2005, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 132 B, 1, p. 24-28 5 p.

Research output: Contribution to journalArticle

29 Scopus citations

Non-coding variability at the APOE locus contributes to the Alzheimer’s risk

Alzheimer’s Disease Neuroimaging Initiative, Dec 1 2019, In : Nature communications. 10, 1, 3310.

Research output: Contribution to journalArticle

Open Access
1 Scopus citations