Tatiana Foroud

  • 42200 Citations
  • 101 h-Index
1976 …2021
If you made any changes in Pure, your changes will be visible here soon.

Publications 1988 2020

Filter
Article
130 Citations (Scopus)

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., 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 2007, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 22, 2, p. 173-183 11 p.

Research output: Contribution to journalArticle

Meta-Analysis
Genome
Spine
Bone and Bones
Chromosomes
56 Citations (Scopus)

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., 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., Mitchell, B. D., Richards, J. B., Kiel, D. P. & Foroud, T., Mar 2013, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 28, 3, p. 547-558 12 p.

Research output: Contribution to journalArticle

Bone Density
Single Nucleotide Polymorphism
Meta-Analysis
Genome
Spine
150 Citations (Scopus)

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 2012, In : Annals of Neurology. 71, 3, p. 370-384 15 p.

Research output: Contribution to journalArticle

Parkinson Disease
Meta-Analysis
Odds Ratio
Disease Susceptibility
Single Nucleotide Polymorphism
2 Citations (Scopus)

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
Genetic Loci
Meta-Analysis
Smoking
Nucleotides
Exome
6 Citations (Scopus)

Michael J. Fox Foundation LRRK2 Consortium: Geographical differences in returning genetic research data to study participants

Alcalay, R. N., Aasly, J., Berg, D., Bressman, S., Brice, A., Brockmann, K., Chan, P., Clark, L., Cormier, F., Corvol, J. C., Durr, A., Facheris, M., Farrer, M., Foroud, T., Gasser, T., Giladi, N., Halter, C., Lang, A., Langston, J. W., Marras, C. & 15 others, Marti-Masso, J. F., Ruiz Martinez, J., Mejia-Santana, H., Mirelman, A., Pont-Sunyer, C., Orr-Urtreger, A., Raymond, D., Saunders-Pullman, R., Schüle, B., Tanner, C., Tolosa, E., Urkowitz, A., Vilas, D., Wise, A. & Marder, K., 2014, In : Genetics in Medicine. 16, 8, p. 644-645 2 p.

Research output: Contribution to journalArticle

60 Citations (Scopus)

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

Asymptomatic Diseases
Huntington Disease
Genes
Alleles
Trinucleotide Repeats

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
Hippocampus
Alzheimer Disease
Biomarkers
Magnetic Resonance Imaging
Diffusion Magnetic Resonance Imaging
43 Citations (Scopus)

Multiple step pattern as a biomarker in Parkinson disease

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

Research output: Contribution to journalArticle

Parkinson Disease
Biomarkers
Saccades
Siblings
Aptitude
1230 Citations (Scopus)

Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura

Levy, G. G., Nichols, W. C., Lian, E. C., Foroud, T., McClintick, J., McGee, B. M., Yang, A. Y., Siemieniak, D. R., Stark, K. R., Gruppo, R., Sarode, R., Shurin, S. B., Chandrasekaran, V., Stabler, S. P., Sabio, H., Bouhassira, E. E., Upshaw, J. D., Ginsburg, D. & Tsai, H. M., Oct 4 2001, In : Nature. 413, 6855, p. 488-494 7 p.

Research output: Contribution to journalArticle

Thrombotic Thrombocytopenic Purpura
Mutation
Genes
von Willebrand Factor
Proteolysis
160 Citations (Scopus)

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., 2013, In : New England Journal of Medicine. 369, 3, p. 233-244 12 p.

Research output: Contribution to journalArticle

Multiple System Atrophy
coenzyme Q10
Mutation
Research
Cerebellar Ataxia
33 Citations (Scopus)

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

Parkinson Disease
Exons
Mutation
Multiplex Polymerase Chain Reaction
Homozygote
120 Citations (Scopus)

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

Glucosylceramidase
Disease Susceptibility
Age of Onset
Parkinson Disease
Mutation
23 Citations (Scopus)

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 2006, In : Movement Disorders. 21, 12, p. 2257-2260 4 p.

Research output: Contribution to journalArticle

Mutation
Parkinson Disease
Pedigree
58 Citations (Scopus)

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., Tischfield, J. A., Porjesz, B., Edenberg, H. & Foroud, T., Dec 2008, In : Alcoholism: Clinical and Experimental Research. 32, 12, p. 2031-2040 10 p.

Research output: Contribution to journalArticle

Neuropeptide Y Receptors
Cocaine-Related Disorders
Cocaine
Alcoholism
Genes
516 Citations (Scopus)

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

Collaborators & 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

Body Fat Distribution
Genetic Loci
Waist-Hip Ratio
Waist Circumference
Hip
18 Citations (Scopus)

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

Informed Consent
Aneuploidy
Patient Education
Down Syndrome
Pregnant Women
29 Citations (Scopus)

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

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 5
GABA-A Receptors
Alcoholism
Genes
Alcohol-Related Disorders

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
loci
Alzheimer Disease
Haplotypes
Endophenotypes
brain

Nonlinear Z-score modeling for improved detection of cognitive abnormality

ARTFL/LEFFTDS consortium, Dec 2019, In : Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring. 11, p. 797-808 12 p.

Research output: Contribution to journalArticle

Open Access
Sex Education

Nonparametric linkage and family-based association studies of a simulated complex disorder

Koller, D. L., Balding, J. & Foroud, T., 1999, In : Genetic Epidemiology. 17, SUPPL. 1

Research output: Contribution to journalArticle

Lod Score
Gene-Environment Interaction
Genetic Loci
Disease Susceptibility
Pedigree
66 Citations (Scopus)

Novel genetic loci associated with hippocampal volume

Hibar, D. P., Adams, H. H. H., Jahanshad, N., Chauhan, G., Stein, J. L., Hofer, E., Renteria, M. E., Bis, J. C., Arias-Vasquez, A., Ikram, M. K., Desrivières, S., Vernooij, M. W., Abramovic, L., Alhusaini, S., Amin, N., Andersson, M., Arfanakis, K., Aribisala, B. S., Armstrong, N. J., Athanasiu, L. & 312 others, Axelsson, T., Beecham, A. H., Beiser, A., Bernard, M., Blanton, S. H., Bohlken, M. M., Boks, M. P., Bralten, J., Brickman, A. M., Carmichael, O., Chakravarty, M. M., Chen, Q., Ching, C. R. K., Chouraki, V., Cuellar-Partida, G., Crivello, F., Den Braber, A., Doan, N. T., Ehrlich, S., Giddaluru, S., Goldman, A. L., Gottesman, R. F., Grimm, O., Griswold, M. E., Guadalupe, T., Gutman, B. A., Hass, J., Haukvik, U. K., Hoehn, D., Holmes, A. J., Hoogman, M., Janowitz, D., Jia, T., Jørgensen, K. N., Karbalai, N., Kasperaviciute, D., Kim, S., Klein, M., Kraemer, B., Lee, P. H., Liewald, D. C. M., Lopez, L. M., Luciano, M., MacAre, C., Marquand, A. F., Matarin, M., Mather, K. A., Mattheisen, M., McKay, D. R., Milaneschi, Y., Muñoz Maniega, S., Nho, K., Nugent, A. C., Nyquist, P., Loohuis, L. M. O., Oosterlaan, J., Papmeyer, M., Pirpamer, L., Pütz, B., Ramasamy, A., Richards, J. S., Risacher, S. L., Roiz-Santiañez, R., Rommelse, N., Ropele, S., Rose, E. J., Royle, N. A., Rundek, T., Sämann, P. G., Saremi, A., Satizabal, C. L., Schmaal, L., Schork, A. J., Shen, L., Shin, J., Shumskaya, E., Smith, A. V., Sprooten, E., Strike, L. T., Teumer, A., Tordesillas-Gutierrez, D., Toro, R., Trabzuni, D., Trompet, S., Vaidya, D., Van Der Grond, J., Van Der Lee, S. J., Van Der Meer, D., Van Donkelaar, M. M. J., Van Eijk, K. R., Van Erp, T. G. M., Van Rooij, D., Walton, E., Westlye, L. T., Whelan, C. D., Windham, B. G., Winkler, A. M., Wittfeld, K., Woldehawariat, G., Wolf, C., Wolfers, T., Yanek, L. R., Yang, J., Zijdenbos, A., Zwiers, M. P., Agartz, I., Almasy, L., Ames, D., Amouyel, P., Andreassen, O. A., Arepalli, S., Assareh, A. A., Barral, S., Bastin, M. E., Becker, D. M., Becker, J. T., Bennett, D. A., Blangero, J., Van Bokhoven, H., Boomsma, D. I., Brodaty, H., Brouwer, R. M., Brunner, H. G., Buckner, R. L., Buitelaar, J. K., Bulayeva, K. B., Cahn, W., Calhoun, V. D., Cannon, D. M., Cavalleri, G. L., Cheng, C. Y., Cichon, S., Cookson, M. R., Corvin, A., Crespo-Facorro, B., Curran, J. E., Czisch, M., Dale, A. M., Davies, G. E., De Craen, A. J. M., De Geus, E. J. C., De Jager, P. L., De Zubicaray, G. I., Deary, I. J., Debette, S., Decarli, C., Delanty, N., Depondt, C., Destefano, A., Dillman, A., Djurovic, S., Donohoe, G., Drevets, W. C., Duggirala, R., Dyer, T. D., Enzinger, C., Erk, S., Espeseth, T., Fedko, I. O., Fernández, G., Ferrucci, L., Fisher, S. E., Fleischman, D. A., Ford, I., Fornage, M., Foroud, T., Fox, P. T., Francks, C., Fukunaga, M., Gibbs, J. R., Glahn, D. C., Gollub, R. L., Göring, H. H. H., Green, R. C., Gruber, O., Gudnason, V., Guelfi, S., Håberg, A. K., Hansell, N. K., Hardy, J., Hartman, C. A., Hashimoto, R., Hegenscheid, K., Heinz, A., Le Hellard, S., Hernandez, D. G., Heslenfeld, D. J., Ho, B. C., Hoekstra, P. J., Hoffmann, W., Hofman, A., Holsboer, F., Homuth, G., Hosten, N., Hottenga, J. J., Huentelman, M., Pol, H. E. H., Ikeda, M., Jack, C. R., Jenkinson, M., Johnson, R., Jönsson, E. G., Jukema, J. W., Kahn, R. S., Kanai, R., Kloszewska, I., Knopman, D. S., Kochunov, P., Kwok, J. B., Lawrie, S. M., Lemaître, H., Liu, X., Longo, D. L., Lopez, O. L., Lovestone, S., Martinez, O., Martinot, J. L., Mattay, V. S., McDonald, C., McIntosh, A. M., McMahon, F. J., McMahon, K. L., Mecocci, P., Melle, I., Meyer-Lindenberg, A., Mohnke, S., Montgomery, G. W., Morris, D. W., Mosley, T. H., Mühleisen, T. W., Müller-Myhsok, B., Nalls, M. A., Nauck, M., Nichols, T. E., Niessen, W. J., Nöthen, M. M., Nyberg, L., Ohi, K., Olvera, R. L., Ophoff, R. A., Pandolfo, M., Paus, T., Pausova, Z., Penninx, B. W. J. H., Pike, G. B., Potkin, S. G., Psaty, B. M., Reppermund, S., Rietschel, M., Roffman, J. L., Romanczuk-Seiferth, N., Rotter, J. I., Ryten, M., Sacco, R. L., Sachdev, P. S., Saykin, A., Schmidt, R., Schmidt, H., Schofield, P. R., Sigursson, S., Simmons, A., Singleton, A., Sisodiya, S. M., Smith, C., Smoller, J. W., Soininen, H., Steen, V. M., Stott, D. J., Sussmann, J. E., Thalamuthu, A., Toga, A. W., Traynor, B. J., Troncoso, J., Tsolaki, M., Tzourio, C., Uitterlinden, A. G., Hernández, M. C. V., Van Der Brug, M., Van Der Lugt, A., Van Der Wee, N. J. A., Van Haren, N. E. M., Van 'T Ent, D., Van Tol, M. J., Vardarajan, B. N., Vellas, B., Veltman, D. J., Völzke, H., Walter, H., Wardlaw, J. M., Wassink, T. H., Weale, M. E., Weinberger, D. R., Weiner, M. W., Wen, W., Westman, E., White, T., Wong, T. Y., Wright, C. B., Zielke, R. H., Zonderman, A. B., Martin, N. G., Van Duijn, C. M., Wright, M. J., Longstreth, W. T., Schumann, G., Grabe, H. J., Franke, B., Launer, L. J., Medland, S. E., Seshadri, S., Thompson, P. M. & Ikram, M. A., Jan 18 2017, In : Nature Communications. 8, 13624.

Research output: Contribution to journalArticle

Genetic Loci
loci
Hippocampus
Genes
Episodic Memory
64 Citations (Scopus)

Novel genetic loci underlying human intracranial volume identified through genome-wide association

Adams, H. H. H., Hibar, D. P., Chouraki, V., Stein, J. L., Nyquist, P. A., Rentería, M. E., Trompet, S., Arias-Vasquez, A., Seshadri, S., Desrivières, S., Beecham, A. H., Jahanshad, N., Wittfeld, K., van der Lee, S. J., Abramovic, L., Alhusaini, S., Amin, N., Andersson, M., Arfanakis, K., Aribisala, B. S. & 322 others, Armstrong, N. J., Athanasiu, L., Axelsson, T., Beiser, A., Bernard, M., Bis, J. C., Blanken, L. M. E., Blanton, S. H., Bohlken, M. M., Boks, M. P., Bralten, J., Brickman, A. M., Carmichael, O., Chakravarty, M. M., Chauhan, G., Chen, Q., Ching, C. R. K., Cuellar-Partida, G., Braber, A. D., Doan, N. T., Ehrlich, S., Filippi, I., Ge, T., Giddaluru, S., Goldman, A. L., Gottesman, R. F., Greven, C. U., Grimm, O., Griswold, M. E., Guadalupe, T., Hass, J., Haukvik, U. K., Hilal, S., Hofer, E., Hoehn, D., Holmes, A. J., Hoogman, M., Janowitz, D., Jia, T., Kasperaviciute, D., Kim, S., Klein, M., Kraemer, B., Lee, P. H., Liao, J., Liewald, D. C. M., Lopez, L. M., Luciano, M., Macare, C., Marquand, A., Matarin, M., Mather, K. A., Mattheisen, M., Mazoyer, B., McKay, D. R., McWhirter, R., Milaneschi, Y., Mirza-Schreiber, N., Muetzel, R. L., Maniega, S. M., Nho, K., Nugent, A. C., Loohuis, L. M. O., Oosterlaan, J., Papmeyer, M., Pappa, I., Pirpamer, L., Pudas, S., Pütz, B., Rajan, K. B., Ramasamy, A., Richards, J. S., Risacher, S. L., Roiz-Santiañez, R., Rommelse, N., Rose, E. J., Royle, N. A., Rundek, T., Sämann, P. G., Satizabal, C. L., Schmaal, L., Schork, A. J., Shen, L., Shin, J., Shumskaya, E., Smith, A. V., Sprooten, E., Strike, L. T., Teumer, A., Thomson, R., Tordesillas-Gutierrez, D., Toro, R., Trabzuni, D., Vaidya, D., van der Grond, J., van der Meer, D., van Donkelaar, M. M. J., van Eijk, K. R., van Erp, T. G. M., van Rooij, D., Walton, E., Westlye, L. T., Whelan, C. D., Windham, B. G., Winkler, A. M., Woldehawariat, G., Wolf, C., Wolfers, T., Xu, B., Yanek, L. R., Yang, J., Zijdenbos, A., Zwiers, M. P., Agartz, I., Aggarwal, N. T., Almasy, L., Ames, D., Amouyel, P., Andreassen, O. A., Arepalli, S., Assareh, A. A., Barral, S., Bastin, M. E., Becker, D. M., Becker, J. T., Bennett, D. A., Blangero, J., van Bokhoven, H., Boomsma, D. I., Brodaty, H., Brouwer, R. M., Brunner, H. G., Buckner, R. L., Buitelaar, J. K., Bulayeva, K. B., Cahn, W., Calhoun, V. D., Cannon, D. M., Cavalleri, G. L., Chen, C., Cheng, C. Y., Cichon, S., Cookson, M. R., Corvin, A., Crespo-Facorro, B., Curran, J. E., Czisch, M., Dale, A. M., Davies, G. E., de Geus, E. J. C., de Jager, P. L., de Zubicaray, G. I., Delanty, N., Depondt, C., DeStefano, A. L., Dillman, A., Djurovic, S., Donohoe, G., Drevets, W. C., Duggirala, R., Dyer, T. D., Erk, S., Espeseth, T., Evans, D. A., Fedko, I. O., Fernández, G., Ferrucci, L., Fisher, S. E., Fleischman, D. A., Ford, I., Foroud, T. M., Fox, P. T., Francks, C., Fukunaga, M., Gibbs, J. R., Glahn, D. C., Gollub, R. L., Göring, H. H. H., Grabe, H. J., Green, R. C., Gruber, O., Gudnason, V., Guelfi, S., Hansell, N. K., Hardy, J., Hartman, C. A., Hashimoto, R., Hegenscheid, K., Heinz, A., Le Hellard, S., Hernandez, D. G., Heslenfeld, D. J., Ho, B. C., Hoekstra, P. J., Hoffmann, W., Hofman, A., Holsboer, F., Homuth, G., Hosten, N., Hottenga, J. J., Pol, H. E. H., Ikeda, M., Ikram, M. K., Jr, C. R. J., Jenkinson, M., Johnson, R., Jönsson, E. G., Jukema, J. W., Kahn, R. S., Kanai, R., Kloszewska, I., Knopman, D. S., Kochunov, P., Kwok, J. B., Lawrie, S. M., Lemaître, H., Liu, X., Longo, D. L., Jr, W. T. L., Lopez, O. L., Lovestone, S., Martinez, O., Martinot, J. L., Mattay, V. S., McDonald, C., McIntosh, A. M., McMahon, K. L., McMahon, F. J., Mecocci, P., Melle, I., Meyer-Lindenberg, A., Mohnke, S., Montgomery, G. W., Morris, D. W., Mosley, T. H., Mühleisen, T. W., Müller-Myhsok, B., Nalls, M. A., Nauck, M., Nichols, T. E., Niessen, W. J., Nöthen, M. M., Nyberg, L., Ohi, K., Olvera, R. L., Ophoff, R. A., Pandolfo, M., Paus, T., Pausova, Z., Penninx, B. W. J. H., Pike, G. B., Potkin, S. G., Psaty, B. M., Reppermund, S., Rietschel, M., Roffman, J. L., Romanczuk-Seiferth, N., Rotter, J. I., Ryten, M., Sacco, R. L., Sachdev, P. S., Saykin, A. J., Schmidt, R., Schofield, P. R., Sigurdsson, S., Simmons, A., Singleton, A., Sisodiya, S. M., Smith, C., Smoller, J. W., Soininen, H., Srikanth, V., Steen, V. M., Stott, D. J., Sussmann, J. E., Thalamuthu, A., Tiemeier, H., Toga, A. W., Traynor, B. J., Troncoso, J., Turner, J. A., Tzourio, C., Uitterlinden, A. G., Hernández, M. C. V., van der Brug, M., van der Lugt, A., van der Wee, N. J. A., van Duijn, C. M., van Haren, N. E. M., van ′t Ent, D., van Tol, M. J., Vardarajan, B. N., Veltman, D. J., Vernooij, M. W., Völzke, H., Walter, H., Wardlaw, J. M., Wassink, T. H., Weale, M. E., Weinberger, D. R., Weiner, M. W., Wen, W., Westman, E., White, T., Wong, T. Y., Wright, C. B., Zielke, H. R., Zonderman, A. B., Deary, I. J., DeCarli, C., Schmidt, H., Martin, N. G., de Craen, A. J. M., Wright, M. J., Launer, L. J., Schumann, G., Fornage, M., Franke, B., Debette, S., Medland, S. E., Ikram, M. A. & Thompson, P. M., Oct 3 2016, (Accepted/In press) In : Nature Neuroscience.

Research output: Contribution to journalArticle

Genetic Loci
Genome
Genome-Wide Association Study
Phosphatidylinositol 3-Kinases
Cognition
5 Citations (Scopus)

Novel recruitment strategy to enrich for lrrk2 mutation carriers

Foroud, T., Smith, D., Jackson, J., Verbrugge, J., Halter, C., Wetherill, L., Sims, K., Xin, W., Arnedo, V., Lasch, S. & Marek, K., Jan 1 2015, In : Molecular Genetics and Genomic Medicine. 3, 5, p. 404-412 9 p.

Research output: Contribution to journalArticle

Open Access
Mutation
Parkinson Disease
Internet
Biomarkers
Clinical Trials
62 Citations (Scopus)

Oculomotor control in asymptomatic and recently diagnosed individuals with the genetic marker for Huntington's disease

Blekher, T. M., Yee, R. D., Kirkwood, S. C., Hake, A., Stout, J. C., Weaver, M. R. & Foroud, T., Oct 2004, In : Vision Research. 44, 23, p. 2729-2736 8 p.

Research output: Contribution to journalArticle

Saccades
Huntington Disease
Genetic Markers
Optokinetic Nystagmus
Genes
5 Citations (Scopus)

Ondansetron blocks wild-type and p.F503l variant small-conductance Ca2+-activated K+ channels

Ko, J. S., Guo, S., Hassel, J., Celestino-Soper, P., Lynnes, T. C., Tisdale, J. E., Zheng, J. J., Taylor, S. E., Foroud, T., Murray, M., Kovacs, R., Li, X., Lin, S-F., Chen, Z., Vatta, M., Chen, P-S. & Rubart-von der Lohe, M., Aug 1 2018, In : American Journal of Physiology - Heart and Circulatory Physiology. 315, 2, p. H375-H388

Research output: Contribution to journalArticle

Calcium-Activated Potassium Channels
Ondansetron
Long QT Syndrome
Serotonin 5-HT3 Receptor Antagonists
Receptors, Serotonin, 5-HT3
1 Citation (Scopus)

Parametric linkage analysis and disequilibrium methods to identify loci for complex disease

McClintick, J., Koller, D. L., Pankratz, N., Kirkwood, S. C., Naughton, B. & Foroud, T., 2001, In : Genetic Epidemiology. 21, SUPPL. 1

Research output: Contribution to journalArticle

Linkage Disequilibrium
Haplotypes
Phenotype
Base Pairing
Alleles
237 Citations (Scopus)

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

Perry, J. R. B., Day, F., Elks, C. E., Sulem, P., Thompson, D. J., Ferreira, T., He, C., Chasman, D. I., Esko, T., Thorleifsson, G., Albrecht, E., Ang, W. Q., Corre, T., Cousminer, D. L., Feenstra, B., Franceschini, N., Ganna, A., Johnson, A. D., Kjellqvist, S., Lunetta, K. L. & 178 others, McMahon, G., Nolte, I. M., Paternoster, L., Porcu, E., Smith, A. V., Stolk, L., Teumer, A., Tšernikova, N., Tikkanen, E., Ulivi, S., Wagner, E. K., Amin, N., Bierut, L. J., Byrne, E. M., Hottenga, J. J., Koller, D. L., Mangino, M., Pers, T. H., Yerges-Armstrong, L. M., Zhao, J. H., Andrulis, I. L., Anton-Culver, H., Atsma, F., Bandinelli, S., Beckmann, M. W., Benitez, J., Blomqvist, C., Bojesen, S. E., Bolla, M. K., Bonanni, B., Brauch, H., Brenner, H., Buring, J. E., Chang-Claude, J., Chanock, S., Chen, J., Chenevix-Trench, G., Collée, J. M., Couch, F. J., Couper, D., Coviello, A. D., Cox, A., Czene, K., D'adamo, A. P., Smith, G. D., De Vivo, I., Demerath, E. W., Dennis, J., Devilee, P., Dieffenbach, A. K., Dunning, A. M., Eiriksdottir, G., Eriksson, J. G., Fasching, P. A., Ferrucci, L., Flesch-Janys, D., Flyger, H., Foroud, T., Franke, L., Garcia, M. E., García-Closas, M., Geller, F., De Geus, E. E. J., Giles, G. G., Gudbjartsson, D. F., Gudnason, V., Guénel, P., Guo, S., Hall, P., Hamann, U., Haring, R., Hartman, C. A., Heath, A. C., Hofman, A., Hooning, M. J., Hopper, J. L., Hu, F. B., Hunter, D. J., Karasik, D., Kiel, D. P., Knight, J. A., Kosma, V. M., Kutalik, Z., Lai, S., Lambrechts, D., Lindblom, A., Mägi, R., Magnusson, P. K., Mannermaa, A., Martin, N. G., Masson, G., McArdle, P. F., McArdle, W. L., Melbye, M., Michailidou, K., Mihailov, E., Milani, L., Milne, R. L., Nevanlinna, H., Neven, P., Nohr, E. A., Oldehinkel, A. J., Oostra, B. A., Palotie, A., Peacock, M., Pedersen, N. L., Peterlongo, P., Peto, J., Pharoah, P. D. P., Postma, D. S., Pouta, A., Pylkäs, K., Radice, P., Ring, S., Rivadeneira, F., Robino, A., Rose, L. M., Rudolph, A., Salomaa, V., Sanna, S., Schlessinger, D., Schmidt, M. K., Southey, M. C., Sovio, U., Stampfer, M. J., Stöckl, D., Storniolo, A. M., Timpson, N. J., Tyrer, J., Visser, J. A., Vollenweider, P., Völzke, H., Waeber, G., Waldenberger, M., Wallaschofski, H., Wang, Q., Willemsen, G., Winqvist, R., Wolffenbuttel, B. H. R., Wright, M. J., Boomsma, D. I., Econs, M., Khaw, K. T., Loos, R. J. F., McCarthy, M. I., Montgomery, G. W., Rice, J. P., Streeten, E. A., Thorsteinsdottir, U., Van Duijn, C. M., Alizadeh, B. Z., Bergmann, S., Boerwinkle, E., Boyd, H. A., Crisponi, L., Gasparini, P., Gieger, C., Harris, T. B., Ingelsson, E., Järvelin, M. R., Kraft, P., Lawlor, D., Metspalu, A., Pennell, C. E., Ridker, P. M., Snieder, H., Sørensen, T. I. A., Spector, T. D., Strachan, D. P., Uitterlinden, A. G., Wareham, N. J., Widen, E., Zygmunt, M., Murray, A., Easton, D. F., Stefansson, K., Murabito, J. M. & Ong, K. K., Oct 2 2014, In : Nature. 514, 7520, p. 92-97 6 p.

Research output: Contribution to journalArticle

Menarche
Puberty
Aminobutyrates
Cytoplasmic and Nuclear Receptors
Rare Diseases
27 Citations (Scopus)

PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease

Beecham, G. W., Dickson, D. W., Scott, W. K., Martin, E. R., Schellenberg, G., Nuytemans, K., Larson, E. B., Buxbaum, J. D., Trojanowski, J. Q., Van Deerlin, V. M., Hurtig, H. I., Mash, D. C., Beach, T. G., Troncoso, J. C., Pletnikova, O., Frosch, M. P., Ghetti, B., Foroud, T., Honig, L. S., Marder, K. & 12 others, Vonsattel, J. P., Goldman, S. M., Vinters, H. V., Ross, O. A., Wszolek, Z. K., Wang, L., Dykxhoorn, D. M., Pericak-Vance, M. A., Montine, T. J., Leverenz, J. B., Dawson, T. M. & Vance, J. M., Mar 10 2015, In : Neurology. 84, 10, p. 972-980 9 p.

Research output: Contribution to journalArticle

Parkinson Disease
Genome-Wide Association Study
Haplotypes
Genetic Heterogeneity
Chromosomes, Human, Pair 1
52 Citations (Scopus)

Parkin dosage mutations have greater pathogenicity in familial PD than simple sequence mutations

Pankratz, N., Kissell, D. K., Pauciulo, M. W., Halter, C. A., Rudolph, A., Pfeiffer, R. F., Marder, K. S., Foroud, T. & Nichols, W. C., Jul 2009, In : Neurology. 73, 4, p. 279-286 8 p.

Research output: Contribution to journalArticle

Parkinson Disease
Virulence
Mutation
Haploinsufficiency
Age of Onset
2 Citations (Scopus)

Pattern Discovery in Brain Imaging Genetics via SCCA Modeling with a Generic Non-convex Penalty

Du, L., Liu, K., Yao, X., Yan, J., Risacher, S. L., Han, J., Guo, L., Saykin, A., Shen, L., Weiner, M. W., Aisen, P., Petersen, R., Jack, C. R., Jagust, W., Trojanowki, J. Q., Toga, A. W., Beckett, L., Green, R. C., Morris, J., Shaw, L. M. & 293 others, Khachaturian, Z., Sorensen, G., Carrillo, M., Kuller, L., Raichle, M., Paul, S., Davies, P., Fillit, H., Hefti, F., Holtzman, D., Mesulam, M. M., Potter, W., Snyder, P., Schwartz, A., Montine, T., Thomas, R. G., Donohue, M., Walter, S., Gessert, D., Sather, T., Jiminez, G., Balasubramanian, A. B., Mason, J., Sim, I., 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., Franklin, E., Taylor-Reinwald, L., Lee, V., Korecka, M., Figurski, M., Crawford, K., Neu, S., Foroud, T., Potkin, S., Faber, K., Kim, S., Nho, K., Thal, L., Buckholtz, N., Albert, M., Frank, R., Hsiao, J., Kaye, J., Quinn, J., Silbert, L., Lind, B., Carter, R., Dolen, S., Schneider, L. S., Pawluczyk, S., Beccera, M., Teodoro, L., Spann, B. M., Brewer, J., Vanderswag, H., Fleisher, A., Heidebrink, J. L., Lord, J. L., Mason, S. S., Albers, C. S., Knopman, D., Johnson, K., Doody, R. S., Villanueva-Meyer, J., Pavlik, V., Shibley, V., Chowdhury, M., Rountree, S., Dang, M., Stern, Y., Honig, L. S., Bell, K. L., Ances, B., Carroll, M., Creech, M. L., Franklin, E., Mintun, M. A., Schneider, S., Oliver, A., Marson, D., Geldmacher, D., Love, M. N., Griffith, R., Clark, D., Brockington, J., Roberson, E., Grossman, H., Mitsis, E., Shah, R. C., Detoledo-Morrell, L., Duara, R., Greig-Custo, M. T., Barker, W., Onyike, C., D'Agostino, D., Kielb, S., Sadowski, M., Sheikh, M. O., Ulysse, A., Gaikwad, M., Murali Doraiswamy, P., Petrella, J. R., Borges-Neto, S., Wong, T. Z., Coleman, E., Arnold, S. E., Karlawish, J. H., Wolk, D. A., Clark, C. M., Smith, C. D., Jicha, G., Hardy, P., Sinha, P., Oates, E., Conrad, G., Lopez, O. L., Oakley, M. A., Simpson, D. M., Porsteinsson, A. P., Goldstein, B. S., Martin, K., Makino, K. M., Ismail, M. S., Brand, C., Preda, A., Nguyen, D., Womack, K., Mathews, D., Quiceno, M., Levey, A. I., Lah, J. J., Cellar, J. S., Burns, J. M., Swerdlow, R. H., Brooks, W. M., Apostolova, L., Tingus, K., Woo, E., Silverman, D. H. S., Lu, P. H., Bartzokis, G., Graff-Radford, N. R., Parfitt, F., Poki-Walker, K., Farlow, M., Hake, A., Matthews, B., Brosch, J. R., Herring, S., Van Dyck, C. H., Carson, R. E., MacAvoy, M. G., Varma, P., Chertkow, H., Bergman, H., Hosein, C., Black, S., Stefanovic, B., Caldwell, C., Robin Hsiung, G. Y., Mudge, B., Sossi, V., Feldman, H., Assaly, M., Finger, E., Pasternack, S., Rachisky, I., Rogers, J., Trost, D., Kertesz, A., Bernick, C., Munic, D., Rogalski, E., Lipowski, K., Weintraub, S., Bonakdarpour, B., Kerwin, D., Wu, C. K., Johnson, N., Sadowsky, C., Villena, T., Scott Turner, R., Johnson, K., Reynolds, B., Sperling, R. A., Johnson, K. A., Marshall, G., Yesavage, J., Taylor, J. L., Lane, B., Rosen, A., Tinklenberg, J., Sabbagh, M. N., Belden, C. M., Jacobson, S. A., Sirrel, S. A., Kowall, N., Killiany, R., Budson, A. E., Norbash, A., Lynn Johnson, P., Obisesan, T. O., Wolday, S., Allard, J., Lerner, A., Ogrocki, P., Tatsuoka, C., Fatica, P., Fletcher, E., Maillard, P., Olichney, J., Decarli, C., Carmichael, O., Kittur, S., Borrie, M., Lee, T. Y., Bartha, R., Johnson, S., Asthana, S., Carlsson, C. M., Tariot, P., Burke, A., Milliken, A. M., Trncic, N., Fleisher, A., Reeder, S., Bates, V., Capote, H., Rainka, M., Scharre, D. W., Kataki, M., Kelly, B., Zimmerman, E. A., Celmins, D., Brown, A. D., Pearlson, G. D., Blank, K., Anderson, K., Flashman, L. A., Seltzer, M., Hynes, M. L., Santulli, R. B., Sink, K. M., Gordineer, L., Williamson, J. D., Garg, P., Watkins, F., Ott, B. R., Tremont, G., Daiello, L. A., Salloway, S., Malloy, P., Correia, S., Rosen, H. J., Miller, B. L., Perry, D., Mintzer, J., Spicer, K., Bachman, D., Pomara, N., Hernando, R., Sarrael, A., Schultz, S. K., Ekstam Smith, K., Koleva, H., Nam, K. W., Shim, H., Relkin, N., Chaing, G., Lin, M., Ravdin, L., Smith, A., Ashok Raj, B. & Fargher, K., Dec 1 2017, In : Scientific Reports. 7, 1, 14052.

Research output: Contribution to journalArticle

Brain
Imaging techniques
Neuroimaging
Biomarkers
Feature extraction
51 Citations (Scopus)

Pdgfra protects against ethanol-induced craniofacial defects in a zebrafish model of FASD

Mccarthy, N., Wetherill, L., Lovely, C. B., Swartz, M. E., Foroud, T. & Eberhart, J. K., Aug 1 2013, In : Development (Cambridge). 140, 15, p. 3254-3265 12 p.

Research output: Contribution to journalArticle

Fetal Alcohol Spectrum Disorders
Platelet-Derived Growth Factor alpha Receptor
Zebrafish
Ethanol
Neural Crest
51 Citations (Scopus)

Peak bone mineral density at the hip is linked to chromosomes 14q and 15q

Peacock, M., Koller, D. L., Hui, S., Johnston, C. C., Foroud, T. & Econs, M., Jun 2004, In : Osteoporosis International. 15, 6, p. 489-496 8 p.

Research output: Contribution to journalArticle

Bone Density
Hip
Chromosomes
Siblings
African Americans
28 Citations (Scopus)

Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestry

for the Michael J. Fox LRRK2 Cohort Consortium, Oct 1 2017, In : Movement Disorders. 32, 10, p. 1432-1438 7 p.

Research output: Contribution to journalArticle

Penetrance
Leucine
Phosphotransferases
Mutation
Jews
47 Citations (Scopus)

Peroxisome Proliferator-Activated Receptors α and γ are Linked with Alcohol Consumption in Mice and Withdrawal and Dependence in Humans

Blednov, Y. A., Benavidez, J. M., Black, M., Ferguson, L. B., Schoenhard, G. L., Goate, A. M., Edenberg, H., Wetherill, L., Hesselbrock, V., Foroud, T. & Adron Harris, R., Jan 1 2015, In : Alcoholism: Clinical and Experimental Research. 39, 1, p. 136-145 10 p.

Research output: Contribution to journalArticle

Peroxisome Proliferator-Activated Receptors
Alcohol Drinking
Alcohols
Alcoholism
Association reactions
1 Citation (Scopus)

Persistent Changes in Stress-Regulatory Genes in Pregnant Women or Children Exposed Prenatally to Alcohol

Sarkar, D. K., Gangisetty, O., Wozniak, J. R., Eckerle, J. K., Georgieff, M. K., Foroud, T., Wetherill, L., Wertelecki, W., Chambers, C. D., Riley, E., Zymak-Zakutnya, N. & Yevtushok, L., Sep 1 2019, In : Alcoholism: Clinical and Experimental Research. 43, 9, p. 1887-1897 11 p.

Research output: Contribution to journalArticle

Regulator Genes
Pregnant Women
Genes
Alcohols
Pro-Opiomelanocortin
70 Citations (Scopus)

Phenotypic Dissection of Bone Mineral Density Reveals Skeletal Site Specificity and Facilitates the Identification of Novel Loci in the Genetic Regulation of Bone Mass Attainment

Kemp, J. P., Medina-Gomez, C., Estrada, K., St Pourcain, B., Heppe, D. H. M., Warrington, N. M., Oei, L., Ring, S. M., Kruithof, C. J., Timpson, N. J., Wolber, L. E., Reppe, S., Gautvik, K., Grundberg, E., Ge, B., van der Eerden, B., van de Peppel, J., Hibbs, M. A., Ackert-Bicknell, C. L., Choi, K. & 13 others, Koller, D. L., Econs, M., Williams, F. M. K., Foroud, T., Carola Zillikens, M., Ohlsson, C., Hofman, A., Uitterlinden, A. G., Davey Smith, G., Jaddoe, V. W. V., Tobias, J. H., Rivadeneira, F. & Evans, D. M., 2014, In : PLoS Genetics. 10, 6, e1004423.

Research output: Contribution to journalArticle

Genetic Loci
dissection
bone density
Bone Density
Dissection
25 Citations (Scopus)

PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation

Jun, G., Asai, H., Zeldich, E., Drapeau, E., Chen, C., Chung, J., Park, J. H., Kim, S., Haroutunian, V., Foroud, T., Kuwano, R., Haines, J. L., Pericak-Vance, M. A., Schellenberg, G. D., Lunetta, K. L., Kim, J. W., Buxbaum, J. D., Mayeux, R., Ikezu, T., Abraham, C. R. & 1 others, Farrer, L. A., Sep 1 2014, In : Annals of Neurology. 76, 3, p. 379-392 14 p.

Research output: Contribution to journalArticle

Alzheimer Disease
Phosphorylation
Serum Amyloid A Protein
Protein Isoforms
Transfection
46 Citations (Scopus)

Polygenic Risk for Externalizing Disorders: Gene-by-Development and Gene-by-Environment Effects in Adolescents and Young Adults

Salvatore, J. E., Aliev, F., Bucholz, K., Agrawal, A., Hesselbrock, V., Hesselbrock, M., Bauer, L., Kuperman, S., Schuckit, M. A., Kramer, J. R., Edenberg, H., Foroud, T. & Dick, D. M., Mar 1 2015, In : Clinical Psychological Science. 3, 2, p. 189-201 13 p.

Research output: Contribution to journalArticle

Young Adult
Impulsive Behavior
Genes
Psychopathology
Genome-Wide Association Study
12 Citations (Scopus)

Polygenic risk scores in familial Alzheimer disease

Tosto, G., Bird, T. D., Tsuang, D., Bennett, D. A., Boeve, B. F., Cruchaga, C., Faber, K., Foroud, T., Farlow, M., Goate, A. M., Bertlesen, S., Graff-Radford, N. R., Medrano, M., Lantigua, R., Manly, J., Ottman, R., Rosenberg, R., Schaid, D. J., Schupf, N., Stern, Y. & 2 others, Sweet, R. A. & Mayeux, R., Mar 21 2017, In : Neurology. 88, 12, p. 1180-1186 7 p.

Research output: Contribution to journalArticle

Alzheimer Disease
National Institute on Aging (U.S.)
Age of Onset
Hispanic Americans
Single Nucleotide Polymorphism
20 Citations (Scopus)

Polygenic Scores for Major Depressive Disorder and Risk of Alcohol Dependence

Andersen, A. M., Pietrzak, R. H., Kranzler, H. R., Ma, L., Zhou, H., Liu, X., Kramer, J., Kuperman, S., Edenberg, H., Nurnberger, J., Rice, J. P., Tischfield, J. A., Goate, A., Foroud, T., Meyers, J. L., Porjesz, B., Dick, D. M., Hesselbrock, V., Boerwinkle, E., Southwick, S. M. & 6 others, Krystal, J. H., Weissman, M. M., Levinson, D. F., Potash, J. B., Gelernter, J. & Han, S., Nov 1 2017, In : JAMA Psychiatry. 74, 11, p. 1153-1160 8 p.

Research output: Contribution to journalArticle

Major Depressive Disorder
Alcoholism
Genome-Wide Association Study
Veterans
Meta-Analysis
13 Citations (Scopus)

Polymorphisms in the bone morphogenetic protein 2 (BMP2) gene do not affect bone mineral density in white men or women

Ichikawa, S., Johnson, M. L., Koller, D. L., Lai, D., Xuei, X., Edenberg, H., Hui, S., Foroud, T., Peacock, M. & Econs, M., Apr 2006, In : Osteoporosis International. 17, 4, p. 587-592 6 p.

Research output: Contribution to journalArticle

Bone Morphogenetic Protein 2
Bone Density
Genes
Haplotypes
Single Nucleotide Polymorphism
40 Citations (Scopus)

Polymorphisms in the estrogen receptor β (ESR2) gene are associated with bone mineral density in Caucasian men and women

Ichikawa, S., Koller, D. L., Peacock, M., Johnson, M. L., Lai, D., Hui, S., Johnston, C. C., Foroud, T. & Econs, M., Nov 2005, In : Journal of Clinical Endocrinology and Metabolism. 90, 11, p. 5921-5927 7 p.

Research output: Contribution to journalArticle

Polymorphism
Estrogen Receptors
Bone Density
Minerals
Bone
70 Citations (Scopus)

Polymorphisms in the PON gene cluster are associated with Alzheimer disease

Erlich, P. M., Lunetta, K. L., Cupples, L. A., Huyck, M., Green, R. C., Baldwin, C. T., Farrer, L. A., Auerbach, S., Akomolafe, A., 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., Jan 1 2006, In : Human Molecular Genetics. 15, 1, p. 77-85 9 p.

Research output: Contribution to journalArticle

Multigene Family
Single Nucleotide Polymorphism
Alzheimer Disease
African Americans
Aryldialkylphosphatase
119 Citations (Scopus)
Alcoholism
Single Nucleotide Polymorphism
Genome
Alcohols
Gene Frequency
51 Citations (Scopus)

Possible localization of a major gene for cleft lip and palate to 4q

Beiraghi, S., Foroud, T., Diouhy, S., Bixler, D., Conneally, P. M., Delozier-Blanchet, D. & Hodes, M. E., 1994, In : Clinical Genetics. 46, 3, p. 255-256 2 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 4
Cleft Lip
Cleft Palate
Polymerase Chain Reaction
Genes
52 Citations (Scopus)

Potential outcome measures and trial design issues for multiple system atrophy

May, S., Gilman, S., Sowell, B. B., Thomas, R. G., Stern, M. B., Colcher, A., Tanner, C. M., Huang, N., Novak, P., Reich, S. G., Jankovic, J., Ondo, W. G., Low, P. A., Sandroni, P., Lipp, A., Marshall, F. J., Wooten, F., Shults, C. W., Masliah, E., Thomas, R. & 8 others, Tanner, C., Kukull, W., Lee, V., Trojanowski, J., Low, P., Shoulson, I., Ozelius, L. & Foroud, T., Dec 2007, In : Movement Disorders. 22, 16, p. 2371-2377 7 p.

Research output: Contribution to journalArticle

Multiple System Atrophy
Outcome Assessment (Health Care)
Health Surveys
Sample Size
Cerebellar Ataxia
8 Citations (Scopus)

Predicting Alzheimer’s disease progression using multi-modal deep learning approach

for Alzheimer’s Disease Neuroimaging Initiative, Dec 1 2019, In : Scientific Reports. 9, 1, 1952.

Research output: Contribution to journalArticle

Open Access
Disease Progression
Alzheimer Disease
Learning
Neuroimaging
Area Under Curve
68 Citations (Scopus)

Predicting sensation seeking from dopamine genes: A candidate-system approach

Derringer, J., Krueger, R. F., Dick, D. M., Saccone, S., Grucza, R. A., Agrawal, A., Lin, P., Almasy, L., Edenberg, H., Foroud, T., Nurnberger, J., Hesselbrock, V. M., Kramer, J. R., Kuperman, S., Porjesz, B., Schuckit, M. A. & Bierut, L. J., Sep 2010, In : Psychological Science. 21, 9, p. 1282-1290 9 p.

Research output: Contribution to journalArticle

Dopamine
Single Nucleotide Polymorphism
Genes
Observational Studies
Personality
2 Citations (Scopus)

Predicting Short-term MCI-to-AD Progression Using Imaging, CSF, Genetic Factors, Cognitive Resilience, and Demographics

for the Alzheimer’s Disease Neuroimaging Initiative, Dec 1 2019, In : Scientific Reports. 9, 1, 2235.

Research output: Contribution to journalArticle

Open Access
Disease Progression
Alzheimer Disease
Demography
Complement C1
Prodromal Symptoms
40 Citations (Scopus)

Predictive accuracy of serial transvaginal cervical lengths and quantitative vaginal fetal fibronectin levels for spontaneous preterm birth among nulliparous women

Esplin, M. S., Elovitz, M. A., Iams, J. D., Parker, C. B., Wapner, R. J., Grobman, W. A., Simhan, H. N., Wing, D. A., Haas, D., Silver, R. M., Hoffman, M. K., Peaceman, A. M., Caritis, S. N., Parry, S., Wadhwa, P., Foroud, T., Mercer, B. M., Hunter, S. M., Saade, G. R. & Reddy, U. M., Mar 14 2017, In : JAMA - Journal of the American Medical Association. 317, 10, p. 1047-1056 10 p.

Research output: Contribution to journalArticle

Premature Birth
Fibronectins
Pregnancy
Term Birth
Infant Mortality