Tatiana Foroud

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

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Psychosocial moderation of polygenic risk for cannabis involvement: the role of trauma exposure and frequency of religious service attendance

Meyers, J. L., Salvatore, J. E., Aliev, F., Johnson, E. C., McCutcheon, V. V., Su, J., Kuo, S. I. C., Lai, D., Wetherill, L., Wang, J. C., Chan, G., Hesselbrock, V., Foroud, T., Bucholz, K. K., Edenberg, H. J., Dick, D. M., Porjesz, B. & Agrawal, A., Dec 1 2019, In : Translational psychiatry. 9, 1, 269.

Research output: Contribution to journalArticle

Open Access
Cannabis
Wounds and Injuries
Genome-Wide Association Study
Multifactorial Inheritance
Masks
137 Citations (Scopus)

Quantitative trait loci analysis of human event-related brain potentials: P3 voltage

Begleiter, H., Porjesz, B., Reich, T., Edenberg, H., Goate, A., Blangero, J., Almasy, L., Foroud, T., Van Eerdewegh, P., Polich, J., Rohrbaugh, J., Kuperman, S., Bauer, L. O., O'Connor, S., Chorlian, D. B., Li, T. K., Conneally, P. M., Hesselbrock, V., Rice, J. P., Schuckit, M. A. & 4 others, Cloninger, R., Nurnberger, J., Crowe, R. & Bloom, F. E., Apr 1998, In : Electroencephalography and Clinical Neurophysiology/ Evoked Potentials. 108, 3, p. 244-250 7 p.

Research output: Contribution to journalArticle

P300 Event-Related Potentials
Quantitative Trait Loci
Evoked Potentials
Brain
Genetic Loci
3 Citations (Scopus)
Chromosomes, Human, Pair 4
Quantitative Trait Loci
Neuropeptide Y
Corticotropin-Releasing Hormone
body weight
7 Citations (Scopus)

R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation

Nichols, W. C., Marek, D. K., Pauciulo, M. W., Pankratz, N., Halter, C. A., Rudolph, A., Shults, C. W., Wojcieszek, J., Foroud, T., Shults, C., Marshall, F., Oakes, D., Rudolph, A., Shinaman, A., Marder, K., Conneally, P. M., Foroud, T., Halter, C., Lyons, K., Siemers, E. & 199 others, Factor, S., Higgins, D., Evans, S., 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., Marder, K., 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., Panisset, M., Hall, 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., Wolff, M., Fernandez, M., Hubble, J., Kostyk, S., Campbell, A., Reider, C., Camicioli, R., Carter, J., Andrews, P., Morehouse, S., Stone, C., Mendis, T., Grimes, D., Gray, P., Haas, K., Sutton, J., Hutchinson, B., Young, J., Rajput, A., Rajput, A., Klassen, L., Shirley, T., Manyam, B., Simpson, P., Whetteckey, J., Wulbrecht, B., Truong, D., Pathak, M., Luong, N., Tra, T., Tran, A., Vo, J., Lang, A., Kleiner-Fisman, G., Nieves, A., So, J., Podskalny, G., Giffin, L., Atchison, P., Allen, C., Martin, W., Wieler, M., Suchowersky, O., Klimek, M., Hermanowicz, N., Niswonger, S., Shults, C., Fontaine, D., Aminoff, M., Christine, C., Diminno, M., Hevezi, J., Dalvi, A., Kang, U., Richman, J., Uy, S., Young, J., Dalvi, A., Sahay, A., Schwieterman, D., Leehey, M., Culver, S., Derian, T., Demarcaida, T., Belber, S., Rodnitzky, R., Dobson, J., Pahwa, R., Lyons, K., Gales, T., Thomas, S., Shulman, L., Weiner, W., Dustin, K., Singer, C., Koller, W., Lyons, K., Weiner, W., Zelaya, L., Tuite, P., Hagen, V., Rolandelli, S., Schacherer, R., Gordon, P., Werner, J., Serrano, C., Roque, S., Kurlan, R., Berry, D., Gardiner, I., Hauser, R., Sanchez-Ramos, J., Zesiewicz, T., Delgado, H., Price, K., Rodriguez, P., Pfeiffer, R., Davis, L., Pfeiffer, B., Dewey, R., Hayward, B., Meacham, M., Walker, F., Hunt, V., Racette, B., Good, L., Rundle, M., Oakes, D., Watts, A., Wang, A., Ross, T., Bennett, S., Kamp, D. & Julian-Baros, E., Jan 15 2007, In : Movement Disorders. 22, 2, p. 254-257 4 p.

Research output: Contribution to journalArticle

Parkinson Disease
Mutation
Guanine Nucleotides
Adenine
Glutamine
11 Citations (Scopus)

Racial disparities in adverse pregnancy outcomes and psychosocial stress

Eunice Kennedy Shriver National Institute of Child Health and Human Development Nulliparous Pregnancy Outcomes Study: Monitoring Mothers-to-Be (nuMoM2b) Network, Feb 1 2018, In : Obstetrics and Gynecology. 131, 2, p. 328-335 8 p.

Research output: Contribution to journalArticle

Pregnancy Outcome
Premature Birth
Gestational Age
Pregnancy
Parturition
187 Citations (Scopus)

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

Sims, R., Van Der Lee, S. J., Naj, A. C., Bellenguez, C., Badarinarayan, N., Jakobsdottir, J., Kunkle, B. W., Boland, A., Raybould, R., Bis, J. C., Martin, E. R., Grenier-Boley, B., Heilmann-Heimbach, S., Chouraki, V., Kuzma, A. B., Sleegers, K., Vronskaya, M., Ruiz, A., Graham, R. R., Olaso, R. & 429 others, Hoffmann, P., Grove, M. L., Vardarajan, B. N., Hiltunen, M., Nöthen, M. M., White, C. C., Hamilton-Nelson, K. L., Epelbaum, J., Maier, W., Choi, S. H., Beecham, G. W., Dulary, C., Herms, S., Smith, A. V., Funk, C. C., Derbois, C., Forstner, A. J., Ahmad, S., Li, H., Bacq, D., Harold, D., Satizabal, C. L., Valladares, O., Squassina, A., Thomas, R., Brody, J. A., Qu, L., Sánchez-Juan, P., Morgan, T., Wolters, F. J., Zhao, Y., Garcia, F. S., Denning, N., Fornage, M., Malamon, J., Naranjo, M. C. D., Majounie, E., Mosley, T. H., Dombroski, B., Wallon, D., Lupton, M. K., Dupuis, J., Whitehead, P., Fratiglioni, L., Medway, C., Jian, X., Mukherjee, S., Keller, L., Brown, K., Lin, H., Cantwell, L. B., Panza, F., McGuinness, B., Moreno-Grau, S., Burgess, J. D., Solfrizzi, V., Proitsi, P., Adams, H. H., Allen, M., Seripa, D., Pastor, P., Cupples, L. A., Price, N. D., Hannequin, D., Frank-García, A., Levy, D., Chakrabarty, P., Caffarra, P., Giegling, I., Beiser, A. S., Giedraitis, V., Hampel, H., Garcia, M. E., Wang, X., Lannfelt, L., Mecocci, P., Eiriksdottir, G., Crane, P. K., Pasquier, F., Boccardi, V., Henández, I., Barber, R. C., Scherer, M., Tarraga, L., Adams, P. M., Leber, M., Chen, Y., Albert, M. S., Riedel-Heller, S., Emilsson, V., Beekly, D., Braae, A., Schmidt, R., Blacker, D., Masullo, C., Schmidt, H., Doody, R. S., Spalletta, G., Jr, W. T. L., Fairchild, T. J., Bossù, P., Lopez, O. L., Frosch, M. P., Sacchinelli, E., Ghetti, B., Yang, Q., Huebinger, R. M., Jessen, F., Li, S., Kamboh, M. I., Morris, J., Sotolongo-Grau, O., Katz, M. J., Corcoran, C., Dunstan, M., Braddel, A., Thomas, C., Meggy, A., Marshall, R., Gerrish, A., Chapman, J., Aguilar, M., Taylor, S., Hill, M., Fairén, M. D., Hodges, A., Vellas, B., Soininen, H., Kloszewska, I., Daniilidou, M., Uphill, J., Patel, Y., Hughes, J. T., Lord, J., Turton, J., Hartmann, A. M., Cecchetti, R., Fenoglio, C., Serpente, M., Arcaro, M., Caltagirone, C., Orfei, M. D., Ciaramella, A., Pichler, S., Mayhaus, M., Gu, W., Lleó, A., Fortea, J., Blesa, R., Barber, I. S., Brookes, K., Cupidi, C., Maletta, R. G., Carrell, D., Sorbi, S., Moebus, S., Urbano, M., Pilotto, A., Kornhuber, J., Bosco, P., Todd, S., Craig, D., Johnston, J., Gill, M., Lawlor, B., Lynch, A., Fox, N. C., Hardy, J., Albin, R. L., Apostolova, L. G., Arnold, S. E., Asthana, S., Atwood, C. S., Baldwin, C. T., Barnes, L. L., Barral, S., Beach, T. G., Becker, J. T., Bigio, E. H., Bird, T. D., Boeve, B. F., Bowen, J. D., Boxer, A., Burke, J. R., Burns, J. M., Buxbaum, J. D., Cairns, N. J., Cao, C., Carlson, C. S., Carlsson, C. M., Carney, R. M., Carrasquillo, M. M., Carroll, S. L., Diaz, C. C., Chui, H. C., Clark, D. G., Cribbs, D. H., Crocco, E. A., Decarli, C., Dick, M., Duara, R., Evans, D. A., Faber, K. M., Fallon, K. B., Fardo, D. W., Farlow, M., Ferris, S., Foroud, T., Galasko, D. R., Gearing, M., Geschwind, D. H., Gilbert, J. R., Graff-Radford, N. R., Green, R. C., Growdon, J. H., Hamilton, R. L., Harrell, L. E., Honig, L. S., Huentelman, M. J., Hulette, C. M., Hyman, B. T., Jarvik, G. P., Abner, E., Jin, L. W., Jun, G., Karydas, A., Kaye, J. A., Kim, R., Kowall, N. W., Kramer, J. H., Laferla, F. M., Lah, J. J., Leverenz, J. B., Levey, A. I., Li, G., Lieberman, A. P., Lunetta, K. L., Lyketsos, C. G., Marson, D. C., Martiniuk, F., Mash, D. C., Masliah, E., McCormick, W. C., McCurry, S. M., McDavid, A. N., McKee, A. C., Mesulam, M., Miller, B. L., Miller, C. A., Miller, J. W., Morris, J. C., Murrell, J. R., Myers, A. J., O'Bryant, S., Olichney, J. M., Pankratz, V. S., Parisi, J. E., Paulson, H. L., Perry, W., Peskind, E., Pierce, A., Poon, W. W., Potter, H., Quinn, J. F., Raj, A., Raskind, M., Reisberg, B., Reitz, C., Ringman, J. M., Roberson, E. D., Rogaeva, E., Rosen, H. J., Rosenberg, R. N., Saykin, A., Saykin, A. J., Schneider, J. A., Schneider, L. S., Seeley, W. W., Smith, A. G., Sonnen, J. A., Spina, S., Stern, R. A., Swerdlow, R. H., Tanzi, R. E., Thornton-Wells, T. A., Trojanowski, J. Q., Troncoso, J. C., Van Deerlin, V. M., Van Eldik, L. J., Vinters, H. V., Vonsattel, J. P., Weintraub, S., Welsh-Bohmer, K. A., Wilhelmsen, K. C., Williamson, J., Wingo, T. S., Woltjer, R. L., Wright, C. B., Yu, C. E., Yu, L., Garzia, F., Golamaully, F., Septier, G., Engelborghs, S., Vandenberghe, R., De Deyn, P. P., Fernadez, C. M., Benito, Y. A., Thonberg, H., Forsell, C., Lilius, L., Kinhult-Stählbom, A., Kilander, L., Brundin, R., Concari, L., Helisalmi, S., Koivisto, A. M., Haapasalo, A., Dermecourt, V., Fievet, N., Hanon, O., Dufouil, C., Brice, A., Ritchie, K., Dubois, B., Himali, J. J., Keene, C. D., Tschanz, J., Fitzpatrick, A. L., Kukull, W. A., Norton, M., Aspelund, T., Larson, E. B., Munger, R., Rotter, J. I., Lipton, R. B., Bullido, M. J., Hofman, A., Montine, T. J., Coto, E., Boerwinkle, E., Petersen, R. C., Alvarez, V., Rivadeneira, F., Reiman, E. M., Gallo, M., O'Donnell, C. J., Reisch, J. S., Bruni, A. C., Royall, D. R., Dichgans, M., Sano, M., Galimberti, D., St George-Hyslop, P., Scarpini, E., Tsuang, D. W., Mancuso, M., Bonuccelli, U., Winslow, A. R., Daniele, A., Wu, C. K., Peters, O., Nacmias, B., Riemenschneider, M., Heun, R., Brayne, C., Rubinsztein, D. C., Bras, J., Guerreiro, R., Al-Chalabi, A., Shaw, C. E., Collinge, J., Mann, D., Tsolaki, M., Clarimón, J., Sussams, R., Lovestone, S., O'Donovan, M. C., Owen, M. J., Behrens, T. W., Mead, S., Goate, A. M., Uitterlinden, A. G., Holmes, C., Cruchaga, C., Ingelsson, M., Bennett, D. A., Powell, J., Golde, T. E., Graff, C., De Jager, P. L., Morgan, K., Ertekin-Taner, N., Combarros, O., Psaty, B. M., Passmore, P., Younkin, S. G., Berr, C., Gudnason, V., Rujescu, D., Dickson, D. W., Dartigues, J. F., Destefano, A. L., Ortega-Cubero, S., Hakonarson, H., Campion, D., Boada, M., Kauwe, J. K., Farrer, L. A., Van Broeckhoven, C., Ikram, M. A., Jones, L., Haines, J. L., Tzourio, C., Launer, L. J., Escott-Price, V., Mayeux, R., Deleuze, J. F., Amin, N., Holmans, P. A., Pericak-Vance, M. A., Amouyel, P., Van Duijn, C. M., Ramirez, A., Wang, L. S., Lambert, J. C., Seshadri, S., Williams, J. & Schellenberg, G. D., Sep 1 2017, In : Nature Genetics. 49, 9, p. 1373-1384 12 p.

Research output: Contribution to journalArticle

Innate Immunity
Gene Frequency
Alzheimer Disease
Odds Ratio
Microglia
163 Citations (Scopus)

Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families

Cruchaga, C., Chakraverty, S., Mayo, K., Vallania, F. L. M., Mitra, R. D., Faber, K., Williamson, J., Bird, T., Diaz-Arrastia, R., Foroud, T., Boeve, B. F., Graff-Radford, N. R., St. Jean, P., Lawson, M., Ehm, M. G., Mayeux, R., Goate, A. M. & for the NIA-LOAD - NCRAD Family Study Consortium, T. NIA-LOAD. . NCRAD. F. S. C., Feb 1 2012, In : PLoS One. 7, 2, e31039.

Research output: Contribution to journalArticle

Alzheimer disease
Alzheimer Disease
Genes
mutation
Mutation
20 Citations (Scopus)

Rarity of the alzheimer disease-protective APP A673T variant in the United States

National Institute on Aging-Late-Onset Alzheimer's Disease (NIA-LOAD) Family Study & Alzheimer's Disease Genetics Consortium, Feb 1 2015, In : JAMA Neurology. 72, 2, p. 209-216 8 p.

Research output: Contribution to journalArticle

Amyloid beta-Protein Precursor
Alzheimer Disease
Genes
Sweden
Alanine
44 Citations (Scopus)

Recent drinking history: Association with family history of alcoholism and the acute response to alcohol during a 60 mg% clamp

Ramchandani, V. A., Flury, L., Morzorati, S., Kareken, D., Blekher, T., Foroud, T., Li, T. K. & O'Connor, S., Nov 2002, In : Journal of Studies on Alcohol. 63, 6, p. 734-744 11 p.

Research output: Contribution to journalArticle

Clamping devices
genealogy
alcoholism
Alcoholism
Drinking
7 Citations (Scopus)

Regsnps: A strategy for prioritizing regulatory single nucleotide substitutions

Teng, M., Ichikawa, S., Padgett, L. R., Wang, Y., Mort, M., Cooper, D. N., Koller, D. L., Foroud, T., Edenberg, H., Econs, M. & Liu, Y., Jul 2012, In : Bioinformatics. 28, 14, p. 1879-1886 8 p., bts275.

Research output: Contribution to journalArticle

Nucleotides
Single Nucleotide Polymorphism
Substitution
Informatics
Substitution reactions
13 Citations (Scopus)

Relation Over Time Between Facial Measurements and Cognitive Outcomes in Fetal Alcohol-Exposed Children

Foroud, T., Wetherill, L., Vinci-Booher, S., Moore, E. S., Ward, R. E., Hoyme, H. E., Robinson, L. K., Rogers, J., Meintjes, E. M., Molteno, C. D., Jacobson, J. L. & Jacobson, S. W., Sep 2012, In : Alcoholism: Clinical and Experimental Research. 36, 9, p. 1634-1646 13 p.

Research output: Contribution to journalArticle

Fetal Alcohol Spectrum Disorders
Alcohols
Ear
Central Nervous System
Logistic Models
59 Citations (Scopus)

Relationship of age of first drink to child behavioral problems and family psychopathology

Kuperman, S., Chan, G., Kramer, J. R., Bierut, L., Bucholz, K. K., Fox, L., Hesselbrock, V., Nurnberger, J., Reich, T., Reich, W., Schuckit, M. A., Edenberg, H., Connealfy, P. M., Foroud, T., Crowe, R., Porjesz, B., Begleiter, H., Rice, J., Goate, A., Taylor, R. & 2 others, Tischfield, J. & Almasy, L., Oct 2005, In : Alcoholism: Clinical and Experimental Research. 29, 10, p. 1869-1876 8 p.

Research output: Contribution to journalArticle

Psychopathology
Alcoholism
Alcohols
Antisocial Personality Disorder
Child Behavior
27 Citations (Scopus)

Reliability of reported age at onset of Parkinson's disease

Reider, C. R., Halter, C. A., Castelluccio, P. F., Oakes, D., Nichols, W. C., Foroud, T., Wolff, A., Dewey, R., Jones, M., Hermanowicz, N., Feigin, A., Shannon, B., Calabresse, V., Roberge, P., Sutton, J., Hutchinson, B., Ajax, T., Mannetter, J., Podakalny, G. D., Giffin, L. & 6 others, Suchowersky, O., Klimek, M. L., Uitti, R., Foster Turk, M., Shulman, L. & Dustin, K., Mar 1 2003, In : Movement Disorders. 18, 3, p. 275-279 5 p.

Research output: Contribution to journalArticle

Age of Onset
Parkinson Disease
Medical Records
History
Observation
3 Citations (Scopus)

Replicating genetic linkage in the collaborative study on the genetics of alcoholism (COGA)

Reich, T., Goate, A., Edenberg, H., Rice, J., Foroud, T., Hesselbrock, V., Schuckit, M., Porjesz, B., Nurnberger, J., Crowe, R. & Begleiter, H., Nov 6 1998, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 81, 6, p. 478-479 2 p.

Research output: Contribution to journalArticle

Genetic Linkage
Alcoholism
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 4
Phenotype
17 Citations (Scopus)
Genome-Wide Association Study
Bone Density
Single Nucleotide Polymorphism
Femur Neck
Spine

Replication of suggestive linkage on chromosomes 5 and 16 in the NIMH genetics initiative bipolar pedigrees

Dick, D. M., Nurnberger, J., Edenberg, H., McInnis, M. G., Reich, T., Gershon, E. S. & Foroud, T., Oct 8 2001, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 105, 7, p. 592 1 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 3
Pedigree

Reply from the Authors

Nichols, W. C., Elsaesser, V. E., Pankratz, N., Pauciulo, M. W., Marek, D. K., Halter, C. A., Rudolph, A. & Foroud, T., Jun 10 2008, In : Neurology. 70, 24, p. 2348-2349 2 p.

Research output: Contribution to journalArticle

Response

Brown, R. D., Huston, J., Hornung, R., Foroud, T., Kallmes, D. F., Kleindorfer, D., Meissner, I., Woo, D., Sauerbeck, L. & Broderick, J., Jun 2008, In : Journal of Neurosurgery. 108, 6, p. 1131 1 p.

Research output: Contribution to journalArticle

29 Citations (Scopus)

Root resorption associated with orthodontic force in IL-1B knockout mouse

Al-Qawasmi, R. A., Hartsfield, J. K., Everett, E. T., Weaver, M. R., Foroud, T. & Roberts, W. E., Dec 2004, In : Journal of Musculoskeletal Neuronal Interactions. 4, 4, p. 383-385 3 p.

Research output: Contribution to journalArticle

Orthodontic Appliances
Root Resorption
Tooth Root
Animal Disease Models
Mechanical Stress
38 Citations (Scopus)

Root resorption associated with orthodontic force in inbred mice: Genetic contributions

Al-Qawasmi, R. A., Hartsfield, J. K., Everett, E. T., Weaver, M. R., Foroud, T., Faust, D. M. & Roberts, W. E., Feb 2006, In : European Journal of Orthodontics. 28, 1, p. 13-19 7 p.

Research output: Contribution to journalArticle

Root Resorption
Orthodontics
Inbred Strains Mice
Orthodontic Appliances
Tooth
92 Citations (Scopus)

Saccades in presymptomatic and early stages of Huntington disease

Blekher, T., Johnson, S. A., Marshall, J., White, K., Hui, S., Weaver, M., Gray, J., Yee, R., Stout, J. C., Beristain, X., Wojcieszek, J. & Foroud, T., Aug 2006, In : Neurology. 67, 3, p. 394-399 6 p.

Research output: Contribution to journalArticle

Saccades
Huntington Disease
Eye Movements
Biomarkers
Eye Abnormalities
29 Citations (Scopus)

Saccadic eye movements are associated with a family history of alcoholism at baseline and after exposure to alcohol

Blekher, T., Ramchandani, V. A., Flury, L., Foroud, T., Kareken, D., Yee, R. D., Li, T. K. & O'Connor, S., Oct 2002, In : Alcoholism: Clinical and Experimental Research. 26, 10, p. 1568-1573 6 p.

Research output: Contribution to journalArticle

Eye movements
Saccades
Alcoholism
Alcohols
Placebos
54 Citations (Scopus)

Screening for brain aneurysm in the Familial Intracranial Aneurysm study: Frequency and predictors of lesion detection

Brown, R. D., Huston, J., Hornung, R., Foroud, T., Kallmes, D. F., Kleindorfer, D., Meissner, I., Woo, D., Sauerbeck, L. & Broderick, J., Jun 2008, In : Journal of Neurosurgery. 108, 6, p. 1132-1138 7 p.

Research output: Contribution to journalArticle

Intracranial Aneurysm
Aneurysm
Magnetic Resonance Angiography
Smoking
Odds Ratio
56 Citations (Scopus)

Serum Iron Levels and the Risk of Parkinson Disease: A Mendelian Randomization Study

Pichler, I., Del Greco, M. F., Gögele, M., Lill, C. M., Bertram, L., Do, C. B., Eriksson, N., Foroud, T., Myers, R. H., Nalls, M., Keller, M. F., Benyamin, B., Whitfield, J. B., Pramstaller, P. P., Hicks, A. A., Thompson, J. R. & Minelli, C., Jun 2013, In : PLoS Medicine. 10, 6, e1001462.

Research output: Contribution to journalArticle

Random Allocation
Parkinson Disease
Iron
Serum
Meta-Analysis
59 Citations (Scopus)

Sex-specific and non-sex-specific quantitative trait loci contribute to normal variation in bone mineral density in men

Peacock, M., Koller, D. L., Fishburn, T., Krishnan, S., Lai, D., Hui, S., Johnston, C. C., Foroud, T. & Econs, M., May 2005, In : Journal of Clinical Endocrinology and Metabolism. 90, 5, p. 3060-3066 7 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Bone Density
Minerals
Bone
Spine
22 Citations (Scopus)

Sex-specific association of apolipoprotein e with cerebrospinal fluid levels of tau

Alzheimer's Disease Genetics Consortium and the Alzheimer's Disease Neuroimaging Initiative, Aug 1 2018, In : JAMA Neurology. 75, 8, p. 989-998 10 p.

Research output: Contribution to journalArticle

Apolipoproteins
Apolipoproteins E
Cerebrospinal Fluid
Alzheimer Disease
Neurofibrillary Tangles
9 Citations (Scopus)
Genetic Loci
Quantitative Trait Loci
Femur Neck
Bone and Bones
Chromosomes, Human, Pair 1
13 Citations (Scopus)

Sex-specific genetic predictors of Alzheimer’s disease biomarkers

Alzheimer’s Disease Neuroimaging Initiative (ADNI) & The Alzheimer Disease Genetics Consortium (Adgc), Jul 2 2018, (Accepted/In press) In : Acta Neuropathologica. p. 1-16 16 p.

Research output: Contribution to journalArticle

Alzheimer Disease
Biomarkers
Genome-Wide Association Study
Amyloid
Endophenotypes
32 Citations (Scopus)

Sex-specific quantitative trait loci contribute to normal variation in bone structure at the proximal femur in men

Peacock, M., Koller, D. L., Lai, D., Hui, S., Foroud, T. & Econs, M., Oct 2005, In : Bone. 37, 4, p. 467-473 7 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Femur
Bone and Bones
Chromosomes
Thigh
22 Citations (Scopus)

Shared genetic contribution to ischemic stroke and Alzheimer's disease

Traylor, M., Adib-Samii, P., Harold, D., Dichgans, M., Williams, J., Lewis, C. M., Markus, H. S., Fornage, M., Holliday, E. G., Sharma, P., Bis, J. C., Psaty, B. M., Seshadri, S., Nalls, M. A., Devan, W. J., Boncoraglio, G., Malik, R., Mitchell, B. D., Kittner, S. J., Ikram, M. A. & 188 others, Clarke, R., Rosand, J., Meschia, J. F., Sudlow, C., Rothwell, P. M., Levi, C., Bevan, S., Kilarski, L. L., Walters, M., Thijs, V., Slowik, A., Lindgren, A., De Bakker, P. I. W., Lambert, J. C., Ibrahim-Verbaas, C. A., Naj, A. C., Sims, R., Bellenguez, C., Jun, G., Destefano, A. L., Beecham, G. W., Grenier-Boley, B., Russo, G., Thornton-Wells, T. A., Jones, N., Smith, A. V., Chouraki, V., Thomas, C., Zelenika, D., Vardarajan, B. N., Kamatani, Y., Lin, C. F., Gerrish, A., Schmidt, H., Kunkle, B., Dunstan, M. L., Ruiz, A., Bihoreau, M. T., Choi, S. H., Reitz, C., Pasquier, F., Hollingworth, P., Ramirez, A., Hanon, O., Fitzpatrick, A. L., Buxbaum, J. D., Campion, D., Crane, P. K., Baldwin, C., Becker, T., Gudnason, V., Cruchaga, C., Craig, D., Amin, N., Berr, C., Lopez, O. L., De Jager, P. L., Deramecourt, V., Johnston, J. A., Evans, D., Lovestone, S., Letenneur, L., Morón, F. J., Rubinsztein, D. C., Eiriksdottir, G., Sleegers, K., Goate, A. M., Fiçvet, N., Huentelman, M. J., Gill, M., Brown, K., Kamboh, M. I., Keller, L., Barberger-Gateau, P., McGuinness, B., Larson, E. B., Green, R., Myers, A. J., Dufouil, C., Todd, S., Wallon, D., Love, S., Rogaeva, E., Gallacher, J., St George-Hyslop, P., Clarimon, J., Lleo, A., Bayer, A., Tsuang, D. W., Yu, L., Tsolaki, M., Bossù, P., Spalletta, G., Proitsi, P., Collinge, J., Sorbi, S., Sanchez-Garcia, F., Fox, N. C., Hardy, J., Deniz Naranjo, M. C., Bosco, P., Brayne, C., Galimberti, D., Mancuso, M., Matthews, F., Moebus, S., Mecocci, P., Del Zompo, M., Maier, W., Hampel, H., Pilotto, A., Bullido, M., Panza, F., Caffarra, P., Nacmias, B., Gilbert, J. R., Mayhaus, M., Lannfelt, L., Hakonarson, H., Pichler, S., Carrasquillo, M. M., Ingelsson, M., Beekly, D., Alvarez, V., Zou, F., Valladares, O., Younkin, S. G., Coto, E., Hamilton-Nelson, K. L., Gu, W., Razquin, C., Pastor, P., Mateo, I., Owen, M. J., Faber, K. M., Jonsson, P. V., Combarros, O., O'Donovan, M. C., Cantwell, L. B., Soininen, H., Blacker, D., Mead, S., Mosley, T. H., Bennett, D. A., Harris, T. B., Fratiglioni, L., Holmes, C., De Bruijn, R. F. A. G., Passmore, P., Montine, T. J., Bettens, K., Rotter, J. I., Brice, A., Morgan, K., Foroud, T. M., Kukull, W. A., Hannequin, D., Powell, J. F., Nalls, M. A., Ritchie, K., Lunetta, K. L., Kauwe, J. S. K., Boerwinkle, E., Riemenschneider, M., Boada, M., Hiltunen, M., Martin, E. R., Schmidt, R., Rujescu, D., Wang, L. S., Dartigues, J. F., Mayeux, R., Tzourio, C., Hofman, A., Nöthen, M. M., Graff, C., Jones, L., Haines, J. L., Holmans, P. A., Lathrop, M., Pericak-Vance, M. A., Launer, L. J., Farrer, L. A., Van Duijn, C. M., Van Broeckhoven, C., Moskvina, V., Schellenberg, G. D. & Amouyel, P., May 1 2016, In : Annals of Neurology. 79, 5, p. 739-747 9 p.

Research output: Contribution to journalArticle

Alzheimer Disease
Stroke
Genome-Wide Association Study
Single Nucleotide Polymorphism
Meta-Analysis
10 Citations (Scopus)

Shared genetic risk factors of intracranial, abdominal, and thoracic aneurysms

Aneurysm Consortium, Vascular Research Consortium of New Zealand, Jul 1 2016, In : Journal of the American Heart Association. 5, 7, e002603.

Research output: Contribution to journalArticle

Abdominal Aortic Aneurysm
Thoracic Aortic Aneurysm
Intracranial Aneurysm
Aneurysm
Thorax
5 Citations (Scopus)

SIBLING family genes and bone mineral density: Association and allele-specific expression in humans

Alam, I., Padgett, L. R., Ichikawa, S., Alkhouli, M., Koller, D. L., Lai, D., Peacock, M., Xuei, X., Foroud, T., Edenberg, H. & Econs, M., 2014, In : Bone. 64, p. 166-172 7 p.

Research output: Contribution to journalArticle

Bone Density
Alleles
Single Nucleotide Polymorphism
Femur Neck
Genes
54 Citations (Scopus)

Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus

Takacs, I., Koller, D. L., Peacock, M., Christian, J. C., Hui, S. L., Conneally, P. M., Johnston, C. C., Foroud, T. & Econs, M. J., 1999, In : Journal of Clinical Endocrinology and Metabolism. 84, 12, p. 4467-4471 5 p.

Research output: Contribution to journalArticle

Insulin-Like Growth Factor I
Bone Density
Minerals
Siblings
Bone
23 Citations (Scopus)
Proton Pumps
Chromosomes, Human, Pair 13
Osteoclasts
Chromosomes
Bone Density
31 Citations (Scopus)

Sib pair linkage and association studies between bone mineral density and the interleukin-6 gene locus

Takacs, I., Koller, D. L., Peacock, M., Christian, J. C., Evans, W. E., Hui, S., Conneally, P. M., Johnston, C. C., Foroud, T. & Econs, M., Jul 2000, In : Bone. 27, 1, p. 169-173 5 p.

Research output: Contribution to journalArticle

Bone Density
Interleukin-6
Osteoporosis
Genes
Alleles
122 Citations (Scopus)

Significant linkage of Parkinson disease to chromosome 2q36-37

Pankratz, N., Nichols, W. C., Uniacke, S. K., Halter, C., Rudolph, A., Shults, C., Conneally, P. M., Foroud, T., Golbe, L., Koller, W., Lyons, K., Marder, K., Marshall, F., Oakes, D., Shinaman, A., Siemers, E., Wojcieszek, J., Belden, J., Carter, J., Camicioli, R. & 79 others, 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., Ramos, C. S., 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., Blindauer, K., Petit, J., Simon, D., Scollins, L., Pullman, R. S., Boyar, K., Gordon, P. & Werner, J., Apr 1 2003, In : American Journal of Human Genetics. 72, 4, p. 1053-1057 5 p.

Research output: Contribution to journalArticle

Parkinson Disease
Chromosomes
Pedigree
Disease Susceptibility
Neurodegenerative Diseases
51 Citations (Scopus)

Single-nucleotide polymorphisms in corticotropin releasing hormone receptor 1 gene (CRHR1) are associated with quantitative trait of event-related potential and alcohol dependence

Chen, A. C. H., Manz, N., Tang, Y., Rangaswamy, M., Almasy, L., Kuperman, S., Nurnberger, J., O'Connor, S., Edenberg, H., Schuckit, M. A., Tischfield, J., Foroud, T., Bierut, L. J., Rohrbaugh, J., Rice, J. P., Goate, A., Hesselbrock, V. & Porjesz, B., 2010, In : Alcoholism: Clinical and Experimental Research. 34, 6, p. 988-996 9 p.

Research output: Contribution to journalArticle

Corticotropin-Releasing Hormone Receptors
Polymorphism
Evoked Potentials
Alcoholism
Single Nucleotide Polymorphism
113 Citations (Scopus)

Singleton deletions throughout the genome increase risk of bipolar disorder

Zhang, D., Cheng, L., Qian, Y., Alliey-Rodriguez, N., Kelsoe, J. R., Greenwood, T., Nievergelt, C., Barrett, T. B., McKinney, R., Schork, N., Smith, E. N., Bloss, C., Nurnberger, J., Edenberg, H., Foroud, T., Sheftner, W., Lawson, W. B., Nwulia, E. A., Hipolito, M., Coryell, W. & 16 others, Rice, J., Byerley, W., McMahon, F., Schulze, T. G., Berrettini, W., Potash, J. B., Belmonte, P. L., Zandi, P. P., McInnis, M. G., Zöllner, S., Craig, D., Szelinger, S., Koller, D., Christian, S. L., Liu, C. & Gershon, E. S., Apr 2009, In : Molecular Psychiatry. 14, 4, p. 376-380 5 p.

Research output: Contribution to journalArticle

Bipolar Disorder
Genome
Single Nucleotide Polymorphism
Genomic Structural Variation
Age of Onset
53 Citations (Scopus)

Specific psychiatric manifestations among preclinical huntington disease mutation carriers

Marshall, J., White, K., Weaver, M., Flury Wetherill, L., Hui, S., Stout, J. C., Johnson, S. A., Beristain, X., Gray, J., Wojcieszek, J. & Foroud, T., Jan 2007, In : Archives of Neurology. 64, 1, p. 116-121 6 p.

Research output: Contribution to journalArticle

Huntington Disease
Psychiatry
Mutation
Checklist
Depression
22 Citations (Scopus)

Spheroid body myopathy revisited

Goebel, H. H., D'Agostino, A. N., Wilson, J., Cole, G., Foroud, T., Koller, D., Farlow, M., Azzarelli, B. & Muller, J., 1997, In : Muscle and Nerve. 20, 9, p. 1127-1136 10 p.

Research output: Contribution to journalArticle

Muscles
Crystallins
Desmin
Ubiquitin
Spheroid body myopathy
1 Citation (Scopus)

Standard linkage and association methods identify the mechanism of four susceptibility genes for a simulated complex disease

Pankratz, N., Edenberg, E. & Foroud, T., Dec 30 2005, In : BMC Genetics. 6, SUPPL.1, S142.

Research output: Contribution to journalArticle

Single Nucleotide Polymorphism
Chromosomes, Human, Pair 3
Genes
Chromosomes, Human, Pair 1
Phenotype
6 Citations (Scopus)

Steroid Pathway Genes and Neonatal Respiratory Distress after Betamethasone Use in Anticipated Preterm Birth

Haas, D., Lai, D., Sharma, S., Then, J., Kho, A., Flockhart, D. A., Tantisira, K. & Foroud, T., 2015, In : Reproductive Sciences. 23, 5, p. 680-686 7 p.

Research output: Contribution to journalArticle

Betamethasone
Premature Birth
Single Nucleotide Polymorphism
Steroids
Mothers
10 Citations (Scopus)

Stoppage: An issue for segregation analysis

Slager, S. L., Foroud, T., Haghighi, F., Spence, M. A. & Hodge, S. E., 2001, In : Genetic Epidemiology. 20, 3, p. 328-339 12 p.

Research output: Contribution to journalArticle

Parents
Viverridae
Autistic Disorder
Nuclear Family
Early Diagnosis
44 Citations (Scopus)

Stress-response pathways are altered in the hippocampus of chronic alcoholics

McClintick, J., Xuei, X., Tischfield, J. A., Goate, A., Foroud, T., Wetherill, L., Ehringer, M. A. & Edenberg, H., Nov 2013, In : Alcohol. 47, 7, p. 505-515 11 p.

Research output: Contribution to journalArticle

Alcoholics
alcoholism
Hippocampus
Genes
Alcoholism
17 Citations (Scopus)

Subjective Perceptions Associated with the Ascending and Descending Slopes of Breath Alcohol Exposure Vary with Recent Drinking History

Wetherill, L., Morzorati, S., Foroud, T., Windisch, K., Darlington, T., Zimmerman, U. S., Plawecki, M. H. & O'Connor, S., Jun 2012, In : Alcoholism: Clinical and Experimental Research. 36, 6, p. 1050-1057 8 p.

Research output: Contribution to journalArticle

Drinking
Alcohols
Alcoholism
Young Adult
Emotions
106 Citations (Scopus)

Subtle changes among presymptomatic carriers of the Huntington's disease gene

Kirkwood, S. C., Siemers, E., Hodes, M. E., Conneally, P. M., Christian, J. C. & Foroud, T., 2000, In : Journal of Neurology, Neurosurgery and Psychiatry. 69, 6, p. 773-779 7 p.

Research output: Contribution to journalArticle

Huntington Disease
Genes
Reaction Time
Intelligence
Stretch Reflex
61 Citations (Scopus)

Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees

Foroud, T., Castelluccio, P. F., Koller, D. L., Edenberg, H., Miller, M., Bowman, E., Rau, N. L., Smiley, C., Rice, J. P., Goate, A., Armstrong, C., Bierut, L. J., Reich, T., Detera-Wadleigh, S. D., Goldin, L. R., Badner, J. A., Guroff, J. J., Gershon, E. S., McMahon, F. J., Simpson, S. & 6 others, MacKinnon, D., McInnis, M., Stine, O. C., DePaulo, J. R., Blehar, M. C. & Nurnberger, J., Feb 7 2000, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 96, 1, p. 18-23 6 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Lod Score
Pedigree
Depressive Disorder
Mood Disorders
72 Citations (Scopus)

Suggestive linkage on chromosome 1 for a quantitative alcohol-related phenotype

Dick, D. M., Nurnberger, J., Edenberg, H., Goate, A., Crowe, R., Rice, J., Bucholz, K. K., Kramer, J., Schuckit, M. A., Smith, T. L., Porjesz, B., Begleiter, H., Hesselbrock, V. & Foroud, T., Oct 2002, In : Alcoholism: Clinical and Experimental Research. 26, 10, p. 1453-1460 8 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 1
Chromosomes
Alcoholism
Alcohols
Phenotype
16 Citations (Scopus)

Targeted neurogenesis pathway-based gene analysis identifies ADORA2A associated with hippocampal volume in mild cognitive impairment and Alzheimer's disease

Alzheimer's Disease Neuroimaging Initiative (ADNI), Dec 1 2017, In : Neurobiology of Aging. 60, p. 92-103 12 p.

Research output: Contribution to journalArticle

Neurogenesis
Alzheimer Disease
Genes
Social Adjustment
Parahippocampal Gyrus
25 Citations (Scopus)

Telephone assessment of cognitive function in the late-onset Alzheimer's disease family study

Wilson, R. S., Leurgans, S. E., Foroud, T., Sweet, R. A., Graff-Radford, N., Mayeux, R. & Bennett, D. A., Jul 2010, In : Archives of Neurology. 67, 7, p. 855-861 7 p.

Research output: Contribution to journalArticle

Telephone
Cognition
Alzheimer Disease
Episodic Memory
Short-Term Memory