Tatiana Foroud

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

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99 Citations (Scopus)

α-Synuclein maps to a quantitative trait locus for alcohol preference and is differentially expressed in alcohol-preferring and -nonpreferring rats

Liang, T., Spence, J., Liu, L., Strother, W. N., Chang, H. W., Ellison, J. A., Lumeng, L., Li, T. K., Foroud, T. & Carr, L. G., Apr 15 2003, In : Proceedings of the National Academy of Sciences of the United States of America. 100, 8, p. 4690-4695 6 p.

Research output: Contribution to journalArticle

Synucleins
Quantitative Trait Loci
Alcohols
3' Untranslated Regions
Hippocampus
28 Citations (Scopus)

Whole-genome scan for linkage to bone strength and structure in inbred Fischer 344 and Lewis rats

Alam, I., Sun, Q., Liu, L., Koller, D. L., Fishburn, T., Carr, L. G., Econs, M., Foroud, T. & Turner, C. H., Sep 2005, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 20, 9, p. 1589-1596 8 p.

Research output: Contribution to journalArticle

Inbred Lew Rats
Inbred F344 Rats
Genome
Femur
Bone and Bones
217 Citations (Scopus)

Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort

Shen, L., Kim, S., Risacher, S. L., Nho, K., Swaminathan, S., West, J. D., Foroud, T., Pankratz, N., Moore, J. H., Sloan, C. D., Huentelman, M. J., Craig, D. W., DeChairo, B. M., Potkin, S. G., Jack, C. R., Weiner, M. W. & Saykin, A., Nov 2010, In : NeuroImage. 53, 3, p. 1051-1063 13 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Genome-Wide Association Study
Neuroimaging
Single Nucleotide Polymorphism
Cohort Studies
8 Citations (Scopus)

Whole exome sequencing of intracranial aneurysm

Foroud, T., Jan 2013, In : Stroke. 44, SUPPL. 1

Research output: Contribution to journalArticle

Exome
Genome-Wide Association Study
Intracranial Aneurysm
Human Genome
Pedigree
25 Citations (Scopus)

Whole-exome sequencing in familial Parkinson disease

Farlow, J. L., Robak, L. A., Hetrick, K., Bowling, K., Boerwinkle, E., Coban-Akdemir, Z. H., Gambin, T., Gibbs, R. A., Gu, S., Jain, P., Jankovic, J., Jhangiani, S., Kaw, K., Lai, D., Lin, H., Ling, H., Liu, Y., Lupski, J. R., Muzny, D., Porter, P. & 6 others, Pugh, E., White, J., Doheny, K., Myers, R. M., Shulman, J. M. & Foroud, T., Jan 1 2016, In : JAMA Neurology. 73, 1, p. 68-75 8 p.

Research output: Contribution to journalArticle

Exome
Parkinson Disease
Genes
Age of Onset
Disease Susceptibility
48 Citations (Scopus)

Whole-exome sequencing and imaging genetics identify functional variants for rate of change in hippocampal volume in mild cognitive impairment

Nho, K., Corneveaux, J. J., Kim, S., Lin, H., Risacher, S. L., Shen, L., Swaminathan, S., Ramanan, V. K., Liu, Y., Foroud, T., Inlow, M. H., Siniard, A. L., Reiman, R. A., Aisen, P. S., Petersen, R. C., Green, R. C., Jack, C. R., Weiner, M. W., Baldwin, C. T., Lunetta, K. & 14 others, Farrer, L. A., Furney, S. J., Lovestone, S., Simmons, A., Mecocci, P., Vellas, B., Tsolaki, M., Kloszewska, I., Soininen, H., McDonald, B., Farlow, M., Ghetti, B., Huentelman, M. J. & Saykin, A., Jul 2013, In : Molecular Psychiatry. 18, 7, p. 781-787 7 p.

Research output: Contribution to journalArticle

Apolipoprotein E3
Exome
Atrophy
Neuroimaging
Alzheimer Disease
168 Citations (Scopus)

Voxelwise genome-wide association study (vGWAS)

Stein, J. L., Hua, X., Lee, S., Ho, A. J., Leow, A. D., Toga, A. W., Saykin, A., Shen, L., Foroud, T., Pankratz, N., Huentelman, M. J., Craig, D. W., Gerber, J. D., Allen, A. N., Corneveaux, J. J., DeChairo, B. M., Potkin, S. G., Weiner, M. W. & Thompson, P. M., Nov 2010, In : NeuroImage. 53, 3, p. 1160-1174 15 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Brain
Neuroimaging
Alzheimer Disease
Genome
81 Citations (Scopus)

Voxelwise gene-wide association study (vGeneWAS): Multivariate gene-based association testing in 731 elderly subjects

Hibar, D. P., Stein, J. L., Kohannim, O., Jahanshad, N., Saykin, A., Shen, L., Kim, S., Pankratz, N., Foroud, T., Huentelman, M. J., Potkin, S. G., Jack, C. R., Weiner, M. W., Toga, A. W. & Thompson, P. M., Jun 15 2011, In : NeuroImage. 56, 4, p. 1875-1891 17 p.

Research output: Contribution to journalArticle

Genes
Brain
Single Nucleotide Polymorphism
Genome
Neuroimaging
13 Citations (Scopus)

Visual scanning and cognitive performance in prediagnostic and early-stage Huntington's disease

Blekher, T., Weaver, M. R., Marshall, J., Hui, S., Jackson, J. G., Stout, J. C., Beristain, X., Wojcieszek, J., Yee, R. D. & Foroud, T., Mar 15 2009, In : Movement Disorders. 24, 4, p. 533-540 8 p.

Research output: Contribution to journalArticle

Huntington Disease
Eye Movements
Genes
12 Citations (Scopus)

Visual perception in prediagnostic and early stage Huntington's disease

O'Donnell, B., Blekhert, T. M., Weaver, M., White, K. M., Marshall, J., Beristain, X., Stout, J. C., Gray, J., Wojcieszek, J. & Foroud, T., May 2008, In : Journal of the International Neuropsychological Society. 14, 3, p. 446-453 8 p.

Research output: Contribution to journalArticle

Visual Perception
Huntington Disease
Contrast Sensitivity
Genes
Visual Pathways
9 Citations (Scopus)

Visual function in Hungtington's disease patients and presymptomatic gene carriers

O'Donnell, B., Wilt, M. A., Hake, A., Stout, J. C., Kirkwood, S. C. & Foroud, T., Sep 1 2003, In : Movement Disorders. 18, 9, p. 1027-1034 8 p.

Research output: Contribution to journalArticle

Asymptomatic Diseases
Huntington Disease
Contrast Sensitivity
Genes
Motion Perception
476 Citations (Scopus)

Variations in GABRA2, Encoding the α2 Subunit of the GABA A Receptor, Are Associated with Alcohol Dependence and with Brain Oscillations

Edenberg, H., Dick, D. M., Xuei, X., Tian, H., Almasy, L., Bauer, L. O., Crowe, R. R., Goate, A., Hesselbrock, V., Jones, K., Kwon, J., Li, T. K., Nurnberger, J., O'Connor, S., Reich, T., Rice, J., Schuckit, M. A., Porjesz, B., Foroud, T. & Begleiter, H., Apr 2004, In : American Journal of Human Genetics. 74, 4, p. 705-714 10 p.

Research output: Contribution to journalArticle

GABA-A Receptors
Alcoholism
Single Nucleotide Polymorphism
Brain
Genes
3 Citations (Scopus)
Chromatin Assembly and Disassembly
Alcoholism
Chromatin
Sucrose
Alcohols
33 Citations (Scopus)

Variation in GIGYF2 is not associated with Parkinson disease

Nichols, W. C., Kissell, D. K., Pankratz, N., Pauciulo, M. W., Elsaesser, V. E., Clark, K. A., Halter, C. A., Rudolph, A., Wojcieszek, J., Pfeiffer, R. F. & Foroud, T., Jun 2 2009, In : Neurology. 72, 22, p. 1886-1892 7 p.

Research output: Contribution to journalArticle

Parkinson Disease
Chromosomes
Mutation
Genes
18 Citations (Scopus)

Variants located upstream of CHRNB4 on chromosome 15q25.1 are associated with age at onset of daily smoking and habitual smoking

Kapoor, M., Wang, J. C., Bertelsen, S., Bucholz, K., Budde, J. P., Hinrichs, A., Agrawal, A., Brooks, A., Chorlian, D., Dick, D., Hesselbrock, V., Foroud, T., Kramer, J., Kuperman, S., Manz, N., Nurnberger, J., Porjesz, B., Rice, J., Tischfield, J., Xuei, X. & 4 others, Schuckit, M., Edenberg, H., Bierut, L. J. & Goate, A. M., Mar 16 2012, In : PLoS One. 7, 3, e33513.

Research output: Contribution to journalArticle

alcohol abuse
Chromosomes
young adults
Age of Onset
Genes
191 Citations (Scopus)

Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein e ε4, and the risk of late-onset Alzheimer disease in African Americans

Reitz, C., Jun, G., Naj, A., Rajbhandary, R., Vardarajan, B. N., Wang, L. S., Valladares, O., Lin, C. F., Larson, E. B., Graff-Radford, N. R., Evans, D., De Jager, P. L., Crane, P. K., Buxbaum, J. D., Murrell, J. R., Raj, T., Ertekin-Taner, N., Logue, M., Baldwin, C. T., Green, R. C. & 22 others, Barnes, L. L., Cantwell, L. B., Fallin, M. D., Go, R. C. P., Griffith, P., Obisesan, T. O., Manly, J. J., Lunetta, K. L., Kamboh, M. I., Lopez, O. L., Bennett, D. A., Hendrie, H., Hall, K., Goate, A. M., Byrd, G. S., Kukull, W. A., Foroud, T., Haines, J. L., Farrer, L. A., Pericak-Vance, M. A., Schellenberg, G. D. & Mayeux, R., Apr 10 2013, In : Journal of the American Medical Association. 309, 14, p. 1483-1492 10 p.

Research output: Contribution to journalArticle

ATP-Binding Cassette Transporters
Apolipoproteins
African Americans
Alzheimer Disease
Single Nucleotide Polymorphism
422 Citations (Scopus)

Variants in nicotinic receptors and risk for nicotine dependence

Bierut, L. J., Stitzel, J. A., Wang, J. C., Hinrichs, A. L., Grucza, R. A., Xuei, X., Saccone, N. L., Saccone, S. F., Bertelsen, S., Fox, L., Horton, W. J., Breslau, N., Budde, J., Cloninger, C. R., Dick, D. M., Foroud, T., Hatsukami, D., Hesselbrock, V., Johnson, E. O., Kramer, J. & 13 others, Kuperman, S., Madden, P. A. F., Mayo, K., Nurnberger, J., Pomerleau, O., Porjesz, B., Reyes, O., Schuckit, M., Swan, G., Tischfield, J. A., Edenberg, H., Rice, J. P. & Goate, A. M., Sep 2008, In : American Journal of Psychiatry. 165, 9, p. 1163-1171 9 p.

Research output: Contribution to journalArticle

Tobacco Use Disorder
Nicotinic Receptors
Smoking
Population
Amino Acids
63 Citations (Scopus)
Inbred Strains Rats
Genetic Models
Femur Neck
Bone and Bones
Alleles
1 Citation (Scopus)

Use of variable marker density, principal components, and neural networks in the dissection of disease etiology.

Pankratz, N., Kirkwood, S. C., Flury, L., Koller, D. L. & Foroud, T., 2001, In : Genetic Epidemiology. 21 Suppl 1

Research output: Contribution to journalArticle

Quantitative Trait Loci
Dissection
Phenotype
Principal Component Analysis
Genome
36 Citations (Scopus)

Update on chromosomal locations for psychiatric disorders: Report of the interim meeting of chromosome workshop chairpersons from the VIIth World Congress of Psychiatric Genetics, Monterey; California, October 14-18, 1999

DeLisi, L. E., Craddock, N. J., Detera-Wadleigh, S., Foroud, T., Gejman, P., Kennedy, J. L., Lendon, C., Macciardi, F., McKeon, P., Mynett-Johnson, L., Nurnberger, J., Paterson, A., Schwab, S., Van Broeckhoven, C., Wildenauer, D. & Crow, T. J., Jun 12 2000, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 96, 3, p. 434-449 16 p.

Research output: Contribution to journalArticle

Psychiatry
Chromosomes
Education
Autistic Disorder
Bipolar Disorder
55 Citations (Scopus)

Unique facial features distinguish fetal alcohol syndrome patients and controls in diverse ethnic populations

Moore, E. S., Ward, R. E., Wetherill, L. F., Rogers, J. L., Autti-Rämö, I., Fagerlund, Å., Jacobson, S. W., Robinson, L. K., Hoyme, H. E., Mattson, S. N., Foroud, T., Riley, E., Autti-Rämö, I., Fagerlund, Å., Korkman, M., Jacobson, S. W., Robinson, L. K. & Mattson, S. N., Oct 2007, In : Alcoholism: Clinical and Experimental Research. 31, 10, p. 1707-1713 7 p.

Research output: Contribution to journalArticle

Fetal Alcohol Spectrum Disorders
Alcohols
Population
Anthropometry
Orbits
4 Citations (Scopus)

Understanding the effects of prenatal alcohol exposure using threedimensional facial imaging

Wetherill, L. & Foroud, T., 2011, In : Alcohol Research and Health. 34, 1, p. 38-41 4 p.

Research output: Contribution to journalArticle

Prenatal Exposure Delayed Effects
Fetal Alcohol Spectrum Disorders
Three-Dimensional Imaging
Alcohol Drinking
Alcohols
12 Citations (Scopus)

Uncovering the heterogeneity and temporal complexity of neurodegenerative diseases with Subtype and Stage Inference

The Genetic FTD Initiative (GENFI) & The Alzheimer’s Disease Neuroimaging Initiative (ADNI), Dec 1 2018, In : Nature Communications. 9, 1, 4273.

Research output: Contribution to journalArticle

Neurodegenerative diseases
inference
Neurodegenerative Diseases
Aptitude
Genotype
2 Citations (Scopus)

Type 2 diabetes mellitus, brain atrophy, and cognitive decline

Moran, C., Beare, R., Wang, W., Callisaya, M., Srikanth, V., 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., Liu, E., Montine, T., Gamst, A., Thomas, R. G. & 234 others, Donohue, M., Walter, S., Gessert, D., Sather, T., Harvey, D., Kornak, J., Dale, A., Bernstein, M., Felmlee, J., Fox, N., Thompson, P., Schuff, N., Alexander, G., Decarli, C., Bandy, D., Koeppe, R. A., Foster, N., Reiman, E. M., Chen, K., Mathis, C., Cairns, N. J., Taylor-Reinwald, L., Trojanowki, J. Q., Shaw, L., Lee, V. M. Y., Korecka, M., Crawford, K., Neu, S., Foroud, T. M., Potkin, S., Shen, L., Kachaturian, Z., Frank, R., Snyder, P. J., Molchan, S., Kaye, J., Quinn, J., Lind, B., Dolen, S., Schneider, L. S., Pawluczyk, S., Spann, B. M., Brewer, J., Vanderswag, H., Heidebrink, J. L., Lord, J. L., Johnson, K., Doody, R. S., Villanueva-Meyer, J., Chowdhury, M., Stern, Y., Honig, L. S., Bell, K. L., Morris, J. C., Ances, B., Carroll, M., Leon, S., Mintun, M. A., Schneider, S., Marson, D., Griffith, R., Clark, D., Grossman, H., Mitsis, E., Romirowsky, A., Detoledo-Morrell, L., Shah, R. C., Duara, R., Varon, D., Roberts, P., Albert, M., Onyike, C., Kielb, S., Rusinek, H., De Leon, M. J., Glodzik, L., De Santi, S., Doraiswamy, P. M., Petrella, J. R., Coleman, R. E., Arnold, S. E., Karlawish, J. H., Wolk, D., Smith, C. D., Jicha, G., Hardy, P., Lopez, O. L., Oakley, M., Simpson, D. M., Porsteinsson, A. P., Goldstein, B. S., Martin, K., Makino, K. M., Ismail, M. S., Brand, C., Mulnard, R. A., Thai, G., McAdams-Ortiz, C., Womack, K., Mathews, D., Quiceno, M., Diaz-Arrastia, R., King, R., Weiner, M., Martin-Cook, K., Devous, M., Levey, A. I., Lah, J. J., Cellar, J. S., Burns, J. M., Anderson, H. S., Swerdlow, R. H., Apostolova, L., Lu, P. H., Bartzokis, G., Silverman, D. H. S., Graff-Radford, N. R., Parfitt, F., Johnson, H., Farlow, M. R., Hake, A. M., Matthews, B. R., Herring, S., Van Dyck, C. H., Carson, R. E., Macavoy, M. G., Chertkow, H., Bergman, H., Hosein, C., Black, S., Stefanovic, B., Caldwell, C., Robin Hsiung, G. Y., Feldman, H., Mudge, B., Assaly, M., Kertesz, A., Rogers, J., Trost, D., Bernick, C., Munic, D., Kerwin, D., Mesulam, M. M., Lipowski, K., Wu, C. K., Johnson, N., Sadowsky, C., Martinez, W., Villena, T., Turner, R. S., Johnson, K., Reynolds, B., Sperling, R. A., Johnson, K. A., Marshall, G., Frey, M., Yesavage, J., Taylor, J. L., Lane, B., Rosen, A., Tinklenberg, J., Sabbagh, M., Belden, C., Jacobson, S., Kowall, N., Killiany, R., Budson, A. E., Norbash, A., Johnson, P. L., Obisesan, T. O., Wolday, S., Bwayo, S. K., Lerner, A., Hudson, L., Ogrocki, P., Fletcher, E., Carmichael, O., Olichney, J., Kittur, S., Borrie, M., Bartha, D. R., Johnson, S., Asthana, S., Carlsson, C. M., Potkin, S. G., Preda, A., Nguyen, D., Tariot, P., Fleisher, A., Reeder, S., Bates, V., Capote, H., Rainka, M., Scharre, D. W., Kataki, M., Zimmerman, E. A., Celmins, D., Brown, A. D., Pearlson, G. D., Blank, K., Anderson, K., Santulli, R. B., Schwartz, E. S., Sink, K. M., Williamson, J. D., Garg, P., Watkins, F., Ott, B. R., Querfurth, H., Tremont, G., Salloway, S., Malloy, P., Correia, S., Rosen, H. J., Miller, B. L., Mintzer, J., Longmire, C. F., Spicer, K., Finger, E., Rachinsky, I., Drost, D., Pomara, N., Hernando, R., Sarrael, A., Schultz, S. K., Boles Ponto, L. L., Shim, H., Smith, K. E., Relkin, N., Chaing, G., Raudin, L., Smith, A., Fargher, K. & Raj, B. A., Feb 19 2019, In : Neurology. 92, 8, p. E823-E830

Research output: Contribution to journalArticle

Type 2 Diabetes Mellitus
Atrophy
Brain
Cognition
Cognitive Reserve
48 Citations (Scopus)

Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans

Logue, M. W., Schu, M., Vardarajan, B. N., Farrell, J., Bennett, D. A., Buxbaum, J. D., Byrd, G. S., Ertekin-Taner, N., Evans, D., Foroud, T., Goate, A., Graff-Radford, N. R., Kamboh, M. I., Kukull, W. A., Manly, J. J., Hainesm, J. L., Mayeuxl, R., Pericak-Vancen, M. A., Schellenbergo, G. D., Lunettab, K. L. & 3 others, Baldwina, C. T., Daniele Fallinp, M. & Farrer, L. A., Nov 1 2014, In : Alzheimer's and Dementia. 10, 6, p. 609-618 10 p.

Research output: Contribution to journalArticle

Exome
African Americans
Alzheimer Disease
Single Nucleotide Polymorphism
17 Citations (Scopus)

Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans

Alzheimer's Disease Genetics Consortium, Feb 1 2017, In : Alzheimer's and Dementia. 13, 2, p. 119-129 11 p.

Research output: Contribution to journalArticle

African Americans
Genome-Wide Association Study
Alzheimer Disease
Single Nucleotide Polymorphism
Genome
61 Citations (Scopus)

Two gene co-expression modules differentiate psychotics and controls

Chen, C., Cheng, L., Grennan, K., Pibiri, F., Zhang, C., Badner, J. A., Kelsoe, J. R., Greenwood, T. A., Nievergelt, C. M., Barrett, T. B., McKinney, R., Shilling, P. D., Schork, N. J., Smith, E. N., Bloss, C. S., Nurnberger, J., Edenberg, H., Foroud, T., Koller, D. L., Scheftner, W. & 18 others, Lawson, W. B., Nwulia, E. A., Hipolito, M., Coryell, W., Rice, J., Byerley, W., McMahon, F., Chen, D. T. W., Schulze, T. G., Berrettini, W., Potash, J. B., Zandi, P. P., Mahon, P. B., McInnis, M., Craig, D., Szelinger, S., Gershon, E. S. & Liu, C., Dec 2013, In : Molecular Psychiatry. 18, 12, p. 1308-1314 7 p.

Research output: Contribution to journalArticle

Bipolar Disorder
Schizophrenia
Gene Expression
Neurons
Cerebral Cortex

Twelfth Annual Symposia on Etiology, Pathogenesis, and Treatment of Parkinson's Disease and Etiology, Pathogenesis, and Treatment of Huntington's Disease, Queen Elizabeth Hotel, Montreal, Canada, 18 October 1998

Kieburtz, K., Frey, K., Albin, R., Marek, K., Bates, G., Aylward, E., Guttman, M., Rouleau, G., Baehr, M., Pahwa, R., Lyons, K. E., Wilkinson, S. B., Kieltyka, J., Koller, W. C., Bertoni, J. M., Strickland, D., Eberly, C., Seeland, M., Brewer, M., Stacy, M. & 57 others, Ellgring, H., Pfeiffer, B., Ulm, G., Factor, S. A., Seibyl, J., Innis, R., Marek, K., Frey, K. A., Bohnen, N. I., Elmer, L. W., Koeppe, R. A., Kilbourn, M. R., Lyons, K. E., Troster, A. I., DeCarti, C., Paulson, G. W., Sax, D. S., Kornetsky, C., Siemers, E. R., Hubble, J., Tuite, P., Comella, C., Kompoliti, K., Oakes, D., Wojcieszek, J., Foroud, T., Conneally, P. M., Takanashi, M., Abe, K., Yanagihara, T., Weiner, W. J., Minagar, A., Shulman, L. M., Zakzanis, K. K., Kaplan, E., Leach, L., Freedman, M., Zesiewicz, T. A., Cardoza, F., Malik, A., Willing, A., Sanchez-Ramos, J., Hauser, R. A., Cha, J. H. J., Frey, A. S., Menon, A. S., Chung, W. M., Alsdorf, S. A., Mangiarini, L., Davies, S. W., Penney, J. B., Bates, G. P., Young, A. B., Moskowitz, C. B., Quinn, L., Francis, K. & Schwartz, R., 1998, In : Movement Disorders. 13, 5, p. 858-863 6 p.

Research output: Contribution to journalArticle

62 Citations (Scopus)

TREM2 is associated with increased risk for Alzheimer's disease in African Americans

Jin, S. C., Carrasquillo, M. M., Benitez, B. A., Skorupa, T., Carrell, D., Patel, D., Lincoln, S., Krishnan, S., Kachadoorian, M., Reitz, C., Mayeux, R., Wingo, T. S., Lah, J. J., Levey, A. I., Murrell, J., Hendrie, H., Foroud, T., Graff-Radford, N. R., Goate, A. M., Cruchaga, C. & 1 others, Ertekin-Taner, N., Apr 10 2015, In : Molecular Neurodegeneration. 10, 1, 19.

Research output: Contribution to journalArticle

African Americans
Alzheimer Disease
Linkage Disequilibrium
Myeloid Cells
Mutation
175 Citations (Scopus)

Translation initiator EIF4G1 mutations in familial parkinson disease

Chartier-Harlin, M. C., Dachsel, J. C., Vilariño-Güell, C., Lincoln, S. J., Leprêtre, F., Hulihan, M. M., Kachergus, J., Milnerwood, A. J., Tapia, L., Song, M. S., Le Rhun, E., Mutez, E., Larvor, L., Duflot, A., Vanbesien-Mailliot, C., Kreisler, A., Ross, O. A., Nishioka, K., Soto-Ortolaza, A. I., Cobb, S. A. & 30 others, Melrose, H. L., Behrouz, B., Keeling, B. H., Bacon, J. A., Hentati, E., Williams, L., Yanagiya, A., Sonenberg, N., Lockhart, P. J., Zubair, A. C., Uitti, R. J., Aasly, J. O., Krygowska-Wajs, A., Opala, G., Wszolek, Z. K., Frigerio, R., Maraganore, D. M., Gosal, D., Lynch, T., Hutchinson, M., Bentivoglio, A. R., Valente, E. M., Nichols, W. C., Pankratz, N., Foroud, T., Gibson, R. A., Hentati, F., Dickson, D. W., Destée, A. & Farrer, M. J., Sep 9 2011, In : American Journal of Human Genetics. 89, 3, p. 398-406 9 p.

Research output: Contribution to journalArticle

Parkinsonian Disorders
Parkinson Disease
Mutation
Eukaryotic Initiation Factor-4G
Lewy Body Disease
3 Citations (Scopus)
Translational Medical Research
Epidemiology
33 Citations (Scopus)

Transethnic genome-wide scan identifies novel Alzheimer's disease loci

Jun, G. R., Chung, J., Mez, J., Barber, R., Beecham, G. W., Bennett, D. A., Buxbaum, J. D., Byrd, G. S., Carrasquillo, M. M., Crane, P. K., Cruchaga, C., De Jager, P., Ertekin-Taner, N., Evans, D., Fallin, M. D., Foroud, T. M., Friedland, R. P., Goate, A. M., Graff-Radford, N. R., Hendrie, H. & 31 others, Hall, K. S., Hamilton-Nelson, K. L., Inzelberg, R., Kamboh, M. I., Kauwe, J. S. K., Kukull, W. A., Kunkle, B. W., Kuwano, R., Larson, E. B., Logue, M. W., Foroud, T., Martin, E. R., Hendrie, H., Hall, K., Naj, A., Reiman, E. M., Reitz, C., Sherva, R., St. George-Hyslop, P. H., Thornton, T., Younkin, S. G., Vardarajan, B. N., Wang, L. S., Wendlund, J. R., Winslow, A. R., Haines, J., Mayeux, R., Pericak-Vance, M. A., Schellenberg, G., Lunetta, K. L. & Saykin, A., 2017, (Accepted/In press) In : Alzheimer's and Dementia.

Research output: Contribution to journalArticle

Alzheimer Disease
Genome
Single Nucleotide Polymorphism
Genome-Wide Association Study
Genetic Loci
44 Citations (Scopus)

Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

23andMe Research Team, Dec 1 2018, In : Nature Neuroscience. 21, 12, p. 1656-1669 14 p.

Research output: Contribution to journalArticle

Open Access
Genome-Wide Association Study
Alcoholism
Psychiatry
Genome
Drinking Behavior
313 Citations (Scopus)

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

Elks, C. E., Perry, J. R. B., Sulem, P., Chasman, D. I., Franceschini, N., He, C., Lunetta, K. L., Visser, J. A., Byrne, E. M., Cousminer, D. L., Gudbjartsson, D. F., Esko, T., Feenstra, B., Hottenga, J. J., Koller, D. L., Kutalik, Z., Lin, P., Mangino, M., Marongiu, M., McArdle, P. F. & 154 others, Smith, A. V., Stolk, L., Van Wingerden, S. H., Zhao, J. H., Albrecht, E., Corre, T., Ingelsson, E., Hayward, C., Magnusson, P. K. E., Smith, E. N., Ulivi, S., Warrington, N. M., Zgaga, L., Alavere, H., Amin, N., Aspelund, T., Bandinelli, S., Barroso, I., Berenson, G. S., Bergmann, S., Blackburn, H., Boerwinkle, E., Buring, J. E., Busonero, F., Campbell, H., Chanock, S. J., Chen, W., Cornelis, M. C., Couper, D., Coviello, A. D., D'Adamo, P., De Faire, U., De Geus, E. J. C., Deloukas, P., Döring, A., Smith, G. D., Easton, D. F., Eiriksdottir, G., Emilsson, V., Eriksson, J., Ferrucci, L., Folsom, A. R., Foroud, T., Garcia, M., Gasparini, P., Geller, F., Gieger, C., Gudnason, V., Hall, P., Hankinson, S. E., Ferreli, L., Heath, A. C., Hernandez, D. G., Hofman, A., Hu, F. B., Illig, T., Järvelin, M. R., Johnson, A. D., Karasik, D., Khaw, K. T., Kiel, D. P., Kilpelänen, T. O., Kolcic, I., Kraft, P., Launer, L. J., Laven, J. S. E., Li, S., Liu, J., Levy, D., Martin, N. G., McArdle, W. L., Melbye, M., Mooser, V., Murray, J. C., Murray, S. S., Nalls, M. A., Navarro, P., Nelis, M., Ness, A. R., Northstone, K., Oostra, B. A., Peacock, M., Palmer, L. J., Palotie, A., Paré, G., Parker, A. N., Pedersen, N. L., Peltonen, L., Pennell, C. E., Pharoah, P., Polasek, O., Plump, A. S., Pouta, A., Porcu, E., Rafnar, T., Rice, J. P., Ring, S. M., Rivadeneira, F., Rudan, I., Sala, C., Salomaa, V., Sanna, S., Schlessinger, D., Schork, N. J., Scuteri, A., Segrè, A. V., Shuldiner, A. R., Soranzo, N., Sovio, U., Srinivasan, S. R., Strachan, D. P., Tammesoo, M. L., Tikkanen, E., Toniolo, D., Tsui, K., Tryggvadottir, L., Tyrer, J., Uda, M., Van Dam, R. M., Van Meurs, J. B. J., Vollenweider, P., Waeber, G., Wareham, N. J., Waterworth, D. M., Weedon, M. N., Wichmann, H. E., Willemsen, G., Wilson, J. F., Wright, A. F., Young, L., Zhai, G., Zhuang, W. V., Bierut, L. J., Boomsma, D. I., Boyd, H. A., Crisponi, L., Demerath, E. W., Van Duijn, C. M., Econs, M., Harris, T. B., Hunter, D. J., Loos, R. J. F., Metspalu, A., Montgomery, G. W., Ridker, P. M., Spector, T. D., Streeten, E. A., Stefansson, K., Thorsteinsdottir, U., Uitterlinden, A. G., Widen, E., Murabito, J. M., Ong, K. K. & Murray, A., Dec 1 2010, In : Nature Genetics. 42, 12, p. 1077-1085 9 p.

Research output: Contribution to journalArticle

Menarche
Genome-Wide Association Study
Meta-Analysis
Genes
Biological Phenomena
32 Citations (Scopus)

The tachykinin receptor 3 is associated with alcohol and cocaine dependence

Foroud, T., Wetherill, L. F., Kramer, J., Tischfield, J. A., Nurnberger, J., Schuckit, M. A., Xuei, X. & Edenberg, H., Jun 2008, In : Alcoholism: Clinical and Experimental Research. 32, 6, p. 1023-1030 8 p.

Research output: Contribution to journalArticle

Tachykinin Receptors
Cocaine-Related Disorders
Cocaine
Alcoholism
Alcohols
21 Citations (Scopus)

The Systemic Synuclein Sampling Study: Toward a biomarker for Parkinson's disease

Visanji, N. P., Mollenhauer, B., Beach, T. G., Adler, C. H., Coffey, C. S., Kopil, C. M., Dave, K. D., Foroud, T., Chahine, L. & Jennings, D., Apr 1 2017, In : Biomarkers in Medicine. 11, 4, p. 359-368 10 p.

Research output: Contribution to journalArticle

Synucleins
Sampling Studies
Biomarkers
Parkinson Disease
Sampling
49 Citations (Scopus)

The search for genetic risk factors associated with suicidal behavior

Hesselbrock, V., Dick, D., Hesselbrock, M., Foroud, T., Schuckit, M., Edenberg, H., Bucholz, K., Kramer, J., Reich, T., Goate, A., Bierut, L., Rice, J. P. & Nurnberger, J., May 2004, In : Alcoholism: Clinical and Experimental Research. 28, 5 SUPPL.

Research output: Contribution to journalArticle

Chromosomes
Suicide
Alcohols
Lod Score
Alcoholism
164 Citations (Scopus)

The role of GABRA2 in risk for conduct disorder and alcohol and drug dependence across developmental stages

Dick, D. M., Bierut, L., Hinrichs, A., Fox, L., Bucholz, K. K., Kramer, J., Kuperman, S., Hesselbrock, V., Schuckit, M., Almasy, L., Tischfield, J., Porjesz, B., Begleiter, H., Nurnberger, J., Xuei, X., Edenberg, H. & Foroud, T., Jul 2006, In : Behavior Genetics. 36, 4, p. 577-590 14 p.

Research output: Contribution to journalArticle

drug abuse
Conduct Disorder
alcohol abuse
developmental stage
Alcoholism
19 Citations (Scopus)

The role of cardiovascular risk factors and stroke in familial Alzheimer disease

Tosto, G., Bird, T. D., Bennett, D. A., Boeve, B. F., Brickman, A. M., Cruchaga, C., Faber, K., Foroud, T., Farlow, M., Goate, A. M., Graff-Radford, N. R., Lantigua, R., Manly, J., Ottman, R., Rosenberg, R., Schaid, D. J., Schupf, N., Stern, Y., Sweet, R. A. & Mayeux, R., Oct 1 2016, In : JAMA Neurology. 73, 10, p. 1231-1237 7 p.

Research output: Contribution to journalArticle

Alzheimer Disease
Stroke
Odds Ratio
Apolipoprotein E4
Cardiovascular Diseases
83 Citations (Scopus)

The role of apolipoprotein E (APOE) genotype in early mild cognitive impairment (E-MCI)

Risacher, S. L., Kim, S., Shen, L., Nho, K., Foroud, T., Green, R. C., Petersen, R. C., Jack, C. R., Aisen, P. S., Koeppe, R. A., Jagust, W. J., Shaw, L. M., Trojanowski, J. Q., Weiner, M. W. & Saykin, A., 2013, In : Frontiers in Aging Neuroscience. 5, APR, Article 11.

Research output: Contribution to journalArticle

Apolipoproteins E
Cerebrospinal Fluid
Genotype
Apolipoprotein E4
Amyloid
37 Citations (Scopus)

The relationship between smoking and replicated sequence variants on chromosomes 8 and 9 with familial intracranial aneurysm

Deka, R., Koller, D. L., Lai, D., Indugula, S. R., Sun, G., Woo, D., Sauerbeck, L., Moomaw, C. J., Hornung, R., Connolly, E. S., Anderson, C., Rouleau, G., Meissner, I., Bailey-Wilson, J. E., Huston, J., Brown, R. D., Kleindorfer, D. O., Flaherty, M. L., Langefeld, C. D., Foroud, T. & 1 others, Broderick, J. P., Jun 2010, In : Stroke. 41, 6, p. 1132-1137 6 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 8
Chromosomes, Human, Pair 9
Intracranial Aneurysm
Smoking
Single Nucleotide Polymorphism
2 Citations (Scopus)

The Promise and Pitfalls of Facebook Advertising: a Genetic Counselor’s Perspective

Verbrugge, J., Rumbaugh, M., Cook, L., Schulze, J., Miller, M., Heathers, L., Arnedo, V., Kuhl, M. M. G. & Foroud, T., Apr 1 2018, In : Journal of Genetic Counseling. 27, 2, p. 326-328 3 p.

Research output: Contribution to journalArticle

Research
Internet
Parkinson Disease
Biomarkers
Counselors
8 Citations (Scopus)

The Parkinson's progression markers initiative (PPMI) – establishing a PD biomarker cohort

the Parkinson's Progression Markers Initiative, Jan 1 2018, (Accepted/In press) In : Annals of Clinical and Translational Neurology.

Research output: Contribution to journalArticle

Parkinson Disease
Biomarkers
Dopamine Plasma Membrane Transport Proteins
Cerebrospinal Fluid
Synucleins
57 Citations (Scopus)

The opioid system in alcohol and drug dependence: Family-based association study

Xuei, X., Flury-Wetherill, L., Bierut, L., Dick, D., Nurnberger, J., Foroud, T. & Edenberg, H., Oct 5 2007, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 144, 7, p. 877-884 8 p.

Research output: Contribution to journalArticle

Pro-Opiomelanocortin
Opioid Analgesics
Alcoholism
Substance-Related Disorders
Single Nucleotide Polymorphism
54 Citations (Scopus)

The North American Multiple System Atrophy Study Group

Gilman, S., May, S. J., Shults, C. W., Tanner, C. M., Kukull, W., Lee, V. M. Y., Masliah, E., Low, P., Sandroni, P., Trojanowski, J. Q., Ozelius, L. & Foroud, T., Dec 2005, In : Journal of Neural Transmission. 112, 12, p. 1687-1694 8 p.

Research output: Contribution to journalArticle

Multiple System Atrophy
alpha-Synuclein
Levodopa
Research Personnel
Cerebellar Diseases
11 Citations (Scopus)
Drinking
Trajectories
Alcohols
Genes
Alcoholism
5 Citations (Scopus)

The genetics of dementia

Farlow, J. L. & Foroud, T., 2013, In : Seminars in Neurology. 33, 4, p. 417-422 6 p.

Research output: Contribution to journalArticle

Dementia
Genes
Frontotemporal Lobar Degeneration
Exome
Inborn Genetic Diseases
157 Citations (Scopus)

The genetics of alcoholism: Identifying specific genes through family studies

Edenberg, H. & Foroud, T., Sep 2006, In : Addiction Biology. 11, 3-4, p. 386-396 11 p.

Research output: Contribution to journalArticle

Alcoholism
Genes
Phenotype
Single Nucleotide Polymorphism
Research Personnel
47 Citations (Scopus)

The Familial Intracranial Aneurysm (FIA) study protocol

Broderick, J. P., Sauerbeck, L. R., Foroud, T., Huston, J., Pankratz, N., Meissner, I. & Brown, R. D., Apr 26 2005, In : BMC Medical Genetics. 6, 17.

Research output: Contribution to journalArticle

Intracranial Aneurysm
Ruptured Aneurysm
Aneurysm
Rupture
Genome
294 Citations (Scopus)

The ENIGMA Consortium: Large-scale collaborative analyses of neuroimaging and genetic data

Thompson, P. M., Stein, J. L., Medland, S. E., Hibar, D. P., Vasquez, A. A., Renteria, M. E., Toro, R., Jahanshad, N., Schumann, G., Franke, B., Wright, M. J., Martin, N. G., Agartz, I., Alda, M., Alhusaini, S., Almasy, L., Almeida, J., Alpert, K., Andreasen, N. C., Andreassen, O. A. & 269 others, Apostolova, L. G., Appel, K., Armstrong, N. J., Aribisala, B., Bastin, M. E., Bauer, M., Bearden, C. E., Bergmann, Ø., Binder, E. B., Blangero, J., Bockholt, H. J., Bøen, E., Bois, C., Boomsma, D. I., Booth, T., Bowman, I. J., Bralten, J., Brouwer, R. M., Brunner, H. G., Brohawn, D. G., Buckner, R. L., Buitelaar, J., Bulayeva, K., Bustillo, J. R., Calhoun, V. D., Cannon, D. M., Cantor, R. M., Carless, M. A., Caseras, X., Cavalleri, G. L., Chakravarty, M. M., Chang, K. D., Ching, C. R. K., Christoforou, A., Cichon, S., Clark, V. P., Conrod, P., Coppola, G., Crespo-Facorro, B., Curran, J. E., Czisch, M., Deary, I. J., de Geus, E. J. C., den Braber, A., Delvecchio, G., Depondt, C., de Haan, L., de Zubicaray, G. I., Dima, D., Dimitrova, R., Djurovic, S., Dong, H., Donohoe, G., Duggirala, R., Dyer, T. D., Ehrlich, S., Ekman, C. J., Elvsåshagen, T., Emsell, L., Erk, S., Espeseth, T., Fagerness, J., Fears, S., Fedko, I., Fernández, G., Fisher, S. E., Foroud, T., Fox, P. T., Francks, C., Frangou, S., Frey, E. M., Frodl, T., Frouin, V., Garavan, H., Giddaluru, S., Glahn, D. C., Godlewska, B., Goldstein, R. Z., Gollub, R. L., Grabe, H. J., Grimm, O., Gruber, O., Guadalupe, T., Gur, R. E., Gur, R. C., Göring, H. H. H., Hagenaars, S., Hajek, T., Hall, G. B., Hall, J., Hardy, J., Hartman, C. A., Hass, J., Hatton, S. N., Haukvik, U. K., Hegenscheid, K., Heinz, A., Hickie, I. B., Ho, B. C., Hoehn, D., Hoekstra, P. J., Hollinshead, M., Holmes, A. J., Homuth, G., Hoogman, M., Hong, L. E., Hosten, N., Hottenga, J. J., Hulshoff Pol, H. E., Hwang, K. S., Jack, C. R., Jenkinson, M., Johnston, C., Jönsson, E. G., Kahn, R. S., Kasperaviciute, D., Kelly, S., Kim, S., Kochunov, P., Koenders, L., Krämer, B., Kwok, J. B. J., Lagopoulos, J., Laje, G., Landen, M., Landman, B. A., Lauriello, J., Lawrie, S. M., Lee, P. H., Le Hellard, S., Lemaître, H., Leonardo, C. D., Li, C. S., Liberg, B., Liewald, D. C., Liu, X., Lopez, L. M., Loth, E., Lourdusamy, A., Luciano, M., Macciardi, F., Machielsen, M. W. J., MacQueen, G. M., Malt, U. F., Mandl, R., Manoach, D. S., Martinot, J. L., Matarin, M., Mather, K. A., Mattheisen, M., Mattingsdal, M., Meyer-Lindenberg, A., McDonald, C., McIntosh, A. M., McMahon, F. J., McMahon, K. L., Meisenzahl, E., Melle, I., Milaneschi, Y., Mohnke, S., Montgomery, G. W., Morris, D. W., Moses, E. K., Mueller, B. A., Muñoz Maniega, S., Mühleisen, T. W., Müller-Myhsok, B., Mwangi, B., Nauck, M., Nho, K., Nichols, T. E., Nilsson, L. G., Nugent, A. C., Nyberg, L., Olvera, R. L., Oosterlaan, J., Ophoff, R. A., Pandolfo, M., Papalampropoulou-Tsiridou, M., Papmeyer, M., Paus, T., Pausova, Z., Pearlson, G. D., Penninx, B. W., Peterson, C. P., Pfennig, A., Phillips, M., Pike, G. B., Poline, J. B., Potkin, S. G., Pütz, B., Ramasamy, A., Rasmussen, J., Rietschel, M., Rijpkema, M., Risacher, S. L., Roffman, J. L., Roiz-Santiañez, R., Romanczuk-Seiferth, N., Rose, E. J., Royle, N. A., Rujescu, D., Ryten, M., Sachdev, P. S., Salami, A., Satterthwaite, T. D., Savitz, J., Saykin, A., Scanlon, C., Schmaal, L., Schnack, H. G., Schork, A. J., Schulz, S. C., Schür, R., Seidman, L., Shen, L., Shoemaker, J. M., Simmons, A., Sisodiya, S. M., Smith, C., Smoller, J. W., Soares, J. C., Sponheim, S. R., Sprooten, E., Starr, J. M., Steen, V. M., Strakowski, S., Strike, L., Sussmann, J., Sämann, P. G., Teumer, A., Toga, A. W., Tordesillas-Gutierrez, D., Trabzuni, D., Trost, S., Turner, J., Van den Heuvel, M., van der Wee, N. J., van Eijk, K., van Erp, T. G. M., van Haren, N. E. M., van 't Ent, D., van Tol, M. J., Valdés Hernández, M. C., Veltman, D. J., Versace, A., Völzke, H., Walker, R., Walter, H., Wang, L., Wardlaw, J. M., Weale, M. E., Weiner, M. W., Wen, W., Westlye, L. T., Whalley, H. C., Whelan, C. D., White, T., Winkler, A. M., Wittfeld, K., Woldehawariat, G., Wolf, C., Zilles, D., Zwiers, M. P., Thalamuthu, A., Schofield, P. R., Freimer, N. B., Lawrence, N. S. & Drevets, W., 2014, In : Brain Imaging and Behavior. 8, 2, p. 153-182 30 p.

Research output: Contribution to journalArticle

Neuroimaging
Meta-Analysis
Genome-Wide Association Study
Brain
Attention Deficit Disorder with Hyperactivity