Tatiana Foroud

  • 42200 Citations
  • 101 h-Index
1976 …2021
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Publications 1988 2020

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20 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Exome
aneurysm
Inborn Genetic Diseases
Intracranial Aneurysm
genetic disorders
766 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Parkinson Disease
Meta-Analysis
Genome
Odds Ratio
Genome-Wide Association Study
20 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

polymorphism
nucleotides
Genomics
Polymorphism
Single Nucleotide Polymorphism
834 Citations (Scopus)

Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

Sklar, P., Ripke, S., Scott, L. J., Andreassen, O. A., Cichon, S., Craddock, N., Edenberg, H., Nurnberger, J., Rietschel, M., Blackwood, D., Corvin, A., Flickinger, M., Guan, W., Mattingsdal, M., McQuillin, A., Kwan, P., Wienker, T. F., Daly, M., Dudbridge, F., Holmans, P. A. & 152 others, Lin, D., Burmeister, M., Greenwood, T. A., Hamshere, M. L., Muglia, P., Smith, E. N., Zandi, P. P., Nievergelt, C. M., McKinney, R., Shilling, P. D., Schork, N. J., Bloss, C. S., Foroud, T., Koller, D. L., Gershon, E. S., Liu, C., Badner, J. A., Scheftner, W. A., Lawson, W. B., Nwulia, E. A., Hipolito, M., Coryell, W., Rice, J., Byerley, W., McMahon, F. J., Schulze, T. G., Berrettini, W., Lohoff, F. W., Potash, J. B., Mahon, P. B., McInnis, M. G., Zöllner, S., Zhang, P., Craig, D. W., Szelinger, S., Barrett, T. B., Breuer, R., Meier, S., Strohmaier, J., Witt, S. H., Tozzi, F., Farmer, A., McGuffin, P., Strauss, J., Xu, W., Kennedy, J. L., Vincent, J. B., Matthews, K., Day, R., Ferreira, M. A., O'Dushlaine, C., Perlis, R., Raychaudhuri, S., Ruderfer, D., Lee, P. H., Smoller, J. W., Li, J., Absher, D., Bunney, W. E., Barchas, J. D., Schatzberg, A. F., Jones, E. G., Meng, F., Thompson, R. C., Watson, S. J., Myers, R. M., Akil, H., Boehnke, M., Chambert, K., Moran, J., Scolnick, E., Djurovic, S., Melle, I., Morken, G., Gill, M., Morris, D., Quinn, E., Mühleisen, T. W., Degenhardt, F. A., Mattheisen, M., Schumacher, J., Maier, W., Steffens, M., Propping, P., Nöthen, M. M., Anjorin, A., Bass, N., Gurling, H., Kandaswamy, R., Lawrence, J., McGhee, K., McIntosh, A., McLean, A. W., Muir, W. J., Pickard, B. S., Breen, G., St. Clair, D., Caesar, S., Gordon-Smith, K., Jones, L., Fraser, C., Green, E. K., Grozeva, D., Jones, I. R., Kirov, G., Moskvina, V., Nikolov, I., O'Donovan, M. C., Owen, M. J., Collier, D. A., Elkin, A., Williamson, R., Young, A. H., Nicol Ferrier, I., Stefansson, K., Stefansson, H., Porgeirsson, P., Steinberg, S., Gustafsson, Ó., Bergen, S. E., Nimgaonkar, V., Hultman, C., Landén, M., Lichtenstein, P., Sullivan, P., Schalling, M., Osby, U., Backlund, L., Frisén, L., Langstrom, N., Jamain, S., Leboyer, M., Etain, B., Bellivier, F., Petursson, H., Sigurdsson, E., Müller-Mysok, B., Lucae, S., Schwarz, M., Fullerton, J. M., Schofield, P. R., Martin, N., Montgomery, G. W., Lathrop, M., Óskarsson, H., Bauer, M., Wright, A., Mitchell, P. B., Hautzinger, M., Reif, A., Kelsoe, J. R. & Purcell, S. M., Oct 2011, In : Nature Genetics. 43, 10, p. 977-985 9 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Bipolar Disorder
Single Nucleotide Polymorphism
Calcium Channels
Sample Size
29 Citations (Scopus)

Lack of association of alcohol dependence and habitual smoking with catechol-O-methyltransferase

Foroud, T., Wetherill, L. F., Dick, D. M., Hesselbrock, V., Nurnberger, J., Kramer, J., Tischfield, J., Schuckit, M., Bierut, L. J., Xuei, X. & Edenberg, H., Nov 2007, In : Alcoholism: Clinical and Experimental Research. 31, 11, p. 1773-1779 7 p.

Research output: Contribution to journalArticle

Catechol O-Methyltransferase
Alcoholism
Smoking
Alcohols
Polymorphism
4 Citations (Scopus)

L1 coupling to ankyrin and the spectrin-actin cytoskeleton modulates ethanol inhibition of L1 adhesion and ethanol teratogenesis

Dou, X., Menkari, C., Mitsuyama, R., Foroud, T., Wetherill, L., Hammond, P., Suttie, M., Chen, X., Chen, S. Y. & Charness, M. E., Mar 1 2018, In : FASEB Journal. 32, 3, p. 1364-1374 11 p.

Research output: Contribution to journalArticle

Ankyrins
Teratogenesis
Spectrin
Actin Cytoskeleton
Actins
156 Citations (Scopus)

Joint multipoint linkage analysis of multivariate qualitative and quantitative trait. II. Alcoholism and event-related potentials

Williams, J. T., Begleiter, H., Porjesz, B., Edenberg, H., Foroud, T., Reich, T., Goate, A., Van Eerdewegh, P., Almasy, L. & Blangero, J., 1999, In : American Journal of Human Genetics. 65, 4, p. 1148-1160 13 p.

Research output: Contribution to journalArticle

Evoked Potentials
Alcoholism
Multivariate Analysis
Joints
P300 Event-Related Potentials
98 Citations (Scopus)

Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder

Cross-Disorder Working Group of the Psychiatric Genomics Consortium, Feb 5 2015, In : American Journal of Human Genetics. 96, 2, p. 283-294 12 p.

Research output: Contribution to journalArticle

Major Depressive Disorder
Bipolar Disorder
Psychiatry
Schizophrenia
Sample Size
30 Citations (Scopus)

Is there a genetic relationship between alcoholism and depression?

Nurnberger, J., Foroud, T., Flury, L., Meyer, E. T. & Wiegand, R., 2002, In : Alcohol Research and Health. 26, 3, p. 233-240 8 p.

Research output: Contribution to journalArticle

Alcoholism
Depression
Phenotype
Chromosomes, Human, Pair 1
Genes
1 Citation (Scopus)

Introduction to genetic linkage analysis

Foroud, T., 1997, In : Cancer Investigation. 15, 6, p. 548-552 5 p.

Research output: Contribution to journalArticle

Genetic Linkage
Neurofibromatoses
Chromosome Mapping
Huntington Disease
Cystic Fibrosis
2 Citations (Scopus)

Interpretation of Genetic Linkage Findings (multiple letters)

Liu, Y., Xu, F., Recker, R. R., Deng, H. W., Koller, D. L., White, K., Liu, G., Hui, S., Conneally, P. M., Johnston, C. C., Econs, M., Foroud, T. & Peacock, M., Nov 2003, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 18, 11, p. 2077-2080 4 p.

Research output: Contribution to journalArticle

Lod Score
Genetic Linkage
Chromosome Mapping
Quantitative Trait Loci
Reproducibility of Results

Interactive feature visualization and detection for 3D face classification

McLaughlin, J., Fang, S., Jacobson, S. W., Hoyme, H. E., Robinson, L. & Foroud, T., Apr 2011, In : International Journal of Cognitive Informatics and Natural Intelligence. 5, 2, p. 1-16 16 p.

Research output: Contribution to journalArticle

Visualization
Alcohols
Lighting
Decision making
Geometry
8 Citations (Scopus)

Integration of bioinformatics and imaging informatics for identifying rare PSEN1 variants in Alzheimer's disease

Nho, K., Horgusluoglu, E., Kim, S., Risacher, S. L., Kim, D., Foroud, T., Aisen, P. S., Petersen, R. C., Jack, C. R., Shaw, L. M., Trojanowski, J. Q., Weiner, M. W., Green, R. C., Toga, A. W. & Saykin, A., Aug 12 2016, In : BMC Medical Genomics. 9, 30.

Research output: Contribution to journalArticle

Informatics
Computational Biology
Endophenotypes
Cerebrospinal Fluid
Alzheimer Disease
34 Citations (Scopus)

Integrating mRNA and miRNA weighted gene co-expression networks with eQTLs in the nucleus accumbens of subjects with alcohol dependence

Mamdani, M., Williamson, V., McMichael, G. O., Blevins, T., Aliev, F., Adkins, A., Hack, L., Bigdeli, T., Van Der Vaart, A. D., Web, B. T., Bacanu, S. A., Kalsi, G., Kendler, K. S., Miles, M. F., Dick, D., Riley, B. P., Dumur, C., Vladimirov, V. I., Hesselbrock, V., Edenberg, H. & 29 others, Nurnberger, J., Foroud, T., Kuperman, S., Kramer, J., Porjesz, B., Bierut, L., Goate, A., Rice, J., Bucholz, K., Schuckit, M., Tischfield, J., Almasy, L., Taylor, R., Dick, D., Bauer, L., Koller, D., O'Connor, S., Wetherill, L., Xuei, X., Chan, G., Kang, S., Manz, N., Rangaswamy, M., Rohrbaugh, J., Wang, J. C., Brooks, A., Aliev, F., Parsian, A. & Reilly, M., Sep 18 2015, In : PLoS One. 10, 9, e0137671.

Research output: Contribution to journalArticle

Nucleus Accumbens
alcohol abuse
MicroRNAs
microRNA
Alcoholism
143 Citations (Scopus)

Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: Chromosomes 3, 5, 15, 16, 17, and 22

Edenberg, H., Foroud, T., Conneally, P. M., Sorbel, J. J., Carr, K., Crose, C., Willig, C., Zhao, J., Miller, M., Bowman, E., Mayeda, A., Rau, N. L., Smiley, C., Rice, J. P., Goate, A., Reich, T., Stine, O. C., McMahon, F., DePaulo, J. R., Meyers, D. & 5 others, Detera-Wadleigh, S. D., Goldin, L. R., Gershon, E. S., Blehar, M. C. & Nurnberger, J., 1997, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 74, 3, p. 238-246 9 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 5
Chromosomes, Human, Pair 3
Pedigree
Alleles
93 Citations (Scopus)

Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: Chromosomes 2, 11, 13, 14, and x

Stine, O. C., McMahon, F. J., Chen, L. S., Xu, J., Meyers, D. A., MacKinnon, D. F., Simpson, S., McInnis, M. G., Rice, J. P., Goate, A., Reich, T., Edenberg, H., Foroud, T., Nurnberger, J., Detera-Wadleigh, S. D., Goldin, L. R., Guroff, J., Gershon, E. S., Blehar, M. C. & DePaulo, J. R., 1997, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 74, 3, p. 263-269 7 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 11
Chromosomes, Human, Pair 2
Pedigree
Bipolar Disorder
114 Citations (Scopus)

Initial genome scan of the NIMH genetics initiative bipolar pedigrees: Chromosomes 4, 7, 9, 18, 19, 20, and 21q

Detera-Wadleigh, S. D., Badner, J. A., Yoshikawa, T., Sanders, A. R., Goldin, L. R., Turner, G., Rolling, D. Y., Moses, T., Guroff, J. J., Kazuba, D., Maxwell, M. E., Edenberg, H., Foroud, T., Lahiri, D., Nurnberger, J., Stine, O. C., McMahon, F., Meyers, D. A., MacKinnon, D., Simpson, S. & 7 others, McInnis, M., DePaulo, J. R., Rice, J., Goate, A., Reich, T., Blehar, M. C. & Gershon, E. S., 1997, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 74, 3, p. 254-262 9 p.

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Chromosomes, Human, Pair 4
Chromosomes, Human, Pair 7
Pedigree
Alleles
109 Citations (Scopus)

Initial genome scan of the nimh genetics initiative bipolar pedigrees: Chromosomes 1, 6, 8, 10, and 12

Rice, J. P., Goate, A., Williams, J. T., Bierut, L., Dorr, D., Wu, W., Shears, S., Gopalakrishnan, G., Edenberg, H., Foroud, T., Nurnberger, J., Gershon, E. S., Detera-Wadleigh, S. D., Goldin, L. R., Guroff, J. J., McMahon, F. J., Simpson, S., MacKinnon, D., McInnis, M., Stine, O. C. & 3 others, DePaulo, J. R., Blehar, M. C. & Reich, T., 1997, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 74, 3, p. 247-253 7 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 6
Chromosomes, Human, Pair 1
Pedigree
Lod Score
Genome
14 Citations (Scopus)

Inheritance of susceptibility to root resorption associated with orthodontic force in mice

Abass, S. K., Hartsfield, J. K., Al-Qawasmi, R. A., Everett, E. T., Foroud, T. & Roberts, W. E., Dec 2008, In : American Journal of Orthodontics and Dentofacial Orthopedics. 134, 6, p. 742-750 9 p.

Research output: Contribution to journalArticle

Root Resorption
Orthodontics
Multifactorial Inheritance
Inheritance Patterns
Genetic Heterogeneity
42 Citations (Scopus)

Influence of Genetic Variation on Plasma Protein Levels in Older Adults Using a Multi-Analyte Panel

Kim, S., Swaminathan, S., Inlow, M., Risacher, S. L., Nho, K., Shen, L., Foroud, T., Petersen, R. C., Aisen, P. S., Soares, H., Toledo, J. B., Shaw, L. M., Trojanowski, J. Q., Weiner, M. W., McDonald, B., Farlow, M., Ghetti, B. & Saykin, A., Jul 23 2013, In : PLoS One. 8, 7, e70269.

Research output: Contribution to journalArticle

blood proteins
Blood Proteins
Polymorphism
Single Nucleotide Polymorphism
genetic variation
48 Citations (Scopus)

Influence of ADH1B polymorphism on alcohol use and its subjective effects in a Jewish population

Carr, L. G., Foroud, T., Stewart, T., Castelluccio, P., Edenberg, H. & Li, T. K., Oct 1 2002, In : American Journal of Medical Genetics. 112, 2, p. 138-143 6 p.

Research output: Contribution to journalArticle

Alcohol Drinking
Alcohols
Population
Alleles
Alcohol Dehydrogenase
16 Citations (Scopus)

Inflammatory profile in LRRK2-associated prodromal and clinical PD

Brockmann, K., Apel, A., Schulte, C., Schneiderhan-Marra, N., Pont-Sunyer, C., Vilas, D., Ruiz-Martinez, J., Langkamp, M., Corvol, J. C., Cormier, F., Knorpp, T., Joos, T. O., Gasser, T., Schüle, B., Aasly, J. O., Foroud, T., Marti-Masso, J. F., Brice, A., Tolosa, E., Marras, C. & 2 others, Berg, D. & Maetzler, W., May 24 2016, In : Journal of Neuroinflammation. 13, 1, 122.

Research output: Contribution to journalArticle

Parkinson Disease
Prodromal Symptoms
Mutation
Brain-Derived Neurotrophic Factor
Inflammation
13 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Parkinson Disease
Macrophage Inflammatory Proteins
Chemokine CCL2
Brain-Derived Neurotrophic Factor
Interleukin-8
3 Citations (Scopus)

Individualized atrophy scores predict dementia onset in familial frontotemporal lobar degeneration

ARTFL/LEFFTDS consortium, Jan 1 2019, In : Alzheimer's and Dementia.

Research output: Contribution to journalArticle

Open Access
Frontotemporal Lobar Degeneration
Atrophy
Dementia
Logistic Models
Brain
35 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Amyloid beta-Protein Precursor
Protein Transport
Alzheimer Disease
Single Nucleotide Polymorphism
Genes
47 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Age of Onset
Tobacco Products
Smoking
Alleles
Odds Ratio
24 Citations (Scopus)

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

Maier, R. M., Zhu, Z., Lee, S. H., Trzaskowski, M., Ruderfer, D. M., Stahl, E. A., Ripke, S., Wray, N. R., Yang, J., Visscher, P. M., Robinson, M. R., Forstner, A. J., Mcquillin, A., Trubetskoy, V., Wang, W., Wang, Y., Coleman, J. R. I., Gaspar, H. A., De Leeuw, C. A., Whitehead Pavlides, J. M. & 221 others, Olde Loohuis, L. M., Pers, T. H., Lee, P. H., Charney, A. W., Dobbyn, A. L., Huckins, L., Boocock, J., Giambartolomei, C., Roussos, P., Mullins, N., Awasthi, S., Agerbo, E., Als, T. D., Pedersen, C. B., Grove, J., Kupka, R., Regeer, E. J., Anjorin, A., Casas, M., Mahon, P. B., Allardyce, J., Escott-Price, V., Forty, L., Fraser, C., Kogevinas, M., Frank, J., Streit, F., Strohmaier, J., Treutlein, J., Witt, S. H., Kennedy, J. L., Strauss, J. S., Garnham, J., O'donovan, C., Slaney, C., Steinberg, S., Thorgeirsson, T. E., Hautzinger, M., Steffens, M., Perlis, R. H., Sánchez-Mora, C., Hipolito, M., Lawson, W. B., Nwulia, E. A., Levy, S. E., Foroud, T., Jamain, S., Young, A. H., Mckay, J. D., Albani, D., Zandi, P., Potash, J. B., Zhang, P., Raymond Depaulo, J., Bergen, S. E., Juréus, A., Karlsson, R., Kandaswamy, R., Mcguffin, P., Rivera, M., Lissowska, J., Cruceanu, C., Lucae, S., Cervantes, P., Budde, M., Gade, K., Heilbronner, U., Pedersen, M. G., Morris, D. W., Weickert, C. S., Weickert, T. W., Macintyre, D. J., Lawrence, J., Elvsåshagen, T., Smeland, O. B., Djurovic, S., Xi, S., Green, E. K., Czerski, P. M., Hauser, J., Xu, W., Vedder, H., Oruc, L., Spijker, A. T., Gordon, S. D., Medland, S. E., Curtis, D., Mühleisen, T. W., Badner, J., Scheftner, W. A., Sigurdsson, E., Schork, N. J., Schatzberg, A. F., Bækvad-Hansen, M., Bybjerg-Grauholm, J., Hansen, C. S., Knowles, J. A., Szelinger, S., Montgomery, G. W., Boks, M., Adolfsson, A. N., Hoffmann, P., Bauer, M., Pfennig, A., Leber, M., Kittel-Schneider, S., Reif, A., Del-Favero, J., Fischer, S. B., Herms, S., Reinbold, C. S., Degenhardt, F., Koller, A. C., Maaser, A., Ori, A., Dale, A. M., Fan, C. C., Greenwood, T. A., Nievergelt, C. M., Shehktman, T., Shilling, P. D., Byerley, W., Bunney, W., Alliey-Rodriguez, N., Clarke, T. K., Liu, C., Coryell, W., Akil, H., Burmeister, M., Flickinger, M., Li, J. Z., Mcinnis, M. G., Meng, F., Thompson, R. C., Watson, S. J., Zollner, S., Guan, W., Green, M. J., Craig, D., Sobell, J. L., Milani, L., Gordon-Smith, K., Knott, S. V., Perry, A., Parra, J. G., Mayoral, F., Rivas, F., Rice, J. P., Barchas, J. D., Børglum, A. D., Mortensen, P. B., Mors, O., Grigoroiu-Serbanescu, M., Bellivier, F., Etain, B., Leboyer, M., Ramos-Quiroga, J. A., Agartz, I., Amin, F., Azevedo, M. H., Bass, N., Black, D. W., Blackwood, D. H. R., Bruggeman, R., Buccola, N. G., Choudhury, K., Cloninger, C. R., Corvin, A., Craddock, N., Daly, M. J., Datta, S., Donohoe, G. J., Duan, J., Dudbridge, F., Fanous, A., Freedman, R., Freimer, N. B., Friedl, M., Gill, M., Gurling, H., De Haan, L., Hamshere, M. L., Hartmann, A. M., Holmans, P. A., Kahn, R. S., Keller, M. C., Kenny, E., Kirov, G. K., Krabbendam, L., Krasucki, R., Lencz, T., Levinson, D. F., Lieberman, J. A., Lin, D. Y., Linszen, D. H., Magnusson, P. K. E., Maier, W., Malhotra, A. K., Mattheisen, M., Mattingsdal, M., Mccarroll, S. A., Medeiros, H., Melle, I., Milanova, V., Myin-Germeys, I., Neale, B. M., Ophoff, R. A., Owen, M. J., Pimm, J., Purcell, S. M., Puri, V., Quested, D. J., Rossin, L., Sanders, A. R., Shi, J., Sklar, P., St Clair, D., Stroup, T. S., Van Os, J., Wiersma, D. & Zammit, S., Dec 1 2018, In : Nature Communications. 9, 1, 02769-6.

Research output: Contribution to journalArticle

Phenotype
Precision Medicine
Genome-Wide Association Study
Genomics
predictions
11 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Fetal Alcohol Spectrum Disorders
dictionary
alcohol
Alcohols
Research Personnel
7 Citations (Scopus)

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

Beach, T. G., Serrano, G. E., Kremer, T., Canamero, M., Dziadek, S., Sade, H., Derkinderen, P., Corbillé, A. G., Letournel, F., Munoz, D. G., White, C. L., Schneider, J., Crary, J. F., Sue, L. I., Adler, C. H., Glass, M. J., Intorcia, A. J., Walker, J. E., Foroud, T., Coffey, C. S. & 13 others, Ecklund, D., Riss, H., Goßmann, J., König, F., Kopil, C. M., Arnedo, V., Riley, L., Linder, C., Dave, K. D., Jennings, D., Seibyl, J., Mollenhauer, B. & Chahine, L., Jan 1 2018, In : Journal of Neuropathology and Experimental Neurology. 77, 9, p. 793-802 10 p.

Research output: Contribution to journalArticle

Synucleins
Sampling Studies
Glass
Parkinson Disease
Pathology
86 Citations (Scopus)

Identification of TMEM230 mutations in familial Parkinson's disease

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

Research output: Contribution to journalArticle

Parkinson Disease
Mutation
Synaptic Vesicles
Chromosomes, Human, Pair 20
Neurons
39 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Quantitative Trait Loci
drinking
Alcohol Drinking
alcohol
quantitative trait loci
28 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

alcohol
quantitative trait loci
alcohols
Alcohols
Chromosomes, Human, Pair 9
107 Citations (Scopus)

Identification of pathways for bipolar disorder: A meta-analysis

Nurnberger, J., Koller, D. L., Jung, J., Edenberg, H., Foroud, T., Guella, I., Vawter, M. P. & Kelsoe, J. R., 2014, In : JAMA Psychiatry. 71, 6, p. 657-664 8 p.

Research output: Contribution to journalArticle

Bipolar Disorder
Meta-Analysis
Genes
Genome-Wide Association Study
Psychiatry
4 Citations (Scopus)

Identification of genes for complex disease using longitudinal phenotypes.

Pankratz, N., Mukhopadhyay, N., Huang, S., Foroud, T. & Kirkwood, S. C., 2003, In : BMC Genetics. 4 Suppl 1, S58.

Research output: Contribution to journalArticle

Phenotype
Genes
Information Dissemination
Genome
Education
6 Citations (Scopus)

Identification of functional variants from whole-exome sequencing, combined with neuroimaging genetics

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. 739 1 p.

Research output: Contribution to journalArticle

Exome
Genome-Wide Association Study
Neuroimaging
Atrophy
Hippocampus
388 Citations (Scopus)

Identification of common variants associated with human hippocampal and intracranial volumes

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

Research output: Contribution to journalArticle

Brain
Temporal Lobe Epilepsy
Genome-Wide Association Study
Neuroimaging
Cognition
23 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 4
Quantitative Trait Loci
Femur Neck
Bone Density
Phenotype
4 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Linkage Disequilibrium
Chromosomes
Single Nucleotide Polymorphism
Genes
Spine
61 Citations (Scopus)

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

Ichikawa, S., Koller, D. L., Johnson, M. L., Lai, D., Xuei, X., Edenberg, H., Klein, R. F., Orwoll, E. S., Hui, S., Foroud, T., Peacock, M. & Econs, M., Apr 2006, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 21, 4, p. 556-564 9 p.

Research output: Contribution to journalArticle

Spine
Genes
Single Nucleotide Polymorphism
Haplotypes
Osteoporosis
4 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Bone Density
Genome
Single Nucleotide Polymorphism
Phenotype
Haplotypes
1050 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Germ-Line Mutation
Type II Bone Morphogenetic Protein Receptors
Penetrance
Protein-Serine-Threonine Kinases
Pulmonary Artery
175 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Parkinson Disease
Mutation
Genes
Age of Onset
Alleles
12 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Chromosome Mapping
Animal Models
Bone and Bones
Phenotype
Inbred Strains Rats
38 Citations (Scopus)

Heterogeneity in hereditary pancreatitis

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

Research output: Contribution to journalArticle

Trypsinogen
Mutation
Chronic Pancreatitis
Radiation Hybrid Mapping
Genes
40 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Alzheimer Disease
Episodic Memory
Short-Term Memory
Semantics
Endophenotypes
22 Citations (Scopus)
Femur Neck
Siblings
Bone and Bones
Weights and Measures
Body Weight
48 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Genome-Wide Association Study
Amyloid
Transcriptional Activation
Alzheimer Disease
Interleukin-1 Receptor Accessory Protein
86 Citations (Scopus)

Guidelines for the standardization of preanalytic variables for blood-based biomarker studies in Alzheimer's disease research

O'Bryant, S. E., Gupta, V., Henriksen, K., Edwards, M., Jeromin, A., Lista, S., Bazenet, C., Soares, H., Lovestone, S., Hampel, H., Montine, T., Blennow, K., Foroud, T., Carrillo, M., Graff-Radford, N., Laske, C., Breteler, M., Shaw, L., Trojanowski, J. Q., Schupf, N. & 8 others, Rissman, R. A., Fagan, A. M., Oberoi, P., Umek, R., Weiner, M. W., Grammas, P., Posner, H. & Martins, R., May 1 2015, In : Alzheimer's and Dementia. 11, 5, p. 549-560 12 p.

Research output: Contribution to journalArticle

Alzheimer Disease
Biomarkers
Guidelines
Research
Neuroimaging
89 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Intracranial Aneurysm
Rupture
Angiography
Cerebral Angiography
Ruptured Aneurysm
18 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Glutathione Transferase
Rats
Alcohols
Third Ventricle
Brain