Tatiana Foroud

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

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Article

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
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
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
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
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
155 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
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
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
824 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
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
750 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
19 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
14 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Hispanic Americans
Alzheimer Disease
Multigene Family
Nervous System
Joints
108 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Linkage Disequilibrium
Cognition
Single Nucleotide Polymorphism
Electroencephalography
P300 Event-Related Potentials
229 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Aminobutyrates
Linkage Disequilibrium
Automatic Data Processing
Electroencephalography
Brain
6 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Monoamine Oxidase
Chromosomes
Platelets
Lod Score
Blood Platelets
32 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 4
Chromosome Mapping
Chromosomes, Human, Pair 15
Electroencephalography
Chromosomes, Human, Pair 1
1 Citation (Scopus)

Linkage of an alcoholism-related severity phenotype to chromosome 16

Foroud, T., Bucholz, K. K., Edenberg, H., Goate, A., Neuman, R. J., Porjesz, B., Koller, D. L., Rice, J., Reich, T., Bierut, L. J., Cloninger, C. R., Nurnberger, J., Li, T. K., Conneally, P. M., Tischfield, J. A., Crowe, R., Hesselbrock, V., Schuckit, M. & Begleiter, H., Nov 6 1998, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 81, 6, p. 479 1 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 16
Alcoholism
Phenotype
Lod Score
Alcoholics
59 Citations (Scopus)

Linkage of an alcoholism-related severity phenotype to chromosome 16

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

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 16
Chromosomes
Alcoholism
Genes
Alcohols
120 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 13
Bone Density
Osteoporosis
Genes
Population
39 Citations (Scopus)

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

Koller, D. L., White, K., Liu, G., Hui, S., Conneally, P. M., Johnston, C. C., Econs, M., Foroud, T. & Peacock, M., Jun 1 2003, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 18, 6, p. 1057-1065 9 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 3
Chromosomes, Human, Pair 7
Thigh
Femur
Chromosomes, Human, Pair 19
176 Citations (Scopus)

Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene

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

Research output: Contribution to journalArticle

Prion Diseases
Codon
Valine
Genes
Lod Score
14 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Cystinuria
Alleles
Lod Score
Phenotype
Chromosomes
53 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

alcoholism
Alcoholism
Substance-Related Disorders
drug dependence
alcohol
7 Citations (Scopus)

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

Koller, D. L., Liu, L., Alam, I., Sun, Q., Econs, M., Foroud, T. & Turner, C. H., Sep 2008, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 23, 9, p. 1382-1388 7 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Phenotype
Chromosomes, Human, Pair 1
Femur
Inbred Strains Animals
48 Citations (Scopus)

Linkage stratification and mutation analysis at the parkin locus identifies mutation positive Parkinson's disease families [1]

Nichols, W. C., Pankratz, N., Uniacke, S. K., Pauciulo, M. W., Halter, C., Rudolph, A., Conneally, P. M., Foroud, T., Carter, J., Camicioli, R., Wojcieszek, J., Fernandez, M., Hubble, J., Rajput, A., Panisset, M., Mendis, T., Grimes, D. A., Serrano Ramos, C., Reich, S., Hauser, R. & 53 others, Sanchez-Ramos, J., Zesiewicz, T., Pfeiffer, R., Friedman, J., Fernandez, H., Shults, C., Seeberger, L., O'Brien, C., Pahwa, R., Elmer, L., Jennings, D., Marek, K., Truong, D., Pathak, M., Rodnitzyk, R., Kurlan, R., Tuite, P., Aminoff, M., Marder, K., Lewitt, P., Koller, W., Martin, W., Jankovic, J., Bertoni, J., Factor, S., Walker, F., Jung Kang, U., Stacy, M., Simon, D., Blindauer, K., Manyam, B., Nieves, A., Velickovic, M., Gordon, M. F., Leehey, M., Gordon, P., Rao, J., Dalvi, A., Racette, B., Sethi, K., Sudarsky, L., Saunders Pullman, R., Simuni, T., Dewey, R., Hermanowicz, N., Feigin, A., Calabresse, V., Sutton, J., Ajax, T., Podakalny, G. D., Suchowersky, O., Uitti, R. & Shulman, L., 2002, In : Journal of Medical Genetics. 39, 7, p. 489-492 4 p.

Research output: Contribution to journalArticle

509 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Ataxia Telangiectasia
Chromosomes
Genes
Heterozygote
Lymphocytes
42 Citations (Scopus)

Localization of an ataxia-telangiectasia locus to a 3-cM interval on chromosome 11q23: Linkage analysis of 111 families by an international consortium

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

Research output: Contribution to journalArticle

Ataxia Telangiectasia
Chromosomes
Lod Score
Monte Carlo Method
Neural Cell Adhesion Molecules
218 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Lod Score
Chromosomes
Pulmonary Artery
Genes
Chromosomes, Human, Pair 2
57 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

National Institute of Mental Health (U.S.)
Pedigree
Mood Disorders
Bipolar Disorder
Chromosomes
15 Citations (Scopus)

Locus heterogeneity of autosomal dominant osteopetrosis (ADO)

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

Research output: Contribution to journalArticle

Osteopetrosis
Chromosomes
Genes
Microsatellite Repeats
Bone
16 Citations (Scopus)

Longitudinal change of clinical and biological measures in early Parkinson's disease: Parkinson's progression markers initiative cohort

Simuni, T., Siderowf, A., Lasch, S., Coffey, C. S., Caspell-Garcia, C., Jennings, D., Tanner, C. M., Trojanowski, J. Q., Shaw, L. M., Seibyl, J., Schuff, N., Singleton, A., Kieburtz, K., Toga, A. W., Mollenhauer, B., Galasko, D., Chahine, L. M., Weintraub, D., Foroud, T., Tosun, D. & 6 others, Poston, K., Arnedo, V., Frasier, M., Sherer, T., Chowdhury, S. & Marek, K., Jan 1 2018, (Accepted/In press) In : Movement Disorders.

Research output: Contribution to journalArticle

Dopamine Plasma Membrane Transport Proteins
Parkinson Disease
Disease Progression
Corpus Striatum
Sample Size
89 Citations (Scopus)

Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers

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

Research output: Contribution to journalArticle

Asymptomatic Diseases
Huntington Disease
Optokinetic Nystagmus
Genes
Nervous System
49 Citations (Scopus)

Longitudinal personality changes among presymptomatic Huntington disease gene carriers

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

Research output: Contribution to journalArticle

Asymptomatic Diseases
MMPI
Huntington Disease
Personality
Hostility
13 Citations (Scopus)

LRRK2: Both a cause and a risk factor for Parkinson disease?

Foroud, T., Sep 13 2005, In : Neurology. 65, 5, p. 664-665 2 p.

Research output: Contribution to journalArticle

Parkinson Disease
44 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Leucine
Parkinson Disease
Phosphotransferases
Mutation
Genes
88 Citations (Scopus)

Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease

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

Research output: Contribution to journalArticle

Parkinsonian Disorders
Parkinson Disease
Age of Onset
Leucine
Mutation
20 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

saccharin
Saccharin
Quantitative Trait Loci
alcohol
quantitative trait loci
91 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Gene-Environment Interaction
Marital Status
marital status
Alcoholism
Genes
21 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Mitochondrial DNA
Parkinson Disease
Mutation
Age of Onset
Maternal Inheritance
11 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Marijuana Abuse
Cocaine-Related Disorders
Diagnostic and Statistical Manual of Mental Disorders
Alcoholism
Substance-Related Disorders

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

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

Research output: Contribution to journalArticle

Inborn Genetic Diseases
Meta-Analysis
Alcohols
Alcoholics
Attention Deficit Disorder with Hyperactivity
279 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Apolipoproteins E
Meta-Analysis
Alzheimer Disease
Genotype
Single Nucleotide Polymorphism
1550 Citations (Scopus)

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

European Alzheimer's Disease Initiative (EADI), Genetic and Environmental Risk in Alzheimer's Disease (GEGERAD), Alzheimer's Disease Genetic Consortium (ADGCDGCDGC) & Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGEGE), Dec 1 2013, In : Nature Genetics. 45, 12, p. 1452-1458 7 p.

Research output: Contribution to journalArticle

Meta-Analysis
Alzheimer Disease
Genome-Wide Association Study
Single Nucleotide Polymorphism
Inborn Genetic Diseases
5 Citations (Scopus)

Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity

Edwards, A. C., Deak, J. D., Gizer, I. R., Lai, D., Chatzinakos, C., Wilhelmsen, K. P., Lindsay, J., Heron, J., Hickman, M., Webb, B. T., Bacanu, S. A., Foroud, T., Kendler, K. S., Dick, D. M. & Schuckit, M. A., Jan 1 2018, (Accepted/In press) In : Alcoholism: Clinical and Experimental Research.

Research output: Contribution to journalArticle

Meta-Analysis
Genes
Alcohols
Single Nucleotide Polymorphism
Polymorphism
129 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle