Tatiana Foroud

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

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171 Citations (Scopus)

Autosomal genomic scan for loci linked to obesity and energy metabolism in Pima Indians

Norman, R. A., Tataranni, P. A., Pratley, R., Thompson, D. B., Hanson, R. L., Prochazka, M., Baier, L., Ehm, M. G., Sakul, H., Foroud, T., Garvey, W. T., Burns, D., Knowler, W. C., Bennett, P. H., Bogardus, C. & Ravussin, E., Mar 1998, In : American Journal of Human Genetics. 62, 3, p. 659-668 10 p.

Research output: Contribution to journalArticle

Potassium Iodide
Energy Metabolism
Obesity
Adipose Tissue
Siblings
95 Citations (Scopus)

A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors

Duan, Q. L., Nikpoor, B., Dubé, M. P., Molinaro, G., Meijer, I. A., Dion, P., Rochefort, D., Saint-Onge, J., Flury, L., Brown, N. J., Gainer, J. V., Rouleau, J. L., Agostoni, A., Cugno, M., Simon, P., Clavel, P., Potier, J., Wehbe, B., Benarbia, S., Marc-Aurèle, J. & 4 others, Chanard, J., Foroud, T., Adam, A. & Rouleau, G. A., Oct 2005, In : American Journal of Human Genetics. 77, 4, p. 617-626 10 p.

Research output: Contribution to journalArticle

Angioedema
Angiotensin-Converting Enzyme Inhibitors
Single Nucleotide Polymorphism
Pedigree
Microsatellite Repeats
20 Citations (Scopus)

Bone mineral density variation in men is influenced by sex-specific and non sex-specific quantitative trait loci

Peacock, M., Koller, D. L., Lai, D., Hui, S., Foroud, T. & Econs, M., Sep 2009, In : Bone. 45, 3, p. 443-448 6 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Bone Density
Hip
Siblings
Spine
15 Citations (Scopus)

Brief report: Genetics of alcoholic Cirrhosis-GenomALC multinational study

the GenomALC Consortium, May 1 2015, In : Alcoholism: Clinical and Experimental Research. 39, 5, p. 836-842 7 p.

Research output: Contribution to journalArticle

Alcoholic Liver Cirrhosis
Alcohols
Liver
Liver Diseases
Fathers
64 Citations (Scopus)

C9orf72 hexanucleotide repeat expansions in clinical alzheimer disease

Harms, M., Benitez, B. A., Cairns, N., Cooper, B., Cooper, P., Mayo, K., Carrell, D., Faber, K., Williamson, J., Bird, T., Diaz-Arrastia, R., Foroud, T., Boeve, B. F., Graff-Radford, N. R., Mayeux, R., Chakraverty, S., Goate, A. M. & Cruchaga, C., 2013, In : JAMA Neurology. 70, 6, p. 736-741 6 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 9
Open Reading Frames
Alzheimer Disease
National Institute on Aging (U.S.)
Frontotemporal Dementia
9 Citations (Scopus)

Calcium-sensing receptor genotype and response to cinacalcet in patients undergoing hemodialysis

Moe, S., Wetherill, L., Decker, B., Lai, D., Abdalla, S., Long, J., Vatta, M., Foroud, T. & Chertow, G. M., Jul 7 2017, In : Clinical Journal of the American Society of Nephrology. 12, 7, p. 1128-1138 11 p.

Research output: Contribution to journalArticle

Calcium-Sensing Receptors
Single Nucleotide Polymorphism
Renal Dialysis
Genotype
Alleles

Cancer outcomes among Parkinson's disease patients with leucine rich repeat kinase 2 mutations, idiopathic Parkinson's disease patients, and nonaffected controls

Agalliu, I., Ortega, R. A., Luciano, M. S., Mirelman, A., Pont-Sunyer, C., Brockmann, K., Vilas, D., Tolosa, E., Berg, D., Warø, B., Glickman, A., Raymond, D., Inzelberg, R., Ruiz-Martinez, J., Mondragon, E., Friedman, E., Hassin-Baer, S., Alcalay, R. N., Mejia-Santana, H., Aasly, J. & 5 others, Foroud, T., Marder, K., Giladi, N., Bressman, S. & Saunders-Pullman, R., Sep 1 2019, In : Movement disorders : official journal of the Movement Disorder Society. 34, 9, p. 1392-1398 7 p.

Research output: Contribution to journalArticle

Leucine
Parkinson Disease
Phosphotransferases
Mutation
Neoplasms
179 Citations (Scopus)

Candidate genes for alcohol dependence: A review of genetic evidence from human studies

Dick, D. M. & Foroud, T., May 1 2003, In : Alcoholism: Clinical and Experimental Research. 27, 5, p. 868-879 12 p.

Research output: Contribution to journalArticle

Nerve Tissue Proteins
Dopamine Plasma Membrane Transport Proteins
GABA Receptors
Membrane Transport Proteins
Alcohol Dehydrogenase
1 Citation (Scopus)

Characteristic patterns of inter- and intra-hemispheric metabolic connectivity in patients with stable and progressive mild cognitive impairment and Alzheimer’s disease

for the Alzheimer’s Disease Neuroimaging Initiative, Dec 1 2018, In : Scientific Reports. 8, 1, 13807.

Research output: Contribution to journalArticle

Alzheimer Disease
Metabolic Networks and Pathways
Brain
Fluorodeoxyglucose F18
Occipital Lobe
5 Citations (Scopus)

Characteristics of Bipolar I patients grouped by externalizing disorders

Swaminathan, S., Koller, D. L., Foroud, T., Edenberg, H., Xuei, X., Niculescu, A. & Nurnberger, J., Jul 1 2015, In : Journal of Affective Disorders. 178, p. 206-214 9 p., 7324.

Research output: Contribution to journalArticle

Mood Disorders
Calcium Channels
Bipolar Disorder
Genes
Single Nucleotide Polymorphism
12 Citations (Scopus)

Charcot-Marie-Tooth gene, SBF2, associated with taxaneinduced peripheral neuropathy in African Americans

Schneider, B., Lai, D., Shen, F., Jiang, G., Radovich, M., Li, L., Gardner, L., Miller, K., O'Neill, A., Sparano, J. A., Xue, G., Foroud, T. & Sledge, G. W., 2016, In : Oncotarget. 7, 50, p. 82244-82253 10 p.

Research output: Contribution to journalArticle

Peripheral Nervous System Diseases
African Americans
Tooth
Genes
Paclitaxel
71 Citations (Scopus)

Chloride channel 7 (CLCN7) gene mutations and autosomal dominant osteopetrosis, type II

Waguespack, S. G., Koller, D. L., White, K., Fishburn, T., Carn, G., Buckwalter, K., Johnson, M., Kocisko, M., Evans, W. E., Foroud, T. & Econs, M., Aug 2003, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 18, 8, p. 1513-1518 6 p.

Research output: Contribution to journalArticle

Osteopetrosis
Chloride Channels
Mutation
Genes
Penetrance
3 Citations (Scopus)

Chromosome 5 and Parkinson disease

Foroud, T., Pankratz, N. & Martinez, M., Oct 2006, In : European Journal of Human Genetics. 14, 10, p. 1106-1110 5 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 5
Parkinson Disease
Age of Onset
Chromosomes
Disease Susceptibility
6 Citations (Scopus)

Chromosome 6 workshop

Nurnberger, J. & Foroud, T., 1998, In : Psychiatric Genetics. 8, 2, p. 79-83 5 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 6
Psychiatry
Education
34 Citations (Scopus)

Chromosome 6 workshop report

Nurnberger, J. & Foroud, T., Jun 18 1999, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 88, 3, p. 233-238 6 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 6
Psychiatry
Schizophrenia
Education
Bipolar Disorder
14 Citations (Scopus)

Cis-regulatory variants affect CHRNA5 mRNA expression in populations of African and European ancestry

Wang, J. C., Spiegel, N., Bertelsen, S., Le, N., McKenna, N., Budde, J. P., Harari, O., Kapoor, M., Brooks, A., Hancock, D., Tischfield, J., Foroud, T., Bierut, L. J., Steinbach, J. H., Edenberg, H., Traynor, B. J. & Goate, A. M., Nov 26 2013, In : PLoS One. 8, 11, e80204.

Research output: Contribution to journalArticle

ancestry
Genes
Multigene Family
Messenger RNA
Alleles
5 Citations (Scopus)

CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white men

Chu, K., Koller, D. L., Ichikawa, S., Snyder, R., Curry, L., Lai, D., Austin, A., Xuei, X., Edenberg, H., Hui, S., Foroud, T., Peacock, M. & Econs, M., Dec 2008, In : Bone. 43, 6, p. 995-998 4 p.

Research output: Contribution to journalArticle

Chloride Channels
Bone Density
Genes
Femur Neck
Osteopetrosis
16 Citations (Scopus)

Clinical/Scientific Notes: The Alzheimer's disease sequencing project: Study design and sample selection

Beecham, G. W., Bis, J. C., Martin, E. R., Choi, S. H., DeStefano, A. L., Van Duijn, C. M., Fornage, M., Gabriel, S. B., Koboldt, D. C., Larson, D. E., Naj, A. C., Psaty, B. M., Salerno, W., Bush, W. S., Foroud, T., Wijsman, E., Farrer, L. A., Goate, A., Haines, J. L., Pericak-Vance, M. A. & 4 others, Boerwinkle, E., Mayeux, R., Seshadri, S. & Schellenberg, G., Oct 1 2017, In : Neurology: Genetics. 3, 5, e194.

Research output: Contribution to journalArticle

Alzheimer Disease
26 Citations (Scopus)

Clinical correlates of depressive symptoms in familial Parkinson's disease

Pankratz, N., Marder, K. S., Halter, C. A., Rudolph, A., Shults, C. W., Nichols, W. C. & Foroud, T., Nov 15 2008, In : Movement Disorders. 23, 15, p. 2216-2223 8 p.

Research output: Contribution to journalArticle

Parkinson Disease
Depression
Geriatrics
Activities of Daily Living
Logistic Models
71 Citations (Scopus)

Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations

Ishihara, L., Warren, L., Gibson, R., Amouri, R., Lesage, S., Dürr, A., Tazir, M., Wszolek, Z. K., Uitti, R. J., Nichols, W. C., Griffith, A., Hattori, N., Leppert, D., Watts, R., Zabetian, C. P., Foroud, T., Farrer, M. J., Brice, A., Middleton, L. & Hentati, F., 2006, In : Archives of Neurology. 63, 9, p. 1250-1254 5 p.

Research output: Contribution to journalArticle

Leucine
Parkinson Disease
Phosphotransferases
Mutation
Gene Dosage
21 Citations (Scopus)

Clinical-genetic associations in the Prospective Huntington at Risk Observational Study (PHAROS) implications for clinical trials

The Huntington Study Group PHAROS Investigators, Jan 1 2016, In : JAMA Neurology. 73, 1, p. 102-110 9 p.

Research output: Contribution to journalArticle

Open Access
Cytosine
Guanine
Adenine
Huntington Disease
Observational Studies
15 Citations (Scopus)

Clinical implications of gene discovery in Parkinson's disease and parkinsonism

Wider, C., Foroud, T. & Wszolek, Z. K., 2010, In : Movement Disorders. 25, SUPPL. 1

Research output: Contribution to journalArticle

Genetic Association Studies
Parkinsonian Disorders
Parkinson Disease
Genes
Mutation
111 Citations (Scopus)

Cognitive performance and neuropsychiatric symptoms in early, untreated Parkinson's disease

Parkinson's Progression Markers Initiative, Jun 1 2015, In : Movement Disorders. 30, 7, p. 919-927 9 p.

Research output: Contribution to journalArticle

Parkinson Disease
Disruptive, Impulse Control, and Conduct Disorders
Apathy
Aptitude
Psychotic Disorders
110 Citations (Scopus)

Cognitive scores in carriers of Huntington's disease gene compared to noncarriers

Foroud, T., Siemers, E., Kleindorfer, D., Bill, D. J., Hodes, M. E., Norton, J. A., Conneally, P. M. & Christian, J. C., May 1995, In : Annals of Neurology. 37, 5, p. 657-664 8 p.

Research output: Contribution to journalArticle

Huntington Disease
Genes
Alleles
Trinucleotide Repeats
Chromosomes, Human, Pair 4
56 Citations (Scopus)

Collaborative initiative on fetal alcohol spectrum disorders: Methodology of clinical projects

Mattson, S. N., Foroud, T., Sowell, E. R., Jones, K. L., Coles, C. D., Fagerlund, Å., Autti-Rämö, I., May, P. A., Adnams, C. M., Konovalova, V., Wetherill, L., Arenson, A. D., Barnett, W. K. & Riley, E. P., Nov 2010, In : Alcohol. 44, 7-8, p. 635-641 7 p.

Research output: Contribution to journalArticle

Fetal Alcohol Spectrum Disorders
alcohol
Alcohols
Imaging techniques
Three-Dimensional Imaging
1 Citation (Scopus)

Collagen COL22A1 maintains vascular stability and mutations in COL22A1 are potentially associated with intracranial aneurysms

Ton, Q. V., Leino, D., Mowery, S. A., Bredemeier, N. O., Lafontant, P. J., Lubert, A., Gurung, S., Farlow, J. L., Foroud, T., Broderick, J. & Sumanas, S., Dec 12 2018, In : Disease models & mechanisms. 11, 12

Research output: Contribution to journalArticle

Intracranial Aneurysm
Blood Vessels
Collagen
Embryonic Structures
Mutation
162 Citations (Scopus)

Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q

McQueen, M. B., Devlin, B., Faraone, S. V., Nimgaonkar, V. L., Sklar, P., Smoller, J. W., Jamra, R. A., Albus, M., Bacanu, S. A., Baron, M., Barrett, T. B., Berrettini, W., Blacker, D., Byerley, W., Cichon, S., Coryell, W., Craddock, N., Daly, M. J., DePaulo, J. R., Edenberg, H. & 33 others, Foroud, T., Gill, M., Gilliam, T. C., Hamshere, M., Jones, I., Jones, L., Juo, S. H., Kelsoe, J. R., Lambert, D., Lange, C., Lerer, B., Liu, J., Maier, W., MacKinnon, J. D., McInnis, M. G., McMahon, F. J., Murphy, D. L., Nöthen, M. M., Nurnberger, J., Pato, C. N., Pato, M. T., Potash, J. B., Propping, P., Pulver, A. E., Rice, J. P., Rietschel, M., Scheftner, W., Schumacher, J., Segurado, R., Van Steen, K., Xie, W., Zandi, P. P. & Laird, N. M., Oct 2005, In : American Journal of Human Genetics. 77, 4, p. 582-595 14 p.

Research output: Contribution to journalArticle

Bipolar Disorder
Chromosomes
Meta-Analysis
Genotype
Genome
4 Citations (Scopus)

Combined Face-Brain Morphology and Associated Neurocognitive Correlates in Fetal Alcohol Spectrum Disorders

Suttie, M., Wozniak, J. R., Parnell, S. E., Wetherill, L., Mattson, S. N., Sowell, E. R., Kan, E., Riley, E. P., Jones, K. L., Coles, C., Foroud, T. & Hammond, P., Jan 1 2018, (Accepted/In press) In : Alcoholism: Clinical and Experimental Research.

Research output: Contribution to journalArticle

Fetal Alcohol Spectrum Disorders
Caudate Nucleus
Brain
Corpus Callosum
Alcohols
92 Citations (Scopus)

Combined sequence-based and genetic mapping analysis of complex traits in outbred rats

Baud, A., Hermsen, R., Guryev, V., Stridh, P., Graham, D., McBride, M. W., Foroud, T., Calderari, S., Diez, M., Ockinger, J., Beyeen, A. D., Gillett, A., Abdelmagid, N., Guerreiro-Cacais, A. O., Jagodic, M., Tuncel, J., Norin, U., Beattie, E., Huynh, N., Miller, W. H. & 50 others, Koller, D. L., Alam, I., Falak, S., Osborne-Pellegrin, M., Martinez-Membrives, E., Canete, T., Blazquez, G., Vicens-Costa, E., Mont-Cardona, C., Diaz-Moran, S., Tobena, A., Hummel, O., Zelenika, D., Saar, K., Patone, G., Bauerfeind, A., Bihoreau, M. T., Heinig, M., Lee, Y. A., Rintisch, C., Schulz, H., Wheeler, D. A., Worley, K. C., Muzny, D. M., Gibbs, R. A., Lathrop, M., Lansu, N., Toonen, P., Ruzius, F. P., De Bruijn, E., Hauser, H., Adams, D. J., Keane, T., Atanur, S. S., Aitman, T. J., Flicek, P., Malinauskas, T., Jones, E. Y., Ekman, D., Lopez-Aumatell, R., Dominiczak, A. F., Johannesson, M., Holmdahl, R., Olsson, T., Gauguier, D., Hubner, N., Fernandez-Teruel, A., Cuppen, E., Mott, R. & Flint, J., Jul 2013, In : Nature Genetics. 45, 7, p. 767-775 9 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Phenotype
Genes
Multiple Sclerosis
Heart Diseases
5 Citations (Scopus)

Common and specific factors in the familial transmission of substance dependence

Bierut, L., Rice, J., Goate, A., Foroud, T., Edenberg, H., Crowe, R., Hesselbrock, V., Li, T. K., Nurnberger, J., Porjesz, B., Schuckit, M., Begleiter, H. & Reich, T., Aug 7 2000, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 96, 4, p. 459 1 p.

Research output: Contribution to journalArticle

Alcoholism
Substance-Related Disorders
Marijuana Abuse
Smoking
Cocaine-Related Disorders
17 Citations (Scopus)

Common biological networks underlie genetic risk for alcoholism in African- and European-American populations

Kos, M. Z., Yan, J., Dick, D. M., Agrawal, A., Bucholz, K. K., Rice, J. P., Johnson, E. O., Schuckit, M., Kuperman, S., Kramer, J., Goate, A. M., Tischfield, J. A., Foroud, T., Nurnberger, J., Hesselbrock, V., Porjesz, B., Bierut, L. J., Edenberg, H. & Almasy, L., Jul 2013, In : Genes, Brain and Behavior. 12, 5, p. 532-542 11 p.

Research output: Contribution to journalArticle

African Americans
Alcoholism
Genome-Wide Association Study
Population
Genes
972 Citations (Scopus)

Common genetic determinants of vitamin D insufficiency: A genome-wide association study

Wang, T. J., Zhang, F., Richards, J. B., Kestenbaum, B., Van Meurs, J. B., Berry, D., Kiel, D. P., Streeten, E. A., Ohlsson, C., Koller, D. L., Peltonen, L., Cooper, J. D., O'Reilly, P. F., Houston, D. K., Glazer, N. L., Vandenput, L., Peacock, M., Shi, J., Rivadeneira, F., McCarthy, M. I. & 56 others, Anneli, P., De Boer, I. H., Mangino, M., Kato, B., Smyth, D. J., Booth, S. L., Jacques, P. F., Burke, G. L., Goodarzi, M., Cheung, C. L., Wolf, M., Rice, K., Goltzman, D., Hidiroglou, N., Ladouceur, M., Wareham, N. J., Hocking, L. J., Hart, D., Arden, N. K., Cooper, C., Malik, S., Fraser, W. D., Hartikainen, A. L., Zhai, G., Macdonald, H. M., Forouhi, N. G., Loos, R. J. F., Reid, D. M., Hakim, A., Dennison, E., Liu, Y., Power, C., Stevens, H. E., Jaana, L., Vasan, R. S., Soranzo, N., Bojunga, J., Psaty, B. M., Lorentzon, M., Foroud, T., Harris, T. B., Hofman, A., Jansson, J. O., Cauley, J. A., Uitterlinden, A. G., Gibson, Q., Järvelin, M. R., Karasik, D., Siscovick, D. S., Econs, M., Kritchevsky, S. B., Florez, J. C., Todd, J. A., Dupuis, J., Hyppönen, E. & Spector, T. D., 2010, In : The Lancet. 376, 9736, p. 180-188 9 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Vitamin D
Genome
Genotype
Luminescent Measurements

Common genetic determinants of vitamin D insufficiency: A genome-wide association study

Wang, T. J., Zhang, F., Richards, J. B., Kestenbaum, B., Van Meurs, J. B., Berry, D., Kiel, D. P., Streeten, E. A., Ohlsson, C., Koller, D. L., Peltonen, L., Cooper, J. D., O'Reilly, P. F., Houston, D. K., Glazer, N. L., Vandenput, L., Peacock, M., Shi, J., Rivadeneira, F., McCarthy, M. I. & 56 others, Anneli, P., De Boer, I. H., Mangino, M., Kato, B., Smyth, D. J., Booth, S. L., Jacques, P. F., Burke, G. L., Goodarzi, M., Cheung, C. L., Wolf, M., Rice, K., Goltzman, D., Hidiroglou, N., Ladouceur, M., Wareham, N. J., Hocking, L. J., Hart, D., Arden, N. K., Cooper, C., Malik, S., Fraser, W. D., Hartikainen, A. L., Zhai, G., MacDonald, H. M., Forouhi, N. G., Loos, R. J. F., Reid, D. M., Hakim, A., Dennison, E., Liu, Y., Power, C., Stevens, H. E., Jaana, L., Vasan, R. S., Soranzo, N., Bojunga, J., Psaty, B. M., Lorentzon, M., Foroud, T., Harris, T. B., Hofman, A., Jansson, J. O., Cauley, J. A., Uitterlinden, A. G., Gibson, Q., Järvelin, M. R., Karasik, D., Siscovick, D. S., Econs, M., Kritchevsky, S. B., Florez, J. C., Todd, J. A., Dupuis, J., Hyppönen, E. & Spector, T. D., Feb 2011, In : Obstetrical and Gynecological Survey. 66, 2, p. 91-93 3 p.

Research output: Contribution to journalArticle

340 Citations (Scopus)

Common genetic variants influence human subcortical brain structures

Hibar, D. P., Stein, J. L., Renteria, M. E., Arias-Vasquez, A., Desrivières, S., Jahanshad, N., Toro, R., Wittfeld, K., Abramovic, L., Andersson, M., Aribisala, B. S., Armstrong, N. J., Bernard, M., Bohlken, M. M., Boks, M. P., Bralten, J., Brown, A. A., Mallar Chakravarty, M., Chen, Q., Ching, C. R. K. & 267 others, Cuellar-Partida, G., Den Braber, A., Giddaluru, S., Goldman, A. L., Grimm, O., Guadalupe, T., Hass, J., Woldehawariat, G., Holmes, A. J., Hoogman, M., Janowitz, D., Jia, T., Kim, S., Klein, M., Kraemer, B., Lee, P. H., Olde Loohuis, L. M., Luciano, M., MacAre, C., Mather, K. A., Mattheisen, M., Milaneschi, Y., Nho, K., Papmeyer, M., Ramasamy, A., Risacher, S. L., Roiz-Santiañez, R., Rose, E. J., Salami, A., Sämann, P. G., Schmaal, L., Schork, A. J., Shin, J., Strike, L. T., Teumer, A., Van Donkelaar, M. M. J., Van Eijk, K. R., Walters, R. K., Westlye, L. T., Whelan, C. D., Winkler, A. M., Zwiers, M. P., Alhusaini, S., Athanasiu, L., Ehrlich, S., Hakobjan, M. M. H., Hartberg, C. B., Haukvik, U. K., Heister, A. J. G. A. M., Hoehn, D., Kasperaviciute, D., Liewald, D. C. M., Lopez, L. M., Makkinje, R. R. R., Matarin, M., Naber, M. A. M., Reese McKay, D., Needham, M., Nugent, A. C., Pütz, B., Royle, N. A., Shen, L., Sprooten, E., Trabzuni, D., Van Der Marel, S. S. L., Van Hulzen, K. J. E., Walton, E., Wolf, C., Almasy, L., Ames, D., Arepalli, S., Assareh, A. A., Bastin, M. E., Brodaty, H., Bulayeva, K. B., Carless, M. A., Cichon, S., Corvin, A., Curran, J. E., Czisch, M., De Zubicaray, G. I., Dillman, A., Duggirala, R., Dyer, T. D., Erk, S., Fedko, I. O., Ferrucci, L., Foroud, T., Fox, P. T., Fukunaga, M., Raphael Gibbs, J., Göring, H. H. H., Green, R. C., Guelfi, S., Hansell, N. K., Hartman, C. A., Hegenscheid, K., Heinz, A., Hernandez, D. G., Heslenfeld, D. J., Hoekstra, P. J., Holsboer, F., Homuth, G., Hottenga, J. J., Ikeda, M., Jack, C. R., Jenkinson, M., Johnson, R., Kanai, R., Keil, M., Kent, J. W., Kochunov, P., Kwok, J. B., Lawrie, S. M., Liu, X., Longo, D. L., McMahon, K. L., Meisenzahl, E., Melle, I., Mohnke, S., Montgomery, G. W., Mostert, J. C., Mühleisen, T. W., Nalls, M. A., Nichols, T. E., Nilsson, L. G., Nöthen, M. M., Ohi, K., Olvera, R. L., Perez-Iglesias, R., Bruce Pike, G., Potkin, S. G., Reinvang, I., Reppermund, S., Rietschel, M., Romanczuk-Seiferth, N., Rosen, G. D., Rujescu, D., Schnell, K., Schofield, P. R., Smith, C., Steen, V. M., Sussmann, J. E., Thalamuthu, A., Toga, A. W., Traynor, B. J., Troncoso, J., Turner, J. A., Valdés Hernández, M. C., Van 'T Ent, D., Van Der Brug, M., Van Der Wee, N. J. A., Van Tol, M. J., Veltman, D. J., Wassink, T. H., Westman, E., Zielke, R. H., Zonderman, A. B., Ashbrook, D. G., Hager, R., Lu, L., McMahon, F. J., Morris, D. W., Williams, R. W., Brunner, H. G., Buckner, R. L., Buitelaar, J. K., Cahn, W., Calhoun, V. D., Cavalleri, G. L., Crespo-Facorro, B., Dale, A. M., Davies, G. E., Delanty, N., Depondt, C., Djurovic, S., Drevets, W. C., Espeseth, T., Gollub, R. L., Ho, B. C., Hoffmann, W., Hosten, N., Kahn, R. S., Le Hellard, S., Meyer-Lindenberg, A., Müller-Myhsok, B., Nauck, M., Nyberg, L., Pandolfo, M., Penninx, B. W. J. H., Roffman, J. L., Sisodiya, S. M., Smoller, J. W., Van Bokhoven, H., Van Haren, N. E. M., Völzke, H., Walter, H., Weiner, M. W., Wen, W., White, T., Agartz, I., Andreassen, O. A., Blangero, J., Boomsma, D. I., Brouwer, R. M., Cannon, D. M., Cookson, M. R., De Geus, E. J. C., Deary, I. J., Donohoe, G., Fernández, G., Fisher, S. E., Francks, C., Glahn, D. C., Grabe, H. J., Gruber, O., Hardy, J., Hashimoto, R., Hulshoff Pol, H. E., Jönsson, E. G., Kloszewska, I., Lovestone, S., Mattay, V. S., Mecocci, P., McDonald, C., McIntosh, A. M., Ophoff, R. A., Paus, T., Pausova, Z., Ryten, M., Sachdev, P. S., Saykin, A., Simmons, A., Singleton, A., Soininen, H., Wardlaw, J. M., Weale, M. E., Weinberger, D. R., Adams, H. H. H., Launer, L. J., Seiler, S., Schmidt, R., Chauhan, G., Satizabal, C. L., Becker, J. T., Yanek, L., Van Der Lee, S. J., Ebling, M., Fischl, B., Longstreth, W. T., Greve, D., Schmidt, H., Nyquist, P., Vinke, L. N., Van Duijn, C. M., Xue, L., Mazoyer, B., Bis, J. C., Gudnason, V., Seshadri, S., Ikram, M. A., Martin, N. G., Wright, M. J., Schumann, G., Franke, B., Thompson, P. M. & Medland, S. E., Apr 9 2015, In : Nature. 520, 7546, p. 224-229 6 p.

Research output: Contribution to journalArticle

Putamen
Brain
Developmental Genes
Transport Vesicles
Caudate Nucleus
139 Citations (Scopus)

Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis

Whitcomb, D. C., LaRusch, J., Krasinskas, A. M., Klei, L., Smith, J. P., Brand, R. E., Neoptolemos, J. P., Lerch, M. M., Tector, M., Sandhu, B. S., Guda, N. M., Orlichenko, L., Alkaade, S., Amann, S. T., Anderson, M. A., Baillie, J., Banks, P. A., Conwell, D., Coté, G. A., Cotton, P. B. & 178 others, DiSario, J., Farrer, L. A., Forsmark, C. E., Johnstone, M., Gardner, T. B., Gelrud, A., Greenhalf, W., Haines, J. L., Hartman, D. J., Hawes, R. A., Lawrence, C., Lewis, M., Mayerle, J., Mayeux, R., Melhem, N. M., Money, M. E., Muniraj, T., Papachristou, G. I., Pericak-Vance, M. A., Romagnuolo, J., Schellenberg, G. D., Sherman, S., Simon, P., Singh, V. P., Slivka, A., Stolz, D., Sutton, R., Weiss, F. U., Wilcox, C. M., Zarnescu, N. O., Wisniewski, S. R., O'Connell, M. R., Kienholz, M. L., Roeder, K., Barmada, M. M., Yadav, D., Devlin, B., Albert, M. S., Albin, R. L., Apostolova, L. G., Arnold, S. E., Baldwin, C. T., Barber, R., Barnes, L. L., Beach, T. G., Beecham, G. W., Beekly, D., Bennett, D. A., Bigio, E. H., Bird, T. D., Blacker, D., Boxer, A., Burke, J. R., Buxbaum, J. D., Cairns, N. J., Cantwell, L. B., Cao, C., Carney, R. M., Carroll, S. L., Chui, H. C., Clark, D. G., Cribbs, D. H., Crocco, E. A., Cruchaga, C., DeCarli, C., Demirci, F. Y., Dick, M., Dickson, D. W., Duara, R., Ertekin-Taner, N., Faber, K. M., Fallon, K. B., Farlow, M., Ferris, S., Foroud, T., Frosch, M. P., Galasko, D. R., Ganguli, M., Gearing, M., Geschwind, D. H., Ghetti, B., Gilbert, J. R., Gilman, S., Glass, J. D., Goate, A. M., Graff-Radford, N. R., Green, R. C., Growdon, J. H., Hakonarson, H., Hamilton-Nelson, K. L., Hamilton, R. L., Harrell, L. E., Head, E., Honig, L. S., Hulette, C. M., Hyman, B. T., Jicha, G. A., Jin, L. W., Jun, G., Kamboh, M. I., Karydas, A., Kaye, J. A., Kim, R., Koo, E. H., Kowall, N. W., Kramer, J. H., Kramer, P., Kukul, W. A., LaFerla, F. M., Lah, J. J., Leverenz, J. B., Levey, A. I., Li, G., Lin, C. F., Lieberman, A. P., Lopez, O. L., Lunetta, K. L., Lyketsos, C. G., MacK, W. J., Marson, D. C., Martin, E. R., Martiniuk, F., Mash, D. C., Masliah, E., McKee, A. C., Mesulam, M., Miller, B. L., Miller, C. A., Miller, J. W., Montine, T. J., Morris, J. C., Murrel, J. R., Naj, A. C., Olichney, J. M., Parisi, J. E., Peskind, E., Petersen, R. C., Pierce, A., Poon, W. W., Potter, H., Quinn, J. F., Raj, A., Raskind, M., Reiman, E. M., Reisberg, B., Reitz, C., Ringman, J. M., Roberson, E. D., Rosen, H. J., Rosenberg, R. N., Sano, M., Saykin, A., Schneider, J. A., Schneider, L. S., Seeley, W. W., Smith, A. G., Sonnen, J. A., Spina, S., Stern, R. A., Tanzi, R. E., Trojanowski, J. Q., Troncoso, J. C., Tsuang, D. W., Valladares, O., Van Deerlin, V. M., Van Eldik, L. J., Vardarajan, B. N., Vinters, H. V., Vonsatte, J. P., Wang, L. S., Weintraub, S., Welsh-Bohmer, K. A., Williamson, J., Woltjer, R. L., Wright, C. B., Younkin, S. G., Yu, C. E. & Yu, L., Dec 2012, In : Nature Genetics. 44, 12, p. 1349-1354 6 p.

Research output: Contribution to journalArticle

Pancreatitis
Alcohols
Claudin-2
Hemizygote
Alleles
1094 Citations (Scopus)

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

Naj, A. C., Jun, G., Beecham, G. W., Wang, L. S., Vardarajan, B. N., Buros, J., Gallins, P. J., Buxbaum, J. D., Jarvik, G. P., Crane, P. K., Larson, E. B., Bird, T. D., Boeve, B. F., Graff-Radford, N. R., De Jager, P. L., Evans, D., Schneider, J. A., Carrasquillo, M. M., Ertekin-Taner, N., Younkin, S. G. & 135 others, Cruchaga, C., Kauwe, J. S. K., Nowotny, P., Kramer, P., Hardy, J., Huentelman, M. J., Myers, A. J., Barmada, M. M., Demirci, F. Y., Baldwin, C. T., Green, R. C., Rogaeva, E., George-Hyslop, P. S., Arnold, S. E., Barber, R., Beach, T., Bigio, E. H., Bowen, J. D., Boxer, A., Burke, J. R., Cairns, N. J., Carlson, C. S., Carney, R. M., Carroll, S. L., Chui, H. C., Clark, D. G., Corneveaux, J., Cotman, C. W., Cummings, J. L., Decarli, C., Dekosky, S. T., Diaz-Arrastia, R., Dick, M., Dickson, D. W., Ellis, W. G., Faber, K. M., Fallon, K. B., Farlow, M., Ferris, S., Frosch, M. P., Galasko, D. R., Ganguli, M., Gearing, M., Geschwind, D. H., Ghetti, B., Gilbert, J. R., Gilman, S., Giordani, B., Glass, J. D., Growdon, J. H., Hamilton, R. L., Harrell, L. E., Head, E., Honig, L. S., Hulette, C. M., Hyman, B. T., Jicha, G. A., Jin, L. W., Johnson, N., Karlawish, J., Karydas, A., Kaye, J. A., Kim, R., Koo, E. H., Kowall, N. W., Lah, J. J., Levey, A. I., Lieberman, A. P., Lopez, O. L., MacK, W. J., Marson, D. C., Martiniuk, F., Mash, D. C., Masliah, E., McCormick, W. C., McCurry, S. M., McDavid, A. N., McKee, A. C., Mesulam, M., Miller, B. L., Miller, C. A., Miller, J. W., Parisi, J. E., Perl, D. P., Peskind, E., Petersen, R. C., Poon, W. W., Quinn, J. F., Rajbhandary, R. A., Raskind, M., Reisberg, B., Ringman, J. M., Roberson, E. D., Rosenberg, R. N., Sano, M., Schneider, L. S., Seeley, W., Shelanski, M. L., Slifer, M. A., Smith, C. D., Sonnen, J. A., Spina, S., Stern, R. A., Tanzi, R. E., Trojanowski, J. Q., Troncoso, J. C., Van Deerlin, V. M., Vinters, H. V., Vonsattel, J. P., Weintraub, S., Welsh-Bohmer, K. A., Williamson, J., Woltjer, R. L., Cantwell, L. B., Dombroski, B. A., Beekly, D., Lunetta, K. L., Martin, E. R., Kamboh, M. I., Saykin, A., Reiman, E. M., Bennett, D. A., Morris, J. C., Montine, T. J., Goate, A. M., Blacker, D., Tsuang, D. W., Hakonarson, H., Kukull, W. A., Foroud, T., Haines, J. L., Mayeux, R., Pericak-Vance, M. A., Farrer, L. A. & Schellenberg, G. D., May 2011, In : Nature Genetics. 43, 5, p. 436-443 8 p.

Research output: Contribution to journalArticle

Alzheimer Disease
Meta-Analysis
Genome-Wide Association Study
Disease Susceptibility
Genome
17 Citations (Scopus)

Comparison of Parent, Peer, Psychiatric, and Cannabis Use Influences Across Stages of Offspring Alcohol Involvement: Evidence from the COGA Prospective Study

Bucholz, K. K., McCutcheon, V. V., Agrawal, A., Dick, D. M., Hesselbrock, V. M., Kramer, J. R., Kuperman, S., Nurnberger, J., Salvatore, J. E., Schuckit, M. A., Bierut, L. J., Foroud, T., Chan, G., Hesselbrock, M., Meyers, J. L., Edenberg, H. & Porjesz, B., Feb 1 2017, In : Alcoholism: Clinical and Experimental Research. 41, 2, p. 359-368 10 p.

Research output: Contribution to journalArticle

Cannabis
Psychiatry
Alcohols
Prospective Studies
Wounds and Injuries
19 Citations (Scopus)
Saccades
Huntington Disease
Gray Matter
Parietal Lobe
Caudate Nucleus
16 Citations (Scopus)

Comprehensive gene- and pathway-based analysis of depressive symptoms in older adults

the Alzheimer's Disease Neuroimaging Initiative (ADNI) & Kim, S., 2015, In : Journal of Alzheimer's Disease. 45, 4, p. 1197-1206 10 p.

Research output: Contribution to journalArticle

Depression
Genes
Alzheimer Disease
Genome
Neuronal Plasticity
347 Citations (Scopus)

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDgene database

Lill, C. M., Roehr, J. T., McQueen, M. B., Kavvoura, F. K., Bagade, S., Schjeide, B. M. M., Schjeide, L. M., Meissner, E., Zauft, U., Allen, N. C., Liu, T., Schilling, M., Anderson, K. J., Beecham, G., Berg, D., Biernacka, J. M., Brice, A., DeStefano, A. L., Do, C. B., Eriksson, N. & 34 others, Factor, S. A., Farrer, M. J., Foroud, T., Gasser, T., Hamza, T., Hardy, J. A., Heutink, P., Hill-Burns, E. M., Klein, C., Latourelle, J. C., Maraganore, D. M., Martin, E. R., Martinez, M., Myers, R. H., Nalls, M. A., Pankratz, N., Payami, H., Satake, W., Scott, W. K., Sharma, M., Singleton, A. B., Stefansson, K., Toda, T., Tung, J. Y., Vance, J., Wood, N. W., Zabetian, C. P., Young, P., Tanzi, R. E., Khoury, M. J., Zipp, F., Lehrach, H., Ioannidis, J. P. A. & Bertram, L., Mar 2012, In : PLoS Genetics. 8, 3, e1002548.

Research output: Contribution to journalArticle

Parkinson disease
Parkinson Disease
Meta-Analysis
Genome-Wide Association Study
genome
15 Citations (Scopus)

Confirmation of alcohol preference quantitative trait loci in the replicate high alcohol drinking and low alcohol drinking rat lines

Foroud, T., Ritchotte, A., Spence, J., Liu, L., Lumeng, L., Li, T. K. & Carr, L. G., Sep 2003, In : Psychiatric Genetics. 13, 3, p. 155-161 7 p.

Research output: Contribution to journalArticle

Quantitative Trait Loci
Alcohol Drinking
Alcohols
Chromosomes, Human, Pair 10
Chromosomes, Human, Pair 5
38 Citations (Scopus)

Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15

Young, K., Foroud, T., Williams, P., Jackson, C. E., Beckmann, J. S., Cohen, D., Conneally, P. M., Tischfield, J. & Hodes, M. E., 1992, In : Genomics. 13, 4, p. 1370-1371 2 p.

Research output: Contribution to journalArticle

47 Citations (Scopus)

Confirmation of Linkage to Chromosome 1q for Peak Vertebral Bone Mineral Density in Premenopausal White Women

Econs, M., Koller, D. L., Hui, S., Fishburn, T., Conneally, P. M., Johnston, C. C., Peacock, M. & Foroud, T., Feb 2004, In : American Journal of Human Genetics. 74, 2, p. 223-228 6 p.

Research output: Contribution to journalArticle

Bone Density
Chromosomes
Spine
Siblings
Microsatellite Repeats
62 Citations (Scopus)

Confirmation of subtle motor changes among presymptomatic carriers of the huntington disease gene

Kirhwood, S. C., Siemers, E., Bond, C., Comically, P. M., Christian, J. C. & Foroud, T., Jul 2000, In : Archives of Neurology. 57, 7, p. 1040-1044 5 p.

Research output: Contribution to journalArticle

Huntington Disease
Reaction Time
Genes
Chorea
Neurologic Examination
80 Citations (Scopus)

Contribution of the LRP5 gene to normal variation in peak BMD in women

Koller, D. L., Ichikawa, S., Johnson, M. L., Lai, D., Xuei, X., Edenberg, H., Conneally, P. M., Hui, S., Johnston, C. C., Peacock, M., Foroud, T. & Econs, M., 2005, In : Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research. 20, 1, p. 75-80 6 p.

Research output: Contribution to journalArticle

Low Density Lipoprotein Receptor-Related Protein-5
Single Nucleotide Polymorphism
Genes
Spine
Hip
96 Citations (Scopus)

Convergent genetic and expression data implicate immunity in Alzheimer's disease

International Genomics of Alzheimer's Disease Consortium (IGAP), Jun 1 2015, In : Alzheimer's and Dementia. 11, 6, p. 658-671 14 p.

Research output: Contribution to journalArticle

Genomics
Endocytosis
Immunity
Alzheimer Disease
Cholesterol
103 Citations (Scopus)

Copy-number disorders are a common cause of congenital kidney malformations

Sanna-Cherchi, S., Kiryluk, K., Burgess, K. E., Bodria, M., Sampson, M. G., Hadley, D., Nees, S. N., Verbitsky, M., Perry, B. J., Sterken, R., Lozanovski, V. J., Materna-Kiryluk, A., Barlassina, C., Kini, A., Corbani, V., Carrea, A., Somenzi, D., Murtas, C., Ristoska-Bojkovska, N., Izzi, C. & 36 others, Bianco, B., Zaniew, M., Flogelova, H., Weng, P. L., Kacak, N., Giberti, S., Gigante, M., Arapovic, A., Drnasin, K., Caridi, G., Curioni, S., Allegri, F., Ammenti, A., Ferretti, S., Goj, V., Bernardo, L., Jobanputra, V., Chung, W. K., Lifton, R. P., Sanders, S., State, M., Clark, L. N., Saraga, M., Padmanabhan, S., Dominiczak, A. F., Foroud, T., Gesualdo, L., Gucev, Z., Allegri, L., Latos-Bielenska, A., Cusi, D., Scolari, F., Tasic, V., Hakonarson, H., Ghiggeri, G. M. & Gharavi, A. G., Dec 7 2012, In : American Journal of Human Genetics. 91, 6, p. 987-997 11 p.

Research output: Contribution to journalArticle

Kidney
Population Control
Gene Dosage
Urinary Tract
Databases
7 Citations (Scopus)

Copy number variation accuracy in genome-wide association studies

Lin, P., Hartz, S. M., Wang, J. C., Krueger, R. F., Foroud, T., Edenberg, H., Nurnberger, J., Brooks, A. I., Tischfield, J. A., Almasy, L., Webb, B. T., Hesselbrock, V. M., Porjesz, B., Goate, A. M., Bierut, L. J. & Rice, J. P., Jul 2011, In : Human Heredity. 71, 3, p. 141-147 7 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Research Personnel
Chromosome Duplication
Reproducibility of Results
Software
39 Citations (Scopus)

Copy number variation in familial parkinson disease

Pankratz, N., Dumitriu, A., Hetrick, K. N., Sun, M., Latourelle, J. C., Wilk, J. B., Halter, C., Doheny, K. F., Gusella, J. F., Nichols, W. C., Myers, R. H., Foroud, T. & DeStefano, A. L., 2011, In : PLoS One. 6, 8, e20988.

Research output: Contribution to journalArticle

Parkinson disease
Parkinson Disease
Genes
loci
DNA
65 Citations (Scopus)

Defining alcohol-related phenotypes in humans: The collaborative study on the genetics of alcoholism

Bierut, L. J., Saccone, N. L., Rice, J. P., Goate, A., Foroud, T., Edenberg, H., Almasy, L., Conneally, P. M., Crowe, R., Hesselbrock, V., Li, T. K., Nurnberger, J., Porjesz, B., Schuckit, M. A., Tischfield, J., Begleiter, H. & Reich, T., 2002, In : Alcohol Research and Health. 26, 3, p. 208-213 6 p.

Research output: Contribution to journalArticle

Alcoholism
Alcohols
Phenotype
Alcoholics
Chromosomes