Tatiana Foroud

  • 42505 Citations
  • 101 h-Index
1976 …2021
If you made any changes in Pure, your changes will be visible here soon.

Publications 1988 2020

Filter
Article
6 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

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

Stoppage: An issue for segregation analysis

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

Alcoholics
alcoholism
Hippocampus
Genes
Alcoholism
17 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Drinking
Alcohols
Alcoholism
Young Adult
Emotions
106 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

Telephone
Cognition
Alzheimer Disease
Episodic Memory
Short-Term Memory
2 Citations (Scopus)

Telomere Shortening in the Alzheimer's Disease Neuroimaging Initiative Cohort

Nudelman, K. N. H., Lin, J., Lane, K. A., Nho, K., Kim, S., Faber, K. M., Risacher, S. L., Foroud, T. M., Gao, S., Davis, J. W., Weiner, M. W. & Saykin, A. J., Jan 1 2019, In : Journal of Alzheimer's Disease. 71, 1, p. 33-43 11 p.

Research output: Contribution to journalArticle

Telomere Shortening
Neuroimaging
Telomere
Alzheimer Disease
Disease Progression
44 Citations (Scopus)

Ten-year rate of longitudinal change in neurocognitive and motor function in prediagnosis Huntington disease

Solomon, A. C., Stout, J. C., Weaver, M., Queller, S., Tomusk, A., Whitlock, K. B., Hui, S., Marshall, J., Jackson, J. G., Siemens, E. R., Beristain, X., Wojcieszek, J. & Foroud, T., Oct 15 2008, In : Movement Disorders. 23, 13, p. 1830-1836 7 p.

Research output: Contribution to journalArticle

Huntington Disease
Age of Onset
Longitudinal Studies
20 Citations (Scopus)

Test-retest reliability of saccadic measures in subjects at risk for Huntington disease

Blekher, T., Weaver, M. R., Cai, X., Hui, S., Marshall, J., Jackson, J. G., Wojcieszek, J., Yee, R. D. & Foroud, T., Dec 2009, In : Investigative Ophthalmology and Visual Science. 50, 12, p. 5707-5711 5 p.

Research output: Contribution to journalArticle

Saccades
Huntington Disease
Reproducibility of Results
Biomarkers
Eye Movements
43 Citations (Scopus)

The ATC (ataxia-telangiectasia complementation group C) locus localizes to 11q22-q23

Ziv, Y., Rotman, G., Frydman, M., Dagan, J., Cohen, T., Foroud, T., Gatti, R. A. & Shiloh, Y., 1991, In : Genomics. 9, 2, p. 373-375 3 p.

Research output: Contribution to journalArticle

Ataxia Telangiectasia
Genes
Chromosomes, Human, Pair 11
Restriction Fragment Length Polymorphisms
Chromosomes
2 Citations (Scopus)

The BIN1 rs744373 SNP is associated with increased tau-PET levels and impaired memory

The Alzheimer’s Disease Neuroimaging Initiative (ADNI), Dec 1 2019, In : Nature communications. 10, 1, 1766.

Research output: Contribution to journalArticle

Open Access
integrators
polymorphism
nucleotides
Polymorphism
genes
11 Citations (Scopus)

The effect of shared genetic and environmental factors on periodontal disease parameters in untreated adult siblings in Guatemala

Dowsett, S. A., Archila, L., Foroud, T., Koller, D., Eckert, G. J. & Kowolik, M., Oct 1 2002, In : Journal of Periodontology. 73, 10, p. 1160-1168 9 p.

Research output: Contribution to journalArticle

Guatemala
Periodontal Diseases
Spouses
Siblings
Periodontal Index
300 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

Neuroimaging
Meta-Analysis
Genome-Wide Association Study
Brain
Attention Deficit Disorder with Hyperactivity
48 Citations (Scopus)

The Familial Intracranial Aneurysm (FIA) study protocol

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

Research output: Contribution to journalArticle

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

The genetics of alcoholism: Identifying specific genes through family studies

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

Research output: Contribution to journalArticle

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

The genetics of dementia

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

Research output: Contribution to journalArticle

Dementia
Genes
Frontotemporal Lobar Degeneration
Exome
Inborn Genetic Diseases
11 Citations (Scopus)
Drinking
Trajectories
Alcohols
Genes
Alcoholism
1 Citation (Scopus)

The longitudinal evaluation of familial frontotemporal dementia subjects protocol: Framework and methodology

LEFFTDS Consortium, Jan 1 2019, (Accepted/In press) In : Alzheimer's and Dementia.

Research output: Contribution to journalArticle

Open Access
Frontotemporal Lobar Degeneration
Frontotemporal Dementia
Dementia
tau Proteins
Chromosomes, Human, Pair 9
55 Citations (Scopus)

The North American Multiple System Atrophy Study Group

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

Research output: Contribution to journalArticle

Multiple System Atrophy
alpha-Synuclein
Levodopa
Research Personnel
Cerebellar Diseases
59 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

Research
Internet
Parkinson Disease
Biomarkers
Counselors
38 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

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

The search for genetic risk factors associated with suicidal behavior

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

Research output: Contribution to journalArticle

Chromosomes
Suicide
Alcohols
Lod Score
Alcoholism
23 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

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

The tachykinin receptor 3 is associated with alcohol and cocaine dependence

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

Menarche
Genome-Wide Association Study
Meta-Analysis
Genes
Biological Phenomena

Tracking white matter degeneration in asymptomatic and symptomatic MAPT mutation carriers

LEFFTDS Consortium, Nov 2019, In : Neurobiology of Aging. 83, p. 54-62 9 p.

Research output: Contribution to journalArticle

Microtubule-Associated Proteins
Mutation
Diffusion Tensor Imaging
Anisotropy
Disease Progression
48 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

Alzheimer Disease
Genome
Single Nucleotide Polymorphism
Genome-Wide Association Study
Genetic Loci
4 Citations (Scopus)
Translational Medical Research
Epidemiology
176 Citations (Scopus)

Translation initiator EIF4G1 mutations in familial parkinson disease

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

Research output: Contribution to journalArticle

Parkinsonian Disorders
Parkinson Disease
Mutation
Eukaryotic Initiation Factor-4G
Lewy Body Disease
67 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

African Americans
Alzheimer Disease
Linkage Disequilibrium
Myeloid Cells
Mutation

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

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

Research output: Contribution to journalArticle

62 Citations (Scopus)

Two gene co-expression modules differentiate psychotics and controls

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

Research output: Contribution to journalArticle

Bipolar Disorder
Schizophrenia
Gene Expression
Neurons
Cerebral Cortex
20 Citations (Scopus)

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

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

Type 2 diabetes mellitus, brain atrophy, and cognitive decline

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

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

Understanding the effects of prenatal alcohol exposure using threedimensional facial imaging

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

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

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

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

Research output: Contribution to journalArticle

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

Use of the CDR® plus NACC FTLD in mild FTLD: Data from the ARTFL/LEFFTDS consortium

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

Research output: Contribution to journalArticle

Frontotemporal Lobar Degeneration
Dementia
Language
Personality
Primary Progressive Nonfluent Aphasia
1 Citation (Scopus)

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

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

Research output: Contribution to journalArticle

Quantitative Trait Loci
Dissection
Phenotype
Principal Component Analysis
Genome