Tatiana Foroud

  • 82045 Citations
  • 113 h-Index
1976 …2020

Research output per year

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Publications

Evidence for association between polymorphisms in the cannabinoid receptor 1 (CNR1) gene and cannabis dependence

Agrawal, A., Wetherill, L., Dick, D. M., Xuei, X., Hinrichs, A., Hesselbrock, V., Kramer, J., Nurnberger, J. I., Schuckit, M., Bierut, L. J., Edenberg, H. J. & Foroud, T., Jul 5 2009, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 150, 5, p. 736-740 5 p.

Research output: Contribution to journalArticle

45 Scopus citations

Evidence for a susceptibility locus for bipolar disorder on chromosome 11p11.5

McInnis, M. G., MacKinnon, D. F., McMahon, F. J., Foroud, T., Edenberg, H. J., Goate, A., Detera-Wadleigh, S., Stine, O. C., Rice, J., Blehar, M., Reich, T., Gershon, E., Nurnberger, J. I., Simpson, S. G. & DePaulo, J. R., Nov 6 1998, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 81, 6, 1 p.

Research output: Contribution to journalArticle

3 Scopus citations

Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts

Dick, D. M., Meyers, J., Aliev, F., Nurnberger, J., Kramer, J., Kuperman, S., Porjesz, B., Tischfield, J., Edenberg, H. J., Foroud, T., Schuckit, M., Goate, A., Hesselbrock, V. & Bierut, L., Sep 2010, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153, 6, p. 1179-1188 10 p.

Research output: Contribution to journalArticle

27 Scopus citations

Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index

Children's Hospital of Philadelphia/Price Foundation, GCAN, WTCCC3, GIANT, EGG & Price Foundation Collaborative Group, Feb 1 2017, In : Molecular Psychiatry. 22, 2, p. 192-201 10 p.

Research output: Contribution to journalArticle

28 Scopus citations

Evidence of association between brain-derived neurotrophic factor gene and bipolar disorder

Liu, L., Foroud, T., Xuei, X., Berrettini, W., Byerley, W., Coryell, W., El-Mallakh, R., Gershon, E. S., Kelsoe, J. R., Lawson, W. B., MacKinnon, D. F., McInnis, M., McMahon, F. J., Murphy, D. L., Rice, J., Scheftner, W., Zandi, P. R., Lohoff, F. W., Niculescu, A. B., Meyer, E. T. & 2 others, Edenberg, H. J. & Nurnberger, J. I., Dec 1 2008, In : Psychiatric genetics. 18, 6, p. 267-274 8 p.

Research output: Contribution to journalArticle

44 Scopus citations

Evolution of Alzheimer's Disease Cerebrospinal Fluid Biomarkers in Early Parkinson's Disease

Irwin, D. J., Fedler, J., Coffey, C. S., Caspell-Garcia, C., Kang, J. H., Simuni, T., Foroud, T., Toga, A. W., Tanner, C. M., Kieburtz, K., Chahine, L. M., Reimer, A., Hutten, S., Weintraub, D., Mollenhauer, B., Galasko, D. R., Siderowf, A., Marek, K., Trojanowski, J. Q. & Shaw, L. M., Sep 1 2020, In : Annals of neurology. 88, 3, p. 574-587 14 p.

Research output: Contribution to journalArticle

Open Access

Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study

The Alzheimer’s Disease Genetics Consortium, Dec 1 2020, In : Nature communications. 11, 1, 667.

Research output: Contribution to journalArticle

Open Access
11 Scopus citations

Exome-chip association analysis of intracranial aneurysms

van 't Hof, F. N. G., Lai, D., van Setten, J., Bots, M. L., Vaartjes, I., Broderick, J., Woo, D., Foroud, T., Rinkel, G. J. E., de Bakker, P. I. W. & Ruigrok, Y. M., Feb 4 2020, In : Neurology. 94, 5, p. e481-e488

Research output: Contribution to journalArticle

Exome Chip Meta-analysis Fine Maps Causal Variants and Elucidates the Genetic Architecture of Rare Coding Variants in Smoking and Alcohol Use

CHD Exome+ Consortium & Consortium for Genetics of Smoking Behaviour, Jun 1 2019, In : Biological psychiatry. 85, 11, p. 946-955 10 p.

Research output: Contribution to journalArticle

9 Scopus citations

Exome Sequencing Identifies Candidate Genetic Modifiers of Syndromic and Familial Thoracic Aortic Aneurysm Severity

Landis, B. J., Schubert, J. A., Lai, D., Jegga, A. G., Shikany, A. R., Foroud, T., Ware, S. M. & Hinton, R. B., Aug 1 2017, In : Journal of cardiovascular translational research. 10, 4, p. 423-432 10 p.

Research output: Contribution to journalArticle

9 Scopus citations

Expression profiling and QTL analysis: A powerful complementary strategy in drug abuse research

Spence, J. P., Liang, T., Foroud, T., Lo, D. & Carr, L. G., Mar 2005, In : Addiction Biology. 10, 1, p. 47-51 5 p.

Research output: Contribution to journalArticle

15 Scopus citations

Facial Curvature Detects and Explicates Ethnic Differences in Effects of Prenatal Alcohol Exposure

the CIFASD, Aug 2017, In : Alcoholism: Clinical and Experimental Research. 41, 8, p. 1471-1483 13 p.

Research output: Contribution to journalArticle

9 Scopus citations

Facial dysmorphism across the fetal alcohol spectrum

Suttie, M., Foroud, T., Wetherill, L., Jacobson, J. L., Molteno, C. D., Meintjes, E. M., Hoyme, H. E., Khaole, N., Robinson, L. K., Riley, E. P., Jacobson, S. W. & Hammond, P., Mar 2013, In : Pediatrics. 131, 3, p. e779-e788

Research output: Contribution to journalArticle

62 Scopus citations

False positive rates in association studies as a function of degree of stratification

Koller, D. L., Peacock, M., Lai, D., Foroud, T. & Econs, M. J., Aug 1 2004, In : Journal of Bone and Mineral Research. 19, 8, p. 1291-1295 5 p.

Research output: Contribution to journalArticle

17 Scopus citations

FAM222A encodes a protein which accumulates in plaques in Alzheimer’s disease

The Alzheimer Disease Neuroimaging Initiative, Dec 1 2020, In : Nature communications. 11, 1, 411.

Research output: Contribution to journalArticle

Open Access
2 Scopus citations

Familial intracranial aneurysms: Is anatomic vulnerability heritable?

Mackey, J., Brown, R. D., Moomaw, C. J., Hornung, R., Sauerbeck, L., Woo, D., Foroud, T., Gandhi, D., Kleindorfer, D., Flaherty, M. L., Meissner, I., Anderson, C., Rouleau, G., Connolly, E. S., Deka, R., Koller, D. L., Abruzzo, T., Huston, J. & Broderick, J. P., Jan 2013, In : Stroke. 44, 1, p. 38-42 5 p.

Research output: Contribution to journalArticle

15 Scopus citations

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17

Murrell, J. R., Koller, D., Foroud, T., Goedert, M., Spillantini, M. G., Edenberg, H. J., Farlow, M. R. & Ghetti, B., Nov 1997, In : American Journal of Human Genetics. 61, 5, p. 1131-1138 8 p.

Research output: Contribution to journalArticle

64 Scopus citations

Family-Based Association Analysis of Alcohol Dependence Criteria and Severity

Wetherill, L., Kapoor, M., Agrawal, A., Bucholz, K., Koller, D., Bertelsen, S. E., Le, N., Wang, J. C., Almasy, L., Hesselbrock, V., Kramer, J., Nurnberger, J. I., Schuckit, M., Tischfield, J. A., Xuei, X., Porjesz, B., Edenberg, H. J., Goate, A. M. & Foroud, T., Feb 2014, In : Alcoholism: Clinical and Experimental Research. 38, 2, p. 354-366 13 p.

Research output: Contribution to journalArticle

16 Scopus citations

Family-based association of FKBP5 in bipolar disorder

Willour, V. L., Chen, H., Toolan, J., Belmonte, P., Cutler, D. J., Goes, F. S., Zandi, P. P., Lee, R. S., MacKinnon, D. F., Mondimore, F. M., Schweizer, B., DePaulo, J. R., Gershon, E., McMahon, F. J., Potash, J. B., Miller, E., Pearl, J., Kassem, L., Lopez, V., Nurnberger, J. & 46 others, Miller, M. J., Bowman, E. S., Reich, T., Goate, A., Rice, J., Stine, C., Kazuba, D., Maxwell, E., Rau, N. L., Moe, P. R., Samavedy, N., El-Mallakh, R., Manji, H., Glitz, D. A., Meyer, E. T., Smiley, C., Foroud, T., Flury, L., Dick, D. M., Edenberg, H., Bierut, L., McInnis, M., Avramopoulos, D., Payne, J., Berrettini, W., Byerley, W., Vawter, M., Coryell, W., Crowe, R., Badner, J., Liu, C., Sanders, A., Caserta, M., Dinwiddie, S., Nguyen, T., Harakal, D., Kelsoe, J., McKinney, R., Scheftner, W., Kravitz, H. M., Marta, D., Vaughn-Brown, A., Bederow, L., Detera-Wadleigh, S., Austin, L. & Murphy, D. L., Jan 1 2009, In : Molecular Psychiatry. 14, 3, p. 261-268 8 p.

Research output: Contribution to journalArticle

124 Scopus citations

Family-based association of YWHAH in psychotic bipolar disorder

Grover, D., Verma, R., Goes, F. S., Belmonte Mahon, P. L., Gershon, E. S., McMahon, F. J., Potash, J. B., Steele, J., Kassem, L., Pearl, J., Schulze, T., MacKinnon, D. F., Miller, E., Toolan, J., Zandi, P. P., Simpson, S., Nurnberger, J., Miller, M. J., Bowman, E. S., Reich, T. & 45 others, Goate, A., Rice, J., DePaulo, J. R., Stine, C., Kazuba, D., Maxwell, E., Rau, N. L., Moe, P. R., Samavedy, N., El-Mallakh, R., Manji, H., Glitz, D. A., Meyer, E. T., Smiley, C., Foroud, T., Flury, L., Dick, D. M., Edenberg, H., Bierut, L., McInnis, M., Mondimore, F. M., Avramopoulos, D., Payne, J., Berrettini, W., Byerley, W., Vawter, M., Coryell, W., Crowe, R., Badner, J., Liu, C., Sanders, A., Caserta, M., Dinwiddie, S., Nguyen, T., Harakal, D., Kelsoe, J., McKinney, R., Scheftner, W., Kravitz, H. M., Marta, D., Vaughn-Brown, A., Bederow, L., Detera-Wadleigh, S., Austin, L. & Murphy, D. L., Oct 5 2009, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 150, 7, p. 977-983 7 p.

Research output: Contribution to journalArticle

37 Scopus citations

Family-based genome-wide association study of frontal theta oscillations identifies potassium channel gene KCNJ6

Kang, S. J., Rangaswamy, M., Manz, N., Wang, J. C., Wetherill, L., Hinrichs, T., Almasy, L., Brooks, A., Chorlian, D. B., Dick, D., Hesselbrock, V., Kramer, J., Kuperman, S., Nurnberger, J., Rice, J., Schuckit, M., Tischfield, J., Bierut, L. J., Edenberg, H. J., Goate, A. & 2 others, Foroud, T. & Porjesz, B., Aug 1 2012, In : Genes, Brain and Behavior. 11, 6, p. 712-719 8 p.

Research output: Contribution to journalArticle

44 Scopus citations

Family-based study of the association of the dopamine D2 receptor gene (DRD2) with habitual smoking

Bierut, L. J., Rice, J. P., Edenberg, H. J., Goate, A., Foroud, T., Cloninger, C. R., Begleiter, H., Conneally, P. M., Crowe, R. R., Hesselbrock, V., Li, T. K., Nurnberger, J. I., Porjesz, B., Schuckit, M. A. & Reich, T., 2000, In : American journal of medical genetics. 90, 4, p. 299-302 4 p.

Research output: Contribution to journalArticle

96 Scopus citations

FASTKD2 is associated with memory and hippocampal structure in older adults

Ramanan, V. K., Nho, K., Shen, L., Risacher, S. L., Kim, S., McDonald, B. C., Farlow, M. R., Foroud, T. M., Gao, S., Soininen, H., Kłoszewska, I., Mecocci, P., Tsolaki, M., Vellas, B., Lovestone, S., Aisen, P. S., Petersen, R. C., Jack, C. R., Shaw, L. M., Trojanowski, J. Q. & 7 others, Weiner, M. W., Green, R. C., Toga, A. W., De Jager, P. L., Yu, L., Bennett, D. A. & Saykin, A. J., Oct 29 2015, In : Molecular Psychiatry. 20, 10, p. 1197-1204 8 p.

Research output: Contribution to journalArticle

15 Scopus citations

Feasibility and safety of lumbar puncture in the Parkinson's disease research participants: Parkinson's Progression Marker Initiative (PPMI)

The Parkinson's Progression Markers InitiativeSteering Committee, Study Cores, Site Investigators, Coordinators & Industry and Scientific Advisory Board, May 2019, In : Parkinsonism and Related Disorders. 62, p. 201-209 9 p.

Research output: Contribution to journalArticle

2 Scopus citations

Feasibility and safety of multicenter tissue and biofluid sampling for μ -Synuclein in Parkinson's disease: The systemic synuclein sampling study (S4)

Chahine, L. M., Beach, T. G., Seedorff, N., Caspell-Garcia, C., Coffey, C. S., Brumm, M., Adler, C. H., Serrano, G. E., Linder, C., Mosovsky, S., Foroud, T., Riss, H., Ecklund, D., Seibyl, J., Jennings, D., Arnedo, V., Riley, L., Dave, K. D. & Mollenhauer, B., Jan 1 2018, In : Journal of Parkinson's Disease. 8, 4, p. 517-527 11 p.

Research output: Contribution to journalArticle

3 Scopus citations

Ferritin levels in the cerebrospinal fluid predict Alzheimer's disease outcomes and are regulated by APOE

Alzheimer's Disease Neuroimaging Initiative, May 19 2015, In : Nature communications. 6, 6760.

Research output: Contribution to journalArticle

113 Scopus citations

Fibroblast growth factor 23 genotype and cardiovascular disease in patients undergoing hemodialysis

Schwantes-An, T. H., Liu, S., Stedman, M., Decker, B. S., Wetherill, L., Edenberg, H. J., Vatta, M., Foroud, T. M., Chertow, G. M. & Moe, S. M., Feb 1 2019, In : American journal of nephrology. 49, 2, p. 125-132 8 p.

Research output: Contribution to journalArticle

2 Scopus citations

Finding useful biomarkers for Parkinson s disease

Chen-Plotkin, A. S., Albin, R., Alcalay, R., Babcock, D., Bajaj, V., Bowman, D., Buko, A., Cedarbaum, J., Chelsky, D., Cookson, M. R., Dawson, T. M., Dewey, R., Foroud, T., Frasier, M., German, D., Gwinn, K., Huang, X., Kopil, C., Kremer, T., Lasch, S. & 20 others, Marek, K., Marto, J. A., Merchant, K., Mollenhauer, B., Naito, A., Potashkin, J., Reimer, A., Rosenthal, L. S., Saunders-Pullman, R., Scherzer, C. R., Sherer, T., Singleton, A., Sutherland, M., Thiele, I., Van Der Brug, M., Keuren-Jensen, K. V., Vaillancourt, D., Walt, D., West, A. & Zhang, J., Aug 15 2018, In : Science translational medicine. 10, 454, eaam6003.

Research output: Contribution to journalReview article

22 Scopus citations

Fine mapping and expression of candidate genes within the chromosome 10 QTL region of the high and low alcohol-drinking rats

Bice, P. J., Liang, T., Zhang, L., Graves, T. J., Carr, L. G., Lai, D., Kimpel, M. W. & Foroud, T., Sep 2010, In : Alcohol. 44, 6, p. 477-485 9 p.

Research output: Contribution to journalArticle

16 Scopus citations

Fine mapping of bone structure and strength QTLs in heterogeneous stock rat

Alam, I., Koller, D. L., Cañete, T., Blázquez, G., Mont-Cardona, C., López-Aumatell, R., Martínez-Membrives, E., Díaz-Morán, S., Tobeña, A., Fernández-Teruel, A., Stridh, P., Diez, M., Olsson, T., Johannesson, M., Baud, A., Econs, M. J. & Foroud, T., Dec 1 2015, In : Bone. 81, p. 417-426 10 p.

Research output: Contribution to journalArticle

6 Scopus citations

Fine mapping quantitative trait loci that influence alcohol preference behavior in the high and low alcohol preferring (HAP and LAP) mice

Bice, P. J., Lai, D., Zhang, L. & Foroud, T., Jul 1 2011, In : Behavior Genetics. 41, 4, p. 565-570 6 p.

Research output: Contribution to journalArticle

10 Scopus citations

From QTL to candidate gene: A genetic approach to alcoholism research

Spence, J. P., Liang, T., Liu, L., Johnson, P. L., Foroud, T., Carr, L. G. & Shekhar, A., Jun 2009, In : Current Drug Abuse Reviews. 2, 2, p. 127-134 8 p.

Research output: Contribution to journalArticle

26 Scopus citations

Functional brain architecture is associated with the rate of tau accumulation in Alzheimer’s disease

Alzheimer’s Disease Neuroimaging Initiative (ADNI), Dec 1 2020, In : Nature communications. 11, 1, 347.

Research output: Contribution to journalArticle

Open Access
3 Scopus citations
36 Scopus citations

Functional relevance of human ADH polymorphism

Eriksson, C. J. P., Fukunaga, T., Sarkola, T., Chen, W. J., Chen, C. C., Ju, J. M., Cheng, A. T. A., Yamamoto, H., Kohlenberg-Müller, K., Kimura, M., Murayama, M., Matsushita, S., Kashima, H., Higuchi, S., Carr, L., Viljoen, D., Brooke, L., Stewart, T., Foroud, T., Su, J. & 2 others, Li, T. K. & Whitfield, J. B., Jun 27 2001, In : Alcoholism: Clinical and Experimental Research. 25, 5 SUPPL., p. 157S-163S

Research output: Contribution to journalArticle

66 Scopus citations

Functional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependence

Hinrichs, A. L., Wang, J. C., Bufe, B., Kwon, J. M., Budde, J., Allen, R., Bertelsen, S., Evans, W., Dick, D., Rice, J., Foroud, T., Nurnberger, J., Tischfield, J. A., Kuperman, S., Crowe, R., Hesselbrock, V., Schuckit, M., Almasy, L., Porjesz, B., Edenberg, H. J. & 4 others, Begleiter, H., Meyerhof, W., Bierut, L. J. & Goate, A. M., Jan 2006, In : American Journal of Human Genetics. 78, 1, p. 103-111 9 p.

Research output: Contribution to journalArticle

104 Scopus citations

Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease

Hui, K. Y., Fernandez-Hernandez, H., Hu, J., Schaffner, A., Pankratz, N., Hsu, N. Y., Chuang, L. S., Carmi, S., Villaverde, N., Li, X., Rivas, M., Levine, A. P., Bao, X., Labrias, P. R., Haritunians, T., Ruane, D., Gettler, K., Chen, E., Li, D., Schiff, E. R. & 31 others, Pontikos, N., Barzilai, N., Brant, S. R., Bressman, S., Cheifetz, A. S., Clark, L. N., Daly, M. J., Desnick, R. J., Duerr, R. H., Katz, S., Lencz, T., Myers, R. H., Ostrer, H., Ozelius, L., Payami, H., Peter, Y., Rioux, J. D., Segal, A. W., Scott, W. K., Silverberg, M. S., Vance, J. M., Ubarretxena-Belandia, I., Foroud, T., Atzmon, G., Pe'er, I., Ioannou, Y., McGovern, D. P. B., Yue, Z., Schadt, E. E., Cho, J. H. & Peter, I., Jan 10 2018, In : Science translational medicine. 10, 423, eaai7795.

Research output: Contribution to journalArticle

80 Scopus citations

Further analyses of the NIMH bipolar dataset: Follow up on suggestive linkage results on 1p and 10p

Corbett, J., Rice, J., Saccone, N., Goate, A., Reich, T., Foroud, T., Nurnberger, J., Edenberg, H., DePaulo, J. R. & Gershon, E., Aug 7 2000, In : American Journal of Medical Genetics - Neuropsychiatric Genetics. 96, 4, 1 p.

Research output: Contribution to journalArticle

Further mapping of an ataxia-telangiectasia locus to the chromosome 11q23 region

Sanal, O., Wei, S., Foroud, T., Malhotra, U., Concannon, P., Charmley, P., Salser, W., Lange, K. & Gatti, R. A., Nov 21 1990, In : American Journal of Human Genetics. 47, 5, p. 860-866 7 p.

Research output: Contribution to journalArticle

29 Scopus citations

G2019S mutation in the leucine-rich repeat kinase 2 gene is not associated with multiple system atrophy

Ozelius, L. J., Foroud, T., May, S., Senthil, G., Sandroni, P., Low, P. A., Reich, S., Colcher, A., Stern, M. B., Ondo, W. G., Jankovic, J., Huang, N., Tanner, C. M., Novak, P., Gilman, S., Marshall, F. J., Wooten, G. F., Chelimsky, T. C., Shults, C. W., Masliah, E. & 5 others, Kukull, W., Lee, V., Trojanowski, J., Shoulson, I. & Ozelius, L., Mar 15 2007, In : Movement Disorders. 22, 4, p. 546-549 4 p.

Research output: Contribution to journalArticle

20 Scopus citations

GABRR1 and GABRR2, encoding the GABA-A receptor subunits ρ1 and ρ2, are associated with alcohol dependence

Xuei, X., Flury-Wetherill, L., Dick, D., Goate, A., Tischfield, J., Nurnberger, J., Schuckit, M., Kramer, J., Kuperman, S., Hesselbrock, V., Porjesz, B., Foroud, T. & Edenberg, H. J., Mar 1 2010, In : American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics. 153, 2, p. 418-427 10 p.

Research output: Contribution to journalArticle

38 Scopus citations

Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation

Dumitriu, A., Latourelle, J. C., Hadzi, T. C., Pankratz, N., Garza, D., Miller, J. P., Vance, J. M., Foroud, T., Beach, T. G. & Myers, R. H., Jun 2012, In : PLoS Genetics. 8, 6, e1002794.

Research output: Contribution to journalArticle

43 Scopus citations

Gene mapping using linkage analysis.

Sanal, O., Foroud, T. & Gatti, R. A., Jan 1 1991, In : The Turkish journal of pediatrics. 33, 1, p. 1-12 12 p.

Research output: Contribution to journalArticle

7 Scopus citations

Genes influencing Parkinson disease onset: Replication of PARK3 and identification of novel loci

Pankratz, N., Uniacke, S. K., Halter, C. A., Rudolph, A., Shults, C. W., Conneally, P. M., Foroud, T. & Nichols, W. C., May 11 2004, In : Neurology. 62, 9, p. 1616-1618 3 p.

Research output: Contribution to journalArticle

33 Scopus citations

Genes influencing spinal bone mineral density in inbred F344, LEW, COP, and DA rats

Alam, I., Sun, Q., Koller, D. L., Liu, L., Liu, Y., Edenberg, H. J., Foroud, T. & Turner, C. H., Mar 1 2010, In : Functional and Integrative Genomics. 10, 1, p. 63-72 10 p.

Research output: Contribution to journalArticle

8 Scopus citations

Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease

International Genomics of Alzheimer's Project (IGAP), ARUK Consortium & GERAD/PERADES, CHARGE, ADGC, EADI, Jan 1 2018, In : Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring. 10, p. 595-598 4 p.

Research output: Contribution to journalArticle

Genetically predicted body mass index and Alzheimer's disease-related phenotypes in three large samples: Mendelian randomization analyses

Adult Changes in Thought Study Investigators, Religious Orders Study/Memory and Aging Project Investigators & Alzheimer's Disease Genetics Consortium, Dec 1 2015, In : Alzheimer's and Dementia. 11, 12, p. 1439-1451 13 p.

Research output: Contribution to journalArticle

22 Scopus citations

Genetic analysis of quantitative phenotypes in AD and MCI: Imaging, cognition and biomarkers

Shen, L., Thompson, P. M., Potkin, S. G., Bertram, L., Farrer, L. A., Foroud, T. M., Green, R. C., Hu, X., Huentelman, M. J., Kim, S., Kauwe, J. S. K., Li, Q., Liu, E., Macciardi, F., Moore, J. H., Munsie, L., Nho, K., Ramanan, V. K., Risacher, S. L., Stone, D. J. & 4 others, Swaminathan, S., Toga, A. W., Weiner, M. W. & Saykin, A. J., Jun 2014, In : Brain Imaging and Behavior. 8, 2, p. 183-207 25 p.

Research output: Contribution to journalArticle

86 Scopus citations

Genetic and bioinformatic tools in Parkinson’s disease

Foroud, T. & Pankratz, N., Jan 1 2012, Parkinson's Disease, Second Edition. CRC Press, p. 181-187 7 p.

Research output: Chapter in Book/Report/Conference proceedingChapter