Tatiana Foroud

  • 82045 Citations
  • 113 h-Index
1976 …2020

Research output per year

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Publications

Review article

Analysis of copy number variation in Alzheimer's disease: The NIALOAD/ NCRAD family study

Swaminathan, S., Shen, L., Kim, S., Inlow, M., West, J. D., Faber, K. M., Foroud, T., Mayeux, R. & Saykin, A. J., 2012, In : Current Alzheimer research. 9, 7, p. 801-814 14 p.

Research output: Contribution to journalReview article

44 Scopus citations

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 journalReview article

184 Scopus citations

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 1 2003, In : Psychiatric genetics. 13, 3, p. 155-161 7 p.

Research output: Contribution to journalReview article

15 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
36 Scopus citations

Genetics and alcoholism

Edenberg, H. J. & Foroud, T., Aug 1 2013, In : Nature Reviews Gastroenterology and Hepatology. 10, 8, p. 487-494 8 p.

Research output: Contribution to journalReview article

70 Scopus citations

Genetics of alcoholism: A review of recent studies in human and animal models

Foroud, T. & Li, T. K., Sep 1 1999, In : American Journal on Addictions. 8, 4, p. 261-278 18 p.

Research output: Contribution to journalReview article

45 Scopus citations

Genetics of bipolar affective disorder.

Nurnberger, J. I. & Foroud, T., Apr 2000, In : Current psychiatry reports. 2, 2, p. 147-157 11 p.

Research output: Contribution to journalReview article

43 Scopus citations

Genetics of osteoporosis

Peacock, M., Turner, C. H., Econs, M. J. & Foroud, T., Jan 1 2002, In : Endocrine Reviews. 23, 3, p. 303-326 24 p.

Research output: Contribution to journalReview article

312 Scopus citations

Genetics of Parkinson disease

Pankratz, N. & Foroud, T., Dec 1 2007, In : Genetics in Medicine. 9, 12, p. 801-811 11 p.

Research output: Contribution to journalReview article

63 Scopus citations

Genetic studies of quantitative MCI and AD phenotypes in ADNI: Progress, opportunities, and plans

Saykin, A. J., Shen, L., Yao, X., Kim, S., Nho, K., Risacher, S. L., Ramanan, V. K., Foroud, T. M., Faber, K. M., Sarwar, N., Munsie, L. M., Hu, X., Soares, H. D., Potkin, S. G., Thompson, P. M., Kauwe, J. S. K., Kaddurah-Daouk, R., Green, R. C., Toga, A. W. & Weiner, M. W., Jul 1 2015, In : Alzheimer's and Dementia. 11, 7, p. 792-814 23 p.

Research output: Contribution to journalReview article

101 Scopus citations

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

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

Research output: Contribution to journalReview article

97 Scopus citations

Introduction to genetic linkage analysis

Foroud, T., Jan 1 1997, In : Cancer Investigation. 15, 6, p. 548-552 5 p.

Research output: Contribution to journalReview article

1 Scopus citations

Knowledge gaps and research recommendations for essential tremor

Hopfner, F., Haubenberger, D., Galpern, W. R., Gwinn, K., Van't Veer, A., White, S., Bhatia, K., Adler, C. H., Eidelberg, D., Ondo, W., Stebbins, G. T., Tanner, C. M., Helmich, R. C., Lenz, F. A., Sillitoe, R. V., Vaillancourt, D., Vitek, J. L., Louis, E. D., Shill, H. A., Frosch, M. P. & 7 others, Foroud, T., Kuhlenbäumer, G., Singleton, A., Testa, C. M., Hallett, M., Elble, R. & Deuschl, G., Dec 1 2016, In : Parkinsonism and Related Disorders. 33, p. 27-35 9 p.

Research output: Contribution to journalReview article

23 Scopus citations

Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura

Levy, G. G., Nichols, W. C., Lian, E. C., Foroud, T., McClintick, J. N., McGee, B. M., Yang, A. Y., Siemieniak, D. R., Stark, K. R., Gruppo, R., Sarode, R., Shurin, S. B., Chandrasekaran, V., Stabler, S. P., Sabio, H., Bouhassira, E. E., Upshaw, J. D., Ginsburg, D. & Tsai, H. M., Oct 4 2001, In : Nature. 413, 6855, p. 488-494 7 p.

Research output: Contribution to journalReview article

1267 Scopus citations

Neurology Individualized Medicine: When to Use Next-Generation Sequencing Panels

Klein, C. J. & Foroud, T., Feb 1 2017, In : Mayo Clinic Proceedings. 92, 2, p. 292-305 14 p.

Research output: Contribution to journalReview article

22 Scopus citations

Parkinson's disease biomarkers: Perspective from the NINDS Parkinson's Disease Biomarkers Program

Gwinn, K., David, K. K., Swanson-Fischer, C., Albin, R., Hillaire-Clarke, C. S., Sieber, B. A., Lungu, C., Bowman, F. D., Alcalay, R. N., Babcock, D., Dawson, T. M., Dewey, R. B., Foroud, T., German, D., Huang, X., Petyuk, V., Potashkin, J. A., Saunders-Pullman, R., Sutherland, M., Walt, D. R. & 6 others, West, A. B., Zhang, J., Chen-Plotkin, A., Scherzer, C. R., Vaillancourt, D. E. & Rosenthal, L. S., Jun 2017, In : Biomarkers in Medicine. 11, 6, p. 451-473 23 p.

Research output: Contribution to journalReview article

20 Scopus citations

Prenatal alcohol exposure: Advancing knowledge through international collaborations

Riley, E. P., Guerri, C., Calhoun, F., Charness, M. E., Foroud, T. M., Li, T. K., Mattson, S. N., May, P. A. & Warren, K. R., Jan 1 2003, In : Alcoholism: Clinical and Experimental Research. 27, 1, p. 118-135 18 p.

Research output: Contribution to journalReview article

35 Scopus citations

The genetics of alcoholism: Identifying specific genes through family studies

Edenberg, H. J. & Foroud, T., Sep 1 2006, In : Addiction Biology. 11, 3-4, p. 386-396 11 p.

Research output: Contribution to journalReview article

162 Scopus citations
Letter

Don't give up on GWAS

on behalf of 96 Psychiatric Genetics Investigators, Jan 1 2012, In : Molecular Psychiatry. 17, 1, p. 2-3 2 p.

Research output: Contribution to journalLetter

46 Scopus citations

Interpretation of Genetic Linkage Findings (multiple letters)

Liu, Y., Xu, F., Recker, R. R., Deng, H. W., Koller, D. L., White, K. E., Liu, G., Hui, S. L., Conneally, P. M., Johnston, C. C., Econs, M. J., Foroud, T. & Peacock, M., Nov 2003, In : Journal of Bone and Mineral Research. 18, 11, p. 2077-2078 2 p.

Research output: Contribution to journalLetter

2 Scopus citations

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

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

Research output: Contribution to journalLetter

48 Scopus citations

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

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

Research output: Contribution to journalLetter

6 Scopus citations

Reply from the Authors

Nichols, W. C., Elsaesser, V. E., Pankratz, N., Pauciulo, M. W., Marek, D. K., Halter, C. A., Rudolph, A. & Foroud, T., Jun 10 2008, In : Neurology. 70, 24, p. 2348-2349 2 p.

Research output: Contribution to journalLetter

Tau mutations as a novel risk factor for cancer—letter

the LEFFTDS Consortium, Nov 15 2018, In : Cancer Research. 78, 22, p. 6523-6524 2 p.

Research output: Contribution to journalLetter

1 Scopus citations
Editorial

Assessing the genetic risk for alcohol use disorders

Foroud, T. & Phillips, T. J., 2012, In : Alcohol research : current reviews. 34, 3, p. 266-272 7 p.

Research output: Contribution to journalEditorial

2 Scopus citations

Editorial: The genetics of absorptive hypercalciuria - A note of caution

Econs, M. J. & Foroud, T., Jun 20 2002, In : Journal of Clinical Endocrinology and Metabolism. 87, 4, p. 1473-1475 3 p.

Research output: Contribution to journalEditorial

6 Scopus citations

Genetics and genomics of late-onset Alzheimer's disease and its endophenotypes

Reitz, C., Rogaeva, E., Foroud, T. & Farrer, L. A., 2011, In : International Journal of Alzheimer's Disease. 284728.

Research output: Contribution to journalEditorial

4 Scopus citations

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

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

Research output: Contribution to journalEditorial

13 Scopus citations

Using global team science to identify genetic parkinson's disease worldwide

MJFF Global Genetic Parkinson's Disease Study Group, Aug 2019, In : Annals of neurology. 86, 2, p. 153-157 5 p.

Research output: Contribution to journalEditorial

4 Scopus citations
Conference contribution

A framework for 3D analysis of facial morphology in fetal alcohol syndrome

Wan, J., Shen, L., Fang, S., McLaughlin, J., Autti-Rämö, I., Fagerlund, Å., Riley, E., Hoyme, H. E., Moore, E. S. & Foroud, T., Nov 9 2010, Medical Imaging and Augmented Reality - 5th International Workshop, MIAR 2010, Proceedings. p. 118-127 10 p. (Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics); vol. 6326 LNCS).

Research output: Chapter in Book/Report/Conference proceedingConference contribution

5 Scopus citations

A multinational deployment of 3D laser scanning to study craniofacial dysmorphology in fetal alcohol spectrum disorders

Rogers, J., Wernert, E., Moore, E., Ward, R., Wetherill, L. F. & Foroud, T., Jan 1 2007, Proceedings of SPIE-IS and T Electronic Imaging - Videometrics IX. SPIE, 64910I. (Proceedings of SPIE - The International Society for Optical Engineering; vol. 6491).

Research output: Chapter in Book/Report/Conference proceedingConference contribution

Implementation of a distributed architecture for managing collection and dissemination of data for fetal alcohol spectrum disorders research

Arenson, A., Bakhireva, L., Chambers, T., Deximo, C., Foroud, T., Jacobson, J., Jacobson, S., Jones, K. L., Mattson, S., May, P., Moore, E., Ogle, K., Riley, E., Robinson, L., Rogers, J., Streissguth, A., Tavares, M., Urbanski, J., Yezerets, H. & Stewart, C. A., 2007, Distributed, High-Performance and Grid Computing in Computational Biology International Workshop, GCCB 2006, Proceedings. Springer Verlag, p. 33-44 12 p. (Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics); vol. 4360 LNBI).

Research output: Chapter in Book/Report/Conference proceedingConference contribution

Interactive feature visualization and detection for 3D face classification

McLaughlin, J., Fang, S., Huang, J., Jacobson, S., Hoyme, H. E., Robinson, L. & Foroud, T., Dec 13 2010, Proceedings of the 9th IEEE International Conference on Cognitive Informatics, ICCI 2010. p. 160-167 8 p. 5599748. (Proceedings of the 9th IEEE International Conference on Cognitive Informatics, ICCI 2010).

Research output: Chapter in Book/Report/Conference proceedingConference contribution

Comment/debate

Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing (Nature Genetics, (2019), 51, 3, (414-430), 10.1038/s41588-019-0358-2)

Alzheimer Disease Genetics Consortium (ADGC), The European Alzheimer’s Disease Initiative (EADI), Cohorts for Heart and Aging Research in Genomic Epidemiology Consortium (CHARGE) & Genetic and Environmental Risk in AD/Defining Genetic, Polygenic and Environmental Risk for Alzheimer’s Disease Consortium (GERAD/PERADES), Sep 1 2019, In : Nature genetics. 51, 9, p. 1423-1424 2 p.

Research output: Contribution to journalComment/debate

Open Access
2 Scopus citations

Author Correction: Multimodal hippocampal subfield grading for Alzheimer’s disease classification (Scientific Reports, (2019), 9, 1, (13845), 10.1038/s41598-019-49970-9)

Alzheimer’s Disease Neuroimaging Initiative, Dec 1 2020, In : Scientific reports. 10, 1, 10969.

Research output: Contribution to journalComment/debate

Open Access

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. J., 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 journalComment/debate

Correction: Genetic risk for schizophrenia and psychosis in Alzheimer disease (Molecular Psychiatry, (2018), 23, 4, (963-972), 10.1038/mp.2017.81)

DeMichele-Sweet, M. A. A., Weamer, E. A., Klei, L., Vrana, D. T., Hollingshead, D. J., Seltman, H. J., Sims, R., Foroud, T., Hernandez, I., Moreno-Grau, S., Tárraga, L., Boada, M., Ruiz, A., Williams, J., Mayeux, R., Lopez, O. L., Sibille, E. L., Kamboh, M. I., Devlin, B. & Sweet, R. A., Jan 1 2019, In : Molecular Psychiatry.

Research output: Contribution to journalComment/debate

Open Access

Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer’s disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (Acta Neuropathologica, (2019), 138, 2, (237-250), 10.1007/s00401-019-02026-8)

EADB (Alzheimer Disease European DNA biobank), IFGC (International FTD-Genomics Consortium), IPDGC (The International Parkinson Disease Genomics Consortium), RiMod-FTD (Risk and Modifying factors in Fronto-Temporal Dementia), Netherlands Brain Bank (NBB), The GIFT (Genetic Investigation in Frontotemporal Dementia and Alzheimer’s Disease) Study Group & DESGESCO (Dementia Genetics Spanish Consortium), May 1 2020, In : Acta Neuropathologica. 139, 5, p. 959-962 4 p.

Research output: Contribution to journalComment/debate

Open Access

Erratum: Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus (Journal of Clinical Endocrinology and Metabolism 84 (4467-4471))

Takacs, I., Koller, D. L., Peacock, M., Christian, J. C., Hui, S. L., Conneally, P. M., Johnston, C. C., Foroud, T. & Econs, M. J., Dec 1 2000, In : Journal of Clinical Endocrinology and Metabolism. 85, 1, 1 p.

Research output: Contribution to journalComment/debate

Erratum to: Genome-wide association study identifies loci associated with liability to alcohol and drug dependence that is associated with variability in reward-related ventral striatum activity in African- and European-Americans (Genes, Brain and Behavior, (e12580), 10.1111/gbb.12580)

Wetherill, L., Lai, D., Johnson, E. C., Anokhin, A., Bauer, L., Bucholz, K. K., Dick, D. M., Hariri, A. R., Hesselbrock, V., Kamarajan, C., Kramer, J., Kuperman, S., Meyers, J. L., Nurnberger, J. I., Schuckit, M., Scott, D. M., Taylor, R. E., Tischfield, J., Porjesz, B., Goate, A. M. & 4 others, Edenberg, H. J., Foroud, T., Bogdan, R. & Agrawal, A., Nov 1 2019, In : Genes, Brain and Behavior. 18, 8, e12608.

Research output: Contribution to journalComment/debate

Open Access

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption (Proceedings of the National Academy Sciences of the United States of America (2011) 108, 17, (7119-7124))

Schumann, G., Coin, L. J., Lourdusamy, A., Charoen, P., Berger, K. H., Stacey, D., Desrivières, S., Aliev, F. A., Khan, A. A., Amin, N., Aulchenko, Y. S., Bakalkin, G., Bakker, S. J., Balkau, B., Beulens, J. W., Bilbao, A., De Boer, R. A., Beury, D., Bots, M. L., Breetvelt, E. J. & 96 others, Cauchi, S., Cavalcanti-Proença, C., Chambers, J. C., Clarke, T. K., Dahmen, N., De Geus, E. J., Dick, D., Ducci, F., Easton, A., Edenberg, H. J., Esk, T., Fernández-Medarde, A., Foroud, T., Freimer, N. B., Girault, J. A., Grobbee, D. E., Guarrera, S., Gudbjartsson, D. F., Hartikainen, A. L., Heath, A. C., Hesselbrock, V., Hofman, A., Hottenga, J. J., Isohanni, M. K., Kaprio, J., Khaw, K. T., Kuehnel, B., Laitinen, J., Lobbens, S., Luan, J., Mangino, M., Maroteaux, M., Matullo, G., McCarthy, M. I., Mueller, C., Navis, G., Numans, M. E., Núñez, A., Nyholt, D. R., Onland-Moret, C. N., Oostra, B. A., O'Reilly, P. F., Palkovits, M., Penninx, B. W., Polidoro, S., Pouta, A., Prokopenko, I., Ricceri, F., Santos, E., Smit, J. H., Soranzo, N., Song, K., Sovio, U., Stumvoll, M., Surakk, I., Thorgeirsson, T. E., Thorsteinsdottir, U., Troakes, C., Tyrfingsson, T., Tönjes, A., Uiterwaal, C. S., Uitterlinden, A. G., Van Der Harst, P., Van Der Schouw, Y. T., Staehlin, O., Vogelzangs, N., Vollenweider, P., Waeber, G., Wareham, N. J., Waterworth, D. M., Whitfield, J. B., Wichmann, E. H., Willemsen, G., Witteman, J. C., Yuan, X., Zhai, G., Zhao, J. H., Zhang, W., Martin, N. G., Metspalu, A., Doering, A., Scott, J., Spector, T. D., Loos, R. J., Boomsma, D. I., Mooser, V., Peltonen, L., Stefansson, K., Van Duijn, C. M., Vineis, P., Sommer, W. H., Kooner, J. S., Spanagel, R., Heberlein, U. A., Jarvelin, M. R. & Elliott, P., May 31 2011, In : Proceedings of the National Academy of Sciences of the United States of America. 108, 22, p. 9316 1 p.

Research output: Contribution to journalComment/debate

3 Scopus citations

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

Nho, K., Corneveaux, J. J., Kim, S., Lin, H., Risacher, S. L., Shen, L., Swaminathan, S., Ramanan, V. K., Liu, Y., Foroud, T., Inlow, M. H., Siniard, A. L., Reiman, R. A., Aisen, P. S., Petersen, R. C., Green, R. C., Jack, C. R., Weiner, M. W., Baldwin, C. T., Lunetta, K. & 14 others, Farrer, L. A., Furney, S. J., Lovestone, S., Simmons, A., Mecocci, P., Vellas, B., Tsolaki, M., Kloszewska, I., Soininen, H., McDonald, B. C., Farlow, M. R., Ghetti, B., Huentelman, M. J. & Saykin, A. J., Jul 2013, In : Molecular Psychiatry. 18, 7, p. 739 1 p.

Research output: Contribution to journalComment/debate

7 Scopus citations

Predictive accuracy of serial transvaginal cervical lengths and quantitative vaginal fetal fibronectin levels for spontaneous preterm birth among nulliparous women

Sean Esplin, M., Elovitz, M. A., Iams, J. D., Parker, C. B., Wapner, R. J., Grobman, W. A., Simhan, H. N., Wing, D. A., Haas, D. M., Silver, R. M., Hoffman, M. K., Peaceman, A. M., Caritis, S. N., Parry, S., Wadhwa, P., Foroud, T., Mercer, B. M., Hunter, S. M., Saade, G. R. & Reddy, U. M., Jan 1 2017, In : Obstetrical and Gynecological Survey. 72, 7, p. 397-399 3 p.

Research output: Contribution to journalComment/debate

Response

Brown, R. D., Huston, J., Hornung, R., Foroud, T., Kallmes, D. F., Kleindorfer, D., Meissner, I., Woo, D., Sauerbeck, L. & Broderick, J., Jun 1 2008, In : Journal of neurosurgery. 108, 6, 1 p.

Research output: Contribution to journalComment/debate

4 Scopus citations
Chapter

Complex Genetics of Alcoholism

Edenberg, H. J. & Foroud, T., Feb 2014, Neurobiology of Alcohol Dependence. Elsevier Inc., p. 539-550 12 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

3 Scopus citations

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

Alzheimer’s Disease Neuroimaging Initiative (ADNI), Jan 1 2015, Handbook of Depression in Alzheimer's Disease. IOS Press, p. 313-322 10 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Comprehensive Gene- and Pathway-Based Analysis of Depressive Symptoms in Older Adults

Nho, K., Ramanan, V. K., Horgusluoglu, E., Kim, S., Inlow, M. H., Risacher, S. L., McDonald, B. C., Farlow, M. R., Foroud, T. M., Gao, S., Callahan, C. M., Hendrie, H. C., Niculescu, A. B. & Saykin, A. J., Jan 1 2015, Handbook of Depression in Alzheimer's Disease. Smith, G. S. (ed.). IOS Press, p. 313-322 10 p. (Advances in Alzheimer's Disease; vol. 4).

Research output: Chapter in Book/Report/Conference proceedingChapter

1 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