Home > People > U-M Researchers . Off-Campus . Training . Postdocs . Predocs . Staff . Experts . Disciplines

PSC In The News

RSS Feed icon

Savolainen links antisocial behavior in childhood to disadvantage and poverty in adulthood

Norton et al. put dollar value on relief from chronic pain for Americans age 50+

Seefeldt says TANF restrictions may limit program's help for poor Americans

More News

Highlights

Paula Fomby to succeed Jennifer Barber as Associate Director of PSC

PSC community celebrates Violet Elder's retirement from PSC

Neal Krause wins GSA's Robert Kleemeier Award

U-M awarded $58 million to develop ideas for preventing and treating health problems

More Highlights

Jessica Faul

Research Affiliate, Population Studies Center.

Associate Research Scientist, Survey Research Center, Institute for Social Research.

Ph.D., University of Michigan

Dr. Faul's work focuses on socioeconomic predictors of health and health disparities across the life course. Her research integrates genetic and social science data and uses longitudinal modeling and time-varying predictors in examining determinants of health.

Select Publications

Journal Articles

Direk, Nese, Stephanie Williams, Jennifer A. Smith, Stephan Ripke, Tracy Air, Azmeraw T. Amare, Najaf Amin, Bernhard T. Baune, David A. Bennett, Douglas H. R. Blackwood, Dorret Boomsma, Gerome Breen, Henriette N. Buttenschøn, Enda M. Byrne, Anders D. Børglum, Enrique Castelao, Sven Cichon, Toni-Kim Clarke, Marilyn C. Cornelis, Udo Dannlowski, Philip L. De Jager, Ayse Demirkan, Enrico Domenici, Cornelia M. van Duijn, Erin C. Dunn, Johan G. Eriksson, Tonu Esko, Jessica Faul, Luigi Ferrucci, Myriam Fornage, Eco de Geus, Michael Gill, Scott D. Gordon, Hans Jörgen Grabe, Gerard van Grootheest, Steven P. Hamilton, Catharina A. Hartman, Andrew C. Heath, Karin Hek, Albert Hofman, Georg Homuth, Carsten Horn, Jouke Jan Hottenga, Sharon L. R. Kardia, Stefan Kloiber, Karestan Koenen, Zoltán Kutalik, Karl-Heinz Ladwig, Jari Lahti, Douglas F. Levinson, Cathryn M. Lewis, Glyn Lewis, Qingqin S. Li, David J. Llewellyn, Susanne Lucae, Kathryn L. Lunetta, Donald J. MacIntyre, Pamela Madden, Nicholas G. Martin, Andrew M. McIntosh, Andres Metspalu, Yuri Milaneschi, Grant W. Montgomery, Ole Mors, Thomas H. Mosley Jr, Joanne M. Murabito, Bertram Müller-Myhsok, Markus M. Nöthen, Dale R. Nyholt, Michael C. O'Donovan, Brenda W. Penninx, Michele L. Pergadia, Roy Perlis, James B. Potash, Martin Preisig, Shaun M. Purcell, Jorge A. Quiroz, Katri Räikkönen, John P. Rice, Marcella Rietschel, Margarita Rivera, Thomas G. Schulze, Jianxin Shi, Stanley Shyn, Grant C. Sinnamon, Johannes H. Smit, Jordan W. Smoller, Harold Snieder, Toshiko Tanaka, Katherine E. Tansey, Alexander Teumer, Rudolf Uher, Daniel Umbricht, Sandra Van der Auwera, Erin Bakshis Ware, David Weir, Myrna M. Weissman, Gonneke Willemsen, Jingyun Yang, and Wei Zhao, et al. Forthcoming. "An Analysis of Two Genome-Wide Association Meta-Analyses Identifies a New Locus for Broad Depression Phenotype." Biological psychiatry. DOI. Abstract.

Barban, Nicola, Rick Jansen, Jessica Faul, and David Weir, et al. Forthcoming. "Genome-wide analysis identifies 12 loci influencing human reproductive behavior." Nature Genetics. DOI. Abstract.

Ben-Avraham, Dan, David Karasik, Joe Verghese, Kathryn L. Lunetta, Jennifer A. Smith, John D. Eicher, Rotem Vered, Joris Deelen, Alice M. Arnold, Aron S. Buchman, Toshiko Tanaka, Jessica Faul, Maria Nethander, Myriam Fornage, Hieab H. Adams, Amy M. Matteini, Michele L. Callisaya, Albert V. Smith, Lei Yu, Philip L. De Jager, Denis A. Evans, Vilmundur Gudnason, Albert Hofman, Alison Pattie, Janie Corley, Lenore J. Launer, Davis S. Knopman, Neeta Parimi, Stephen T. Turner, Stefania Bandinelli, Marian Beekman, Danielle Gutman, Lital Sharvit, Simon P. Mooijaart, David C. Liewald, Jeanine J. Houwing-Duistermaat, Claes Ohlsson, Matthijs Moed, Vincent J. Verlinden, Dan Mellstrom, Jos N. van der Geest, Magnus Karlsson, Dena Hernandez, Rebekah McWhirter, Yongmei Liu, Russell Thomson, Gregory J. Tranah, Andre G. Uitterlinden, David Weir, Wei Zhao, John M. Starr, Andrew D. Johnson, M. Arfan Ikram, David A. Bennett, Steven R. Cummings, Ian J. Deary, Tamara B. Harris, Sharon L. R. Kardia, Thomas H. Mosley, Velandai K. Srikanth, Beverly G. Windham, Ann B. Newman, Jeremy D. Walston, Gail Davies, Daniel S. Evans, Eline P. Slagboom, Luigi Ferrucci, Douglas P. Kiel, Joanne M. Murabito, and Gil Atzmon. 2017. "The complex genetics of gait speed: genome-wide meta-analysis approach." Aging, 9(1): 209-246. DOI. Abstract.

Li, M., Y. Li, O. Weeks, V. Mijatovic, A. Teumer, J.E. Huffman, G. Tromp, C. Fuchsberger, M. Gorski, L.P. Lyytikainen, T. Nutile, S. Sedaghat, R. Sorice, A. Tin, Q. Yang, T.S. Ahluwalia, D.E. Arking, N.A. Bihlmeyer, C.A. Boger, R.J. Carroll, D.I. Chasman, M.C. Cornelis, A. Dehghan, Jessica Faul, M.F. Feitosa, G. Gambaro, P. Gasparini, F. Giulianini, I. Heid, J. Huang, M. Imboden, A.U. Jackson, J. Jeff, M.A. Jhun, R. Katz, A. Kifley, T.O. Kilpelainen, A. Kumar, M. Laakso, R. Li-Gao, K. Lohman, Y. Lu, R. Magi, G. Malerba, E. Mihailov, K.L. Mohlke, D.O. Mook-Kanamori, A. Robino, D. Ruderfer, E. Salvi, U.M. Schick, C.A. Schulz, A.V. Smith, Jennifer A. Smith, M. Traglia, L.M. Yerges-Armstrong, W. Zhao, M.O. Goodarzi, A.T. Kraja, C. Liu, J. Wessel, E. Boerwinkle, I.B. Borecki, J. Bork-Jensen, E.P. Bottinger, D. Braga, I. Brandslund, J.A. Brody, A. Campbell, D.J. Carey, C. Christensen, J. Coresh, E. Crook, G.C. Curhan, D. Cusi, I.H. de Boer, A.P. de Vries, J.C. Denny, O. Devuyst, A.W. Dreisbach, K. Endlich, T. Esko, O.H. Franco, T. Fulop, G.S. Gerhard, C. Glumer, O. Gottesman, N. Grarup, V. Gudnason, T.B. Harris, C. Hayward, L. Hocking, A. Hofman, F.B. Hu, L.L. Husemoen, R.D. Jackson, T. Jorgensen, and M.E. Jorgensen, et al. 2017. "SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function." Journal of the American Society of Nephrology : JASN, 28(3): 981-994. DOI. Abstract.

Marouli, Eirini, Mariaelisa Graff, Carolina Medina-Gomez, Ken Sin Lo, Andrew R. Wood, Troels R. Kjaer, Rebecca S. Fine, Yingchang Lu, Claudia Schurmann, Heather M. Highland, Sina Rüeger, Gudmar Thorleifsson, Anne E. Justice, David Lamparter, Kathleen E. Stirrups, Valerie Turcot, Kristin L. Young, Thomas W. Winkler, Tõ Esko, Tugce Karaderi, Adam E. Locke, Nicholas G. D. Masca, Maggie C. Y. Ng, Poorva Mudgal, Manuel A. Rivas, Sailaja Vedantam, Anubha Mahajan, Xiuqing Guo, Goncalo Abecasis, Katja K. Aben, Linda S. Adair, Dewan S. Alam, Eva Albrecht, Kristine H. Allin, Matthew Allison, Philippe Amouyel, Emil V. Appel, Dominique Arveiler, Folkert W. Asselbergs, Paul L. Auer, Beverley Balkau, Bernhard Banas, Lia E. Bang, Marianne Benn, Sven Bergmann, Lawrence F. Bielak, Matthias Blüher, Heiner Boeing, Eric Boerwinkle, Carsten A. Böger, Lori L. Bonnycastle, Jette Bork-Jensen, Michiel L. Bots, Erwin P. Bottinger, Donald W. Bowden, Ivan Brandslund, Gerome Breen, Murray H. Brilliant, Linda Broer, Amber A. Burt, Adam S. Butterworth, David J. Carey, Mark J. Caulfield, John C. Chambers, Daniel I. Chasman, Yii-Der Ida Chen, Rajiv Chowdhury, Cramer Christensen, Audrey Y. Chu, Massimiliano Cocca, Francis S. Collins, James P. Cook, Janie Corley, Jordi Corominas Galbany, Amanda J. Cox, Gabriel Cuellar-Partida, John Danesh, Gail Davies, Paul I. W. de Bakker, Gert J. de Borst, Simon de Denus, Mark C. H. de Groot, Renée de Mutsert, Ian J. Deary, George Dedoussis, Ellen W. Demerath, Anneke I. den Hollander, Joe G. Dennis, Emanuele Di Angelantonio, Fotios Drenos, Mengmeng Du, Alison M. Dunning, Douglas F. Easton, Tapani Ebeling, Todd L. Edwards, Patrick T. Ellinor, Paul Elliott, Evangelos Evangelou, Aliki-Eleni Farmaki, and Jessica Faul, et al. 2017. "Rare and low-frequency coding variants alter human adult height." Nature, 542(7640): 186-190. DOI. Abstract.

Langa, Kenneth M., Eric Larson, Eileen Crimmins, Jessica Faul, Deborah Levine, Mohammed Kabeto, and David Weir. 2017. "A Comparison of the Prevalence of Dementia in the United States in 2000 and 2012." JAMA Internal Medicine, 177(1): 51-58. DOI. Abstract.

Okbay, A., B. Baselmans, J. De Neve, P. Turley, M. Nivard, M. Fontana, S. Meddens, R. Linnér, C. Rietveld, J. Derringer, and Jessica Faul, et al. 2016. "Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses." Nature Genetics, 48(6): 624-633. PMCID: PMC4884152. DOI. Abstract.

View additional select publications of Jessica Faul