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Creswell, Paul, Lauren Wisk, Kristin Litzelman, Adelyn Allchin, and Whitney Witt. 2014. “Parental Depressive Symptoms and Childhood Cancer: The Importance of Financial Difficulties.”. Support Care Cancer 22 (2): 503-11.

Witt, Whitney, Lauren Wisk, Erika Cheng, John Hampton, and Erika Hagen. 2012. “Preconception Mental Health Predicts Pregnancy Complications and Adverse Birth Outcomes: A National Population-Based Study.”. Matern Child Health J 16 (7): 1525-41.

Witt, Whitney, Lauren Wisk, Erika Cheng, John Hampton, Paul Creswell, Erika Hagen, Hilary Spear, Torsheika Maddox, and Thomas DeLeire. 2011. “Poor Prepregnancy and Antepartum Mental Health Predicts Postpartum Mental Health Problems Among US Women: A Nationally Representative Population-Based Study.”. Womens Health Issues 21 (4): 304-13.

Amstutz, Harlan, Michel Le Duff, Patricia Campbell, Thomas Gruen, and Lauren Wisk. 2010. “Clinical and Radiographic Results of Metal-on-Metal Hip Resurfacing With a Minimum Ten-Year Follow-Up.”. J Bone Joint Surg Am 92 (16): 2663-71.

Kurugol, Sila, Moti Freiman, Liran Domachevsky, Onur Afacan, and Simon Warfield. 2015. “Quantitative Diffusion-Weighted MR Imaging of Crohn’s Disease Using a Spatially-Constrained Probability Distribution Model of Incoherent Motion (SPIM)”. ISMRM Diffusion Weighted Imaging Outside Brain Workshop, Boston, MA. April 2015.

Manzini, Chiara, Dimira Tambunan, Sean Hill, Tim Yu, Thomas Maynard, Erin Heinzen, Kevin Shianna, et al. 2012. “Exome Sequencing and Functional Validation in Zebrafish Identify GTDC2 Mutations As a Cause of Walker-Warburg Syndrome.”. Am J Hum Genet 91 (3): 541-7.

Brownstein, Catherine, Alan Beggs, Nils Homer, Barry Merriman, Timothy Yu, Katherine Flannery, Elizabeth Dechene, et al. 2014. “An International Effort towards Developing Standards for Best Practices in Analysis, Interpretation and Reporting of Clinical Genome Sequencing Results in the CLARITY Challenge.”. Genome Biol 15 (3): R53.

Chaste, Pauline, Lambertus Klei, Stephan Sanders, Vanessa Hus, Michael Murtha, Jennifer Lowe, Jeremy Willsey, et al. 2015. “A Genome-Wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?”. Biol Psychiatry 77 (9): 775-84.

Maier, Robert, Gerhard Moser, Guo-Bo Chen, Stephan Ripke, Cross-Disorder Working Group of the Psychiatric Genomics Consortium, William Coryell, James Potash, et al. 2015. “Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder.”. Am J Hum Genet 96 (2): 283-94.

Chao, Yu, Fujisawa, Culotti, Gengyo-Ando, Mitani, Moulder, Barstead, Tessier-Lavigne, and Bargmann. 2001. “C. Elegans Slit Acts in Midline, Dorsal-Ventral, and Anterior-Posterior Guidance via the SAX-3/Robo Receptor.”. Neuron 32 (1): 25-38.