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Rossi, Andrea, Marco Gnesi, Cristina Montomoli, Gaetano Chirico, Laura Malerba, Lotfi Merabet, NAVEG Study Group, and Elisa Fazzi. 2017. “Neonatal Assessment Visual European Grid (NAVEG): Unveiling Neurological Risk”. Infant Behav Dev 49: 21-30.

Wang, Yvonne, Frederick Jakobiec, Fouad Zakka, and Nahyoung Grace Lee. 2017. “A Lacrimal Gland Choristoma of the Lacrimal Sac”. Ophthal Plast Reconstr Surg.

Das, Sayantan, Lukas Forer, Sebastian Schönherr, Carlo Sidore, Adam Locke, Alan Kwong, Scott Vrieze, et al. 2016. “Next-Generation Genotype Imputation Service and Methods”. Nat Genet 48 (10): 1284-87.

Lipson, Mark, Po-Ru Loh, Sriram Sankararaman, Nick Patterson, Bonnie Berger, and David Reich. 2015. “Calibrating the Human Mutation Rate via Ancestral Recombination Density in Diploid Genomes”. PLoS Genet 11 (11): e1005550.

Pickrell, Joseph, Nick Patterson, Chiara Barbieri, Falko Berthold, Linda Gerlach, Tom Güldemann, Blesswell Kure, et al. 2012. “The Genetic Prehistory of Southern Africa”. Nat Commun 3: 1143.

Sümbül, Uygar, Aleksandar Zlateski, Ashwin Vishwanathan, Richard Masland, and Sebastian Seung. 2014. “Automated Computation of Arbor Densities: A Step Toward Identifying Neuronal Cell Types”. Front Neuroanat 8: 139.

Lipson, Mark*, Po-Ru* Loh, Alex Levin, David Reich, Nick Patterson, and Bonnie Berger. 2013. “Efficient Moment-Based Inference of Admixture Parameters and Sources of Gene Flow”. Mol Biol Evol 30 (8): 1788-802.

Bulik-Sullivan, Brendan, Hilary Finucane, Verneri Anttila, Alexander Gusev, Felix Day, Po-Ru Loh, Laramie Duncan, et al. 2015. “An Atlas of Genetic Correlations across Human Diseases and Traits”. Nat Genet 47 (11): 1236-41.

Bulik-Sullivan, Brendan, Po-Ru Loh, Hilary Finucane, Stephan Ripke, Jian Yang, Nick Patterson, Mark Daly, Alkes Price, and Benjamin Neale. 2015. “LD Score Regression Distinguishes Confounding from Polygenicity in Genome-Wide Association Studies”. Nat Genet 47 (3): 291-5.

Dagi, Linda, Laura Tiedemann, Gena Heidary, Caroline Robson, Amber Hall, and David Zurakowski. 2014. “Using Spectral-Domain Optical Coherence Tomography to Detect Optic Neuropathy in Patients With Craniosynostosis.”. J AAPOS 18 (6): 543-9.