Lessons learned: next-generation sequencing applied to undiagnosed genetic diseases by Bryce A. Schuler, Erica T. Nelson, Mary Koziura, Joy D. Cogan, Rizwan Hamid, John A. Phillips III

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Deterministic Writing and Control of the Dark Exciton Spin Using Single Short Optical Pulses by I. Schwartz, E. R. Schmidgall, L. Gantz, D. Cogan, E. Bordo, Y. Don, M. Zielinski, D. Gershoni

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Clinical and molecuar characterization of Brazilian patients with growth hormone gene deletions by I.J.P. Arnhold, M.G.F. Osorio, S.B. Oliveira, V. Estefan, T. Kamijo, M.R.S. Krishnamani, J.D. Cogan, J.A. Phillips III, B.B. Mendonça

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Low-grade albuminuria in pulmonary arterial hypertension by Nils P. Nickel, Vinicio A. de Jesus Perez, Roham T. Zamanian, Joshua P. Fessel, Joy D. Cogan, Rizwam Hamid, James D. West, Mark P. de Caestecker, Haichun Yang, Eric D. Austin

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Ancestral mutation in telomerase causes defects in repeat addition processivity and manifests as familial pulmonary fibrosis. by Jonathan K Alder, Joy D Cogan, Andrew F Brown, Collin J Anderson, William E Lawson, Peter M Lansdorp, John A Phillips, James E Loyd, Julian J-L Chen, Mary Armanios

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Personalized structural biology reveals the molecular mechanisms underlying heterogeneous epileptic phenotypes caused by de novo KCNC2 variants by Souhrid Mukherjee, Thomas A. Cassini, Ningning Hu, Tao Yang, Bian Li, Wangzhen Shen, Christopher W. Moth, David C. Rinker, Jonathan H. Sheehan, Joy D. Cogan, John H. Newman, Rizwan Hamid, Robert L. Macdonald, Dan M. Roden, Jens Meiler, Georg Kuenze, John A. Phillips, John A. Capra

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