Deterministic generation of a cluster state of entangled photons von Schwartz, I., Cogan, D., Schmidgall, E. R., Don, Y., Gantz, L., Kenneth, O., Lindner, N. H., Gershoni, D.

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HACER: an atlas of human active enhancers to interpret regulatory variants von Wang, Jing, Dai, Xizhen, Berry, Lynne D, Cogan, Joy D, Liu, Qi, Shyr, Yu

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Lessons learned: next-generation sequencing applied to undiagnosed genetic diseases von Schuler, Bryce A, Nelson, Erica T, Koziura, Mary, Cogan, Joy D, Hamid, Rizwan, Phillips, 3rd, John A

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

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Extensive phenotyping of individuals at risk for familial interstitial pneumonia reveals clues to the pathogenesis of interstitial lung disease von Kropski, Jonathan A, Pritchett, Jason M, Zoz, Donald F, Crossno, Peter F, Markin, Cheryl, Garnett, Errine T, Degryse, Amber L, Mitchell, Daphne B, Polosukhin, Vasiliy V, Rickman, Otis B, Choi, Leena, Cheng, Dong-Sheng, McConaha, Melinda E, Jones, Brittany R, Gleaves, Linda A, McMahon, Frank B, Worrell, John A, Solus, Joseph F, Ware, Lorraine B, Lee, Jae Woo, Massion, Pierre P, Zaynagetdinov, Rinat, White, Eric S, Kurtis, Jonathan D, Johnson, Joyce E, Groshong, Steve D, Lancaster, Lisa H, Young, Lisa R, Steele, Mark P, Phillips Iii, John A, Cogan, Joy D, Loyd, James E, Lawson, William E, Blackwell, Timothy S

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Short telomeres are a risk factor for idiopathic pulmonary fibrosis von Alder, Jonathan K, Chen, Julian J.-L, Lancaster, Lisa, Danoff, Sonye, Su, Shu-chih, Cogan, Joy D, Vulto, Irma, Xie, Mingyi, Qi, Xiaodong, Tuder, Rubin M, Phillips, John A. III, Lansdorp, Peter M, Loyd, James E, Armanios, Mary Y

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A review of multiple diagnostic approaches in the undiagnosed diseases network to identify inherited metabolic diseases von Furuta, Yutaka, Tinker, Rory J, Hamid, Rizwan, Cogan, Joy D, Ezell, Kimberly M, Oglesbee, Devin, DeBerardinis, Ralph J, Phillips, 3rd, John A

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Alterations in oestrogen metabolism: implications for higher penetrance of familial pulmonary arterial hypertension in females von Austin, E. D, Cogan, J. D, West, J. D, Hedges, L. K, Hamid, R, Dawson, E. P, Wheeler, L. A, Parl, F. F, Loyd, J. E, Phillips, J. A., III

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A Novel Dyskerin ( DKC1 ) Mutation Is Associated With Familial Interstitial Pneumonia von Kropski, Jonathan A., MD, Mitchell, Daphne B., MS, Markin, Cheryl, BS, Polosukhin, Vasiliy V., MD, Choi, Leena, PhD, Johnson, Joyce E., MD, Lawson, William E., MD, Phillips, John A., MD, Cogan, Joy D., PhD, Blackwell, Timothy S., MD, Loyd, James E., MD

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Telomerase Mutations in Families with Idiopathic Pulmonary Fibrosis von Armanios, Mary Y, Chen, Julian J.-L, Cogan, Joy D, Alder, Jonathan K, Ingersoll, Roxann G, Markin, Cheryl, Lawson, William E, Xie, Mingyi, Vulto, Irma, Phillips, John A, Lansdorp, Peter M, Greider, Carol W, Loyd, James E

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TBX4 Transcription Factor Is a Positive Feedback Regulator of Itself and Phospho-SMAD1/5 von Cai, Ying, Yan, Ling, Kielt, Matthew J, Cogan, Joy D, Hedges, Lora K, Nunley, Bethany, West, James, Austin, Eric D, Hamid, Rizwan

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Ancestral mutation in telomerase causes defects in repeat addition processivity and manifests as familial pulmonary fibrosis von Alder, Jonathan K, Cogan, Joy D, Brown, Andrew F, Anderson, Collin J, Lawson, William E, Lansdorp, Peter M, Phillips, 3rd, John A, Loyd, James E, Chen, Julian J-L, Armanios, Mary

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All-optical depletion of dark excitons from a semiconductor quantum dot von Schmidgall, E. R., Schwartz, I., Cogan, D., Gantz, L., Heindel, T., Reitzenstein, S., Gershoni, D.

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Truncating and missense BMPR2 mutations differentially affect the severity of heritable pulmonary arterial hypertension von Austin, Eric D, Phillips, John A, Cogan, Joy D, Hamid, Rizwan, Yu, Chang, Stanton, Krista C, Phillips, Charles A, Wheeler, Lisa A, Robbins, Ivan M, Newman, John H, Loyd, James E

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High Frequency of BMPR2 Exonic Deletions/Duplications in Familial Pulmonary Arterial Hypertension von Cogan, Joy D, Pauciulo, Michael W, Batchman, Amy P, Prince, Melissa A, Robbins, Ivan M, Hedges, Lora K, Stanton, Krista C, Wheeler, Lisa A, Phillips, John A., III, Loyd, James E, Nichols, William C

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Review and metabolomic profiling of unsolved case reveals newly reported autosomal dominant congenital disorder of glycosylation, type Iw formerly thought to only be an autosomal r... von Ezell, Kimberly M., Furuta, Yutaka, Oglesbee, Devin, Pivnick, Eniko K., Rinker, David, Sheehan, Jonathan H., Tinker, Rory J., Hamid, Rizwan, Cogan, Joy D., Rives, Lynette, Neumann, Serena, Corner, Brian, Koziura, Mary, Phillips, John A.

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On-demand source of maximally entangled photon pairs using the biexciton-exciton radiative cascade von Winik, R., Cogan, D., Don, Y., Schwartz, I., Gantz, L., Schmidgall, E. R., Livneh, N., Rapaport, R., Buks, E., Gershoni, D.

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Coaching Olympic Athletes with Sport Psychology von Cogan, Karen D.

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Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis von Fingerlin, Tasha E, Murphy, Elissa, Zhang, Weiming, Peljto, Anna L, Brown, Kevin K, Steele, Mark P, Loyd, James E, Cosgrove, Gregory P, Lynch, David, Groshong, Steve, Collard, Harold R, Wolters, Paul J, Bradford, Williamson Z, Kossen, Karl, Seiwert, Scott D, du Bois, Roland M, Garcia, Christine Kim, Devine, Megan S, Gudmundsson, Gunnar, Isaksson, Helgi J, Kaminski, Naftali, Zhang, Yingze, Gibson, Kevin F, Lancaster, Lisa H, Cogan, Joy D, Mason, Wendi R, Maher, Toby M, Molyneaux, Philip L, Wells, Athol U, Moffatt, Miriam F, Selman, Moises, Pardo, Annie, Kim, Dong Soon, Crapo, James D, Make, Barry J, Regan, Elizabeth A, Walek, Dinesha S, Daniel, Jerry J, Kamatani, Yoichiro, Zelenika, Diana, Smith, Keith, McKean, David, Pedersen, Brent S, Talbert, Janet, Kidd, Raven N, Markin, Cheryl R, Beckman, Kenneth B, Lathrop, Mark, Schwarz, Marvin I, Schwartz, David A

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Mutations in PROP1 cause familial combined pituitary hormone deficiency von Wu, Wei, Cogan, Joy D., Pfäffle, Roland W., Dasen, Jeremy S., Frisch, Herwig, O'Connell, Shawn M., Flynn, Sarah E., Brown, Milton R., Mullis, Primus E., Parks, John S., Phillips III, John A., Rosenfeld, Michael G.

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