Quantifying the polygenic contribution to variable expressivity in eleven rare genetic disorders von Oetjens, M. T., Kelly, M. A., Sturm, A. C., Martin, C. L., Ledbetter, D. H.

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EMR documentation of physician–patient communication following genomic counseling for actionable complex disease and pharmacogenomic results von Sweet, K., Sturm, A.C., Schmidlen, T., Hovick, S., Peng, J., Manickam, K., Salikhova, A., McElroy, J., Scheinfeldt, L., Toland, A.E., Roberts, J.S., Christman, M.

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Simultaneous Interferometric Measurement of Corrosive or Demineralizing Bacteria and Their Mineral Interfaces von Waters, M.S, El-Naggar, M.Y, Hsu, L, Sturm, C.A, Luttge, A, Udwadia, F.E, Cvitkovitch, D.G, Goodman, S.D, Nealson, K.H

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Cardiovascular genetics: are we there yet? von Sturm, A C

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In search of the microbe/mineral interface: quantitative analysis of bacteria on metal surfaces using vertical scanning interferometry von WATERS, M.S, STURM, C.A, EL-NAGGAR, M.Y, LUTTGE, A, UDWADIA, F.E, CVITKOVITCH, D.G, GOODMAN, S.D, NEALSON, K.H

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Population genomic screening of all young adults in Australia to detect familial hypercholesterolemia: a cost-effectiveness analysis von Ademi, Z, Marquina, C, Lacaze, P, Tiller, J, Riaz, M, Sturm, A C, Nelson, M, Ference, B A, Pang, J, Watts, G F, Nicholls, S J, Zoungas, S, Liew, D, McNeil, J

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Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death von Walsh, R, Adler, A, Amin, AS, Abiusi, E, Care, M, Bikker, H, Amenta, S, Feilotter, H, Nannenberg, EA, Mazzarotto, F, Trevisan, V, Garcia, J, Hershberger, RE, Perez, M, Sturm, AC, Ware, JS, Zareba, W, Novelli, V, Wilde, AAM, Gollob, MH

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International Atherosclerosis Society guidance for implementing best practice in the care of familial hypercholesterolaemia von Watts, GF, Gidding, SS, Hegele, RA, Raal, FJ, Sturm, AC, Jones, LK, Sarkies, MN, Al-Rasadi, K, Blom, DJ, Daccord, M, De Ferranti, SD, Folco, E, Libby, P, Mata, P, Nawawi, HM, Ramaswami, U, Ray, KK, Stefanutti, C, Yamashita, S, Pang, J, Thompson, GR, Santos, RD

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Homocysteine and MTHFR Mutations: Relation to Thrombosis and Coronary Artery Disease von Varga, Elizabeth A., Sturm, Amy C., Misita, Caron P., Moll, Stephan

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An international, multicentered evidence-based reappraisal of genes reported to cause congenital long QT syndrome von Adler, A, Novelli, V, Amin, AS, Abiusi, E, Care, M, Nannenberg, EA, Feilotter, H, Amenta, S, Mazza, D, Bikker, H, Sturm, AC, Garcia, J, Ackerman, MJ, Hershberger, RE, Perez, MV, Zareba, W, Ware, J, Wilde, AAM, Gollob, MH

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Reappraisal of reported genes for sudden arrhythmic death: an evidence-based evaluation of gene validity for Brugada syndrome von Hosseini, SM, Kim, R, Udupa, S, Costain, G, Jobling, R, Liston, E, Jamal, SM, Szybowska, M, Morel, CF, Bowdin, S, Garcia, J, Care, M, Sturm, AC, Novelli, V, Ackerman, MJ, Ware, JS, Hershberger, RE, Wilde, AAM, Gollob, MH, NIH-Clinical Genome Resource Consortium

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Woody debris and channel morphology in first- and second-order forested channels in Washington's coast ranges von Jackson, C. Rhett, Sturm, Christopher A.

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Lessons Learned while Developing a Cancer Family History Campaign in the Columbus, Ohio Metropolitan Area von Sturm, Amy C., Sweet, Kevin, Schwirian, Patricia M., Koenig, Clint, Westman, Judith, Kelly, Kimberly M.

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Responsible use of polygenic risk scores in the clinic: potential benefits, risks and gaps von Adeyemo, Adebowale, Balaconis, Mary K., Darnes, Deanna R., Fatumo, Segun, Granados Moreno, Palmira, Hodonsky, Chani J., Inouye, Michael, Kanai, Masahiro, Kato, Kazuto, Knoppers, Bartha M., Lewis, Anna C. F., Martin, Alicia R., McCarthy, Mark I., Meyer, Michelle N., Okada, Yukinori, Richards, J. Brent, Richter, Lucas, Ripatti, Samuli, Rotimi, Charles N., Sanderson, Saskia C., Sturm, Amy C., Verdugo, Ricardo A., Widen, Elisabeth, Willer, Cristen J., Wojcik, Genevieve L., Zhou, Alicia

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TIMBER HARVEST IMPACTS ON SMALL HEADWATER STREAM CHANNELS IN THE COAST RANGES OF WASHINGTON von Jackson, C. Rhett, Sturm, Christopher A., Ward, Jason M.

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Cryptococcal Thyroiditis and Hyperthyroidism von Avram, Anca M., Sturm, Christine A., Michael, Claire W., Sisson, James C., Jaffe, Craig A.

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Beyond gene-disease validity: capturing structured data on inheritance, allelic-requirement, disease-relevant variant classes, and disease mechanism for inherited cardiac condition... von Josephs, KS, Roberts, AM, Theotokis, P, Walsh, R, Ostrowski, PJ, Edwards, M, Fleming, A, Thaxton, C, Roberts, JD, Care, M, Zareba, W, Adler, A, Sturm, AC, Tadros, R, Novelli, V, Owens, E, Bronicki, L, Jarinova, O, Callewaert, B, Peters, S, Lumbers, T, Jordan, E, Asatryan, B, Krishnan, N, Hershberger, RE, Chahal, CAA, Landstrom, AP, James, C, McNally, EM, Judge, DP, Van Tintelen, P, Wilde, A, Gollob, M, Ingles, J, Ware, JS

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Determination and Documentation of the Need for Practice Guidelines von Sturm, Cynthia A, Hancock, Kristin A, Cerbone, Armand R, de La Cancela, Victor, Connell, Mary A, Foote, William E, Galietta, Michele M, James, Larry C, Jerome, Leigh W, Knight, Sara J, Mohr, David C, West, Carolyn M, Witt, Phillip H

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Collateral Circulation and Outcome in Atherosclerotic Versus Cardioembolic Cerebral Large Vessel Occlusion von Guglielmi, Valeria, LeCouffe, Natalie E, Zinkstok, Sanne M, Compagne, Kars C.J, Eker, Reyhan, Tolhuisen, Manon L, van der Worp, H Bart, Jansen, Ivo G.H, van Oostenbrugge, Robert J, Marquering, Henk A, Dippel, Diederik W.J, Emmer, Bart J, Majoie, Charles B.L.M, Roos, Yvo B.W.E.M, Coutinho, Jonathan M, van der Lugt, Aad, van Zwam, Wim H, Boiten, Jelis, A. Vos, Jan, Mulder, Maxim J.H.L, Goldhoorn, Robert-Jan B, Kappelhof, Manon, Schonewille, Wouter J, Vos, Jan A, Wermer, Marieke J.H, van Walderveen, Marianne A.A, Staals, Julie, Hofmeijer, Jeannette, Martens, Jasper M, Lycklama à Nijeholt, Geert J, Roozenbeek, Bob, de Bruijn, Sebastiaan F, van Dijk, Lukas C, Lo, Rob H, van Dijk, Ewoud J, Boogaarts, Hieronymus D, de Kort, Paul L.M, Peluso, Jo P, van den Berg, Jan S.P, van Hasselt, Boudewijn A.A.M, Aerden, Leo A.M, Dallinga, René J, Uyttenboogaart, Maarten, Eshghi, Omid, Schreuder, Tobien H.C.M.L, Heijboer, Roel J.J, Keizer, Koos, Yo, Lonneke S.F, den Hertog, Heleen M, Sturm, Emiel J.C, Sprengers, Marieke E.S, Jenniskens, Sjoerd F.M, van den Berg, René, Yoo, Albert J, Postma, Alida A, Roosendaal, Stefan D, van der Kallen, Bas F.W, van den Wijngaard, Ido R, van Es, Adriaan C.G.M, Bot, Joost, van Doormaal, Pieter-Jan, Flach, H Zwenneke, Lingsma, Hester F, el Ghannouti, Naziha, Sterrenberg, Martin, Puppels, Corina, Pellikaan, Wilma, Sprengers, Rita, Elfrink, Marjan, de Meris, Joke, Vermeulen, Tamara, Geerlings, Annet, van Vemde, Gina, Simons, Tiny, van Rijswijk, Cathelijn, Bongenaar, Hester, Bodde, Karin, Kleijn, Sandra, Lodico, Jasmijn, Droste, Hanneke, Jeurrissen, D, Bos, Ernas, Drabbe, Yvonne, Aaldering, Nicoline, Zweedijk, Berber, Khalilzada, Mostafa, Venema, Esmee, Chalos, Vicky, Geuskens, Ralph R, van Straaten, Tim, Ergezen, Saliha, Harmsma, Roger R.M, Muijres, Daan, de Jong, Anouk, Hinsenveld, Wouter, Berkhemer, Olvert A, Boers, Anna M.M, Huguet, J, Groot, P.F.C, Alves, Heitor

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The “bathroom game”: A systematic program for the elimination of encopretic behavior von Bornstein, Philip H., Balleweg, Bernard J., McLellarn, Robert W., Wilson, Gregory L., Sturm, Cynthia A., Andre, John C., Van Den Pol, Richard A.

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