Weighted gene coexpression network analysis strategies applied to mouse weight von Fuller, Tova F, Ghazalpour, Anatole, Aten, Jason E, Drake, Thomas A, Lusis, Aldons J, Horvath, Steve

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Identification of an ATPase, MsmK, Which Energizes Multiple Carbohydrate ABC Transporters in Streptococcus pneumoniae von MARION, Carolyn, ATEN, Andrew E, WOODIGA, Shireen A, KING, Samantha J

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Exome variant prioritization in a large cohort of hearing-impaired individuals indicates IKZF2 to be associated with non-syndromic hearing loss and guides future research of unsolv... von Velde, Hedwig M., Vaseghi-Shanjani, Maryam, Smits, Jeroen J., Ramakrishnan, Gayatri, Oostrik, Jaap, Wesdorp, Mieke, Astuti, Galuh, Yntema, Helger G., Hoefsloot, Lies, Lanting, Cris P., Huynen, Martijn A., Lehman, Anna, Turvey, Stuart E., Pennings, Ronald J. E., Kremer, Hannie

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Using genetic markers to orient the edges in quantitative trait networks: the NEO software von Aten, Jason E, Fuller, Tova F, Lusis, Aldons J, Horvath, Steve

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De novo variants in CNOT3 cause a variable neurodevelopmental disorder von Martin, R, Splitt, M, Genevieve, D, Aten, E, Collins, A, de Bie, C I, Faivre, L, Foulds, N, Giltay, J, Ibitoye, R, Joss, S, Kennedy, J, Kerr, B, Kivuva, E, Koopmans, M, Newbury-Ecob, R, Jean-Marçais, N, Peeters, E A J, Smithson, S, Tomkins, S, Tranmauthem, F, Piton, A, van Haeringen, A

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OC21.02: The incidence of genetic variants in fetuses with severe congenital heart defects von Nisselrooij, A., Lugthart, M., Santen, G., Aten, E., Clur, S.B., Linskens, I., Pajkrt, E., Rammeloo, L., Van Lith, J., Blom, N., Haak, M.C.

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An Integrative Genetics Approach to Identify Candidate Genes Regulating BMD: Combining Linkage, Gene Expression, and Association von Farber, Charles R, van Nas, Atila, Ghazalpour, Anatole, Aten, Jason E, Doss, Sudheer, Sos, Brandon, Schadt, Eric E, Ingram‐Drake, Leslie, Davis, Richard C, Horvath, Steve, Smith, Desmond J, Drake, Thomas A, Lusis, Aldons J

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Methods to detect CNVs in the human genome von Aten, E., White, S.J., Kalf, M.E., Vossen, R.H.A.M., Thygesen, H.H., Ruivenkamp, C.A., Kriek, M., Breuning, M.H.B., den Dunnen, J.T.

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G.P.91 A new syndrome characterized by demyelinating neuropathy and hydrocephalus caused by a heterozygous mutation in one of the aminoacyl-tRNA synthetase genes von Niks, E.H, Potjer, T.P, Al Momani, R, Sun, Y, Koot, R.W, van Dijk, J.G, Haring, D.A.J, Aten, E, Kriek, M, Santen, G.W.E, Lesnik Oberstein, S.A.M

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The natural history and genotype–phenotype correlations of TMPRSS3 hearing loss: an international, multi-center, cohort analysis von Colbert, Brett M., Lanting, Cris, Smeal, Molly, Blanton, Susan, Dykxhoorn, Derek M., Tang, Pei-Ciao, Getchell, Richard L., Velde, Hedwig, Fehrmann, Mirthe, Thorpe, Ryan, Chapagain, Prem, Elkhaligy, Heidy, Kremer, Hannie, Yntema, Helger, Haer-Wigman, Lonneke, Redfield, Shelby, Sun, Tieqi, Bruijn, Saskia, Plomp, Astrid, Goderie, Thadé, van de Kamp, Jiddeke, Free, Rolien H., Wassink-Ruiter, Jolien Klein, Widdershoven, Josine, Vanhoutte, Els, Rotteveel, Liselotte, Kriek, Marjolein, van Dooren, Marieke, Hoefsloot, Lies, de Gier, Heriette H. W., Schaefer, Amanda, Kolbe, Diana, Azaiez, Hela, Rabie, Grace, Aburayyan, Armal, Kawas, Mariana, Kanaan, Moien, Holder, Jourdan, Usami, Shin-ichi, Chen, Zhengyi, Dai, Pu, Holt, Jeffrey, Nelson, Rick, Choi, Byung Yoon, Shearer, Eliot, Smith, Richard J. H., Pennings, Ronald, Liu, Xue Zhong

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Consensus recommendations on counselling in Phelan-McDermid syndrome, with special attention to recurrence risk and to ring chromosome 22 von Koza, Sylvia A., Tabet, Anne C., Bonaglia, Maria C., Andres, Stephanie, Anderlid, Britt-Marie, Aten, Emmelien, Stiefsohn, Dominique, Evans, D. Gareth, van Ravenswaaij-Arts, Conny M.A., Kant, Sarina G.

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P1785Whole exome sequencing unravels new genes associated with mitral valve prolapse von Van Wijngaarden, A, Hiemstra, Y L, Koopmann, T T, Ruivenkamp, C A L, Aten, E, Bax, J J, Delgado, V, Barge-Schaapveld, D Q C M, Ajmone Marsan, N

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Stable long-term outcomes after cochlear implantation in subjects with TMPRSS3 associated hearing loss: a retrospective multicentre study von Fehrmann, M L A, Huinck, W J, Thijssen, M E G, Haer-Wigman, L, Yntema, H G, Rotteveel, L J C, Widdershoven, J C C, Goderie, T, van Dooren, M F, Hoefsloot, E H, van der Schroeff, M P, Mylanus, E A M, Lanting, C P, Pennings, R J E

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Weighted gene co-expression network analysis identifies biomarkers in glycerol kinase deficient mice von MacLennan, Nicole K., Dong, Jun, Aten, Jason E., Horvath, Steve, Rahib, Lola, Ornelas, Loren, Dipple, Katrina M., McCabe, Edward R.B.

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Genetic dissection of a major mouse obesity QTL (Carfhg2): integration of gene expression and causality modeling von Farber, Charles R, Aten, Jason E, Farber, Emily A, de Vera, Vincent, Gularte, Rodrigo, Islas-Trejo, Alma, Wen, Pengzi, Horvath, Steve, Lucero, Michael, Lusis, Aldons J, Medrano, Juan F

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New techniques to detect genomic variation von Aten, E.

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Genetic islands of Streptococcus agalactiae strains NEM316 and 2603VR and their presence in other Group B streptococcal strains von Herbert, Mark A, Beveridge, Catriona J E, McCormick, David, Aten, Emmelien, Jones, Nicola, Snyder, Lori A S, Saunders, Nigel J

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Consensus recommendations on counselling in Phelan-McDermid syndrome, with special attention to recurrence risk and to ring chromosome 22 von Koza, S.A., Tabet, A.C., Bonaglia, M.C., Andres, S., Anderlid, B.M., Aten, E., Stiefsohn, D., Evans, D.G., Ravenswaaij-Arts, C.M.A. van, Kant, S.G.

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High-yield identification of pathogenic NF1 variants by skin fibroblast transcriptome screening after apparently normal diagnostic DNA testing von Douben, H.C.W., Nellist, M., Unen, L. van, Elfferich, P., Kasteleijn, E., Hoogeveen-Westerveld, M., Louwen, J., Veghel-Plandsoen, M. van, Valk, W. de, Saris, J.J., Hendriks, F., Korpershoek, E., Hoefsloot, L.H., Vliet, M. van, Bever, Y. van, Laar, I. van de, Aten, E., Lachmeijer, A.M.A., Taal, W., Bersselaar, L. van den, Schuurmans, J., Oostenbrink, R., Minkelen, R. van, Ierland, Y. van, Ham, T.J. van

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Pharmacokinetics and Urinary Excretion of Clavulanic Acid After Oral Administration of Amoxicillin and Potassium Clavulanate von FERSLEW, KENNETH E., DAIGNEAULT, ERNEST A., ATEN, EDWARD M., ROSEMAN, JAMES M.

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