Weighted gene coexpression network analysis strategies applied to mouse weight
Fuller, Tova F, Ghazalpour, Anatole, Aten, Jason E, Drake, Thomas A, Lusis, Aldons J, Horvath, Steve
Published in Mammalian genome (01.07.2007)
Published in Mammalian genome (01.07.2007)
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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 unsolved cases
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
Published in Human genetics (01.11.2024)
Published in Human genetics (01.11.2024)
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De novo variants in CNOT3 cause a variable neurodevelopmental disorder
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
Published in European journal of human genetics : EJHG (01.11.2019)
Published in European journal of human genetics : EJHG (01.11.2019)
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Using genetic markers to orient the edges in quantitative trait networks: the NEO software
Aten, Jason E, Fuller, Tova F, Lusis, Aldons J, Horvath, Steve
Published in BMC systems biology (15.04.2008)
Published in BMC systems biology (15.04.2008)
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OC21.02: The incidence of genetic variants in fetuses with severe congenital heart defects
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.
Published in Ultrasound in obstetrics & gynecology (01.10.2019)
Published in Ultrasound in obstetrics & gynecology (01.10.2019)
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An Integrative Genetics Approach to Identify Candidate Genes Regulating BMD: Combining Linkage, Gene Expression, and Association
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
Published in Journal of bone and mineral research (01.01.2009)
Published in Journal of bone and mineral research (01.01.2009)
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Methods to detect CNVs in the human genome
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.
Published in Cytogenetic and genome research (01.01.2008)
Published in Cytogenetic and genome research (01.01.2008)
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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
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
Published in Neuromuscular disorders : NMD (01.10.2012)
Published in Neuromuscular disorders : NMD (01.10.2012)
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Weighted gene co-expression network analysis identifies biomarkers in glycerol kinase deficient mice
MacLennan, Nicole K., Dong, Jun, Aten, Jason E., Horvath, Steve, Rahib, Lola, Ornelas, Loren, Dipple, Katrina M., McCabe, Edward R.B.
Published in Molecular genetics and metabolism (01.10.2009)
Published in Molecular genetics and metabolism (01.10.2009)
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P1785Whole exome sequencing unravels new genes associated with mitral valve prolapse
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
Published in European heart journal (01.10.2019)
Published in European heart journal (01.10.2019)
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Genetic dissection of a major mouse obesity QTL (Carfhg2): integration of gene expression and causality modeling
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
Published in Physiological genomics (13.05.2009)
Published in Physiological genomics (13.05.2009)
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Consensus recommendations on counselling in Phelan-McDermid syndrome, with special attention to recurrence risk and to ring chromosome 22
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.
Published in European journal of medical genetics (01.07.2023)
Published in European journal of medical genetics (01.07.2023)
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Archeological Evidence for Pimple (Prairie) Mound Genesis
Aten, Lawrence E., Bollich, Charles N.
Published in Science (American Association for the Advancement of Science) (18.09.1981)
Published in Science (American Association for the Advancement of Science) (18.09.1981)
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Genetic islands of Streptococcus agalactiae strains NEM316 and 2603VR and their presence in other Group B streptococcal strains
Herbert, Mark A, Beveridge, Catriona J E, McCormick, David, Aten, Emmelien, Jones, Nicola, Snyder, Lori A S, Saunders, Nigel J
Published in BMC microbiology (24.05.2005)
Published in BMC microbiology (24.05.2005)
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Ioversol clinical safety summary
Benamor, M, Aten, E M, McElvany, K D, Lankin, D G, James, M A, Buy-Gandal, T, Harashe, L T, Weinandt, W J
Published in Investigative radiology (01.06.1989)
Published in Investigative radiology (01.06.1989)
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