Search Results - Lukic, Vesna

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  1. 1
    Using familial information for variant filtering in high-throughput sequencing studies

    Using familial information for variant filtering in high-throughput sequencing studies by Bahlo, Melanie, Tankard, Rick, Lukic, Vesna, Oliver, Karen L., Smith, Katherine R.

    Published 2014
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  2. 2
    In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery

    In silico prioritization based on coexpression can aid epileptic encephalopathy gene discovery by Oliver, Karen L., Lukic, Vesna, Freytag, Saskia, Scheffer, Ingrid E., Berkovic, Samuel F., Bahlo, Melanie

    Published 2016
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  3. 3
    Harnessing Gene Expression Networks to Prioritize Candidate Epileptic Encephalopathy Genes

    Harnessing Gene Expression Networks to Prioritize Candidate Epileptic Encephalopathy Genes by Oliver, Karen L., Lukic, Vesna, Thorne, Natalie P., Berkovic, Samuel F., Scheffer, Ingrid E., Bahlo, Melanie

    Published 2014
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  4. 4
    GSTM1-null and GSTT1-active genotypes as risk determinants of primary open angle glaucoma among smokers

    GSTM1-null and GSTT1-active genotypes as risk determinants of primary open angle glaucoma among smokers by Stamenkovic, Miroslav, Lukic, Vesna, Suvakov, Sonja, Simic, Tatjana, Sencanic, Ivan, Pljesa-Ercegovac, Marija, Jaksic, Vesna, Babovic, Sinisa, Matic, Marija, Radosavljevic, Aleksandra, Savic-Radojevic, Ana, Djukic, Tatjana

    Published 2018
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  5. 5
    Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 loss

    Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 loss by Marsh, Ashley P.L., Lukic, Vesna, Pope, Kate, Bromhead, Catherine, Tankard, Rick, Ryan, Monique M., Yiu, Eppie M., Sim, Joe C.H., Delatycki, Martin B., Amor, David J., McGillivray, George, Sherr, Elliott H., Bahlo, Melanie, Leventer, Richard J., Lockhart, Paul J.

    Published 2015
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  6. 6
    A family study implicates GBE1 in the etiology of autism spectrum disorder

    A family study implicates GBE1 in the etiology of autism spectrum disorder by Fanjul-Fernández, Miriam, Brown, Natasha J, Hickey, Peter, Diakumis, Peter, Rafehi, Haloom, Bozaoglu, Kiymet, Green, Cherie C, Rattray, Audrey, Young, Savannah, Alhuzaimi, Dana, Mountford, Hayley S, Gillies, Greta, Lukic, Vesna, Vick, Tanya, Finlay, Keri, Coe, Bradley P, Eichler, Evan E, Delatycki, Martin B, Wilson, Sarah J, Bahlo, Melanie, Scheffer, Ingrid E, Lockhart, Paul J

    Published 2021
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  7. 7
    Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance

    Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance by Marsh, Ashley P L, Heron, Delphine, Edwards, Timothy J, Quartier, Angélique, Galea, Charles, Nava, Caroline, Rastetter, Agnès, Moutard, Marie-Laure, Anderson, Vicki, Bitoun, Pierre, Bunt, Jens, Faudet, Anne, Garel, Catherine, Gillies, Greta, Gobius, Ilan, Guegan, Justine, Heide, Solveig, Keren, Boris, Lesne, Fabien, Lukic, Vesna, Mandelstam, Simone A, McGillivray, George, McIlroy, Alissandra, Méneret, Aurélie, Mignot, Cyril, Morcom, Laura R, Odent, Sylvie, Paolino, Annalisa, Pope, Kate, Riant, Florence, Robinson, Gail A, Spencer-Smith, Megan, Srour, Myriam, Stephenson, Sarah E M, Tankard, Rick, Trouillard, Oriane, Welniarz, Quentin, Wood, Amanda, Brice, Alexis, Rouleau, Guy, Attié-Bitach, Tania, Delatycki, Martin B, Mandel, Jean-Louis, Amor, David J, Roze, Emmanuel, Piton, Amélie, Bahlo, Melanie, de Villemeur, Thierry Billette, Sherr, Elliott H, Leventer, Richard J, Richards, Linda J, Lockhart, Paul J, Depienne, Christel

    Published 2017
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