Resultats de la cerca - Addis, Laura

Purification, crystallization and preliminary X-ray diffraction analysis of human chondroadherin per Pramhed, Anna, Addis, Laura, Tillgren, Viveka, Wenglén, Christina, Heinegård, Dick, Logan, Derek T.

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Identification and Characterization of the Integrin α(2)β(1) Binding Motif in Chondroadherin Mediating Cell Attachment per Haglund, Lisbet, Tillgren, Viveka, Addis, Laura, Wenglén, Christina, Recklies, Anneliese, Heinegård, Dick

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Imaging and Genetics of Language and Cognition in Pediatric Epilepsy per Addis, Laura, Lin, Jack J., Pal, Deb K., Hermann, Bruce, Caplan, Rochelle

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Analysis of rare copy number variation in absence epilepsies per Addis, Laura, Rosch, Richard E., Valentin, Antonio, Makoff, Andrew, Robinson, Robert, Everett, Kate V., Nashef, Lina, Pal, Deb K.

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Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic per Derkach, Andriy, Chiang, Theodore, Gong, Jiafen, Addis, Laura, Dobbins, Sara, Tomlinson, Ian, Houlston, Richard, Pal, Deb K., Strug, Lisa J.

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A Whole-Genome Scan and Fine-Mapping Linkage Study of Auditory-Visual Synesthesia Reveals Evidence of Linkage to Chromosomes 2q24, 5q33, 6p12, and 12p12 per Asher, Julian E., Lamb, Janine A., Brocklebank, Denise, Cazier, Jean-Baptiste, Maestrini, Elena, Addis, Laura, Sen, Mallika, Baron-Cohen, Simon, Monaco, Anthony P.

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The Genetics of Reading Disability in an Often Excluded Sample: Novel Loci Suggested for Reading Disability in Rolandic Epilepsy per Strug, Lisa J., Addis, Laura, Chiang, Theodore, Baskurt, Zeynep, Li, Weili, Clarke, Tara, Hardison, Huntley, Kugler, Steven L., Mandelbaum, David E., Novotny, Edward J., Wolf, Steven M., Pal, Deb K.

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Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses per Addis, Laura, Sproviero, William, Thomas, Sanjeev V, Caraballo, Roberto H, Newhouse, Stephen J, Gomez, Kumudini, Hughes, Elaine, Kinali, Maria, McCormick, David, Hannan, Siobhan, Cossu, Silvia, Taylor, Jacqueline, Akman, Cigdem I, Wolf, Steven M, Mandelbaum, David E, Gupta, Rajesh, van der Spek, Rick A, Pruna, Dario, Pal, Deb K

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Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia per Simpson, Nuala H, Addis, Laura, Brandler, William M, Slonims, Vicky, Clark, Ann, Watson, Jocelynne, Scerri, Thomas S, Hennessy, Elizabeth R, Bolton, Patrick F, Conti-Ramsden, Gina, Fairfax, Benjamin P, Knight, Julian C, Stein, John, Talcott, Joel B, O'Hare, Anne, Baird, Gillian, Paracchini, Silvia, Fisher, Simon E, Newbury, Dianne F, Consortium, SLI

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A microRNA‐328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy per Panjwani, Naim, Wilson, Michael D., Addis, Laura, Crosbie, Jennifer, Wirrell, Elaine, Auvin, Stéphane, Caraballo, Roberto H., Kinali, Maria, McCormick, David, Oren, Caroline, Taylor, Jacqueline, Trounce, John, Clarke, Tara, Akman, Cigdem I., Kugler, Steven L., Mandelbaum, David E., McGoldrick, Patricia, Wolf, Steven M., Arnold, Paul, Schachar, Russell, Pal, Deb K., Strug, Lisa J.

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CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment per Newbury, Dianne F., Winchester, Laura, Addis, Laura, Paracchini, Silvia, Buckingham, Lyn-Louise, Clark, Ann, Cohen, Wendy, Cowie, Hilary, Dworzynski, Katharina, Everitt, Andrea, Goodyer, Ian M., Hennessy, Elizabeth, Kindley, A. David, Miller, Laura L., Nasir, Jamal, O'Hare, Anne, Shaw, Duncan, Simkin, Zoe, Simonoff, Emily, Slonims, Vicky, Watson, Jocelynne, Ragoussis, Jiannis, Fisher, Simon E., Seckl, Jonathon R., Helms, Peter J., Bolton, Patrick F., Pickles, Andrew, Conti-Ramsden, Gina, Baird, Gillian, Bishop, Dorothy V.M., Monaco, Anthony P.

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