Purification, crystallization and preliminary X-ray diffraction analysis of human chondroadherin

بواسطة Pramhed, Anna, Addis, Laura, Tillgren, Viveka, Wenglén, Christina, Heinegård, Dick, Logan, Derek T.
منشور في 2008

Identification and Characterization of the Integrin α(2)β(1) Binding Motif in Chondroadherin Mediating Cell Attachment

بواسطة Haglund, Lisbet, Tillgren, Viveka, Addis, Laura, Wenglén, Christina, Recklies, Anneliese, Heinegård, Dick
منشور في 2011

Imaging and Genetics of Language and Cognition in Pediatric Epilepsy

بواسطة Addis, Laura, Lin, Jack J., Pal, Deb K., Hermann, Bruce, Caplan, Rochelle
منشور في 2012

Analysis of rare copy number variation in absence epilepsies

بواسطة Addis, Laura, Rosch, Richard E., Valentin, Antonio, Makoff, Andrew, Robinson, Robert, Everett, Kate V., Nashef, Lina, Pal, Deb K.
الحاوية / القاعدة Neurol Genet (2016)

Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statistic

بواسطة Derkach, Andriy, Chiang, Theodore, Gong, Jiafen, Addis, Laura, Dobbins, Sara, Tomlinson, Ian, Houlston, Richard, Pal, Deb K., Strug, Lisa J.
منشور في 2014

A Whole-Genome Scan and Fine-Mapping Linkage Study of Auditory-Visual Synesthesia Reveals Evidence of Linkage to Chromosomes 2q24, 5q33, 6p12, and 12p12

بواسطة Asher, Julian E., Lamb, Janine A., Brocklebank, Denise, Cazier, Jean-Baptiste, Maestrini, Elena, Addis, Laura, Sen, Mallika, Baron-Cohen, Simon, Monaco, Anthony P.
منشور في 2009

The Genetics of Reading Disability in an Often Excluded Sample: Novel Loci Suggested for Reading Disability in Rolandic Epilepsy

بواسطة 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.
منشور في 2012

Identification of new risk factors for rolandic epilepsy: CNV at Xp22.31 and alterations at cholinergic synapses

بواسطة 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
الحاوية / القاعدة J Med Genet (2018)

Increased prevalence of sex chromosome aneuploidies in specific language impairment and dyslexia

بواسطة 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
الحاوية / القاعدة Dev Med Child Neurol (2014)

A microRNA‐328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy

بواسطة 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.
الحاوية / القاعدة Ann Clin Transl Neurol (2016)

CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment

بواسطة 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.
منشور في 2009