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.
Publicat 2008

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
Publicat 2011

Imaging and Genetics of Language and Cognition in Pediatric Epilepsy

per Addis, Laura, Lin, Jack J., Pal, Deb K., Hermann, Bruce, Caplan, Rochelle
Publicat 2012

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.
Publicat a Neurol Genet (2016)

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.
Publicat 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

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

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.
Publicat 2012

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
Publicat a J Med Genet (2018)

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
Publicat a Dev Med Child Neurol (2014)

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.
Publicat a Ann Clin Transl Neurol (2016)

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.
Publicat 2009