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

av Pramhed, Anna, Addis, Laura, Tillgren, Viveka, Wenglén, Christina, Heinegård, Dick, Logan, Derek T.
Publicerad 2008

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

av Haglund, Lisbet, Tillgren, Viveka, Addis, Laura, Wenglén, Christina, Recklies, Anneliese, Heinegård, Dick
Publicerad 2011

Imaging and Genetics of Language and Cognition in Pediatric Epilepsy

av Addis, Laura, Lin, Jack J., Pal, Deb K., Hermann, Bruce, Caplan, Rochelle
Publicerad 2012

Analysis of rare copy number variation in absence epilepsies

av Addis, Laura, Rosch, Richard E., Valentin, Antonio, Makoff, Andrew, Robinson, Robert, Everett, Kate V., Nashef, Lina, Pal, Deb K.
I publikationen Neurol Genet (2016)

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

av Derkach, Andriy, Chiang, Theodore, Gong, Jiafen, Addis, Laura, Dobbins, Sara, Tomlinson, Ian, Houlston, Richard, Pal, Deb K., Strug, Lisa J.
Publicerad 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

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

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

av 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.
Publicerad 2012

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

av 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
I publikationen J Med Genet (2018)

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

av 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
I publikationen Dev Med Child Neurol (2014)

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

av 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.
I publikationen Ann Clin Transl Neurol (2016)

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

av 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.
Publicerad 2009