Neurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanisms von Mascheretti, S, De Luca, A, Trezzi, V, Peruzzo, D, Nordio, A, Marino, C, Arrigoni, F

Volltext

The DCDC2 intron 2 deletion impairs illusory motion perception unveiling the selective role of magnocellular-dorsal stream in reading (dis)ability von Gori, Simone, Mascheretti, Sara, Giora, Enrico, Ronconi, Luca, Ruffino, Milena, Quadrelli, Ermanno, Facoetti, Andrea, Marino, Cecilia

Volltext

Sluggish dorsally-driven inhibition of return during orthographic processing in adults with dyslexia von Franceschini, S., Mascheretti, S., Bertoni, S., Trezzi, V., Andreola, C., Gori, S., Facoetti, A.

Volltext

Visual motion and rapid auditory processing are solid endophenotypes of developmental dyslexia von Mascheretti, S., Gori, S., Trezzi, V., Ruffino, M., Facoetti, A., Marino, C.

Volltext

Reconstruction of the Sudden Oak Death epidemic in California through microsatellite analysis of the pathogen Phytophthora ramorum von MASCHERETTI, S, CROUCHER, P.J.P, VETTRAINO, A, PROSPERO, S, GARBELOTTO, M

Volltext

An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia von Mascheretti, S., Bureau, A., Trezzi, V., Giorda, R., Marino, C.

Volltext

Population genetic analyses provide insights on the introduction pathway and spread patterns of the North American forest pathogen Heterobasidion irregulare in Italy von Garbelotto, M., Guglielmo, F., Mascheretti, S., Croucher, P. J. P., Gonthier, P.

Volltext

Genetic epidemiology of the Sudden Oak Death pathogen Phytophthora ramorum in California von Mascheretti, S, Croucher, P.J.P, Kozanitas, M, Baker, L, Garbelotto, M

Volltext

A First Generation Heterobasidion Hybrid Discovered in Larix lyalli in Montana von Lockman, B, Mascheretti, S, Schechter, S, Garbelotto, M

Volltext

An assessment of gene‐by‐environment interactions in developmental dyslexia‐related phenotypes von Mascheretti, S., Bureau, A., Battaglia, M., Simone, D., Quadrelli, E., Croteau, J., Cellino, M. R., Giorda, R., Beri, S., Maziade, M., Marino, C.

Volltext

Monoamine oxidase A polymorphism moderates stability of attention problems and susceptibility to life stress during adolescence von Zohsel, K., Bianchi, V., Mascheretti, S., Hohm, E., Schmidt, M. H., Esser, G., Brandeis, D., Banaschewski, T., Nobile, M., Laucht, M.

Volltext

Mediterranean Europe as an area of endemism for small mammals rather than a source for northwards postglacial colonization von Bilton, David T., Mirol, Patricia M., Mascheretti, Silvia, Fredga, Karl, Zima, Jan, Searle, Jeremy B.

Volltext

Pharmacogenetic investigation of the TNF TNF-receptor system in patients with chronic active Crohn's disease treated with infliximab von Mascheretti, S, Hampe, J, Kühbacher, T, Herfarth, H, Krawczak, M, Fölsch, U R, Schreiber, S

Volltext

Genetic variants in the CCR gene cluster and spontaneous viral elimination in hepatitis C‐infected patients von MASCHERETTI, S., HINRICHSEN, H., ROSS, S., BUGGISCH, P., HAMPE, J., FOELSCH, U. R., SCHREIBER, S.

Volltext

The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease von Cuthbert, Andrew P., Fisher, Sheila A., Mirza, Muddassar M., King, Kathy, Hampe, Jochen, Roucher, Peter J.P., Mascheretti, Silvia, Sanderson, Jeremy, Forbes, Alastair, Mansfield, John, Schreiber, Stefan, Lewis, Cathryn M., Mathew, Christopher G.

Volltext

Pharmacogenetics of inflammatory bowel disease von Mascheretti, Silvia, Croucher, Peter J.P, Schreiber, Stefan

Volltext

Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations von Hampe, Jochen, Cuthbert, Andrew, Croucher, Peter JP, Mirza, Muddassar M, Mascheretti, Silvia, Fisher, Sheila, Frenzel, Henning, King, Kathy, Hasselmeyer, Anja, MacPherson, Andrew JS, Bridger, Stephen, van Deventer, Sander, Forbes, Alastair, Nikolaus, Susanna, Lennard-Jones, John E, Foelsch, Ulrich R, Krawczak, Michael, Lewis, Cathryn, Schreiber, Stefan, Mathew, Christopher G

Volltext

Transmission disequilibrium test of stromelysin-1 gene variation in relation to Crohn’s disease von Pender, S L F, Croucher, P J P, Mascheretti, S, Prothero, J D, Fisher, S A, MacDonald, T T, Schreiber, S, Ye, Shu

Volltext

DCDC2 genetic variants and susceptibility to developmental dyslexia von Marino, Cecilia, Meng, Haiying, Mascheretti, Sara, Rusconi, Marianna, Cope, Natalie, Giorda, Roberto, Molteni, Massimo, Gruen, Jeffrey R

Volltext

Genetic testing in Crohn disease: utility in individualizing patient management von Mascheretti, Silvia, Schreiber, Stefan

Volltext