Subtle structural abnormalities in genotype positive phenotype ‘negative’ patients with pre-clinical hypertrophic cardiomyopathy (HCM): a blinded, controlled cardiovascular magneti...

Por Deva, Djeven, Gruner, Christiane, Care, Melanie, Wintersperger, Bernd J, Rakowski, Harry, Crean, Andrew M
Publicado em 2012

Incremental predictive value of deep crypts in the basal inferoseptum in the setting of hypertrophic cardiomyopathy

Por Deva, Djeven P, Williams, Lynne K, Care, Melanie, Siminovitch, Katherine A, Moshonov, Hadas, Wintersperger, Bernd J, Rakowski, Harry, Crean, Andrew M
Publicado em 2013

Knowledge of genetic testing for hereditary kidney cancer in Canada is lacking: The results of the Canadian national hereditary kidney cancer needs assessment survey

Por Violette, Philippe D., Kamel-Reid, Suzanne, Graham, Gail E., Reaume, M. Neil, Jewett, Michael A., Care, Melanie, Basiuk, Joan, Pautler, Stephen E.
Publicado no Can Urol Assoc J (2014)

Structured assessment and followup for patients with hereditary kidney tumour syndromes

Por Lattouf, Jean-Baptiste, Pautler, Stephen E., Reaume, M. Neil, Kim, Raymond H., Care, Melanie, Green, Jane, So, Alan, Violette, Philippe D., Saliba, Issam, Major, Philippe, Silver, Shane, Leicht, Richard, Basiuk, Joan, Tanguay, Simon, Jewett, Michael A.S., Drachenberg, Darrel
Publicado no Can Urol Assoc J (2016)

The Cardiac Myosin Binding Protein C Arg502Trp Mutation: A Common Cause of Hypertrophic Cardiomyopathy

Por Saltzman, Adam J., Mancini-DiNardo, Debora, Li, Chumei, Chung, Wendy K., Ho, Carolyn Y., Hurst, Stephanie, Wynn, Julia, Care, Melanie, Hamilton, Robert M., Seidman, Gregor W., Gorham, Joshua, McDonough, Barbara, Sparks, Elizabeth, Seidman, Jonathan G., Seidman, Christine E., Rehm, Heidi L.
Publicado em 2010

Genetic Testing for Dilated Cardiomyopathy in Clinical Practice

Por Lakdawala, Neal K., Funke, Birgit H., Baxter, Samantha, Cirino, Allison L., Roberts, Amy E., Judge, Daniel P., Johnson, Nicole, Mendelsohn, Nancy J., Morel, Chantal, Care, Melanie, Chung, Wendy K., Jones, Carolyn, Psychogios, Apostolos, Duffy, Elizabeth, Rehm, Heidi L., White, Emily, Seidman, J.G., Seidman, Christine E., Ho, Carolyn Y.
Publicado em 2012

Canadian guideline on genetic screening for hereditary renal cell cancers

Por Reaume, M. Neil, Graham, Gail E., Tomiak, Eva, Kamel-Reid, Suzanne, Jewett, Michael A.S., Bjarnason, Georg A., Blais, Normand, Care, Melanie, Drachenberg, Darryl, Gedye, Craig, Grant, Ronald, Heng, Daniel Y.C., Kapoor, Anil, Kollmannsberger, Christian, Lattouf, Jean-Baptiste, Maher, Eamonn R., Pause, Arnim, Ruether, Dean, Soulieres, Denis, Tanguay, Simon, Turcotte, Sandra, Violette, Philippe D., Wood, Lori, Basiuk, Joan, Pautler, Stephen E.
Publicado em 2013

Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia

Por Moreno-De-Luca, Daniel, Mulle, Jennifer G., Kaminsky, Erin B., Sanders, Stephan J., Myers, Scott M., Adam, Margaret P., Pakula, Amy T., Eisenhauer, Nancy J., Uhas, Kim, Weik, LuAnn, Guy, Lisa, Care, Melanie E., Morel, Chantal F., Boni, Charlotte, Salbert, Bonnie Anne, Chandrareddy, Ashadeep, Demmer, Laurie A., Chow, Eva W.C., Surti, Urvashi, Aradhya, Swaroop, Pickering, Diane L., Golden, Denae M., Sanger, Warren G., Aston, Emily, Brothman, Arthur R., Gliem, Troy J., Thorland, Erik C., Ackley, Todd, Iyer, Ram, Huang, Shuwen, Barber, John C., Crolla, John A., Warren, Stephen T., Martin, Christa L., Ledbetter, David H.
Publicado em 2010

Deletion 17q12 Is a Recurrent Copy Number Variant that Confers High Risk of Autism and Schizophrenia

Por Moreno-De-Luca, Daniel, Mulle, Jennifer G., Kaminsky, Erin B., Sanders, Stephan J., Myers, Scott M., Adam, Margaret P., Pakula, Amy T., Eisenhauer, Nancy J., Uhas, Kim, Weik, LuAnn, Guy, Lisa, Care, Melanie E., Morel, Chantal F., Boni, Charlotte, Salbert, Bonnie Anne, Chandrareddy, Ashadeep, Demmer, Laurie A., Chow, Eva W.C., Surti, Urvashi, Aradhya, Swaroop, Pickering, Diane L., Golden, Denae M., Sanger, Warren G., Aston, Emily, Brothman, Arthur R., Gliem, Troy J., Thorland, Erik C., Ackley, Todd, Iyer, Ram, Huang, Shuwen, Barber, John C., Crolla, John A., Warren, Stephen T., Martin, Christa L., Ledbetter, David H.
Publicado em 2011