Beckwith-Wiedemann syndrome by Choufani, Sanaa, Shuman, Cheryl, Weksberg, Rosanna

Get full text

Discovery of cross-reactive probes and polymorphic CpGs in the Illumina Infinium HumanMethylation450 microarray by Chen, Yi-an, Lemire, Mathieu, Choufani, Sanaa, Butcher, Darci T., Grafodatskaya, Daria, Zanke, Brent W., Gallinger, Steven, Hudson, Thomas J., Weksberg, Rosanna

Get full text

Anatomy of DNA methylation signatures: Emerging insights and applications by Chater-Diehl, Eric, Goodman, Sarah J., Cytrynbaum, Cheryl, Turinsky, Andrei L., Choufani, Sanaa, Weksberg, Rosanna

Get full text

Molecular Findings in Beckwith-Wiedemann Syndrome by CHOUFANI, SANAA, SHUMAN, CHERYL, WEKSBERG, ROSANNA

Get full text

Screening for genes that accelerate the epigenetic aging clock in humans reveals a role for the H3K36 methyltransferase NSD1 by Martin-Herranz, Daniel E, Aref-Eshghi, Erfan, Bonder, Marc Jan, Stubbs, Thomas M, Choufani, Sanaa, Weksberg, Rosanna, Stegle, Oliver, Sadikovic, Bekim, Reik, Wolf, Thornton, Janet M

Get full text

P837: DNA methylation profiling in Kabuki syndrome: Steps towards improved classification of variants of uncertain significance by Choufani, Sanaa, Weksberg, Rosanna

Get full text

Basic concepts of epigenetics by Inbar-Feigenberg, Michal, M.D, Choufani, Sanaa, Ph.D, Butcher, Darci T., Ph.D, Roifman, Maian, M.D, Weksberg, Rosanna, M.D., Ph.D

Get full text

Functional impact of global rare copy number variation in autism spectrum disorders by Gillberg, Christopher, Kolevzon, Alexander, Nelson, Stanley F, Sansom, Katherine, Casallo, Guillermo, Miller, Judith, Brennan, Sean, Leboyer, Marion, Bacchelli, Elena, Delorme, Richard, Fombonne, Eric, Hallmayer, Joachim, Green, Jonathan, Pickles, Andrew, Heron, Elizabeth A, Salt, Jeff, Battaglia, Agatino, Klauck, Sabine M, McDougle, Christopher J, Mahoney, William, Noor, Abdul, Cytrynbaum, Cheryl, Sato, Daisuke, Almeida, Joana, Korvatska, Olena, Dawson, Geraldine, Bierut, Laura J, Coon, Hilary, Rickaby, Jessica, Freitag, Christine M, Roeder, Kathryn, Bader, Gary D, Wijsman, Ellen M, Vincent, John B, Hakonarson, Hakon, Segurado, Ricardo, Paton, Tara, Roge, Bernadette, Ennis, Sean, Kim, Cecilia, Monaco, Anthony P, Paterson, Andrew D, Crossett, Andrew, McGrath, Jane, Carson, Andrew R, Le Couteur, Ann, Cook, Edwin H, Chung, Brian H.Y, Cuccaro, Michael L, Van Engeland, Herman, Conroy, Judith, Holt, Richard, Strawbridge, Christina, Kustanovich, Vlad, Migita, Ohsuke, Stoppioni, Vera, Igliozzi, Roberta, Poustka, Fritz, Stein, Olaf, Posey, David J, Sheffield, Val C, Duque, Frederico, Parrini, Barbara, Berney, Tom, Hus, Vanessa, Baird, Gillian, Duketis, Eftichia, Soorya, Latha, Corsello, Christina, Drmic, Irene, Sousa, Inês, Abrahams, Brett S, Thomson, Susanne, Lajonchere, Clara M, Tsiantis, John, Pinto, Dalila, Green, Andrew, Hughes, Gillian, Mantoulan, Carine, Betancur, Catalina, Volkmar, Fred, Poustka, Annemarie, Shah, Naisha, Bryson, Susan E, Munson, Jeff, Tancredi, Raffaella, Nygren, Gudrun, Wittemeyer, Kerstin, Merikangas, Alison, Oliveira, Guiomar, Farrar, Penny, Maestrini, Elena, Liu, Xiao-Qing, Gallagher, Louise, McConachie, Helen, Zurawiecki, Danielle, Schellenberg, Gerard D, Glessner, Joseph T, Lord, Catherine, Piven, Joseph

Get full text

Diagnostic yield of genetic testing in epileptic encephalopathy in childhood by Mercimek‐Mahmutoglu, Saadet, Patel, Jaina, Cordeiro, Dawn, Hewson, Stacy, Callen, David, Donner, Elizabeth J., Hahn, Cecil D., Kannu, Peter, Kobayashi, Jeff, Minassian, Berge A., Moharir, Mahendranath, Siriwardena, Komudi, Weiss, Shelly K., Weksberg, Rosanna, Snead, O. Carter

Get full text

Exposure to Gestational Diabetes Mellitus (GDM) alters DNA methylation in placenta and fetal cord blood by Awamleh, Zain, Butcher, Darci T., Hanley, Anthony, Retnakaran, Ravi, Haertle, Larissa, Haaf, Thomas, Hamilton, Jill, Weksberg, Rosanna

Get full text

DNA Methylation of the Oxytocin Receptor Across Neurodevelopmental Disorders by Siu, Michelle T., Goodman, Sarah J., Yellan, Isaac, Butcher, Darci T., Jangjoo, Maryam, Grafodatskaya, Daria, Rajendram, Rageen, Lou, Youliang, Zhang, Rujun, Zhao, Chunhua, Nicolson, Rob, Georgiades, Stelios, Szatmari, Peter, Scherer, Stephen W., Roberts, Wendy, Anagnostou, Evdokia, Weksberg, Rosanna

Get full text

Integrative approach to interpret DYRK1A variants, leading to a frequent neurodevelopmental disorder by Courraud, Jérémie, Chater-Diehl, Eric, Durand, Benjamin, Vincent, Marie, Del Mar Muniz Moreno, Maria, Boujelbene, Imene, Drouot, Nathalie, Genschik, Loréline, Schaefer, Elise, Nizon, Mathilde, Gerard, Bénédicte, Abramowicz, Marc, Cogné, Benjamin, Bronicki, Lucas, Burglen, Lydie, Barth, Magalie, Charles, Perrine, Colin, Estelle, Coubes, Christine, David, Albert, Delobel, Bruno, Demurger, Florence, Passemard, Sandrine, Denommé, Anne-Sophie, Faivre, Laurence, Feger, Claire, Fradin, Mélanie, Francannet, Christine, Genevieve, David, Goldenberg, Alice, Guerrot, Anne-Marie, Isidor, Bertrand, Johannesen, Katrine M, Keren, Boris, Kibæk, Maria, Kuentz, Paul, Mathieu-Dramard, Michèle, Demeer, Bénédicte, Metreau, Julia, Steensbjerre Møller, Rikke, Moutton, Sébastien, Pasquier, Laurent, Pilekær Sørensen, Kristina, Perrin, Laurence, Renaud, Mathilde, Saugier, Pascale, Rio, Marlène, Svane, Joane, Thevenon, Julien, Tran Mau Them, Frédéric, Tronhjem, Cathrine Elisabeth, Vitobello, Antonio, Layet, Valérie, Auvin, Stéphane, Khachnaoui, Khaoula, Birling, Marie-Christine, Drunat, Séverine, Bayat, Allan, Dubourg, Christèle, El Chehadeh, Salima, Fagerberg, Christina, Mignot, Cyril, Guipponi, Michel, Bienvenu, Thierry, Herault, Yann, Thompson, Julie, Willems, Marjolaine, Mandel, Jean-Louis, Weksberg, Rosanna, Piton, Amélie

Get full text

Inhibition of DNA methylation during chronic obstructive bladder disease (COBD) improves function, pathology and expression by Sidler, Martin, Aitken, K J, Jiang, Jia-Xin, Yadav, Priyank, Lloyd, Erin, Ibrahim, Malak, Choufani, Sanaa, Weksberg, Rosanna, Bägli, Darius

Get full text

Isolation of MECP2-nuLl Rett Syndrome patient hiPS cells and isogenic controls through X-chromosome inactivation by CHEUNG, Aaron Y. L, HORVATH, Lindsay M, GRAFODATSKAYA, Daria, PASCERI, Peter, WEKSBERG, Rosanna, HOTTA, Akitsu, CARREL, Laura, ELLIS, James

Get full text

Comparison of genome-wide and gene-specific DNA methylation between ART and naturally conceived pregnancies by Melamed, Nir, Choufani, Sanaa, Wilkins-Haug, Louise E, Koren, Gideon, Weksberg, Rosanna

Get full text

Clinically and biologically relevant subgroups of Wilms tumour defined by genomic and epigenomic analyses by Brzezinski, Jack, Choufani, Sanaa, Romao, Rodrigo, Shuman, Cheryl, Chen, Haiying, Cunanan, Joanna, Bagli, Darius, Grant, Ronald, Lorenzo, Armando, Weksberg, Rosanna

Get full text

Clinically relevant copy number variations detected in cerebral palsy by Oskoui, Maryam, Gazzellone, Matthew J, Thiruvahindrapuram, Bhooma, Zarrei, Mehdi, Andersen, John, Wei, John, Wang, Zhuozhi, Wintle, Richard F, Marshall, Christian R, Cohn, Ronald D, Weksberg, Rosanna, Stavropoulos, Dimitri J, Fehlings, Darcy, Shevell, Michael I, Scherer, Stephen W

Get full text

DNA Methylation Signature for EZH2 Functionally Classifies Sequence Variants in Three PRC2 Complex Genes by Choufani, Sanaa, Gibson, William T., Turinsky, Andrei L., Chung, Brian H.Y., Wang, Tianren, Garg, Kopal, Vitriolo, Alessandro, Cohen, Ana S.A., Cyrus, Sharri, Goodman, Sarah, Chater-Diehl, Eric, Brzezinski, Jack, Brudno, Michael, Ming, Luk Ho, White, Susan M., Lynch, Sally Ann, Clericuzio, Carol, Temple, I. Karen, Flinter, Frances, McConnell, Vivienne, Cushing, Tom, Bird, Lynne M., Splitt, Miranda, Kerr, Bronwyn, Scherer, Stephen W., Machado, Jerry, Imagawa, Eri, Okamoto, Nobuhiko, Matsumoto, Naomichi, Testa, Guiseppe, Iascone, Maria, Tenconi, Romano, Caluseriu, Oana, Mendoza-Londono, Roberto, Chitayat, David, Cytrynbaum, Cheryl, Tatton-Brown, Katrina, Weksberg, Rosanna

Get full text

Structural Variation of Chromosomes in Autism Spectrum Disorder by Marshall, Christian R., Noor, Abdul, Vincent, John B., Lionel, Anath C., Feuk, Lars, Skaug, Jennifer, Shago, Mary, Moessner, Rainald, Pinto, Dalila, Ren, Yan, Thiruvahindrapduram, Bhooma, Fiebig, Andreas, Schreiber, Stefan, Friedman, Jan, Ketelaars, Cees E.J., Vos, Yvonne J., Ficicioglu, Can, Kirkpatrick, Susan, Nicolson, Rob, Sloman, Leon, Summers, Anne, Gibbons, Clare A., Teebi, Ahmad, Chitayat, David, Weksberg, Rosanna, Thompson, Ann, Vardy, Cathy, Crosbie, Vicki, Luscombe, Sandra, Baatjes, Rebecca, Zwaigenbaum, Lonnie, Roberts, Wendy, Fernandez, Bridget, Szatmari, Peter, Scherer, Stephen W.

Get full text

P369: Acute lymphocytic leukemia in a child with Beckwith Wiedemann syndrome: Coincidence or related to loss of CDKN1C function? by Martin, Nicole, Choufani, Sanaa, Weksberg, Rosanna

Get full text