Noonan syndrome von Roberts, Amy E, Dr, Allanson, Judith E, Prof, Tartaglia, Marco, PhD, Gelb, Bruce D, Prof

Volltext

Genetic Basis for Congenital Heart Disease: Revisited: A Scientific Statement From the American Heart Association von Pierpont, Mary Ella, Brueckner, Martina, Chung, Wendy K., Garg, Vidu, Lacro, Ronald V., McGuire, Amy L., Mital, Seema, Priest, James R., Pu, William T., Roberts, Amy, Ware, Stephanie M., Gelb, Bruce D., Russell, Mark W.

Volltext

De novo mutations in histone-modifying genes in congenital heart disease von Zaidi, Samir, Choi, Murim, Wakimoto, Hiroko, Ma, Lijiang, Jiang, Jianming, Overton, John D., Romano-Adesman, Angela, Bjornson, Robert D., Breitbart, Roger E., Brown, Kerry K., Carriero, Nicholas J., Cheung, Yee Him, Deanfield, John, DePalma, Steve, Fakhro, Khalid A., Glessner, Joseph, Hakonarson, Hakon, Italia, Michael J., Kaltman, Jonathan R., Kaski, Juan, Kim, Richard, Kline, Jennie K., Lee, Teresa, Leipzig, Jeremy, Lopez, Alexander, Mane, Shrikant M., Mitchell, Laura E., Newburger, Jane W., Parfenov, Michael, Pe’er, Itsik, Porter, George, Roberts, Amy E., Sachidanandam, Ravi, Sanders, Stephan J., Seiden, Howard S., State, Mathew W., Subramanian, Sailakshmi, Tikhonova, Irina R., Wang, Wei, Warburton, Dorothy, White, Peter S., Williams, Ismee A., Zhao, Hongyu, Seidman, Jonathan G., Brueckner, Martina, Chung, Wendy K., Gelb, Bruce D., Goldmuntz, Elizabeth, Seidman, Christine E., Lifton, Richard P.

Volltext

The Congenital Heart Disease Genetic Network Study: Cohort description von Hoang, Thanh T, Goldmuntz, Elizabeth, Roberts, Amy E, Chung, Wendy K, Kline, Jennie K, Deanfield, John E, Giardini, Alessandro, Aleman, Adolfo, Gelb, Bruce D, Mac Neal, Meghan, Porter, Jr, George A, Kim, Richard, Brueckner, Martina, Lifton, Richard P, Edman, Sharon, Woyciechowski, Stacy, Mitchell, Laura E, Agopian, A J

Volltext

Short sleep duration, glucose dysregulation and hormonal regulation of appetite in men and women von St-Onge, Marie-Pierre, O'Keeffe, Majella, Roberts, Amy L, RoyChoudhury, Arindam, Laferrère, Blandine

Volltext

The threat of invasive species to IUCN-listed critically endangered species: A systematic review von Dueñas, Manuel-Angel, Hemming, David J., Roberts, Amy, Diaz-Soltero, Hilda

Volltext

Noonan Syndrome: Clinical Features, Diagnosis, and Management Guidelines von ROMANO, Alicia A, ALLANSON, Judith E, DAHLGREN, Jovanna, GELB, Bruce D, HALL, Bryan, PIERPONT, Mary Ella, ROBERTS, Amy E, ROBINSON, Wanda, TAKEMOTO, Clifford M, NOONAN, Jacqueline A

Volltext

The Genetics of Neurodevelopment in Congenital Heart Disease von Patt, Eli, Singhania, Asmita, Roberts, Amy E., Morton, Sarah U.

Volltext

Sleep restriction leads to increased activation of brain regions sensitive to food stimuli von ST-ONGE, Marie-Pierre, MCREYNOLDS, Andrew, TRIVEDI, Zalak B, ROBERTS, Amy L, SY, Melissa, HIRSCH, Joy

Volltext

Phenotypic Manifestations of Arrhythmogenic Cardiomyopathy in Children and Adolescents von DeWitt, Elizabeth S., Chandler, Stephanie F., Hylind, Robyn J., Beausejour Ladouceur, Virginie, Blume, Elizabeth D., VanderPluym, Christina, Powell, Andrew J., Fynn-Thompson, Francis, Roberts, Amy E., Sanders, Stephen P., Bezzerides, Vassilios, Lakdawala, Neal K., MacRae, Calum A., Abrams, Dominic J.

Volltext

Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project von Ceyhan-Birsoy, Ozge, Murry, Jaclyn B., Machini, Kalotina, Lebo, Matthew S., Yu, Timothy W., Fayer, Shawn, Genetti, Casie A., Schwartz, Talia S., Agrawal, Pankaj B., Parad, Richard B., Holm, Ingrid A., McGuire, Amy L., Green, Robert C., Rehm, Heidi L., Beggs, Alan H., Agrawal, Pankaj B., Beggs, Alan H., Betting, Wendi N., Ceyhan-Birsoy, Ozge, Christensen, Kurt D., Dukhovny, Dmitry, Fayer, Shawn, Frankel, Leslie A., Genetti, Casie A., Graham, Chet, Green, Robert C., Guiterrez, Amanda M., Harden, Maegan, Holm, Ingrid A., Krier, Joel B., Lebo, Matthew S., Levy, Harvey L., Lu, Xingquan, Machini, Kalotina, McGuire, Amy L., Murry, Jaclyn B., Naik, Medha, Nguyen, Tiffany T., Parad, Richard B., Peoples, Hayley A., Pereira, Stacey, Petersen, Devan, Ramamurthy, Uma, Ramanathan, Vivek, Rehm, Heidi L., Roberts, Amy, Robinson, Jill O., Roumiantsev, Serguei, Schwartz, Talia S., Truong, Tina K., VanNoy, Grace E., Waisbren, Susan E., Yu, Timothy W.

Volltext

The Anglo-Saxon migration and the formation of the early English gene pool von Gretzinger, Joscha, Sayer, Duncan, Justeau, Pierre, Altena, Eveline, Pala, Maria, Dulias, Katharina, Edwards, Ceiridwen J., Jodoin, Susanne, Lacher, Laura, Sabin, Susanna, Vågene, Åshild J., Haak, Wolfgang, Ebenesersdóttir, S. Sunna, Moore, Kristjan H. S., Radzeviciute, Rita, Schmidt, Kara, Brace, Selina, Bager, Martina Abenhus, Patterson, Nick, Papac, Luka, Broomandkhoshbacht, Nasreen, Callan, Kimberly, Harney, Éadaoin, Iliev, Lora, Lawson, Ann Marie, Michel, Megan, Stewardson, Kristin, Zalzala, Fatma, Rohland, Nadin, Kappelhoff-Beckmann, Stefanie, Both, Frank, Winger, Daniel, Neumann, Daniel, Saalow, Lars, Krabath, Stefan, Beckett, Sophie, Van Twest, Melanie, Faulkner, Neil, Read, Chris, Barton, Tabatha, Caruth, Joanna, Hines, John, Krause-Kyora, Ben, Warnke, Ursula, Schuenemann, Verena J., Barnes, Ian, Dahlström, Hanna, Clausen, Jane Jark, Richardson, Andrew, Popescu, Elizabeth, Dodwell, Natasha, Ladd, Stuart, Phillips, Tom, Mortimer, Richard, Sayer, Faye, Swales, Diana, Stewart, Allison, Powlesland, Dominic, Kenyon, Robert, Ladle, Lilian, Peek, Christina, Grefen-Peters, Silke, Ponce, Paola, Daniels, Robin, Spall, Cecily, Woolcock, Jennifer, Jones, Andy M., Roberts, Amy V., Symmons, Robert, Rawden, Anooshka C., Cooper, Alan, Bos, Kirsten I., Booth, Tom, Schroeder, Hannes, Thomas, Mark G., Helgason, Agnar, Richards, Martin B., Reich, David, Krause, Johannes, Schiffels, Stephan

Volltext

Short sleep duration increases energy intakes but does not change energy expenditure in normal-weight individuals von ST-ONGE, Marie-Pierre, ROBERTS, Amy L, JINYA CHEN, KELLEMAN, Michael, O'KEEFFE, Majella, ROYCHOUDHURY, Arindam, JONES, Peter Jh

Volltext

Interferon inducible X-linked gene CXorf21 may contribute to sexual dimorphism in Systemic Lupus Erythematosus von Odhams, Christopher A., Roberts, Amy L., Vester, Susan K., Duarte, Carolina S. T., Beales, Charlie T., Clarke, Alexander J., Lindinger, Sonja, Daffern, Samuel J., Zito, Antonino, Chen, Lingyan, Jones, Leonardo L., Boteva, Lora, Morris, David L., Small, Kerrin S., Fernando, Michelle M. A., Cunninghame Graham, Deborah S., Vyse, Timothy J.

Volltext

Cardio-facio-cutaneous syndrome: clinical features, diagnosis, and management guidelines von Pierpont, Mary Ella M, Magoulas, Pilar L, Adi, Saleh, Kavamura, Maria Ines, Neri, Giovanni, Noonan, Jacqueline, Pierpont, Elizabeth I, Reinker, Kent, Roberts, Amy E, Shankar, Suma, Sullivan, Joseph, Wolford, Melinda, Conger, Brenda, Santa Cruz, Molly, Rauen, Katherine A

Volltext

De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies von Homsy, Jason, Zaidi, Samir, Shen, Yufeng, Ware, James S., Samocha, Kaitlin E., Karczewski, Konrad J., DePalma, Steven R., McKean, David, Wakimoto, Hiroko, Gorham, Josh, Jin, Sheng Chih, Deanfield, John, Giardini, Alessandro, Porter, George A., Kim, Richard, Bilguvar, Kaya, López-Giráldez, Francesc, Tikhonova, Irina, Mane, Shrikant, Romano-Adesman, Angela, Qi, Hongjian, Vardarajan, Badri, Ma, Lijiang, Daly, Mark, Roberts, Amy E., Russell, Mark W., Mital, Seema, Newburger, Jane W., Gaynor, J. William, Breitbart, Roger E., Iossifov, Ivan, Ronemus, Michael, Sanders, Stephan J., Kaltman, Jonathan R., Seidman, Jonathan G., Brueckner, Martina, Gelb, Bruce D., Goldmuntz, Elizabeth, Lifton, Richard P., Seidman, Christine E., Chung, Wendy K.

Volltext

Insights Into the Pathogenesis of Catecholaminergic Polymorphic Ventricular Tachycardia From Engineered Human Heart Tissue von Park, Sung-Jin, Zhang, Donghui, Qi, Yan, Li, Yifei, Lee, Keel Yong, Bezzerides, Vassilios J, Yang, Pengcheng, Xia, Shutao, Kim, Sean L, Liu, Xujie, Lu, Fujian, Pasqualini, Francesco S, Campbell, Patrick H, Geva, Judith, Roberts, Amy E, Kleber, Andre G, Abrams, Dominic J, Pu, William T, Parker, Kevin Kit

Volltext

Modeling the mitochondrial cardiomyopathy of Barth syndrome with induced pluripotent stem cell and heart-on-chip technologies von Wang, Gang, McCain, Megan L, Yang, Luhan, He, Aibin, Pasqualini, Francesco Silvio, Agarwal, Ashutosh, Yuan, Hongyan, Jiang, Dawei, Zhang, Donghui, Zangi, Lior, Geva, Judith, Roberts, Amy E, Ma, Qing, Ding, Jian, Chen, Jinghai, Wang, Da-Zhi, Li, Kai, Wang, Jiwu, Wanders, Ronald J A, Kulik, Wim, Vaz, Frédéric M, Laflamme, Michael A, Murry, Charles E, Chien, Kenneth R, Kelley, Richard I, Church, George M, Parker, Kevin Kit, Pu, William T

Volltext

Inducible Pluripotent Stem Cell–Derived Cardiomyocytes Reveal Aberrant Extracellular Regulated Kinase 5 and Mitogen-Activated Protein Kinase Kinase 1/2 Signaling Concomitantly Prom... von Jaffré, Fabrice, Miller, Clint L, Schänzer, Anne, Evans, Todd, Roberts, Amy E, Hahn, Andreas, Kontaridis, Maria I

Volltext

Escape from X-inactivation in twins exhibits intra- and inter-individual variability across tissues and is heritable von Zito, Antonino, Roberts, Amy L, Visconti, Alessia, Rossi, Niccolo', Andres-Ejarque, Rosa, Nardone, Stefano, El-Sayed Moustafa, Julia S, Falchi, Mario, Small, Kerrin S

Volltext