Resultados da pesquisa - Hanson, Ellen
- A mostrar 1 - 20 resultados de 20
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Genetic Variants of Coagulation Factor XI Show Association with Ischemic Stroke Up to 70 Years of Age Por Hanson, Ellen, Nilsson, Staffan, Jood, Katarina, Norrving, Bo, Engström, Gunnar, Blomstrand, Christian, Lindgren, Arne, Melander, Olle, Jern, Christina
Publicado em 2013Text -
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Novel ALDH5A1 variants and genotype: Phenotype correlation in SSADH deficiency Por DiBacco, Melissa L., Pop, Ana, Salomons, Gajja S., Hanson, Ellen, Roullet, Jean-Baptiste, Gibson, K. Michael, Pearl, Phillip L.
Publicado em 2020Text -
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Language characterization in 16p11.2 deletion and duplication syndromes Por Kim, So Hyun, Green-Snyder, LeeAnne, Lord, Catherine, Bishop, Somer, Steinman, Kyle J., Bernier, Raphael, Hanson, Ellen, Goin-Kochel, Robin P., Chung, Wendy K.
Publicado em 2020Text -
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Comment on “Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients” Por Eran, Alal, Graham, Kaitlin R., Vatalaro, Kayla, McCarthy, Jillian, Collins, Christin, Peters, Heather, Brewster, Stephanie J., Hanson, Ellen, Hundley, Rachel, Rappaport, Leonard, Holm, Ingrid A., Kohane, Isaac S., Kunkel, Louis M.
Publicado em 2009Text -
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Impacting Development in Infants with Tuberous Sclerosis Complex: Multidisciplinary Research Collaboration Por Williams, Marian E., Pearson, Deborah A., Capal, Jamie K., Byars, Anna W., Murray, Donna S., Speaks, Autism, Kissinger, Robin, O’Kelley, Sarah E., Hanson, Ellen, Bing, Nicole M., Kent, Bridget, Wu, Joyce Y., Northrup, Hope, Bebin, E. Martina, Sahin, Mustafa, Krueger, Darcy
Publicado em 2019Text -
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Scalp EEG spikes predict impending epilepsy in TSC infants: A longitudinal observational study Por Wu, Joyce Y., Goyal, Monisha, Peters, Jurriaan M., Krueger, Darcy, Sahin, Mustafa, Northrup, Hope, Au, Kit S., O’Kelley, Sarah, Williams, Marian, Pearson, Deborah A., Hanson, Ellen, Byars, Anna W., Krefting, Jessica, Beasley, Mark, Cutter, Gary, Limdi, Nita, Bebin, E. Martina
Publicado em 2019Text -
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Characteristics and Predictive Value of Blood Transcriptome Signature in Males with Autism Spectrum Disorders Por Kong, Sek Won, Collins, Christin D., Shimizu-Motohashi, Yuko, Holm, Ingrid A., Campbell, Malcolm G., Lee, In-Hee, Brewster, Stephanie J., Hanson, Ellen, Harris, Heather K., Lowe, Kathryn R., Saada, Adrianna, Mora, Andrea, Madison, Kimberly, Hundley, Rachel, Egan, Jessica, McCarthy, Jillian, Eran, Ally, Galdzicki, Michal, Rappaport, Leonard, Kunkel, Louis M., Kohane, Isaac S.
Publicado em 2012Text -
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Psychiatric disorders in children with 16p11.2 deletion and duplication Por Niarchou, Maria, Chawner, Samuel J. R. A., Doherty, Joanne L., Maillard, Anne M., Jacquemont, Sébastien, Chung, Wendy K., Green-Snyder, LeeAnne, Bernier, Raphael A., Goin-Kochel, Robin P., Hanson, Ellen, Linden, David E. J., Linden, Stefanie C., Raymond, F. Lucy, Skuse, David, Hall, Jeremy, Owen, Michael J., Bree, Marianne B. M. van den
Publicado em 2019Text -
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Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication Por Niarchou, Maria, Chawner, Samuel J. R. A., Doherty, Joanne L., Maillard, Anne M., Jacquemont, Sébastien, Chung, Wendy K., Green-Snyder, LeeAnne, Bernier, Raphael A., Goin-Kochel, Robin P., Hanson, Ellen, Linden, David E. J., Linden, Stefanie C., Raymond, F. Lucy, Skuse, David, Hall, Jeremy, Owen, Michael J., van den Bree, Marianne B. M.
Publicado em 2019Text -
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Influence of Seizures on Early Development in Tuberous Sclerosis Complex Por Capal, Jamie K, Bernardino-Cuesta, Beatriz, Horn, Paul S., Murray, Donna, Byars, Anna Weber, Bing, Nicole M., Kent, Bridget, Pearson, Deborah A., Sahin, Mustafa, Krueger, Darcy A., O’Kelley, Sarah, Mansour, Rosleen, Williams, Marian E., Hanson, Ellen M., Peters, Jurriaan, Goyal, Monisha, Walsh, Amy, Bruns, Stephanie, Filip-Dhima, Rajna, Mitchell, Terry, Cutter, Gary, Northrup, Hope, Wu, Joyce Y., Bebin, Martina
Publicado em 2017Text -
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Utility of the Autism Observation Scale for Infants in Early Identification of Autism in Tuberous Sclerosis Complex Por Capal, Jamie K, Horn, Paul S., Murray, Donna S., Byars, Anna Weber, Bing, Nicole M., Kent, Bridget, Bucher, Lindsey A., Williams, Marian E., O’Kelley, Sarah, Pearson, Deborah A., Sahin, Mustafa, Krueger, Darcy A., Mansour, Rosleen, Hanson, Ellen M., Peters, Jurriaan, Goyal, Monisha, Walsh, Amy, Bruns, Stephanie, Filip-Dhima, Rajna, Mitchell, Terry, Cutter, Gary, Northrup, Hope, Wu, Joyce Y., Bebin, Martina
Publicado em 2017Text -
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Clinical phenotype of the recurrent 1q21.1 copy-number variant Por Bernier, Raphael, Steinman, Kyle J., Reilly, Beau, Wallace, Arianne Stevens, Sherr, Elliott H., Pojman, Nicholas, Mefford, Heather C., Gerdts, Jennifer, Earl, Rachel, Hanson, Ellen, Goin-Kochel, Robin P., Berry, Leandra, Kanne, Stephen, Snyder, LeeAnne Green, Spence, Sarah, Ramocki, Melissa B., Evans, David W., Spiro, John E., Martin, Christa L., Ledbetter, David H., Chung, Wendy K.
Publicado em 2015Text -
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The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population Por Hanson, Ellen, Bernier, Raphael, Porcheª, Ken, Jackson, Frank I., Goin-Kochel, Robin P., Snyder, LeeAnne Green, Snow, Anne V., Wallace, Arianne Stevens, Campe, Katherine L., Zhang, Yuan, Chen, Qixuan, D’Angelo, Debra, Moreno-De-Luca, Andres, Orr, Patrick T., Boomer, K.B., Evans, David W., Kanne, Stephen, Berry, Leandra, Miller, Fiona K., Olson, Jennifer, Sheer, Elliot, Martin, Christa L., Ledbetter, David H., Spiro, John E., Chung, Wendy K.
Publicado em 2014Text -
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A Multi-Site Study of the Clinical Diagnosis of Different Autism Spectrum Disorders Por Lord, Catherine, Petkova, Eva, Hus, Vanessa, Gan, Weijin, Lu, Feihan, Martin, Donna M., Ousley, Opal, Guy, Lisa, Bernier, Raphael, Gerdts, Jennifer, Algermissen, Molly, Whitaker, Agnes, Sutcliffe, James S., Warren, Zachary, Klin, Ami, Saulnier, Celine, Hanson, Ellen, Hundley, Rachel, Piggot, Judith, Fombonne, Eric, Steiman, Mandy, Miles, Judith, Kanne, Stephen M., Goin-Kochel, Robin P., Peters, Sarika U., Cook, Edwin H., Guter, Stephen, Tjernagel, Jennifer, Green-Snyder, Lee Anne, Bishop, Somer, Esler, Amy, Gotham, Katherine, Luyster, Rhiannon, Miller, Fiona, Olson, Jennifer, Richler, Jennifer, Risi, Susan
Publicado em 2011Text -
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Deletions of NRXN1 (Neurexin-1) Predispose to a Wide Spectrum of Developmental Disorders Por Ching, Michael SL, Shen, Yiping, Tan, Wen-Hann, Jeste, Shafali S, Morrow, Eric M, Chen, Xiaoli, Mukaddes, Nahit M, Yoo, Seung-Yun, Hanson, Ellen, Hundley, Rachel, Austin, Christina, Becker, Ronald E, Berry, Gerard T, Driscoll, Katherine, Engle, Elizabeth C, Friedman, Sandra, Gusella, James F, Hisama, Fuki M, Irons, Mira B, Lafiosca, Tina, LeClair, Elaine, Miller, David T, Neessen, Michael, Picker, Jonathan D, Rappaport, Leonard, Rooney, Cynthia M, Sarco, Dean P, Stoler, Joan M, Walsh, Christopher A, Wolff, Robert R, Zhang, Ting, Nasir, Ramzi H, Wu, Bai-Lin
Publicado em 2010Text -
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A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders Por Zufferey, Flore, Sherr, Elliott H, Beckmann, Noam D, Hanson, Ellen, Maillard, Anne M, Hippolyte, Loyse, Macé, Aurélien, Ferrari, Carina, Kutalik, Zoltán, Andrieux, Joris, Aylward, Elizabeth, Barker, Mandy, Bernier, Raphael, Bouquillon, Sonia, Conus, Philippe, Delobel, Bruno, Faucett, W Andrew, Goin-Kochel, Robin P, Grant, Ellen, Harewood, Louise, Hunter, Jill V, Lebon, Sébastien, Ledbetter, David H, Martin, Christa Lese, Männik, Katrin, Martinet, Danielle, Mukherjee, Pratik, Ramocki, Melissa B, Spence, Sarah J, Steinman, Kyle J, Tjernagel, Jennifer, Spiro, John E, Reymond, Alexandre, Beckmann, Jacques S, Chung, Wendy K, Jacquemont, Sébastien
Publicado em 2012Text -
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A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants Por Chawner, Samuel J.R.A., Doherty, Joanne L., Anney, Richard, Antshel, Kevin M., Kushan, Leila, Bearden, Carrie E., Bernier, Raphael, Chung, Wendy K., Clements, Caitlin C., Curran, Sarah R., Cuturilo, Goran, Fiksinski, Ania M., Gallagher, Louise, Goin-Kochel, Robin P., Kushan, Leila, Gur, Raquel E., Hanson, Ellen, Jacquemont, Sebastien, Kates, Wendy R., Maillard, Anne M., McDonald-McGinn, Donna M., Mihaljevic, Marina, Miller, Judith S, Moss, Hayley, Pejovic-Milovancevic, Milica, Schultz, Robert T., Green-Snyder, LeeAnne, Vorstman, Jacob A., Wenger, Tara L., Hall, Jeremy, Owen, Michael J., van den Bree, Marianne B.M.
Publicado em 2021Text -
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Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities Por D’Angelo, Debra, Lebon, Sébastien, Chen, Qixuan, Martin-Brevet, Sandra, Snyder, LeeAnne Green, Hippolyte, Loyse, Hanson, Ellen, Maillard, Anne M., Faucett, W. Andrew, Macé, Aurélien, Pain, Aurélie, Bernier, Raphael, Chawner, Samuel J. R. A., David, Albert, Andrieux, Joris, Aylward, Elizabeth, Baujat, Genevieve, Caldeira, Ines, Conus, Philippe, Ferrari, Carrina, Forzano, Francesca, Gérard, Marion, Goin-Kochel, Robin P., Grant, Ellen, Hunter, Jill V., Isidor, Bertrand, Jacquette, Aurélia, Jønch, Aia E., Keren, Boris, Lacombe, Didier, Caignec, Cédric Le, Martin, Christa Lese, Männik, Katrin, Metspalu, Andres, Mignot, Cyril, Mukherjee, Pratik, Owen, Michael J., Passeggeri, Marzia, Rooryck-Thambo, Caroline, Rosenfeld, Jill A., Spence, Sarah J., Steinman, Kyle J., Tjernagel, Jennifer, Van Haelst, Mieke, Shen, Yiping, Draganski, Bogdan, Sherr, Elliott H., Ledbetter, David H., van den Bree, Marianne B. M., Beckmann, Jacques S., Spiro, John E., Reymond, Alexandre, Jacquemont, Sébastien, Chung, Wendy K.
Publicado em 2016Text