檢索結果 - Hanson, Ellen

A pilot study to improve venipuncture compliance in children and adolescents with Autism Spectrum Disorders 由 Davit, Caroline J., Hundley, Rachel J., Bacic, Janine D., Hanson, Ellen M.

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Genetic Variants of Coagulation Factor XI Show Association with Ischemic Stroke Up to 70 Years of Age 由 Hanson, Ellen, Nilsson, Staffan, Jood, Katarina, Norrving, Bo, Engström, Gunnar, Blomstrand, Christian, Lindgren, Arne, Melander, Olle, Jern, Christina

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Novel ALDH5A1 variants and genotype: Phenotype correlation in SSADH deficiency 由 DiBacco, Melissa L., Pop, Ana, Salomons, Gajja S., Hanson, Ellen, Roullet, Jean-Baptiste, Gibson, K. Michael, Pearl, Phillip L.

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SSADH Deficiency: Review of the Natural History Study 由 Pearl, Phillip L, DiBacco, Melissa L, Papadelis, Christos, Opladen, Thomas, Hanson, Ellen, Roullet, Jean-Baptiste, Gibson, K. Michael

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Language characterization in 16p11.2 deletion and duplication syndromes 由 Kim, So Hyun, Green-Snyder, LeeAnne, Lord, Catherine, Bishop, Somer, Steinman, Kyle J., Bernier, Raphael, Hanson, Ellen, Goin-Kochel, Robin P., Chung, Wendy K.

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Comment on “Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients” 由 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.

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Impacting Development in Infants with Tuberous Sclerosis Complex: Multidisciplinary Research Collaboration 由 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

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Scalp EEG spikes predict impending epilepsy in TSC infants: A longitudinal observational study 由 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

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Characteristics and Predictive Value of Blood Transcriptome Signature in Males with Autism Spectrum Disorders 由 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.

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Psychiatric disorders in children with 16p11.2 deletion and duplication 由 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

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Correction: Psychiatric disorders in children with 16p11.2 deletion and duplication 由 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.

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Influence of Seizures on Early Development in Tuberous Sclerosis Complex 由 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

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Utility of the Autism Observation Scale for Infants in Early Identification of Autism in Tuberous Sclerosis Complex 由 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

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Clinical phenotype of the recurrent 1q21.1 copy-number variant 由 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.

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The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population 由 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.

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A Multi-Site Study of the Clinical Diagnosis of Different Autism Spectrum Disorders 由 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

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Deletions of NRXN1 (Neurexin-1) Predispose to a Wide Spectrum of Developmental Disorders 由 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

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A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders 由 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

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A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants 由 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.

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Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities 由 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.

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