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Wendy R. Kates

Albert Einstein College of Medicine

53H指数
166论文数
8.2K被引数
收录论文 77
发表时间
Unique Functional Neuroimaging Signatures of Genetic Versus Clinical High Risk for Psychosis
err2025-01-01
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errOAAI
errSchleifer, Charles H.; Chang, Sarah E.; Amir, Carolyn M.; O'Hora, Kathleen P.; Fung, Hoki; Kang, Jee Won D.; Kushan-Wells, Leila; Daly, Eileen; Di Fabio, Fabio; Frascarelli, Marianna; Gudbrandsen, Maria; Kates, Wendy R.; Murphy, Declan; Addington, Jean; Anticevic, Alan; Cadenhead, Kristin S.; Cannon, Tyrone D.; Cornblatt, Barbara A.; Keshavan, Matcheri; Mathalon, Daniel H.; Perkins, Diana O.; Stone, William S.; Walker, Elaine; Woods, Scott W.; Uddin, Lucina Q.; Kumar, Kuldeep; Hoftman, Gil D.; Bearden, Carrie E.
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Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome基于源的形态计量学揭示了22 q11.2缺失综合征的结构性脑模式异常
err2024-01-12
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errOAAI
errGe, Ruiyang; Ching, Christopher R. K.; Bassett, Anne S.; Kushan, Leila; Antshel, Kevin M.; van Amelsvoort, Therese; Bakker, Geor; Butcher, Nancy J.; Campbell, Linda E.; Chow, Eva W. C.; Craig, Michael; Crossley, Nicolas A.; Cunningham, Adam; Daly, Eileen; Doherty, Joanne L.; Durdle, Courtney A.; Emanuel, Beverly S.; Fiksinski, Ania; Forsyth, Jennifer K.; Fremont, Wanda; Goodrich-Hunsaker, Naomi J.; Gudbrandsen, Maria; Gur, Raquel E.; Jalbrzikowski, Maria; Kates, Wendy R.; Lin, Amy; Linden, David E. J.; Mccabe, Kathryn L.; McDonald-McGinn, Donna; Moss, Hayley; Murphy, Declan G.; Murphy, Kieran C.; Owen, Michael J.; Villalon-Reina, Julio E.; Repetto, Gabriela M.; Roalf, David R.; Ruparel, Kosha; Schmitt, J. Eric; Schuite-Koops, Sanne; Angkustsiri, Kathleen; Sun, Daqiang; Vajdi, Ariana; van den Bree, Marianne; Vorstman, Jacob; Thompson, Paul M.; Vila-Rodriguez, Fidel; Bearden, Carrie E.
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Brief Report: Sensory Features Associated with Autism After Controlling for ADHD Symptoms
err2023-07-01
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PREAI
errMasters, Ellen C. C.; Antshel, Kevin M. M.; Kates, Wendy R. R.; Russo, Natalie
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Smaller subcortical volumes and enlarged lateral ventricles are associated with higher global functioning in young adults with 22q11.2 deletion syndrome with prodromal symptoms of schizophrenia
err2021-07-01
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PREAI
errHeller, Carina; Weiss, Thomas; del Re, Elisabetta C.; Swago, Sophia; Coman, Ioana L.; Antshel, Kevin M.; Fremont, Wanda; Bouix, Sylvain; Kates, Wendy R.; Kubicki, Marek R.; Kikinis, Zora
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Inter-rater reliability of subthreshold psychotic symptoms in individuals with 22q11.2 deletion syndrome患有22 q11.2缺失综合征的个体的阈下精神病症状的评分者间可靠性
err2021-06-14
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errMoore, Tyler M.; Salzer, Deby; Bearden, Carrie E.; Calkins, Monica E.; Kates, Wendy R.; Kushan, Leila; Gallagher, Robert Sean; Frumer, Dafna Sofrin; Weinberger, Ronnie; McDonald-McGinn, Donna M.; Gur, Raquel E.; Gothelf, Doron
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A normative chart for cognitive development in a genetically selected population在遗传选择的人群中认知发展的规范性图表
err2021-03-29
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errOAAI
errFiksinski, Ania M.; Bearden, Carrie E.; Bassett, Anne S.; Kahn, Rene S.; Zinkstok, Janneke R.; Hooper, Stephen R.; Tempelaar, Wanda; McDonald-McGinn, Donna; Swillen, Ann; Emanue, Beverly; Morrow, Bernice; Gur, Raquel; Chow, Eva; van den Bree, Marianne; Vermeesch, Joris; Warren, Stephen; Owen, Michael; van Amelsvoor, Therese; Eliez, Stephan; Gothelf, Doron; Celso, Arango; Kates, Wendy; Simon, Tony; Murphy, Kieran; Repetto, Gabriela; Sune, Damian Heine; Vicar, Stefano; Cubells, Joseph; Armando, Marco; Philip, Nicole; Campbell, Linda; Garcia-Minaur, Sixto; Schneider, Maude; Shashi, Vandana; Vorstman, Jacob; Breetvelt, Elemi J.
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A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants剖析自闭症异质性的遗传学优先方法: 自闭症风险拷贝数变异的表型比较
err2021-01-01
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errChawner, Samuel J. R. A.; Doherty, Joanne L.; Anney, Richard J. L.; Antshel, Kevin M.; 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.; Gur, Raquel E.; Hanson, Ellen; Jacquemont, Sebastien; Kates, Wendy R.; Kushan, Leila; 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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Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome使用常见的遗传变异来检查22 q11.2缺失综合征的表型表达和风险预测
err2020-11-09
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errDavies, Robert W.; Fiksinski, Ania M.; Breetvelt, Elemi J.; Williams, Nigel M.; Hooper, Stephen R.; Monfeuga, Thomas; Bassett, Anne S.; Owen, Michael J.; Gur, Raquel E.; Morrow, Bernice E.; McDonald-McGinn, Donna M.; Swillen, Ann; Chow, Eva W. C.; van den Bree, Marianne; Emanuel, Beverly S.; Vermeesch, Joris R.; van Amelsvoort, Therese; Arango, Celso; Armando, Marco; Campbell, Linda E.; Cubells, Joseph F.; Eliez, Stephan; Garcia-Minaur, Sixto; Gothelf, Doron; Kates, Wendy R.; Murphy, Kieran C.; Murphy, Clodagh M.; Murphy, Declan G.; Philip, Nicole; Repetto, Gabriela M.; Shashi, Vandana; Simon, Tony J.; Suner, Damian Heine; Vicari, Stefano; Scherer, Stephen W.; Bearden, Carrie E.; Vorstman, Jacob A. S.
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Abnormalities in white matter tracts in the fronto-striatal-thalamic circuit are associated with verbal performance in 22q11.2DS
err2020-10-01
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errHeller, Carina; Steinmann, Saskia; Levitt, James J.; Makris, Nikos; Antshel, Kevin M.; Fremont, Wanda; Coman, Ioana L.; Schweinberger, Stefan R.; Weiss, Thomas; Bouix, Sylvain; Kubicki, Marek R.; Kates, Wendy R.; Kikinis, Zora
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Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness
err2020-07-01
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errChing, Christopher R. K.; Gutman, Boris A.; Sun, Daqiang; Reina, Julio Villalon; Ragothaman, Anjanibhargavi; Isaev, Dmitry; Zavaliangos-Petropulu, Artemis; Lin, Amy; Jonas, Rachel K.; Kushan, Leila; Pacheco-Hansen, Laura; Vajdi, Ariana; Forsyth, Jennifer K.; Jalbrzikowski, Maria; Bakker, Geor; van Amelsvoort, Therese; Antshel, Kevin M.; Fremont, Wanda; Kates, Wendy R.; Campbell, Linda E.; McCabe, Kathryn L.; Craig, Michael C.; Daly, Eileen; Gudbrandsen, Maria; Murphy, Clodagh M.; Murphy, Declan G.; Murphy, Kieran C.; Fiksinski, Ania; Koops, Sanne; Vorstman, Jacob; Crowley, T. Blaine; Emanuel, Beverly S.; Gur, Raquel E.; McDonald-McGinn, Donna M.; Roalf, David R.; Ruparel, Kosha; Schmitt, J. Eric; Zackai, Elaine H.; Durdle, Courtney A.; Goodrich-Hunsaker, Naomi J.; Simon, Tony J.; Bassett, Anne S.; Butcher, Nancy J.; Chow, Eva W. C.; Vila-Rodriguez, Fidel; Cunningham, Adam; Doherty, Joanne; Linden, David E.; Moss, Hayley; Owen, Michael J.; van den Bree, Marianne; Crossley, Nicolas A.; Repetto, Gabriela M.; Thompson, Paul M.; Bearden, Carrie E.
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Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion
err2020-02-03
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errOAAI
errCleynen, Isabelle; Engchuan, Worrawat; Hestand, Matthew S.; Heung, Tracy; Holleman, Aaron M.; Johnston, H. Richard; Monfeuga, Thomas; McDonald-McGinn, Donna M.; Gur, Raquel E.; Morrow, Bernice E.; Swillen, Ann; Vorstman, Jacob A. S.; Bearden, Carrie E.; Chow, Eva W. C.; van den Bree, Marianne; Emanuel, Beverly S.; Vermeesch, Joris R.; Warren, Stephen T.; Owen, Michael J.; Chopra, Pankaj; Cutler, David J.; Duncan, Richard; Kotlar, Alex, V; Mulle, Jennifer G.; Voss, Anna J.; Zwick, Michael E.; Diacou, Alexander; Golden, Aaron; Guo, Tingwei; Lin, Jhih-Rong; Wang, Tao; Zhang, Zhengdong; Zhao, Yingjie; Marshall, Christian; Merico, Daniele; Jin, Andrea; Lilley, Brenna; Salmons, Harold, I; Oanh Tran; Holmans, Peter; Pardinas, Antonio; Walters, James T. R.; Demaerel, Wolfram; Boot, Erik; Butcher, Nancy J.; Costain, Gregory A.; Lowther, Chelsea; Evers, Rens; van Amelsvoort, Therese A. M. J.; van Duin, Esther; Vingerhoets, Claudia; Breckpot, Jeroen; Devriendt, Koen; Vergaelen, Elfi; Vogels, Annick; Crowley, T. Blaine; McGinn, Daniel E.; Moss, Edward M.; Sharkus, Robert J.; Unolt, Marta; Zackai, Elaine H.; Calkins, Monica E.; Gallagher, Robert S.; Gur, Ruben C.; Tang, Sunny X.; Fritsch, Rosemarie; Ornstein, Claudia; Repetto, Gabriela M.; Breetvelt, Elemi; Duijff, Sasja N.; Fiksinski, Ania; Moss, Hayley; Niarchou, Maria; Murphy, Kieran C.; Prasad, Sarah E.; Daly, Eileen M.; Gudbrandsen, Maria; Murphy, Clodagh M.; Murphy, Declan G.; Buzzanca, Antonio; Di Fabio, Fabio; Digilio, Maria C.; Pontillo, Maria; Marino, Bruno; Vicari, Stefano; Coleman, Karlene; Cubells, Joseph F.; Ousley, Opal Y.; Carmel, Miri; Gothelf, Doron; Mekori-Domachevsky, Ehud; Michaelovsky, Elena; Weinberger, Ronnie; Weizman, Abraham; Kushan, Leila; Jalbrzikowski, Maria; Armando, Marco; Eliez, Stephan; Sandini, Corrado; Schneider, Maude; Bena, Frederique Sloan; Antshel, Kevin M.; Fremont, Wanda; Kates, Wendy R.; Belzeaux, Raoul; Busa, Tiffany; Philip, Nicole; Campbell, Linda E.; McCabe, Kathryn L.; Hooper, Stephen R.; Schoch, Kelly; Shashi, Vandana; Simon, Tony J.; Tassone, Flora; Arango, Celso; Fraguas, David; Garcia-Minaur, Sixto; Morey-Canyelles, Jaume; Rosell, Jordi; Suner, Damia H.; Raventos-Simic, Jasna; Epstein, Michael P.; Williams, Nigel M.; Bassett, Anne S.
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Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects
err2020-01-01
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errOAAI
errZhao, Yingjie; Diacou, Alexander; Johnston, H. Richard; Musfee, Fadi I.; McDonald-McGinn, Donna M.; McGinn, Daniel; Crowley, T. Blaine; Repetto, Gabriela M.; Swillen, Ann; Breckpot, Jeroen; Vermeesch, Joris R.; Kates, Wendy R.; Digilio, M. Cristina; Unolt, Marta; Marino, Bruno; Pontillo, Maria; Armando, Marco; Di Fabio, Fabio; Vicari, Stefano; van den Bree, Marianne; Moss, Hayley; Owen, Michael J.; Murphy, Kieran C.; Murphy, Clodagh M.; Murphy, Declan; Schoch, Kelly; Shashi, Vandana; Tassone, Flora; Simon, Tony J.; Shprintzen, Robert J.; Campbell, Linda; Philip, Nicole; Heine-Suner, Damian; Garcia-Minaur, Sixto; Fernandez, Luis; Bearden, Carrie E.; Vingerhoets, Claudia; van Amelsvoort, Therese; Eliez, Stephan; Schneider, Maude; Vorstman, Jacob A. S.; Gothelf, Doron; Zackai, Elaine; Agopian, A. J.; Gur, Raquel E.; Bassett, Anne S.; Emanuel, Beverly S.; Goldmuntz, Elizabeth; Mitchell, Laura E.; Wang, Tao; Morrow, Bernice E.
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Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study
err2019-07-29
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errVillalon-Reina, Julio E.; Martinez, Kenia; Qu, Xiaoping; Ching, Christopher R. K.; Nir, Talia M.; Kothapalli, Deydeep; Corbin, Conor; Sun, Daqiang; Lin, Amy; Forsyth, Jennifer K.; Kushan, Leila; Vajdi, Ariana; Jalbrzikowski, Maria; Hansen, Laura; Jonas, Rachel K.; van Amelsvoort, Therese; Bakker, Geor; Kates, Wendy R.; Antshel, Kevin M.; Fremont, Wanda; Campbell, Linda E.; McCabe, Kathryn L.; Daly, Eileen; Gudbrandsen, Maria; Murphy, Clodagh M.; Murphy, Declan; Craig, Michael; Emanuel, Beverly; McDonald-McGinn, Donna M.; Vorstman, Jacob A. S.; Fiksinski, Ania M.; Koops, Sanne; Ruparel, Kosha; Roalf, David; Gur, Raquel E.; Schmitt, J. Eric; Simon, Tony J.; Goodrich-Hunsaker, Naomi J.; Durdle, Courtney A.; Doherty, Joanne L.; Cunningham, Adam C.; van den Bree, Marianne; Linden, David E. J.; Owen, Michael; Moss, Hayley; Kelly, Sinead; Donohoe, Gary; Murphy, Kieran C.; Arango, Celso; Jahanshad, Neda; Thompson, Paul M.; Bearden, Carrie E.
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Novel Diffusion MRI Measures in 22q Deletion Syndrome: Large-Scale International Studies by the ENIGMA-22q Consortium
err2019-05-01
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PREAI
errVillalon, Julio; Ching, Christopher; Nir, Talia; Jahanshad, Neda; Kothapalli, Deydeep; Sun, Daqiang; Lin, Amy; Forsyth, Jennifer; Kushan, Leila; Vajdi, Ariana; Jalbrzikowski, Maria; van Amelsvoort, Therese; Bakker, Geor; Kates, Wendy R.; Antshel, Kevin M.; Fremont, Wanda; Campbell, Linda; McCabe, Kathryn; Eileen, Daly; Maria, Gudbrandsen; Murphy, Clodagh; Murphy, Declan. G. M.; Craig, Michael C.; Emanuel, Beverly; McDonald-McGinn, Donna; Ruparel, Kosha; Schmitt, Eric; Simon, Tony; Thompson, Paul M.; Bearden, Carrie
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Abnormalities in gray matter microstructure in young adults with 22q11.2 deletion syndrome
err2019-01-01
err7
errOAAI
errKikinis, Zora; Makris, Nikos; Sydnor, Valerie J.; Bouix, Sylvain; Pasternak, Ofer; Coman, Ioana L.; Antshel, Kevin M.; Fremont, Wanda; Kubicki, Marek R.; Shenton, Martha E.; Kates, Wendy R.; Rathi, Yogesh
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A GENETIC FIRST APPROACH TO DISSECTING THE HETEROGENEITY OF AUTISM: PHENOTYPIC COMPARISON OF AUTISM RISK COPY NUMBER VARIANTS
err2019-01-01
err4
PREAI
errChawner, Samuel; Doherty, Joanne; Moss, Hayley; Bearden, Carrie; Chung, Wendy; Curran, Sarah; Hall, Jeremy; Jacquemont, Sebastien; Kates, Wendy; Vorstman, Jacob; Owen, Michael; Van den Bree, Marianne
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Specific differences in temporal binding aspects of the attentional blink in Chromosome 22q11.2 Deletion Syndrome
errCORTEX
IF3.3
err2018-11-01
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errOAAI
errKopec, Justin; Russo, Natalie; Antshel, Kevin M.; Fremont, Wanda; Kates, Wendy R.
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Trajectories of psychiatric diagnoses and medication usage in youth with 22q11.2 deletion syndrome: a 9-year longitudinal study22 q11.2缺失综合征青年的精神病诊断和药物使用轨迹: 一项为期9年的纵向研究
err2018-09-18
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PREAI
errKates, Wendy R.; Mariano, Margaret A.; Antshel, Kevin M.; Chandra, Shanel; Gamble, Hilary; Giordano, Mark; MacMaster, Eric; Mattar, Mirabelle; St Fleur, Diane; Faraone, Stephen V.; Fremont, Wanda P.
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Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size
err2018-06-13
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errSun, Daqiang; Ching, Christopher R. K.; Lin, Amy; Forsyth, Jennifer K.; Kushan, Leila; Vajdi, Ariana; Jalbrzikowski, Maria; Hansen, Laura; Villalon-Reina, Julio E.; Qu, Xiaoping; Jonas, Rachel K.; van Amelsvoort, Therese; Bakker, Geor; Kates, Wendy R.; Antshel, Kevin M.; Fremont, Wanda; Campbell, Linda E.; McCabe, Kathryn L.; Daly, Eileen; Gudbrandsen, Maria; Murphy, Clodagh M.; Murphy, Declan; Craig, Michael; Vorstman, Jacob; Fiksinski, Ania; Koops, Sanne; Ruparel, Kosha; Roalf, David R.; Gur, Raquel E.; Schmitt, J. Eric; Simon, Tony J.; Goodrich-Hunsaker, Naomi J.; Durdle, Courtney A.; Bassett, Anne S.; Chow, Eva W. C.; Butcher, Nancy J.; Vila-Rodriguez, Fidel; Doherty, Joanne; Cunningham, Adam; van den Bree, Marianne B. M.; Linden, David E. J.; Moss, Hayley; Owen, Michael J.; Murphy, Kieran C.; McDonald-McGinn, Donna M.; Emanuel, Beverly; van Erp, Theo G. M.; Turner, Jessica A.; Thompson, Paul M.; Bearden, Carrie E.
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Heterogeneity in Cortical Microstructure is Associated With Cognition
err2018-05-01
err0
PREAI
errKikinis, Zora; Makris, Nikos; Sydnor, Valerie J.; Bouix, Sylvain; Coman, Ioana L.; Antshel, Kevin M.; Fremont, Wanda; Kubicki, Marek; Shenton, Martha; Kates, Wendy; Rathi, Yogesh
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