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  9. Kates, Amy; Snow, Charles C.; Obel, Børge

    Introduction

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    Det Kgl. Bibliotek/Royal Danish Library, 2013

    Published in: Journal of Organization Design, 2 (2013) 3, Seite 1

  12. Bukata, Susan V.; DiGiovanni, Benedict F.; Friedman, Susan M.; Hoyen, Harry; Kates, Amy; Kates, Stephen L.; Mears, Simon C.; Mendelson, Daniel A.; Serna, Fernando H.; Sieber, Frederick E.; Tyler, Wakenda K.

    A Guide to Improving the Care of Patients With Fragility Fractures

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    SAGE Publications, 2011

    Published in: Geriatric Orthopaedic Surgery & Rehabilitation, 2 (2011) 1, Seite 5-37

  14. Olszewski, Amy K.; Kikinis, Zora; Gonzalez, Christie S.; Coman, Ioana L.; Makris, Nikolaos; Gong, Xue; Rathi, Yogesh; Zhu, Anni; Antshel, Kevin M.; Fremont, Wanda; Kubicki, Marek R.; Bouix, Sylvain; Shenton, Martha E.; Kates, Wendy R.

    The social brain network in 22q11.2 deletion syndrome: a diffusion tensor imaging study

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    Springer Science and Business Media LLC, 2017

    Published in: Behavioral and Brain Functions, 13 (2017) 1

  15. Felix Chu; Michael Harbell; Amy Manning-Bog; Alexander Scholz; Ngan Nguyen; Norman Greenberg; William Robinson; Daniel Emerling; Tito Serafini; Wei Cao; Yvonne Leung; Nikhil Vad; Anne Ye; Daniel Santos; Cathrin Czupalla; John Vivian; Carlene Williams; Judevin Sapugay; Shaun Lippow; Chantia Carroll; Lance Kates; Benjamin Haugen; Gary Bolton; Mark Armanini; [...]

    689 ATRC-101 Drives Potent Single-Agent Activity in Mouse Syngeneic Tumor Models via a Novel Cellular Mechanism of Action

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    2020

    Published in: Journal for ImmunoTherapy of Cancer, 8 (2020)

  16. Mlynarski, Elisabeth E.; Xie, Michael; Taylor, Deanne; Sheridan, Molly B.; Guo, Tingwei; Racedo, Silvia E.; McDonald-McGinn, Donna M.; Chow, Eva W. C.; Vorstman, Jacob; Swillen, Ann; Devriendt, Koen; Breckpot, Jeroen; Digilio, Maria Cristina; Marino, Bruno; Dallapiccola, Bruno; Philip, Nicole; Simon, Tony J.; Roberts, Amy E.; Piotrowicz, Małgorzata; Bearden, Carrie E.; Eliez, Stephan; Gothelf, Doron; Coleman, Karlene; Kates, Wendy R.; [...]

    Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome

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    Springer Science and Business Media LLC, 2016

    Published in: Human Genetics, 135 (2016) 3, Seite 273-285

  17. Mlynarski, Elisabeth E.; Sheridan, Molly B.; Xie, Michael; Guo, Tingwei; Racedo, Silvia E.; McDonald-McGinn, Donna M.; Gai, Xiaowu; Chow, Eva W.C.; Vorstman, Jacob; Swillen, Ann; Devriendt, Koen; Breckpot, Jeroen; Digilio, Maria Cristina; Marino, Bruno; Dallapiccola, Bruno; Philip, Nicole; Simon, Tony J.; Roberts, Amy E.; Piotrowicz, Małgorzata; Bearden, Carrie E.; Eliez, Stephan; Gothelf, Doron; Coleman, Karlene; Kates, Wendy R.; [...]

    Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion Syndrome

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    Elsevier BV, 2015

    Published in: The American Journal of Human Genetics, 96 (2015) 5, Seite 753-764

  18. Heldman, Madeleine R.; Kates, Olivia S.; Haydel, Brandy M; Florman, Sander S.; Rana, Meenakshi M.; Chaudhry, Zohra S.; Ramesh, Mayur S.; Safa, Kassem; Kotton, Camille N.; Blumberg, Emily A.; Besharatian, Behdad D.; Tanna, Sajal D.; Ison, Michael G.; Malinis, Maricar; Azar, Marwan M.; Rakita, Robert M.; Morillas, Jose A.; Majeed, Aneela; Sait, Afrah S.; Spaggiari, Mario; Hemmige, Vagish; Mehta, Sapna A.; Neumann, Henry; Badami, Abbasali; [...]

    Healthcare resource use among solid organ transplant recipients hospitalized with COVID‐19

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    Wiley, 2021

    Published in: Clinical Transplantation, 35 (2021) 2

  19. Ge, 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; [...]

    Source‐based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome

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    Wiley, 2024

    Published in: Human Brain Mapping, 45 (2024) 1

  20. Forsyth, Jennifer K; Mennigen, Eva; Lin, Amy; Sun, Daqiang; Vajdi, Ariana; Kushan-Wells, Leila; Ching, Christopher R K; Villalon-Reina, Julio E; Thompson, Paul M; Jonas, Rachel K; Pacheco-Hansen, Laura; 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; [...]

    Prioritizing Genetic Contributors to Cortical Alterations in 22q11.2 Deletion Syndrome Using Imaging Transcriptomics

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    Oxford University Press (OUP), 2021

    Published in: Cerebral Cortex, 31 (2021) 7, Seite 3285-3298