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  1. Magee, Audrey [Author]

    The undertaking - [1. publ.]

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    London: Atlantic Books, 2014

  5. Feuillet, Vincent; Semichon, Monique; Restouin, Audrey; Harriague, Julie; Janzen, Julia; Magee, Anthony; Collette, Yves; Bismuth, Georges

    The distinct capacity of Fyn and Lck to phosphorylate Sam68 in T cells is essentially governed by SH3/SH2-catalytic domain linker interactions

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    Springer Science and Business Media LLC, 2002

    Published in: Oncogene, 21 (2002) 47, Seite 7205-7213

  7. Haggarty, Alison; Henshall, Audrey; Grove, Richard; Cowie, Trevor; Foxon, Andrew; McCullagh, Roderick; Jordan, David; Moffat, Brian; Lehane-Magee, Daragh

    Machrie Moor, Arran: recent excavations at two stone circles

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    Society of Antiquaries of Scotland, 1992

    Published in: Proceedings of the Society of Antiquaries of Scotland, 121 (1992), Seite 51-94

  8. Waheed, Abdul; McCloskey, Audrey; Kennedy, Frank; Seraj, Siamak M; Khan, Jaffar; Nama, Noor; Johnson, Omari; Lo, Peter; Magee, Harres; Akbar, Wazir; Ullah, Asad; Cason, Frederick D

    Colorectal Cancer Screening Challenges in the Recent Afghan Refugee Population: A Comprehensive Review Article

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    Springer Science and Business Media LLC, 2022

    Published in: Cureus (2022)

  9. Simpson, Nicholas B.; Shankar-Hari, Manu; Rowan, Kathryn M.; Cecconi, Maurizio; von Dadelszen, Peter; Huning, Emily Y-S.; Magee, Laura A.; Payne, Beth A.; Quinn, Audrey C.; Harrison, David A.

    Maternal Risk Modeling in Critical Care—Development of a Multivariable Risk Prediction Model for Death and Prolonged Intensive Care*

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    Ovid Technologies (Wolters Kluwer Health), 2020

    Published in: Critical Care Medicine, 48 (2020) 5, Seite 663-672

  10. DeLong, Stephanie M.; Graham, Laurie M.; Magee, Erin P.; Treves-Kagan, Sarah; Gray, Christine L.; McClay, Alison M.; Zarnick, Samantha M.; Kupper, Lawrence L.; Macy, Rebecca J.; Ashley, Olivia S.; Pettifor, Audrey; Moracco, Kathryn E.; Martin, Sandra L.

    Starting the Conversation: Are Campus Sexual Assault Policies Related to the Prevalence of Campus Sexual Assault?

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    SAGE Publications, 2018

    Published in: Journal of Interpersonal Violence, 33 (2018) 21, Seite 3315-3343

  11. Magee, Ciara N.; Murakami, Naoka; Borges, Thiago J.; Shimizu, Tetsunosuke; Safa, Kassem; Ohori, Shunsuke; Cai, Songjie; Uffing, Audrey; Azzi, Jamil; Elyaman, Wassim; Charbonnier, Louis-Marie; Liu, Kaifeng; Toprak, Demet; Visner, Gary; Chatila, Talal A.; Siebel, Christian W.; Najafian, Nader; Riella, Leonardo V.

    Notch-1 Inhibition Promotes Immune Regulation in Transplantation Via Regulatory T Cell–Dependent Mechanisms

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    Ovid Technologies (Wolters Kluwer Health), 2019

    Published in: Circulation, 140 (2019) 10, Seite 846-863

  12. Gordon, Christopher T; Xue, Shifeng; Yigit, Gökhan; Filali, Hicham; Chen, Kelan; Rosin, Nadine; Yoshiura, Koh-ichiro; Oufadem, Myriam; Beck, Tamara J; McGowan, Ruth; Magee, Alex C; Altmüller, Janine; Dion, Camille; Thiele, Holger; Gurzau, Alexandra D; Nürnberg, Peter; Meschede, Dieter; Mühlbauer, Wolfgang; Okamoto, Nobuhiko; Varghese, Vinod; Irving, Rachel; Sigaudy, Sabine; Williams, Denise; Ahmed, S Faisal; [...]

    De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development

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    Springer Science and Business Media LLC, 2017

    Published in: Nature Genetics, 49 (2017) 2, Seite 249-255

  13. Banka, Siddharth; Veeramachaneni, Ratna; Reardon, William; Howard, Emma; Bunstone, Sancha; Ragge, Nicola; Parker, Michael J; Crow, Yanick J; Kerr, Bronwyn; Kingston, Helen; Metcalfe, Kay; Chandler, Kate; Magee, Alex; Stewart, Fiona; McConnell, Vivienne P M; Donnelly, Deirdre E; Berland, Siren; Houge, Gunnar; Morton, Jenny E; Oley, Christine; Revencu, Nicole; Park, Soo-Mi; Davies, Sally J; Fry, Andrew E; [...]

    How genetically heterogeneous is Kabuki syndrome?: MLL2 testing in 116 patients, review and analyses of mutation and phenotypic spectrum

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    Springer Science and Business Media LLC, 2012

    Published in: European Journal of Human Genetics, 20 (2012) 4, Seite 381-388

  14. Martin, Hilary C.; Gardner, Eugene J.; Samocha, Kaitlin E.; Kaplanis, Joanna; Akawi, Nadia; Sifrim, Alejandro; Eberhardt, Ruth Y.; Tavares, Ana Lisa Taylor; Neville, Matthew D. C.; Niemi, Mari E. K.; Gallone, Giuseppe; McRae, Jeremy; Borras, Silvia; Clark, Caroline; Dean, John; Miedzybrodzka, Zosia; Ross, Alison; Tennant, Stephen; Dabir, Tabib; Donnelly, Deirdre; Humphreys, Mervyn; Magee, Alex; McConnell, Vivienne; McKee, Shane; [...]

    The contribution of X-linked coding variation to severe developmental disorders

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    Springer Science and Business Media LLC, 2021

    Published in: Nature Communications, 12 (2021) 1

  15. Kaplanis, Joanna; Samocha, Kaitlin E.; Wiel, Laurens; Zhang, Zhancheng; Arvai, Kevin J.; Eberhardt, Ruth Y.; Gallone, Giuseppe; Lelieveld, Stefan H.; Martin, Hilary C.; McRae, Jeremy F.; Short, Patrick J.; Torene, Rebecca I.; de Boer, Elke; Danecek, Petr; Gardner, Eugene J.; Huang, Ni; Lord, Jenny; Martincorena, Iñigo; Pfundt, Rolph; Reijnders, Margot R. F.; Yeung, Alison; Yntema, Helger G.; Borras, Silvia; Clark, Caroline; [...]

    Evidence for 28 genetic disorders discovered by combining healthcare and research data

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    Springer Science and Business Media LLC, 2020

    Published in: Nature, 586 (2020) 7831, Seite 757-762

  16. Blok, Lot Snijders; Rousseau, Justine; Twist, Joanna; Ehresmann, Sophie; Takaku, Motoki; Venselaar, Hanka; Rodan, Lance H.; Nowak, Catherine B.; Douglas, Jessica; Swoboda, Kathryn J.; Steeves, Marcie A.; Sahai, Inderneel; Stumpel, Connie T. R. M.; Stegmann, Alexander P. A.; Wheeler, Patricia; Willing, Marcia; Fiala, Elise; Kochhar, Aaina; Gibson, William T.; Cohen, Ana S. A.; Agbahovbe, Ruky; Innes, A. Micheil; Au, P. Y. Billie; Rankin, Julia; [...]

    Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

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    Springer Science and Business Media LLC, 2019

    Published in: Nature Communications, 10 (2019) 1

  17. Snijders Blok, Lot; Rousseau, Justine; Twist, Joanna; Ehresmann, Sophie; Takaku, Motoki; Venselaar, Hanka; Rodan, Lance H.; Nowak, Catherine B.; Douglas, Jessica; Swoboda, Kathryn J.; Steeves, Marcie A.; Sahai, Inderneel; Stumpel, Connie T. R. M.; Stegmann, Alexander P. A.; Wheeler, Patricia; Willing, Marcia; Fiala, Elise; Kochhar, Aaina; Gibson, William T.; Cohen, Ana S. A.; Agbahovbe, Ruky; Innes, A. Micheil; Au, P. Y. Billie; Rankin, Julia; [...]

    Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

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    Springer Science and Business Media LLC, 2019

    Published in: Nature Communications, 10 (2019) 1

  18. O’Donnell-Luria, Anne H.; Pais, Lynn S.; Faundes, Víctor; Wood, Jordan C.; Sveden, Abigail; Luria, Victor; Abou Jamra, Rami; Accogli, Andrea; Amburgey, Kimberly; Anderlid, Britt Marie; Azzarello-Burri, Silvia; Basinger, Alice A.; Bianchini, Claudia; Bird, Lynne M.; Buchert, Rebecca; Carre, Wilfrid; Ceulemans, Sophia; Charles, Perrine; Cox, Helen; Culliton, Lisa; Currò, Aurora; Demurger, Florence; Dowling, James J.; Duban-Bedu, Benedicte; [...]

    Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

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    Elsevier BV, 2019

    Published in: The American Journal of Human Genetics, 104 (2019) 6, Seite 1210-1222

  19. Snijders Blok, Lot; Rousseau, Justine; Twist, Joanna; Ehresmann, Sophie; Takaku, Motoki; Venselaar, Hanka; Rodan, Lance H.; Nowak, Catherine B.; Douglas, Jessica; Swoboda, Kathryn J.; Steeves, Marcie A.; Sahai, Inderneel; Stumpel, Connie T. R. M.; Stegmann, Alexander P. A.; Wheeler, Patricia; Willing, Marcia; Fiala, Elise; Kochhar, Aaina; Gibson, William T.; Cohen, Ana S. A.; Agbahovbe, Ruky; Innes, A. Micheil; Au, P. Y. Billie; Rankin, Julia; [...]

    CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

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    Springer Science and Business Media LLC, 2018

    Published in: Nature Communications, 9 (2018) 1

  20. Faundes, Víctor; Newman, William G.; Bernardini, Laura; Canham, Natalie; Clayton-Smith, Jill; Dallapiccola, Bruno; Davies, Sally J.; Demos, Michelle K.; Goldman, Amy; Gill, Harinder; Horton, Rachel; Kerr, Bronwyn; Kumar, Dhavendra; Lehman, Anna; McKee, Shane; Morton, Jenny; Parker, Michael J.; Rankin, Julia; Robertson, Lisa; Temple, I. Karen; Banka, Siddharth; Adam, Shelin; du Souich, Christèle; Elliott, Alison M.; [...]

    Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders

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    Elsevier BV, 2018

    Published in: The American Journal of Human Genetics, 102 (2018) 1, Seite 175-187