Loeys–Dietz syndrome caused by 1q41 deletion including TGFB2 is associated with a neurodevelopmental phenotype

Authors: Fry, Deanna, Groepper, Daniel, MacCarrick, Gretchen, Demo, Erin M., Thomas, Matthew J., Wilkes, Margaret J., Lyons, Michael J., Tucker, Megan E., Steding, Catherine, Fleischer, Julie

Source: American journal of medical genetics.Part A. 188(7):2237-2241

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100153540427.0x000001&indx=1&recIds=ETOCvdc_100153540427.0x000001

Heme and sensory neuropathy: insights from novel mutations in the heme exporter feline leukemia virus subgroup C receptor 1

Authors: Bertino, Francesca, Firestone, Kyra, Bellacchio, Emanuele, Jackson, Kelly E., Asamoah, Alexander, Hersh, Joseph, Fiorito, Veronica, Destefanis, Francesca, Gonser, Rusty, Tucker, Megan E., Altruda, Fiorella, Tolosano, Emanuela, Chiabrando, Deborah

Source: Pain. 160(12):2766-2775

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100174982236.0x000001&indx=1&recIds=ETOCvdc_100174982236.0x000001

Movement of Genetic Counselors from Clinical to Non-clinical Positions: Identifying Driving Forces

Authors: Cohen, Stephanie A., Tucker, Megan E.

Source: Journal of genetic counseling. 27(4):792-799

Availability: http://explore.bl.uk/primo_library/libweb/action/display.do?tabs=detailsTab&gathStatTab=true&ct=display&fn=search&doc=ETOCvdc_100127698913.0x000001&indx=1&recIds=ETOCvdc_100127698913.0x000001

21 - Psychiatric disorders

Authors: Tucker, Megan E.

Source: In Handbook of Clinical Adult Genetics and Genomics 2020:339-352

List of contributors

Authors: Abramson, Ruth K., Addison, Jeffrey, Alsadah, Adnan, Balasubramanyam, Ashok, Bekheirnia, Mir Reza, Bekheirnia, Nasim, Berens, John Christopher, Bergstrom, Katie Lee, Bird, Thomas D., Blazo, Maria, Brunetti-Pierri, Nicola, Burrage, Lindsay, Darilek, Sandra, Dhar, Shweta U., Dietz, Harry C., III, Eble, Tanya N., Esplin, Edward D., Flannery, David, Gabrielsen, J. Scott, Ganesh, Jaya, Garcia, Aixa Gonzalez, Giovanni, Monica, Glinton, Kevin E., Guerrini, Christi J., Hadley, Trevor D., Hause, Jessica, Hipp, Lauren E., Hisama, Fuki M., Huguenard, Sarah, Jones, Krystal M., Lamb, Dolores J., Lazaro-Munoz, Gabriel, Lee, Brendan, Levy, Moise L., MacCarrick, Gretchen, Marom, Ronit, McGuire, Amy L., Mestroni, Luisa, Mody, Avni, Murdock, David R., Murray, Michael F., Nagamani, Sandesh C.S., Peacock, Cynthia, Posey, Jennifer E., Rana, Huma, Rosenfeld, Jill A., Samson, Susan L., Scaglia, Fernando, Small, Aeron M., Taylor, Matthew R.G., Tucker, Megan E., Uhlmann, Wendy R., Van den Veyver, Ignatia B., Vengoechea, Jaime, Weiss, Jennifer, Winograd, Dina, Wiszniewski, Wojciech, Yellapragada, Sarvari, Zakas, Anna, Zhang, Lilei

Source: In Handbook of Clinical Adult Genetics and Genomics 2020:xv-xix

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