Search Results - "Genetics in Medicine Open"

An evaluation of genetic predisposition to congenital anomalies and pediatric cancer supports KAT6B as a novel neuroblastoma susceptibility gene by Gu, Hyunjung, Yu, Yao, Sisoudiya, Saumya Dushyant, Mishra, Pamela, Li, He, Schraw, Jeremy M., Scheurer, Michael E., Muzny, Donna M., Mitchell, Danielle, Taylor, Olga, Jhangiani, Shalini N., Dugan-Perez, Shannon, Wu, Yifan, Doddapaneni, Harsha, Bhamidipati, Sravya Venkata, Gingras, Marie-Claude, Posey, Jennifer E., Gibbs, Richard A., Huff, Chad D., Plon, Sharon E., Lupo, Philip J., Sabo, Aniko

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Pilot Implementation Study of a Default Genetic Referral Process for Patients with Early-Onset Colorectal Cancer by Lau-Min, Kelsey S., Rochester, Shavon, Grabill, Megan, Long, Jessica M., McKenna, Danielle B., Powers, Jacqueline, Bracy, Danny, Boisseau, Leland, Gabriel, Peter, Oyer, Randall, Domchek, Susan M., Rendle, Katharine A., Nathanson, Katherine L., Katona, Bryson W.

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Genome Sequencing Enhances the Diagnostic Yield and Expands the Genetic Landscape of Male Breast Cancer by Wen, Wen, Zhao, Sen, Jiang, Yiwen, Ou, Chengzhu, Guo, Changyuan, Jia, Ziqi, Li, Jiayi, Huang, Yansong, Xu, Hengyi, Pu, Pengming, Shang, Tongxuan, Cong, Lin, Wang, Xiang, Wu, Nan, Liu, Jiaqi

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Frequency and Reasons that Parents Decline Genetic Testing for Critically Ill Neonates by Callahan, Katharine Press, Mueller, Rebecca, Crew, Karen, Brothers, Kyle, Munson, David, Joffe, Steven, Feudtner, Chris

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Genetic counseling development and milestone in Oman by Al-Kharusi, Khalsa, Van Wyk, Chantel, Al Hinai, Mariya, Al-Fori, Amel, Bruwer, Zandre

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Cancer genetic counseling in Chile: Addressing barriers, confronting challenges, and seizing opportunities in an underserved Latin American Community by Fernández-Ramires, Ricardo, Morales-Pison, Sebastián, Rucatti, Guilherme Gischkow, Echeverría, César, San Martín, Esteban, Cammarata, Francisco, Salas-Burgos, Alexis, Adorno-Farias, Daniela, González-Arriagada, Wilfredo Alejandro, Benavides, Claudio, Espinosa-Parrilla, Yolanda, Zapata, Daniela, Norese, Gabriela, Lázaro, Conxi, González, Sara, Pujana, Miguel Angel, Sullcahuaman, Yasser, Margarit, Sonia

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Large-scale evaluation of outcomes after a genetic diagnosis in children with severe developmental disorders by Copeland, Harriet, Low, Karen J., Wynn, Sarah L., Ahmed, Ayesha, Arthur, Victoria, Balasubramanian, Meena, Bennett, Katya, Berg, Jonathan, Bertoli, Marta, Bryson, Lisa, Bucknall, Catrin, Campbell, Jamie, Chandler, Kate, Chauhan, Jaynee, Clarkson, Amy, Coles, Rachel, Conti, Hector, Costello, Philandra, Coupar, Tessa, Craig, Amy, Dean, John, Dillon, Amy, Dixit, Abhijit, Drew, Kathryn, Eason, Jacqueline, Forzano, Francesca, Foulds, Nicola, Gardham, Alice, Ghali, Neeti, Green, Andrew, Hanna, William, Harrison, Rachel, Hegarty, Mairead, Higgs, Jenny, Holder, Muriel, Irving, Rachel, Jain, Vani, Johnson, Katie, Jolley, Rachel, Jones, Wendy D., Jones, Gabriela, Joss, Shelagh, Kalinauskiene, Ruta, Kanani, Farah, Kavanagh, Karl, Khan, Mahmudur, Khan, Naz, Kivuva, Emma, Lahiri, Nayana, Lakhani, Neeta, Lampe, Anne, Lynch, Sally Ann, Mansour, Sahar, Marsden, Alice, Massey, Hannah, McKee, Shane, Mohammed, Shehla, Naik, Swati, Nesarajah, Mithushanaa, Newbury-Ecob, Ruth, Osborne, Fiona, Parker, Michael J., Patterson, Jenny, Pottinger, Caroline, Prapa, Matina, Prescott, Katrina, Quinn, Shauna, Radley, Jessica A., Robart, Sarah, Ross, Alison, Rosti, Giulia, Sansbury, Francis H., Sarkar, Ajoy, Searle, Claire, Shannon, Nora, Shears, Debbie, Smithson, Sarah, Stewart, Helen, Suri, Mohnish, Tadros, Shereen, Theobald, Rachel, Thomas, Rhian, Tsoulaki, Olga, Vasudevan, Pradeep, Rodriguez, Maribel Verdesoto, Vittery, Emma, Whyte, Sinead, Woods, Emily, Wright, Thomas, Zocche, David, Firth, Helen V., Wright, Caroline F.

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iKNOW—Supporting the counseling of women with hereditary risk of breast and ovarian cancer with digital technologies: A randomized controlled trial by Feufel, Markus A., Speiser, Dorothee, Schüürhuis, Stephen, Neumann, Konrad, Keinert, Marie, Stegen, Steffi, Rauwolf, Gudrun, Heibges, Maren, Westfal, Viola, Besch, Laura, Olbrich, Christine, Klein, Katharina, Witzel, Isabell, Kendel, Friederike

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Casgevy (exagamglogene autotemcel) and Lyfgenia (lovotibeglogene autotemcel) for individuals 12 years and older with sickle cell disease (SCD) and recurrent vaso-occlusive crises (VOC): A therapeutics bulletin of the American College of Medical Genetics and Genomics (ACMG) by Lesmana, Harry, Kim, Sun Young, Corado, Andrés Morales, Poskanzer, Sheri A.

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Developing medical genetics in a low-income country: Unveiling the journey of the Pakistani Society of Medical Genetics and Genomics (PSMG) by Furqan, Aisha, Ahmed, Syed A., Naeem, Rizwan, Ashfaq, Myla

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Promoting international, locally focused, and patient-oriented genetic counseling by Weil, Jon, Alaeddin, Dina, Awwad, Rawan, Chanouha, Nour, Elbassiouny, Batoul, Furqan, Aisha, Jacobs, Michelle F., Kavanaugh, Grace, Neogi, Arpita, Rao, Smita K., Sebastin, Monisha

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The global status of genetic counselors in 2023: What has changed in the past 5 years? by Ormond, Kelly E., Abad, Peter James, MacLeod, Rhona, Nishigaki, Masakazu, Wessels, Tina-Marié

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“A Call To Action”: The need for genetic counseling in Uganda by Adžemović, Tessa, Kabbale, Kisakye Diana, Katagirya, Eric, Mukisa, John, Wayengera, Misaki

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The role of the Latin American Professional Society of Genetic Counseling (SPLAGen): Advancing genetic counseling in Latin America by Diaz Caro, D., Simone, L.

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Rapid genomic testing in critically ill pediatric patients: Genetic counseling lessons from a national program by Boggs, Kirsten, Lynch, Fiona, Ward, Michelle, Bouffler, Sophie E., Ayres, Samantha, Forbes, Robin, Springer, Amanda, de Silva, Michelle G., Lynch, Elly, Gallacher, Lyndon, Davis, Tenielle, Rakonjac, Ana, Stallard, Kirsty, Brett, Gemma R., Stark, Zornitza

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Qatar’s genetic counseling landscape: Current insights and future prospects by Abiib, Sumaya, Khodjet-El-khil, Houssein, El-Akouri, Karen, Bux, Reem Ibrahim, Rezoug, Zoulikha, Abualainin, Wafa, Alkowari, Moza, Musa, Sara Osman, Al Mulla, Mariam, Al Saleh, Rehab, Shahbeck, Noora, Farag, Maria, Ismail, Said I., Al Sulaiman, Reem, Ben-Omran, Tawfeg, Al-Thani, Asma, Al-Shafai, Mashael

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The impact of English-centric training for multilingual genetic counseling practice: A commentary by Altemura, C., Diaz Caro, D., Fife, N., Giacomazzi, V., Sumarroca, M.

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A mixed-methods assessment of the Australasian Society of Genetic Counselors (ASGC) Mentor Program by Canton, Holly, Macintosh, Rebecca, Sweeting, Joanna, Mountain, Helen, Ingles, Jodie, Nisselle, Amy, Turbitt, Erin, McEwen, Alison, Yeates, Laura

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Reflections on my international genetic counseling rotations: Contrasts in practice between India and the United States by Jadeja, Niharika, Rajakumar, Nivedita, Reddy, Neeraja, Ali, Nadia, Lichten, Lauren

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Addressing the need for genetic cancer risk assessment in Mexico: From establishment of a formal program to delivery innovation and expansion by Chávarri-Guerra, Yanin, Rodríguez-Olivares, José Luis, Ramírez-González, Alfredo, Moreno-Mirón, José Manuel, Lagunas-Medina, Alex, Peñafort-Zamora, José Carlos, Arteaga-Vázquez, Jazmin, Quintero-Beuló, Gregorio, Sánchez-Reyes, Roberto, Weitzel, Jeffrey N.

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