Family History and Warning Symptoms Precede Sudden Cardiac Death in Arrhythmogenic Right Ventricular Cardiomyopathy (from a Nationwide Study in Sweden)

Authors: Delgado-Vega, Angelica Maria, Kommata, Varvara, Svennblad, Bodil, Wisten, Aase, Hagström, Emil, Stattin, Eva-Lena

Source: In The American Journal of Cardiology 1 September 2022 178:124-130

Occurrence of cancer in Marfan syndrome: Report of two patients with neuroblastoma and review of the literature.

Authors: Maya‐González, Carolina¹, carolina.maya.gonzalez@ki.se, Delgado‐Vega, Angelica Maria^1,2, Taylan, Fulya^1,2, Lagerstedt Robinson, Kristina^1,2, Hansson, Lina³, Pal, Niklas⁴, Fagman, Henrik^5,6, Puls, Florian⁶, Wessman, Sandra^7,8, Stenman, Jakob⁹, Georgantzi, Kleopatra¹⁰, Fransson, Susanne^5,11, Díaz De Ståhl, Teresita^7,8, Ek, Torben¹², Palmer, Ruth¹³, Tesi, Bianca^1,2,14, Kogner, Per¹⁰, Martinsson, Tommy^5,11, Nordgren, Ann^1,2,5,11, ann.nordgren@ki.se

Source: American Journal of Medical Genetics. Part A; Dec2024, Vol. 194 Issue 12, p1-8, 8p

Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon

Authors: Delgado-Vega, Angelica Maria, Cederroth, Helene, Taylan, Fulya, Ekholm, Katja, Ek, Marlene, Thonberg, Håkan, Jemt, Anders, Nilsson, Daniel, Eisfeldt, Jesper, Bilgrav Saether, Kristine, Höijer, Ida, Akgun-Dogan, Ozlem, Asano, Yui, Barakat, Tahsin Stefan, Batkovskyte, Dominyka, Baynam, Gareth, Bodamer, Olaf, Chetruengchai, Wanna, Corcoran, Pádraic, Couse, Madeline, Danis, Daniel, Demidov, German, Dohi, Eisuke, Erhardsson, Mattias, Fernandez-Luna, Luis, Fujiwara, Toyofumi, Garg, Neha, Giugliani, Roberto, Gonzaga-Jauregui, Claudia, Grigelioniene, Giedre, Groza, Tudor, Gunnarsson, Cecilia, Hammarsjö, Anna, Hammond, Charles Kumi, Hatirnaz Ng, Özden, Hesketh, Sirisha, Hettiarachchi, Dineshani, Johansson Soller, Maria, Kirmani, Umn Ahmed, Kjellberg, Martin, Kvarnung, Malin, Kvlividze, Oleg, Lagerstedt-Robinson, Kristina, Lasko, Paul, Lassmann, Timo, Lau, Lynette Y. S., Laurie, Steven, Lim, Weng Khong, Liu, Zhandong, Lysenkova Wiklander, Mariya, Makay, Prince, Maiga, Alassane Baneye, Maya-González, Carolina, Meyn, M. Stephen, Neethiraj, Ramprasad, Nigro, Vincenzo, Nordgren, Felix, Nordlund, Jessica, Orrsjö, Sara, Ottosson, Jesper, Ozbek, Ugur, Özdemir, Özkan, Partin, Clyde, Pearce, David A., Peck, Raquel, Pedersen, Annie, Pettersson, Maria, Pongpanich, Monnat, Posada de la Paz, Manuel, Ramani, Arun, Romero, Juan Andres, Romero, Vanessa I., Rosenquist, Richard, Saw, Aung Min, Spencer, Matthew, Stattin, Eva-Lena, Srichomthong, Chalurmpon, Tapia-Paez, Isabel, Taruscio, Domenica, Taylor, Julie P., Tkemaladze, Tinatin, Tully, Ian, Tümer, Zeynep, van Zelst-Stams, Wendy A. G., Verloes, Alain, Västerviga, Emma, Wang, Sailan, Yang, Rachel, Yamamoto, Shinya, Yépez, Vicente A., Zhang, Qing, Shotelersuk, Vorasuk, Wiafe, Samuel Agyei, Alanay, Yasemin, Botto, Lorenzo D., Kirmani, Salman, Lumaka, Aimé, Palmer, Elizabeth Emma, Puri, Ratna Dua, Wirta, Valtteri, Lindstrand, Anna, Buske, Orion J., Cederroth, Mikk, Nordgren, Ann

Source: Nature Genetics; November 2024, Vol. 56 Issue: 11 p2287-2294, 8p

Equity in action: The Diagnostic Working Group of The Undiagnosed Diseases Network International.

Authors: Palmer, Elizabeth Emma, Cederroth, Helene, Cederroth, Mikk, Delgado-Vega, Angelica Maria, Roberts, Natalie, Taylan, Fulya, Nordgren, Ann, Botto, Lorenzo D.

Source: NPJ Genomic Medicine; 7/5/2024, Vol. 9 Issue 1, p1-7, 7p

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