Abstract
In the first-ever Undiagnosed Hackathon, nearly 100 experts from 28 countries combined advanced phenotyping and genomic techniques for 48 hours, ultimately providing diagnoses to 40% of the previously undiagnosed families. This inspiring model demonstrates the power of multidisciplinary collaboration and patient partnership in precision diagnostics.
Original language | English |
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Journal | Nature Genetics |
Volume | 56 |
Issue number | 11 |
Pages (from-to) | 2287-2294 |
Number of pages | 8 |
ISSN | 1061-4036 |
DOIs |
|
Publication status | Published - 2024 |
Bibliographical note
Publisher Copyright:© Springer Nature America, Inc. 2024.
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Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon. / 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.
In: Nature Genetics, Vol. 56, No. 11, 2024, p. 2287-2294.Research output: Contribution to journal › Comment/debate › Research › peer-review
}
TY - JOUR
T1 - Pushing the boundaries of rare disease diagnostics with the help of the first Undiagnosed Hackathon
AU - Delgado-Vega, Angelica Maria
AU - Cederroth, Helene
AU - Taylan, Fulya
AU - Ekholm, Katja
AU - Ek, Marlene
AU - Thonberg, Håkan
AU - Jemt, Anders
AU - Nilsson, Daniel
AU - Eisfeldt, Jesper
AU - Bilgrav Saether, Kristine
AU - Höijer, Ida
AU - Akgun-Dogan, Ozlem
AU - Asano, Yui
AU - Barakat, Tahsin Stefan
AU - Batkovskyte, Dominyka
AU - Baynam, Gareth
AU - Bodamer, Olaf
AU - Chetruengchai, Wanna
AU - Corcoran, Pádraic
AU - Couse, Madeline
AU - Danis, Daniel
AU - Demidov, German
AU - Dohi, Eisuke
AU - Erhardsson, Mattias
AU - Fernandez-Luna, Luis
AU - Fujiwara, Toyofumi
AU - Garg, Neha
AU - Giugliani, Roberto
AU - Gonzaga-Jauregui, Claudia
AU - Grigelioniene, Giedre
AU - Groza, Tudor
AU - Gunnarsson, Cecilia
AU - Hammarsjö, Anna
AU - Hammond, Charles Kumi
AU - Hatirnaz Ng, Özden
AU - Hesketh, Sirisha
AU - Hettiarachchi, Dineshani
AU - Johansson Soller, Maria
AU - Kirmani, Umn Ahmed
AU - Kjellberg, Martin
AU - Kvarnung, Malin
AU - Kvlividze, Oleg
AU - Lagerstedt-Robinson, Kristina
AU - Lasko, Paul
AU - Lassmann, Timo
AU - Lau, Lynette Y.S.
AU - Laurie, Steven
AU - Lim, Weng Khong
AU - Liu, Zhandong
AU - Lysenkova Wiklander, Mariya
AU - Makay, Prince
AU - Maiga, Alassane Baneye
AU - Maya-González, Carolina
AU - Meyn, M. Stephen
AU - Neethiraj, Ramprasad
AU - Nigro, Vincenzo
AU - Nordgren, Felix
AU - Nordlund, Jessica
AU - Orrsjö, Sara
AU - Ottosson, Jesper
AU - Ozbek, Ugur
AU - Özdemir, Özkan
AU - Partin, Clyde
AU - Pearce, David A.
AU - Peck, Raquel
AU - Pedersen, Annie
AU - Pettersson, Maria
AU - Pongpanich, Monnat
AU - Posada de la Paz, Manuel
AU - Ramani, Arun
AU - Romero, Juan Andres
AU - Romero, Vanessa I.
AU - Rosenquist, Richard
AU - Saw, Aung Min
AU - Spencer, Matthew
AU - Stattin, Eva Lena
AU - Srichomthong, Chalurmpon
AU - Tapia-Paez, Isabel
AU - Taruscio, Domenica
AU - Taylor, Julie P.
AU - Tkemaladze, Tinatin
AU - Tully, Ian
AU - Tümer, Zeynep
AU - van Zelst-Stams, Wendy A.G.
AU - Verloes, Alain
AU - Västerviga, Emma
AU - Wang, Sailan
AU - Yang, Rachel
AU - Yamamoto, Shinya
AU - Yépez, Vicente A.
AU - Zhang, Qing
AU - Shotelersuk, Vorasuk
AU - Wiafe, Samuel Agyei
AU - Alanay, Yasemin
AU - Botto, Lorenzo D.
AU - Kirmani, Salman
AU - Lumaka, Aimé
AU - Palmer, Elizabeth Emma
AU - Puri, Ratna Dua
AU - Wirta, Valtteri
AU - Lindstrand, Anna
AU - Buske, Orion J.
AU - Cederroth, Mikk
AU - Nordgren, Ann
N1 - Publisher Copyright: © Springer Nature America, Inc. 2024.
PY - 2024
Y1 - 2024
N2 - In the first-ever Undiagnosed Hackathon, nearly 100 experts from 28 countries combined advanced phenotyping and genomic techniques for 48 hours, ultimately providing diagnoses to 40% of the previously undiagnosed families. This inspiring model demonstrates the power of multidisciplinary collaboration and patient partnership in precision diagnostics.
AB - In the first-ever Undiagnosed Hackathon, nearly 100 experts from 28 countries combined advanced phenotyping and genomic techniques for 48 hours, ultimately providing diagnoses to 40% of the previously undiagnosed families. This inspiring model demonstrates the power of multidisciplinary collaboration and patient partnership in precision diagnostics.
U2 - 10.1038/s41588-024-01941-1
DO - 10.1038/s41588-024-01941-1
M3 - Comment/debate
C2 - 39433890
AN - SCOPUS:85208710649
VL - 56
SP - 2287
EP - 2294
JO - Nature Genetics
JF - Nature Genetics
SN - 1061-4036
IS - 11
ER -