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Research Interests

Papers共 5 篇Author StatisticsCo-AuthorSimilar Experts

By YearBy Citation主题筛选期刊级别筛选合作者筛选合作机构筛选
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期刊级别
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Pushing the Boundaries of Rare Disease Diagnostics with the Help of the First Undiagnosed Hackathon
Angelica Maria Delgado-Vega,Helene Cederroth,Fulya Taylan,Katja Ekholm,Marlene Ek,Håkan Thonberg,Anders Jemt,Daniel Nilsson,Jesper Eisfeldt,Kristine Bilgrav Saether,Ida Höijer,Ozlem Akgun-Dogan, Yui Asano,Tahsin Stefan Barakat,Dominyka Batkovskyte,Gareth Baynam,Olaf Bodamer,Wanna Chetruengchai,Pádraic Corcoran,Madeline Couse,Daniel Danis,German Demidov,Eisuke Dohi,Mattias Erhardsson, Luis Fernandez-Luna,Toyofumi Fujiwara, Neha Garg,Roberto Giugliani,Claudia Gonzaga-Jauregui,Giedre Grigelioniene,Tudor Groza,Cecilia Gunnarsson,Anna Hammarsjö, Charles Kumi Hammond,Özden Hatirnaz Ng, Sirisha Hesketh,Dineshani Hettiarachchi,Maria Johansson Soller, Umn Ahmed Kirmani, Martin Kjellberg,Malin Kvarnung,Oleg Kvlividze,Kristina Lagerstedt-Robinson,Paul Lasko,Timo Lassmann, Lynette Y S Lau,Steven Laurie,Weng Khong Lim,Zhandong Liu,Mariya Lysenkova Wiklander,Prince Makay, Alassane Baneye Maiga,Carolina Maya-González,M Stephen Meyn,Ramprasad Neethiraj,Vincenzo Nigro, Felix Nordgren,Jessica Nordlund,Sara Orrsjö,Jesper Ottosson,Ugur Ozbek,Özkan Özdemir,Clyde Partin,David A Pearce, Raquel Peck,Annie Pedersen,Maria Pettersson,Monnat Pongpanich,Manuel Posada de la Paz,Arun Ramani, Juan Andres Romero,Vanessa I Romero,Richard Rosenquist, Aung Min Saw, Matthew Spencer,Eva-Lena Stattin,Chalurmpon Srichomthong,Isabel Tapia-Paez,Domenica Taruscio,Julie P Taylor,Tinatin Tkemaladze,Ian Tully,Zeynep Tümer, Wendy A G van Zelst-Stams,Alain Verloes, Emma Västerviga,Sailan Wang, Rachel Yang,Shinya Yamamoto,Vicente A Yépez, Qing Zhang,Vorasuk Shotelersuk,Samuel Agyei Wiafe,Yasemin Alanay,Lorenzo D Botto,Salman Kirmani,Aimé Lumaka,Elizabeth Emma Palmer,Ratna Dua Puri,Valtteri Wirta,Anna Lindstrand,Orion J Buske, Mikk Cederroth,Ann Nordgren
Nature geneticsno. 11 (2024): 2287-2294
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Recommendations for Bioinformatics in Clinical Practice
Ksenia Lavrichenko, Emilie Sofie Engdal, Rasmus L. Marvig,Anders Jemt, Jone Marius Vignes, Henrikki Almusa,Kristine Bilgrav Saether, Eirikur Briem, Eva Caceres, Edda Maria Elvarsdottir,Magnus Halldor Gislason,Maria K. Haanpaa, Viktor Henmyr, Ronja Hotakainen, Eevi Kaasinen, Roan Kanninga, Sofia Khan, Mary Gertrude Lie-Nielsen, Majbritt Busk Madsen, Niklas Mahler,Khurram Maqbool,Ramprasad Neethiraj, Karl Nyren, Minna Paavola, Peter Pruisscher,Ying Sheng,Ashish Kumar Singh, Aashish Srivastava, Thomas K. Stautland, Daniel T. Andreasen,Esmee ten Berk de Boer,Soren Vang,Valtteri Wirta,Frederik Otzen Bagger
biorxiv（2024）
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A community developed pipeline for rare disease diagnostics
Anders Jemt,Ramprasad Neethiraj,Mei Wu, Lauri Mesilaakso,Annick Renevey,Gwenna Breton,Subazini Thankaswamy Kosalai, Sima Rahimi, Emil Bertilsson, Viktor Henmyr,Valtteri Wirta,Henrik Stranneheim
EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 614-614
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Author Statistics

#Papers: 5

#Citation: 0

H-Index: 0

G-Index: 0

Sociability: 5

Diversity: 1

Activity: 2

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