日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Long-read genome sequencing enhances diagnostics of pediatric neurological disorders

长读长基因组测序可提高儿童神经系统疾病的诊断率。

Ek, Marlene; Kvarnung, Malin; Ten Berk de Boer, Esmee; La Fleur, Linnéa; Ljöstad, Lena; Lyander, Anna; Faergeman, Søren Lejsted; Drue, Simon Opstrup; Thonberg, Håkan; Nordgren, Ann; Soller, Maria Johansson; Wirta, Valtteri; Eisfeldt, Jesper; Lindstrand, Anna

The genomic medicine center Karolinska 10-year report on genome sequencing for rare diseases and a strategy for stepwise clinical implementation

卡罗林斯卡基因组医学中心关于罕见病基因组测序的十年报告及分阶段临床实施策略

Lindstrand, Anna; Lagerstedt-Robinson, Kristina; Jemt, Anders; Kvarnung, Malin; Ygberg, Sofia; Vonlanthen, Sofie; Oscarson, Mikael; Nilsson, Daniel; Lesko, Nicole; Mantero, Angelo Salazar; Anderlid, Britt-Marie; Arnell, Henrik; Arthur, Cecilia; Bajalica-Lagercrantz, Svetlana; Barbaro, Michela; Bergman, Peter; Björck, Erik; Picard, Oda Blomqvist; Bruhn, Helene; Carlsten, Jonas; Correia, Sandrina P; De Geer, Karl; Delgado Vega, Angelica M; Ehn, Emma; Eisfeldt, Jesper; Ek, Marlene; Elvers, Ingegerd; Engvall, Martin; Freyer, Christoph; Frisk, Sofia; Graff, Caroline; Grigelioniené, Giedré; Gustafsson, Peter; Hammarsjö, Anna; Helgadottir, Hafdis T; Hellström Pigg, Maritta; Henry, Olivia J; Hägglund, Moa; Iwarsson, Erik; Janvid, Vincent; Soller, Maria Johansson; Sundin, Leif; Kuchinskaya, Ekaterina; Kämpe, Anders; Leinfelt, Anna; Liedén, Agne; Lindelöf, Hillevi; Lyander, Anna; Malmgren, Helena; Mannila, Maria; Marits, Per; Naess, Karin; Neethiraj, Ramprasad; Nyren, Karl; Pappas, Christoforos; Paucar, Martin; Pekkola Pacheco, Nadja; Peña Perez, Lucia; Pettersson, Maria; Pruisscher, Peter; Rasi, Chiara; Renevey, Annick; Rössner, Sophia; Sahlin, Ellika; Stenund, Erik; Stödberg, Tommy; Sundin, Mikael; Svärd, Karl; Tesi, Bianca; Tham, Emma; Thonberg, Håkan; Töhönen, Virpi; Ueberschär, Malin; Wallander, Karin; Westenius, Eini; Winberg, Johanna; Winblad, Nerges; Wincent, Josephine; Winerdal, Malin; Wredenberg, Anna; Zetterlund, Anna; Zetterström, Rolf H; Öfverholm, Ingegerd; Nordgren, Ann; Stranneheim, Henrik; Wirta, Valtteri; Wedell, Anna

The novel ITPR1 p.Phe2566Ser variant impairs IP(3)R1-mediated Ca(2+) release and is associated with ataxia and miosis

新型ITPR1 p.Phe2566Ser变异体损害IP(3)R1介导的Ca(2+)释放,并与共济失调和瞳孔缩小有关。

Wincent, Josephine; Zhang, Songbai; Nolan, Andrew; Kanatani, Shigeaki; Nordin, Frida; Kvarnung, Malin; Uhlén, Per; Paucar, Martin; Eidhof, Ilse

Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition.

SMARCA1 中的致病变异会导致 X 连锁神经发育障碍,该障碍受 NURF 复合物组成调节。

Mirzaa Ghayda M, Yan Keqin, Relator Raissa, Levesque Mathieu, Jayasinghe Pranisha, Timpano Sara, Yalcin Binnaz, Collins Stephan, Ziegler Alban, Pao Emily, Oyama Nora, Brischoux-Boucher Elise, Piard Juliette, Monaghan Kristin G, Guillen Sacoto Maria J, Dobyns William B, Park Kristen L, Fernández-Mayoralas Daniel Martin, Fernández-Jaén Alberto, Jayakar Parul, Palomares-Bralo María, Santos-Simarro Fernando, Brusco Alfredo, Antona Vincenzo, Giorgio Elisa, Kvarnung Malin, Isidor Bertrand, Conrad Solène, Cogné Benjamin, Deb Wallid, Stuurman Kyra E, Štěrbová Katalin, Smal Noor, Weckhuysen Sarah, Oegema Renske, Innes A Micheil, Koboldt Daniel C, Ben-Omran Tawfeg, Yeh Rebecca C, Kruer Michael C, Bakhtiari Somayeh, Papavasiliou Antigone, Moutton Sébastien, Nambot Sophie, Chanprasert Sirisak, Paolucci Sarah A, Miller Kait, Burton Barbara, Kim Katherine, O'Heir Emily, Bruwer Zandre, Donald Kirsten A, Kleefstra Tjitske, Goldstein Amy, Angle Brad, Bontempo Kelly, Miny Peter, Joset Pascal, Demurger Florence, Hobson Emma, Pang Lewis, Carpenter Lori, Li Dong, Bonneau Dominique, Sadikovic Bekim, Picketts David J

Identification of biallelic POLA2 variants in two families with an autosomal recessive telomere biology disorder

在两个患有常染色体隐性端粒生物学疾病的家族中鉴定出双等位基因POLA2变异。

Kvarnung, Malin; Pettersson, Maria; Chun-On, Pattra; Rafati, Maryam; McReynolds, Lisa J; Norberg, Anna; Moura, Pedro Luis; Pesonen, Ida; Chaireti, Roza; Grönros Söderholm, Boa; Burlin, Julia; Rydén, Jenny; Lindberg, Eva Hellström; Giri, Neelam; Savage, Sharon A; Agarwal, Suneet; Nordgren, Ann; Tesi, Bianca

Genome sequencing in a cohort of 32 fetuses with genetic skeletal disorders

对32例患有遗传性骨骼疾病的胎儿进行基因组测序

Lindelöf, Hillevi; Hammarsjö, Anna; Voss, Ulrika; Gaetana Piticchio, Serena; Conner, Peter; Papadogiannakis, Nikos; Batkovskyte, Dominyka; Orellana, Laura; Kvarnung, Malin; Malmgren, Helena; Lagerstedt Robinson, Kristina; Nordgren, Ann; Lindstrand, Anna; Nishimura, Gen; Grigelioniene, Giedre

Diagnostic yield of 1000 trio analyses with exome and genome sequencing in a clinical setting

在临床环境下,采用外显子组和基因组测序对1000例三联体分析进行诊断的产出率

Malmgren, Helena; Kvarnung, Malin; Gustafsson, Peter; Anderlid, Britt-Marie; Arthur, Cecilia; Carlsten, Jonas; De Geer, Karl; Ehn, Emma; Grigelioniené, Giedre; Hammarsjö, Anna; Helgadottir, Hafdis T; Hellström-Pigg, Maritta; Iwarsson, Erik; Kuchinskaya, Ekaterina; Lindelöf, Hillevi; Mannila, Maria; Nilsson, Daniel; Pettersson, Maria; Rudd, Eva; Sahlin, Ellika; Tesi, Bianca; Tham, Emma; Thonberg, Håkan; Westenius, Eini; Winberg, Johanna; Winerdal, Max; Nordenskjöld, Magnus; Johansson-Soller, Maria; Wirta, Valtteri; Nordgren, Ann; Lindstrand, Anna; Lagerstedt-Robinson, Kristina

The value of age of onset and family history as predictors of molecular diagnosis in a Swedish cohort of inherited retinal disease.

发病年龄和家族史作为瑞典遗传性视网膜疾病队列分子诊断预测指标的价值

De Geer Karl, Löfgren Stefan, Lindstrand Anna, Kvarnung Malin, Björck Erik

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

借助首届“未确诊疾病黑客马拉松”,突破罕见病诊断的界限

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

A Novel Type of Autosomal Dominant Episodic Nystagmus Segregating with a Variant in the FRMD5 Gene

一种新型常染色体显性遗传性发作性眼球震颤,与FRMD5基因变异相关

Hammar, Björn; Paulsson, Sofia; Helgadottir, Hafdis T; Albinsson, John; Naumovska, Magdalena; Sheikh, Rafi; Kvarnung, Malin