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Elísabet Einarsdóttir

kth royal institute of technology

31H指数
140论文数
3.4K被引数
收录论文 58
发表时间
Fetal Pathogenesis of Scoliosis Suggested by Asymmetry of Gene Expression in Paravertebral Muscles脊柱侧凸胎儿期病理机制:椎旁肌肉基因表达不对称性的提示
err2026-09-03
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errOAAI
errTian Cheng; Gamze Yazgeldi Gunaydin; Elisabet Einarsdottir; Sini Ezer; Juha Kere; Shintaro Katayama; Paul Gerdhem
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Genetic Adaptation to Brackish Water and Spawning Season in European Cisco欧洲雅罗鱼对咸淡水和产卵季节的遗传适应
err2025-09-03
err0
errOAAI
errQiaoling Deng; Jake Goodall; Mikaela Bergenius Nord; Ignas Bunikis; Arianna Cocco; Bo Delling; Elisabet Einarsdottir; Julia Heintz; Henrik Lantz; Kerstin Lindblad-Toh; Mai-Britt Mosbech; Remi-Andre Olsen; Stefan Palm; Mats E. Pettersson; Martin Pippel; Lucile Soler; Anti Vasemägi; Olga Vinnere Pettersson; Leif Andersson
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Rare and low-frequency variants in families with otitis media链球菌性中耳炎家庭中的罕见和低频变异
err2025-04-04
err0
PREAI
errSantos-Cortez, Regie Lyn P.; Elling, Christina L.; Gomez, Helen Z.; Einarsdottir, Elisabet; Kere, Juha; Mattila, Petri S.; Hafren, Lena; Ryan, Allen F.
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Pain in idiopathic scoliosis not associated with known genetic variants for pain特发性脊柱侧凸的疼痛与已知的疼痛遗传变异无关
err2025-02-01
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errOAAI
errCheng, Tian; Diarbakerli, Elias; Simony, Ane; Andersen, Mikkel Osterheden; Danielsson, Aina; Kere, Juha; Einarsdottir, Elisabet; Gerdhem, Paul
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Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis
err2024-01-26
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errOAAI
errYu, Hao; Khanshour, Anas M.; Ushiki, Aki; Otomo, Nao; Koike, Yoshinao; Einarsdottir, Elisabet; Fan, Yanhui; Antunes, Lilian; Kidane, Yared H.; Cornelia, Reuel; Sheng, Rory R.; Zhang, Yichi; Pei, Jimin; Grishin, Nick, V; Evers, Bret M.; Cheung, Jason Pui Yin; Herring, John A.; Terao, Chikashi; Song, You-qiang; Gurnett, Christina A.; Gerdhem, Paul; Ikegawa, Shiro; Rios, Jonathan J.; Ahituv, Nadav; Wise, Carol A.
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Long-chain polyphosphates inhibit type I interferon signaling and augment LPS-induced cytokine secretion in human leukocytes长链多磷酸盐抑制人白细胞中I型干扰素信号传导并增加LPS诱导的细胞因子分泌
err2023-05-24
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errOAAI
errPirttiniemi, Anniina; Adeshara, Krishna; Happonen, Natalie; Einarsdottir, Elisabet; Katayama, Shintaro; Salmenkari, Hanne; Horkko, Sohvi; Kere, Juha; Groop, Per-Henrik; Lehto, Markku
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Human endometrial cell-type-specific RNA sequencing provides new insights into the embryo-endometrium interplay人类子宫内膜细胞类型特异性RNA测序为胚胎-子宫内膜相互作用提供了新见解
err2022-10-13
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errOAAI
errKoel, Mariann; Krjutskov, Kaarel; Saare, Merli; Samuel, Kulli; Lubenets, Dmitri; Katayama, Shintaro; Einarsdottir, Elisabet; Vargas, Eva; Sola-Leyva, Alberto; Lalitkumar, Parameswaran Grace; Gemzell-Danielsson, Kristina; Blesa, David; Simon, Carlos; Lanner, Fredrik; Kere, Juha; Salumets, Andres; Altmae, Signe
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Idiopathic scoliosis: a systematic review and meta-analysis of heritability
err2022-06-01
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errOAAI
errCheng, Tian; Einarsdottir, Elisabet; Kere, Juha; Gerdhem, Paul
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Viral infection-related gene upregulation in monocytes in children with signs of β-cell autoimmunity
err2022-04-25
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errOAAI
errValta, Milla; Yoshihara, Masahito; Einarsdottir, Elisabet; Pahkuri, Sirpa; Ezer, Sini; Katayama, Shintaro; Knip, Mikael; Veijola, Riitta; Toppari, Jorma; Ilonen, Jorma; Kere, Juha; Lempainen, Johanna
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Hereditary palmoplantar keratoderma - phenotypes and mutations in 64 patients
err2021-05-21
err9
PREAI
errHarjama, L.; Karvonen, V.; Kettunen, K.; Elomaa, O.; Einarsdottir, E.; Heikkila, H.; Kivirikko, S.; Ellonen, P.; Saarela, J.; Ranki, A.; Kere, J.; Hannula-Jouppi, K.
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Distinct whole-blood transcriptome profile of children with metabolic healthy overweight/obesity compared to metabolic unhealthy overweight/obesity
err2020-11-23
err14
PREAI
errPlaza-Florido, Abel; Altmae, Signe; Esteban, Francisco J.; Cadenas-Sanchez, Cristina; Aguilera, Concepcion M.; Einarsdottir, Elisabet; Katayama, Shintaro; Krjutskov, Kaarel; Kere, Juha; Zaldivar, Frank; Radom-Aizik, Shlomit; Ortega, Francisco B.
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Multi-omic studies on missense PLG variants in families with otitis media
err2020-09-14
err7
errOAAI
errBootpetch, Tori C.; Hafren, Lena; Elling, Christina L.; Baschal, Erin E.; Manichaikul, Ani W.; Pine, Harold S.; Szeremeta, Wasyl; Scholes, Melissa A.; Cass, Stephen P.; Larson, Eric D.; Chan, Kenny H.; Ishaq, Rafaqat; Prager, Jeremy D.; Shaikh, Rehan S.; Gubbels, Samuel P.; Yousaf, Ayesha; Wine, Todd M.; Bamshad, Michael J.; Yoon, Patricia J.; Jenkins, Herman A.; Nickerson, Deborah A.; Streubel, Sven-Olrik; Friedman, Norman R.; Frank, Daniel N.; Einarsdottir, Elisabet; Kere, Juha; Riazuddin, Saima; Daly, Kathleen A.; Leal, Suzanne M.; Ryan, Allen F.; Mattila, Petri S.; Ahmed, Zubair M.; Sale, Michele M.; Chonmaitree, Tasnee; Santos-Cortez, Regie Lyn P.
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Nagashima-type palmoplantar keratosis in Finland caused by a SERPINB7 founder mutation由SERPINB7创始人突变引起的芬兰长岛型掌跖角化病
err2020-08-01
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errHannula-Jouppi, Katariina; Harjama, Liisa; Einarsdottir, Elisabet; Elomaa, Outi; Kettunen, Kaisa; Saarela, Janna; Soronen, Minna; Bouchard, Laura; Lappalainen, Katriina; Heikkila, Hannele; Kivirikko, Sirpa; Seppanen, Mikko R. J.; Kere, Juha; Ranki, Annamari
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Otitis media susceptibility and shifts in the head and neck microbiome due to SPINK5 variants
err2020-07-24
err19
errOAAI
errFrank, Daniel N.; Giese, Arnaud P. J.; Hafren, Lena; Bootpetch, Tori C.; Yarza, Talitha Karisse L.; Steritz, Matthew J.; Pedro, Melquiadesa; Labra, Patrick John; Daly, Kathleen A.; Tantoco, Ma Leah C.; Szeremeta, Wasyl; Reyes-Quintos, Maria Rina T.; Ahankoob, Niaz; Llanes, Erasmo Gonzalo d, V; Pine, Harold S.; Yousaf, Sairah; Ir, Diana; Einarsdottir, Elisabet; de la Cruz, Rhodieleen Anne R.; Lee, Nanette R.; Nonato, Rachelle Marie A.; Robertson, Charles E.; Ong, Kimberly Mae C.; Magno, Jose Pedrito M.; Chiong, Alessandra Nadine E.; Espiritu-Chiong, Ma Carmina; San Agustin, Maria Luz; Cruz, Teresa Luisa G.; Abes, Generoso T.; Bamshad, Michael J.; Cutiongco-de la Paz, Eva Maria; Kere, Juha; Nickerson, Deborah A.; Mohlke, Karen L.; Riazuddin, Saima; Chan, Abner; Mattila, Petri S.; Leal, Suzanne M.; Ryan, Allen F.; Ahmed, Zubair M.; Chonmaitree, Tasnee; Sale, Michele M.; Chiong, Charlotte M.; Santos-Cortez, Regie Lyn P.
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Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma
err2020-01-01
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errHarjama, Liisa; Kettunen, Kaisa; Elomaa, Outi; Einarsdottir, Elisabet; Heikkila, Hannele; Kivirikko, Sirpa; Lappalainen, Katriina; Saarela, Janna; Alby, Caroline; Ranki, Annamari; Kere, Juha; Hadj-Rabia, Smail; Hannula-Jouppi, Katariina
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Novel TMEM173 Mutation and the Role of Disease Modifying Alleles新的TMEM173突变和疾病修饰等位基因的作用
err2019-12-05
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errKeskitalo, Salla; Haapaniemi, Emma; Einarsdottir, Elisabet; Rajamaki, Kristiina; Heikkila, Hannele; Ilander, Mette; Poyhonen, Minna; Morgunova, Ekaterina; Hokynar, Kati; Lagstrom, Sonja; Kivirikko, Sirpa; Mustjoki, Satu; Eklund, Kari; Saarela, Janna; Kere, Juha; Seppanen, Mikko R. J.; Ranki, Annamari; Hannula-Jouppi, Katariina; Varjosalo, Markku
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Gain-of-function CEBPE mutation causes noncanonical autoinflammatory inflammasomopathy
err2019-11-01
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errGoos, Helka; Fogarty, Christopher L.; Sahu, Biswajyoti; Plagnol, Vincent; Rajamaki, Kristiina; Nurmi, Katariina; Liu, Xiaonan; Einarsdottir, Elisabet; Jouppila, Annukka; Pettersson, Tom; Vihinen, Helena; Krjutskov, Kaarel; Saavalainen, Paivi; Jarvinen, Asko; Muurinen, Mari; Greco, Dario; Scala, Giovanni; Curtis, James; Nordstrom, Dan; Flaumenhaft, Robert; Vaarala, Outi; Kovanen, Panu E.; Keskitalo, Salla; Ranki, Annamari; Kere, Juha; Lehto, Markku; Notarangelo, Luigi D.; Nejentsev, Sergey; Eklund, Kari K.; Varjosalo, Markku; Taipale, Jussi; Seppanen, Mikko R. J.
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Acute wheeze-specific gene module shows correlation with vitamin D and asthma medication
err2019-10-16
err11
errOAAI
errKatayama, Shintaro; Hammar, Katarina Stenberg; Krjutskov, Kaarel; Einarsdottir, Elisabet; Hedlin, Gunilla; Kere, Juha; Soderhall, Cilia
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The human long non-coding RNA gene RMRP has pleiotropic effects and regulates cell-cycle progression at G2
err2019-09-24
err24
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errVakkilainen, Svetlana; Skoog, Tiina; Einarsdottir, Elisabet; Middleton, Anna; Pekkinen, Minna; Ohman, Tiina; Katayama, Shintaro; Krjutskov, Kaarel; Kovanen, Panu E.; Varjosalo, Markku; Lindqvist, Arne; Kere, Juha; Makitie, Outi
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Characterization of novel TMEM173 mutation causing a lupus- and SAVI-like phenotype, modified by polymorphisms in TMEM173 and IFIH1
err2019-09-01
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errKeskitalo, S.; Haapaniemi, E.; Einarsdottir, E.; Rajamaki, K.; Saarela, J.; Kere, J.; Seppanen, M.; Ranki, A.; Hannula-Jouppi, K.; Varjosalo, M.
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