ANNI SAARELA
Clinical Lecturer
Contact info
Organization
School of Medicine, Institute of Clinical Medicine
anni.saarela@kuh.fi
Phone
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Publications
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Järvelä, Irma; Määttä, Tuomo; Acharya, Anushree; Leppälä, Juha; Jhangiani, Shalini N; Arvio, Maria; Siren, Auli; Kankuri-Tammilehto, Minna; Kokkonen, Hannaleena; Palomäki, Maarit; Varilo, Teppo; Fang, Mary; Hadley, Trevor D; Jolly, Angad; Linnankivi, Tarja; Paetau, Ritva; Saarela, Anni; Kälviäinen, Reetta; Olme, Jan; Nouel-Saied, Liz M et al.. 2021. Exome sequencing reveals predominantly de novo variants in disorders with intellectual disability (ID) in the founder population of Finland Human genetics 140 7: 1011-1029. 2021
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Koko, Mahmoud; Krause, Roland; Sander, Thomas; Bobbili, Dheeraj Reddy; Nothnagel, Michael; May, Patrick; Lerche, Holger; Epi25 Collaborative [incl. Kälviäinen, Reetta; Auvinen, Pia; Saarela, Anni]. 2021. Distinct gene-set burden patterns underlie common generalized and focal epilepsies EBioMedicine 72: 103588. 2021
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Niestroj, Lisa-Marie; Perez-Palma, Eduardo; Howrigan, Daniel P; Zhou, Yadi; Cheng, Feixiong; Saarentaus, Elmo; Nürnberg, Peter; Stevelink, Remi; Daly, Mark J; Palotie, Aarno; Lal, Dennis; Epi25 Collaborative (incl. Kälviäinen, Reetta; Auvinen, Pia; Saarela, Anni). 2020. Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects Brain 143 7: 2106-2118. 2020
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Leu, Costin; Stevelink, Remi; Smith, Alexander W; Goleva, Slavina B; Kanai, Masahiro; Ferguson, Lisa; Campbell, Ciaran; Kamatani, Yoichiro; Okada, Yukinori; Sisodiya, Sanjay M; Cavalleri, Gianpiero L; Koeleman, Bobby PC; Lerche, Holger; Jehi, Lara; Davis, Lea K; Najm, Imad M; Palotie, Aarno; Epi25 Consortium (incl. Kälviäinen, Reetta; Auvinen, Pia; Saarela, Anni). 2019. Polygenic burden in focal and generalized epilepsies Brain 142 11: 3473-3481. 2019