Jonna Männistö
Vieraileva tutkija
Kliinisen lääketieteen yksikkö, Lääketieteen laitos, Terveystieteiden tiedekunta
jmsaarel@uef.fi
Julkaisut
8/8 kappaletta-
Chromosome 20p11.2 deletions cause congenital hyperinsulinism via the loss of FOXA2 or its regulatory elements
Laver, Thomas W.; Wakeling, Matthew N.; Caswell, Richard C.; Bunce, Benjamin; Yau, Daphne; Männistö, Jonna M.E.; Houghton, Jayne A.L.; Hopkins, Jasmin J.; Weedon, Michael N.; Saraff, Vrinda; Kershaw, Melanie; Honey, Engela M.; Murphy, Nuala; Giri, Dinesh; Nath, Stuart; Tangari Saredo, Ana; Banerjee, Indraneel; Hussain, Khalid; Owens, Nick D.L.; Flanagan, Sarah E.. 2024. European journal of human genetics. 32: 813-818 -
Precision treatment of beta-cell monogenic diabetes: a systematic review
Naylor, Rochelle N; Patel, Kashyap A; Kettunen, Jarno L T; Männistö, Jonna M E; Stoy, Julie; Beltrand, Jacques; Polak, Michel; Vilsbøll, Tina; Greeley, Siri A W; Hattersley, Andrew T; Tuomi, Tiinamaija; ADA/EASD PMDI. 2024. Communications medicine. 4: -
Second international consensus report on gaps and opportunities for the clinical translation of precision diabetes medicine
Tobias, Deirdre K; Merino, Jordi; Ahmad, Abrar; Aiken, Catherine; Benham, Jamie L; Bodhini, Dhanasekaran; Clark, Amy L; Colclough, Kevin; Corcoy, Rosa; Cromer, Sara J; Duan, Daisy; Felton, Jamie L; Francis, Ellen C; Gillard, Pieter; Gingras, Véronique; Gaillard, Romy; Haider, Eram; Hughes, Alice; Ikle, Jennifer M; Jacobsen, Laura M; Kahkoska, Anna R; Kettunen, Jarno L T; Kreienkamp, Raymond J; Lim, Lee-Ling; Männistö, Jonna M E; Massey, Robert; Mclennan, Niamh-Maire; Miller, Rachel G; Morieri, M. 2023. Nature medicine. 29: 2428-2457 -
Increased referrals for congenital hyperinsulinism genetic testing in children with trisomy 21 reflects the high burden of non-genetic risk factors in this group
Hewat, Thomas I; Laver, Thomas W; Houghton, Jayne AL; Männistö, Jonna ME; Alvi, Sabah; Brearey, Stephen P; Cody, Declan; Dastamani, Antonia; De los Santos La Torre, Miguel; Murphy, Nuala; Rami-Merhar, Birgit; Wefers, Birgit; Huopio, Hanna; Banerjee, Indraneel; Johnson, Matthew B; Flanagan, Sarah E. 2022. Pediatric diabetes. 23: 457-461 -
Congenital Hyperinsulinism in Finland : Manifestation, Genetics and Long-term Outcome
Männistö, Jonna. 2021. Publications of the University of Eastern Finland. Dissertations in Health Sciences -
Long-Term Outcome and Treatment in Persistent and Transient Congenital Hyperinsulinism: A Finnish Population-Based Study
Männistö, Jonna ME; Jääskeläinen, Jarmo; Otonkoski, Timo; Huopio, Hanna. 2021. Journal of clinical endocrinology and metabolism. 106: e1542-e1551 -
Clinical and Genetic Characterization of 153 Patients with Persistent or Transient Congenital Hyperinsulinism
Männistö, Jonna; Maria, Maleeha; Raivo, Joose; Kuulasmaa, Teemu; Otonkoski, Timo; Huopio, Hanna; Laakso, Markku. 2020. Journal of clinical endocrinology and metabolism. 105: 1-9 -
Health-Related Quality of Life in Children With Congenital Hyperinsulinism
Männistö, Jonna ME, Jääskeläinen, Jarmo; Huopio, Hanna. 2019. Frontiers in endocrinology. 10: 670