J
Julius Juodakis
Researcher at University of Gothenburg
Publications - 36
Citations - 772
Julius Juodakis is an academic researcher from University of Gothenburg. The author has contributed to research in topics: Biology & Gestational age. The author has an hindex of 9, co-authored 22 publications receiving 460 citations. Previous affiliations of Julius Juodakis include Norwegian Institute of Public Health.
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Journal ArticleDOI
Genetic Associations with Gestational Duration and Spontaneous Preterm Birth
Ge Zhang,Bjarke Feenstra,Jonas Bacelis,Xueping Liu,Lisa M. Muglia,Julius Juodakis,Daniel Miller,Nadia K. Litterman,Pan Pan Jiang,Laura Russell,David A. Hinds,Youna Hu,Matthew T. Weirauch,Xiaoting Chen,Arun R. Chavan,Günter P. Wagner,Günter P. Wagner,Mihaela Pavlicev,Mauris C. Nnamani,Jamie Maziarz,Minna K. Karjalainen,Minna K. Karjalainen,Mika Rämet,Mika Rämet,Verena Sengpiel,Frank Geller,Heather A. Boyd,Aarno Palotie,Aarno Palotie,Aarno Palotie,Allison Momany,Bruce Bedell,Kelli K Ryckman,Johanna M. Huusko,Johanna M. Huusko,Johanna M. Huusko,Carmy Forney,Leah C. Kottyan,Mikko Hallman,Mikko Hallman,Mikko Hallman,Kari Teramo,Ellen A. Nohr,George Davey Smith,Mads Melbye,Mads Melbye,Mads Melbye,Bo Jacobsson,Louis J. Muglia +48 more
TL;DR: It is found that variants at the EBF1, EEFSEC, AGTR2, WNT4, ADCY5, and RAP2C loci were associated with gestational duration and variants atThe EBF 1, EE FSEC, and AG TR2 loci with preterm birth.
Journal ArticleDOI
Genetic Associations with Gestational Duration and Spontaneous Preterm Birth
Ge Zhang,Bjarke Feenstra,Jonas Bacelis,Xueping Liu,Lisa M. Muglia,Julius Juodakis,Daniel Miller,Nadia K. Litterman,Pan Pan Jiang,Laura Russell,David A. Hinds,Youna Hu,Matthew T. Weirauch,Xiaoting Chen,Arun R. Chavan,Günter P. Wagner,Günter P. Wagner,Mihaela Pavlicev,Mihaela Pavlicev,Mauris C. Nnamani,Jamie Maziarz,Minna K. Karjalainen,Minna K. Karjalainen,Mika Rämet,Mika Rämet,Verena Sengpiel,Frank Geller,Heather A. Boyd,Aarno Palotie,Aarno Palotie,Aarno Palotie,Allison Momany,Bruce Bedell,Kelli K Ryckman,Johanna M. Huusko,Johanna M. Huusko,Johanna M. Huusko,Carmy Forney,Leah C. Kottyan,Mikko Hallman,Mikko Hallman,Kari Teramo,Ellen A. Nohr,George Davey Smith,Mads Melbye,Mads Melbye,Bo Jacobsson,Bo Jacobsson,Louis J. Muglia +48 more
TL;DR: A genomewide association study in a discovery set of samples obtained from 43,568 women of European ancestry using gestational duration as a continuous trait and term or preterm (<37 weeks) birth as a dichotomous outcome is performed.
Journal ArticleDOI
Genome-wide association study reveals dynamic role of genetic variation in infant and early childhood growth
Øyvind Helgeland,Øyvind Helgeland,Marc Vaudel,Petur Benedikt Juliusson,Petur Benedikt Juliusson,Petur Benedikt Juliusson,Oddgeir L. Holmen,Julius Juodakis,Jonas Bacelis,Jonas Bacelis,Bo Jacobsson,Bo Jacobsson,Haakon Lindekleiv,Kristian Hveem,Rolv T. Lie,Gun Peggy Knudsen,Camilla Stoltenberg,Camilla Stoltenberg,Per Magnus,Per Magnus,Jørn V. Sagen,Jørn V. Sagen,Anders Molven,Anders Molven,Stefan Johansson,Stefan Johansson,Pål R. Njølstad,Pål R. Njølstad +27 more
TL;DR: Both signals are protein quantitative trait loci for soluble-LEPR and LEP in plasma in adults independent from adult traits mapped to the respective genes, suggesting key roles of common variation in the leptin signaling pathway for healthy infant growth.
Journal ArticleDOI
Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration
Xueping Liu,Dorte Helenius,Dorte Helenius,Line Skotte,Robin N Beaumont,Matthias Wielscher,Frank Geller,Julius Juodakis,Anubha Mahajan,Jonathan P. Bradfield,Frederick T.J. Lin,Suzanne Vogelezang,Mariona Bustamante,Tarunveer S. Ahluwalia,Niina Pitkänen,Carol A. Wang,Jonas Bacelis,Maria Carolina Borges,Ge Zhang,Bruce Bedell,Robert M. Rossi,Robert M. Rossi,Kristin Skogstrand,Kristin Skogstrand,Shouneng Peng,Wesley K. Thompson,Wesley K. Thompson,Vivek Appadurai,Vivek Appadurai,Debbie A Lawlor,Ilkka Kalliala,Ilkka Kalliala,Christine Power,Mark I. McCarthy,Heather A. Boyd,Mary L. Marazita,Hakon Hakonarson,M. Geoffrey Hayes,Denise M. Scholtens,Fernando Rivadeneira,Vincent W. V. Jaddoe,Rebecca K. Vinding,Hans Bisgaard,Bridget A. Knight,Katja Pahkala,Olli T. Raitakari,Øyvind Helgeland,Øyvind Helgeland,Øyvind Helgeland,Stefan Johansson,Stefan Johansson,Pål R. Njølstad,Pål R. Njølstad,João Fadista,João Fadista,Andrew J. Schork,Andrew J. Schork,Ron Nudel,Ron Nudel,Daniel Miller,Xiaoting Chen,Matthew T. Weirauch,Preben Bo Mortensen,Preben Bo Mortensen,Anders D. Børglum,Anders D. Børglum,Merete Nordentoft,Merete Nordentoft,Merete Nordentoft,Ole Mors,Ole Mors,Ke Hao,Kelli K. Ryckman,David M. Hougaard,David M. Hougaard,Leah C. Kottyan,Leah C. Kottyan,Craig E. Pennell,Leo-Pekka Lyytikäinen,Klaus Bønnelykke,Martine Vrijheid,Janine F. Felix,William L. Lowe,Struan F.A. Grant,Elina Hyppönen,Elina Hyppönen,Bo Jacobsson,Bo Jacobsson,Marjo-Riitta Järvelin,Marjo-Riitta Järvelin,Louis J. Muglia,Louis J. Muglia,Louis J. Muglia,Jeffrey C. Murray,Rachel M. Freathy,Thomas Werge,Thomas Werge,Thomas Werge,Mads Melbye,Mads Melbye,Mads Melbye,Alfonso Buil,Alfonso Buil,Bjarke Feenstra +103 more
TL;DR: A fetal genome-wide association meta-analysis is performed and it is found that a locus on chromosome 2q13 is associated with pregnancy duration and further show that the lead SNP rs7594852 changes the binding properties of transcriptional repressor HIC1.
Journal ArticleDOI
The genetic architecture of sporadic and multiple consecutive miscarriage.
Triin Laisk,Ana Luiza Gonçalves Soares,Teresa Ferreira,Jodie N. Painter,Jenny C Censin,Samantha Laber,Jonas Bacelis,Chia-Yen Chen,Chia-Yen Chen,Maarja Lepamets,Kuang Lin,Siyang Liu,Iona Y Millwood,Iona Y Millwood,Avinash Ramu,J Southcombe,Marianne Andersen,Ling Yang,Ling Yang,Christian M. Becker,Anders D. Børglum,Anders D. Børglum,Scott D. Gordon,Jonas Bybjerg-Grauholm,Jonas Bybjerg-Grauholm,Øyvind Helgeland,Øyvind Helgeland,David M. Hougaard,David M. Hougaard,Xin Jin,Stefan Johansson,Stefan Johansson,Julius Juodakis,Christiana Kartsonaki,Christiana Kartsonaki,Viktorija Kukushkina,Penelope A. Lind,Andres Metspalu,Grant W. Montgomery,Andrew P. Morris,Andrew P. Morris,Andrew P. Morris,Ole Mors,Ole Mors,Preben Bo Mortensen,Preben Bo Mortensen,Pål R. Njølstad,Pål R. Njølstad,Merete Nordentoft,Merete Nordentoft,Dale R. Nyholt,Margaret F. Lippincott,Stephanie B. Seminara,Andres Salumets,Harold Snieder,Krina T. Zondervan,Thomas Werge,Thomas Werge,Thomas Werge,Zhengming Chen,Donald F. Conrad,Bo Jacobsson,Bo Jacobsson,Liming Li,Nicholas G. Martin,Benjamin M. Neale,Benjamin M. Neale,Rasmus Nielsen,Rasmus Nielsen,Robin G Walters,Robin G Walters,Ingrid Granne,Sarah E. Medland,Reedik Mägi,Debbie A Lawlor,Cecilia M. Lindgren,Cecilia M. Lindgren +76 more
TL;DR: The results show that miscarriage etiopathogenesis is partly driven by genetic variation potentially related to placental biology, and illustrate the utility of large-scale biobank data for understanding this pregnancy complication.