Kristiina Tammimies (K Tammimies)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 25

Top Venues

PloS one

Journal of child psychology and psychiatry, and allied disciplines

Nature communications

Molecular genetics & genomic medicine

Karolinska Institutet (PHD)

This page only lists publications with an associated author ORCID identifier.

Education History

Karolinska Institutet Oct 01 2007 - Dec 27 2011

Sweden

PHD :: Biosciences and Nutrition

University of Oulu Sep 01 2002 - Apr 29 2007

Finland

MSC :: Department of Biology

Publications

Abishek Arora, Francesca Mastropasqua, Sven Bölte, Kristiina Tammimies
Urine metabolomic profiles of autism and autistic traits-A twin study. PloS one 19 (9) (2024)
Abishek Arora, Francesca Mastropasqua, Sven Bölte, Kristiina Tammimies
Urine metabolomic profiles of autism and autistic traits-A twin study. PloS one 19 (9) (2024)
Abishek Arora, Francesca Mastropasqua, Sven Bölte, Kristiina Tammimies
Urine metabolomic profiles of autism and autistic traits-A twin study. PloS one 19 (9) (2024)
Ana Maria Portugal, Charlotte Viktorsson, Mark J Taylor, Luke Mason, Kristiina Tammimies, Angelica Ronald, Terje Falck-Ytter
Infants' looking preferences for social versus non-social objects reflect genetic variation. Nature human behaviour (2023)
Francesca Mastropasqua, Marika Oksanen, Cristina Soldini, Shemim Alatar, Abishek Arora, Roberto Ballarino, Maya Molinari, Federico Agostini, Axel Poulet, Michelle Watts, Ielyzaveta Rabkina, Martin Becker, Danyang Li, Britt-Marie Anderlid, Vladislav Ruchkin, Karl Lundin Remnelius, Mohsen Moslem, Yannick Jacob, Anna Falk, Nicola Crosetto, Magda Bienko, Emanuela Santini, Anders Borgkvist, Sven Bölte, Kristiina Tammimies
Deficiency of the Heterogeneous Nuclear Ribonucleoprotein U locus leads to delayed hindbrain neurogenesis. Biology open 12 (10) (2023)
Lina Jonsson, Joanna Martin, Paul Lichtenstein, Patrik K E Magnusson, Sebastian Lundström, Lars Westberg, Kristiina Tammimies
Examining neurodevelopmental problems in 15q11.2 (BP1-BP2) copy number variation carriers at ages 9/12 and 18 in a Swedish twin sample. Molecular genetics & genomic medicine (2023)
Michelle E Watts, Marika Oksanen, Sanna Lejerkrans, Francesca Mastropasqua, Myriam Gorospe, Kristiina Tammimies
Circular RNAs arising from synaptic host genes during human neuronal differentiation are modulated by SFPQ RNA-binding protein. BMC biology 21 (1) (2023)
Ada J S Chan, Worrawat Engchuan, Miriam S Reuter, Zhuozhi Wang, Bhooma Thiruvahindrapuram, Brett Trost, Thomas Nalpathamkalam, Carol Negrijn, Sylvia Lamoureux, Giovanna Pellecchia, Rohan V Patel, Wilson W L Sung, Jeffrey R MacDonald, Jennifer L Howe, Jacob A S Vorstman, Neal Sondheimer, Nicole Takahashi, Judith H Miles, Evdokia Anagnostou, Kristiina Tammimies, Mehdi Zarrei, Daniele Merico, Dimitri J Stavropoulos, Ryan K C Yuen, Bridget A Fernandez, Stephen W Scherer
Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder. Nature communications 13 (1) (2022)
Charlotte Viktorsson, Ana Maria Portugal, Danyang Li, Maja Rudling, Monica Siqueiros Sanchez, Kristiina Tammimies, Mark J Taylor, Angelica Ronald, Terje Falck-Ytter
Preferential looking to eyes versus mouth in early infancy: heritability and link to concurrent and later development. Journal of child psychology and psychiatry, and allied disciplines (2022)
Zhiqiang Sha, Daan van Rooij, Evdokia Anagnostou, Celso Arango, Guillaume Auzias, Marlene Behrmann, Boris C Bernhardt, Sven Bölte, Geraldo F Busatto, Sara Calderoni, Rosa Calvo, Eileen Daly, Christine Deruelle, Meiyu Duan, Fabio Luis de Souza Duran, Sarah Durston, Christine Ecker, Stefan Ehrlich, Damien Fair, Jennifer Fedor, Jacqueline Fitzgerald, Dorothea L Floris, Barbara Franke, Christine Margarete Freitag, Louise Gallagher, David C Glahn, Shlomi Haar, Liesbeth Hoekstra, Neda Jahanshad, Maria Jalbrzikowski, Joost Janssen, Joseph A King, Luisa Lazaro, Beatriz Luna, Jane McGrath, Sarah E Medland, Filippo Muratori, Declan G M Murphy, Janina Neufeld, Kirsten O'Hearn, Bob Oranje, Mara Parellada, Jose C Pariente, Merel C Postema, Karl Lundin Remnelius, Alessandra Retico, Pedro Gomes Penteado Rosa, Katya Rubia, Devon Shook, Kristiina Tammimies, Margot J Taylor, Michela Tosetti, Gregory L Wallace, Fengfeng Zhou, Paul M Thompson, Simon E Fisher, Jan K Buitelaar, Clyde Francks
Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium. Molecular psychiatry 27 (4) (2022)
Danyang Li, Nora Choque Olsson, Martin Becker, Abishek Arora, Hong Jiao, Nina Norgren, Ulf Jonsson, Sven Bölte, Kristiina Tammimies
Rare variants in the outcome of social skills group training for autism. Autism research : official journal of the International Society for Autism Research 15 (3) (2021)
Anna Hellquist, Kristiina Tammimies
Access, utilization, and awareness for clinical genetic testing in autism spectrum disorder in Sweden: A survey study. Autism : the international journal of research and practice 26 (7) (2021)
Ana Maria Portugal, Mark J Taylor, Charlotte Viktorsson, Pär Nyström, Danyang Li, Kristiina Tammimies, Angelica Ronald, Terje Falck-Ytter
Pupil size and pupillary light reflex in early infancy: heritability and link to genetic liability to schizophrenia. Journal of child psychology and psychiatry, and allied disciplines 63 (9) (2021)
Lynnea Myers, Britt-Marie Anderlid, Ann Nordgren, Karl Lundin, Ralf Kuja-Halkola, Kristiina Tammimies, Sven Bölte
Clinical versus automated assessments of morphological variants in twins with and without neurodevelopmental disorders. American journal of medical genetics. Part A 182 (5) (2020)
Danyang Li, Nora Choque-Olsson, Hong Jiao, Nina Norgren, Ulf Jonsson, Sven Bölte, Kristiina Tammimies
The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorder. NPJ genomic medicine 5 (1) (2020)
Evelyn Susanto, Ana Marin Navarro, Leilei Zhou, Anders Sundström, Niek F H N van Bree, Marina Stantic, Mohsen Moslem, Jignesh Tailor, Jonne Rietdijk, Veronica Zubillaga, Jens-Martin Hübner, Holger Weishaupt, Johanna Wolfsberger, Irina Alafuzoff, Ann Nordgren, Thierry Magnaldo, Peter Siesjö, John Inge Johnsen, Marcel Kool, Kristiina Tammimies, Anna Darabi, Fredrik J Swartling, Anna Falk, Margareta T Wilhelm
Modeling SHH-driven medulloblastoma with patient iPS cell-derived neural stem cells. Proceedings of the National Academy of Sciences of the United States of America 117 (33) (2020)
Danyang Li, Nora Choque-Olsson, Hong Jiao, Nina Norgren, Ulf Jonsson, Sven Bölte, Kristiina Tammimies
The influence of common polygenic risk and gene sets on social skills group training response in autism spectrum disorder. NPJ genomic medicine 5 (2020)
Martin Becker, Francesca Mastropasqua, Jan Philipp Reising, Simon Maier, Mai-Lan Ho, Ielyzaveta Rabkina, Danyang Li, Janina Neufeld, Lea Ballenberger, Lynnea Myers, Viveka Moritz, Malin Kele, Josephine Wincent, Charlotte Willfors, Rouslan Sitnikov, Eric Herlenius, Britt-Marie Anderlid, Anna Falk, Sven Bölte, Kristiina Tammimies
Presynaptic dysfunction in CASK-related neurodevelopmental disorders. Translational psychiatry 10 (1) (2020)
Vide Ohlsson Gotby, Olle Söder, Louise Frisén, Eva Serlachius, Sven Bölte, Catarina Almqvist, Henrik Larsson, Paul Lichtenstein, Kristiina Tammimies
Hypogonadotrophic hypogonadism, delayed puberty and risk for neurodevelopmental disorders. Journal of neuroendocrinology 31 (11) (2019)
Lynnea Myers, Moira Blyth, Kamran Moradkhani, Dubravka Hranilović, Sam Polesie, Johan Isaksson, Ann Nordgren, Maja Bucan, Marie Vincent, Sven Bölte, Britt-Marie Anderlid, Kristiina Tammimies
Variable neurodevelopmental and morphological phenotypes of carriers with 12q12 duplications. Molecular genetics & genomic medicine 8 (1) (2019)
Christine Austin, Paul Curtin, Austen Curtin, Chris Gennings, Manish Arora, Kristiina Tammimies, Johan Isaksson, Charlotte Willfors, Sven Bölte
Dynamical properties of elemental metabolism distinguish attention deficit hyperactivity disorder from autism spectrum disorder. Translational psychiatry 9 (1) (2019)
Kristiina Tammimies, Danyang Li, Ielyzaveta Rabkina, Sofia Stamouli, Martin Becker, Veronika Nicolaou, Steve Berggren, Christina Coco, Torbjörn Falkmer, Ulf Jonsson, Nora Choque-Olsson, Sven Bölte
Association between Copy Number Variation and Response to Social Skills Training in Autism Spectrum Disorder. Scientific reports 9 (1) (2019)
L D'Abate, S Walker, Ryan K C Yuen, Kristiina Tammimies, J A Buchanan, R W Davies, B Thiruvahindrapuram, J Wei, J Brian, S E Bryson, K Dobkins, J Howe, R Landa, J Leef, D Messinger, S Ozonoff, I M Smith, W L Stone, Z E Warren, G Young, L Zwaigenbaum, S W Scherer
Predictive impact of rare genomic copy number variations in siblings of individuals with autism spectrum disorders. Nature communications 10 (1) (2019)
Paul Curtin, Christine Austin, Austen Curtin, Chris Gennings, Manish Arora, null null, Kristiina Tammimies, Charlotte Willfors, Steve Berggren, Paige Siper, Dheeraj Rai, Kristin Meyering, Alexander Kolevzon, Josephine Mollon, Anthony S David, Glyn Lewis, Stanley Zammit, Lynne Heilbrun, Raymond F Palmer, Robert O Wright, Sven Bölte, Abraham Reichenberg
Dynamical features in fetal and postnatal zinc-copper metabolic cycles predict the emergence of autism spectrum disorder. Science advances 4 (5) (2018)
N Kalnak, S Stamouli, M Peyrard-Janvid, I Rabkina, M Becker, T Klingberg, J Kere, H Forssberg, Kristiina Tammimies
Enrichment of rare copy number variation in children with developmental language disorder. Clinical genetics 94 (3-4) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Kristiina Tammimies (K Tammimies)