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Annamari Tuulio-Henriksson

Annamari Tuulio-Henriksson

D-Index & Metrics

Social Sciences and Humanities

D-Index
59
Citations
16906
World Ranking
1544
National Ranking
15

Overview

Annamari Tuulio-Henriksson is affiliated with the University of Helsinki in Finland. Their research primarily spans the field of Medicine, with a specialized focus on Psychiatry and Mental Health, Genetics, Neurology, Pediatrics, Perinatology and Child Health, and Clinical Psychology.

The scientist's work frequently addresses topics such as Schizophrenia Research and Treatment, Long-Term Effects of COVID-19, Genomics and Rare Diseases, Genetic Associations and Epidemiology, Infant Development and Preterm Care, Intensive Care Unit Cognitive Disorders, and Child and Adolescent Psychosocial and Emotional Development.

Their recent scientific publications include the following papers:

  • Long-term cognitive functioning is impaired in ICU-treated COVID-19 patients: a comprehensive controlled neuropsychological study, 2022, Critical Care
  • Psychotic-like experiences of young adults in the general population predict mental disorders, 2022, Psychiatry Research
  • The impact of rare protein coding genetic variation on adult cognitive function, 2023, Nature Genetics
  • Incidence of and Characteristics Associated With Long-term Benzodiazepine Use in Finland, 2020, JAMA Network Open
  • Associations of subjective and objective cognitive functioning after COVID-19: A six-month follow-up of ICU, ward, and home-isolated patients, 2023, Brain Behavior & Immunity - Health

Frequent coauthors include:

  • Erkki Isometsä
  • Jaana Suvisaari
  • Jari Tiihonen
  • Laura Hokkanen
  • Asko Wegelius

Key publication venues for their work are:

  • Schizophrenia Research
  • Brain Behavior & Immunity - Health
  • Research in Developmental Disabilities
  • Critical Care
  • Psychiatry Research

Best Publications

  • Large recurrent microdeletions associated with schizophrenia

    Hreinn Stefansson;Dan Rujescu;Sven Cichon;Olli P. H. Pietilainen

  • Common variants conferring risk of schizophrenia

    Hreinn Stefansson;Hreinn Stefansson;Roel A. Ophoff;Roel A. Ophoff;Roel A. Ophoff;Stacy Steinberg;Stacy Steinberg;Ole A. Andreassen

  • Lifetime Prevalence of Psychotic and Bipolar I Disorders in a General Population

    Jonna Perälä;Jaana Suvisaari;Samuli I. Saarni;Kimmo Kuoppasalmi

  • A review on cognitive impairments in depressive and anxiety disorders with a focus on young adults.

    Anu E. Castaneda;Annamari Tuulio-Henriksson;Mauri Marttunen;Jaana Suvisaari

  • Disruption of the neurexin 1 gene is associated with schizophrenia

    Dan Rujescu;Andres Ingason;Andres Ingason;Sven Cichon;Olli P.H. Pietiläinen

  • The inheritance of neuropsychological dysfunction in twins discordant for schizophrenia

    Tyrone D. Cannon;Matti O. Huttunen;Jouko Lonnqvist;Annamari Tuulio-Henriksson

  • Childhood developmental abnormalities in schizophrenia: evidence from high-risk studies

    Laura T Niemi;Jaana M Suvisaari;Annamari Tuulio-Henriksson;Jouko K Lönnqvist

  • Association of DISC1/TRAX haplotypes with schizophrenia, reduced prefrontal gray matter, and impaired short- and long-term memory.

    Tyrone D. Cannon;William Hennah;Theo G. M. van Erp;Paul M. Thompson

  • Copy number variations of chromosome 16p13.1 region associated with schizophrenia

    A. Ingason;A. Ingason;D. Rujescu;S. Cichon;E. Sigurdsson

  • Long-term use of benzodiazepines: Definitions, prevalence and usage patterns – a systematic review of register-based studies

    T.A.T. Kurko;T.A.T. Kurko;L.K. Saastamoinen;S. Tähkäpää;A. Tuulio-Henriksson

  • Depressive Symptoms in Adolescence as Predictors of Early Adulthood Depressive Disorders and Maladjustment

    Terhi Aalto-Setälä;Mauri Marttunen;Annamari Tuulio-Henriksson;Kari Poikolainen

  • Common variants at VRK2 and TCF4 conferring risk of schizophrenia

    Stacy Steinberg;Simone de Jong;Ole A. Andreassen;Thomas Werge

  • Major depressive disorder and white matter abnormalities: A diffusion tensor imaging study with tract-based spatial statistics

    Tuula Kieseppä;Mervi Eerola;Riitta Mäntylä;Tuomas Neuvonen

  • Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders

    Georg Stoll;Olli P.H. Pietiläinen;Olli P.H. Pietiläinen;Olli P.H. Pietiläinen;Bastian Linder;Jaana Suvisaari

  • Expanding the range of ZNF804A variants conferring risk of psychosis

    S. Steinberg;O. Mors;A.D. Borglum;A.D. Borglum;O. Gustafsson;O. Gustafsson

  • A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia

    W Hennah;A Tuulio-Henriksson;T Paunio;J Ekelund

  • Mental disorders in young adulthood.

    J. Suvisaari;T. Aalto-Setälä;A. Tuulio-Henriksson;T. Härkänen

  • Memory and verbal learning functions in twins with bipolar-I disorder, and the role of information-processing speed.

    Tuula Kieseppä;Annamari Tuulio-Henriksson;Jari Haukka;Theo Van Erp

  • Association of distinct allelic haplotypes of DISC1 with psychotic and bipolar spectrum disorders and with underlying cognitive impairments

    Outi M. Palo;Mervi Antila;Kaisa Silander;William Hennah

  • Having a Male Co-Twin Masculinizes Mental Rotation Performance in Females

    Eero Vuoksimaa;Jaakko Kaprio;Jaakko Kaprio;William S. Kremen;William S. Kremen;Laura Hokkanen

  • Lifetime prevalence of psychotic and bipolar I disorders in a general population. Commentary

    John J. Mcgrath;Jonna Perälä;Jaana Suvisaari;Samuli I. Saarni

Frequent Co-Authors

Mauri Marttunen
Mauri Marttunen University of Helsinki
Samuli I. Saarni
Samuli I. Saarni Tampere University
Jan-Erik Lönnqvist
Jan-Erik Lönnqvist University of Helsinki
Erkki Isometsä
Erkki Isometsä University of Helsinki
Leena Peltonen
Leena Peltonen University of Helsinki
Roel A. Ophoff
Roel A. Ophoff University of California, Los Angeles
Jari Tiihonen
Jari Tiihonen Karolinska Institute
Tellervo Korhonen
Tellervo Korhonen University of Helsinki
Richard J. Rose
Richard J. Rose Indiana University
Hreinn Stefansson
Hreinn Stefansson deCODE Genetics (Iceland)

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