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  • PL 20 (Tukholmankatu 8)

    00014

    Finland

20102019
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Personal profile

Fields of Science

  • 1182 Biochemistry, cell and molecular biology
  • 1184 Genetics, developmental biology, physiology

International and National Collaboration Publications and projects within past five years.

Publications 2010 2019

Primary Immunodeficiency, a Possible Cause of Neutrophilic Necrotizing Dermatosis

Kaustio, M., Hautala, T. & Seppänen, M. R. J., Jul 2019, In : Jama dermatology. 155, 7, p. 863-864 5 p.

Research output: Contribution to journalLetterScientificpeer-review

ADA2 deficiency: Clonal lymphoproliferation in a subset of patients

Trotta, L., Martelius, T., Siitonen, T., Hautala, T., Hämäläinen, S., Juntti, H., Taskinen, M., Ilander, M., Andersson, E. I., Zavialov, A., Kaustio, M., Keski-Filppula, R., Hershfield, M., Mustjoki, S., Tapiainen, T., Seppänen, M. & Saarela, J., Apr 2018, In : Journal of Allergy and Clinical Immunology. 141, 4, p. 1534-+ 12 p.

Research output: Contribution to journalLetterScientificpeer-review

Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypes

Kaustio, M., Haapaniemi, E., Göös, H., Hautala, T., Park, G., Syrjänen, J., Einarsdottir, E., Sahu, B., Kilpinen, S., Rounioja, S., Fogarty, C. L., Glumoff, V., Kulmala, P., Katayama, S., Tamene, F., Trotta, L., Morgunova, E., Krjutskov, K., Nurmi, K., Eklund, K. & 9 othersLagerstedt, A., Helminen, M., Martelius, T., Mustjoki, S., Taipale, J., Saarela, J., Kere, J., Varjosalo, M. & Seppanen, M., Sep 2017, In : Journal of Allergy and Clinical Immunology. 140, 3, p. 782-796 15 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

Constant B cell lymphocytosis since early age in a patient with CARD11 mutation: A 20-year follow-up

Outinen, T., Syrjanen, J., Rounioja, S., Saarela, J., Kaustio, M. & Helminen, M., Apr 2016, In : Clinical Immunology. 165, p. 19-20 2 p.

Research output: Contribution to journalArticleScientific

Open Access
File

Enrichment of rare variants in population isolates: single AICDA mutation responsible for hyper-IgM syndrome type 2 in Finland

Trotta, L., Hautala, T., Hamalainen, S., Syrjanen, J., Viskari, H., Almusa, H., Lepisto, M., Kaustio, M., Porkka, K., Palotie, A., Seppanen, M. & Saarela, J., Oct 2016, In : European Journal of Human Genetics. 24, 10, p. 1473-1478 6 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

Activities 2012 2016

  • 9 Organisation and participation in conferences, workshops, courses, seminars
  • 1 Types for other activities - External teaching and subject coordination

FIMM Peer Mentoring in Soft Skills

Jaakko Leinonen (Teacher), Elina Parri (Teacher), Meri Kyllikki Kaustio (Teacher), Arnoldus Johannes van Adrichem (Teacher)
2016 → …

Activity: Other activity typesTypes for other activities - External teaching and subject coordination

European Society of Human Genetics (ESHG) 2015 meeting

Meri Kaustio (Attendee)
6 Jun 20159 Jun 2015

Activity: Participating in or organising an event typesOrganisation and participation in conferences, workshops, courses, seminars

The 17th EMBL PhD Symposium

Meri Kaustio (Attendee)
22 Oct 201524 Oct 2015

Activity: Participating in or organising an event typesOrganisation and participation in conferences, workshops, courses, seminars

American Society of Human Genetics (ASHG) 2014 Annual Meeting

Meri Kaustio (Attendee)
18 Oct 201422 Oct 2014

Activity: Participating in or organising an event typesOrganisation and participation in conferences, workshops, courses, seminars

15th EMBL PhD Symposium: Competition in Biology

Meri Kaustio (Attendee)
21 Nov 201323 Nov 2013

Activity: Participating in or organising an event typesOrganisation and participation in conferences, workshops, courses, seminars