No photo of Päivi Lahermo

Päivi Lahermo

  • PL 20 (Tukholmankatu 8)

    00014

    Finland

19982018
If you made any changes in Pure these will be visible here soon.

Personal profile

Keywords

  • 1184 Genetics, developmental biology, physiology

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

Publications 1998 2018

Breakpoint mapping and haplotype analysis of translocation t(1;12)(q43;q21.1) in two apparently independent families with vascular phenotypes

Luukkonen, T. M., Mehrjouy, M. M., Pöyhönen, M., Anttonen, A-K., Lahermo, P., Ellonen, P., Paulin, L., Tommerup, N., Palotie, A. & Varilo, T., Jan 2018, In : Molecular Genetics & Genomic Medicine. 6, 1, p. 56-68 13 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

Two missense mutations in KCNQ1 cause pituitary hormone deficiency and maternally inherited gingival fibromatosis

Tommiska, J., Känsäkoski, J., Skibsbye, L., Vaaralahti, K., Liu, X., Lodge, E. J., Tang, C., Yuan, L., Fagerholm, R., Kanters, J. K., Lahermo, P., Kaunisto, M., Keski-Filppula, R., Vuoristo, S., Pulli, K., Ebeling, T., Valanne, L., Sankila, E-M., Kivirikko, S., Lääperi, M. & 15 othersCasoni, F., Giacobini, P., Phan-Hug, F., Buki, T., Tena-Sempere, M., Pitteloud, N., Veijola, R., Lipsanen-Nyman, M., Kaunisto, K., Mollard, P., Andoniadou, C. L., Hirsch, J. A., Varjosalo, M., Jespersen, T. & Raivio, T., 3 Nov 2017, In : Nature Communications. 8, 11 p., 1289.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

High-resolution SNP array analysis of patients with developmental disorder and normal array CGH result (vol 13, 84, 2012)

Siggberg, L., Ala-Mello, S., Linnankivi, T., Avela, K., Scheinin, I., Kristiansson, K., Lahermo, P., Hietala, M., Metsähonkala, L., Kuusinen, E., Laaksonen, M., Saarela, J. & Knuutila, S., 18 Nov 2014, In : BMC Medical Genetics. 15, 1 p., 124.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

High-resolution SNP array analysis of patients with developmental disorder and normal array CGH results

Siggberg, L., Ala-Mello, S., Linnankivi, T., Avela, K., Scheinin, I., Kristiansson, K., Lahermo, P., Hietala, M., Metsähonkala, E-L., Kuusinen, E., Laaksonen, M., Saarela, J. & Knuutila, S., 2012, In : BMC Medical Genetics. 13, 10 p., 84.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

Mutations of complement lectin pathway genes MBL2 and MASP2 associated with placental malaria

Holmberg, V., Onkamo, P., Lahtela, L. E., Lahermo, P., Bedu-Addo, G., Mockenhaupt, F. P. & Meri, S., 2012, In : Malaria Journal. 11, art. no 61, p. - 9 p.

Research output: Contribution to journalArticleScientificpeer-review

Open Access
File

Activities 2005 2016

Genotyping Unit Data and Quality management day

Päivi Lahermo (Attendee)
7 Jun 2016

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

FIMM Scientific Retreat 2016

Päivi Lahermo (Attendee)
2 May 20163 May 2016

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

SPR Veripalvelu

Päivi Lahermo (Visiting researcher)
2 Dec 2016

Activity: Visiting an external institution typesAcademic visit to other institution

Janika Sirjalan insinöörityön ohjaus, Metropolia

Päivi Lahermo (Supervisor)
1 Dec 201631 Mar 2017

Activity: Examination typesSupervision of other thesis (Master's, Licentiate)

FIMM Scientific Direction Discussion

Päivi Lahermo (Attendee)
15 Aug 2016

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