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Komulainen-Ebrahim, Jonna
15  Ergebnisse:
Personensuche X
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1

The Role of Digital Care Pathway for Epilepsy on Patients' ..:

, In: Communications in Computer and Information Science; Digital Health and Wireless Solutions,
Polus, Manria ; Keikhosrokiani, Pantea ; Uusimaa, Johanna... - p. 257-268 , 2024
Link: https://doi.org/10.1007/..
 
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2

Design Sustainability Goals for Digital Care Pathway for Ep..:

, In: Communications in Computer and Information Science; Digital Health and Wireless Solutions,
Khan, Sehrish ; Keikhosrokiani, Pantea ; Uusimaa, Johanna... - p. 269-283 , 2024
Link: https://doi.org/10.1007/..
 
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3

Evidence for the additivity of rare and common variant burd..:

Urpa, Lea ; Kurki, Mitja I. ; Rahikkala, Elisa...
European Journal of Human Genetics.  32 (2024)  5 - p. 576-583 , 2024
Link: https://doi.org/10.1038/..
 
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4

A novel pathogenic SLC12A5 missense variant in epilepsy of ..:

Järvelä, Viivi ; Hamze, Mira ; Komulainen-Ebrahim, Jonna...
Frontiers in Molecular Neuroscience.  17 (2024)  - p. , 2024
Link: https://doi.org/10.3389/..
 
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5

Novel variants and phenotypes widen the phenotypic spectrum..:

Komulainen-Ebrahim, Jonna ; Schreiber, John M. ; Kangas, Salla M....
Seizure.  69 (2019)  - p. 99-104 , 2019
Link: https://doi.org/10.1016/..
 
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6

HIDEA syndrome is caused by biallelic, pathogenic, rare or ..:

Kraatari-Tiri, Minna ; Soikkonen, Leila ; Myllykoski, Matti Aukusti...
urn:issn:0009-9163.  , 2022
Link: https://hdl.handle.net/1..
 
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7

HIDEA syndrome is caused by biallelic, pathogenic, rare or ..:

Kraatari-Tiri, M. (Minna) ; Soikkonen, L. (Leila) ; Myllykoski, M. (Matti)... , 2022
Link: http://urn.fi/urn:nbn:fi..
 
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8

Ei-epileptiset kohtausoireet imeväiässä:

Komulainen-Ebrahim, J. (Jonna) ; Jonsson, H. (Henna) , 2020
Link: http://urn.fi/urn:nbn:fi..
 
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9

Genetic aetiologies and phenotypic variations of childhood-..:

Komulainen-Ebrahim, J. (Jonna)
info:eu-repo/semantics/altIdentifier/pissn/0355-3221.  , 2019
Link: http://urn.fi/urn:isbn:9..
 
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10

Contribution of rare and common variants to intellectual di..:

Kurki, Mitja I ; Saarentaus, Elmo Christian ; Pietiläinen, Olli...
10.1038/s41467-018-08262-y.  , 2019
Link: http://hdl.handle.net/10..
 
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11

Ataxia-pancytopenia syndrome with SAMD9L mutations:

Gorcenco, Sorina ; Komulainen-Ebrahim, Jonna ; Nordborg, Karin...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5570676/.  , 2017
Link: http://www.ncbi.nlm.nih...
 
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12

Gain-of-function SAMD9L mutations cause a syndrome of cytop..:

Tesi, Bianca ; Davidsson, Josef ; Voss, Matthias...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5399482/.  , 2017
Link: http://www.ncbi.nlm.nih...
 
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13

Ataxia-pancytopenia syndrome with SAMD9L mutations:

Gorcenco, S. (Sorina) ; Komulainen- Ebrahim, J. (Jonna) ; Nordborg, K. (Karin)...
info:eu-repo/semantics/altIdentifier/eissn/2376-7839.  , 2017
Link: http://urn.fi/urn:nbn:fi..
 
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14

Gain-of-Function SAMD9L Mutations Cause a Syndrome of Cytop..:

Tesi, B. ; Davidsson, J. ; Voss, M....
Leukemia Research.  55 (2017)  - p. S11-S12 , 2017
Link: https://doi.org/10.1016/..
 
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15

Social music services in teenage life : a case study:

, In: Proceedings of the 22nd Conference of the Computer-Human Interaction Special Interest Group of Australia on Computer-Human Interaction,
Komulainen, Sari ; Karukka, Minna ; Häkkilä, Jonna - p. 364-367 , 2010
Link: https://dl.acm.org/doi/1..
 
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