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Duodecim; Laaketieteellinen Aikakauskirja
|
December 6, 2017
Who would benefit from exome sequencing?
Janna Saarela, Kaisa Kettunen
Molecular Genetics & Genomic Medicine
|
August 18, 2022
A novel partial de novo duplication of JARID2 gene causing a neurodevelopmental phenotype
Liisa Viitasalo, Kaisa Kettunen, Matti Kankainen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 4, 2024
Estimation of carrier frequencies of autosomal and X-linked recessive genetic conditions based on gnomAD v4.0 data in different ancestries
Ronja Hotakainen, Timo Järvinen, Kaisa Kettunen, et al.
European Clinical Respiratory Journal
|
December 18, 2015
Prevalence of PI*Z and PI*S alleles of alpha-1-antitrypsin deficiency in Finland
Jan Häggblom, Kaisa Kettunen, Jussi Karjalainen, et al.
International Journal of Dentistry
|
June 1, 2018
SNP Analysis of Caries and Initial Caries in Finnish Adolescents
Teija Raivisto, AnnaMaria Heikkinen, Leena Kovanen, et al.
BMC Infectious Diseases
|
May 12, 2019
A nearly fatal primary Epstein-Barr virus infection associated with low NK-cell counts in a patient receiving azathioprine: a case report and review of literature
Minna Honkila, Riitta Niinimäki, Mervi Taskinen, et al.
Journal of Clinical and Diagnostic Research : JCDR
|
September 13, 2017
Periodontal Initial Radiological Findings of Genetically Predisposed Finnish Adolescents
Anna Maria Heikkinen, Elmira Pakbaznejad Esmaeili, Leena Kovanen, et al.
Clinical and Experimental Dental Research
|
May 11, 2018
Inflammatory mediator polymorphisms associate with initial periodontitis in adolescents
Anna Maria Heikkinen, Kaisa Kettunen, Leena Kovanen, et al.
BMJ Open Ophthalmology
|
September 14, 2024
Recurrent ocular toxoplasmosis is associated with interferon-gamma deficiency possibly due to genetic origin
Nina Maria Hautala, Maija Joensuu, Teija Paakkola, et al.
American Journal of Medical Genetics. Part A
|
October 11, 2025
The HRAS Variant c.175G>A (p.Ala59Thr) Causes a Predominantly Ectodermal Phenotype Lacking Classic Costello Syndrome Features
Nikole Rautiainen, Eveliina Brandt, Kaisa Kettunen, et al.
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Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
Duodecim; Laaketieteellinen Aikakauskirja
|
December 6, 2017
Who would benefit from exome sequencing?
Janna Saarela, Kaisa Kettunen
Molecular Genetics & Genomic Medicine
|
August 18, 2022
A novel partial de novo duplication of JARID2 gene causing a neurodevelopmental phenotype
Liisa Viitasalo, Kaisa Kettunen, Matti Kankainen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 4, 2024
Estimation of carrier frequencies of autosomal and X-linked recessive genetic conditions based on gnomAD v4.0 data in different ancestries
Ronja Hotakainen, Timo Järvinen, Kaisa Kettunen, et al.
European Clinical Respiratory Journal
|
December 18, 2015
Prevalence of PI*Z and PI*S alleles of alpha-1-antitrypsin deficiency in Finland
Jan Häggblom, Kaisa Kettunen, Jussi Karjalainen, et al.
International Journal of Dentistry
|
June 1, 2018
SNP Analysis of Caries and Initial Caries in Finnish Adolescents
Teija Raivisto, AnnaMaria Heikkinen, Leena Kovanen, et al.
BMC Infectious Diseases
|
May 12, 2019
A nearly fatal primary Epstein-Barr virus infection associated with low NK-cell counts in a patient receiving azathioprine: a case report and review of literature
Minna Honkila, Riitta Niinimäki, Mervi Taskinen, et al.
Journal of Clinical and Diagnostic Research : JCDR
|
September 13, 2017
Periodontal Initial Radiological Findings of Genetically Predisposed Finnish Adolescents
Anna Maria Heikkinen, Elmira Pakbaznejad Esmaeili, Leena Kovanen, et al.
Clinical and Experimental Dental Research
|
May 11, 2018
Inflammatory mediator polymorphisms associate with initial periodontitis in adolescents
Anna Maria Heikkinen, Kaisa Kettunen, Leena Kovanen, et al.
BMJ Open Ophthalmology
|
September 14, 2024
Recurrent ocular toxoplasmosis is associated with interferon-gamma deficiency possibly due to genetic origin
Nina Maria Hautala, Maija Joensuu, Teija Paakkola, et al.
American Journal of Medical Genetics. Part A
|
October 11, 2025
The HRAS Variant c.175G>A (p.Ala59Thr) Causes a Predominantly Ectodermal Phenotype Lacking Classic Costello Syndrome Features
Nikole Rautiainen, Eveliina Brandt, Kaisa Kettunen, et al.
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of 2