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Katariina Hannula‐Jouppi | Researchclopedia

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Katariina Hannula‐Jouppi

University of Helsinki ORCID

87

Works

6,446

Citations

30

h-index

50

i10-index

Research Topics

Skin and Cellular Biology Research Epigenetics and DNA Methylation Genetic Syndromes and Imprinting

Affiliations

University of Helsinki1998–2025

Helsinki University Hospital2013–2025

Karolinska Institutet2003–2003

AbbVie (United States)2020–2020

Sanofi (France)2021–2021

Top Works

A candidate gene for developmental dyslexia encodes a nuclear tetratricopeptide repeat domain protein dynamically regulated in brain

Mikko Taipale,Nina Kaminen‐Ahola,et al.

2003377 citations

Prenatal Screening and Diagnostics

Genetic Associations and Epidemiology

The Axon Guidance Receptor Gene ROBO1 Is a Candidate Gene for Developmental Dyslexia

Katariina Hannula‐Jouppi,Nina Kaminen‐Ahola,et al.

2005332 citations

The mutation spectrum in RECQL4 diseases

H. Annika Siitonen,Jenni Sotkasiira,et al.

2008231 citations

Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal Dyspraxia

Lars Feuk,Aino Kalervo,et al.

2006185 citations

A Narrow Segment of Maternal Uniparental Disomy of Chromosome 7q31-qter in Silver-Russell Syndrome Delimits a Candidate Gene Region

Katariina Hannula‐Jouppi,Marita Lipsanen‐Nyman,et al.

2001127 citations

Submicroscopic genomic alterations in Silver–Russell syndrome and Silver–Russell-like patients

R. Douglas Bruce,Katariina Hannula‐Jouppi,et al.

2009113 citations

Uniting biobank resources reveals novel genetic pathways modulating susceptibility for atopic dermatitis

Eeva Sliz,Laura Huilaja,et al.

2021103 citations

Clinically Distinct Epigenetic Subgroups in Silver-Russell Syndrome: The Degree of<i>H19</i>Hypomethylation Associates with Phenotype Severity and Genital and Skeletal Anomalies

Sara Bruce,Katariina Hannula‐Jouppi,et al.

200896 citations

Monoallelic Mutations in the Translation Initiation Codon of KLHL24 Cause Skin Fragility

Yinghong He,Kristin Maier,et al.

201686 citations