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Juha Kere

University of Helsinki · FI
Area of research
Genetics · Physiology
Research interest
Research interests include Asthma and respiratory diseases, Epigenetics and DNA Methylation, Pregnancy and preeclampsia studies, and Genetics and Neurodevelopmental Disorders.
h-index
112
citations
50,019
works
912
NIH funding
primary concept
email

Recent publications

Nanodiamonds Interact with Primary Human Macrophages and Dendritic Cells Evoking a Vigorous Interferon Response
ACS Nano 2025cited by 8position: middledoi
An atlas of transcribed enhancers across helper T cell diversity for decoding human diseases
Science 2024cited by 27position: middledoi
Primary cilia promote the differentiation of human neurons through the WNT signaling pathway
BMC Biology 2024cited by 21position: middledoi
Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy
JAMA Cardiology 2023cited by 124position: middledoi
Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human
Genome Medicine 2023cited by 14position: middledoi
DUX4 is a multifunctional factor priming human embryonic genome activation
iScience 2022cited by 55position: lastdoi
Biomarkers of nanomaterials hazard from multi-layer data
Nature Communications 2022cited by 45position: middledoi
Transient DUX4 expression in human embryonic stem cells induces blastomere-like expression program that is marked by SLC34A2
Stem Cell Reports 2022cited by 40position: lastdoi
Long-term follow up of families with pathogenic NFKB1 variants reveals incomplete penetrance and frequent inflammatory sequelae
Clinical Immunology 2022cited by 22position: middledoi
Human endometrial cell-type-specific RNA sequencing provides new insights into the embryo–endometrium interplay
Human Reproduction Open 2022cited by 15position: middledoi
Influence of FLG loss-of-function mutations in host–microbe interactions during atopic skin inflammation
Journal of Dermatological Science 2022cited by 3position: middledoi
Dog colour patterns explained by modular promoters of ancient canid origin
Nature Ecology & Evolution 2021cited by 57position: middledoi
Single-cell analysis of human ovarian cortex identifies distinct cell populations but no oogonial stem cells
Nature Communications 2020cited by 370position: middledoi
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women
Nature Communications 2020cited by 190position: middledoi
Epigenome-wide meta-analysis of blood DNA methylation in newborns and children identifies numerous loci related to gestational age
Genome Medicine 2020cited by 148position: middledoi
Fetal HLA-G mediated immune tolerance and interferon response in preeclampsia
EBioMedicine 2020cited by 48position: lastdoi
Epigenetic alterations in skin homing CD4+CLA+ T cells of atopic dermatitis patients
Scientific Reports 2020cited by 47position: middledoi
Microbial and transcriptional differences elucidate atopic dermatitis heterogeneity across skin sites
Allergy 2020cited by 25position: middledoi
Microbe-host interplay in atopic dermatitis and psoriasis
Nature Communications 2019cited by 408position: middledoi
Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweight
Nature Communications 2019cited by 261position: middledoi
Prenatal Particulate Air Pollution and DNA Methylation in Newborns: An Epigenome-Wide Meta-Analysis
Environmental Health Perspectives 2019cited by 159position: middledoi
NET-CAGE characterizes the dynamics and topology of human transcribed cis-regulatory elements
Nature Genetics 2019cited by 121position: middledoi
Cationic gold nanoparticles elicit mitochondrial dysfunction: a multi-omics study
Scientific Reports 2019cited by 85position: middledoi
Novel TMEM173 Mutation and the Role of Disease Modifying Alleles
Frontiers in Immunology 2019cited by 68position: middledoi
Gain-of-function CEBPE mutation causes noncanonical autoinflammatory inflammasomopathy
Journal of Allergy and Clinical Immunology 2019cited by 55position: middledoi
DNA Methylation Trajectories During Pregnancy
Epigenetics Insights 2019cited by 55position: middledoi
The human long non-coding RNA gene RMRP has pleiotropic effects and regulates cell-cycle progression at G2
Scientific Reports 2019cited by 39position: middledoi
Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions
Nature Communications 2019cited by 22position: middledoi
DNA methylation in childhood asthma: an epigenome-wide meta-analysis
The Lancet Respiratory Medicine 2018cited by 252position: middledoi
Epigenome-wide meta-analysis of DNA methylation and childhood asthma
Journal of Allergy and Clinical Immunology 2018cited by 208position: middledoi

Grants

No grants ingested yet.

Frequent collaborators

Shintaro Katayama · University of Helsinki22 papers (2013–2025)Kaarel Krjutškov · Competence Centre on Health Technologies (Estonia)13 papers (2016–2022)Elísabet Einarsdóttir · Science for Life Laboratory11 papers (2015–2022)Cilla Söderhäll · Karolinska University Hospital10 papers (2012–2020)Annika Scheynius · Stockholm South General Hospital9 papers (2012–2020)Erik Melén · Karolinska Institutet7 papers (2012–2019)Lovisa E. Reinius · Karolinska Institutet7 papers (2012–2016)Nathalie Acevedo · University of Cartagena7 papers (2012–2020)Göran Pershagen · Svenska Örtmedicinska Institute6 papers (2012–2019)Eeva‐Mari Jouhilahti · University of Helsinki6 papers (2015–2022)Dario Greco · University of Helsinki6 papers (2012–2020)Outi Hovatta · Karolinska Institutet6 papers (2014–2020)Hannele Laivuori · Stockholm Health Care Services5 papers (2012–2020)Virpi Töhönen · Karolinska University Hospital5 papers (2013–2017)Sten Linnarsson · Karolinska Institutet5 papers (2013–2016)Mikael Knip · and Helsinki University Hospital4 papers (2013–2015)Fredrik Lanner · Karolinska University Hospital4 papers (2016–2022)Masahito Yoshihara · Tokyo Medical and Dental University4 papers (2020–2024)Eero Kajantie · University of Helsinki4 papers (2012–2020)Tiina Skoog · Karolinska Institutet4 papers (2016–2020)