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Author Details
Full Name
Juha Kere
Affiliation
Folkhalsan Research Center, University of Helsinki
ORCID
Career Start Year
1987
Papers
569
H Index
88
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
37684051
A novel SERPINA12 variant and first European patients with diffuse palmoplantar keratoderma.
J Eur Acad Dermatol Venereol
2024
37715654
Effects of exercise on whole-blood transcriptome profile in children with overweight/obesity.
Am J Hum Biol
2024
36153824
The Continued Absence of Functional Germline Stem Cells in Adult Ovaries.
Stem Cells
2023
37708664
Hypertensive pregnancy complications and maternal characteristics as predictors of cardiovascular health within ten years after delivery.
Pregnancy Hypertens
2023
37478859
Transcriptomic differences between human 8-cell-like cells reprogrammed with different methods.
Stem Cell Reports
2023
37726790
CRISPR/Cas9-mediated activation of NR5A1 steers female human embryonic stem cell-derived bipotential gonadal-like cells towards a steroidogenic cell fate.
J Ovarian Res
2023
37285119
Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy.
JAMA Cardiol
2023
37314922
Optimized single-cell RNA sequencing protocol to study early genome activation in mammalian preimplantation development.
STAR Protoc
2023
37237337
Genetic and protein interaction studies between the ciliary dyslexia candidate genes DYX1C1 and DCDC2.
BMC Mol Cell Biol
2023
37164541
Human LUHMES and NES cells as models for studying primary cilia in neurons.
Methods Cell Biol
2023
37224571
Long-chain polyphosphates inhibit type I interferon signaling and augment LPS-induced cytokine secretion in human leukocytes.
J Leukoc Biol
2023
36853658
Computational approach to evaluate scRNA-seq data quality and gene body coverage with SkewC.
STAR Protoc
2023
36472571
In Reply: Revisiting Claims of the Continued Absence of Functional Germline Stem Cells in Adult Ovaries.
Stem Cells
2023
36876139
Comprehensive characterization of the embryonic factor LEUTX.
iScience
2023
36356849
Long-term follow up of families with pathogenic NFKB1 variants reveals incomplete penetrance and frequent inflammatory sequelae.
Clin Immunol
2023
36260239
Characterization of Expanded Gamma Delta T Cells from Atypical X-SCID Patient Reveals Preserved Function and IL2RG-Mediated Signaling.
J Clin Immunol
2023
34929557
Characteristics of preeclampsia in donor cell gestations.
Pregnancy Hypertens
2022
35445468
A novel desmoplakin mutation causes dilated cardiomyopathy with palmoplantar keratoderma as an early clinical sign.
J Eur Acad Dermatol Venereol
2022
35537882
Influence of FLG loss-of-function mutations in host-microbe interactions during atopic skin inflammation.
J Dermatol Sci
2022
35402882
<i>DUX4</i> is a multifunctional factor priming human embryonic genome activation.
iScience
2022
35638601
Idiopathic scoliosis: a systematic review and meta-analysis of heritability.
EFORT Open Rev
2022
35419920
Viral infection-related gene upregulation in monocytes in children with signs of β-cell autoimmunity.
Pediatr Diabetes
2022
35862124
Increased Risk of Preeclampsia in Women With a Genetic Predisposition to Elevated Blood Pressure.
Hypertension
2022
35778420
Biomarkers of nanomaterials hazard from multi-layer data.
Nat Commun
2022
35777358
Transient DUX4 expression in human embryonic stem cells induces blastomere-like expression program that is marked by SLC34A2.
Stem Cell Reports
2022
36824489
Transcriptomic Profiling of JEG-3 cells using human leiomyoma derived matrix.
Biomater Biosyst
2022
36339249
Human endometrial cell-type-specific RNA sequencing provides new insights into the embryo-endometrium interplay.
Hum Reprod Open
2022
35998220
Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people.
Proc Natl Acad Sci U S A
2022
35961773
Deep sequencing of short capped RNAs reveals novel families of noncoding RNAs.
Genome Res
2022
35146392
SkewC: Identifying cells with skewed gene body coverage in single-cell RNA sequencing data.
iScience
2022
35063129
CRISPR activation enables high-fidelity reprogramming into human pluripotent stem cells.
Stem Cell Reports
2022
32754889
Association of Maternal DNA Methylation and Offspring Birthweight.
Reprod Sci
2021
33898616
Nasal upregulation of <i>CST1</i> in dog-sensitised children with severe allergic airway disease.
ERJ Open Res
2021
33606121
A missense variant in IFT122 associated with a canine model of retinitis pigmentosa.
Hum Genet
2021
33914963
Hereditary palmoplantar keratoderma - phenotypes and mutations in 64 patients.
J Eur Acad Dermatol Venereol
2021
34950881
Generation of RNA sequencing libraries for transcriptome analysis of globin-rich tissues of the domestic dog.
STAR Protoc
2021
34675070
Embryonic LTR retrotransposons supply promoter modules to somatic tissues.
Genome Res
2021
34102276
Cystatin B-deficiency triggers ectopic histone H3 tail cleavage during neurogenesis.
Neurobiol Dis
2021
34322716
The role of CDHR3 in susceptibility to otitis media.
J Mol Med (Berl)
2021
34340992
Small RNA expression and miRNA modification dynamics in human oocytes and early embryos.
Genome Res
2021
33955087
Founder effects facilitate the use of a genotyping-based approach to molecular diagnosis in Swedish patients with familial hypercholesterolaemia.
J Intern Med
2021
34050622
HLA-G expression correlates with histological grade but not with prognosis in colorectal carcinoma.
HLA
2021
34026454
Toxicogenomic Profiling of 28 Nanomaterials in Mouse Airways.
Adv Sci (Weinh)
2021
33971943
High-resolution targeted bisulfite sequencing reveals blood cell type-specific DNA methylation patterns in IL13 and ORMDL3.
Clin Epigenetics
2021
31991411
Motor Function Deficits in the Estrogen Receptor Beta Knockout Mouse: Role on Excitatory Neurotransmission and Myelination in the Motor Cortex.
Neuroendocrinology
2021
33057169
Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia.
Mol Psychiatry
2021
33454404
Children at risk for dyslexia show deficient left-hemispheric memory representations for new spoken word forms.
Neuroimage
2021
33230195
Distinct whole-blood transcriptome profile of children with metabolic healthy overweight/obesity compared to metabolic unhealthy overweight/obesity.
Pediatr Res
2021
33466918
DNA Methylation Levels in Mononuclear Leukocytes from the Mother and Her Child Are Associated with IgE Sensitization to Allergens in Early Life.
Int J Mol Sci
2021
33001460
Microbial and transcriptional differences elucidate atopic dermatitis heterogeneity across skin sites.
Allergy
2021
1 - 50 of 569
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12
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12
Peter Arner
Karolinska Institutet at Karolinska Hospital-Huddinge
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12
Markus M N??then
Institute of Human Genetics, University Hospital Bonn
Co-authored papers
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Kristiina Tammimies
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Elisabeth Widen
Co-authored papers
10
Janna Saarela
Co-authored papers
10
Anna Rautanen
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10
Johannes Schumacher
Philipps University of Marburg
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10
Richard C Trembath
Co-authored papers
9
Carsten O Daub
International Institute of Molecular and Cell Biology in Warsaw
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8
Bertram M??ller-Myhsok
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Fred Nyberg
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Per Hoffmann
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