Juha K Kere


Ontology type: schema:Person     


Person Info

NAME

Juha K

SURNAME

Kere

Publications in SciGraph latest 50 shown

  • 2022-10-19 Characterization of Expanded Gamma Delta T Cells from Atypical X-SCID Patient Reveals Preserved Function and IL2RG-Mediated Signaling in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2022-07-01 Biomarkers of nanomaterials hazard from multi-layer data in NATURE COMMUNICATIONS
  • 2021-07-28 The role of CDHR3 in susceptibility to otitis media in JOURNAL OF MOLECULAR MEDICINE
  • 2021-05-10 High-resolution targeted bisulfite sequencing reveals blood cell type-specific DNA methylation patterns in IL13 and ORMDL3 in CLINICAL EPIGENETICS
  • 2021-02-19 A missense variant in IFT122 associated with a canine model of retinitis pigmentosa in HUMAN GENETICS
  • 2020-11-23 Distinct whole-blood transcriptome profile of children with metabolic healthy overweight/obesity compared to metabolic unhealthy overweight/obesity in PEDIATRIC RESEARCH
  • 2020-10-22 Epigenetic alterations in skin homing CD4+CLA+ T cells of atopic dermatitis patients in SCIENTIFIC REPORTS
  • 2020-10-14 Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia in MOLECULAR PSYCHIATRY
  • 2020-09-14 Multi-omic studies on missense PLG variants in families with otitis media in SCIENTIFIC REPORTS
  • 2020-08-04 Association of Maternal DNA Methylation and Offspring Birthweight in REPRODUCTIVE SCIENCES
  • 2020-05-22 Dyslexia Candidate Gene and Ciliary Gene Expression Dynamics During Human Neuronal Differentiation in MOLECULAR NEUROBIOLOGY
  • 2020-05-01 Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia: a case report in BMC MEDICAL GENOMICS
  • 2020-04-15 Congenital chloride diarrhea and Pendred syndrome: case report of siblings with two rare recessive disorders of SLC26 family genes in BMC MEDICAL GENOMICS
  • 2020-03-02 Single-cell analysis of human ovarian cortex identifies distinct cell populations but no oogonial stem cells in NATURE COMMUNICATIONS
  • 2020-03-02 Epigenome-wide meta-analysis of blood DNA methylation in newborns and children identifies numerous loci related to gestational age in GENOME MEDICINE
  • 2020-02-19 Novel Hemizygous IL2RG p.(Pro58Ser) Mutation Impairs IL-2 Receptor Complex Expression on Lymphocytes Causing X-Linked Combined Immunodeficiency in JOURNAL OF CLINICAL IMMUNOLOGY
  • 2019-12-13 Discovery of increased epidermal DNAH10 expression after regeneration of dermis in a randomized with-in person trial — reflections on psoriatic inflammation in SCIENTIFIC REPORTS
  • 2019-10-16 Microbe-host interplay in atopic dermatitis and psoriasis in NATURE COMMUNICATIONS
  • 2019-09-24 The human long non-coding RNA gene RMRP has pleiotropic effects and regulates cell-cycle progression at G2 in SCIENTIFIC REPORTS
  • 2019-09-02 NET-CAGE characterizes the dynamics and topology of human transcribed cis-regulatory elements in NATURE GENETICS
  • 2019-08-13 Guide for library design and bias correction for large-scale transcriptome studies using highly multiplexed RNAseq methods in BMC BIOINFORMATICS
  • 2019-06-27 Dominant TOM1 mutation associated with combined immunodeficiency and autoimmune disease in NPJ GENOMIC MEDICINE
  • 2019-06-10 Pleomorphic Adenoma Gene 1 Is Needed For Timely Zygotic Genome Activation and Early Embryo Development in SCIENTIFIC REPORTS
  • 2019-04-23 Meta-analysis of epigenome-wide association studies in neonates reveals widespread differential DNA methylation associated with birthweight in NATURE COMMUNICATIONS
  • 2019-03-27 Myoglobinopathy is an adult-onset autosomal dominant myopathy with characteristic sarcoplasmic inclusions in NATURE COMMUNICATIONS
  • 2019-03-13 Cationic gold nanoparticles elicit mitochondrial dysfunction: a multi-omics study in SCIENTIFIC REPORTS
  • 2019-02-21 A multiethnic meta-analysis defined the association of rs12946942 with severe adolescent idiopathic scoliosis in JOURNAL OF HUMAN GENETICS
  • 2019-02-11 Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia in TRANSLATIONAL PSYCHIATRY
  • 2018-12-18 TAC-seq: targeted DNA and RNA sequencing for precise biomarker molecule counting in NPJ GENOMIC MEDICINE
  • 2018-11-27 Phylogenetic and mutational analyses of human LEUTX, a homeobox gene implicated in embryogenesis in SCIENTIFIC REPORTS
  • 2018-08-01 A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis in SCIENTIFIC REPORTS
  • 2018-07-21 MANF protects human pancreatic beta cells against stress-induced cell death in DIABETOLOGIA
  • 2018-07-06 Human pluripotent reprogramming with CRISPR activators in NATURE COMMUNICATIONS
  • 2018-06-04 Intracellular signalling pathways and cytoskeletal functions converge on the psoriasis candidate gene CCHCR1 expressed at P-bodies and centrosomes in BMC GENOMICS
  • 2018-03-16 An international meta-analysis confirms the association of BNC2 with adolescent idiopathic scoliosis in SCIENTIFIC REPORTS
  • 2018-03-06 Characterization of the human RFX transcription factor family by regulatory and target gene analysis in BMC GENOMICS
  • 2017-11-16 Hypomethylation of HOXA4 promoter is common in Silver-Russell syndrome and growth restriction and associates with stature in healthy children in SCIENTIFIC REPORTS
  • 2017-10-27 A missense mutation in SLC26A3 is associated with human male subfertility and impaired activation of CFTR in SCIENTIFIC REPORTS
  • 2017-09-13 Acute doses of caffeine shift nervous system cell expression profiles toward promotion of neuronal projection growth in SCIENTIFIC REPORTS
  • 2017-08-29 FANTOM5 CAGE profiles of human and mouse samples in SCIENTIFIC DATA
  • 2017-08-24 Identification of NCAN as a candidate gene for developmental dyslexia in SCIENTIFIC REPORTS
  • 2017-04-19 Ketogenic diet attenuates hepatopathy in mouse model of respiratory chain complex III deficiency caused by a Bcs1l mutation in SCIENTIFIC REPORTS
  • 2017-03-31 Sequence analysis of pooled bacterial samples enables identification of strain variation in group A streptococcus in SCIENTIFIC REPORTS
  • 2017-01-05 The emerging landscape of dynamic DNA methylation in early childhood in BMC GENOMICS
  • 2016-11-22 High-specificity bioinformatics framework for epigenomic profiling of discordant twins reveals specific and shared markers for ACPA and ACPA-positive rheumatoid arthritis in GENOME MEDICINE
  • 2016-11-11 Targeted high-throughput sequencing of candidate genes for chronic obstructive pulmonary disease in BMC PULMONARY MEDICINE
  • 2016-09-16 Genome-wide association analysis reveals variants on chromosome 19 that contribute to childhood risk of chronic otitis media with effusion in SCIENTIFIC REPORTS
  • 2016-09-16 Investigation of rare and low-frequency variants using high-throughput sequencing with pooled DNA samples in SCIENTIFIC REPORTS
  • 2016-09-02 Erratum: Corrigendum: Characterization and target genes of nine human PRD-like homeobox domain genes expressed exclusively in early embryos in SCIENTIFIC REPORTS
  • 2016-08-24 An RGS2 3′UTR polymorphism is associated with preeclampsia in overweight women in BMC GENOMIC DATA
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