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Children at risk for dyslexia show deficient left-hemispheric memory representations for new spoken word forms

NeuroImage (Orlando, Fla.), 2021-04, Vol.229, p.117739-117739, Article 117739

2021

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Single-cell transcriptome analysis of endometrial tissue

Human reproduction (Oxford), 2016-04, Vol.31 (4), p.844-853

2016

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Distinct whole-blood transcriptome profile of children with metabolic healthy overweight/obesity compared to metabolic unhealthy overweight/obesity

Pediatric research, 2021-05, Vol.89 (7), p.1687-1694

2021

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Factors predisposing to acute and recurrent bacterial non-necrotizing cellulitis in hospitalized patients: a prospective case–control study

Clinical microbiology and infection, 2010-06, Vol.16 (6), p.729-734

2010

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Acute wheeze-specific gene module shows correlation with vitamin D and asthma medication

The European respiratory journal, 2020-01, Vol.55 (1), p.1901330

2020

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Founder effects facilitate the use of a genotyping‐based approach to molecular diagnosis in Swedish patients with familial hypercholesterolaemia

Journal of internal medicine, 2021-08, Vol.290 (2), p.404-415

2021

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A novel SERPINA12 variant and first European patients with diffuse palmoplantar keratoderma

Journal of the European Academy of Dermatology and Venereology, 2024-02, Vol.38 (2), p.413-418

2024

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

Journal of medical genetics, 2010-12, Vol.47 (12), p.816-822

2010

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Introduction of complementary foods in infancy and atopic sensitization at the age of 5 years: timing and food diversity in a Finnish birth cohort

Allergy (Copenhagen), 2013-04, Vol.68 (4), p.507-516

2013

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DYX1C1 functions in neuronal migration in developing neocortex

Neuroscience, 2006-12, Vol.143 (2), p.515-522

2006

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Hereditary palmoplantar keratoderma – phenotypes and mutations in 64 patients

Journal of the European Academy of Dermatology and Venereology, 2021-09, Vol.35 (9), p.1874-1880

2021

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The human GIMAP5 gene has a common polyadenylation polymorphism increasing risk to systemic lupus erythematosus

Journal of medical genetics, 2007-05, Vol.44 (5), p.314-321

2007

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CELSR2 is a candidate susceptibility gene in idiopathic scoliosis

PloS one, 2017-12, Vol.12 (12), p.e0189591-e0189591

2017

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A novel desmoplakin mutation causes dilated cardiomyopathy with palmoplantar keratoderma as an early clinical sign

Journal of the European Academy of Dermatology and Venereology, 2022-08, Vol.36 (8), p.1349-1358

2022

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The molecular genetics and neurobiology of developmental dyslexia as model of a complex phenotype

Biochemical and biophysical research communications, 2014-09, Vol.452 (2), p.236-243

Kere, Juha

2014

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Genetic Analysis of PSORS1 Distinguishes Guttate Psoriasis and Palmoplantar Pustulosis

Journal of investigative dermatology, 2003-04, Vol.120 (4), p.627-632

2003

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High-throughput mutational screening adds clinically important information in myelodysplastic syndromes and secondary or therapy-related acute myeloid leukemia

Haematologica (Roma), 2015-06, Vol.100 (6), p.e223-e225

2015

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Replication of GWAS-identified systemic lupus erythematosus susceptibility genes affirms B-cell receptor pathway signalling and strengthens the role of IRF5 in disease susceptibility in a Northern European population

Rheumatology (Oxford, England), 2012-01, Vol.51 (1), p.87-92

2012

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The PSORS1 locus gene CCHCR1 affects keratinocyte proliferation in transgenic mice

Human molecular genetics, 2008-04, Vol.17 (7), p.1043-1051

2008

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Enrichment of rare copy number variation in children with developmental language disorder

Clinical genetics, 2018-10, Vol.94 (3-4), p.313-320

2018

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The Roots of Autism and ADHD Twin Study in Sweden (RATSS)

Twin research and human genetics, 2014-06, Vol.17 (3), p.164-176

2014

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Evidence of streptococcal origin of acute non-necrotising cellulitis: a serological study

European journal of clinical microbiology & infectious diseases, 2015-04, Vol.34 (4), p.669-672

2015

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Pool-seq driven proteogenomic database for Group G Streptococcus

Journal of proteomics, 2019-06, Vol.201, p.84-92

2019

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Single-cell analysis of human ovarian cortex identifies distinct cell populations but no oogonial stem cells

Nature communications, 2020-03, Vol.11 (1), p.1147-1147, Article 1147

2020

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Mechanisms of inactivation of MLH1 in hereditary nonpolyposis colorectal carcinoma : a novel approach

Oncogene, 2007-07, Vol.26 (31), p.4541-4549

2007

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Children at risk for dyslexia show deficient left-hemispheric memory representations for new spoken word forms

Single-cell transcriptome analysis of endometrial tissue

Distinct whole-blood transcriptome profile of children with metabolic healthy overweight/obesity compared to metabolic unhealthy overweight/obesity

Factors predisposing to acute and recurrent bacterial non-necrotizing cellulitis in hospitalized patients: a prospective case–control study

Acute wheeze-specific gene module shows correlation with vitamin D and asthma medication

Founder effects facilitate the use of a genotyping‐based approach to molecular diagnosis in Swedish patients with familial hypercholesterolaemia

A novel SERPINA12 variant and first European patients with diffuse palmoplantar keratoderma

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

Introduction of complementary foods in infancy and atopic sensitization at the age of 5 years: timing and food diversity in a Finnish birth cohort

DYX1C1 functions in neuronal migration in developing neocortex

Hereditary palmoplantar keratoderma – phenotypes and mutations in 64 patients

The human GIMAP5 gene has a common polyadenylation polymorphism increasing risk to systemic lupus erythematosus

CELSR2 is a candidate susceptibility gene in idiopathic scoliosis

A novel desmoplakin mutation causes dilated cardiomyopathy with palmoplantar keratoderma as an early clinical sign

The molecular genetics and neurobiology of developmental dyslexia as model of a complex phenotype

Genetic Analysis of PSORS1 Distinguishes Guttate Psoriasis and Palmoplantar Pustulosis

High-throughput mutational screening adds clinically important information in myelodysplastic syndromes and secondary or therapy-related acute myeloid leukemia

Replication of GWAS-identified systemic lupus erythematosus susceptibility genes affirms B-cell receptor pathway signalling and strengthens the role of IRF5 in disease susceptibility in a Northern European population

The PSORS1 locus gene CCHCR1 affects keratinocyte proliferation in transgenic mice

Enrichment of rare copy number variation in children with developmental language disorder

The Roots of Autism and ADHD Twin Study in Sweden (RATSS)

Evidence of streptococcal origin of acute non-necrotising cellulitis: a serological study

Pool-seq driven proteogenomic database for Group G Streptococcus

Single-cell analysis of human ovarian cortex identifies distinct cell populations but no oogonial stem cells

Mechanisms of inactivation of MLH1 in hereditary nonpolyposis colorectal carcinoma : a novel approach

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