A. Liedén

发表

Gene expression and genetic association studies in eczema.

A. Liedén, 2007 .

Malassezia sympodialis stimulation differently affects gene expression in dendritic cells from atopic dermatitis patients and healthy individuals.

M. D’Amato, S. Gabrielsson, A. Scheynius, 2004, Acta dermato-venereologica.

Rare copy number variants are common in young children with autism spectrum disorder

C. Gillberg, E. Fernell, B. Anderlid, 2015, Acta paediatrica.

Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability.

Philippe M Campeau, Tiziana Granata, Ronnie Wright, 2016, American journal of human genetics.

Association of a Tagging Single Nucleotide Polymorphism in the Androgen Receptor Gene Region with Susceptibility to Severe Hypospadias in a Caucasian Population

T. Adamović, A. Nordenskjöld, H.T.T. Thai, 2013, Sexual Development.

TSHZ3 deletion causes an autism syndrome and defects in cortical projection neurons

P. Gubellini, B. Jacq, N. Šestan, 2016, Nature Genetics.

From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability

P. Georgii‐Hemming, A. Nordgren, J. Eisfeldt, 2019, Genome Medicine.

Lack of association between filaggrin gene mutations and onset of psoriasis in childhood

M. Nordenskjöld, P. Nikamo, M. Winge, 2013, Journal of the European Academy of Dermatology and Venereology : JEADV.

Genome sequencing is a sensitive first-line test to diagnose individuals with intellectual disability.

L. Levin, H. Helgadottir, A. Nordgren, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Molecular and Cytogenetic Analysis in Stillbirth: Results from 481 Consecutive Cases

M. Nordenskjöld, E. Sahlin, E. Iwarsson, 2014, Fetal Diagnosis and Therapy.

Replicative and non-replicative mechanisms in the formation of clustered CNVs are indicated by whole genome characterization

O. Mäkitie, Z. Tümer, N. Tommerup, 2018, PLoS genetics.

JARID2 haploinsufficiency is associated with a clinically distinct neurodevelopmental syndrome

Frédérick A. Mallette, Dagmar Glatz, V. Aggarwal, 2020, Genetics in Medicine.

Identification of putative pathogenic single nucleotide variants (SNVs) in genes associated with heart disease in 290 cases of stillbirth

D. Nilsson, M. Nordenskjöld, E. Sahlin, 2019, PloS one.

Intragenic duplication—A novel causative mechanism for SATB2‐associated syndrome

M. Kvarnung, E. Sahlin, A. Liedén, 2014, American journal of medical genetics. Part A.

Cell‐free tumour DNA testing for early detection of cancer – a potential future tool

R. Rosenquist, M. Nordenskjöld, B. Tesi, 2019, Journal of internal medicine.

Novel filaggrin mutation but no other loss‐of‐function variants found in Ethiopian patients with atopic dermatitis

M. Nordenskjöld, M. Winge, M. Bradley, 2011, The British journal of dermatology.

Nasal speech and hypothyroidism are common hallmarks of 12q15 microdeletions

G. Mortier, B. Menten, S. Lyonnet, 2011, European Journal of Human Genetics.

Deletion of Wiskott–Aldrich syndrome protein triggers Rac2 activity and increased cross-presentation by dendritic cells

S. Snapper, Marisa A. P. Baptista, A. Worth, 2016, Nature Communications.

A genome-wide association study of atopic dermatitis identifies loci with overlapping effects on asthma and psoriasis

L. Liang, J. Kere, S. Heath, 2013, Human molecular genetics.

Genetic variation in the inflammasome and atopic dermatitis susceptibility.

P. Söderkvist, M. Winge, M. Bradley, 2013, The Journal of investigative dermatology.

No evidence for mosaic pathogenic copy number variations in cardiac tissue from patients with congenital heart malformations.

A. Nordgren, H. Berggren, J. Winberg, 2015, European journal of medical genetics.

Cornulin, a marker of late epidermal differentiation, is down‐regulated in eczema

I. Kockum, C. Palmer, M. D’Amato, 2009, Allergy.

DNA Methylation Signature for JARID2-Neurodevelopmental Syndrome

R. Pfundt, Philippe M. Campeau, B. Isidor, 2022, International journal of molecular sciences.

Characterization of Stem-Like Cells in Mucoepidermoid Tracheal Paediatric Tumor

G. Lemon, T. Luedde, P. Macchiarini, 2014, PloS one.

Ataxia in Patients With Bi-Allelic NFASC Mutations and Absence of Full-Length NF186

A. Nordgren, B. Birnir, D. Nilsson, 2019, Front. Genet..

Loss-of-function variants of the filaggrin gene are associated with atopic eczema and associated phenotypes in Swedish families.

I. Kockum, J. Link, C. Palmer, 2008, Acta Dermato-Venereologica.

Skin Barrier Function and Staphylococcus aureus Colonization in Vestibulum Nasi and Fauces in Healthy Infants and Infants with Eczema: A Population-Based Cohort Study

Petter Gjersvik, Håvard Ove Skjerven, Petter Mowinckel, 2015, PloS one.

Partial tetrasomy 14 associated with multiple malformations

A. Nordgren, C. Graff, B. Anderlid, 2013, American journal of medical genetics. Part A.

Cell-free tumour DNA analysis detects copy number alterations in gastro-oesophageal cancer patients

J. Eisfeldt, D. Nilsson, Kenny Billiau, 2021, PloS one.

Solute carriers (SLC) in inflammatory bowel disease: a potential target of probiotics?

M. D’Amato, S. Pettersson, V. Trinchieri, 2008, Journal of Clinical Gastroenterology.

Vitamin D levels and atopic eczema in infancy and early childhood in Norway: a cohort study

K. Lødrup Carlsen, P. Gjersvik, L. Sandvik, 2016, The British journal of dermatology.

Novel point mutation in the STS gene in a patient with X-linked recessive ichthyosis.

B. Berne, M. Nordenskjöld, M. Winge, 2011, Journal of dermatological science.

Whole-exome sequencing of Ethiopian patients with ichthyosis vulgaris and atopic dermatitis.

D. Nilsson, M. Nordenskjöld, S. Asad, 2015, The Journal of allergy and clinical immunology.

Prognosis of Preschool Eczema and Factors of Importance for Remission.

C. Söderhäll, T. Lind, S. Asad, 2018, Acta dermato-venereologica.

Genetic Variation in the Epidermal Transglutaminase Genes Is Not Associated with Atopic Dermatitis

T. Illig, A. Franke, I. Kockum, 2012, PloS one.

Nasal speech in patients with 12q15 microdeletions

G. Mortier, B. Menten, S. Lyonnet, 2011, European Journal of Human Genetics.

Rare copy number variants are common in young children with autism spectrum disorder

C. Gillberg, E. Fernell, B. Anderlid, 2015, Acta paediatrica.

Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability.

A. Nordgren, B. Kerr, S. Banka, 2016, American journal of human genetics.

Loss-of-function variants of the filaggrin gene are associated with atopic eczema and associated phenotypes in Swedish families.

I. Kockum, J. Link, M. D’Amato, 2008, Acta dermato-venereologica.

Cornulin, a marker of late epidermal differentiation, is down‐regulated in eczema

C. Wahlgren, I. Kuo, M. Nordensköld, 2009, Allergy.