Citation Impact
Citing Papers
The MR-Base platform supports systematic causal inference across the human phenome
2018 Standout
Single-cell transcriptome landscape of circulating CD4+ T cell populations in autoimmune diseases
2024 StandoutNobel
Multiple sclerosis
2012
Persistent kallikrein 5 activation induces atopic dermatitis-like skin architecture independent of PAR2 activity
2017 StandoutNobel
Neurotrophin regulation of neural circuit development and function
2012 Standout
Mechanisms Underlying Inflammation in Neurodegeneration
2010 Standout
Hexose-6-phosphate dehydrogenase: a new risk gene for multiple sclerosis
2009
Human Genetics Shape the Gut Microbiome
2014 Standout
Autoinflammatory Disease Reloaded: A Clinical Perspective
2010 Standout
The evolving landscape of biomarkers for checkpoint inhibitor immunotherapy
2019 Standout
Atopic dermatitis
2015 Standout
Epidermal Barrier Dysfunction in Atopic Dermatitis
2009
Mitochondrial Dysfunction in C. elegans Activates Mitochondrial Relocalization and Nuclear Hormone Receptor-Dependent Detoxification Genes
2019 StandoutNobel
Atopic Dermatitis: Global Epidemiology and Risk Factors
2015 Standout
An update on the genetics of atopic dermatitis: Scratching the surface in 2009
2010
Filaggrin mutations that confer risk of atopic dermatitis confer greater risk for eczema herpeticum
2009
Human genetic variation and its contribution to complex traits
2009
Molecular diagnostic tests to predict the risk of progressive multifocal leukoencephalopathy in natalizumab-treated multiple sclerosis patients
2014
Eczema severity in preadolescent children and its relation to sex, filaggrin mutations, asthma, rhinitis, aggravating factors and topical treatment: a report from the BAMSE birth cohort
2013
Association between suppressors of cytokine signalling, T‐helper type 1/T‐helper type 2 balance and allergic sensitization in children
2007
Sclerostin: how human mutations have helped reveal a new target for the treatment of osteoporosis
2013 StandoutNobel
Common SNPs explain a large proportion of the heritability for human height
2010 Standout
Genetics of primary progressive multiple sclerosis
2014
Cellular and Molecular Mechanisms of Pain
2009 StandoutNobel
SOCS regulation of the JAK/STAT signalling pathway
2008 Standout
Molecular Motors in Neurons: Transport Mechanisms and Roles in Brain Function, Development, and Disease
2010
Molecular genetics of migraine
2009
Recent Developments in Mendelian Randomization Studies
2017
Sequencing technologies — the next generation
2009 Standout
From genes to function: the next challenge to understanding multiple sclerosis
2009
Guidelines on the Use of Therapeutic Apheresis in Clinical Practice – Evidence‐Based Approach from the Writing Committee of the American Society for Apheresis: The Eighth Special Issue
2019 Standout
How neuroinflammation contributes to neurodegeneration
2016 StandoutScience
Epistasis and immunity: the role of genetic interactions in autoimmune diseases
2012
The return of metabolism: biochemistry and physiology of the pentose phosphate pathway
2014 Standout
Works of Jenny Link being referenced
JC Polyomavirus Infection Is Strongly Controlled by Human Leucocyte Antigen Class II Variants
2014
Elevated Expression and Genetic Association Links the SOCS3 Gene to Atopic Dermatitis
2006
Loss-of-function Variants of the Filaggrin Gene are Associated with Atopic Eczema and Associated Phenotypes in Swedish Families
2008
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis
2008
Mendelian randomization shows a causal effect of low vitamin D on multiple sclerosis risk
2016