- Home
- Publications
- Publication Search
- Publication Details
Title
What does acne genetics teach us about disease pathogenesis?
Authors
Keywords
-
Journal
BRITISH JOURNAL OF DERMATOLOGY
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2019-03-11
DOI
10.1111/bjd.17721
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Novel POFUT1 mutation associated with hidradenitis suppurativa-Dowling-Degos disease firm up a role for Notch signalling in the pathogenesis of this disorder: reply from the authors
- (2018) M. Pavlovsky et al. BRITISH JOURNAL OF DERMATOLOGY
- Novel POFUT1 mutation associated with hidradenitis suppurativa-Dowling-Degos disease firm up a role for Notch signalling in the pathogenesis of this disorder
- (2018) I. González-Villanueva et al. BRITISH JOURNAL OF DERMATOLOGY
- Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotype
- (2018) Ivo J H M de Vos et al. HUMAN MOLECULAR GENETICS
- Tks adaptor proteins at a glance
- (2018) Priyanka Saini et al. JOURNAL OF CELL SCIENCE
- Exome sequencing and rare variant analysis reveals multiple filaggrin mutations in Bangladeshi atopic eczema families and additional risk genes
- (2018) Manuela Pigors et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- Cutaneous Scarring: Basic Science, Current Treatments, and Future Directions
- (2018) Clement D. Marshall et al. Advances in Wound Care
- Analysis of Hidradenitis Suppurativa-Linked Mutations in Four genes and the Effects of PSEN1-P242LfsX11 on Cytokine and Chemokine Expression in Macrophages
- (2018) Airong Li et al. HUMAN MOLECULAR GENETICS
- Altered Notch signaling in Dowling-Degos disease: Additional mutations in POGLUT1 and further insights into disease pathogenesis
- (2018) Damian J. Ralser et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- Genome-wide meta-analysis implicates mediators of hair follicle development and morphogenesis in risk for severe acne
- (2018) Christos Petridis et al. Nature Communications
- Identification of two novel SH3PXD2B gene mutations in Frank-Ter Haar syndrome by exome sequencing: Case report and review of the literature
- (2017) Abdelali Zrhidri et al. GENE
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- (2017) Damian J. Ralser et al. JOURNAL OF CLINICAL INVESTIGATION
- Acne and Telomere Length: A New Spectrum between Senescence and Apoptosis Pathways
- (2017) Simone Ribero et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- PSENEN Mutation Carriers with Co-manifestation of Acne Inversa (AI) and Dowling-Degos Disease (DDD): Is AI or DDD the Subphenotype?
- (2017) Chengrang Li et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- Genetic architecture of acne vulgaris
- (2017) R. Lichtenberger et al. JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
- Heritability and GWAS Analyses of Acne in Australian Adolescent Twins
- (2017) Angela Mina-Vargas et al. Twin Research and Human Genetics
- Somatic Mutations in NEK9 Cause Nevus Comedonicus
- (2016) Jonathan L. Levinsohn et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Novel Mutations in PSENEN Gene in Two Chinese Acne Inversa Families Manifested as Familial Multiple Comedones and Dowling-Degos Disease
- (2016) Jian-Zhong Zhang et al. CHINESE MEDICAL JOURNAL
- Expanding the spectrum ofγ-secretase gene mutation-associated phenotypes: two novel mutations segregating with familial hidradenitis suppurativa (acne inversa) and acne conglobata
- (2016) Uppala Ratnamala et al. EXPERIMENTAL DERMATOLOGY
- Association of TNF-alpha, IL-6 and IL-1beta gene polymorphisms with polycystic ovary syndrome: a meta-analysis
- (2015) Renyong Guo et al. BMC GENETICS
- A global perspective on the epidemiology of acne
- (2015) J.K.L. Tan et al. BRITISH JOURNAL OF DERMATOLOGY
- Blaschko line acne on pre-existent hypomelanosis reflecting a mosaicFGFR2mutation
- (2015) D. Kiritsi et al. BRITISH JOURNAL OF DERMATOLOGY
- Genome-wide association study identified new susceptibility loci for polycystic ovary syndrome
- (2015) Hyejin Lee et al. HUMAN REPRODUCTION
- Associations between TNF-α and interleukin gene polymorphisms with polycystic ovary syndrome risk: a systematic review and meta-analysis
- (2015) Haijing Wu et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- Variants inSELL,MRPS36P2,TP63,DDB2,CACNA1H,ADAM19,GNAI1,CDH13andGABRG2interact to confer risk of acne in Chinese population
- (2015) HongYan Wang et al. JOURNAL OF DERMATOLOGY
- Understanding innate immunity and inflammation in acne: implications for management
- (2015) B. Dreno et al. JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
- Whole-exome SNP array identifies 15 new susceptibility loci for psoriasis
- (2015) Xianbo Zuo et al. Nature Communications
- Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations
- (2015) M. Geoffrey Hayes et al. Nature Communications
- Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome
- (2015) Felix R. Day et al. Nature Communications
- Dynamics of Lgr6 + Progenitor Cells in the Hair Follicle, Sebaceous Gland, and Interfollicular Epidermis
- (2015) Anja Füllgrabe et al. Stem Cell Reports
- The interleukin-6 and interleukin-1A gene promoter polymorphism is associated with the pathogenesis of acne vulgaris
- (2014) S. Younis et al. ARCHIVES OF DERMATOLOGICAL RESEARCH
- Podosomes are disrupted in PAPA syndrome
- (2014) I. Maridonneau-Parini BLOOD
- The F-BAR protein PSTPIP1 controls extracellular matrix degradation and filopodia formation in macrophages
- (2014) T. W. Starnes et al. BLOOD
- The Pro12Ala polymorphism of the gene for peroxisome proliferator activated receptor-gamma is associated with a lower Global Acne Grading System score in patients with acne vulgaris
- (2014) K. Amr et al. CLINICAL AND EXPERIMENTAL DERMATOLOGY
- Interleukin-6 levels in relation with hormonal and metabolic profile in patients with polycystic ovary syndrome
- (2014) Mert Küçük et al. GYNECOLOGICAL ENDOCRINOLOGY
- Serum tumor necrosis factor-α, interleukin-6, monocyte chemotactic protein-1 and paraoxonase-1 profiles in women with endometriosis, pcos, or unexplained infertility
- (2014) Abdelmoneim Younis et al. JOURNAL OF ASSISTED REPRODUCTION AND GENETICS
- TNF -308 G/A Polymorphism and Risk of Acne Vulgaris: A Meta-Analysis
- (2014) Jian-Kang Yang et al. PLoS One
- Genome-wide association study identifies three novel susceptibility loci for severe Acne vulgaris
- (2014) Alexander A. Navarini et al. Nature Communications
- Two new susceptibility loci 1q24.2 and 11p11.2 confer risk to severe acne
- (2014) Li He et al. Nature Communications
- Impact of TNF Haplotypes in the Physical Course of Acne Vulgaris
- (2013) Ioanna Grech et al. DERMATOLOGY
- Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome
- (2013) Gabrielle R Wilson et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- A genome-wide association study of severe teenage acne in European Americans
- (2013) Mingfeng Zhang et al. HUMAN GENETICS
- The Global Burden of Skin Disease in 2010: An Analysis of the Prevalence and Impact of Skin Conditions
- (2013) Roderick J. Hay et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- c-MYC-Induced Sebaceous Gland Differentiation Is Controlled by an Androgen Receptor/p53 Axis
- (2013) Denny L. Cottle et al. Cell Reports
- Cutaneous Notch Signaling in Health and Disease
- (2013) C. Nowell et al. Cold Spring Harbor Perspectives in Medicine
- Prevalence of Acne Vulgaris in Chinese Adolescents and Adults: A Community-based Study of 17,345 Subjects in Six Cities
- (2012) J Zhang et al. ACTA DERMATO-VENEREOLOGICA
- Mutation of Membrane Type-1 Metalloproteinase, MT1-MMP, Causes the Multicentric Osteolysis and Arthritis Disease Winchester Syndrome
- (2012) Brad R. Evans et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Association of interleukin 4 (-590 T/C) and interleukin 4 receptor (Q551R A/G) gene polymorphisms with acne vulgaris
- (2012) Ahmad A. Al Robaee et al. ANNALS OF SAUDI MEDICINE
- Frank-ter Haar syndrome associated with sagittal craniosynostosis and raised intracranial pressure
- (2012) Charlotte L Bendon et al. BMC Medical Genetics
- Epidemiology of acne vulgaris
- (2012) K. Bhate et al. BRITISH JOURNAL OF DERMATOLOGY
- Lrig1: a new master regulator of epithelial stem cells
- (2012) Paloma Ordóñez-Morán et al. EMBO JOURNAL
- Frank-ter Haar Syndrome Protein Tks4 Regulates Epidermal Growth Factor-dependent Cell Migration
- (2012) Gábor Bögel et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- Tumor necrosis factor-α −308 G/A and interleukin 10 −1082 A/G gene polymorphisms in patients with acne vulgaris
- (2012) Hani A. Al-Shobaili et al. JOURNAL OF DERMATOLOGICAL SCIENCE
- Family history, body mass index, selected dietary factors, menstrual history, and risk of moderate to severe acne in adolescents and young adults
- (2012) Anna Di Landro et al. JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY
- Two novel mutations of the NCSTN gene in Chinese familial acne inverse
- (2012) C. Zhang et al. JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
- Lrig1 controls intestinal stem-cell homeostasis by negative regulation of ErbB signalling
- (2012) Vivian W. Y. Wong et al. NATURE CELL BIOLOGY
- Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome
- (2012) Yongyong Shi et al. NATURE GENETICS
- Exome Analysis Identified a Novel Mutation in the RBP4 Gene in a Consanguineous Pedigree with Retinal Dystrophy and Developmental Abnormalities
- (2012) Catherine Cukras et al. PLoS One
- A deletion of FGFR2 creating a chimeric IIIb/IIIc exon in a child with Apert syndrome
- (2011) Aimee L Fenwick et al. BMC Medical Genetics
- Two novel mutations of the nicastrin gene in Chinese patients with acne inversa
- (2011) C.-R. Li et al. BRITISH JOURNAL OF DERMATOLOGY
- Stem cell dynamics in sebaceous gland morphogenesis in mouse skin
- (2011) Daniela Frances et al. DEVELOPMENTAL BIOLOGY
- Nek9 is a Plk1-activated kinase that controls early centrosome separation through Nek6/7 and Eg5
- (2011) M Teresa Bertran et al. EMBO JOURNAL
- Identification of Semaphorin 4B as a Negative Regulator of Basophil-Mediated Immune Responses
- (2011) Y. Nakagawa et al. JOURNAL OF IMMUNOLOGY
- PSENEN and NCSTN Mutations in Familial Hidradenitis Suppurativa (Acne Inversa)
- (2011) Andrew E. Pink et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- Confirmation by Exome Sequencing of the Pathogenic Role of NCSTN Mutations in Acne Inversa (Hidradenitis Suppurativa)
- (2011) Yuan Liu et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- Acne vulgaris
- (2011) Hywel C Williams et al. LANCET
- The Homolog of the Five SH3-Domain Protein (HOFI/SH3PXD2B) Regulates Lamellipodia Formation and Cell Spreading
- (2011) Árpád Lányi et al. PLoS One
- Disruption of the Podosome Adaptor Protein TKS4 (SH3PXD2B) Causes the Skeletal Dysplasia, Eye, and Cardiac Abnormalities of Frank-Ter Haar Syndrome
- (2010) Zafar Iqbal et al. AMERICAN JOURNAL OF HUMAN GENETICS
- TNFα gene polymorphisms in the pathogenesis of acne vulgaris
- (2010) Kornélia Szabó et al. ARCHIVES OF DERMATOLOGICAL RESEARCH
- Impaired podosome formation and invasive migration of macrophages from patients with a PSTPIP1 mutation and PAPA syndrome
- (2010) Christa L. Cortesio et al. ARTHRITIS AND RHEUMATISM
- Association Study of Tumor Necrosis Factor Receptor Type 2 M196R and Toll-Like Receptor 2 Arg753Gln Polymorphisms with Acne Vulgaris in a Chinese Han Ethnic Group
- (2010) Li-Ming Tian et al. DERMATOLOGY
- Hidradenitis suppurativa (or Acne inversa) with autosomal dominant inheritance is not linked to chromosome 1p21.1-1q25.3 region
- (2010) Faiza Mohamed Saleh Al-Ali et al. EXPERIMENTAL DERMATOLOGY
- Increased EFG- and PDGF -receptor signaling by mutant FGF-receptor 2 contributes to osteoblast dysfunction in Apert craniosynostosis
- (2010) H. Miraoui et al. HUMAN MOLECULAR GENETICS
- TNFR 2 M196R polymorphism and acne vulgaris in Han Chinese: A case-control study
- (2010) Liming Tian et al. Journal of Huazhong University of Science and Technology-Medical Sciences
- A novel homozygous MMP2 mutation in a patient with Torg–Winchester syndrome
- (2010) Seon-Yong Jeong et al. JOURNAL OF HUMAN GENETICS
- The epidemiology of adolescent acne in North East China
- (2010) B Wei et al. JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- (2010) W Chen et al. JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
- Comparison of the epidemiology of acne vulgaris among Caucasian, Asian, Continental Indian and African American women
- (2010) A.C. Perkins et al. JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
- Genome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3
- (2010) Zi-Jiang Chen et al. NATURE GENETICS
- Lgr6 Marks Stem Cells in the Hair Follicle That Generate All Cell Lineages of the Skin
- (2010) H. J. Snippert et al. SCIENCE
- -Secretase and Human Disease
- (2010) R. J. Kelleher et al. SCIENCE
- -Secretase Gene Mutations in Familial Acne Inversa
- (2010) B. Wang et al. SCIENCE
- Interleukin-1A +4845(G> T) polymorphism is a factor predisposing to acne vulgaris
- (2010) K. Szabó et al. TISSUE ANTIGENS
- Lrig1 Expression Defines a Distinct Multipotent Stem Cell Population in Mammalian Epidermis
- (2009) Kim B. Jensen et al. Cell Stem Cell
- Common vs. rare allele hypotheses for complex diseases
- (2009) Nicholas J Schork et al. CURRENT OPINION IN GENETICS & DEVELOPMENT
- Prevalence, Severity, and Severity Risk Factors of Acne in High School Pupils: A Community-Based Study
- (2009) S. Zahra Ghodsi et al. JOURNAL OF INVESTIGATIVE DERMATOLOGY
- The Novel Adaptor Protein Tks4 (SH3PXD2B) Is Required for Functional Podosome Formation
- (2009) Matthew D. Buschman et al. MOLECULAR BIOLOGY OF THE CELL
- Association between tumor necrosis factor-alpha gene promoter polymorphism at position -308 and acne in Turkish patients
- (2008) Kıymet Baz et al. ARCHIVES OF DERMATOLOGICAL RESEARCH
- Lack of association between the promoter polymorphisms at positions -238 and -308 of the tumour necrosis factor alpha gene and acne vulgaris in Polish patients
- (2008) M Sobjanek et al. JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreDiscover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversation