H. Hennies

H. Hennies, F. Hildebrandt, M. Attanasio, 2005, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

A gene mutated in nephronophthisis and retinitis pigmentosa encodes a novel protein, nephroretinin, conserved in evolution.

R. Sudbrak, H. Hennies, F. Hildebrandt, 2002, American journal of human genetics.

Increased cutaneous absorption reflects impaired barrier function of reconstructed skin models mimicking keratinisation disorders

Michał R. Radowski, H. Hennies, M. Schäfer-Korting, 2014, Experimental dermatology.

Late-onset Papillon-Lefèvre syndrome without alteration of the cathepsin C gene.

H. Hennies, E. Aberer, A. Truschnegg, 2003, Journal of the American Academy of Dermatology.

Genetic and clinical heterogeneity in transgressive palmoplantar keratoderma.

H. Hennies, A. Reis, P. Frossard, 2001, The Journal of investigative dermatology.

Palmoplantar keratoderma in association with carcinoma of the esophagus maps to chromosome 17q distal to the keratin gene cluster.

H. Hennies, A. Reis, M. Hagedorn, 1995, Genomics.

Annular Epidermolytic Ichthyosis Mimicking Greither Disease: A Case Report and Literature Review

H. Hennies, O. Alakloby, Fatimah J. Almuqarrab, 2022, The American journal of case reports.

Towards characterization of palmoplantar keratoderma caused by gain‐of‐function mutation in loricrin: analysis of a family and review of the literature

H. Hennies, S. Tinschert, H. Traupe, 2006, The British journal of dermatology.

Localization of a locus for the striated form of palmoplantar keratoderma to chromosome 18q near the desmosomal cadherin gene cluster.

H. Hennies, A. Reis, D. Mischke, 1995, Human molecular genetics.

Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC).

J. Weissenbach, D. Bishop, D. Kelsell, 1996, Human molecular genetics.

A second locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 19q13.3.

R. Barrantes, H. Hennies, B. Neundörfer, 2001, American journal of human genetics.

Mutation spectrum in children with primary hemophagocytic lymphohistiocytosis: molecular and functional analyses of PRF1, UNC13D, STX11, and RAB27A

H. Hennies, R. Schneppenheim, U. Stadt, 2006, Human mutation.

Identification of the first AHI1 gene mutations in nephronophthisis-associated Joubert syndrome

M. Eccles, H. Hennies, F. Hildebrandt, 2005, Pediatric Nephrology.

Gerodermia osteodysplastica is caused by mutations in SCYL1BP1, a Rab-6 interacting golgin

P. Kaplan, S. Mundlos, J. Clayton-Smith, 2008, Nature Genetics.

Medullary cystic kidney disease type 1: mutational analysis in 37 genes based on haplotype sharing

H. Hennies, F. Hildebrandt, M. Attanasio, 2006, Human Genetics.

Envoplakin, a possible candidate gene for focal NEPPK/esophageal cancer (TOC): the integration of genetic and physical maps of the TOC region on 17q25.

D. Bishop, D. Kelsell, F. Watt, 1999, Genomics.

Molekulare Charakterisierung der Ichthyosen

H. Hennies, V. Oji, H. Hennies, 2009 .

Molecular characterization of ichthyoses. New aspects of terminology and classification

H. Hennies, V. Oji, H. Traupe, 2009 .

A novel in situ method for the detection of deficient transglutaminase activity in the skin

M. Raghunath, V. Wiebe, H. Hennies, 1998, Archives of Dermatological Research.

Wnt signaling and Dupuytren's disease.

Peter Nürnberg, Andre Franke, Cisca Wijmenga, 2011, The New England journal of medicine.

Sebaceous gland, hair shaft, and epidermal barrier abnormalities in keratosis pilaris with and without filaggrin deficiency.

H. Hennies, P. Elias, D. Crumrine, 2015, The American journal of pathology.

Vitamin D Status in Distinct Types of Ichthyosis: Importance of Genetic Type and Severity of Scaling

H. Hennies, J. Nofer, Mi-ran Kim, 2021, Acta dermato-venereologica.

Neurotological and Neuroanatomical Changes in the Connexin-26-Related HID/KID Syndrome

H. Hennies, D. Basta, A. Ernst, 2006, Audiology and Neurotology.

A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3

I. Glass, H. Hennies, F. Hildebrandt, 2003, Journal of medical genetics.

Mutation analysis of the M6b gene in patients with Pelizaeus-Merzbacher-like syndrome.

H. Hennies, M. Henneke, J. Gärtner, 2004, American journal of medical genetics. Part A.

Rapid detection of homozygous mutations in congenital recessive ichthyosis

J. Lugassy, H. Hennies, M. Indelman, 2008, Archives of Dermatological Research.

Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.

S. Cichon, T. Schulze, T. Wienker, 2005, American journal of human genetics.

Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis

S. Ehl, H. Hennies, C. Klemann, 2017, Journal of Clinical Immunology.

Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areata

M. Nöthen, G. Kirov, W. Peitsch, 2011, European Journal of Human Genetics.

S1 guidelines for the diagnosis and treatment of ichthyoses – update

H. Hennies, J. Fischer, A. Diem, 2017, Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG.

Ichthyosis, follicular atrophoderma, and hypotrichosis caused by mutations in ST14 is associated with impaired profilaggrin processing.

H. Hennies, D. Metze, G. Lestringant, 2009, The Journal of investigative dermatology.

Palmoplantar keratoderma (PPK): acquired and genetic causes of a not so rare disease

H. Hennies, C. Seebode, S. Emmert, 2014, Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG.

Epidermolytic palmoplantar keratoderma of Vörner: re-evaluation of Vörner's original family and identification of a novel keratin 9 mutation

H. Hennies, A. Reis, W. Küster, 2002, Archives of Dermatological Research.

Mutations in AP3D1 associated with immunodeficiency and seizures define a new type of Hermansky-Pudlak syndrome.

A. Schulz, S. Ehl, H. Hennies, 2016, Blood.

Familial hemophagocytic lymphohistiocytosis type 5 (FHL-5) is caused by mutations in Munc18-2 and impaired binding to syntaxin 11.

S. Ehl, H. Hennies, G. Nürnberg, 2009, American journal of human genetics.

Transglutaminase 1 Replacement Therapy Successfully Mitigates the Autosomal Recessive Congenital Ichthyosis Phenotype in Full-Thickness Skin Disease Equivalents.

H. Hennies, S. Hedtrich, K. Eckl, 2019, The Journal of investigative dermatology.

Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.

H. Hennies, E. Sprecher, F. Martínez, 2009, The Journal of investigative dermatology.

Genotype/phenotype correlation in autosomal recessive lamellar ichthyosis.

V. Wiebe, H. Hennies, A. Reis, 1998, American journal of human genetics.

Transglutaminase-1 and bathing suit ichthyosis: molecular analysis of gene/environment interactions.

H. Hennies, C. Becker-Pauly, V. Oji, 2009, The Journal of investigative dermatology.

hiPSC-Derived Epidermal Keratinocytes from Ichthyosis Patients Show Altered Expression of Cornification Markers

H. Hennies, T. Šarić, P. Nürnberg, 2021, International journal of molecular sciences.

Skin Disease Models In Vitro and Inflammatory Mechanisms: Predictability for Drug Development.

H. Hennies, Y. Poumay, 2021, Handbook of experimental pharmacology.

Thermosensitive dendritic polyglycerol-based nanogels for cutaneous delivery of biomacromolecules.

H. Hennies, M. Calderón, W. Friess, 2015, Nanomedicine : nanotechnology, biology, and medicine.

Self-healing collodion baby: a dynamic phenotype explained by a particular transglutaminase-1 mutation.

M. Raghunath, H. Hennies, P. Steinert, 2003, The Journal of investigative dermatology.

Mutations in SNRPE, which encodes a core protein of the spliceosome, cause autosomal-dominant hypotrichosis simplex.

M. Nöthen, H. Hennies, A. Fryer, 2013, American journal of human genetics.

Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma

D. Kelsell, H. Hennies, I. Leigh, 2001, European Journal of Human Genetics.

Assignment of the gene for a new hereditary nail disorder, isolated congenital nail dysplasia, to chromosome 17p13.

H. Hennies, A. Reis, H. Hamm, 2000, The Journal of investigative dermatology.

Characterization of the first supernumerary tricentric ring chromosome 1 mosaicism by conventional and molecular cytogenetic techniques

H. Hennies, H. Tönnies, H. Neitzel, 2004, Cytogenetic and Genome Research.

Keratin 9 gene mutations in epidermolytic palmoplantar keratoderma (EPPK)

Karl Sperling, André Reis, E. Schröck, 1994, Nature Genetics.

MYO15A (DFNB3) mutations in Turkish hearing loss families and functional modeling of a novel motor domain mutation

C. Cremers, E. Krieger, H. Brunner, 2007, American Journal of Medical Genetics. Part A.

Positional cloning uncovers mutations in PLCE1 responsible for a nephrotic syndrome variant that may be reversible

Peter Nürnberg, Thomas Gudermann, Dominik Seelow, 2006, Nature Genetics.

Induced pluripotent mesenchymal stromal cell clones retain donor-derived differences in DNA methylation profiles.

H. Hennies, M. Zenke, T. Šarić, 2013, Molecular therapy : the journal of the American Society of Gene Therapy.

In vitro Modeling of Ryanodine Receptor 2 Dysfunction Using Human Induced Pluripotent Stem Cells

Azra Fatima, Hendrik Milting, Wilhelm Haverkamp, 2011, Cellular Physiology and Biochemistry.

A gene locus for steroid-resistant nephrotic syndrome with deafness maps to chromosome 14q24.2.

H. Hennies, F. Hildebrandt, M. Wolf, 2003, Journal of the American Society of Nephrology : JASN.

Increased activity of coagulation factor XII (Hageman factor) causes hereditary angioedema type III.

S. Cichon, M. Nöthen, T. Renné, 2006, American journal of human genetics.

Meta-Analysis of Genome-Wide Association Studies and Network Analysis-Based Integration with Gene Expression Data Identify New Suggestive Loci and Unravel a Wnt-Centric Network Associated with Dupuytren’s Disease

C. Gieger, K. Strauch, A. Franke, 2016, PloS one.

Linkage of familial hemophagocytic lymphohistiocytosis (FHL) type-4 to chromosome 6q24 and identification of mutations in syntaxin 11.

H. Hennies, P. Nürnberg, J. Henter, 2005, Human molecular genetics.

Identification and localization of a new human myotubularin-related protein gene, mtmr8, on 8p22-p23.

W. Zimmermann, A. Rosenthal, H. Hennies, 2001, Genomics.

Genetic Aspects of Familial Ménière's Disease

H. Hennies, B. Horsthemke, K. Jahnke, 2011, Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology.

Periodontal Ehlers-Danlos Syndrome Is Caused by Mutations in C1R and C1S, which Encode Subcomponents C1r and C1s of Complement

D. Nickerson, M. Dorschner, T. Meitinger, 2016, American journal of human genetics.

Microdissection of GTG-banded chromosomes and PCR-mediated cloning

H. Hennies, A. Reis, B. Horsthemke, 1993 .

The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4

Yan Liu, Michael A Kennedy, Hemant Khanna, 2006, Nature Genetics.

Unknown mutations and genotype/phenotype correlations of autosomal recessive congenital ichthyosis in patients from Saudi Arabia and Pakistan

H. Hennies, P. Nürnberg, J. Altmüller, 2019, Molecular genetics & genomic medicine.

A new syndrome, congenital extraocular muscle fibrosis with ulnar hand anomalies, maps to chromosome 21qter

H. Hennies, H. Kayserili, R. Desnick, 2005, Journal of Medical Genetics.

Bathing suit ichthyosis is caused by transglutaminase-1 deficiency: evidence for a temperature-sensitive phenotype.

H. Hennies, A. Hovnanian, P. Steijlen, 2006, Human molecular genetics.

Genome-wide scan and fine-mapping linkage study of androgenetic alopecia reveals a locus on chromosome 3q26.

M. Nöthen, H. Hennies, A. Hillmer, 2008, American journal of human genetics.

A Genome-wide Association Study of Dupuytren Disease Reveals 17 Additional Variants Implicated in Fibrosis

E. Zeggini, R. Ophoff, A. Franke, 2017, American journal of human genetics.

The Genetic Basis of Dupuytren’s Disease: An Introduction

H. Hennies, G. Dolmans, 2012 .

All is balanced: inter‐α‐trypsin inhibitors as unseen extracellular matrix proteins in epidermal morphology and differentiation

H. Hennies, 2015, Experimental dermatology.

Vestibular dysfunction of patients with mutations of Connexin 26

H. Hennies, D. Basta, A. Ernst, 2005, Neuroreport.

IGFBP7 as a potential therapeutic target in Psoriasis.

O. Sarig, I. Filip, H. Hennies, 2011, The Journal of investigative dermatology.

Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates

H. Hennies, I. Leigh, P. Nürnberg, 2002, Human Genetics.

A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family.

H. Hennies, K. Sperling, J. Hejtmancik, 2006, Molecular vision.

Cohen Syndrome-associated Protein, COH1, Is a Novel, Giant Golgi Matrix Protein Required for Golgi Integrity*

D. Horn, H. Hennies, T. Maritzen, 2011, The Journal of Biological Chemistry.

A novel locus for dilated cardiomyopathy, diffuse myocardial fibrosis, and sudden death on chromosome 10q25-26.

Calum A MacRae, Gregor Krings, Bong-Seok Song, 2006, Journal of the American College of Cardiology.

Network Analysis and Fine-Mapping GWAS Loci to Identify Genes and Functional Variants Involved in the Development of Dupuytren Disease

H. Hennies, P. Nürnberg, Juanjiangmeng Du, 2017 .

47 patients in 14 families with the rare genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer.

H. Haenssle, H. Hennies, S. Emmert, 2003, European journal of dermatology : EJD.

RHBDF2 mutations are associated with tylosis, a familial esophageal cancer syndrome.

D. Bishop, D. Kelsell, V. Plagnol, 2012, American journal of human genetics.

A novel homozygous missense mutation in SLURP1 causing Mal de Meleda with an atypical phenotype.

H. Hennies, M. Schmuth, N. Romani, 2011, Archives of dermatology.

Localization of the gene causing keratolytic winter erythema to chromosome 8p22-p23, and evidence for a founder effect in South African Afrikaans-speakers.

T. Wienker, A. Spurdle, M. Ramsay, 1997, American journal of human genetics.

Identification, by homozygosity mapping, of a novel locus for autosomal recessive congenital ichthyosis on chromosome 17p, and evidence for further genetic heterogeneity.

H. Hennies, A. Reis, P. Frossard, 2001, American journal of human genetics.

University of Groningen Meta-Analysis of Genome-Wide Association Studies and Network Analysis-Based Integration with Gene Expression Data Identify New Suggestive Loci and Unravel a Wnt-Centric Network Associated with Dupuytren ' s Disease

C. Gieger, K. Strauch, A. Franke, 2017 .

A truncating mutation of CEP135 causes primary microcephaly and disturbed centrosomal function.

H. Hennies, A. Noegel, P. Frommolt, 2012, American journal of human genetics.

A novel mutation in GJA8 associated with autosomal dominant congenital cataract in a family of Indian origin.

H. Hennies, K. Sperling, P. Nürnberg, 2006, Molecular vision.

Hallmarks of Atopic Skin Mimicked In Vitro by Means of a Skin Disease Model Based on FLG Knock-down

Monika Schäfer-Korting, Johanna Plendl, Sarah Küchler, 2011, Alternatives to laboratory animals : ATLA.

Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14–q21 by homozygosity mapping

Irene M. Leigh, Howard P. Stevens, André Reis, 1997, Human Genetics.

Sutural cataract associated with a mutation in the ferritin light chain gene (FTL) in a family of Indian origin.

H. Hennies, K. Sperling, P. Nürnberg, 2006, Molecular vision.

Netherton syndrome previously misdiagnosed as hyper IgE syndrome caused by a probable mutation in SPINK5 C.

H. Hennies, M. Atasoy, Kemal Özyurt, 2019, Turkish Journal of Pediatrics.

Physical and transcriptional map of the critical region for keratolytic winter erythema (KWE) on chromosome 8p22-p23 between D8S550 and D8S1759

M. Lovett, W. Zimmermann, M. Ramsay, 2002, European Journal of Human Genetics.

Band-specific localization of the microsatellite at D13S71 by microdissection and enzymatic amplification.

A. Chakravarti, H. Hennies, A. Reis, 1992, American journal of human genetics.

Cohen Syndrome-associated Protein COH1 Physically and Functionally Interacts with the Small GTPase RAB6 at the Golgi Complex and Directs Neurite Outgrowth*

D. Horn, H. Hennies, T. Maritzen, 2014, The Journal of Biological Chemistry.

Keratin 9 gene mutational heterogeneity in patients with epidermolytic palmoplantar keratoderma

H. Hennies, A. Reis, W. Küster, 1994, Human Genetics.

De novo terminal deletion of chromosome 15q26.1 characterised by comparative genomic hybridisation and FISH with locus specific probes

H. Hennies, I. Schulze, L. Neumann, 2001, Journal of medical genetics.

Mutational spectrum of COH1 and clinical heterogeneity in Cohen syndrome

D. Horn, H. Hennies, D. Chitayat, 2005, Journal of Medical Genetics.

Immunodeficiency with susceptibility to lymphoma with complex genotype affecting energy metabolism (FBP1, ACAD9) and vesicle trafficking (RAB27A)

W. Klapper, S. Ehl, H. Hennies, 2023, Frontiers in Immunology.

Homozygosity mapping as a screening tool for the molecular diagnosis of hereditary skin diseases in consanguineous populations.

H. Hennies, M. Indelman, R. Bergman, 2006, Journal of the American Academy of Dermatology.

Mutation analysis of the M6b gene in patients with Pelizaeus–Merzbacher‐like syndrome

H. Hennies, M. Henneke, J. Gärtner, 2004 .

Full-thickness human skin models for congenital ichthyosis and related keratinization disorders.

H. Hennies, K. Eckl, S. Torres, 2011, The Journal of investigative dermatology.

Penetration of normal, damaged and diseased skin--an in vitro study on dendritic core-multishell nanotransporters.

H. Hennies, R. Haag, E. Fleige, 2014, Journal of controlled release : official journal of the Controlled Release Society.

Bathing Suit Variant of Autosomal Recessive Congenital Ichthyosis (ARCI) in Two Indian Patients

H. Hennies, D. Peter, V. Oji, 2018, Case reports in dermatological medicine.

Bathing suit ichthyosis.

H. Hennies, A. Torrelo, I. Hausser, 2010, European journal of dermatology : EJD.

TRANSGLUTAMINASE 1 REPLACEMENT THERAPY SUCCESSFULLY MITIGATES THE ARCI PHENOTYPE IN FULL-THICKNESS SKIN DISEASE EQUIVALENTS SHORT TITLE: SUCCESSFUL TOPICAL TRANSGLUTAMINASE 1 REPLACEMENT

Katja, H. Hennies, Patrick, 2018 .

Long-term faithful recapitulation of transglutaminase 1-deficient lamellar ichthyosis in a skin-humanized mouse model and insights from proteomic studies

F. Larcher, H. Hennies, R. Rice, 2012, The Journal of investigative dermatology.

SPINK1 mutations in chronic pancreatitis.

H. Hennies, H. Witt, M. Becker, 2001, Gastroenterology.

Effective Immunological Guidance of Genetic Analyses Including Exome Sequencing in Patients Evaluated for Hemophagocytic Lymphohistiocytosis

S. Ehl, H. Hennies, C. Klemann, 2017 .

The importance of genetic susceptibility in Dupuytren's disease

H. Hennies, P. Nürnberg, S. Tinschert, 2015, Clinical genetics.

Promoter polymorphism at -238 of the tumor necrosis factor alpha gene is not associated with early onset psoriasis when tested by the transmission disequilibrium test.

T. Wienker, H. Hennies, F. Rüschendorf, 1999, The Journal of investigative dermatology.

Acropectorovertebral dysgenesis (F syndrome) maps to chromosome 2q36

J. Opitz, S. Mundlos, H. Hennies, 2004, Journal of Medical Genetics.

Genetic and immunohistochemical detection of mutations inactivating the keratinocyte transglutaminase in patients with lamellar ichthyosis

M. Raghunath, V. Wiebe, H. Hennies, 1998, Human Genetics.

Focal palmoplantar and gingival keratosis: a distinct palmoplantar ectodermal dysplasia with epidermolytic alterations but lack of mutations in known keratins.

H. Hennies, P. Reichart, G. Kolde, 2005, Journal of the American Academy of Dermatology.

CEDNIK syndrome results from loss‐of‐function mutations in SNAP29

O. Sarig, D. Goldsher, H. Hennies, 2011, The British journal of dermatology.

Bathing suit ichthyosis: A temperature sensitive phenotype

H. Hennies, B. Ahvazi, I. Hausser, 2008 .

Dinucleotide repeat polymorphism at the locus D13S231.

H. Hennies, A. Reis, L. Saksová, 1993, Human Molecular Genetics.

Three dinucleotide microsatellite polymorphisms on human chromosome 13.

H. Hennies, A. Reis, 1993, Human Molecular Genetics.

Hyalinosis cutis et mucosae

A. Enk, H. Hennies, U. Jappe, 2007 .

Hyalinosis cutis et mucosae

A. Enk, H. Hennies, U. Jappe, 2007, Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG.

Evidence for a single genetic locus in Clouston's hidrotic ectodermal dysplasia

H. Hennies, U. Wollina, A. Wilmer, 1999, The British journal of dermatology.

Comparative association analysis reveals that corneodesmosin is more closely associated with psoriasis than HLA-Cw*0602-B*5701 in German families.

T. Wienker, H. Hennies, R. Blasczyk, 2001, Tissue antigens.

Penetration of normal, damaged and diseased skin--an in vitro study on dendritic core-multishell nanotransporters.

H. Hennies, R. Haag, E. Fleige, 2014, Journal of controlled release : official journal of the Controlled Release Society.

Mutations in CSTA, encoding Cystatin A, underlie exfoliative ichthyosis and reveal a role for this protease inhibitor in cell-cell adhesion.

D. Kelsell, H. Hennies, A. Zvulunov, 2011, American journal of human genetics.

A new locus for autosomal recessive non‐syndromic mental retardation maps to 1p21.1–p13.3

H. Hennies, H. Kayserili, G. Nürnberg, 2007, Clinical genetics.

Filaggrin gene variants among Saudi patients with ichthyosis vulgaris

H. Hennies, O. Alakloby, Kholood Alnutaifi, 2023, BMC Medical Genomics.

Cohen Syndrome-associated Protein, COH1, Is a Novel, Giant Golgi Matrix Protein Required for Golgi Integrity*

D. Horn, H. Hennies, V. Haucke, 2011, The Journal of Biological Chemistry.

A novel fan-shaped cataract-microcornea syndrome caused by a mutation of CRYAA in an Indian family.

H. Hennies, J. Hejtmancik, V. Vanita, 2006, Molecular vision.

UNC13D and PRF1 Mutations in Childhood Patients with Hemophagocytic Lymphohistiocytosis.

H. Hennies, R. Schneppenheim, U. Stadt, 2004 .

HID and KID syndromes are associated with the same connexin 26 mutation

H. Hennies, R. Happle, M. Geel, 2002, The British journal of dermatology.

A genome-wide association meta-analysis implicates Hedgehog and Notch signaling in Dupuytren’s disease

H. Hennies, I. Nolte, D. Drichel, 2024, Nature communications.

Sebaceous gland, hair shaft, and epidermal barrier abnormalities in keratosis pilaris with and without filaggrin deficiency.

H. Hennies, P. Elias, D. Crumrine, 2015, The American journal of pathology.