| # | Title | Journal | Year | Citations |
|---|
| 1 | Revised nomenclature and classification of inherited ichthyoses: Results of the First Ichthyosis Consensus Conference in Sorèze 2009 | Journal of the American Academy of Dermatology | 2010 | 610 |
| 2 | ISOTOPIC RESPONSE | International Journal of Dermatology | 1995 | 304 |
| 3 | Desmoglein 1 deficiency results in severe dermatitis, multiple allergies and metabolic wasting | Nature Genetics | 2013 | 289 |
| 4 | Familial Pityriasis Rubra Pilaris Is Caused by Mutations in CARD14 | American Journal of Human Genetics | 2012 | 220 |
| 5 | Drug-Induced Pemphigus | Clinics in Dermatology | 1998 | 165 |
| 6 | Definitions and outcome measures for mucous membrane pemphigoid: Recommendations of an international panel of experts | Journal of the American Academy of Dermatology | 2015 | 133 |
| 7 | Mutations in Three Genes Encoding Proteins Involved in Hair Shaft Formation Cause Uncombable Hair Syndrome | American Journal of Human Genetics | 2016 | 127 |
| 8 | Mechanisms Causing Loss of Keratinocyte Cohesion in Pemphigus | Journal of Investigative Dermatology | 2018 | 113 |
| 9 | Severe dermatitis, multiple allergies, and metabolic wasting syndrome caused by a novel mutation in the N-terminal plakin domain of desmoplakin | Journal of Allergy and Clinical Immunology | 2015 | 103 |
| 10 | Drug-Induced versus Drug-Triggered Pemphigus | Dermatology | 1991 | 90 |
| 11 | RIN2 Deficiency Results in Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis: MACS Syndrome | American Journal of Human Genetics | 2009 | 89 |
| 12 | Laser Treatment of Traumatic Scars and Contractures: 2020 International Consensus Recommendations | Lasers in Surgery and Medicine | 2020 | 89 |
| 13 | Drug-induced pemphigus I. A survey | Clinics in Dermatology | 1993 | 80 |
| 14 | Familial Tumoral Calcinosis: From Characterization of a Rare Phenotype to the Pathogenesis of Ectopic Calcification | Journal of Investigative Dermatology | 2010 | 72 |
| 15 | CONTACT PEMPHIGUS: A SUBGROUP OF INDUCED PEMPHIGUS | International Journal of Dermatology | 1994 | 71 |
| 16 | Physiology of the skin—Differences between women and men | Clinics in Dermatology | 1997 | 70 |
| 17 | Pemphigus vulgaris: a review of treatment over a 19-year period | Journal of the European Academy of Dermatology and Venereology | 2002 | 70 |
| 18 | CEDNIK syndrome results from loss-of-function mutations in SNAP29 | British Journal of Dermatology | 2011 | 69 |
| 19 | Clinical response to ustekinumab in familial pityriasis rubra pilaris caused by a novel mutation inCARD14 | British Journal of Dermatology | 2014 | 68 |
| 20 | Monopathogenic vs multipathogenic explanations of pemphigus pathophysiology | Experimental Dermatology | 2016 | 63 |
| 21 | Recognition of pemphigus antigens in drug-induced pemphigus vulgaris and pemphigus foliaceus | Journal of the American Academy of Dermatology | 1997 | 62 |
| 22 | A Mutation in LIPN, Encoding Epidermal Lipase N, Causes a Late-Onset Form of Autosomal-Recessive Congenital Ichthyosis | American Journal of Human Genetics | 2011 | 62 |
| 23 | Immediate and delayed effects of treatment at the Dead Sea in patients with psoriatic arthritis | Rheumatology International | 2000 | 60 |
| 24 | Narrow band UVB: is it effective and safe for paediatric psoriasis and atopic dermatitis? | Journal of the European Academy of Dermatology and Venereology | 2011 | 60 |
| 25 | The Genetics of Pemphigus Vulgaris | Frontiers in Medicine | 2018 | 60 |
| 26 | Loss-of-function mutations in caspase recruitment domain-containing protein 14 (CARD14) are associated with a severe variant of atopic dermatitis | Journal of Allergy and Clinical Immunology | 2019 | 60 |
| 27 | Severe Acne Vulgaris and Tobacco Smoking in Young Men | Journal of Investigative Dermatology | 2006 | 59 |
| 28 | Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Syndrome Is Caused by a POC1A Mutation | American Journal of Human Genetics | 2012 | 59 |
| 29 | Kindler syndrome complicated by squamous cell carcinoma of the hard palate: successful treatment with high-dose radiation therapy and granulocyte-macrophage colony-stimulating factor | British Journal of Dermatology | 2001 | 58 |
| 30 | Combined culture and metagenomic analyses reveal significant shifts in the composition of the cutaneous microbiome in psoriasis | British Journal of Dermatology | 2019 | 57 |
| 31 | Autosomal dominant inheritance of central centrifugal cicatricial alopecia in black South Africans | Journal of the American Academy of Dermatology | 2014 | 54 |
| 32 | An Active Amide Group in the Molecule of Drugs That Induce Pemphigus: A Casual or Causal Relationship? | Dermatology | 1994 | 53 |
| 33 | Pyoderma gangrenosum, acne and ulcerative colitis in a patient with a novel mutation in thePSTPIP1gene | Clinical and Experimental Dermatology | 2015 | 53 |
| 34 | Penicillamine-induced bullous dermatoses | Journal of the American Academy of Dermatology | 1996 | 52 |
| 35 | Diet and Pemphigus | Archives of Dermatology | 1998 | 52 |
| 36 | The induction of pemphigus by phenol drugs | International Journal of Dermatology | 1999 | 51 |
| 37 | Dapsone: unapproved uses or indications | Clinics in Dermatology | 2000 | 51 |
| 38 | A Mutation in a Skin-Specific Isoform of SMARCAD1 Causes Autosomal-Dominant Adermatoglyphia | American Journal of Human Genetics | 2011 | 51 |
| 39 | Peeling off the genetics of atopic dermatitis–like congenital disorders | Journal of Allergy and Clinical Immunology | 2014 | 51 |
| 40 | Triggered Psoriasis | Advances in Experimental Medicine and Biology | 1999 | 51 |
| 41 | A phenotype combining hidradenitis suppurativa with Dowling-Degos disease caused by a founder mutation in PSENEN | British Journal of Dermatology | 2018 | 48 |
| 42 | <p>Delayed Inflammatory Reactions to Hyaluronic Acid Fillers: A Literature Review and Proposed Treatment Algorithm</p> | Clinical, Cosmetic and Investigational Dermatology | 2020 | 48 |
| 43 | Epidermolysis Bullosa Simplex | Dermatologic Clinics | 2010 | 47 |
| 44 | Olmsted syndrome | Journal of the American Academy of Dermatology | 2005 | 46 |
| 45 | Inflammatory Peeling Skin Syndrome Caused by a Mutation in CDSN Encoding Corneodesmosin | Journal of Investigative Dermatology | 2011 | 46 |
| 46 | Antimalarials: unapproved uses or indications | Clinics in Dermatology | 2000 | 45 |
| 47 | Possible Nutritional Factors in Induced Pemphigus | Dermatology | 1994 | 44 |
| 48 | Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3 | Journal of Investigative Dermatology | 2014 | 44 |
| 49 | Cole Disease Results from Mutations in ENPP1 | American Journal of Human Genetics | 2013 | 41 |
| 50 | Mutations in Recessive Congenital Ichthyoses Illuminate the Origin and Functions of the Corneocyte Lipid Envelope | Journal of Investigative Dermatology | 2019 | 41 |
