Connection

AMIR HOSSEIN SAEIDIAN to Ichthyosis

This is a "connection" page, showing publications AMIR HOSSEIN SAEIDIAN has written about Ichthyosis.
Connection Strength

1.821
  1. Acquired ichthyosis, asteatotic dermatitis or xerosis? An update on pathoetiology and drug-induced associations. J Eur Acad Dermatol Venereol. 2023 Jan; 37(1):47-56.
    View in: PubMed
    Score: 0.201
  2. Inherited ichthyosis as a paradigm of rare skin disorders: Genomic medicine, pathogenesis, and management. J Am Acad Dermatol. 2023 12; 89(6):1215-1226.
    View in: PubMed
    Score: 0.199
  3. Ichthyosis, psoriasiform dermatitis, and recurrent fungal infections in patients with biallelic mutations in PERP. J Eur Acad Dermatol Venereol. 2022 Mar; 36(3):472-479.
    View in: PubMed
    Score: 0.191
  4. Knockdown of SDR9C7 Impairs Epidermal Barrier Function. J Invest Dermatol. 2021 07; 141(7):1754-1764.e1.
    View in: PubMed
    Score: 0.178
  5. Molecular Genetics of Keratinization Disorders - What's New About Ichthyosis. Acta Derm Venereol. 2020 Mar 25; 100(7):adv00095.
    View in: PubMed
    Score: 0.169
  6. Genotype-phenotype correlation in a large English cohort of patients with autosomal recessive ichthyosis. Br J Dermatol. 2020 03; 182(3):729-737.
    View in: PubMed
    Score: 0.162
  7. A novel autosomal recessive GJB2-associated disorder: Ichthyosis follicularis, bilateral severe sensorineural hearing loss, and punctate palmoplantar keratoderma. Hum Mutat. 2019 02; 40(2):217-229.
    View in: PubMed
    Score: 0.154
  8. Erythrokeratoderma: a manifestation associated with multiple types of ichthyoses with different gene defects. Br J Dermatol. 2018 03; 178(3):e219-e221.
    View in: PubMed
    Score: 0.145
  9. A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome. Orphanet J Rare Dis. 2017 12 06; 12(1):176.
    View in: PubMed
    Score: 0.144
  10. Autosomal recessive congenital ichthyosis: CERS3 mutations identified by a next generation sequencing panel targeting ichthyosis genes. Eur J Hum Genet. 2017 11; 25(11):1282-1285.
    View in: PubMed
    Score: 0.141
  11. Gene-Targeted Next-Generation Sequencing Identifies a Novel CLDN1 Mutation in a Consanguineous Family With NISCH Syndrome. Am J Gastroenterol. 2017 Feb; 112(2):396-398.
    View in: PubMed
    Score: 0.136
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.