Connection

AMIR HOSSEIN SAEIDIAN to Infant

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

0.130
  1. Secondary ACMG and non-ACMG genetic findings in a multiethnic cohort of 16,713 pediatric participants. Genet Med. 2024 Nov; 26(11):101225.
    View in: PubMed
    Score: 0.077
  2. Homozygous IL1RN Mutation in Siblings with Deficiency of Interleukin-1 Receptor Antagonist (DIRA). J Clin Immunol. 2020 05; 40(4):637-642.
    View in: PubMed
    Score: 0.014
  3. 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: 0.014
  4. The genetic basis of hyaline fibromatosis syndrome in patients from a consanguineous background: a case series. BMC Med Genet. 2018 05 25; 19(1):87.
    View in: PubMed
    Score: 0.013
  5. 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: 0.012
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.