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Keywords
Last name
Institution

Connection

Co-Authors

This is a "connection" page, showing publications co-authored by Irene Lara-Corrales and Peter Kannu.

 
Connection Strength
 
 
 
2.123
 
  1. Lara-Corrales I, Moazzami M, GarcĂ­a-Romero MT, Pope E, Parkin P, Shugar A, Kannu P. Mosaic Neurofibromatosis Type 1 in Children: A Single-Institution Experience. J Cutan Med Surg. 2017 Sep/Oct; 21(5):379-382.
    View in: PubMed
    Score: 0.780
  2. Earl BR, Szybowska M, Marwaha A, Belostotsky V, Lara-Corrales I, Pope E, Kannu P. Epidermal growth factor receptor deficiency: Expanding the phenotype beyond infancy. J Dermatol. 2020 Aug; 47(8):898-902.
    View in: PubMed
    Score: 0.243
  3. Gabaton N, Kannu P, Pope E, Shugar A, Lara-Corrales I. A novel ENPP1 mutation identified in a multigenerational family affected by Cole disease. Pediatr Dermatol. 2020 Sep; 37(5):868-871.
    View in: PubMed
    Score: 0.243
  4. Marwaha A, Malach J, Shugar A, Hedges S, Weinstein M, Parkin PC, Pope E, Lara-Corrales I, Kannu P. Genotype-phenotype data from a case series of patients with mosaic neurofibromatosis type 1. Br J Dermatol. 2018 11; 179(5):1216-1217.
    View in: PubMed
    Score: 0.215
  5. Jobling RK, Lara-Corrales I, Hsiao MC, Shugar A, Hedges S, Messiaen L, Kannu P. Mosaicism for a SPRED1 deletion revealed in a patient with clinically suspected mosaic neurofibromatosis. Br J Dermatol. 2017 04; 176(4):1077-1078.
    View in: PubMed
    Score: 0.192
  6. Pope V, Dupuis L, Kannu P, Mendoza-Londono R, Sajic D, So J, Yoon G, Lara-Corrales I. Buschke-Ollendorff syndrome: a novel case series and systematic review. Br J Dermatol. 2016 Apr; 174(4):723-9.
    View in: PubMed
    Score: 0.180
  7. Jobling R, D'Souza R, Baker N, Lara-Corrales I, Mendoza-Londono R, Dupuis L, Savarirayan R, Ala-Kokko L, Kannu P. The collagenopathies: review of clinical phenotypes and molecular correlations. Curr Rheumatol Rep. 2014 Jan; 16(1):394.
    View in: PubMed
    Score: 0.155
  8. Hannah-Shmouni F, MacNeil L, Lara-Corrales I, Pope E, Kannu P, Sondheimer N. Whole-exome sequencing identifies a homozygous pathogenic variant in TAT in a girl with palmoplantar keratoderma. Mol Genet Metab Rep. 2019 Dec; 21:100534.
    View in: PubMed
    Score: 0.058
  9. Wang R, Lara-Corrales I, Kannu P, Pope E. Unraveling incontinentia pigmenti: A comparison of phenotype and genotype variants. J Am Acad Dermatol. 2019 Nov; 81(5):1142-1149.
    View in: PubMed
    Score: 0.056
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.