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This is a "connection" page, showing publications co-authored by Susan Blaser and Michal Inbar-Feigenberg.

Connection Strength
  1. Lee W, Costain G, Blaser S, Walker S, Marshall CR, Gonorazky H, Inbar-Feigenberg M. Genome sequencing identifies a rare case of moderate Zellweger spectrum disorder caused by a PEX3 defect: Case report and literature review. Mol Genet Metab Rep. 2020 Dec; 25:100664.
    View in: PubMed
    Score: 0.233
  2. Hannah-Shmouni F, MacNeil L, Potter M, Jobling R, Yoon G, Laughlin S, Blaser S, Inbar-Feigenberg M. Severe cystic degeneration and intractable seizures in a newborn with molybdenum cofactor deficiency type B. Mol Genet Metab Rep. 2019 Mar; 18:11-13.
    View in: PubMed
    Score: 0.205
  3. Inbar-Feigenberg M, Blaser S, Hawkins C, Shannon P, Hewson S, Chitayat D. Mitochondrial POLG related disorder presenting prenatally with fetal cerebellar growth arrest. Metab Brain Dis. 2018 08; 33(4):1369-1373.
    View in: PubMed
    Score: 0.195
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.