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Connection

Anna Biernacka to Neurodevelopmental Disorders

This is a "connection" page, showing publications Anna Biernacka has written about Neurodevelopmental Disorders.
Connection Strength

0.471
  1. AP4B1-associated hereditary spastic paraplegia: expansion of phenotypic spectrum related to homozygous p.Thr387fs variant. J Appl Genet. 2020 May; 61(2):213-218.
    View in: PubMed
    Score: 0.171
  2. Neurodevelopmental phenotype caused by a de novo PTPN4 single nucleotide variant disrupting protein localization in neuronal dendritic spines. Clin Genet. 2018 12; 94(6):581-585.
    View in: PubMed
    Score: 0.155
  3. Novel GNB1 de novo mutation in a patient with neurodevelopmental disorder and cutaneous mastocytosis: Clinical report and literature review. Eur J Med Genet. 2018 Mar; 61(3):157-160.
    View in: PubMed
    Score: 0.146
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.