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Connection

Robert Hufnagel to High-Throughput Nucleotide Sequencing

This is a "connection" page, showing publications Robert Hufnagel has written about High-Throughput Nucleotide Sequencing.
  1. High-throughput custom capture sequencing identifies novel mutations in coloboma-associated genes: Mutation in DNA-binding domain of retinoic acid receptor beta affects nuclear localization causing ocular coloboma. Hum Mutat. 2020 03; 41(3):678-695.
    View in: PubMed
    Score: 0.176
  2. Biallelic Loss-of-Function Variants in UBAP1L and Nonsyndromic Retinal Dystrophies. JAMA Ophthalmol. 2024 Nov 01; 142(11):1081-1086.
    View in: PubMed
    Score: 0.062
  3. Clinical diagnosis of presumed SOX2 gonadosomatic mosaicism. Ophthalmic Genet. 2021 06; 42(3):320-325.
    View in: PubMed
    Score: 0.048
  4. PDE6C: Novel Mutations, Atypical Phenotype, and Differences Among Children and Adults. Invest Ophthalmol Vis Sci. 2020 10 01; 61(12):1.
    View in: PubMed
    Score: 0.046
  5. Identifying core biological processes distinguishing human eye tissues with precise systems-level gene expression analyses and weighted correlation networks. Hum Mol Genet. 2018 10 01; 27(19):3325-3339.
    View in: PubMed
    Score: 0.040
  6. A novel CHST3 allele associated with spondyloepiphyseal dysplasia and hearing loss in Pakistani kindred. Clin Genet. 2016 07; 90(1):90-5.
    View in: PubMed
    Score: 0.033

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