Next Generation Sequencing Competence Network

Next Generation Sequencing Competence Network

e.g. CCGA
(min 2 characters)

Connection

Co-Authors

This is a "connection" page, showing publications co-authored by Dagmar Wieczorek and Harald Surowy.
Connection Strength

1,470
  1. FGF9-Associated Multiple Synostoses Syndrome Type 3 in a Multigenerational Family. Genes (Basel). 2023 03 15; 14(3).
    View in: PubMed
    Score: 0,230
  2. Expanding the spectrum of EEF1D neurodevelopmental disorders: Biallelic variants in the guanine exchange domain. Clin Genet. 2023 04; 103(4):484-491.
    View in: PubMed
    Score: 0,227
  3. Correction to: The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype. J Mol Med (Berl). 2021 Dec; 99(12):1769-1770.
    View in: PubMed
    Score: 0,211
  4. The recurrent missense mutation p.(Arg367Trp) in YARS1 causes a distinct neurodevelopmental phenotype. J Mol Med (Berl). 2021 12; 99(12):1755-1768.
    View in: PubMed
    Score: 0,208
  5. Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin-Siris syndrome-like phenotype. Hum Genet. 2017 03; 136(3):297-305.
    View in: PubMed
    Score: 0,151
  6. Identification of new TRIP12 variants and detailed clinical evaluation of individuals with non-syndromic intellectual disability with or without autism. Hum Genet. 2017 02; 136(2):179-192.
    View in: PubMed
    Score: 0,149
  7. Profound inhibition of CD73-dependent formation of anti-inflammatory adenosine in B cells of SLE patients. EBioMedicine. 2021 Nov; 73:103616.
    View in: PubMed
    Score: 0,052
  8. C2orf69 mutations disrupt mitochondrial function and cause a multisystem human disorder with recurring autoinflammation. J Clin Invest. 2021 06 15; 131(12).
    View in: PubMed
    Score: 0,051
  9. Acute myeloid leukemia-induced functional inhibition of healthy CD34+ hematopoietic stem and progenitor cells. Stem Cells. 2021 09; 39(9):1270-1284.
    View in: PubMed
    Score: 0,051
  10. QRICH1 variants in Ververi-Brady syndrome-delineation of the genotypic and phenotypic spectrum. Clin Genet. 2021 01; 99(1):199-207.
    View in: PubMed
    Score: 0,049
  11. The Macrophage Migration Inhibitory Factor (MIF) Promoter Polymorphisms (rs3063368, rs755622) Predict Acute Kidney Injury and Death after Cardiac Surgery. J Clin Med. 2020 Sep 11; 9(9).
    View in: PubMed
    Score: 0,048
  12. Gene expression profiling in aggressive digital papillary adenocarcinoma sheds light on the architecture of a rare sweat gland carcinoma. Br J Dermatol. 2019 05; 180(5):1150-1160.
    View in: PubMed
    Score: 0,043
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.