Connection

Co-Authors

This is a "connection" page, showing publications co-authored by TANYA EBLE and SHWETA DHAR.
Connection Strength

1.303
  1. The practice of adult genetics: a 7-year experience from a single center. Am J Med Genet A. 2013 Jan; 161A(1):89-93.
    View in: PubMed
    Score: 0.437
  2. Financial barriers in a county genetics clinic: Problems and solutions. J Genet Couns. 2020 08; 29(4):678-688.
    View in: PubMed
    Score: 0.181
  3. Quality improvement of clinic flow for complex genetic conditions: Using Ehlers-Danlos syndrome as a model. Mol Genet Genomic Med. 2018 11; 6(6):993-1000.
    View in: PubMed
    Score: 0.163
  4. POLG mutation in a patient with cataracts, early-onset distal muscle weakness and atrophy, ovarian dysgenesis and 3-methylglutaconic aciduria. Gene. 2012 May 10; 499(1):209-12.
    View in: PubMed
    Score: 0.103
  5. Heterozygous MAP3K20 variants cause ectodermal dysplasia, craniosynostosis, sensorineural hearing loss, and limb anomalies. Hum Genet. 2024 Mar; 143(3):279-291.
    View in: PubMed
    Score: 0.059
  6. Psychometric Properties of the POAGTS: A Tool for Understanding Parents' Perceptions Regarding Autism Spectrum Disorder Genetic Testing. Int J Environ Res Public Health. 2021 03 23; 18(6).
    View in: PubMed
    Score: 0.048
  7. Family Health History-Based Cancer Prevention Training for Community Health Workers. Am J Prev Med. 2021 03; 60(3):e159-e167.
    View in: PubMed
    Score: 0.048
  8. Texas health educators'?practice in basic genomics education and services. Per Med. 2021 01; 18(1):55-66.
    View in: PubMed
    Score: 0.048
  9. Pursuing genetic testing for children with autism spectrum disorders: What do parents think? J Genet Couns. 2021 04; 30(2):370-382.
    View in: PubMed
    Score: 0.047
  10. Genetic Testing Experiences Among Parents of Children with Autism Spectrum Disorder in the United States. J Autism Dev Disord. 2019 Dec; 49(12):4821-4833.
    View in: PubMed
    Score: 0.044
  11. Needs assessment in genetic testing education: A survey of parents of children with autism spectrum disorder in the united states. Autism Res. 2019 08; 12(8):1162-1170.
    View in: PubMed
    Score: 0.043
  12. De novo missense variant in the GTPase effector domain (GED) of DNM1L leads to static encephalopathy and seizures. Cold Spring Harb Mol Case Stud. 2019 06; 5(3).
    View in: PubMed
    Score: 0.043
  13. Development and evaluation of a genomics training program for community health workers in Texas. Genet Med. 2018 09; 20(9):1030-1037.
    View in: PubMed
    Score: 0.039
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.