Connection

SHWETA DHAR to Humans

This is a "connection" page, showing publications SHWETA DHAR has written about Humans.
Connection Strength

0.184
  1. An innovative medical school curriculum to enhance exposure to genetics and genomics: Updates and outcomes. Genet Med. 2022 03; 24(3):722-728.
    View in: PubMed
    Score: 0.020
  2. Financial barriers in a county genetics clinic: Problems and solutions. J Genet Couns. 2020 08; 29(4):678-688.
    View in: PubMed
    Score: 0.018
  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: 0.016
  4. Autism genetic testing: a qualitative study of awareness, attitudes, and experiences among parents of children with autism spectrum disorders. Genet Med. 2013 Apr; 15(4):274-81.
    View in: PubMed
    Score: 0.011
  5. 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: 0.011
  6. 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: 0.010
  7. Outcomes of integrating genetics in management of patients with retinoblastoma. Arch Ophthalmol. 2011 Nov; 129(11):1428-34.
    View in: PubMed
    Score: 0.010
  8. Enhancing exposure to genetics and genomics through an innovative medical school curriculum. Genet Med. 2012 Jan; 14(1):163-7.
    View in: PubMed
    Score: 0.010
  9. Cranio-meta-diaphyseal dysplasia: 25 year follow-up and review of literature. Am J Med Genet A. 2010 Sep; 152A(9):2335-8.
    View in: PubMed
    Score: 0.009
  10. Tetrasomy 13q mosaicism associated with phylloid hypomelanosis and precocious puberty. Am J Med Genet A. 2009 May; 149A(5):993-6.
    View in: PubMed
    Score: 0.008
  11. 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: 0.006
  12. 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: 0.005
  13. 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: 0.005
  14. Texas health educators'?practice in basic genomics education and services. Per Med. 2021 01; 18(1):55-66.
    View in: PubMed
    Score: 0.005
  15. 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: 0.005
  16. 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: 0.004
  17. Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders. Nat Commun. 2019 10 15; 10(1):4679.
    View in: PubMed
    Score: 0.004
  18. 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: 0.004
  19. 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: 0.004
  20. 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: 0.004
  21. A recurrent p.Arg92Trp variant in steroidogenic factor-1 (NR5A1) can act as a molecular switch in human sex development. Hum Mol Genet. 2016 08 15; 25(16):3446-3453.
    View in: PubMed
    Score: 0.003
  22. Autism genetic testing information needs among parents of affected children: A qualitative study. Patient Educ Couns. 2016 06; 99(6):1011-6.
    View in: PubMed
    Score: 0.003
  23. Molecular diagnostic experience of whole-exome sequencing in adult patients. Genet Med. 2016 07; 18(7):678-85.
    View in: PubMed
    Score: 0.003
  24. WDR35 mutation in siblings with Sensenbrenner syndrome: a ciliopathy with variable phenotype. Am J Med Genet A. 2012 Nov; 158A(11):2917-24.
    View in: PubMed
    Score: 0.003
  25. Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements. Cell. 2011 Sep 16; 146(6):889-903.
    View in: PubMed
    Score: 0.002
  26. Genetic testing and cancer risk management recommendations by physicians for at-risk relatives. Genet Med. 2011 Feb; 13(2):148-54.
    View in: PubMed
    Score: 0.002
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.