Connection

SHWETA DHAR to Male

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

0.091
  1. Outcomes of integrating genetics in management of patients with retinoblastoma. Arch Ophthalmol. 2011 Nov; 129(11):1428-34.
    View in: PubMed
    Score: 0.015
  2. 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: 0.014
  3. 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: 0.009
  4. Texas health educators'?practice in basic genomics education and services. Per Med. 2021 01; 18(1):55-66.
    View in: PubMed
    Score: 0.007
  5. 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: 0.006
  6. Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders. Nat Commun. 2019 10 15; 10(1):4679.
    View in: PubMed
    Score: 0.006
  7. 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: 0.006
  8. 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: 0.006
  9. 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: 0.005
  10. 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: 0.005
  11. Molecular diagnostic experience of whole-exome sequencing in adult patients. Genet Med. 2016 07; 18(7):678-85.
    View in: PubMed
    Score: 0.005
  12. 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: 0.004
  13. Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements. Cell. 2011 Sep 16; 146(6):889-903.
    View in: PubMed
    Score: 0.004
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.