Dhanya Yesodharan

Employment

• Amrita Institute of Medical Sciences and Research Centre Dr.
  2010 - Present

Education

Education history is unavailable.

Projects & Funding

Projects & funding information is unavailable.

Publications (22)

• Lipoprotein Lipase Deficiency
  Indian Journal of Pediatrics 2020 DOI: 10.1007/s12098-020-03305-z
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• Turner syndrome in diverse populations
  American Journal of Medical Genetics, Part A 2020 DOI: 10.1002/ajmg.a.61461
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• Founder effects of the homogentisate 1,2-dioxygenase (HGD) gene in a gypsy population and mutation spectrum in the gene among alkaptonuria patients from India
  Clinical Rheumatology 2020 DOI: 10.1007/s10067-020-05020-8
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• Does the clinical phenotype of mucolipidosis-IIIγ differ from its αβ counterpart?: Supporting facts in a cohort of 18 patients
  Clinical Dysmorphology 2019 DOI: 10.1097/MCD.0000000000000249
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• Four novel mutations in EFNB1 in Indian patients with craniofrontonasal syndrome
  Journal of Human Genetics 2019 DOI: 10.1038/s10038-019-0638-9
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• Ptosis as a unique hallmark for autosomal recessive WNT1-associated osteogenesis imperfecta
  American Journal of Medical Genetics, Part A 2019 DOI: 10.1002/ajmg.a.61119
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• Coinheritance of biallelic SLURP1 and SLC39A4 mutations cause a severe genodermatosis with skin peeling and hair loss all over the body
  British Journal of Dermatology 2018 DOI: 10.1111/bjd.16912
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• Cortical atrophy and hypofibrinogenemia due to FGG and TBCD mutations in a single family: A case report
  BMC Medical Genetics 2018 DOI: 10.1186/s12881-018-0597-6
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• Elsahy–Waters syndrome is caused by biallelic mutations in CDH11
  American Journal of Medical Genetics, Part A 2018 DOI: 10.1002/ajmg.a.38568
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• Goltz-Gorlin Syndrome: Revisiting the Clinical Spectrum
  Indian Journal of Pediatrics 2018 DOI: 10.1007/s12098-018-2632-1
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