ambreen asim

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Publications (15)

• Maternal Risk Factors Triggering Congenital Heart Defects in Down Syndrome: A Case-Control Study.
  Pediatric reports 2022 DOI: 10.3390/pediatric14010015
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• Clinical Exome Sequencing in Cases with Autosomal Recessive Cerebellar Ataxia: A Case Control Study
  Juniper Online Journal of Case Studies (JOJCS) 2022 DOI: 10.19080/JOJCS.2022.13.555860
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• Identification of Novel Genomic Variations in Susceptibility to Nonsyndromic Cleft Lip and Palate Patients.
  Pediatric reports 2021 DOI: 10.3390/pediatric13040077
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• Brain exosomes as minuscule information hub for Autism Spectrum Disorder
  Expert Review of Molecular Diagnostics 2021 DOI: 10.1080/14737159.2021.2000395
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• Congenital heart defects among Down's syndrome cases: an updated review from basic research to an emerging diagnostics technology and genetic counselling.
  Journal of genetics 2021 DOI: 10.1007/s12041-021-01296-0
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• Investigation of LOY in Prostate, Pancreatic, and Colorectal Cancers in males: A case–control study
  Expert Review of Molecular Diagnostics 2020 DOI: 10.1080/14737159.2020.1853528
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• Segmental duplication-quantitative fluorescent-polymerase chain reaction: An approach for the diagnosis of Down syndrome in India
  Journal of Turkish Society of Obstetric and Gynecology 2018 DOI: 10.4274/tjod.56244
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• CRELD1 gene variants and atrioventricular septal defects in Down syndrome
  Gene 2018 DOI: 10.1016/j.gene.2017.10.044
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• MTHFR promoter hypermethylation may lead to congenital heart defects in Down syndrome
  Intractable & Rare Diseases Research 2017 DOI: 10.5582/IRDR.2017.01068
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• MTRR gene variants may predispose to the risk of Congenital Heart Disease in Down syndrome patients of Indian origin
  Egyptian Journal of Medical Human Genetics 2017 DOI: 10.1016/J.EJMHG.2016.02.006
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