Akhtar Ali

Employment

• Banaras Hindu University Associate Professor, & Coordinator
  2008 - Present

Education

• Banaras Hindu University Ph.D.
  2004 - 2010

Projects & Funding

Projects & funding information is unavailable.

Publications (9)

• Philadelphia chromosome- positive myelodysplastic syndrome with single lineage dysplasia
  Cancer Genetics 2023 DOI: 10.1016/j.cancergen.2023.05.002
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• Novel GLI3 pathogenic variants in complex pre‐ and postaxial polysyndactyly and Greig cephalopolysyndactyly syndrome
  American Journal of Medical Genetics Part A 2021 DOI: 10.1002/ajmg.a.61919
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• GLI3 mutations in syndromic and non‐syndromic polydactyly in two Indian families
  Congenital Anomalies 2016 DOI: 10.1111/cga.12139
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• Co-occurrence of mosaic supernumerary isochromosome 18p and intermittent 2q13 deletions in a child with multiple congenital anomalies.
  2015 DOI: 10.1016/j.gene.2015.01.042
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• A novel GLI3c.750delC truncation mutation in a multiplex Greig cephalopolysyndactyly syndrome family with an unusual phenotypic combination in a patient.
  2014 DOI: 10.1016/j.mgene.2014.11.002
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• MTHFR C677T predisposes to POAG but not to PACG in a North Indian population: a case control study.
  2014 DOI: 10.1371/journal.pone.0103063
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• Lower incidence of nonsyndromic cleft lip with or without cleft palate in females: is homocysteine a factor?
  2013 DOI: 10.1007/s12038-013-9298-7
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• Coding region of IRF6 gene may not be causal for Van der Woude syndrome in cases from India.
  2009 DOI: 10.1597/08-202.1
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• MTHFR 677TT alone and IRF6 820GG together with MTHFR 677CT, but not MTHFR A1298C, are risks for nonsyndromic cleft lip with or without cleft palate in an Indian population.
  2009 DOI: 10.1089/gtmb.2008.0115
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