• 13303 Citations
  • 57 h-Index
1974 …2019

Research output per year

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Letter
2002

Presence of the genetic marker for Gilbert syndrome is associated with increased level and duration of neonatal jaundice [1]

Roy-Chowdhury, N., Deocharan, B., Bejjanki, H. R., Roy-Chowdhury, J., Koliopoulos, C., Petmezaki, S. & Valaes, T., Jan 1 2002, In : Acta Paediatrica, International Journal of Paediatrics. 91, 1, p. 100-102 3 p.

Research output: Contribution to journalLetter

33 Scopus citations
2001

Interaction of coding region mutations and the Gilbert-type promoter abnormality of the UGT1A1 gene causes moderate degrees of unconjugated hyperbilirubinaemia and may lead to neonatal kernicterus [4]

Kadakol, A., Sappal, B. S., Ghosh, S. S., Lowenheim, M., Chowdhury, A., Chowdhury, S., Santra, A., Arias, I. M., Chowdhury, J. R. & Chowdhury, N. R., Apr 30 2001, In : Journal of medical genetics. 38, 4, p. 244-249 6 p.

Research output: Contribution to journalLetter

52 Scopus citations
1995

Genetic inheritance of Gilbert's syndrome

Bosma, P. J., Roy Chowdhury, J., Jansen, P. H. M., Sato, H., Adachi, Y., Aono, S., Uyama, E., Nanno, T., Keino, H., Yamada, Y. & Koiwai, O., Jul 29 1995, In : The Lancet. 346, 8970, p. 314-315 2 p.

Research output: Contribution to journalLetter

33 Scopus citations