
Number of publications published per year by Kelly, Deirdre A.. (Source : PubMed)

Distribution of publications types for Kelly, Deirdre A.. (Source : PubMed)
(a publication can be of different types, so total may exceed publications count)
Mutations in VIPAR cause an arthrogryposis, renal dysfunction and cholestasis syndrome phenotype with defects in epithelial polarization.
Nat. Genet.
2010;42;4
Childhood autoimmune liver disease: indications and outcome of liver transplantation.
J. Pediatr. Gastroenterol. Nutr.
2010;50;3
Mutations in TTC37 Cause Trichohepatoenteric Syndrome (Phenotypic Diarrhoea of Infancy).
Gastroenterology
2010
Activated Alleles of the Schizosaccharomyces pombe gpa2+ G{alpha} Gene Identify Residues Involved in GDP-GTP Exchange.
Eukaryotic Cell
2010
Liver transplantation in children using non-heart-beating donors (NHBD).
Pediatr Transplant
2010

Biliary atresia.
Lancet
2009;374;9702
Improved outcomes of combined liver and kidney transplants in small children (<15 kg).
Transplantation
2009;88;5

Calcineurin inhibitor minimization in pediatric liver allograft recipients.
Pediatr Transplant
2009;13;6
Renal function recovery in children undergoing combined liver kidney transplants.
Transplantation
2009;87;10
Isolated liver transplant in infants with short bowel syndrome: insights into outcomes and prognostic factors.
J. Pediatr. Gastroenterol. Nutr.
2009;48;3
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means that Kelly, Deirdre A. has 34 papers cited a least 34 times - methodology
Department of Medical and Molecular Genetics, University of Birmingham School of Medicine, Birmingham, B15 2TT, UK and Liver Unit, Birmingham Children's Hospital, Steelhouse Lane, Birmingham, B4 6NH, UK.
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