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Robert Lindeman

Noninvasive measurement and imaging of liver iron concentrations using proton magnetic resonance
2004 · Timothy G. St. Pierre, Paul R. Clark, et al. · Blood · 905
Integrative Genomics Identifies the Molecular Basis of Resistance to Azacitidine Therapy in Myelodysplastic Syndromes
2017 · Ashwin Unnikrishnan, Elli Papaemmanuil, et al. · Cell Reports · 133
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SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathway
2009 · Simon T. Cliffe, Jamie M. Kramer, et al. · Human Molecular Genetics · 122
Single amino acid mutation of FCγ receptor is associated with the development of heparin‐induced thrombocytopenia
1995 · Janette K. Burgess, Robert Lindeman, et al. · British Journal of Haematology · 106
Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease
2006 · Tony Roscioli, Simon T Cliffe, et al. · Nature Genetics · 96
Development of the segmental innervation of the chick forelimb
1979 · A. G. Pettigrew, R. Lindeman, et al. · Development · 80
Glycogen Synthase Kinase-3 β Inhibition Preserves Hematopoietic Stem Cell Activity and Inhibits Leukemic Cell Growth
2008 · Tiffany Holmes, Tracey A. O'Brien, et al. · Stem Cells · 68
Recombinant Activated Factor VII in Cardiac Surgery: Experience From the Australian and New Zealand Haemostasis Registry
2008 · Scott Dunkley, Louise Phillips, et al. · The Annals of Thoracic Surgery · 59
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Quality of Life Related to Oral versus Subcutaneous Iron Chelation: A Time Trade-off Study
2007 · Richard H. Osborne, Richard De Abreu Lourenço, et al. · Value in Health · 59
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Polymerase chain reaction (PCR) mutagenesis enabling rapid non‐radioactive detection of common β‐thalassaemia mutations in Mediterraneans
1991 · R. Lindeman, S. P. Hu, et al. · British Journal of Haematology · 59
Clinical, molecular, and cellular immunologic findings in patients with SP110-associated veno-occlusive disease with immunodeficiency syndrome
2012 · Simon T. Cliffe, Donald B. Bloch, et al. · Journal of Allergy and Clinical Immunology · 54
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Impact of Rapid Molecular Diagnostic Testing of Respiratory Viruses on Outcomes of Adults Hospitalized with Respiratory Illness: a Multicenter Quasi-experimental Study
2018 · Nasir Wabe, Ling Li, et al. · Journal of Clinical Microbiology · 52
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Impact on learning of an e-learning module on leukaemia: a randomised controlled trial
2012 · Yuri Morgulis, Rakesh K Kumar, et al. · BMC Medical Education · 47
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The impact of rapid molecular diagnostic testing for respiratory viruses on outcomes for emergency department patients
2019 · Nasir Wabe, Ling Li, et al. · The Medical Journal of Australia · 42
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A variety of genetic mechanisms are associated with the Prader–Willi syndrome
1994 · Trevor Woodage, Ze‐Min Deng, et al. · American Journal of Medical Genetics · 42
Glycogen synthase kinase−3β inhibitors suppress leukemia cell growth
2010 · Emma Y. Song, Patricia Palladinetti, et al. · Experimental Hematology · 40
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Platelet Function and Constituents of Platelet Rich Plasma
2012 · M. Pelletier, A. Malhotra, et al. · International Journal of Sports Medicine · 36
The Role of Glycogen Synthase Kinase-3β in Normal Haematopoiesis, Angiogenesis and Leukaemia
2008 · T. Holmes, T. O'Brien, et al. · Current Medicinal Chemistry · 29
Rituximab treatment of mild haemophilia A with inhibitors: a proposed treatment protocol
2006 · S. DUNKLEY, G. KERSHAW, et al. · Haemophilia · 28
Delivering safe and effective test-result communication, management and follow-up: a mixed-methods study protocol
2018 · Maria R Dahm, Andrew Georgiou, et al. · BMJ Open · 27
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Exome sequencing identification of a GJB1 missense mutation in a kindred with X-linked spinocerebellar ataxia (SCA-X1)
2013 · M. Caramins, J. G. Colebatch, et al. · Human Molecular Genetics · 25
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Management and clinical outcomes of transfusion‐dependent thalassaemia major in an Australian tertiary referral clinic
2008 · Giselle L Kidson‐Gerber, Sally Francis, et al. · The Medical Journal of Australia · 25
Molecular and cytogenetic studies of the Prader-Willi syndrome.
1991 · R J Trent, F Volpato, et al. · Journal of Medical Genetics · 25
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Dinucleotide repeat polymorphism of D15S10 in the Prader-Willi chromosome region (PWCR)
1991 · R. Lindeman, S. Kouts, et al. · Nucleic Acids Research · 23
Molecular characterisation of Vietnamese HPFH
1993 · Penelope I. Motum, Tracey J. Hamilton, et al. · Human Mutation · 22
Works count: 107
Citation count: 2,682
H-index: 23
I10-index: 49
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