Erna Lim - Concepedia

Author

Erna Lim

Sir Charles Gairdner Hospital

Also Known As

E. Justin Lim, E.J. Lim, Ee Mun Lim, Erna Lim

Publications

210

Citations

H-Index

Concepts

All Affiliations

Sir Charles Gairdner Hospital Leiden University Medical Center Harry Perkins Institute of Medical Research University of Reggio Calabria

About

Erna Lim is an author at Sir Charles Gairdner Hospital specializing in medicine, genetics, and inherited metabolic disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	104
2	Molecular Genetics	2	2	75
3	Pathology	2	2	75
4	Biology	1	1	42
5	Molecular Biology	1	1	33

Erna Lim

Publications

205

Citations

H-Index

Page 1

	Year	Citations
Thalassemia in Western Australia: 11 novel deletions characterized by Multiplex Ligation-dependent Probe Amplification Marion Phylipsen, John F. Prior, Erna Lim, Blood Cells Molecules and Diseases BiologyWestern AustraliaMedicineGeneticsHematology	2010	42
The Prevalence and Molecular Basis of Hemoglobinopathies in Cambodia Benedict P. Carnley, John F. Prior, Anne Gilbert, Hemoglobin	2006	36
Hemoglobin Titusville, a low oxygen affinity variant hemoglobin, in a family of Northern European background Hongyuan Luo, Ian Irving, John F. Prior, American Journal of Hematology	2004	35
Seven novel mutations in carbonic anhydrase II deficiency syndrome identified by SSCP and direct sequencing analysis Peiyi Hu, Erna Lim, Jessica Ciccolella, Human Mutation Molecular Diagnostic TechniquesMendelian DisorderGenetic DisorderGeneticsInherited Metabolic Disease	1997	33
Clinical and molecular heterogeneity in carbonic anhydrase II deficiency and prenatal diagnosis in an Italian family Pietro Strisciuglio, Peiyi Hu, Erna Lim, The Journal of Pediatrics Italian FamilyInherited Metabolic DiseasePediatricsPrenatal DiagnosisMedicine	1998	29
Two New α1-Globin Gene Point Mutations: Hb Nedlands (HBA1:c.86C>T) [α28(B9)Ala→Val] and Hb Queens Park (HBA1:c.98T>A) [α32(B13)Met→Lys] Marion Phylipsen, John F. Prior, Erna Lim, Hemoglobin	2010	17
A Moderately Severe α-Thalassemia Condition Resulting From a Combination of the α2 Polyadenylation Signal (AATA<i>AA</i>→AATA– –) Mutation and a 3.7 Kb α Gene Deletion in an Australian Family John F. Prior, Erna Lim, Neela Lingam, Hemoglobin	2007	13

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